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Informal Consultative Meeting on Antimicrobial Resistance Prevention and Control in Emergencies/Disasters, Manila, Philippines, 29-30 November 2011 : report

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Meeting Report Informal Consultative Meeting on Antimicrobial Resistance Prevention and Control in Emergencies/Disasters 29-30 November 2011 Manila, Philippines WORLD HEALTH ORGANIZATION REGIONAL OFFICE FOR THE WESTERN PACIFIC REPORT INFORMAL CONSULTATIVE MEETING ON ANTIMICROBIAL RESISTANCE PREVENTION AND CONTROL IN EMERGENCIES/DISASTERS Manila, Philippines 29–30 November 2011 WPR/2011/DHS/HSD-E English only Report Series No.: RS/2011/GE/78(PHL) REPORT INFORMAL CONSULTATIVE MEETING ON ANTIMICROBIAL RESISTANCE PREVENTION AND CONTROL IN EMERGENCIES/DISASTERS Convened by: WORLD HEALTH ORGANIZATION REGIONAL OFFICE FOR THE WESTERN PACIFIC Manila, Philippines 29–30 November 2011 Not for sale Printed and distributed by: World Health Organization Regional Office for the Western Pacific Manila, Philippines February 2012 NOTE The views expressed in this report are those of the participants in the Informal Consultative Meeting on Antimicrobial Resistance Prevention and Control in Emergencies/Disasters and do not necessarily reflect the policies of the Organization. This report has been prepared by the World Health Organization Regional Office for the Western Pacific for governments of Members States in the Region and for those who participated in the Informal Consultative Meeting on Antimicrobial Resistance Prevention and Control in Emergencies/Disasters, which was held in Manila, Philippines from 29 to 30 November 2011. CONTENTS Page 1. INTRODUCTION................................................................................................... 1 1.1 Objectives ................................................................................................................ 1 1.2 Opening Remarks .................................................................................................... 1 1.3 Participants .............................................................................................................. 1 1.4 Meeting Structure .................................................................................................... 2 2. PROCEEDINGS...................................................................................................... 2 2.1 WHO’s work in AMR prevention and control ........................................................ 2 2.2 AMR in emergencies ............................................................................................... 2 2.3 Experience from the field ........................................................................................ 2 2.4 Literature review on AMR prevention and control and emergencies ..................... 3 2.5 Urban Health Emergency Management .................................................................. 4 2.6 Managing medicines during emergencies: the role of WHO .................................. 4 2.7 Operational Framework for Health Cluster Response in the Western Pacific Region...................................................................................................................... 4 2.8 Group work.............................................................................................................. 5 3. CONCLUSIONS ..................................................................................................... 6 ANNEXES: ANNEX 1 - LIST OF PARTICIPANTS .........................................................................9 ANNEX 2 - WORKSHOP SCHEDULE.......................................................................13 ANNEX 3 - SUMMARY OF THE LITERATURE REVIEW .....................................15 ANNEX 4 - PRESENTATIONS...................................................................................33 ANNEX 5 - NOTES FROM GROUP WORK............................................................131 Key words: Antimicrobial Resistance (AMR) / Emergency / Disaster Management 1. INTRODUCTION An Informal Consultative Meeting on Antimicrobial Resistance Prevention and Control in Emergencies was held from 29 to 30 November 2011 in Manila, the Philippines, by the World Health Organization (WHO) Western Pacific Regional Office, in collaboration with the WHO Centre for Health Development in Kobe, Japan. Antimicrobial resistance (AMR) has become a serious problem for both developed and developing countries. On World Health Day 2011, WHO launched a worldwide campaign to fight AMR. Although prevention and control of outbreaks of infectious diseases in emergencies and disasters has received a lot of attention, emergency managers have not yet been engaged in national, regional and global efforts to address the issue of AMR in emergencies. As part of the preparation for the meeting, a literature review was conducted to document what is currently known about antimicrobial resistance and emergencies. 1.1 Objectives (1) To understand current knowledge of the prevalence and significance of AMR in emergency situations as presented in the findings of a literature review that was commissioned as part of the preparation for the meeting. (2) To identify the strengths, weaknesses and gaps of the current emergency preparedness response and recovery arrangements in relation to AMR prevention and control in emergency settings. 1.2 Opening remarks The participants were welcomed to the meeting by Dr Takeshi Kasai, Director of the Division of Health Security and Emergencies, WHO Regional Office for the Western Pacific. He explained that an informal consultation is a mechanism often used by WHO to gather the views and opinions of selected experts and practitioners, as part of a wider process of informing WHO decision-makers on how best to take an issue forward. Although AMR is not considered a high priority area in the management of most emergencies, it is an important public health issue that needs to be kept in mind by emergency managers. As such, this meeting was an opportunity for emergency managers and those working on AMR to explore new perspectives. Although the issue needs to be addressed through a long-term strategic approach, immediate action is also needed. As such, Dr Kasai requested participants to share their thoughts on what could be done in both the long and short term. 1.3 Participants Nine experts from three countries joined 13 WHO Regional Office staff from the Division of Health Security and Emergencies and the Division of Health Sector Development, the WHO Kobe Centre in Japan and the WHO Representative’s Office in the Philippines. Two facilitators were recruited to record and document the meeting. See Annex 1 for a list of participants. - 2 - 1.4 Meeting structure To provide background to the discussion, six presentations were made by WHO staff and experts on various aspects of the prevention and control of AMR, and of emergency management. The participants were divided into two groups and given a set of guidance questions to assist in developing their observations. Each day, the work of the groups was presented and discussed in plenary. On the second day, the goal of the plenary was to develop a consensus on AMR prevention and control in emergency settings. See Annex 2 for meeting schedule. 2. PROCEEDINGS The following presentations were given to provide context and background to the discussions. The full text of each presentation is included in Annex 4. 2.1 WHO’s work in AMR prevention and control Dr Madeleine de Rosas-Valera, Technical Officer, Patient Safety, Division of Health Sector Development, WHO Regional Office, presented an overview of WHO’s work in AMR prevention and control. As a follow-up to World Health Day 2011, WHO developed a six-point policy package to address the issue of AMR prevention and control at the global level. To support implementation of this policy in the Western Pacific Region, WHO undertook key informant interviews in 13 countries, which indentified seven priority areas for action. Implementation of the global policy in the Region is constrained by lack of laboratory capacity to confirm AMR and weak surveillance systems to detect it. However, some accomplishments have been made, including: development of a training package on the rational use of antimicrobials for ASEAN countries, conduct of national advocacy workshops on AMR, public advocacy on the rational use of antimicrobials and technical support for pilot implementation of a minimum training package. Future plans include finalization of an AMR Technical Strategic Framework, joint ventures to assist countries developing comprehensive multidisciplinary national plans to address AMR and resource mobilization to support implementation of the AMR Technical Strategic Framework. 2.2 AMR in emergencies Dr Bipin Verma, Special Adviser, Emergency and Humanitarian Action, Division of Health Security and Emergencies, WHO Regional Office, presented an analysis of pharmaceutical needs in emergencies. He showed how needs are based on both the morbidity profiles of different hazards, and the differing needs of the relief and recovery phases of emergency management. In respect to AMR issues, prescriber habits and the appropriateness and/or relevance of case management protocols are the main determinants of the rational use of antimicrobials in emergencies. AMR can also evolve due to efficacy issues, caused by problems in relation to the quantity, quality, storage, wastage and disposal of antimicrobials that are very common in emergency settings. 2.3 Experience from the field Mr Michael Chai, Southeast Asia Coordinator, Action on Antibiotic Resistance (ReAct), gave his views on the issue. He felt that although it is not true to say there is no evidence that AMR is a problem in emergencies, it is certainly true that there is a lack of relevant evidence. For - 3 - example, there are many reports in the literature of foreign victims of disasters developing resistant infections, but these infections are identified and treated in the victims’ home countries, followed by the affected country addressing the issue where the infection was acquired. Prevention and control of AMR is a problem with multiple factors, and to be successful, engagement is needed outside the clinical/ research laboratory fields. Official guidance on rational use on antimicrobials in emergencies may exist, but it is hard to enforce in the complex environment of an emergency, especially with multiple private sector and international actors. An opportunity to address the issue on a global scale could be taken by including AMR on the Rio +20 agenda. Professor Mei Che Pang, Head of the School of Nursing, Hong Kong Polytechnic University, presented the experience of Hong Kong (China). She said that lessons learnt from severe acute respiratory syndrome (SARS) have led to revised guidance on intensive care unit (ICU) facilities and the development of the three “Rs” approach – rationing, restriction and responsibility – to maximize the effectiveness of antimicrobial use. An evaluation of the effectiveness of their community health promotion programme on acute respiratory diseases showed that goal-oriented training for trainers and support for engagement of professional health networks are key to improving community health literacy. With support from the WHO Regional Office, the School of Nursing, Hong Kong Polytechnic University has developed a package to support the prevention and control of health care-associated infections in low-resource countries. The package, which consists of an assessment tool, a toolkit and a training programme, is currently being implemented in the Region. 2.4 Literature review on AMR prevention and control and emergencies Ms Yuki Maehira, Visiting Researcher, Department of Global Health, Medicine and Welfare, Nagasaki University Graduate School of Biomedical Sciences, was commissioned to prepare a literature review of AMR and emergencies. A full report of her findings is attached in Annex 3. The key findings of her review were as follows: (1) There is no internationally accepted guiding framework for AMR prevention and control in emergencies. (2) The priority given to life-saving interventions, and the medical cultural conflict between the curative care of individuals and a public health approach are major determinants of the use of antimicrobials in emergencies. (3) Public health and medical decision-making in emergencies is often based on available resources rather than best practice or public good. (4) Many existing AMR surveillance systems are owned by the private sector, creating issues of conflict of interest, transparency and accountability. (5) Emergency conditions create increased risk for AMR dissemination through treatment provider behaviours, population conditions and reduced capacity of health systems. (6) There is a fundamental lack of information on the prevalence of AMR by location and on the rational use of antimicrobials in emergencies (e.g. prescribing habits, complication rates and treatment failure rates). (7) Detecting and confirming AMR is a highly technical area, requiring extensive surveillance systems, sophisticated laboratories and collaborative partnerships. The issue - 4 - can only be addressed in emergencies through strategic investments in risk assessment, risk communication, advocacy, preparedness and confidence building. 2.5 Urban Health Emergency Management Dr Arturo Pesigan, WHO Kobe Centre, Urban Health Emergency Management, presented an overview of current thinking in the urban aspects of emergency management. Projections indicate that 70% of the global population will be urban by 2050, mostly in low- and middle- income nations. Asia’s urban population made up 32% of the world’s urban population in 1950, and this percentage is expected to increase to 55% by 2030. Given the specificity of the determinants of health status in urban populations, a 10-point checklist has been developed for local governments, covering areas such as organization and coordination of services, risk assessment, safety of infrastructure including health facilities and protection of ecosystems and natural buffers. In each of these 10 areas, specific AMR prevention and control issues could be addressed. The discussions after the presentation highlighted the need to consider context when planning AMR detection and control. Urban and rural areas have differences in pathogen profiles, disease transmission routes and rates, access to primary, secondary and tertiary care, as well as capacities for the detection, reporting and confirmation of resistance. All of these factors need to be taken into account when planning interventions to manage AMR in emergencies. 2.6 Managing medicines during emergencies: the role of WHO Dr Vanchinsuren Lkhagvadorj, Essential Medicines and Health Technologies, WHO Regional Office for the Western Pacific, presented an overview of international and WHO arrangements for managing medical supplies in emergencies and discussed some of the issues around management of drug supplies in emergencies. One of the problems faced by WHO and others is related to logistics and appropriateness – the need to get sufficient quantities of safe, effective and appropriate medicines to the affected population as soon as possible, which includes the effective management of donations. Since 1990, various international initiatives have been taken to address these issues, such as regional stockpiles, the development of specific kits, such as the Interagency Emergency Health Kit, guidelines on making drug donations in emergencies and guidelines on the safe disposal of medicines in emergencies. A discussion after the presentation highlighted the fact that AMR prevention and control is not explicitly addressed in any of the existing instruments. The emergency management community can contribute to global and national processes for the prevention and control of AMR by reviewing and updating current guidance, and developing additional guidance on AMR in emergency and post emergency settings. 2.7 Operational Framework for Health Cluster Response in the Western Pacific Region Dr Li Ailan, Emergency and Humanitarian Action, WHO Regional Office for the Western Pacific, presented an overview of current international coordination arrangements for emergency management. In 2005, the Humanitarian Reform Initiative was implemented as a response to lessons learnt in the Asian tsunami in 2004/2005. As part of the initiative, the Inter-Agency Standing Committee adopted the global cluster system in an attempt to improve coordination between international actors, and between the international community and host governments. WHO was appointed lead agency for the Health Cluster. In August 2011, the WHO Regional Office organized the First Regional Health Cluster Forum on Humanitarian Emergencies in Kobe, Japan. The aim of the forum was to develop a common operational framework for implementing the health cluster approach at country level in the Western Pacific Region. The - 5 - participants developed a governing framework known as “Three plus One”, which organizes health cluster emergency management functions into related areas of Information, Health Services and Resources, as well as Monitoring and Evaluation. As a universally recognized international mechanism for oversight of all international actions in preparing for, responding to and recovering from emergencies, the Health Cluster may have an important role in the prevention and control of AMR, by ensuring that health actions in specific emergencies do not contribute to the development of AMR, and also, under the Information function, by identifying AMR data or information that might contribute to health needs and risk assessments that inform provision of health services during emergencies. However current guidance will need reviewing and updating, and specific guidance on AMR detection and control in emergency and post emergency settings may be needed, particularly for health services at local level. 2.8 Group work The group work on day one focussed on developing problem-and-issue statements based on the knowledge and experience of the participants and on information provided in the presentations. Since the output of these discussions fed directly into the group work of day two, a discussion of day one group work is not included here, but a summary is provided in Annex 5. On day two, the participants worked in groups to develop their observations and findings on how AMR prevention and control in emergencies might be addressed. The conclusions of each group are summarized below. 2.8.1 Group One (1) Advocacy material is needed to convince policy-makers and decision-makers to make investments in AMR prevention and control in emergencies, and this material should be based on evidence. (2) Emergency managers need to be engaged in national AMR prevention and control measures. (3) International and national guidelines and protocols on drug donations and the safe disposal of donations need to be revised and enforced in support of AMR prevention and control. (4) AMR prevention and control issues need to be included in formal emergency management monitoring and evaluation processes at national and international levels. 2.8.2 Group Two (1) A mechanism, such as a task force, is needed at the country level to allow emergency managers and those working on AMR prevention and control to work together to identify and address country-specific needs in their own emergency settings. (2) A mechanism is needed to allow up-to-date information on AMR prevalence and distribution to be made available to emergency managers whenever needed, and to allow emergency managers to contribute information to support AMR prevention and control measures, e.g. by participating in the systematic reporting of unexplained treatment failures in emergency settings. - 6 - (3) To be useful to emergency managers, AMR data need to be disaggregated by location, easily accessed and regularly updated. (4) Information on AMR prevalence and distribution is needed to inform processes to develop, update and revise international guidance and national standard protocols for case management in emergencies, and this information needs to be regularly updated to ensure the appropriateness of first-line treatments is maintained, and to provide up-to-date guidance on appropriate second- and third-line treatments in the event of treatment failure. (5) National protocols for reporting failed treatment in emergency settings, and guidance on the implementation of those protocols at the local level, need to be developed. (6) Based on a review of treatment guidelines, managers of stockpiles and warehouses need to ensure second- and third-line treatment options are procured and maintained in stock. Controls need to be put in place on the release and accounting for second- and third- line treatments. Mechanisms are needed to ensure that managers with responsibilities in AMR prevention and control have access to regularly updated information on trends in the use of second- and third-line treatments in emergency and post emergency settings. 