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The WHO application of ICD-10 to deaths during the perinatal period: ICD-PM

11 août 2016 Organisation mondiale de la santé

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The WHO application of ICD10 to deaths during the perinatal period: ICD-PM [JP1]

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Acknowledgements The WHO application of ICD-10 to deaths during the perinatal period: ICD-perinatal mortality (ICDPM) was developed by the World Health Organization (WHO) Working Group on Perinatal Death Classification. The following individuals (in alphabetical order) participated in the activities of the Working Group: Emma Allanson, Hannah Blencowe, Doris Chou, Jahnavi Daru, Jan Jaap Erwich, Vicki Flenady, Frederik Frøen, Jason Gardosi, Rogelio Gonzalez, A. Metin Gülmezoglu, Kate Kerber, Joy Lawn, Edward A. Liechty, Jaouad Mahjour, Priya Mannava, Matthews Mathai, James Neilson, Robert C. Pattinson, Cynthia Pileggi-Castro, Zahida Qureshi, Cleo Rooney, Lale Say, Ӧzge Tunçalp, Joshua P. Vogel and Khalid Yunis. During the development phase, ICD-PM was piloted in two databases in the United Kingdom and South Africa, with additional contributions from Amanda Quach and Andre Francis.

Furthermore, we thank Vanessa Brizuela, Sarah de Masi, Robert Jakob, Kapila Jayaratne, Olufemi Oladapo, Nathalie Roos and Florina Serbanescu for their technical review and comments on this work.

Emma Allanson and Ӧzge Tunçalp prepared the alpha and beta drafts of this work, based on the guidance provided by the Working Group and the pilot studies. Jan Jaap Erwich, Vicki Flenady, Frederik Frøen, Jason Gardosi, A. Metin Gülmezoglu, James Neilson and Robert C. Pattinson revised the beta draft. The final version of the document was prepared by Emma Allanson, Ӧzge Tunçalp and A. Metin Gülmezoglu.

This work was funded by the United States Agency for International Development (USAID) and the UNDP/UNFPA/UNICEF/WHO/World Bank Special Programme of Research, Development and Research Training in Human Reproduction (HRP).

Editing: Green Ink, United Kingdom (www.greenink.co.uk)

Contents Acknowledgements ............................................................................................................................ ii Abbreviations and acronyms .............................................................................................................v Executive summary ........................................................................................................................... vi 1. Introduction .................................................................................................................................... 1 2. Development of The WHO application of ICD-10 to deaths during the perinatal period: ICD-PM (ICD-perinatal mortality) .................................................................................................... 5 3. ICD-10 procedures for death certificates ................................................................................... 7 3.1 Perinatal cause of death and maternal condition on the death certificate ..................................... 7 3.2 Certification of cause of perinatal death .......................................................................................... 7 3.3 Certification of maternal condition at the time of perinatal death ................................................ 11 3.4 Coding the death certificate ........................................................................................................... 13

4. The WHO application of ICD-10 to deaths during the perinatal period ............................. 14 4.1 Application of ICD-PM to the cause of perinatal death .................................................................. 14 4.2 Application of ICD-PM to the maternal condition in perinatal death............................................. 14 4.3 Summary and tabulation of ICD-PM ............................................................................................... 20

5. Specific conditions........................................................................................................................ 23 5.1 Growth restriction........................................................................................................................... 23 5.2 Preterm labour ................................................................................................................................ 23 5.3 Prematurity ..................................................................................................................................... 24 5.4 Obstructed labour ........................................................................................................................... 25 5.5 HIV and AIDS ................................................................................................................................... 25 5.6 Termination of pregnancy............................................................................................................... 26

6. Case examples............................................................................................................................... 28 6.1 Case 1 .............................................................................................................................................. 28 6.2 Case 2 .............................................................................................................................................. 29 6.3 Case 3 .............................................................................................................................................. 30 6.4 Case 4 .............................................................................................................................................. 31

7. Implications for practice and research ..................................................................................... 32 8. Perinatal audit .............................................................................................................................. 32 9. Conclusion ..................................................................................................................................... 33 References ......................................................................................................................................... 34 Annex A: ICD-PM groups and ICD-10 codes for antepartum deaths ....................................... 36 A1 Congenital malformations, deformations and chromosomal abnormalities .................................. 36 A2 Infection ........................................................................................................................................... 40 A3 Acute antepartum event ................................................................................................................. 42 A4 Other specified antepartum disorder .............................................................................................. 43 A5 Disorders related to length of gestation and fetal growth .............................................................. 46 iii