3. CONCLUSIONS In the closing session of the meeting, the participants reached a consensus on the following points: (1) Although AMR is not a high priority issue in the management of most emergencies, it is an important issue that emergency managers need to keep in mind. The most important elements of a strategic approach to AMR and emergencies are, first, to maintain the effectiveness and capacity of the routine AMR surveillance services, and second, to ensure that institutional mechanisms exist to facilitate the exchange of information between emergency managers and AMR surveillance systems. (2) This group would like to continue to be involved in the WHO planning process on the issue of AMR prevention and control in emergencies. (3) Suspecting, detecting and confirming the existence of AMR is a highly technical area, requiring extensive surveillance systems, sophisticated laboratories and collaborative partnerships. The issue can only be addressed in emergency settings through extensive investments in preparedness. (4) Emergency managers should be invited to join national planning processes for AMR prevention and control, and AMR experts need to participate in high-level public health planning for emergencies. (5) AMR prevention and control issues should be addressed in emergency management protocols, guidelines, training packages and toolkits, wherever appropriate. (6) Advocacy is needed to encourage national authorities to strengthen capacities for preventing, suspecting, detecting, reporting, confirming and controlling AMR in emergencies, but the messages need to be based on convincing evidence. The immediate priorities are as follows: - 7 - (a) form partnerships to continue to collect data and research evidence; (b) advocate and enhance national capacity for AMR prevention and control in emergencies, including rational use of medicines, information collection and risk assessments in emergencies, as appropriate; and (c) develop and use advocacy material to generate support for the national strategy. (7) As a concrete measure, the Department of Health Philippines committed to revising their national guidelines for case management in emergencies to ensure that AMR prevention and control issues are addressed. (8) A commitment was also given by the School of Nursing, Hong Kong Polytechnic University to review their educational and training materials to ensure that AMR prevention and control issues are properly reflected in the content. - 9 - ANNEX 1 LIST OF PARTICIPANTS, RESOURCE PERSONS, AND SECRETARIAT 1. TEMPORARY ADVISORS Dr Carmencita Banatin, Director III, Health Emergency Management Staff, Department of Health, San Lazaro Compound, Sta. Cruz Manila 1003 Philippines Telephone: (632) 651 7800 loc. 2200 Fax: (632) 740 5030 E-mail: carmencita.banatin@yahoo.com Dr Celia Carlos, Chairperson, Research Institute for Tropical Medicine, Department of Health Compound, FILINVEST Corporate City, Alabang, Muntinlupa City 1781 Philippines Telephone: (632) 809 9763 Fax: (632) 809 9763 E-mail: celia.carlos@yahoo.com Mr Michael Chai, Southeast Asia Coordinator, Action on Antibiotic Resistance(ReAct), 97 Jalan SS22A/1, Damansara Jaya, Petaling Jaya 47400 Malaysia Telephone: (601) 639 18787 E-mail: chai.mikael@gmail.com Dr Kenneth Hartigan-Go, Associate Professor, Center for Development Management Asian Institute of Management (AIM), Eugenio Lopez Foundation Building, 123 Paseo de Roxas, MCPO Box 2095, Makati City Philippines Fax: (632) 817 9240 E-mail: KHGo@AIM.EDU Ms Narumi Hori, Assistant Professor, St Luke's College of Nursing, 10-1 Akashi Chuo Tokyo 1040044 Japan Fax: (813) 5550 2255 E-mail: nhori@slcn.ac.jp Dr Hiroyuki Kunishima, Assistant Professor, Department of Regional Cooperation for Infectious Diseases, Tohoku University Graduate School Sendai 980-8574 Japan Telephone: (812) 2717 7373 Fax : (812) 2717 7390 E-mail: h2kuni@med.tohoku.ac.jp Dr Satoko Otsu, Director of Infectious Diseases, Department and Deputy Director of International Medical Relief Department, Japanese Red Cross Society Wakayama Medical Center, 4-20 Komatsubaradori Wakayama 640-8558 Japan Telephone: (817) 3422 4171 Fax: (817) 3426 1168 E-mail: so777manila@gmail.com - 10 - Annex 1 Ms Mei Che (Samantha) Pang, Professor, Head of School of Nursing Hong Kong Polytechnic University (HKPU), GH507 School of Nursing HKPU, Hung Hom, KLN, Hong Kong China Fax: (852) 2330 5140 E-mail: hsspang@inet.polyu.edu.hk Dr Satowa Suzuki, Principal Researcher, Bacterial Pathogenesis and Infection Control National Institute of Infectious Diseases (NIID), Toyama 1-23-1 Shinjuku-ku Tokyo 162-8640 Japan Fax: (814) 2561 0771 extension 3546 E-mail: suzukiss@nih.go.jp 2. RESOURCE PERSONS Ms Yuki Maehira, Visiting Researcher, Department of Global Health, Medicine and Welfare, Nagasaki University Graduate School of Biomedical Sciences, 43-2, Sugoudai, Himeji Hyogo 671-2243 Japan Telephone: (8190) 516 14385 Fax: (8179) 267 0397 E-mail: maehiray@snow.ocn.ne.jp Dr Rodger Doran, Adjunct Professor, Faculty of Public Health, Thammasat University, Rangsit Pathumthani, Thailand Telephone: (668) 7347 5621 E-mail: rodger5591@yahoo.com 3. SECRETARIAT Dr Madeleine de Rosas-Valera, (Responsible Officer) Technical Officer, Patient Safety, Health Services Development, WHO Western Pacific Regional Office, P.O. Box 2932, United Nations Avenue, 1000 Manila Philippines Telephone: (632) 528 9047 Fax: (632) 521 1036 E-mail : derosasvaleram@wpro.who.int Dr Momoe Takeuchi, Technical Officer, Quality and Health Systems Strengthening, Health Services Development, WHO Western Pacific Regional Office, P.O. Box 2932, United Nations Avenue 1000 Manila Philippines Telephone: (632) 528 9084 Fax: (632) 521 1036 E-mail : takeuchim@wpro.who.int - 11 - Annex 1 Dr Takeshi Kasai, Director, Health Security and Emergencies, WHO Western Pacific Regional Office, P.O. Box 2932, United Nations Avenue 1000 Manila Philippines Telephone: (632) 528 9730 Fax: (632) 521 1036 E-mail: kasait@wpro.who.int Dr Bipin Verma, Special Adviser to Emergency and Humanitarian Action WHO Western Pacific Regional Office, P.O. Box 2932 United Nations Avenue 1000 Manila Philippines Telephone: (632) 528 9810 Fax: (632) 521 1036 E-mail: vermab@wpro.who.int Dr Li Ailan, (Responsible Officer) Medical Officer (International Health Regulations), Health Security and Emergencies and Acting Team Leader, Emergency and Humanitarian Action, WHO Western Pacific Regional Office, P.O. Box 2932, United Nations Avenue 1000 Manila Philippines Telephone: (632) 528 9784 Fax: (632) 521 1036 E-mail: lia@wpro.who.int Dr Jeffrey Michael Partridge, Epidemiologist, Emerging Disease Surveillance and Response, WHO Western Pacific Regional Office, P.O. Box 2932 United Nations Avenue 1000 Manila Philippines Telephone: (632) 5289732 Fax: (632) 521 1036 E-mail: partridgej@wpro.who.int Dr Tamano Matsui, Medical Officer (Field Epidemiology Training Programme) Emerging Disease Surveillance and Response, WHO Western Pacific Regional Office, P.O. Box 2932, United Nations Avenue 1000 Manila Philippines Telephone: (632) 528 9828 Fax: (632) 521 1036 E-mail: matsuit@wpro.who.int Mr Thomas Cotter, Intern, Emergency and Humanitarian Action, WHO Western Pacific Regional Office, P.O. Box 2932, United Nations Avenue 1000 Manila Philippines Telephone: (632) 528 8001 local 89348 Fax: (632) 521 1036 E-mail: cottert@wpro.who.int Dr Gerardo Medina, Programme Officer, Emergency and Humanitarian Action WHO Office in the Philippines, National Tuberculosis Centre Building, Second Floor, Bldg. 9, Department of Health, San Lazaro Hospital Compound, Sta. Cruz, 1000 Manila Philippines Telephone: (632) 528 9765 Fax: (632) 731-3914 E-mail: medinag@wpro.who.int - 12 - Annex 1 Dr Arturo Pesigan, Team Leader, Urban Health Emergency Management, WHO Centre for Health Development, 1-5-1 Wakinohama, Kaigandori Chuo-ku, Kobe 651-0073 Japan Telephone: (817) 8230 3100 Fax: (817) 8230 3178 E-mail: pesigana@wkc.who.int - 13 - ANNEX 2 WORKSHOP SCHEDULE TIME ITEM Responsible DAY 1: Tuesday, 29 November 2011 08h00 – 08h30 Registration of participants Secretariat Opening 08h30 – 09h00 Welcome Remarks Introduction of the participants Objectives and expected outcomes of the meeting Organization and schedule of the meeting Group photo Dr Takeshi Kasai All participants WPRO HSD and EHA Rodger Doran Plenary 1: Background of the work 09h00 – 10h00 WHO's work on AMR Overview of health emergencies and disasters "Types of Disasters and Overall Response" Madeleine de Rosas-Valera Bipin Verma Plenary 2: AMR in Emergencies - Perspectives 10h00 – 12h00 Experience from the field Summary of the literature review Michael Chai Samantha Pang Yuki Maehira 12h00 – 13h30 Lunch Break 13h30 – 15h00 Working Group AMR and Emergency Response All participants Plenary 3: Discussion on the group work 15h00 – 16h00 Presentation of the group work Discussion Group Rapporteurs All participants 16h00 – Closing of Day 1 18h00 – 19h00 Welcome Drink (at Sky Lounge, Diamond Hotel) Annex 2 - 14 - TIME ITEM Responsible DAY 2: Wednesday, 30 November 2011 Plenary 4: Emergency tools and guidelines 09h00 – 10h30 Recap of Day 1 Urban Health Emergency Management Managing Medicines during Emergencies: the Role of WHO Operational Framework for Health Cluster Response in the Western Pacific Region Rodger Doran Arturo Pesigan Vanchinsuren Lkhagvadorj Ailan Li 10h30 – 12h00 Working Group AMR and Emergency Preparedness All participants 12h00 – 13h30 Lunch Break Plenary 5: Discussion on the group work 13h30 – 14h00 Presentation of the group work Discussion Group Rapporteurs All participants 14h00 – Closing Session 14h00 – 15h00 Conclusions and recommendations for the way forward 15h00 Closing of Day 2 - 15 - ANNEX 3 SUMMARY OF LITERATURE REVIEW Silent Menace: Emerging Antimicrobial Resistance behind Dedicated Life- saving Efforts Literature Review for Gap Analysis on Antimicrobial Resistance (AMR) Control in Emergencies/Post Disasters OCTOBER 2011 Yuki MAEHIRA As the work for Joint country-WHO collaborative programme for 2010-2011, funded by the Ministry of Health, Labour and Welfare, the Government of Japan - 16 - Annex 3 Table of Contents page List of key acronyms and abbreviations 17 1 Background for literature review 18 2 Methods of literature review and gap analysis 20 3 Summary of literature review; findings and critical lessons learned, issues to be addressed 23 4 Annex List of key references and useful websites 27 - 17 - Annex 3 List of key acronyms and abbreviations AM Antimicrobial (s) MDR-TB Multi-Drug resistant Tuberculosis AMR Antimicrobial Resistance MIC Minimum Inhibitory Concentration ARI Acute respiratory infection MRSA Methicillin-resistant Staphylococcus aureus ART Antiretroviral treatment/therapy MSF Medicins Sans Frontieres ATC Anatomical Therapeutic Classification NDM-1 New Delhi metallo β-lactamase-1 (blaNDM- 1) AUC Area Under the (blood concentration- time) Curve NGO/CSO Non-Governmental/Civil Society Organization BEmOC Basic Emergency Obstetric Care NMCH Neonatal, Maternal and Child Health CE-DAT Complex Emergency Database NTD Neglected Tropical Disease CMR Crude Mortality Rate PHC Primary Health Care CRED Centre for Research on the epidemiology of Disasters PK/PD Pharmacokinetics/Pharmacodynamics CSR/HSE Communicable Diseases Surveillance and Response / Health Security and Environment (Dept. of WHO) PMTCT Prevention of mother to child transmission DDD Defined Daily Dose PRSP Penicillin-resistant Streptococcus pneumoniae DOTS Direct Observed Treatment Short Course R&D Research and Development EDL/EML Essential Drug List/Essential Medicine List STI Sexually transmitted infection EDM/EHT Essential Drugs and Medicines/Essential Health Technology (Dept. of WHO) TDM Therapeutic Drug Monitoring ESBL Extended-spectrum β-lactamase producers UNICEF United Nations (International) Children’s (Emergency) Fund GEJE Great East Japan Earthquake UTI Urinary tract infection HAC Health Action in Crisis (Dept. of WHO) VRE Vancomycin-resistant Escherichia coli HIV/AIDS Human Immunodeficiency Virus /Acquired Immunodeficiency Syndrome VRSA/VISA Vancomycin-resistant/Vancomycin- intermediately resistant Staphylococcus aureus HR Human Resource U5MR Under-5 mortality rate IASC Inter-Agency Standing Committee XDR-TB Extensive Drug Resistant-Tuberculosis IMAI Integrated Management of Adolescent and Adult Illness WB The World Bank IMCI Integrated Management of Childhood Illness WHA World Health Assembly M&E Monitoring and Evaluation WHD World Health Day MDRP Multi-drug resistant Pseudomonas aeruginosa WHO World Health Organization WPRO WHO Office for the Western Pacific - 18 - Annex 3 1. Background for literature review In response to the emphasis of global commitment and public awareness largely promoted on occasion of World Health Day, 7 April 2011, the concerns for AMR prevalence and future impacts to emerge AMR has been raised particularly in cases to use them in both quantitatively and qualitatively different ways for varied characteristics of target population in emergency settings. After the Great East Japan (Tohoku) Earthquake (GEJE) occurred on 11 March 2011, Japan is now confronting difficult restoration, rehabilitation process tackling with multifold challenges due to the earthquake, tsunami and nuclear plant crisis1,2,3, and global concerns about health security in emergencies has been raised to alarming level. This is also because of increased frequency of prolonged complex emergencies associated with political crisis or conflicts worldwide such as the wave of democratization in several countries, which often associated with geophysical environmental changes and de-prioritization of health issues from nation’s development strategies to make it difficult to ensure various infectious diseases control. The GEJE was the particular case which has rarely occurred to result in large-scale evacuation or relocation due to physical loss of housing and radiation emergency. For this case, special attention shall be typically needed for variety of health risks associated with outbreaks probably caused in dense-shelters, polluted and insecure temporary conditions to live. In response to the recent emergency medical needs as such where more AM use would be presumed for both prevention and treatment, the immediate situation review and analysis on AMR in post disaster emergencies are strongly required. Conducting the review work is also supported by the below reasons and contexts which has made AMR control rather difficult in such particular circumstances;  Humanitarian act or emergency relief measures for medical service delivery shall cover larger population with diverse characteristics. Efficiency and effectiveness to provide services is paramount in order to maximize life-saving practices. And the service delivery to cover such hard-to-control populations are now achievable to significant extent by various actors including NGO/CSOs as its capacity has been much enhanced technically and financially. But it is not certain if all of them have received coherent messages to specifically control AMR during and post disasters in a concerted manner.  Majority of disaster victims is in need of pharmaceuticals and healthcare technologies to prevent and control various infections under insecure living environments to which those have to be adapted physically, psychologically with no choice in emergencies4. However the service delivery may be made through alternative or temporary channel to dispense resources without sufficient medical information or guidance. Many patient records may be lost. Under such circumstances, driving forces to enhance more AM use can be accumulated for prevention and treatment, while more probability of emergence or resurgence of ARM pathogens, which is rare, old or new, may be increased.  AM misuse includes the use of sub-standardized and sometime counterfeits or adulterates, intentionally or unconsciously. Prescribers’ empirical use may also be a causative for AMR, because it could often lead overuse for uncovered resistant strains of infection to fear treatment failure particularly in difficulties of timely lab-testing for precise diagnosis. Non-prescribed self-medication practices could also be widely prevailed under poorly- 1 J.P Avouac, Earthquake: The lesson of Tohoku-Oki, Nature, 15;475(7356):3oo-1(June 25 2011) 2 W.A.Bird, E. Grossman, Chemical aftermath: contamination and cleanup following the Tohoku earthquake and tsunami, Environ. Health Perspect., 119(7):A290-301(Jul. 2011) 3 D. Normile, Tohoku-Oki earthquake. Crippled reactors to get cooled and wrapped, Science, 20:332(6032):909 (May 2011) 4 A. J. Linscott, et al. Natural Disasters – a Microbe’s Paradise, Clinical Microbiology Newsletter, 29(8):57-62 (15 Apr. 2007). - 19 - Annex 3 regulated but extremely resource-limited, somewhat coercive health care circumstance. Those favorable conditions are to fuel the emergence of AMR and its transmission can often be associated in various service delivery processes in communities or alternative health care settings 5 particularly after disaster or emergency settings, where unique challenges required for infection prevention. Therefore, clinical practices with the use of pharmaceuticals should be rationalized and optimized in order not to go beyond the threshold of probability6,7 to emerge further AMR.  And it is rather difficult circumstances to do appropriate interventions particularly in developing countries where primary health development in populations has been blocked by unstable, fragile public health systems, even not affected by disasters.  AMR control in emergencies shall be emphasized also because it is rather unfeasible with no doubt to monitor and evaluate whole process to provide preventive measures or treatment throughout the population in a timely manner. Due to such nature of difficulty to conduct epidemiological, operational survey during emergency responses, the data and information cannot be effectively acquired thus assumed useful evidences are scarce.  Active surveillance are prioritized tasks for outbreak control of re-emergence and emergence of pathogens, but limited resources cannot be mobilized for both retrospective, prospective survey to assess AMR threats and investigate its cause-impact relationship.  Reiterated that AMR is common in areas with frequent natural disasters (on prevalence, or probability acquired), subject association has not yet been shown objectively, systematically for generalization on scientific basis.  There may be a possibility that well intentioned public health interventions and actions may in fact exacerbate the diseases burden or impede the diseases eradication8, whereas those are to aim at controlling post-disaster epidemics in the longer term.  According to the above overview, we predicted that there shall be critically substantial gap or pitfalls in research and evidence acquisition by studies conducted to assess the impacts of AMR in emergencies. This should be further strongly addressed in addition to the voices regularly raised for AM resource shortfalls in pharmaceutical R&D lists for future. It is also because the approaches and innovative disease control modeling with environmental (e.g. GIS), ecological health data can benefit to general AMR control and definitive infectious diseases eradication providing guiding framework with information for rather effective resource targeting to counter such emergence with prediction. WHO and relevant inter-agency working groups have had in-depth discussions and developed global strategies and guidelines for AM use and resistance since the 1990s’9, however relevant analytical reviews are mainly based on the resistance emerged through general practices in rather stable, healthcare facility-based detection. Such methodological gap in analysis cannot highlight potentially higher risk and larger vulnerability underestimated in specific post-disaster emergency perspectives, under a remarkably high pressure for urgently required medical assistance beyond to cover diverse needs for life-saving or incentive care. In order not to modest health gains for ones of the most vulnerable populations in such a post disaster environment as well as the general health development with limited pharmaceutical resources, it necessitates urgent review and analysis of potential gap for commitment or shortfalls of emphasis for the specific characteristics, modalities in AMR control in post disaster settings. The expected analytical review results would serve as the useful decision- criteria and rationale for conceptual integration of AMR control in emergency 5 E. Flanagan, T. Chopra, L. Mody, Infection prevention in alternative health care settings, Infect. Dis. Clin. North Am. 25(1):271-83 (2011). 6 M.A. Kohanski, M.A. DePristo, et al. Sublethal antibiotic treatment leads to multidrug resistance via Radical-Induced Mutagenesis, Molecular Cell, 37:311-320 (Feb-12, 2010). 7 M. Hegreness, N. shoresh, et al. Accelerated evolution of resistance in multidrug environments, Proc. Natl. Acad. Sci. USA, 105: 13977-13981 (2008). 8 Do post-disaster public health interventions impede malaria eradication? Editorial, Medical Hypotheses, 74:403-405 (2010). 9 Summary of discussion process to be referred to; WHO Global Strategy for Containment of Antimicrobial Resistance, Executive Summary (p1), Introduction(p12), WHO, Geneva (2001) - 20 - Annex 3 settings, particularly post disasters, into global action plan in health cluster approach10. And the points for intervention of post disaster AMR control should be coordinated strategically as an integral part of essential medical service package needed in the pillar of humanitarian act for emergency response11, by determining the commonality or differences in policies and strategies from general AMR guidelines which are already available. 2. Methods of literature review and gap analysis Comparative desk-top review was conducted during September-October 2011 based on available AM-related literatures, scientific papers, peer journals gray in addition to the guidelines, standards, fact sheets, commentaries and policy documents for coordination, regulation. However, the gray documents or interim, internal reports probably available at institutional level could not been covered in this review work. In addition to the collection of general AMR resources for situation review, web databases were explored by key word search addressing; (antibiotic or antimicrobial + resistance )+ (disaster or emergency or crisis or conflict) (Fig.2). The databases searched were: PubMed, Medline, and major titles including The Lancet, BMJ, JAMA, in order to find global health policy-level comments, suggestions to overview respective trends and analyses. In the review process, we shall be prudent to differentiate various AMR, i.e. antibiotics, antivirals, antiparasites for each different pharmaceutical, microbiological dynamics and’ characteristics, though many papers deal them regardless such differences without clear specifications. For further technical area-specific information and evidences to be aggregated, journal-targeted keyword search was also conducted onto: Disaster Management and Response, Disaster Research, The International Journal of Disaster Medicine, International Journal of Rescue and Disaster Medicine, Conflict and Health, in addition to; Antimicrobial agents and chemotherapy, International Journal of antimicrobial agents, Journal of antimicrobial chemotherapy, Open Antimicrobial Agents Journal, and the AMR-related publications available in hand. Additionally, selective term-specific literature search was conducted to supplement epidemiological, pharmaco-technical information as particularly needed, for instance regarding (laboratory or surveillance) and (PK/PD12 or prophylaxis), in combination with (antibiotic or antimicrobial + resistance) + (disaster or emergency), as probable insufficiency of those area- specific information by the above sequence for search. For gap analysis in  associated factors,  action for interventions,  expected outcomes Disaster Medicine + Emergency Response  /assistance General healthcare  status  resistance disaster factor, risk treatment  strategy/guideline emergency (crisis, conflict) intervention  Antimicrobial + Antibiotic Fig.2, Concept of keywords sequence for literature search 10Inter-Agency Standing Committee (IASC), Health Cluster Guide, A practical guide for country-level implementation of the Health Cluster, provisional version, WHO, Geneva (2009) 11 Eric K. Noji, ABC of conflict and disaster, Pubic health in the aftermath of disasters, BMJ, 330,11June 2005. 12 PK/PD control: pharmacokinetics/pharmacodynamics theory-based antimicrobial dosage control - 21 - Annex 3 After discussions to streamline the process of literature review and analysis, specifically ‘natural, geophysical, hydro-meteorological disasters’ are set as the primary events to lead emergencies in which situational factors like collapse, or weaken governance and leadership may be considered as an important component of health systems strengthening13. The biological disaster itself was not regarded as the primary cause of disaster, but recognized the core process to promote AMR. Moreover, the political humanitarian emergencies in conflicts or warfare were not taken into consideration as primarily essential, core events as direct causes to assess ‘AMR in emergency’. However, we shall keep it in our minds that the disasters and complex emergencies often being associated and interlinked with each other in various dimensions, synergistically, as part of the continuity especially in both cases pre- and post disasters14. Explicitly, there may be some commonalities among the inter-linked risk factors for planning of interventions as seen in the studies on outbreak control during the conflicts particularly in developing countries15. And there are some important observations that reports the lower impact by natural disaster as direct factor for diseases outbreak, but rather higher implication with post-disaster complex emergencies to increase morbidity and mortality rates as seen in the outside-camp populations16, or primarily associated with the characteristics of the displaced populations within the local disease ecology,17,18 whereas each of response phase of ‘post-disaster’ and ‘acute emergency’ cannot be differentiate easily. Respective definitions for ‘disaster’ in general, ‘natural disaster’, ‘complex emergencies’ and ‘epidemics’ are provided with practical data including the median duration19, while the other studies pointed out its complication and difficulty to give clear classification, taxonomy or terminologies for operational comparison20,21. Basic series of term & definitions are available in the Glossary of Humanitarian Terms22. ----- The AMR are a synergic consequence caused in complex in between above disasters and emergencies. Following natural disasters or being de-prioritized from the public interventions in complex emergencies, massive influx of medicines and drugs, including non-qualified, may facilitate the development of resistance. The preliminary criteria and key areas for reference collection were;  Major disease-based, causal agent-specific research papers to overview and identify of commonality in microbiological characteristics and transmission modalities with those potentially associated in emergency settings.  Characteristics of emergency-specific communicable diseases control  Resources describing from viewpoints of humanitarian action, emergency relief and aid coordination to identify AMR-related points of discussion, intervention or strategies for containment  Resources to compare AMR control interventions in developing and developed countries. Annex 3 13 Everybody’s Business, Strengthening Health Systems to Improve Health Outcomes, WHO framework for action, WHO, Geneva (2007) (available at: http://www.who.int/healthsystems/strategy/everybodys_business.pdf/ ) 14 W. V. Damme, et al., Primary health care vs. emergency medical assistance: a conceptual framework, Health policy and Planning, 17(1):49-60 (2002). 15 M. Gayer, et.al. Conflict and Emerging Infectious Diseases, Emerging Infectious Diseases, 13 (11):1625-1631(November 2007). 16 P. Salama, et al., Lessons learned from complex emergencies over past decade, The Lancet, 354: 1801-1813, 13-Nov. (2004). 17 J.T. Watson, et al. Epidemics after Natural Disasters, Emerging Infectious Diseases, 13(1):1-5 18 N. Floret, J.F. Viek et al. Negligible risk for epidemics after geophysical disasters, Emerging. Infectious. Diseases., 12:534- 8(2006). 19 P. Spiegel, et.al. Occurrence and overlap of natural disasters, complex emergencies and epidemics during the past decade (1995-2004), Conflict and Health, 1:2 (2007). 20 CE-DAT, A Database on the Human Impact of Complex Emergencies (available at http://www.cred) 21 R. Below, et al. Disaster Category Classification and peril Terminology for Operational Purposes, Common accord Centre for Research on the Epidemiology of Disasters (CRED) and Munich Reinsurance Company (Munich RE), Working Paper, October 2009. 22 ReliefWeb Project, Glossary of Humanitarian Terms, Draft Version (August 2008) ( http://www.who.int/hac/about/reliefweb- aug2008.pdf) - 22 - Annex 3  Resources by which we can revisit to the factors to promote AMR and relevant outcomes for patients including socio-economic, health impact  Resources to compare health care service delivery settings between general infectious control practices and emergency medical assistance for infectious diseases control.  Resources to provide indicators and characteristics for vulnerability in lab diagnostic, testing capacity in emergencies  Pharmaceutical policies and systems particularly affected in emergencies including the challenges in procurement, stockpiling strategies  Impacts of prophylaxis, vaccination and longer-term AM treatment package (e.g. 6-month treatment package for TB-DOTS) applied to the specific infectious diseases control modality in emergency in comparison with general public health development approaches.  Disaster-type specific outbreak control and treatment modalities to use AMs. For baseline information review, the lists of core reference items were given by WPRO at web-based folder which shares the lists of;  WHO policy papers, guidelines, presentations related to AMR (including the items originated from CSR/HSE, EDM/EHT, HAC)  Diseases-, causal agent-specific survey reports, case studies, situation analysis  2011 World Health Day promotional package composed of the factsheets, policy frameworks, presentations List of useful, key reference items and web links are in the Annex. Predicting the difficulty to extrapolate evidences or findings from one case to another in different emergency settings and response phases, useful data of literature review information was aggregated onto the database matrix to identify pitfalls, gaps between the readily-adapted interventions in conventional AMR control settings. As indicated below, disease- or causal agent-specific information were tabulated on the spreadsheets over time-action series from pre-incident to post-disaster, follow-up stage which may be rephrased as the restoration, reconstruction phase. As well, target population-based points of intervention were searched. The database matrix was created by data-mining with currently available information based on this literature review and situation analysis, in order to compare probable commonality, gaps in identification of purposes or target populations, barriers to interrupt a seamless modality shift of health service delivery. The database matrix sample mentioned in the above section is shown in the Annex. This analytical approaches were taken in reference to the strategic forms of intervention plan described in the below 2 core reference items;  The Race against Drug Resistance (2010)23 ; in a form of the area-specific, politically committed intervention plan.  WHO Global Strategy for Containment of Antimicrobial Resistance (2001)24; in a form of target population-based plan In the meantime, humanitarian action principles for medical response usually employ progressive action frameworks to address the needs to shift respective roles from independently working, tentative ones to locally acceptable, sustainable ones. Modality shift from emergency response to primary health systems development may be implied. Then additionally, we shall examine the gap and possible integration of the concepts of AMR in emergencies into;  Health Cluster Guide (2009), A practical guide for country-level implementation of the Health Cluster, by which humanitarian operational guidelines are being coordinated in a Annex 3 comprehensive cluster approach identifying respective institutional roles of work and 23 R. Nugent, et al.,The Race Against Drug Resistance, A Report of the Center for Global Development’s Drug Resistance Working Group (2010) (available at: http://www.cgdev.org/files/1424207_file_CGD_DRWG_FINAL.pdf/ ) 24 WHO Global Strategy for Containment of Antimicrobial Resistance, WHO CDS/CSR/DRS (2001) - 23 - Annex 4 functionality-explored plan of intervention for output generation over the progressive work phases. Since the concept of AMR control has not well linked with humanitarian priorities in projects so far, it strongly necessitate to rephrase the issues boldly to address its critical impacts on AMR emergence and transmission rates for pragmatic global commitment, in conjunction with the voices for conventional AMR control needs. Ti m e c ou rs e – ar ea  of  w or k (la bo ra to ry  ca pa cit y, s ur ve ill an ce , ph ar m ac eu tic al  res ou rc e a cc es sib ili ty , et c. ) Disease‐, causal agent‐, type of natural disaster‐specific information (ARI, diarrhea, TB, Malaria, HIV/AIDS, STI/UTI, Meningitis, surgical infection, floods, radiation, etc.) Ro le  of  ac to rs  ‐t ar ge t po pu la tio ns  for  int er ve nt io n (p Currently available research evidences (mostly based on general AMR or infectious disease control settings 3. Summary of literature review; findings and critical lessons learned, issues to be addressed In summary, there is very limited number of papers to describe the specific modalities or characteristics of AMR control in post disaster settings, and even found, almost all of them only refer it as one point for consideration in the whole procedure to implement communicable disease outbreak control. So, in supporting our prediction as mentioned in the background for this literature review, we can reiterate or rephrase the points reconfirmed as below;  Most of currently available references on disaster- or emergency medical response related are only to provide list of major infectious diseases which shall be tackled with special emphasis due to its high morbidity and mortality observed in many cases of emergencies (though not specified as ‘directly’ related to the disasters). The diseases targeted usually in emergency medical responses are diarrheal diseases, acute respiratory infections caused by a variety of pathogens 25 . Vector/reservoir control and causal pathogens are listed particularly as the points for intervention after geographical disasters, sometime along with possible impacts by each seasonal climate changes in Annex 3 25 B.L.Ligon, Infectious Diseases That Pose Specific Challenges after Natural Disasters: A review, Seminars in Pediatric Infectious Diseases, 17:36-45 (2006). la nn er , ph ar m ac eu tic al  ind us tr ie s, a ca de m ic s oc ie tie s, p at ie nt s,  pre sc rib er s, e tc .) available available available available available available available not found not found not found not found not found not found ) Id en tif ic at io n o f po te nt ia l ga p a nd  int er ve nt io n p oi nt s Area‐focus gap? Resource delivery  environment OK? Only focus on elderly? HR can be secured? Just institutional  case studies? Adherence ensured in emergency settings? Fig.3 Concept of gap analysis in comparison with generic AMR control by data-mining of available literature review information - 24 - Annex 4 general 26 . Some also addressed the resurgence or emergence of rare, old pathogens including haemorrhagic agents,16,27 however, the trauma case management is not referred within the infectious diseases control in post-disaster emergencies, while tetanus is addressed in some literatures. (though its treatment is not by AM but with immune globulin28)  However, few literatures have been found which document the characteristics of particular AMR pathogens, its proportions in specific human populations in emergencies.29,30,31,32 Most of those identified as the review of emergency response, it only pointed the awareness needed for future AMR emergence due to AM misuse (but not much mentioned to its quantitative, qualitative indicators or aspects to cause AMR). AMR prevalence reviews are substantial, primary data needed for optimal measures to predict the AMR trend in affected population for treatment as mentioned e.g. in Rwandan refugee camps (S. dysenteriae type-1 isolation: 3/7 were resistant to nalidixic acid)33 or TB resistance in refugee and non-refugee populations in northeast Kenya (18% vs 5% resistance in refugee and non-refugee populations)34 or Somalia (14.5% defaulted treatment)35.  Clinical, biological research papers related to AMR are mostly the case report of susceptibility/insusceptibility assessment or highlights of epidemiological event of newly emerged or reemerged old strains and clinical features for treatment on the health facility basis. And there is a fundamental gap for acquisition of research and scientific evidences, operational assessments in developing countries36.  Outstanding research interests have been evolved for comparative assessments with community-acquired and migrated population-base settings from public health development perspectives, recently. Expanded research concept of ‘healthcare associated’ AMR has also been developed for comparative assessment between the AMR strains in health facilities and those identified as ‘community-acquired’.37 And relevant study results indicated the needs to have further comprehensive views to perform medical practices in and outside health facilities for infection control.  There are no specific interventions for AMR control in emergencies suggested concretely in the form of guidelines or action plan. Just as the same level to address within the scope of general infectious diseases case management including alternative AM use for unsusceptible cases, such as the recommendation only to prescribe minimum use of ‘antibiotics’ by which the individuals can be completely treated within the duration the disaster medical service team could support on site.38 This probably means that emergency health care intervention measures for AMR control can only focus as part of the case management to treat infections effectively at each clinical site and it may only rely on individual prescribers’ empirical capacities and technical skills, like an unwritten Annex 3 26 B. Widner, et al. (ed.) Environmental health in emergencies and disasters: a practical guide, WHO (2002). 27 M.A. Connolly, et al., Communicable diseases in complex emergencies: impact and challenges, The Lancet, 364:1974- 1983(2004). 28 S.C. Waring, et al. The Threat of Communicable Diseases Following Natural Disasters: A Public Health Response, Disaster Management & Response, 41-47 (April-June 2005). 29 I. Uçkay, et al. Multi-resistant infections in repatriated patients after natural disasters: lessons learned from the 2004 tsunami for hospital infection control, J. Hospital Infection, 68:1-8 (2008) 30 K. Ebisawa, N. Yamada, et al. Combined legionella and Escherichia coli lung infection after a tsunami disaster, Intern. Med., 50(19):2233-6 (2011). 31 I.N. Miskin, et al. Antimicrobial Therapy for Wound Infections after Catastrophic Earthquake, NEJM, 363:2571-73 (Dec. 23 2010). 32 Xu J., Liu ZG., et al. Analysis of Pulmonary Infection of Hospitalized Patients Injured in the Wenchuan Earthquake in China, Life Science Journal, 7(2)):28-34 (2010). 33 C. Paquet, et al. An outbreak of Shigella dysenteriae type 1 in a refugee camp in Rwanda, Sante, 5:181-184 (1995) (in French) 34 W.A. Githui, et al. Surveillance of drug-resistant tuberculosis and molecular evaluation of transmission of resistant strains in refugee and non-refugee populations in North-Eastern Kenya, Int. J. Tuberculosis and Lung Diseases, 4:947-55(2000). 35 W.O. Agutu, Short-course tuberculosis chemotherapy in rural Somalia, East Afr. Med. J, 74: 348-52(1997) 36 P. Shears, Poverty and infection in the developing world: healthcare-related infections and infection control in the tropics, J. Hosp. Infect., 67(3): 217-224 (Nov. 2007). 37 T.S. Naimi, et al. Comparison of Community and Health care-Associated Methicillin-Resistant Staphylococcus aureus infection, JAMA, 290 (22):2976-2984 (Dec. 2003). 38 Activity Manual for Japan Medical Team for Disaster Relief, p55 (revised 2010, in Japanese only) - 25 - Annex 4 role as impossible to standardize all AM care services. TB or malaria case management is referred in each particular treatment guidelines in general.  The uses of other AMs are only referred in the particular-diseases control guidelines such as the Integrated Management of Childhood Illness (IMCI) 39 , 40 or the Integrated Management of Adolescent and Adult illness (IMAI) to treat specific, immunocompromised patients like HIV/AIDS infection.  Reference of anti-parasites (other than Malaria) has only been identified on each prevalence, epidemiological data related to migration in post-disaster emergencies; e.g. trypanosomiasis41, leishmaniasis,42,43 but no concrete association with AMR is indicated.  Therefore, eventually it revealed difficult to find either uniqueness or commonalities for AMR control in emergencies, in comparison with general AMR control policies, intervention frameworks, capacity development strategies for both patients and prescribers. Regarding more area-specific issues for AMR control in emergencies, the below points are considerable as important issues;  While attention paid to the fatal ravage of childhood dysentery, pneumonia or malaria due to infection of resistant strains, yet insufficient emphasis on Newborn-Maternal-Child Health (NMCH) perspectives to use AMs in post-disaster emergencies. There is lack of scientific evidences to quantify and alert AMR impacts as well on NMCH aspects in emergencies.  NMCH issues of AMR are mostly referred as vulnerability in primary health care settings, e.g. diarrhea, ARIs and pneumonia, ear infections, or malaria (fever) in link with nutritional management and parasites in the treatment guides or system in IMCI which has been actively used as key NMCH treatment strategies in developing countries 44 , 45 . Specific guidance on pediatric HIV care and treatment refers to the choice, duration of AM (antibiotics) use but not enough like ART resistance control, the cases of TB or HBV co- infection. The particular issues of IMCI are providing concrete guidance for AMR control. But AMR issues in emergencies are not particularly mentioned as well in IMAI.  AM use is critical to prevent infection during delivery and newborn care as part of basic emergency obstetric care (BEmOC), consistently in any health care settings. This remark could be extended to the Prevention of Mother to Child Transmission (PMTCT) procedures for control of vertical HIV transmission, and this shall be stressed as longer prophylaxis with single AM dose 46 , without jeopardizing the effort to maximize the treatment for elimination of pediatric HIV, as well as sustainable ART coverage for those living with HIV/AIDS based on the revised WHO guidelines, even under emergency settings.  WHO guidelines to control MDR/XDR-TB, Malaria and HIV/AIDS certainly address its particular needs of AMR resistance control implying the poor health system function Annex 3 particularly in developing countries where the vast majority of patients are tackling to 39 Manual on Paediatric HIV care and Treatment for District Hospitals, IMCI, WHO (2011). (IMCI documents available at http://www.who.int/child_adolescent_health/documents/imci/en/index.html# ) 40 WHO Recommendations on the management of diarrhoea and pneumonia in HIV-infected infants and children, IMCI, WHO (2010) 41 L.B. Ford, Civil conflict and sleeping sickness in Africa in general and Uganda in particular, Conflict and Health, 1:6, doc:10.1186/1752-1505-1-6 (2007) 42 M. Rowland, A. Munir, et al. An outbreak of cutaneous leishmaniasis in an Afghan refugee settlement in north-west Pakistan, Trans. Royal. Soc. Trop. Med. Hyg., 93:133-36(1999) 43 M.V.L. Marlet, D.K. Sang, et al. Emergence or re-emergence of visceral leishmaniasis in areas of Somalia, north eastern Kenya, and south eastern Ethiopia in 2000-01, Trans. Royal Soc. Trop. Med. Hyg., 97:515-518 (2003). 