A6 Antepartum death of unspecified cause ......................................................................................... 47

Annex B: ICD-PM groups and ICD-10 codes for intrapartum deaths ....................................... 48 I1 Congenital malformations, deformations and chromosomal abnormalities ................................... 48 I2 Birth trauma ...................................................................................................................................... 52 I3 Acute intrapartum event .................................................................................................................. 54 I4 Infection ............................................................................................................................................ 55 I5 Other specified intrapartum disorder ............................................................................................... 56 I6 Disorders related to fetal growth ..................................................................................................... 58 I7 Intrapartum death of unspecified cause........................................................................................... 60

Annex C: ICD-PM groups and ICD-10 codes for neonatal deaths ............................................. 61 N1 Congenital malformations, deformations and chromosomal abnormalities .................................. 61 N2 Disorders related to fetal growth .................................................................................................... 65 N3 Birth trauma .................................................................................................................................... 66 N4 Complications of intrapartum events.............................................................................................. 69 N5 Convulsions and disorders of cerebral status ................................................................................. 70 N6 Infection........................................................................................................................................... 71 N7 Respiratory and cardiovascular disorders ....................................................................................... 76 N8 Other neonatal conditions .............................................................................................................. 79 N9 Low birth weight and prematurity .................................................................................................. 86 N10 Miscellaneous ................................................................................................................................ 87 N11 Neonatal death of unspecified cause ............................................................................................ 88

Annex D: ICD-PM groups and ICD-10 codes for maternal conditions in perinatal death .... 89 M1 Complications of placenta, cord and membranes .......................................................................... 89 M2 Maternal complications of pregnancy ............................................................................................ 91 M4 Maternal medical and surgical conditions...................................................................................... 93 M5 No maternal condition.................................................................................................................... 95

Abbreviations and acronyms ABO HRP ABO (ABH) blood group system UNDP/UNFPA/UNICEF/WHO/World Bank Special Programme of Research, Development and Research Training in Human Reproduction International Statistical Classification of Diseases and Related Health Problems ICD, 10th revision The WHO application of ICD-10 to deaths during pregnancy, childbirth and the puerperium: ICD-maternal mortality The WHO application of ICD-10 to deaths during the perinatal period: ICDperinatal mortality not otherwise specified termination of pregnancy United Nations Development Programme United Nations Population Fund United Nations Children’s Fund United States Agency for International Development World Health Organization

ICD ICD-10 ICD-MM

ICD-PM

NOS TOP UNDP UNFPA UNICEF USAID WHO

Executive summary

With more than 5 million perinatal deaths occurring globally each year, ending preventable stillbirths and neonatal deaths will continue to form a significant part of the international public health agenda beyond 2015. The Every Newborn Action Plan clearly highlights that we will get a triple return on our investment if we focus on high coverage of care during birth and in the immediate neonatal period, resulting in saving the lives of both mothers and babies, alongside the prevention of stillbirth. In the regions with the highest mortality burden, perinatal deaths are poorly recorded and are therefore most likely to be unaccounted for. The first step in targeting programmes that address perinatal mortality is the accurate capture and classification of the causes of those deaths across all settings, using a globally applicable and comparable system.

The WHO application of ICD-10 to deaths during the perinatal period: ICD-perinatal mortality (ICDPM) is modelled on The WHO application of ICD-10 to deaths during pregnancy, childbirth and the puerperium: ICD-maternal mortality (ICD-MM). ICD-PM, in the same vein as ICD-MM, is based on the 10th revision of the International Statistical Classification of Diseases and Related Health Problems (ICD-10) and its coding rules. It is intended to facilitate the consistent collection, analysis and interpretation of information on perinatal deaths. Improved reporting will also facilitate the coding of conditions.

This document presents:   a brief summary of the development of this guide; a grouping system for identification of perinatal deaths using existing ICD-10 codes, which countries can immediately implement.

ICD-PM is intended to be used by those who assist health-care providers and those charged with death certification, to guide them in correctly documenting the pertinent information by clarifying which conditions should be considered underlying causes of death, thus improving accurate death attribution. As a result, it will improve the information available to coders, programme managers, statistical offices and academics/researchers. vi

This document can help to clarify the application of ICD-10 and to standardize the identification of perinatal deaths. Its principles should be applicable for categorizing deaths via data collected through civil registration, surveys, hospital information systems, verbal autopsies, confidential enquires and other special studies.