44 Handbook: IMCI Integrated Management of Childhood Illness Handbook, WHO, UNICEF (2005) 45 Technical Update of the Guideline on the Integrated Management of Childhood Illness (IMCI), WHO(2005) 46 New recommendation in 2009 WHO PMTCT guideline; To start AZT prophylaxis at the beginning of 2nd trimester (14 - 16 wks gestation) or as soon after as possible, and then continue with SD NVP and a "tail" of 7 days of AZT/3TC at labour and delivery. And for breastfeeding, to provide up to 12 months of daily infant Nevirapine to the baby, or until the end of breastfeeding if earlier, while alternative recommendations can be considered by countries, and the guideline committee. - 26 - Annex 4 survive under persistently limited resource availability. However, there is no clear linkage of strategic interventions with the post disaster settings and AMR control.  TB-DOTS strategies have been widely implemented in countries, and it is essential to sustain the outreach systems in healthy community with effective human-to-human inter- linkage for treatment observation (rephrased as prescriber-patient linkage). But such valued mechanism in communities would easily be collapsed in emergencies. Treatment adherence and compliance to the role in DOTS mechanism shall be maintained by the substituted health workers, probably under the pressure of limited pharmaceutical resources and its logistics. Treatment adherence issues are certainly critical for all of the immuno-compromised patients including HIV/AIDS. Messaging strategies for preventive measures including Malaria infection control would also be failed in shelters or insecure living conditions in emergencies.  Vulnerability for AMR (for both emergence and transmission), the immuno-compromised patients are repeatedly addressed for special AM use and strategies. Underlying diseases- specific case reports are many, but the population-based impact on AMR has not been assessed, which could be attributed by the high percentage of patients under treatment of HIV/AIDS, TB or chronic illness including diabetes, hypertension or malnutrition, etc. (Moreover, such vulnerable population-specific assessment in emergency settings has not been found yet even as the general public health impacts to attribute to the morbidity or mortality in general populations) Thus there are yet some room to promote awareness either for major infectious diseases control in consideration of AMR and that in emergency settings.  Differentiating the group living settings (i.e. in camp versus non-camp, surrounding communities, etc)16,47, emergency medical response framework of intervention addressed the outreach strategies, importance of risk communication and networking to maximize access to ‘available’ health services and best possible number of patients’ survival as a humanitarian priority.  Situation review on diagnostic technologies in emergencies has not been identified by which pragmatic approaches or simplified measures could be suggested preferably at the point-of-dispensary. Various rapid testing kits are available, but not many studies have been done to assess its efficacy for diagnosis, or other operational aspects including costing for the use in emergencies.  Syndromic(event-based) and routine (indicator-based) surveillance of infectious diseases and its reporting-networking systems have been examined to ensure its function and identify the pitfalls, on occasion of specific environments like mass gathering such as the world football games48 or political gatherings, but there are not clear objectives to detect epidemiological AMR information. There may be a potential to identify some commonality for AMR control in emergencies between the ‘mass gathering medicine’ 49 as large impact made by mass population movement. The time-lag distribution for disease- specific strategies has been addressed to improve the surveillance and reporting systems50.  There is a lack of the contextual analysis with comprehensive evidence acquisition for emergence of AMR linking the horizontal data. For example, identification of XDR-TB strongly addressed the threats to deliberately be used, for which active surveillance and medical R&D shall be encouraged involving many political arguments particularly led by developed countries’ security concerns. Now, global AMR threat awareness on other Annex 3 potential biological agents such as ‘NDM-1 superbug51,52 has just been elevated but yet 47 P. B. Spiegel, et al. Health-care needs of people affected by conflict: future trends and changing frameworks, The Lancet, 375(9711:341-345 (23-29 Jan. 2010). 48 C.J. Williams, et al. FIFA World Cup 2006 in Germany: enhanced surveillance improved timeliness detection, Epidemiol. Infect. 137(4):597-605 (Apr. 2009). Various sources in Eurosurveillance available at 49 P. Arbon, et al. Mass gathering medicine: a predictive model for patient presentation and transport rates, Prehosp. Diseaster Med. 16(3):150-158 (Jul.-Sep. 2001). 50 Y. Hyo-Soon, et al. Timeliness of national notifiable disease surveillance system in Korea; a cross-sectional study, BMC Public Health, 2:93-101 (2009). doi:10.1186/1471-2458-9-93 51 Y. Guo, A structural view of the antibiotic degradation enzyme NDM-1 from superbug, Protein & Cell, 2(5):384-94. doi: - 27 - Annex 4 preoccupied with evidence-scarce invalid accusation against AM misuse which is thought to be originated from so-called ‘less-prudent’ countries. It may be true that AM misuse in countries can bring the threats into other countries irrespective to the man-made borders where various factors of responsibilities should be shared not criticizing AMR-favorable environments in developing countries. The factors such as international travel history53 or patient repatriation30, 54 should be considered for AMR control in relation to recent globalization including the emergency settings. And this mass population movement issues are to be referred to the first responders, aid workers or medical response teams particularly in emergencies post large-scale disasters.  The 1st line regimens (or 2nd line if 1st line is not applicable) are recommended in many guidelines of infectious diseases control, but it is presumed that the most of affordable conventional list of AMs as categorized for the 1st options may have already conquered by at least one resistant strain for susceptibility or not available in emergency medicine lists. There are no concrete availability-priority mapping efforts to update AM use in line with the essential drug list or emergency medicinal guidelines. Though there may be a room to retrieve further case studies on disease-specific analytical basis, this analytical review on literatures and references highlights the lack or shortfall in AMR information in post-disaster emergencies and implies critical bottlenecks or barriers to coordinate comprehensive medical strategies for intervention to interpret AMR issues in conventional healthcare settings into that in emergencies. This is probably because of the challenges to understand contextual factors for cause and impact assessment in time-series manner to link with the situation of AM use and the AMR emergence in geographically different environments. There may be some counterproductive policies in emergency health care framework and those should be clearly remarked to pursue comprehensive AMR control. And related challenges and complex in intervention coordination shall be recognized for proper attention in order not to lose the greatly valued pharmaceutical resources and waste our tremendous efforts for treatment and public health gain to safe and prolong lives with huge investments. 4. Annex List of key references and useful web links Key references Policies, commentaries for strategies A Safer Future, Global Public Health Security in the 21st Century, The World Health Report 2007, p22-23, World Health Organization(2007). Alanis AJ., Resistance to Antibiotics: Are We in the post-Antibiotic Era? Archives of Med. Res., 36:697-705 (2005). Checchi F., et al. Humanitarian Practice Network (HPN), Public Health in crisis-affected populations, A practical guide for decision-makers, No. 61 (Dec 2007). Connolly MA., Heymann DL., Deadly comrades: war and infectious diseases, The Lancet, supplement 360:s23-24 (2002). Connolly MA., et al. Communicable diseases in complex emergencies: impact and challenges, The Lancet, 364: 1974-1983 (27 Nov. 2004) Annex 3 10.1007/s13238-011-1055-9(2011 May) 52R.K. Srivastava, Superbug –the so called NDM-1,Indian J. Med. Res.,133(5):458-60 (May 2011) 53 A. Wilder-Smith, Meningococcal disease: risk for international travelers and vaccine strategies, Travel Med. Infect. Dis. 6(4):182- 186 (Jul.2008). J.N. Zuckerman, 2010 FIFA world cup South Africa: travel health issues and new options for protection against meningococcal disease, Travel Med. Infect. Dis. 8(2):68-73 (Mar. 2010). 54 B.A Rogers, et al. Country-to-Country Transfer of Patients and the Risk of Multi-Resistant Bacterial Infection, CID, 53: 49-56 (1 July 2011). - 28 - Annex 4 Floret N., et al. Negligible Risk for Epidemics after Geophysical Disasters, Emerging Infectious Diseases, 12(4):543-548 (4 Apr. 2010). Gayer M., et al. Conflict and Emerging Infectious Diseases, Emerging Infectious Diseases, 13(11):1625-1631 (Nov. 2007). Heymann DL., Resistance to Anti-Infective Drugs and the Threat to Public Health, Cell 124, Feb.24(2006). Ligon BL., Infectious Diseases that Pose Specific Challenges After Natural Disasters: A Review, Seminars in Pediatric Infectious Diseases, doi: 10.1053/j.spid.2006.01.002 (2006). Linscott AJ., et al. Natural Disasters- A Microbe’s Paradise, Clinical Microbiology Newsletter, 29(8):57-62 (15 Apr. 2007). Noji EK., ABC of conflict and disaster, Public health in the aftermath of disasters, BMJ, 330:1379-1381 (11 June 2005). Salama P., et al. Lessons learned from complex emergencies over past decade, The Lancet, 364: 1801-1813 (13 Nov. 2004). Schwartz B., et al. Preventing the Emergence of Antimicrobial Resistance, JAMA, 278(11):944-945 (1997). Sondorp E., et al. Editorial: Beyond emergency care: challenges to health planning in complex emergencies, Tropical Med. Intern. Health, 6(12):965-970(Dec. 2001) Spiegel PB., et al. Occurrence and overlap of natural disasters, complex emergencies and epidemics during the past decade (1995-2004), Conflict and Health, 1:2, doi: 10.1186/1752- 1505-1-2 (2007). Spiegel PB., et al. Health-care needs of people affected by conflict: future trends and changing frameworks, The Lancet, 375(9711:341-345 (23-29 Jan. 2010). Waring SC., et al. The Threat of Communicable Diseases Following Natural Disasters: A Public Health Response, Disaster Management & Response, 41-47 (April-June 2005). Watson JT., et al. Epidemics after Natural Disasters, Emerging Infectious Diseases, 13(1): 1-5 (January 2007). Wise R., Antimicrobial resistance: priorities for action, J. Antimicrobial Chemotherapy, 49:585-586 (2002). Area-specific policies and situation reviews An evaluation of Drug Resistant TB Treatment Scale-up, Medicins Sans Frontiers, Partners in Health, Treatment Action Group (July 2011). Population monitoring in radiation emergencies: a guide for state and local public health planners, CDC (Aug. 2007). Review of HIV Drug Resistance Assessment and Prevention Activities in Approved Round 7-9 Grants, World Health Organization, The Global Fund (March 2010) Ahern M., et al. Global Health Impacts of Floods: Epidemiologic Evidence, Epidemiologic Reviews, 27:36-46 (2005). Bellos A., et al. The burde of acute respiratory infections in crisis-affected populations; a systematic review, Conflict and Health, 4:3-14 (2010). Bremer R., Policy Development in Disaster Preparedness and Management: Lessons Learned from the January 2001 Earthquake in Gujarat, India, Prehospital and Disaster Medicine,18(4):370-382 (Oct-Dec. 2003) Cinti S., Pandemic Influenza: Are We Ready?, Disaster Management & Response, 61-67 (July- Sep. 2005). De Luca A., et al. Resistance considerations in sequencing of antiretroviral therapy in low- middle income countries with currently available options, Current Opinion in HIV and AIDS, 5:27-37 (2010). Ford LB., Civil conflict and sleeping sickness in Africa in general and Uganda in particular, Conflict and Health, 1-6 (2007). Doi:10.1186/1752-1505-1-6. Annex 3 - 29 - Annex 4 Hick JL., et al. Health Care System Planning for and Response to a Nuclear Detonation, American Medical Association, Disaster Medicine and Public Health Preparedness, s73-88 (2011). Khaw A., et al. HIV prevention and control in emergency affected populations, Disasters, 24:181-197 (2000). Ku J., et al. Analysis of Pulmonary Infection of Hospitalized Patients Injured in the Wenchuan Earthquake in China, Life Science Journal, 7(2):28-34 (2010) Miskin IN., et al. Antimicrobial Therapy for Wound Infections after Catastrophic Earthquakes, Correspondence, NEJM, 363(26):2571-2573 (23 Dec. 2010). Monzote L., Current Treatment of Leishmaniasis: A Review, Te Open Antimicrobial Agents J., 1:9-10(2009). Perlman SE., et al. Short-term and medium-term health effects of 9/11, The Lancet, 378:925- 934 (2011). (other 9/11 related situation reviews available on The Lancet, 379 (9794). Sack DA., How many cholera deaths can be averted in Haiti?, The Lancet, 377(9773):1214- 1216 (Apr. 2011). Sutherst RW., Global Change and Human Vulnerability to Vector-borne Diseases, Clinical Microbiology Reviews, 17(1):136-173 (2004). Weinstein P., Do post-disaster public health interventions impede malaria eradications?, Medical Hypotheses, 74(3):403-405 (Mar. 201). Laboratory capacity and Surveillance Bruckner C., et al. Detection of infectious disease outbreaks in twenty-two fragile states, 2000- 2010: A systematic review, Conflict and Health, 5:13, doi:10.1186/1752-1505-5-13 (2011). Williams RJ., et al. Surveillance of antimicrobial resistance – an international perspective, BMJ, 317: 651 (1998). Risk factors and Impacts of AMR in developing country perspective An Approach to the Evaluation of Quality Indicators of the Outcome of Care in Hospitalized Patients, With a Focus on Nosocomial Infection Indicators, Infection Control and Hospital Epidemiology, 308-316 (May 1995). Bhatia R., Narain JP., The growing challenges of antimicrobial resistance in the South-East Asia Region-Are we losing the battle?, Indian J. Med. Res. 132;482-486 (Nov. 2010) Byarugaba DK., A view on antimicrobial resistance in developing countries and responsible risk factors, Int. J. Antimicrobial Agents, 24:105-110 (2004). Cosgrove SE., The Relationship between antimicrobial Resistance and Patient Outcomes: Mortality, Length of Hospital Stay, and Health Care Costs, CID, 42 (suppl. 2) s82-88 (2006). Damme WV., et al. Primary health care vs. emergency medical assistance: a conceptual framework, Health Policy and Planning, 17(1):49-60 (2002). DiazGranados CA., et al. Antimicrobial resistance: international control strategies, with a focus on limited-resource settings, Int. J. Antimicrobial Agents, 32:1-9 (2008). Gangly NK., Global Antibiotic Resistance Partnership –India National Working Groups, Situation Analysis: Antibiotic use and resistance in India (2010) (http://www.cddep.org/sites/cddep.org/files/publication_files/India-report- web.pdf?issuusl=ignore ) Okeke IN., et al. Antimicrobial resistance in developing countries, Part 1: recent trends and current status, The Lancet Infectious Diseases, 5:481-493(Aug. 2005). Okeke IN., et al. Antimicrobial resistance in developing countries. Part 2: strategies for containment, The Lancet Infectious Diseases, 5:568-180 (Sep. 2005). Safdar N., et al. The Commonality of risk factors for nosocomial colonization and infection with antimicrobial-resistant Staphylococcus aureus, enterococcus, gram-negative Clsotridium difficile, and Candida, Ann. Intern. Med., 136(11):834-844 (4 Jun. 2002). Annex 3 - 30 - Annex 4 Shears P., Antibiotic resistance in the tropics, Epidemiology and surveillance of antimicrobial resistance in the tropics, Meeting at Manson House, 18 May 2000, London, Trans. Royal Society of Trop. Med. & Hygiene, 95:127-130 (2001). Shears P., Poverty and infection in the developing world: healthcare-related infections and infection control in the tropics, J. Hosp. Infect., 67(3): 217-224 (Nov. 2007). Sirinavin S., et al. Antimicrobial Resistance in Countries with Limited Resources: Unique challenges and Limited Alternatives, Seminars in Pediatric Inf. Dis., 15(2):94-98 (Apr. 2004). Virk A., et al. Clinical aspects of antimicrobial resistance, Mayo Clin. Proc., 75(2):200-214 (Feb. 2000). Epidemiology, characteristics in population and its movement Allan R., Medicine for refugees, The Lancet Extreme medicine, 362:s34-35 (Dec. 2003). Caron WP., et al. Prevention strategies for antimicrobial resistance: a systematic review of the literature, Infection and Drug Resistance, 3:25-33 (2010). Fluit AC., et al. Muti-resistance to antimicrobial agents for the ten most frequently isolated bacterial pathogens, Int. J. Antimicrobial Agents, 18:147-160(2001). Lynch J., et al. Disasters and Their Effects on Children, Advances in Pediatrics, 57(1:7-31 (2010). Naimi TS., et al. Comparison of Community and Health care-Associated Methicillin-Resistant Staphylococcus aureus infection, JAMA, 290 (22):2976-2984 (Dec. 2003). Ouellette M., et al. Microbial multidrug resistance, Int. J. Antimicrobial Agents, 8:179-187 (1997). Quinn JP., et al. Antibiotic policies in neonatal intensive-care units, The Lancet, 355:946-947 (18 Mar. 2000). Ran YC., et al. Microbiological study of pathogenic bacteria isolated from pediatric wound infections following the 2008 Wenchuan earthquake, Scand. J. Infect. Dis., 42(5):347-350 (2010). Rogers BA., et al. Country-to-Country Transfer of Patients and the Risk of Multi-Resistant Bacterial Infection, CID, 53: 49-56 (1 July 2011). Uçkay I, et al. Multi-resistant infections in repatriated patients after natural disasters: lessons learned from the 2004 tsunami for hospital infection control, J. Hospital Infection, 68:1-8 (2008). van de Sande-Bruinsma N., et al. Antimicrobial Drug Use and Resistance in Europe, Emerging Infectious Diseases, 14(11):1722-1730 (Nov. 2008). Waltzman M., et al. Preparing for Natural Disasters, Clin. Pediatric Emergency Medicine, 10(3):144-148 (Sep. 2009). Health economics re. AMR Howard DH., Resistance-induced Antibiotic Substitution, Health Economics, 13:585- 595(2004). Larson E., Factors associated with variation in estimates of the cost of resistant infections, NIH public Access, Med. Care, 48 (9):767-775 (Sep. 2010). Smith RD., et al. Antimicrobial resistance: a global response, Bulletin of the World Health Organization, 80(2): 126-133 (2002). AMR as pharmaceutical issues Counterfeit Drugs. A Global Health Risk, Pharmaceutical Forum, IFPMA (2004). Essential Drugs MONITOR, No. 28 & 29 (double issue), World Health Organization (2000). Substandard and Counterfeit Medicines, WHO (2003). Quality assurance of pharmaceuticals. A compendium of guidelines and related materials, vol.2, Updated Edition, WHO (2004). Annex 3 - 31 - Annex 4 Pinheiro CP., Drug donations: what lies beneath, Bulletin of the World Health Organization, 86 (8):580-581(Aug. 2008). AM R&D Global Antibiotic Resistance Partnership (http://www.cddep.org/projects/global_antibiotic_resistance_partnership ) Infectious Diseases Society of America, The 10 x ’20 Initiative: Pursuing a Global Commitment to Develop 10 New Antibacterial Drugs by 2020, CID, 50:1081-1083 (15 Apr. 2010). Urgently needed: new antibiotics, Editorial, The Lancet, 374:1868 (5 Dec. 2009). The need for new antibiotics, Correspondence, The Lancet, 375:637-638 (27 Feb. 2010). Self-medication and quality assurance Gossens H., et al. Outpatient antibiotic use in Europe and association with resistance: a cross- national database study, The Lancet, 365: 579-587 (12 Feb. 2005). Grigoryann L., et al. Self-medication with antibiotics in Europe: a case for action, Curr. Drug Saf. 5(4):329-332 (Oct. 2010). Hämmerlein A., et al. Survey of drug-related problems identified by community pharmacies, Ann. Parmacother., 41(11): 1825-1832 (2007). Seiter A., Pharmaceuticals: Quality Assurance in the Distribution Chain, Health, Nutrition and Population (HNP) Brief No. 6, World Bank (July 2005). AM use in food production Antimicrobial resistance: monitoring the quantities of antimicrobials used in animal husbandry, Rev. Sci. Tech. 20:841-847(2001). Guidelines: Antimicrobial resistance: responsible and prudent use of antimicrobial agents in veterinary medicine, Rev Sci. Tech. 2:22-28(2003). WHO Use of antimicrobials outside Human Medicine and Resultant Antimicrobial Resistance in Human (2002). http://www.foodinsight.org/Resources/Detail.aspx?topic=Animal_Antibiotics_and_Food_ Safety_What_you_Should_Know Key guidelines, Manuals Clinical Guidelines, Diagnosis and Treatment Manual, for curative programmes in hospitals and dispensaries, guidance for prescribing, 2010 Edition, Medicins Sans Frontiers (Jan. 2010). Containing Antimicrobial Resistance: Review of the literature and Report of a WHO Workshop on the Development of a Global Strategy for the Containment of Antimicrobial Resistance, WHO/CDS/CSR/DRS (1999). Critically Important Antimicrobials for Human Medicine, 2nd Revision, World Health Organization (2009). Essential Drugs, Practical Guidelines, intended for physicians, pharmacists, nurses and medical auxiliaries, 2010 Edition. Flooding and communicable diseases fact sheet: risk assessment and preventive measures, Communicable