There are three distinct features of ICD-PM: 1. It captures the time of a perinatal death in relation to its occurrence in the antepartum (before the onset of labour), intrapartum (during labour but before delivery) or neonatal period (up to day 7 of postnatal life). Note: While ICD-PM is designed to be used for all antepartum, intrapartum and early neonatal deaths, it can also be used for late neonatal deaths, which – although falling outside the perinatal period according to ICD – may be a consequence of events in the perinatal period. 2. It applies a multilayered approach to the classification of cause of death, such that it reflects varying levels of available information depending on the setting. By using ICD-PM, mutually exclusive clinical conditions that lead to the identification of a single cause of perinatal death are determined and linked with an ICD code. 3. It links the contributing maternal condition, if any, with perinatal death, reflecting that the condition of the mother at the time of the death is closely linked with perinatal death, given that a maternal condition is frequently found in the context of a perinatal death.

By identifying the timing of death as part of a multilayered approach to classification, ICD-PM applies ICD-10 in such a way that it reflects locally available information. By requiring that a maternal condition be documented for every perinatal death (even if it is “no maternal condition”), the system reflects the inherently linked health outcomes of these two groups of patients.

Capturing the chain of events that led to the perinatal death, from both the maternal and the perinatal side, informs the design and development of preventative and therapeutic measures. vii

Doing this imparts obvious benefit to both mother and baby when advocating for programmes aimed at one unifying pathology (e.g. hypertension) or clinical scenario (e.g. intrapartum care). ICDPM draws on this evidence and logic to make capturing maternal condition an integral part of the classification of perinatal death. This also aligns with the recommendation in the Every Newborn Action Plan that encourages capturing maternal complications as part of perinatal death registration.

This document, the annexes and tables are intended to:    facilitate consistent reporting of the clinical conditions in perinatal death identify codes for perinatal death according to the timing of death identify the conditions and codes for the maternal condition contributing to the perinatal outcome.

Ultimately, standardization of the attribution of cause of death will improve:     interpretation of data on perinatal mortality interpretation of data on the maternal condition in the context of perinatal mortality analysis of the causes of perinatal mortality allocation of resources to both mother and baby programmes intended to address mortality.

Applying ICD-PM will decrease errors in coding and improve attribution of cause of perinatal death. This will enhance the usability and comparability of perinatal mortality statistics generated from ICD data. It is recommended that countries adopt ICD-PM, and that statistical offices and academics collect data according to it.

[START SHADED BOX] This guide should always be used in conjunction with the three volumes of ICD-10. The suggested code should be verified, and possible additional information should be coded using the full ICD-10,

viii

volumes 1 and 3; rules for selection of underlying cause of death and certification of death apply in the way they are described in ICD-10 volume 2.1 [END SHADED BOX]

All online versions of ICD-10 are available at: http://www.who.int/classifications/icd/icdonlineversions/en/; the current 2016 version is available at: http://apps.who.int/classifications/icd10/browse/2016/en

1. Introduction

With more than 5 million perinatal deaths occurring globally each year (1, 2), ending preventable stillbirths and neonatal deaths will continue to form a significant part of the international public health agenda beyond 2015 (3). In the regions with the highest mortality burden, perinatal deaths are poorly recorded and are therefore most likely to be unaccounted for (3). The first step in targeting programmes that address perinatal mortality is the accurate capture and classification of the causes of those deaths across all settings, using a globally applicable and comparable system. Perinatal outcomes are also intricately linked to maternal condition, and targeted programmes for reducing perinatal mortality may also affect maternal mortality, as the underlying causes are so entwined. Ideally programmes aimed at improving the health outcomes of these two groups should be integrated. Applying a classification system for perinatal death in such a way that the perinatal deaths are linked to maternal conditions and maternal death enables this process. The WHO application of ICD-10 to deaths during the perinatal period: ICD-perinatal mortality (ICD-PM) is outlined in this document.

ICD-PM is based on the 10th revision of the International Statistical Classification of Diseases and Related Health Problems (ICD-10) (4) and follows all rules for mortality coding as described in ICD-10 volume 2: instruction manual (5). ICD-PM is a programmatically driven system with several advantageous features in the way the existing ICD-10 codes are applied. The relevance of existing codes is clarified, and there is meaningful grouping of ICD categories to enable both consistent application of ICD coding and rules, and analysis of that application to drive programmes aimed at reducing mortality.