Disease Working Group on Emergency, WHO. Guideline for Cholera control, WHO (1993). Guidelines for Drug Donations, World Health Organization (Revised 1999). Guidelines for epidemic preparedness and response to measles outbreaks, WHO (1999). Guidelines for Safe Disposal of Unwanted Pharmaceuticals in and after Emergencies, World Health Organization (1999). Health Cluster Guide, A practical Guide for Country-level Implementation of the Health Cluster, Inter-Agency Standing Committee, World Health Organization (2009). HIV-IMAI publications ( http://www.who.int/hiv/topics/capacity/en/index.html ) Annex 3 - 32 - Annex 4 IMCI guidelines and publications ( http://www.who.int/child_adolescent_health/documents/imci/en/index.html# ) Infant Feeding in Emergencies, EURO/WHO, (http://www.ennonline.net/pool/files/ife/guide- for-mothers-english-who-1997.pdf ) (Revised Sep. 1997) Inter-agency Field Manual on Reproductive Health in Humanitarian Settings, 2010 Revision for Field Review, UNHCR(2010) Inter-Agency Standing Committee (IASC) on HIV/AIDS. Guidelines for HIV/AIDS Interventions in emergency settings (2003) (http://data.unaids.org/publications/External- Documents/iasc_guidelines-emergency-settings_en.pdf) Interagency standing committee (IASC) on HIV/AIDS in emergency settings. Matrix of HIV/AIDS interventions in emergencies (2002:12) , Guidelines for HIV/AIDS interventions in emergencies (2004). Management of Acute Malnutrition in Infant (MAMI) Project, Summary Report (Oct. 2009) (http://www.actionagainsthunger.org/sites/default/files/publications/Management-Acute- Malnutrition-Infants-Report.pdf ) Management of nutrition in major emergencies, WHO (2000). Mass Medical Care with Scarce Resources, A Community Planning Guide, Bioterrorism and Other Public Health Emergencies, Tools and Models for Planning and Preparedness, Agency for Healthcare Research and Quality (AHRQ), USA (Feb. 2007). Nugent R., et al. The Race against Drug Resistance, A report of the Center for Global Development’s Drug Resistance Working Group, UK (2010). Save the Children, Emergency Health and Nutrition Forum, Issue 1: the Emergency Nutrition Portfolio, March 2007. The Sphare Project, Humanitarian Charter and Minimum Standards in Humanitarian Response, 2011 Edition (2010). USAID, FANTA-2, Community-based Management of Acute Malnutrition (CMAM)Reports (http://www.fantaproject.org/publications/home_titles.shtml ) WHO Global Strategy for Containment of Antimicrobial Resistance, WHO/CDS/CSR/DRS (2001). Useful websites In general http://www.cochrane.org/cochrane-reviews/evidence-aid-project http://emedicine.medscape.com/emergency_medicine http://www.nlm.nih.gov/docline/intlresources.html http://www.dmphp.org/ http://highwire.stanford.edu/lists/devecon.dtl http://www.cdc.gov/std/ http://sis.nlm.nih.gov/dimrc/disasters.html http://www.healthnet.org/essential-links/emergency-medicine-and-trauma#a_1101 Area-specific: Emergency and essential surgical care: http://www.who.int/surgery/publications/imeesc/en/index.html http://www.worldwidewounds.com/ Radiation: http://www.who.int/ionizing_radiation/a_e/en/ http://www.remm.nlm.gov/sns.htm#kinds http://www.annals.org/content/140/12/1037.full http://www.uptodate.com/contents/treatment-of-radiation-injury-in-the- adult?source=search_result&selectedTitle=4%7E150 http://science.thomsonreuters.jp/announce/20110317/0318data/ TB: http://www.who.int/tb/data/ http://whqlibdoc.who.int/hq/1997/who_tb_97.221.pdf http://who.int/tb/challenges/xdr/xdr_map_june08.pdf/ http://desastres.unanleon.edu.ni/pdf/2003/enero/pdf/eng/doc8955/doc8955.htm Malaria: http://rbm.who.int/cmc_upload/0/000/015/366/RBMInfosheet_7.htm/ Surveillance: http://www.ecdc.europa.eu/en/activities/surveillance/EARS-Net/Pages/index.aspx http://www.cgdev.org/section/initiatives/_active/drugresistanceglobalhealth/resources Disaster-related database: http://www.cred.be/projects http://www.cred.be/publications Mass prophylaxis: http://archive.ahrq.gov/research/cbmprophyl/ - 33 - ANNEX 4 PRESENTATIONS I. WHO's work on AMR Dr. Henk Bekedam Chairperson, WPRO AMR-TWG Global AMR Meeting, 28-29 Nov 2011 Geneva Contents of the presentation • AMR Six Policy Package • Results of key informant interviews in 12 WPR Countries • Status of the AMR policy package in the WP Region – Comprehensive financed AMR plans – Surveillance and laboratory capacity – Access to quality assured essential medicines – Regulation and promotion of medicines, including in animal husbandry – Infection prevention and control – Innovations, research and new tools • Conclusions and next steps WHO Western Pacific Region - 34 - Annex 4 - 35 - Annex 4 WHD 2011 Core Product: Policy Package 1. Commit to a comprehensive, financed national plan with accountability and civil society engagement 2. Strengthen surveillance and laboratory capacity 3. Ensure uninterrupted access to quality essential medicine 4. Regulate and promote rational use of medicines, including in animal husbandry, and ensure proper patient care 5. Enhance infection prevention & control 6. Foster innovations and research & development of new tools WHO Western Pacific Region Key Informant Interviews on AMR in 12 Western Pacific countries Majority of respondents stressed need for – Budgeted national AMR plans which address both prevention and management of AMR – Laboratory capacity building – Surveillance system for AMR and drug consumption – Legislation to reduce use of antimicobials in food animals – Promoting and enforcing Rational Prescription – Inclusion of infection prevention and control (IPC) as part of accreditation and registration of health institutions – Basic research into new diagnostics and antimicrobials. WHO Western Pacific Region - 36 - Annex 4 Status of AMR policy package in Western Pacific Region • comprehensive financed national AMR plans lacking • No complete oversight of AB use in animal husbandry • Many achievements and initiatives in the field of – surveillance and lab – Uninterrupted access to quality assured drugs – Rational use of medicines – Infection control and prevention – Research and development for new tools WHO Western Pacific Region Surveillance and laboratory capacity Issues and challenges 1. Insufficient laboratory testing • Access to QA methods for all relevant markers • Reporting on testing and outcomes • Technical skills and retention of qualified staff • Funding shortages 2. Weak or absent surveillance capacity • Weak national surveillance systems • Establishing functioning national networks • Laboratory network design in view of new tools • External quality assurance WHO Western Pacific Region - 37 - Annex 4 But many activities ongoing to strengthen surveillance and lab capacity • Capacity building on drug susceptibility testing (DST) – Training lab techniques & training of trainers in member states – Countries rolling out new (crosscutting) laboratory tools – Development and use of training modules and SOPs – Supportive role of supranational laboratories for EQA and TA • Normative guidance – Data analysis software; WHO endorsement of new techniques – Guidelines on representative sampling techniques • Surveillance – Strengthening of AMR surveillance networks (malaria, HIV, TB) – Anti-viral resistance monitoring WHO Western Pacific Region Example: Antiviral resistance • WHO CCs routinely test for antiviral resistance in all viruses submitted by National Influenza Centres and other labs. • As per a 2010 survey of 12 of the NICs in WPR, 9 (75%) were conducting antiviral resistance testing • The proportion of A(H1N1)pdm09 viruses determined to be oseltamivir (Tamiflu) resistant is about 1%, with the majority of resistant viruses isolated from patients with a history of treatment with antivirals, WHO Western Pacific Region - 38 - Annex 4 37 – Countries & Areas 3 – WHO Collaborating Centers 21 – National Influenza Centers in 15 countries GISRS* in WHO’s Western Pacific Region *Global Influenza Surveillance and Response System 11 Example 2: Gonococcal Antimicrobial Surveillance Programme - WPR/SEAR 2009 • Gonococcal Antimicrobial Surveillance Programme (GASP)  since 1992 ‐ long term surveillance of AMR in Neisseria gonorrhoeae • 8,704 N. gonorrhoeae examined for  their susceptibility to  one or more antibiotics used for gonorrhoeae treatment by  EQAS controlled methods in 2009 – High rates of penicillin, tetracycline, and quinolone resistance  – Increasing reports of clinical treatment failures and  decreased susceptibility to cephalosporins, the last line  treatment for gonorrhoea raising concerns that  gonorrhoea may become untreatable. WHO Western Pacific Region - 39 - Annex 4 Surveillance and laboratory capacity: Selection of next steps • Establishing national AMR surveillance programs • Support to lab network design and introduction new tools • Develop guidelines for establishing national AMR surveillance • Build capacity for EAQ AMR network in member states • Link surveillance data to health system action • Close monitoring of bacterial and AMR patterns in children given increased coverage of vaccination with HIB and pneumococcal vaccin • MDR/XDR surveillance in all previous treated patients • Children: DST for meningitis, typhoid fever, dysentery WHO Western Pacific Region Essential Medicines: Challenges 1. Lack of regulatory control on the availability and distribution of antimicrobials in the market. 2. Wide spread irrational use in health facilities and communities. 3. Sub standard quality of products in the market (malaria, TB, and widely used AB) 4. Lack of awareness on the danger of irrational use of antimicrobials. 5. Lack of systematic program to monitor and promote rational use of antimicrobials WHO Western Pacific Region - 40 - Annex 4 Essential Medicines: Some accomplishments and plans Accomplishments  Training on Rational Use of Antimicrobials & Containing AMR for ASEAN countries (Brunei November/December 2011).  National advocacy workshops on antimicrobial resistance  Public advocacy on the rational use of antimicrobials  Technical support for pilot implementation of MTP Planned activities  Promoting and monitoring rational use of antimicrobials in hospitals through therapeutics committee.  National workshops (in context of national AMR plans) WHO Western Pacific Region Regulate and promote rational use of medicines: a real challenge • Major differences between countries, with some addressing causes of AMR and some with an uncontrolled private sector and weak national regulatory authorities Examples of challenges: • Malaria: Oral artemisinin monotherapy, fake and counterfeit drugs • TB: huge sales and uncontrolled use of TB drugs in private sector Examples of interventions from disease programmes • Containment of artemisinin resistance and prevention of further emergence (focus on Mekong: huge operations) • Public private mix models and insurance schemes linked to quality • Monitoring of MDR-programmes through WHO and partners (GLC) • Normative: evidence based guidelines, tools, SOPs WHO Western Pacific Region - 41 - Annex 4 Infection Prevention an control Challenges: • Simple effective ‘administrative control’ neglected in comparison with expensive environmental measures (equipment/infrastructure) • Translating disease specific guidelines into integrated IC approaches at all levels of the health system • Capacity building and funds for implementation Initiatives and plans • Regional inventory of the situation in 7 countries (TB) • Training and training of trainers for HCW capacity building • Establishment of facility IPC committees ; SOPs • Normative guidance: criteria for equipment and maintenance • Training of engineers WHO Western Pacific Region Innovations, research and development Challenges • In country capacity, timelines, developing evidence based guidelines and country operations, funding Opportunities in WPR • Strong academic environment; some active countries; numbers Examples • Drug and vaccine trials ; new diagnostic tools (TB, malaria,..) • Linking disease programmes with academic partners • Drug consumption in relation to disease burden • Cross border projects (malaria, TB) • Private sector issues (prescription, over counter sales, quality drugs) WHO Western Pacific Region - 42 - Annex 4 Many efforts, many initiatives, but need for better coordination of initiatives to combat AMR WHO Western Pacific Region Technology “Menu” Regional Laboratories 1. TB Rif / INH 2. TB Fluoroquinolones/Inject Aminoglycosides 3. EID/HIV District/Subdistrict Laboratories 1. TB Rif 2. TB Fluoroquinolones/Inject Aminoglycosides 3. STD/Viral load HIV 4. MRSA 5. Others: Hepatitis B/C Microscopy Centres 1. TB 2. Malaria 3. HAT 4. EID/HIV Microscopy Centres 1. TB 2. HAT 3. Malaria For instance: improving cost-effectiveness by shared technology platforms - 43 - Annex 4 General Conclusions for WPR • Surveillance data show worrisome levels of drug resistance for STD, TB and Malaria and other drugs • Countries show different levels of AMR awareness and control efforts, both encouraging and challenging • More advocacy necessary with politicians, professionals (medical associations) and general public • Major opportunities for technical and operational collaboration between sectors and disease programmes • WPRO AMR WG exchange was an important first step, but needs to be ‘translated’ to comprehensive actions WHO Western Pacific Region Current and next steps for WHO WPRO – Finalization of crosscutting AMR Technical Strategic Framework (TSF) • Based on AMR Policy Package • Results, targets, indicators, responsibilities, funding gaps • Identification of partners – Joint ventures to assist countries developing comprehensive multidisciplinary costed AMR plans based on a generic assessment tool – Resource mobilization for implementation AMR-TSF WHO Western Pacific Region - 44 - Annex 4 II. Gap Analysis on Antimicrobial Resistance (AMR) Control in Emergencies Gap Analysis on Antimicrobial Resistance (AMR) Control in Emergencies Dr. Bipin Verma WHO-Emergency and Humanitarian Action (EHA)  Drug Needs  Drug Availability – Emergency, Relief and Recovery Phases  Appropriate drug use during Emergencies - Prescription habits, Treatment protocols  Drug Efficacy – Quantity, Quality issues, Storage, Wastage & Disposal - 45 - Annex 4 Health Sector Disaster Issues (First 5 Days) • Large number of Injured/Deaths/drowned. • Extensive infrastructure damage. • Health Facilities damaged. • Medical supplies and equipment damaged, lost or non-functional due to absence of essential back-up service support - no electricity, water supply, waste disposal etc. • Health sector related rumors. • Health Manpower also affected (dead/injured/missing). • Families of Medical and Para- medical manpower also affected; needs attention - 46 - Annex 4 24.12109Total 1.105Nerve Injury (Brach. Plexus) 0.884Head Injury 0.884Abdominal Injury 1.115Chest Injury 1.999Paraplegia 2.2118Clavicle fracture 3.3215Spinal Injury 3.9818Multi. fracture 4.2819L. Limb Injury 4.4228U. Limb Injury Percentag e TotalIndoor adm ission  Total Affected Populatio n – 167, 457  Death – 12 %  Injuries – 4.8 % 1. Maharashtra Instt. Of Medical Sciences and Research (Pvt. Med. Coll.) Latur 2. Pvt. Medical Camp, Latur r n Variable Public Health Impacti l i l 1993 Latu (Maharashtra) Earthquake (I juryI Pattern - (30.9 .93 to 6.10.93). t Variable Post Emergency Drug Needs Energy Partition i i Fallout 10% Blast 50% Thermal 35% Initial Radiation 5% Standard Fission / Fusiont a i i / s ita d r F s on u i AFRRI, F M edical Ef fect s o f Nu clea r We apo nsi E f r a , “Blast an d T he rmal Ef fect sr f ” L ect ure, 19 90.u Systemic Effects of Radiation:  Prodromal  Hematologic  Gastronintestinal  Pulmonary  Cutaneous  Neurovascular  Combined Injury Natural Hazard Radiation emergencies 24.12109Total 1.105erve Injury (Brach. Plexus) 0.884ead Injury 0.884Abdo inal Injury 1.115Chest Injury 1.999Paraplegia 2.2118Clavicle fracture 3.3215Spinal Injury 3.9818ulti. fracture 4.2819L. Li b Injury 4.4228U. Li b Injury Total Affected Populatio n – 167, 457 eath – 12 Injuries – 4.8 1. aharashtra Instt. f edical Sciences and Research (Pvt. ed. Coll.) Latur 2. Pvt. edical Ca p, Latur Percentag e TotalIndoor ad ission Variable Public ealth I pacti l i l m 1993 Latur ( aharashtra) EarthquakeM (InjuryI Pattern - (30.9 .93 to 6.10.93). t i l t r rt tEne gy Pa i ion Fallout 10 Blast 50 Ther al 35 Initial Radiation 5 t n d i si / F ionSta dar Fis ion / usit i AFRRI, F M edical Ef fect s o f Nu clea r We apo nsi E f r a , “Blast an d T he rmal Ef fect sr f ” L ect ure, 19 90.u t i ff t f i ti :S s E e ad on r r lP od a t l ie a o og c tr i t ti las on n es na l rP na y t s r l r eu ovascu a i I j rn d u y at ral azar a iati e er e cies Variable Post Emergency Drug Needs Protection of high -risk groups Ca se m an ag em en t an d in fe ct io n co nt ro lMigratory birds Infected poultry Ri sk co m m un ica tio n fo r t he p ub lic Man Disease Surveillance Key Strategies surveillance Prevent exposure Ou tbr ea k c on tro l in po ult ry Transparency in operation and information Credit: MoPH., Thailand Bhopal Industrial Accident 1984  Conjunctival xerosis.  Corneal opacities,  Lenticular opacities  Corneal Opacities in the ‘exposed areas’ were nearly three times more than in the ‘control areas’. Ocular changes in MIC / toxic gas exposed population Abortions, peri-natal and neonatal mortality were significantly higher in the toxic gas affected areas than the control areas. However, there was no significant difference in the incidence of congenital malformations. Pregnancy outcome in women exposed to MIC/toxic gas  Chronic bronchitis -17% (exposed patients) vs 7% (control);  Bronchial asthma - 12% vs 5% classified as “reactive airway dysfunction syndrome (RADS)”;  Unspecified lung disease including small airway disease - 57% vs 0.2%;  Chest Radiography - 80% showed abnormalities like linear, reticulonodular opacities, honey-combing and hyperinflation etc  Mortuary Findings 18 in 86; 17 in 87; 47 in 1988 - progressive pulmonary damage, including desquamative pneumonitis or fibrosing alveolitis or its variants. Respiratory Diseases SUMMARY FINDINGSHEALTH ISSUES Biological Hazard - 47 - Annex 4 - 48 - Annex 4 Enhanced Public Health Needs Compromised Health Infrastructure - 49 - Annex 4 Public Health Needs - an example Army Field Hospital Experience (Gujarat, India- 2001 Earthquake) – First 28 Days • 26,654 Victims were provided treatment • 2, 002 Major operations performed • • 3, 004 Patients referred from Bhuj to other hospitals 7,528 Minor operations performed 1222 300 0 500 1000 1500 2000 2500 3000 3500 J a n - 2 6 J a n - 2 7 J a n - 2 8 J a n - 2 9 J a n - 3 0 J a n - 3 1 F e b - 1 F e b - 2 F e b - 3 F e b - 4 F e b - 5 F e b - 6 F e b - 7 F e b - 8 F e b - 9 F e b - 1 0 F e b - 1 1 F e b - 1 2 F e b - 1 3 F e b - 1 4 F e b - 1 5 F e b - 1 6 F e b - 1 7 F e b - 1 8 F e b - 1 9 F e b - 2 0 F e b - 2 1 F e b - 2 2 F e b - 2 3 F e b - 2 4 Major Surgeries Minor Surgeries - 50 - Annex 4 Army Field Hospital Experience (during First three days)  Hospital building badly damaged & unsafe for occupation.  Make-shifts operation theatre in tents with electric supply from generators.  Large influx of casualties mostly with contaminated wound soiled with foreign material, dirt and mud.  Shortage of water, hosp beds & clean linen.  Water & electricity supply disrupted.  Shortage of disposables & disinfectants  Absence of laundry services & other support services.  Health hazards - large quantity of biomedical waste & human refuse generated SAM PANTHKEY Army Field Hospital Experience (during First three days)  Inadequate crowd control.  Documentation of injured influx not possible with the existing manpower  Disruption of Communication Network ( Partial Restoration after two days and full restoration after 3 days).  