In essence, the features of ICD-PM are: 1. It identifies the time of death as antepartum (before the onset of labour), intrapartum (during labour but before delivery) or neonatal (up to day 7 of postnatal life). Note: While ICD-PM is designed to be used for all antepartum, intrapartum and early neonatal deaths, it can also be used for late neonatal deaths, which – although falling

outside the perinatal period according to ICD – may be a consequence of events in the perinatal period. 2. It is multilayered such that the depth of classification can reflect the locally available intensity of investigation (this reflects the current ICD-10 system where cause of death is assigned in a stepwise process, following the progression of underlying clinical conditions leading to death). 3. It links the contributing maternal condition, if any, with perinatal death.

Ultimately all of these features allow easy identification of where a programme intervention should be targeted to improve both maternal and perinatal outcomes.

The timing of a perinatal death may be the only piece of information captured when classifying a death in poorly resourced settings, where the burden of disease is the greatest (6). In such settings, the data on timing can be used to make international comparisons as well as programmatic decisions to focus local efforts and interventions. Moreover, bringing stillbirth and neonatal death together in a standardized system of definitions and coding rules not only allows comparability but, given the widespread use of ICD (117 countries use ICD for mortality reporting), it has great potential to bring to the foreground those deaths that have previously gone unnoticed.

ICD-PM is designed to be used for all antepartum, intrapartum and early neonatal deaths. The early neonatal deaths fall within the perinatal period as defined by ICD-10, and therefore should always be classified using ICD-PM. Late neonatal deaths, while falling outside the period defined as perinatal by ICD, may occur as a consequence of events in the perinatal period; therefore, the benefit of using ICD-PM for these cases is the same as for the early neonatal deaths. Using the principles of ICD-PM in these late neonatal deaths and linking the condition of the baby and the mother is valuable from both a classification and a programmatic point of view. A good example of this is obstructed labour in a term pregnancy that results in hypoxic ischaemic encephalopathy, where the neonatal death occurs on day 8. With regard to capturing perinatal cause of death and maternal condition, there is little distinction between this case and a case with the same clinical scenario but where the neonatal death occurs on day 6. There is, however, a group of late neonatal deaths that are remote from the perinatal events and thus not necessarily adequately captured by

using the ICD-PM-linked ICD codes that apply to perinatal deaths. For example, a neonate that has an uncomplicated antepartum, intrapartum and early neonatal period but returns to hospital on day 21 and subsequently dies following a diarrhoeal illness. As such, the members of the WHO Working Group on Perinatal Death Classification (who developed ICD-PM) decided that ICD-PM should always be used for early neonatal deaths, and can be used for late neonatal deaths.

It is critical that a standardized classification system is globally relevant. Therefore, a great deal of consideration has gone into ensuring that ICD-PM is applicable in low-resource settings, where the burden of perinatal mortality is greatest, and also in high-resource settings, where perinatal mortality is lower but present across all three time periods (7). Accordingly, the ICD-PM approach to classification of cause of death allows deaths to be captured in settings where investigations such as post-mortem or placental histology alongside deaths are not feasible.

Reporting of results should be standardized while also reflecting local priorities. This allows standardized reporting of the causes of perinatal deaths and contributing maternal conditions. The structure of ICD-PM also allows local health-care facilities, districts and countries to investigate perinatal deaths based on local priorities. It is possible to look at deaths at the broad level of timing or ICD-PM groups, or to extract very specific causes of deaths and specific ICD-10 codes. ICD-PM will be made available through an interactive Excel-based system, which will be accessible via the website of the World Health Organization (WHO) Department of Reproductive Health and Research2 and on request by contacting the department at mpa-info@who.int.

Training and education are integral to the implementation of the classification system. During pilottesting of ICD-PM, clinicians and researchers who were not involved in the development of the system were trained in its use. What was learnt from that process informed the further development and the planned roll-out of ICD-PM (this document). In addition to this, WHO has developed the Making every baby count: audit and review of stillbirths and neonatal deaths at facility tool (8). To classify stillbirths and neonatal deaths as part of audit and review, ICD-PM is embedded within this tool and addressed in the training and education being done along with its dissemination. 2

Available at: http://www.who.int/reproductivehealth/en/

2. Development of The WHO application of ICD-10 to deaths during the perinatal period: ICD-PM (ICD-perinatal mortality)

The guide and groupings described here, based on ICD-10 (4), were developed through a consultative process. WHO established a technical Working Group on Perinatal Death Classification, including obstetricians, neonatologists, epidemiologists and public health professionals from developing and developed countries to prepare this standard guide for capturing information relating to perinatal deaths.