Restricted food, tentage & fuel  AIIMS super-specialty medical teams from Delhi reported without equipment & Personal administration - 51 - Annex 4 Health Sector Disaster Issues from day 2 to day 30 • People sheltered all around. Gradually moving to camps with only consideration of safety. • Camps established with no proper water supply, cooking facilities, latrines, waste disposal arrangement leading to mosquito/flies breeding. • Overcrowding in camps with possibility of fast-spread of potential disease outbreaks – Measles, water & food-related diseases. • Outbreak of Potential diseases • Increase of mosquito breeding sites. • Disruption of chronic disease control measures like T.B., Malaria, HIV surveillance, Dengue and other vector- control measures. • Disruption of normal medical services for diseases like hypertension, other cardio-vascular diseases, asthma, peptic ulcer etc. - 52 - Annex 4 0 500 1000 1500 2000 2500 3000 3500 26 /01 /20 02 27 /01 /20 02 28 /01 /20 02 29 /01 /20 02 30 /01 /20 02 31 /01 /20 02 01 /02 /20 02 02 /02 /20 02 03 /02 /20 02 04 /02 /20 02 05 /02 /20 02 Minor Major Trends - Selected Syndromes Post-disaster Disease Surveillance, Kutch Govt. of Gujarat and WHO 0 1000 2000 3000 4000 5000 6000 7000 8000 9000 12 13 14 15 16 17 Post disaster week N o . o f c a s e s Bloody Diarrhoea Watery Diarrhoea Acute Respiratory Infections Fever "Outbreak of Reporting", Post-earthquake Disease Surveillance, Kutch 0 20 40 60 80 100 120 140 160 180 3 4 5 6 7 8 9 10 11 12 13 14 15 16 Post Disaster Week R e p o r t i n g U n i t s ( R U ) 0 1000 2000 3000 4000 5000 6000 7000 8000 9000 A c u t e R e s p i r a t o r y I n f e c t i o n s ( A R I ) c a s e s RU ARI 0 500 1000 1500 2000 2500 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 Malaria Cases in Kutch District Post Emergency Changing Drug Needs - 53 - Annex 4 0 1 2 3 4 5 6 Se p Oc t No v De c Water Borne Respiratory Nut. Deficiency SkinSource: DHS Gujarat I n T h o u s a n d s Year 1987 Disease Pattern 1987 Draught - Gujarat Post Emergency Changing Drug Needs - 54 - Annex 4 • Sleep disturbance • Hunting of memory • Digestive problems • Disenabled and injured people • Keep thinking of past • Lack of interest • Lack of emotional resp • Irritable / angry Psycho-Somatic Manifestations – Special Drug Needs Kutch 2001(Gujarat Earthquake) Interviewed 26,000 people in targeted 45 villages after 3 months of EQ (March – Nov 2001) • 47% were not affected • 28% were Mildly affected • 15% were Moderately • 10% were Severely affected Post Emergency Special Drug Needs 2%119Mentally ill people 33%1684 School going children at the risk of abuse & exploitation 11%574 People experiencing chronic illnesses 18%902Elderly citizens (over 60) 8%405 Single parent with preschool children or infants 13%686Lactating mothers 10%20Youth addicted to drugs 5%244Persons with disabilities 3%134Pregnant women Post Tsunami Sri Lanka – Southern Province 0%0Special Groups Source: Basic needs, an NGO working in Southern Province - 55 - Annex 4 Drug Needs for routine care during post Emergency period Hypertension, Diabetes, Asthma etc. Routine Immunization Coverage Vector Borne Diseases DOTS Treatment 1 week 4 Week 2 Month 3 Month Injuries A.R.I. PUO Diar. Disea. Vector Borne Adolescent, Maternal, Neonatal & Child Health Issues – 1 week onwards day 1 Psycho-social & Mental Health Issues – 4/6 weeks Chronic Medical Diseases & Long- standing public health issues like TB – day 1 Post-Emergency Public Health Risks – A summary P at ie n t s - 56 - Annex 4 Health Sector Disaster Issues beyond 30 days • New town/village planning sites including housing rehabilitation sites to consider including issues relating to the potential public health risks- location, accessibility. • Proper Housing Faculties must consider including the adequate essential services important to prevent the potential public health risk like proper water supply system, latrines, sanitation including waste-disposal systems. • New health facilities to be rebuild must be able to remain functional during future disaster situations. • Introspection of existing health sector disaster contingency plans and its up- dating. • Documentation of best-practices and inadequacies. • Re-training of health sector manpower. Appropriate Drug Use during Emergencies - Prescription habits, Treatment protocols - 57 - Annex 4 Drug Efficacy – Quantity, Quality issues, Storage, Wastage & disposal • MSD storage capacity was constrained. Special bottleneck in shipping and receiving area due to lack of space. • Many RMSD/Institution stores at or near full capacity, which was further aggravated by emergency Tsunami shipments and donations. • Warehouse conditions at some locations needed considerable improvement (facilities, temperature, shelving, organization). Some stores were set up in hospital rooms or in tents. • Batch traceability and shelf life monitoring were not adequate at MSD and periphery facilities due to lack of physical storage capacity, manual book keeping and/or lack of appropriate procedures. • Proper cold storage capacity (cold rooms) is needed at many locations, currently using multiple household refrigerators without proper monitoring and backup systems. Post-tsunami Scenario (Sri Lanka) - 58 - Annex 4 Observations • Inventory Control System though adequate at Colombo, but programming was needed to include periphery stores, and warehouses. • General lack of written procedures and manuals. • Outside of Colombo, the entire supply chain was paper based. • Limited number of computers, computer software and expertise available at RMSD/Institutions. • Very limited internet/e-mail access. Limited data communication capabilities between periphery and Colombo. • No Local Area Networks available at DPDHS and institutions. Post-tsunami Scenario (Sri Lanka) Variable Post-Emergency Drug Needs (Summary) Vector borne disease - Malaria etc.Endemic disease Hypertension, diabètes, Peptic Ulcer, Asthma etc. Non-communicable diseases prevalent in community  Reproductive, adolescent, Maternal, Neonatal and Child Health, Sexual Violence, HIV etc, Disabled, Elderly etc  Psychological distress Special Group Drug Needs  Acute Respiratory infections  Pyrexia Unknown Origin  Food & Water Born Diseases  Viral Diseases – Measles, Chicken Pox Outbreak of potential Communicable Diseases in temporary shelters  Hypothermia - Hyperthermia  Crush injury and crush syndrome  Hypovolemia shock  Airway obstruction  Airway contamination/ respiratory diseases  Pneumothorax  Abdominal injuries  Dehydration  Near drowning  Burns  Chemical injuries and asphyxia  Pain control and sedation Injury Care AilmentsDrug Needs for - 59 - Annex 4 III. Experience from the field: Infection Control and Prevention: Hong Kong Experience Infection Control & Prevention:  Hong Kong Experience Samantha Mei‐che Pang  Professor & Head School of Nursing The Hong Kong Polytechnic University What we have learned from SARS - 60 - Annex 4 • SARS transmission, risk factors, and  prevention in Hong Kong (Lau et al, 2004) Risk factors: – Visited mainland China – Hospitals – Amoy Garden Protective factors:  – Frequent mask use in public venues – Frequent hand washing & disinfecting the living  quarters  • Why did SARS syndrome occur in some hospital  wards but not in others? (Yu et al 2007) – Minimum distance between beds of < 1 m – Availability of washing or changing facilities for  staff – Resuscitation was ever performed in the ward – Staff members worked while experiencing  symptoms – Host patients required oxygen therapy – Host patients required bi‐level positive airway  pressure ventilation  - 61 - Annex 4 • Recommendations on expanding ICU facilities  based on SARS experience (Gomersall et al  2006) – To base expansion plans on estimates of feasibility  rather than estimates of requirements (iatrogenic  injury, over‐dilution) – A step‐down approach to err on the side of  caution (in absence of knowledge, assume to be  spread by contact and airborne transmission) – Temporary expansion has to meet minimum  standards (infrastructure, ventilation) – Protocol for donning and removing PPE – Staffing level, staff mix, well‐being, and training  Three “R”s ethical challenges: Rationing, Restriction, Responsibility • Lifeboat ethics: The access to and distribution of limited or scarce  lifesaving resources • Principle for resource distribution: Preserving the functioning of  society, priority will be individuals who are essential to the provision  of health care, public safety • Creation of hospital surge capacity : triage • Balancing community interests and individual liberties • Human resource surge capacity: Delegation of responsibility and  authority to perform procedures and interventions customarily  carried out by certain professionals to other less formally qualified  individuals  - 62 - Annex 4 Infection control plan  for influenza epidemic outbreak • Department of Health • Hospital Authority of Hong Kong • Other Institutions  Evaluating the effectiveness of an Acute Respiratory  Diseases (ARDs) community health promotional  programme in Hong Kong Acknowledgement This project is supported by a seed money grant from the WHO. The  authors would like to thank our nursing colleagues, students from  The Hong Kong Polytechnic University and all professional health workers and community staff from Hong Kong, Macau, and  mainland China for their active participation in the ARDs programme.  - 63 - Annex 4 Objective • Based on the World Health Organization (WHO)  Trainers’ and Trainees’ Guides on infection control  measures for the health care of ARDs in a community  setting, a culturally‐specific train‐the‐trainer (TOT)  programme was developed for professional health  workers and community workers in Hong Kong., with  an aim to enhance the health literacy of the Chinese‐ speaking community in the prevention and control of  the spread of ARDs. Method The training programme incorporates infection  control measures into a workshop on two case‐based  scenarios that emphasize the application of  knowledge and skills in prevention and control of the  spread of ARDs in daily living.  With a 3‐ and a 6‐hour learning package for  professional health workers and community  healthcare workers respectively.  - 64 - Annex 4 Evaluation A pre‐post survey was designed to evaluate changes in level of  knowledge about ARDs prevention and control after the  workshop. The competencies of participants to re‐run the programme  were reviewed by the ARDs team within 3 months of the  workshop. - 65 - Annex 4 Implementation  (March to September 2009) A total of 15 sessions of TOT workshops were  conducted, and 49 workshops were re‐run in the  community.  One workshop was held for healthcare professionals in  Macau, and 32 and 16 workshops were re‐run in Hong  Kong elderly centers and schools respectively.  A total of 880 trainers were trained and 2244  professional health workers and community workers  participated in the TOT programme. Disaster Management Continuum ICN (2009) - 66 - Annex 4 (Chan et al., 2010) - 67 - Annex 4 Conclusion This programme was effective in enhancing the  participants’ knowledge of ARDs prevention and  control using the WHO guidelines. Participants were equipped to conduct health  promotional activities in the community.  The health literacy of the community can be enhanced  through goal‐oriented TOT workshops and good  networks with professional health workers and  community partners. Bi‐regional Training Course for Staff Managing  Healthcare‐Associated Infection (HAI) with  Minimal Resources Authors’ Name and Affiliations Peggy Or1, Eric Chan2, Danny Tong3, Meyrick Chow4, Patricia Ching5, WH Seto6,  Samantha Pang7, Kathleen Fritsch8 1,4 School of Nursing, The Hong Kong Polytechnic University, Hong Kong, China 2 Nursing Division, Hospital Authority 3 Infectious Disease Centre, Hospital Authority 5,6 World Health Organization Collaborating Centre for Infection Control, Hospital Authority 7 World Health Organization Collaborating Centre for Community Health Services,  The Hong Kong Polytechnic University 8 World Health Organization Western Pacific Region, Manila, Philippine  Reference World Health Organization. (2002). Prevention of hospital acquired  infections – A practical guide. Geneva: WHO (Document no.  WHO/CDS/EPH/2002.12). - 68 - Annex 4 Background To prevent and control Healthcare‐Associated Infection  (HAI), it is necessary to have adequately trained staff  and substantial financial resources. The aim of this  training was to train personnel at various levels in the  healthcare system in multifaceted infection control  practices specifically for situations where resources are  limited. A Regional Infection Control Assessment Toolkit was  developed for low resource countries, consisting of  3 components:  An assessment tool, toolkit and training programme.  The training programme will be held in November  2010 in Hong Kong. Target course participants are  healthcare workers from different countries with an  infection control background. The teaching materials  and training activities are under revision. - 69 - Annex 4 Thank you Method The training programme consisted of lectures, interactive  group work using the PPRR (Prevention, Preparedness,  Response and Recovery) model on infectious diseases  (figure 1), a skills test on Personal Protective Equipment  (PPE), and a written test.  Each participant was required to complete the infection  control assessment checklist. Participants were also  required to prepare an action plan for developing effective  infection control in their countries. - 70 - Annex 4 The pilot training programme was held in November 2010 in Hong Kong 69 health care professionals from 16 countries. In  their home countries, 37 (53.6%) worked in  hospitals; 31 (44.5%) worked in Ministry of  Health agencies, and 6 (8.7%) were on teaching  faculties of universities. 21 (59.4%) participants  had some previous training in infection control.  The highest score on the written test was 46 out of 50  and the lowest score was 27 out of 50 (Figure 2). Participants strongly agreed that the course was  relevant and rewarding; they were satisfied with the  training method. - 71 - Annex 4 Conclusion Further consolidate the training material into a  toolkit and establish a network with our course  participants in order to support and facilitate  their work in their home countries. Infection  Control Elluminate is held every two weeks to  share and review their work. - 72 - Annex 4 IV. Literature Review Literature review and situation analysis on AMR in emergencies/disasters Yuki MAEHIRA Visiting Researcher / Pharmacist Department of Global Health, Medicine and Welfare Nagasaki University Graduate School of Biomedical Sciences, Japan 1 Informal Consultative Meeting on Antimicrobial Resistance (AMR) Prevention and Control  in Emergencies/Disasters Manila, Philippines, 29‐30 November 2011 Photos :Dr Md. Manirul Islam, icddr,b PURPOSE of LITERATURE REVIEW  WHAT we exactly know on AMR for general, routine control related to AMR? HOW much impact on AMR made during emergencies?  HOW we can assess the gap/differences  and its  backgrounds (WHY) ? WHAT currently available resources /tools can be used  for AMR control in emergencies? WHAT & HOW emergency‐specific AMR issues to be addressed?  - 73 - Annex 4 Key findings: Routine AMR control  • Control policy framework available • Plenty of medical, clinical evidences on diseases,  agent‐specific case prevalence and treatment  models • Bulk data to accumulate all AMR cases in separate  Surveillance‐PJs (country‐wise, diseases/agent‐ based trends  & data – mostly sentinel) • Diseases trend & ecological factors for health  predictable • Actors & service target population predictable • Not solid evidences of AMR to attribute to mortality  & morbidity • Lack of evidences in developing countries & further  contextual analyses • Not definite solution‐based guidelines (awareness  promotion level) • Global awareness for commitment not effective  without strategic info. AMR in emergencies • No guiding framework  • Priority is on: quantitative life‐saving and case  management for tentative cure • Resource availability dependent – decision  making • Mass population movement is particularly  critical aspect to potentially accelerate AMR  emerge – transmission cycle • Works & efforts in fragmentation (mainly at  health dispensary points – passive?) • Fundamental lack of information:  (1) AMR prevalence on sites & its horizontal  aggregation (2) AM use in emergencies • Following to general AMR control procedures  of case management (not population‐based) (Reference: D. Haymann, Resistance to Anti‐Infective Drugs and the Threat to Public Health, Cell, 124 (2006) Wide range variety of AMR prevalence  on disease‐based surveillance data - 74 - Annex 4 Top 10 Causes of death (2008) ‐ World Health Statistics 2011 •More than 2,500 annual death in US  (more than death toll of AIDS) •Approx. 2,500 annual death in EUR  How much Mortality- based info can show for AMR? - 75 - Annex 4 BASIC SOURCES OF INFORMATION Trend of AMR prevalence : advance in surveillance   - Alexander Project (1992~, by GlaxoSmithKline, community‐acquired S.  pneumonia, H. influenzae, M. catarrhalis) superseded by Alexander Network  since 2002 - LIBRA Initiative (by Bayer)  - Prosctive Resistant Organism Tracking and Epidemiology for the Ketolide Telithromycin (PROTEKT), (1999~, by Abentis, agent, diseases‐specific: respiratory  tract pathogens) - SENTRY (1997~, by the Bristol‐Myers Squibb) - Tracking Resistance in the US Today (TRUST)  (by Ortho‐McNeil) - The Surveillance Network (TSN) (by Focus Diagnostics Inc.) - European Antimicrobial Resistance Surveillance System (EARSS) - European  Surveillance of Antimicrobial Consumption (ESAC) - Asian Network for Surveillance of Resistance Pathogens (ANSORP) - FluNET, EuroFlu (Influenza antiviral susceptibility) Issues on accountability, transparency and availability of commitment for  collaborative coordination  OK?  Enough? - 76 - Annex 4 SENTRY data: Hospital and community‐acquired infections (Source: Bell, Turnridge, Comm. Dis. Intelligence 2003) Penicillin‐resistant Strep pneumoniae <Respiratory isolates> <Blood isolates> Ciprofloxacin‐resistant E. coliOxacillin‐resistant S. aureus - 77 - Annex 4 ESAC‐EARSS data - 78 - Annex 4 AM USE  ‐ accelerate AMR Quantitative: overuse , duration Qualitative : drug selection, non‐prescribed, single or  combined,  counterfeited/adulterated  Annex 4 SEASONAL VARIATION – OUTPATIENT ANTIBIOTIC USE (10 EUR countries) Source: Goossens H., et al. Outpatient antibiotic use in Europe and association with resistance: cross‐national database study, The Lancet, 365: 579‐587 (2005). - 79 - - 80 - Annex 4 Context of AMR prevalence – information available?  AMR proportion in Mortality vs. Morbidity   Quantification of disaster/emergency impact on AMR  AMR case containment vs. future AMR control on sites  Factors of AMR; AM dose/volume of usage vs. compliance (interruption) Self‐medication, empirical/presumptive medication Food safety  Variety in; diseases, pathogens, socio‐economic/ecological aspects  (WHERE, WHAT/WHICH ) pharmaceuticals, lab‐technologies, surveillance, logistics                  (HOW)  purpose to use (priorities, policies) (WHY) actors, target for services (by/for WHOM) Among those, how many of:  Failing/Insusceptible cases of AM treatment involved? hospital‐acquired?  Community‐acquired? Elderly or children? Immuno‐compromised? AND.. How many of: Disaster /emergency‐related? Failing/Insusceptible cases of AM treatment involved? FACTS IN MORTALITY & MORBIDITY Even as for general AMR control situation, many  information hidden and not clearly presented as evidences.       l                  l       - 81 - Annex 4 Source: Felmingham D., et al. The Alexander Project: the benefits from a decade of surveillance,  J.  Antimicro. Chemother.  56: s13‐21  (2005). Potential of  AMR Surveillances Differentiation between  agents/classes of  AMs Mechanism of AMRDrivers of AMR Pathogen evolution &  coronal spreadChanges in susceptibility  over time Clinical relevance  of AMR Quantitative MIC  data Geographical differences in  AMR prevalence Application of PK/PD based  breakpoints Strategies to  combat AMR - 82 - Annex 4 Surveillance Networking PJ ‐ data utilization CHALLENGES Different aspects among institutions, organizations, countries: Definitions Technical consideration – denominators, choice of populations, numbers/types of  samples,  Role and responsibility allocation Potential collaboration:  Enlarge lab‐diagnostic network horizontally and vertically Quality control and manufacture standards in veterinary / food production societies Action needed? Pitfall or gap identification in the already existing surveillance systems Ex. more behavioural surveillance  The role of antimicrobial pressure from agricultural use remains to be evaluated, but there  is no evidence to suggest that errors committed in developed countries will not be  replicated. Inadequate surveillance means that resistance prevalence and trends are  largely understudied and that baseline data for evaluating potential interventions are  unlikely to be sufficient.   (Okeke I.N., et al. Antimicrobial resistance in developing countries. Part I: recent trends and current status, The Lancet, 5: 481‐493  (2005) - 83 - Annex 4 AMR Source: Containing Antimicrobial Resistance: review of the literature and report of a WHO workshop on the Development of a Global Strategy for the Containment of  Antimicrobial Resistance, WHO , Geneva, 4‐5 Feb(1999) Generic factors associated with AMR prevalence EMERGENCE TRANSMISSION Many behavioural factors or process indicators - 84 - Annex 4 Driving Forces: governance & regulatory mechanism collapse, mass prophylaxis, AM overuse,  lack of lab‐diagnosis, mass population movement, poor assessment & surveillance,  lack of  case follow‐up, barriers for sustainability Annex 4 Psychology for prescribers:   ‘the more substitution of  treatment induced, the less   resistance’ …. what would happen in  future?   …. Only cost issues? In many cases, physicians prescribe antibiotics without knowing whether an individual  patient is infected with a susceptible or resistant pathogen. As the proportion of resistant  organisms in a community increases, physicians substitute away from older‐inexpensive  drugs to newer, more expensive agents as first line therapy. Source: Howard D.H., Resistance‐induced Antibiotic Substitution, Health Economics, 13:585‐595(2004). Economic pressure on AM use   ‐ ‘Choice of drug’ issue - 85 - - 86 - Annex 4 What AMR shall we look at in emergencies for  control?  Prevalence on emergency health service delivery sites & target  populations as part of comprehensive case management  Subsequent AMR in near future due to AM misuse in post‐ disaster/emergency settings  Differentiation of approaches OR standing on currently available systems  which could be strengthened with  operational review 5W‐1H in emergencies to associate with AM use  • Population characteristics  • Diseases trends • Ecological changes • Resource availability • Medical service delivery structure • Policies, priority settings for public health outcomes AMR‐favoring environment:  potential factors • Mass population movement • Larger immuno‐compromised mixed‐up • More pathogens contaminations in environmental  devastation • Vulnerable governance and regulatory mechanism for  pharmaceuticals • Poor function of lab & surveillance networks • Limitation in AM & other medicinal resources • Loss of medical records, treatment follow‐up  Scale of impact may vary in emergencies,  strategic approaches to control  AMR  can provide better useful  channels to highlight AMR issues,  examples of practices, tools either for application to conventional AMR  control in general, primary health settings.  l    i      i   i ,   i       l       i     l   l     i li    i ,  l     i ,  l   i     li i     i l    l i   l,  i   l   i .  - 87 - Annex 4 Category indicator primary health care (PHC) emergency medical assistance (EMA) Paradigms Aim Health as a condition for human development and well being Physical survival as pre-condition for human development Relation to context In harmony with other sectors of society Part of a package of 'emergency relief measures' Resource use Use 'reasonable share' of all available Use 'all' that can be mobilized Technical dimension(rationalization) Optimization of effectiveness, efficiency Maximization Social dimension Autonomy and participation (responsiveness) Dignity and compliance Time perspectives Long Short Characteristics of care Objectives Cure, care and autonomy Cure is dominant over care and autonomy Qualitative points for approach Optimal balance between being effective, integrated, continuous and holistic Effectiveness takes precedence over other characteristics Determinant of care components Care provided is a compromise between need and demand Need get precedence over demand Characteristics of health services Accessibility(temporal, geographical) Permanent facilities are mandatory for curative activities and for emergencies; preventive activities can be intermittent Financial accessibility A balance to be struck between financial participation and financial accessibility Free of charge services Polyvalent or Specialized polyvalence for integrated, holistic care Specialized services Clients-provider relationship Whole range of valued aspects to be aimed at Quality of relationship to subordinate to other characteristics. Decentralization of health systems 1st line Polyvalent health centers to cover a defined population (1/5000~15000) Curative health posts (1/3000~5000) 2nd line District hospitals Referral hospitals Exceptions to two-tier system Peripheral extensions and intermediate can be justified. Community health workers seldom adequate. Home visitors and intermediate structures often needed. Vertical services Mobile team sometime justified Mobile teams and feeding centers often needed Articulation of services Two-tier integrated district health system, avoiding gap and overlap. A rational referral system to be encouraged. Often parallel health system; marginally linked to pre-existing health system. A strict referral system to be imposed. Management of decentralized health systems Management structure Team of professionals with autonomy over the different health facilities in a health district Team of professionals with full operational, administrative authority, high degree of autonomy. Logic in management Balancing medico-technical, administrative and sociological type of logic Medico-technical logic paramount Responsiveness to epidemic alerts Important Paramount Pre-established objectives May be counterproductive May be necessary Measures to improve resource mobilization Good quality of care, empathic relationship Relatively coercive methods can be justifiedAdherence to treatment strategies Structural dialogue with the community during care Conceptual gap analysis of 2 health service delivery approaches; primary health care (PHC) and emergency medical assistance (EMA) - 88 - Annex 4 Category indicator primary health care (PHC) emergency medical assistance (EMA) Sustainability Programme vs, Project Programme format preferable Project format preferable Institutional strengthening Managerial sustainability to be obtained Low priority Cost constraints (importance) Often paramount; sustainable health services to be organized at 'affordable' cost Limited; funding from international donors. Sustainability is not an aim. Funding sources Cost-sharing between government, international donors and users. Often exclusively funded by international donors. Actors Identity of decision-makers Local Often outsiders Relation with local authorities Collaboration needed Some links needed Role of central MoH To allocate resources, set norms and regulate (Stewardship) Often very limited Role of foreign assistance Mainly as technical assistance Substitution is often needed Manpower policy Staffs mainly constituted of health professionals on log-term contracts. Training is important. Staffs often recruited among beneficiaries, with short-term contracts. Training geared to perform standardized tasks Balance of private and public Increasingly, managers have to come to terms with private healthcare, both non-profit, and for-profit. Dominated by private, non-profit actors Conceptual gap analysis of 2 health service delivery approaches; primary health care (PHC) and emergency medical assistance (EMA) (continued) Variety Predictable, and streamlined to access to disease-specific health care services. Unpredictable, as mixed phases of population not based on the conventional community structure Mobility Urbanization, globalization (intentional) Migration, evacuation, isolation, marginalization(unintended) Health modality Predictable burden following to usual trend of diseases prevalence Target populations Unpredictable high burden with high probability of exposure to various diseases under psycho- physical pressure - 89 - Annex 4 Vector/rodent‐borne diseases (in emergencies/disasters) Specific  aspects / indicators/factors Characteristics of AMR Categories of  disaster/emergency Characteristics of  population in treatment  needs leadership / responsibility  / guidelines Malaria‐AM resistance  globally prevailed Direct impact on Hydro‐ meteorological,  geophysical landscape  changes (flood, cyclone,  earthquake, etc.) Possibility of Re‐ Infection/recurrence  Vaccination coverage  varied Impact from agricultural,  mining industries to be  considered (some also  related to food security) Resistant‐NTD agents: lack  of resistance info. Hantavirus, leptospirosis,  leishmaniasis, etc. Mobility of  vector/reservoir pop. In  addition to Human pop.  movement Urban vulnerability Increased exposure by  trade/travel, population  pressures, civil unrests  (including PH‐HR  deployment) IHR application ? Lack of basic treatment  measures  Preventive medication  prevailed pr co hly virulent  Psychological panic  Market pharmaceuticals  imarily poor regulatory  ntrol Resistance transmission  cycle with animals Possibility of hig haemorrhagic  infections  control  in population sometime  needed Lack of technical resources  on specific NTDs. WE CAN WORK MORE ON SUCH  CASE ASSESSMENT  Ref.: Sutherst RW., Global Change and Human Vulnerability to Vecor‐Borne Diseases, Clinical Microbiology Reviews, 17(1):136‐173(2004) - 90 - Annex 4 (Source: Price RN., et al. Vivax malaria: neglected  and not benign, Trop Med Hyg, 77: 79‐87 (2007) - 91 - Annex 4 Time No. of death Cumulative No. of infection(all diseases) Rainy season Higher temp. season Cold, dry season Crush injuries, trauma,  drowning, burn Diarrhea  Malaria ARI  Influenza Disaster Cumulative AM use  (rational + empirical, alternative + preventive) V ARI Time‐series model of AM use and diseases prevalence post disasters  (in the same population, one disaster‐basis) - 92 - Annex 4 Surgical infection for crush‐related wounds, injuries, blunt trauma (in emergencies/disasters) Specific  aspects / indicators/factors Characteristics of AMR Categories of  disaster/emergency Characteristics of  population in treatment  needs leadership / responsibility  / guidelines Water, soil contamination  of unusual pathogens,  polimicrobial Cases in almost type of  emergencies Probably larger  geographical coverage. Not always seeking  treatment services. Emergency response team  –project level approach Clostridium difficile, non‐ fermenting species,  enterobacteria. Large involvement of  gram(‐) pathogens. Case management burden  huge. Both community‐based,  health facility‐based  infection control needed Daily treatment may be  performed by non‐ specialist Many cases  repatriated or  evacuated . Sometime in  mix‐up with non‐injuries  but immuno‐suppressed  groups. As integral parts of routine  case management at health  facility base Ref.: Antimicrobial Therapy for Wound Infection after Catastrophic Earthquakes, NEJM, 363(26):2571‐73(2010) . Natural hazards‐specific  assessment may also be  useful - 93 - Annex 4 Disaster‐ 3 Disaster‐ 4 Disaster‐ 5 C u m u l a t i v e   A M   u s e /   N o .   o f   i n f e c t i o n Population growth/urbanization, globalization Time  Worsen scenario Better scenario No disaster scenario Disaster‐ 1 Disaster‐ 2 Time‐series model of cumulative AM use / No. of infection (longer perspective) A v o i d a b l e ? U n a v o i d a b l e ? C u m u l a t i v e   r i s k   f o r   e m e r g e n c e   a n d   t r a n s m i s s i o n   o f   A M R Generic AMR  control target? Baseline (ideal) - 94 - Annex 4 Changes required in ways of approach?  Priority settings –differences to be recognized for strategically, active  control  Time concept  (task shifting, resource allocation, etc.) Work components & structure  (‘preparedness’ or ‘response  measures’)  In which operational guidelines to address the AMR in emergencies?  ‐ Emergency Prep & Medical Response guidelines ‐ AMR control guidelines ‐ Diseases‐specific treatment guidelines ‐ Medicine lists  Lab‐diagnostic & surveillance issues need to be well highlighted for further solid evidence collection, strengthening currently available systems &  mechanisms  R&D priorities in which, how to be promoted - 95 - Annex 4 Health system building blocks service delivery/infrastructure, health workforce, health information, medical products,  financing, leadership & governance  Capacity development Education Clinical  interventions Protective  interventions Enabling  environment Socio economic  factors T a r g e t   p o p u l a t i o n ‐ b a s e d   r e v i e w   &   a n a l y s i s Diagnosis and treatment of immuno‐compromised cases: malnutrition, HIV/AIDS, TB, Malaria, NTDs, those with chronic diseases AMR surveillance (TB‐DOTS, HIV‐ART/PMTCT, malaria control, etc.) Management of  childhood illness Immunization, prophylaxis (MR, Hib, Cholera vaccines, Malaria‐IPT, PMTCT) Vector control (ex Malaria‐ LLINs, indoor spraying) Sanitation and Hygiene Surgical Infection control STI control , Reproductive Health Promoting Breast Feeding Chronic Diseases screening Nutritional support :Vitamin‐A and micro nutrients Prudent diagnosis and treatment  strategies for rational use of drugs Continuum of rational AM use for care feasible over time course ?  Prescriber & consumer education for proper medication, compliance Postpartum/ Newborn Care D i s e a s e ‐ s p e c i f i c   ( c a u s a l   a g e n t ‐ s p e c i f i c )   r e v i e w   &   a n a l y s i s health care  facility‐based community‐ based Laboratory  and  surveillance capacity strengthening Food security Points of Intervention TIME CONCEPT TARGET FOR INTERVENTION (POP. & Behavioral) Downstream – disease-specific area to be worked on in the particular guidelines SYSTEM DEVELOPMENT APPROACH Acknowledgements • Researchers, experts contributed to plenty of scientific evidences & resources to  address AMR issues • Meeting participants for valued contribution and fruitful discussion to develop our  recommendations, action plans. • WPRO colleagues HSD/HSE team; Dr Hendrik Bekedam, Dr Momoe Takeuchi, Dr Madeleine de Rosas‐ Valera DSE team;  Dr Alian Li, Dr Bipin Kumar Verma Dr Jeffrey M Partridge, Mr Thomas Cotter Dr Takeshi Kasai,  and  Secretaries: Ms Dyann Severo, Ms Mary Ann Gamilla, Ms Daisy Mae Soan, and  relevant support staffs • WPRO AMR working group members • WKC‐UHEM team; Dr Arturo Pesigan, Dr Jostacio Lapitan • Dr Rodger Doran, Thammasat University - 96 - Annex 4 - 97 - Annex 4 V. Urban Health Emergency Management Emergency and Humanitarian Action WHO Philippines Urban Health Emergency Management Dr Art Pesigan WHO Kobe Centre Urban Health is recognized as a global public health issue - 98 - Annex 4 Urbanization • Proportion of global population living in cities has increased dramatically in past century – 1900: 15% – Now : 50% and increasing • One third of the total urban population live in slums (1 billion) • 70% of urban population of developing countries live in slums 50% of the world is urban. 60% by 2025. 70% by 2050. United Nations World Urbanization Prospects (2007 Revision) - 99 - Annex 4 Recent Major Emergencies Affecting Cities  2010 – Chile (8.8) – Haiti  2011 – Great East Japan Earthquake (9.0) “While urban living continues to offer many opportunities, including potential access to better healthcare, today’s urban environments can concentrate health risks and introduce new hazards.” - 100 - Annex 4 Special Considerations…Urban Areas (1)  Concentration of population, homes and buildings, transportation  More ‘government’ in urban than in rural areas—more rules and regulations  Market pressures—low-income groups struggle to find affordable accommodation and health services Special Considerations…Urban Areas (2)  2010 – 2.5 billion urban dwellers in low- and middle-income nations  Africa considered predominantly rural but its urban population is now much larger than that of North America  Most of the world’s largest cities are low- and middle-income nations - 101 - Annex 4 Cities in Low Income Nations Face high levels of risk  Not because of monetary value of exposed assets  Due to inadequacies in their infrastructure  Poor quality of housing  Weakness of city institutions Projections 2010-2030  Almost all the growth in the world’s population will be in urban centres in low- and middle –income nations  Asia will undergo massive urban growth  Most of the urban population in low- and middle-income nations  Asia with 32% of world’s urban population in 1950 to 55% in 2030 - 102 - Annex 4 Health Challenges in Urban Areas  Water  Environment  Violence and injury  NCDs  Unhealthy diets and physical inactivity  Harmful use of alcohol  Risks associated with disease outbreak Health of Children in Urban Areas  Higher prevalence rate of diarrhea  Diarrheal diseases account for nearly 2 million deaths out of a total of almost 10 M among children under age of 5  1990 to 2006: – Industrialized countries: drop of under-5 mortality rates from 10 to 6 per 1 000 live births – Developing countries: drop of 103 to 79 per 1 000 live births - 103 - Annex 4 Communicable Diseases  Diarrheal diseases, parasitic infection or diseases associated with inadequate water and sanitation – Lancet (2005) • Nearly half of the urban population in Africa, Asia and Latin America  TB incidence – New York has 4x the national average TB infection rate – Some parts of London, TB incidence is higher than in China Indoor air pollution  Use solid fuels for household heating and cooking – 25 of city dwellers in developing countries – 70% of city dwellers in least developed countries  Exposure to indoor pollution (2004) – Estimated to cause about 2 M deaths globally (pneumonia, chronic lung disease, cancer) - 104 - Annex 4 Health effects •Temperature-related illness and death •Extreme weather- related health effects •Air pollution-related health effects •Water and food-borne diseases •Vector-borne and rodent- borne diseases •Effects of food and water shortages •Effects of population displacement CLIMATE CHANGE Based on Patz et al, 2000 The health effects of climate change Climate Change Risk Vulnerability of low-income urban residents  Greater exposure to hazards (living in unsafe sites)  Lack of hazard-reducing infrastructure  Less adaptive capacity  Less state provision of assistance  Less legal and financial protection - 105 - Annex 4 Disaster Impact Vulnerability gap in urban areas  Lack of knowledge and financial capacity of urban authorities to reduce risks and vulnerabilities  High proportion of urban households and communities limited in their capacity to reduce risk by – inadequate incomes, limited political influence, high land prices and corrupt practices in land-use management Making Cities Resilient  10 point Checklist for Local Governments 1. Organization and coordination 2. Budget 3. Risk assessments 4. Critical infrastructure that reduces risk 5. Safety of all schools and health facilities 6. Risk compliant building regulations and land-use planning 7. Education programmes and training 8. Protect ecosystems and natural buffers 9. Early warning systems and emergency management 10. Post disaster: needs of survivors at centre of reconstruction - 106 - Annex 4 What Cities Should Do  Assessment of vulnerabilities and capacity  Risk Management  Policy development  Response plan  Training/Human resource development  Stockpiling Good Practice Cities in Africa, Asia and Latin America Disaster risks reduced  Provision of basic infrastructure and services  Local governments map disaster risk  Action in partnership with local communities  Quality and effectiveness of urban government - 107 - Annex 4 VI. Managing medicines during emergencies: the role of WHO Managing medicines during emergencies: the role of WHO Outline • WHO’s contribution to managing medicines during emergencies • Medicine-issues during and after emergencies - 108 - Annex 4 Managing medicines: the problem Note: most experience in developing countries Two recurrent problems: – Needed medicines and medical supplies do not reach patients – Shipments of donated medicines and supplies that are not useful are being received Interagency Emergency Health Kit (IEHK) • Launched in 1990; revised in 2006. • Endorsed by: Ecumenical Pharmaceutical Network, International Committee of the Red Cross, International Dispensary Association (IDA), International Federation of Red Cross and Red Crescent Societies, International Organization for Migration, Medecins Sans Frontieres (MSF), Merlin, UNFPA, UNHCR, UNICEF, and WHO. • IEHK 2006 is designed principally to meet the first primary health care needs of a displaced population without medical facilities. – Its content is a compromise and there will always be some items which do not completely meet requirements. – An ideal kit can only be designed with an exact knowledge of the population characteristics, disease prevalence, morbidity patterns and level of training of those using the kit. - 109 - Annex 4 Interagency Emergency Health Kit (IEHK) • not designed for immunization or nutritional programmes. • not designed for reproductive health services. • does not include medicines against communicable diseases such as HIV/AIDS, tuberculosis or leprosy.  these may be ordered separately after an assessment of needs. • will always be supplied with a patient post-exposure prophylaxis (PEP) module; • will always be supplied with malaria modules  unless there is a specific request not to include these items at the time of ordering. IEHK 10 basic units: can be used by health care workers with limited training 1 supplementary unit: for use by physicians or senior healthcare workers Total: about 1000 kg and 4m3 - 110 - Annex 4 IEHK 2006: basic unit (for 1,000 persons for 3 months) Medicines Unit Quantity • albendazole, chewable tab 400mg tab 200 • aluminium hydroxide + magnesium hydroxide tab 1,000 • amoxicillin, tab 250 mg tab 3,000 • benzyl benzoate, lotion 25%5 bottle,1 litre 1 • chlorhexidine gluconate, solution 5% bottle,1 litre 1 • ferrous sulfate + folic acid, tab 200 + 0.4 mg tab 2,000 • gentian violet, powder 25 g 4 • ibuprofen, scored tab 400 mg tab 2,000 • ORS (oral rehydration salts) sachet for 1 litre 200 • paracetamol, tab 100 mg tab 1,000 • paracetamol, tab 500 mg tab 2,000 • tetracycline, eye ointment 1% tube, 5 g 50 • zinc sulfate, dispersible tab 20 mg tab 1,000 • Malaria module (can be withheld upon request) – artemether + lumefantrine, tab 20 + 120 mg assorted packages – quinine sulfate, tab 300 mg tab 2,000 IEHK 2006: basic unit – cont. Medical devices, renewable Unit Quantity • rapid diagnostic tests unit 800 • lancet for blood sampling (sterile) unit 1,000 • safety box for used lancets, 5 litres unit 2 • bandage, elastic, 7.5 cm x 5 m, roll unit 20 • bandage, gauze, 8 cm x 4 m, roll unit 200 • compress, gauze, 10 cm x 10 cm, non-sterile unit 500 • cotton wool, 500 g, roll, non-sterile unit 2 • gloves, examination, latex, medium, disposable unit 100 • soap, toilet, bar, approximately 110 g, wrapped unit 10 • tape, adhesive, zinc oxide, 2.5 cm x 5 m unit 30 Basic stationery (health card, pen) Treatment guidelines Medical devices/equipment (scissors, thermometer) - 111 - Annex 4 Drug donations have often created considerable challenges for the recipient country. Drug donations have often created considerable challenges for the recipient country.  Interagency Guidelines for Drug Donations. Developed and endorsed by: Caritas Internationalis, Churches Action for Health of the World Council of Churches, International Committee of the Red Cross, International Federation of Red Cross and Red Crescent Societies, International Pharmaceutical Federation, Medecins Sans Frontieres (MSF), Oxfam, Pharmaciens Sans Frontieres, UNAIDS, UNDP, UNFPA, UNHCR, UNICEF, World Bank and WHO. - 112 - Annex 4 Good Donation Practices • Why good donations practices? – Donated drugs are often not relevant for the emergency situation, for the disease pattern or for the level of care that is available – Drugs are unsorted and labelled in a language which is not easily understood – Double standards of drugs (donating returned drugs…) – Drugs arrive just before their expiry date etc … Guidelines for drug donations Core principles: 1. Donations should benefit the recipient 2. Respect wishes and authority of recipient 3. No double standards in quality 4. Communication between donor and recipients is essential - 113 - Annex 4 Examples of problems with medicine donations • Unknown products labelled in a language that is not understood Some women (temporarily) lost eyesight after being given a donated, veterinary drug (Lithuania, 1993) • Products may be useless or unnecessary A donation to Southern Sudan contained contact lens solution and appetite stimulants (Sudan, 1990) • Medicines may be sub-standard or expired 17,000 tons of inappropriate donations; estimated disposal cost 34 million US$ (Bosnia and Herzegovina, 1992-1996) • Inappropriate quantities and/or unsorted medicines 5,000 tons of drugs and supplies received – it took 50 people six months to obtain an overview of what had been received (Armenia, 1988) Volunteers trying to sort donated medicines. - 114 - Annex 4 Guidelines for drug donations • Prior information to and consent of recipient • Approved for use in recipient country • Presentation, formulation and strength commonly used in recipient country • Comply with quality standards in both donor and recipient country • No returned drugs or samples • One year remaining shelf-life upon arrival * • Label to contain INN; in language that is understood in recipient country • Preferably large/hospital packs • Proper outer packing & packing list • Value: wholesale price of generic equivalent • Transport, handling, storage etc paid by donor * * Except when recipient explicitly agreed otherwise Sources of obsolete pharmaceuticals: 1. Products damaged by the tsunami; 2. Products provided as aid which are not appropriate; 3. Products in stock that have become or will become obsolete before their likely use. 1. 