A meeting of the Working Group in July 2014 resulted in a consensus decision on the underlying structure of ICD-PM. As part of the background work for the development of ICD-PM, a systematic review of existing classification systems was undertaken (9), which identified more than 80 systems in use between 2009 and 2014. In addition, a Delphi survey of experts from 21 countries was conducted, which identified 17 key characteristics necessary for a perinatal death classification system (10). There was also an exploration of the relationship between these key characteristics and existing classification systems (11).

In developing ICD-PM, the approach of the Working Group involved three main principles: the system should be globally applicable, follow existing ICD-10 rules, and be compatible with the upcoming ICD-11 (12).

Following the development of ICD-PM, pilot-testing was undertaken on two perinatal death databases in South Africa and the United Kingdom.3 The steps taken in this process are outlined in Box 1. By undertaking pilot-testing on these databases, we were able to demonstrate the application of ICD-PM, its comparability between settings and its use in considering where programmes could be targeted to potentially address perinatal mortality. In addition, the pilot-testing identified areas where codes can be improved for future versions of ICD (13).

Four articles reporting on the results of this pilot-testing are being published as a mini-series in BJOG, in August 2016 (www.bjog.org).

Box 1: Steps taken in ICD-PM pilot-testing 1. Identification of the denominator population 2. Verification and description of data collection procedures and methods for the original datasets 3. Assignment of cause of perinatal death and maternal condition at the time of perinatal death using ICDPM groupings 4. Assessment of the difficulty/ease of using the proposed system 5. Identification of specific issues that would require further study.

The following sections will describe the ICD-10 procedures for death certificates and how to use ICDPM in detail, as well as information on specific conditions and case examples.

3. ICD-10 procedures for death certificates

3.1 Perinatal cause of death and maternal condition on the death certificate The first step in capturing the perinatal death and the maternal condition is undertaken by the care providers at any given health-care facility. This process is not one of coding, but of capturing all of the important clinical aspects of a perinatal death, telling the entire clinical story about both mother and baby. There is no need to have in-depth knowledge of ICD-10 codes to complete this process. Following documentation of the perinatal cause of death and maternal conditions, ICD-PM can be applied using a step-by-step process, whereby components of the clinical story are grouped into ICDPM groups and linked to the appropriate ICD-10 code without prior knowledge of the codes.

3.2 Certification of cause of perinatal death Cause of death is determined by the medical practitioner or other qualified certifier, who should use his or her clinical judgement in completing the medical certificate of cause of death, including documentation of the morbid conditions and events leading to the perinatal death. It is essential that at this stage all relevant information is recorded in its entirety. Medical certificates of cause of death used in ICD-10 aim to assist the certifier in this process.

A WHO perinatal death certificate has existed for some time, and variations of it are in use in a variety of settings. The relevant part of this certificate for perinatal death is shown in Box 2; it is specific to the disease or conditions in both the fetus or infant and the mother. Alternatively, WHO has a death certificate applicable to all deaths, regardless of age, as shown in Figure 1. The same information as for the perinatal death certificate is captured, but in a slightly different format. Figure 1 highlights the areas that relate to the main disease or condition in the fetus or infant, and to the main maternal disease or condition affecting the fetus or infant in this version of the death certificate.

Box 2. Perinatal death certificate cause of death section Causes of death (a) Main disease or condition in fetus or infant (b) Other diseases of conditions in fetus or infant (c) Main maternal disease or condition affecting fetus or infant (d) Other maternal diseases or conditions affecting fetus or infant

Figure 1. WHO death certificate for all deaths, regardless of age

Main disease or condition in fetus or infant

Main maternal disease or condition affecting fetus or infant 9

The main disease or condition in the fetus or infant is defined in ICD-10 as the disease or condition that initiated the morbid chain of events leading to death. This is the disease or condition that is entered on line (a) of the perinatal death certificate (Box 2, i.e. “main disease or condition in fetus or infant”) or on line (d) of the WHO death certificate (Figure 1, i.e. “the underlying cause”). This is the single identified cause of death and it should be as specific as possible. Multiple other contributing conditions can be entered on line (b) of the perinatal death certificate or on lines (a) to (c) of the WHO death certificate.