3. 2. - 115 - Annex 4 • Damaged, expired, unidentifiable, useless, inappropriate medicines; medicines whose use is not authorized; excess medicines • Pose health risks: when stored in unsecured locations, scavengers may pick them up and they end up circulating and being used, which can result in harm to people • Pose environmental risks: – dangerous per se (e.g. antibiotics), and – due to chemical transformations and reactions, their toxicity could increase Obsolete pharmaceuticals Local disposal of obsolete pharmaceuticals - only if emission control - extract from packaging; labour-intensive - Aceh: need to rebuilt kiln first (takes 2-3 years) cement kiln - Aceh: no emission controls => enters environment - capacity problem (it would take + 8 years) incineration (hosp.) - labour-intensive - increases volume ! - risk of eventual release into environment immobilization - ok for some products e.g. NaCl infusion; volume water-treatment plant - ok for some products e.g. dressings; volume - risk of eventual release into environment engineered landfill - risk of scavenging & public exposure - environmental contamination open dump None of these options seem appropriate - 116 - Annex 4 Landfill- how? – Open uncontrolled non-engineered dump • Untreated waste discharged into an uncontrolled, non-engineered open dump is not recommended • Waste should be discharged after immobilization by encapsulation or inertization • Un immobilized waste must be covered rapidly with large quantities of municipal waste to prevent scavenging • High risk of contamination of drinking water – Engineered landfill: protection from loss of chemicals into the aquifer – Highly engineered landfill • A site that is adequately situated, constructed and managed • An appropriate landfill consist of an evacuated pit isolated from watercourses Landfill- what type of medicines? • Engineered landfill – Waste solids, semi-solids and powders, preferably after immobilization. – PVC (polyvinyl chloride) plastics • Highly engineered landfill – Limited quantities of untreated solids, semi-solids and powders. – Disposal of waste pharmaceutical after immobilization preferable. – PVC plastics - 117 - Annex 4 Incineration- what type of medicines? • High temperature incineration with temperatures greatly in excess of 1200°C: – Solids, semi-solids, – powders, – antineoplastics, – controlled substances • Medium temperature incineration with two-chamber incinerator with minimum temperature of 850°C. – In the absence of high temperature incinerators, solids, semi- solids, powders and – Controlled substances Waste immobilization • Encapsulation: Immobilizing the pharmaceuticals in a solid block within plastic or steel drum. • Drums are filled to 75% capacity with solid and semi-solid pharmaceuticals, and fill up with: – Plastic foam – Bituminous sand – Cement mortar – Clay material • When dry, seal containers and landfill to restrict access to and reduce mobilization of hazardous substances • Encapsulation of antineoplastic drugs require a slightly different technique Solids, semi-solids Powders Liquids Antineoplastics Controlled substances - 118 - Annex 4 Waste immobilization • Method – Remove Packaging – Grind material (Road Roller) – Add Water (5%), Lime (15%) and Cement (15%) – Then, either • When dry, store or landfill or • When wet, decant into municipal waste in landfill • Types of medicines – Solids, semi-solids – Powders – Antineoplastics – Controlled substances Inertization is a variant of encapsulation and involves removing the packaging materials, paper, cardboard and plastic, from the pharmaceuticals Other treatment and disposal methods • Sewer – Some liquid pharmaceuticals, e.g. syrups and IV fluids, can be diluted with water and flushed into the sewers in small quantities Antineoplastics, and undiluted disinfectants, and antiseptics not recommended • Burning in open container – Packaging, paper cardboard Pharmaceuticals and PVC should not be destroyed by burning at low temperature in open containers Chemical decomposition • not recommended unless chemical expertise and materials available • not practical for quantities over 50 kg. - 119 - Annex 4 Disposal method_ summary • Pharmaceuticals are ideally disposed of by high temperature (above 1,200 ºC) incineration. Such incineration facilities, equipped with adequate emission control, are mainly to found in the industrialized world. • Quotations for disposing of the pharmaceutical waste in Croatia and Bosnia and Herzegovina in this way range from US$ 2.2\ kg to US$ 4.1\kg. • To incinerate the stockpile of waste pharmaceuticals in Croatia (1992- 1996) would therefore cost between US$4.4 million and US$ 8.2 million. • To dispose 17,000 metric tons of inappropriate donations were received with an estimated disposal cost of US$34 million. Bad medicines donation pharmaceutical waste • Tsunami relief in Indonesia– In 30 October 2005 newsletter the Pharmaciens Sans Frontières Comité International (PSF-CI - see www.psfci.org) reports on its assessment of medicine donations to Banda Aceh province in Indonesia after the 26 December 2004 tsunami: – medicines were donated by 140 donors, of which 53 were national organisations and 48 were international organisations from 39 countries – 4000 tonnes of medicine were received for a population of less than 2 million people – medicines were labelled in more than 16 foreign languages – nearly 60% were not on the national List of Essential Drugs – 10% had expired before they reached Banda Aceh – 30% were due to expire in less than 6 months or had missing expiry dates – those medicine that were appropriate were received in quantities equivalent to 6- 8 years' use – 345 tonnes (1150 cubic metres) have been identified for destruction, which will cost an estimated Euro 1.4 million (75 cubic metres of donated medicines were destroyed in February 2005) - 120 - Annex 4 To sum up 1. Drug donations can be essential in alleviating suffering. 2. Some donors have knowingly sent expired stocks. How can this be prevented? 3. Large consignments of obsolete drugs are a threat to human health and to the environment. They need to be secured, inventoried/segregated and disposed off safely. 4. Safe disposal of obsolete drug donations costs 2000- 5000 US$ per tonne. Who will pay? 5. Adherence to WHO Guidelines on Drug Donations would help to prevent this problem from recurring in future emergencies, but is voluntary. - 121 - Annex 4 VII. Operational Framework for Health Cluster Response in the Western Pacific Region Health Cluster Operational Framework: “Three Plus One” Functional Areas Division of Health Security and Emergencies (DSE) WHO Western Pacific Regional Office (WPRO) 2Division of Health Security and Emergencies (DSE)WHO Western Pacific Regional Office (WPRO) Emergency & disaster situation… - 122 - Annex 4 3Division of Health Security and Emergencies (DSE)WHO Western Pacific Regional Office (WPRO) Humanitarian Reform in 2005 • Recommendations to improve – Predictability – Accountability – Leadership – Partnership • 3 pillars of reform Improved Humanitarian Response Partnerships St re ng th en ed H C S ys te m Im pr ov ed   fin an ci ng Cl us te r  A pp ro ac h 4Division of Health Security and Emergencies (DSE)WHO Western Pacific Regional Office (WPRO) “In the event of a sudden major new emergency requiring a multi‐sectoral response with the  participation of a wide range of international  humanitarian actors, the cluster approach should be  used from the start in planning and organizing the  international response.“ IASC Guidance Note When do we use Clusters? - 123 - Annex 4 5Division of Health Security and Emergencies (DSE)WHO Western Pacific Regional Office (WPRO) WHO: Health Cluster Lead 6Division of Health Security and Emergencies (DSE)WHO Western Pacific Regional Office (WPRO) How to operationalize health cluster approach? b - 124 - Annex 4 7Division of Health Security and Emergencies (DSE)WHO Western Pacific Regional Office (WPRO) Regional Health Cluster Forum • First Regional Health Cluster Forum on  Humanitarian Emergencies, 22‐24 August 2011,  Kobe, Japan • Aimed to develop a simply, common  operational framework for health cluster  response at the country level 8Division of Health Security and Emergencies (DSE)WHO Western Pacific Regional Office (WPRO) Why Framework? • Emergency and disaster management requires a  multidimensional approach involving in multiple  actors • A cluster approach developed to improve the  efficiency and effectiveness of humanitarian  response • Various policies, guides and tools related to the  global health cluster approach are in place - 125 - Annex 4 9Division of Health Security and Emergencies (DSE)WHO Western Pacific Regional Office (WPRO) Why Framework? • However, the health cluster approach and global  guidelines are not fully operationalized in a systematic  way, taking consideration of region context • In the Western Pacific Region – Health security threats from various diseases, public health  emergencies and disasters – Relatively strong government system in place  – Enhanced existing programme such as EIDs 10Division of Health Security and Emergencies (DSE)WHO Western Pacific Regional Office (WPRO) Process of developing an operational framework… Implementation Operational  Framework Guidelines GuidelinesPolicyPolicy ExperienceExperiences  - 126 - Annex 4 11Division of Health Security and Emergencies (DSE)WHO Western Pacific Regional Office (WPRO) From various expected outcomes to  “Three in One” functional area 12Division of Health Security and Emergencies (DSE)WHO Western Pacific Regional Office (WPRO) “Three plus One” Functional Areas Service  delivery Information   Resource Health Cluster  M&E  - 127 - Annex 4 13Division of Health Security and Emergencies (DSE)WHO Western Pacific Regional Office (WPRO) Information for action • Disasters often change health needs and remain  dynamic at the different phases  • Information is the key to assessing heath needs and  public heath risks that inform appropriate  public  health actions • Many ways of collecting, organizing, assessing and  using information before, during and after disasters • Need to operationalize and simplify the process of  collecting and using information for health  assessments and actions   14Division of Health Security and Emergencies (DSE)WHO Western Pacific Regional Office (WPRO) Proposed framework for information - 128 - Annex 4 15Division of Health Security and Emergencies (DSE)WHO Western Pacific Regional Office (WPRO) Action‐oriented modification  1. Pre‐event basic information • Country profile (district‐level)  2. Preliminary health needs assessment • Within 24‐72 hours for immediate health intervention • Jointly with the Ministry of Health, whenever possible 3. Continuing health needs and risks assessments • Jointly with health cluster partners • Information includes “health service delivery” 16Division of Health Security and Emergencies (DSE)WHO Western Pacific Regional Office (WPRO) Health Service in Emergency • Post‐disaster health needs depend on many factors – Type and extent of disasters – Stage of emergency and disaster response – Population and geographical locations affected • Various way of categorizing heath services – IASC Global Health Cluster Guide 2009 – Sphere Handbook 2011 – Many others - 129 - Annex 4 17Division of Health Security and Emergencies (DSE)WHO Western Pacific Regional Office (WPRO) 18Division of Health Security and Emergencies (DSE)WHO Western Pacific Regional Office (WPRO) Recommended health service grouping… 1. Clinical services (including injury) 2. Child health 3. Nutrition  4. Communicable diseases 5. STI & HIV/AIDs 6. Maternal and new‐born health 7. Sexual violence 8. Non‐communicable diseases 9. Mental health and psychosocial support (MHPSS) 10. Environmental health - 131 - ANNEX 5 NOTES FROM GROUP WORK I. Group Work Discussion Questions (Day 1): 1. Are there any AMR issues to be addressed during an emergency response? • Are AMR issues different in emergency settings than in normal ("peace time") settings? • What are some of the main issues related to drug use during emergencies? • Are there examples how AMR issues could be exacerbated during emergencies? 2. How can emergency and disaster response include AMR prevention and control considerations? • Is it feasible to address AMR issues during emergency situation? Why? GROUP‐1 Work on Q‐1 - 132 - Annex 5 Question‐1: (1)  Yes,  – Information/data for more solid evidence in  emergency settings for any decision‐making – Surveillance improvement needed: appropriately  designed for AMR in emergencies (advocacy more on  AMR needed) – Difficulties on definition(bioterrorism issues  included?), target agents, type of hazards, time‐phase  for operation Question‐1: (2) Main issues to related to drug use – Control of drug supply (shortage‐influx) with appropriate  standards, coordination/ regulatory mechanism (donation  protocol, …)  – Need for establishment of knowledge base body to facilitate  national guidelines to follow – Counterfeit drug  (even in normal situation, donation) – Coordination among external & local organizations  (systematically by some facilitator(s) (coordinating bodies) – Patients’ compliance, record keeping – Drug disposal: environmental contamination (incinerator  management)  – Animal husbandry: Research‐agenda - 133 - Annex 5 Question‐1: (3) Examples to exacerbate during emergences – Interruption of medical treatment  eg. TB treatment  Issues to be addressed: – Research agenda: Scale of target populations,  definitions of  AMR, cause of AMR, monitor the  capacity of organizations in disaster, medical disposal – Best practices sharing  ‐ to reflect to bigger technical  frameworks – Recording systems to keep track of care – Lab‐support – Training capacity  even during emergencies  – More risk communication mechanism Question‐2 Is it feasible t address AMR issues during emergency  situation? Not necessary to develop emergency‐specific   by complying to standard guidelines used for  routine AM use – Prevention is more important! - 134 - Annex 5 WHO Western Pacific Region Informal Consultative Meeting on AMR Prevention and Control in Emergencies/Disasters Group 2 Discussion on Response – Day 1 Manila, 29 November 2011 WHO Western Pacific Region AMR issues to be addressed  during emergency response ? • Need to resolve whether treatment guidelines should be  different in “emergency, field” situation than during  “peacetime” situation. • There are no AMR guidelines (as to antibiotic choices, doses,  duration of treatment) for emergency situations. • It will be difficult to decide on appropriate guidelines in an  “emergency, field” situation; different types of hazards (i.e.  trauma, flooding, volcanic eruptions) produce different  medical problems and different types of infections - 135 - Annex 5 WHO Western Pacific Region AMR issues to be addressed  during emergency response ? • There are many priority health issues to be managed  during emergency response, there may be a  challenge to put AMR as a priority • Different types of emergencies and disasters may  have different types of diseases with treatment  needs • An important AMR issue to be addressed is “need  different types of treatment guidance during  emergencies” (especially for the field e.g. camps)  – No lab capacity to support diagnosis  WHO Western Pacific Region Comparison of “peacetime” vs. “emergency  field” situation Parameter Emergency field Emergency Intact  hospital Peacetime Lab testing Not available Available Available Drug formulary Modified (ex.  Hongkong) _>  potential misuse  (overuse,  underuse) Standard Standard Availability of  Antibiotics Limited  availability in  terms of quantity,  quality (ideal  antibiotics not  available);  antibiotics for  pediatrics may be  short Generally  available Generally  available - 136 - Annex 5 WHO Western Pacific Region Comparison of “peacetime” vs. “emergency  field” situation Parameter Emergency field Emergency Intact  hospital Peacetime Health care  worker 1) Limited  availability of  physicians ‐ >  inappropriate  use of  antibiotics 2) Health care  workers who  are themselves  victims of the  disaster are  physically &  mentally  overburdened  1) Generally  available 2) Generally less  physically and  mentally  overburdened 1)Generally  available 2) Generally less  physically and  mentally  overburdened WHO Western Pacific Region Comparison of “peacetime” vs. “emergency  field” situation Parameter Emergency field Emergency Intact  hospital Peacetime Environment Dirty environment  ‐> multiple  infections  requiring  antibiotics with  broader coverage Normal clean Normal clean Standard  treatment  protocol Daily shifting of  physicians ‐> may  be following  different  treatment  protocols Stable pool of  physicians ‐>  follow same  treatment  protocols Stable pool of  physicians ‐>  follow same  treatment  protocols - 137 - Annex 5 WHO Western Pacific Region Comparison of “peacetime” vs. “emergency  field” situation Parameter Emergency field Emergency Intact  hospital Peacetime Infection control  protocols Usually  overlooked (no  water, no linen,  no disinfectants);  PPE Initially none  for first 2‐3 days  then become so  many Implemented well Implemented well Quality of  antibiotics  Antibiotics may be  improperly stored Antibiotics kept  properly stored Antibiotics kept  properly in the  pharmacy WHO Western Pacific Region AMR issues to be addressed  during emergency response ? • AMR issues may be different in emergency settings  than in “peace time” – Treatment habits (e.g. due to frequent change of medical  personnel) – Mental and psychosocial effects of affected medical  practitioners  – Inappropriate use of drug due to lifesaving purpose – Availability and quality of drug during an emergency – Lack of medical records – Risk environment and behaviours – ICP practice - 138 - Annex 5 WHO Western Pacific Region AMR issues to be addressed  during emergency response ? • AMR work contributing to emergency response  – Research on AMR (e.g. data and evidence) • Feasibility of addressing some priority AMR issues – E.g. Treatment guideline - 139 - Annex 5 II. Group Work Discussion Questions (Day 2): 1. What needs to be put in place during "peace time" in order to support responses to emergencies that take AMR prevention and control into consideration? • What system capacities need to be in place? • Is data needed? If so, what kind of data is needed? • Are there SOPs or guidelines that need to be developed? GROUP WORK‐DAY2: Group 1 1) How can AMR programme managers support and facilitate the  network of emergency managers? (strategy + immediate actions) Routine  Systems to be strengthened ‐Information Systems  (central, local health information management systems) Surveillance systems Advocacy to highlight further on AMR in use of the evidences on  emergencies Help emergency managers (EM) to understand AMR Provide guidelines /protocols on drug donations for AMR control Provide M&E guidelines 2) How emergency programme managers contribute to AMR  prevention and control? (strategy+immediate actions) • IASC to include AMR programme managers • EM programme managers to disseminate treatment/donation  guidelines, protocols to enforce them • EM programme managers to conduct, collect data needed 3) NO  single AMR programme managers per country – coordinating body in country on AMR • Inquire among managers ‐> AMR country focal points - 140 - Annex 5 Recommendations for the Next Steps 1. Research agenda=gather and have the evidences  first. “what the research agenda would be?” 2. Develop advocacy plans: ongoing advocacy on AMR  to continue & strengthen capacity of structure on  lab, surveillance , training, etc. Group Work Day 2: Group 2 (written on a flipchart) AMR Contribution to Emergencies * AMR data/pre-event info on AB use, etc made available as part of profiling * AMR group proactively participate in the decision for drug formula for emergencies and needs/risks assessment * Emergencies team consult the "AMR Group" for planning, assessment * Strengthen routine AMR surveillance, coordination mechanism, one entry point for AMR group Preparedness = use routine system and information Versus Readiness = task force * Increase response capacity including AMR information: e.g. policy, GL, mechanism, training, exercise * SOP for failed treatment (index case) AMR Surveillance: gives ideas for suspicious cases? Possible in the emergency, field situation ICP: need scale up in emergencies? Universal precaution Needs: 1. Information 2. Task force 3. Initiate action for what's lacking

Informations clés
Type de document Technical Documents
Date d'adoption
Source Organisation mondiale de la santé