In addition to the main disease or condition in the fetus or infant, knowing the timing of the perinatal death is critical to ICD-PM. WHO proposes the collection of a minimum set of perinatal indicators around the time of all births and perinatal deaths (Box 3), which includes the timing of death.

Box 3[JP2]. Collection of a minimum set of perinatal indicators

3.3 Certification of maternal condition at the time of perinatal death The clinical team determines the main maternal condition at the time of presentation of the perinatal death. It should be a condition that would reasonably be considered to be part of the pathway leading to perinatal death (e.g. hypertensive disease in macerated stillbirth, breech extraction in acute intrapartum event). The main maternal condition is entered on line (c) of the perinatal death certificate (Box 2, i.e. “main maternal disease or condition affecting fetus or infant”) or in the highlighted section in the lower half of the WHO death certificate (Figure 1, i.e. “conditions of mother that affected the fetus and newborn”). Multiple other contributing conditions can be entered on line (d) of the perinatal death certificate or in the same highlighted section of the WHO death certificate (following the main condition, which should be documented first).

If the woman is assessed by the clinicians as having no recognizable condition, and there were no maternal complications of labour and delivery (e.g. malpresentation), then the maternal condition of “no maternal condition” needs to be recorded. This clearly documents the absence of any maternal condition or deviation from standard intrapartum progress.

There are some maternal conditions that occur in mothers who are apparently healthy, and health workers need to consider this when completing the section on the main maternal disease or condition affecting the fetus or infant. For example, a woman may have had no known conditions throughout her pregnancy and may be otherwise clinically healthy when she presents with idiopathic preterm labour and whose baby subsequently dies in the neonatal period from hyaline membrane disease, which is an abnormal occurrence/complication of labour and delivery. In the interest of linking perinatal and maternal interventions, it is important that this woman is recorded as having the maternal condition of preterm spontaneous labour with preterm delivery.

Knowing the maternal condition as a component of the perinatal death adds information that may improve the accuracy of the “death story”, particularly in settings where investigation is limited and verbal autopsy forms the mainstay of classification. For example, in the instance of a macerated antepartum stillbirth where the mother has tuberculosis, the perinatal death without autopsy or placental histology may be classified as “unexplained”. However, there is a reasonable temporal relationship between tuberculosis and perinatal death, and recording the maternal condition at the time of perinatal death allows more information related to an otherwise unexplained perinatal death to be captured.

The other major benefit of requiring the recording of the maternal condition is to encourage the development of programmes and public health policies that would help both mother and baby. For example, in cases of pre-eclampsia, antepartum stillbirths could be reduced through increased antepartum surveillance for hypertension. Likewise, neonatal deaths following abnormal labour in otherwise healthy mothers could be reduced by training health workers in intrapartum emergency obstetric care.

3.4 Coding the death certificate Coding the main and other disease(s) or condition(s) in the fetus or infant A trained coder codes the conditions mentioned on the death certificate, applying ICD-10 rules. To summarize the process, one first considers coding a disease or condition using a specific ICD-10 fourcharacter code. In most cases this is a letter and three numbers (e.g. P26.1, which is the code for massive pulmonary haemorrhage originating in the perinatal period). This can then be more broadly grouped in an ICD-10 three-character code group (e.g. P26, which is the code group for pulmonary haemorrhage originating in the perinatal period).

Coding rules mandate that the disease or condition recorded on line (a) of the perinatal death certificate (Box 2) or line (d) of the WHO death certificate (Figure 1) – in both cases the main perinatal cause of death – is coded to one of the codes in the range of P05–P96 (perinatal conditions) or Q00–Q99 (congenital anomalies). There are a small number of exceptions where other codes can be used; for example, neonatal tetanus is always coded to A33 tetanus neonatorum. Assignment of the conditions in each section follows the rules for perinatal mortality coding in ICD-10 volume 2 (5).

Line (a) of the perinatal death certificate or line (d) of the WHO death certificate is the underlying cause of death, which in ICD terminology is defined as the disease or condition that initiated the morbid chain of events leading to death. This is the main identified cause of death and it should be as specific as possible.

Coding the maternal disease(s) and condition(s) affecting the fetus or infant The assignment of three- and four-character codes for the main maternal condition is the same as for the perinatal cause of death. The condition entered on line (c) of the perinatal death certificate (Box 2) or in the highlighted area for the maternal condition on the WHO death certificate (Figure 1) can only be coded to P00–P04 (i.e. the codes for fetus and newborn affected by maternal factors and by complications of pregnancy, labour and delivery). These same codes must also be used for any other maternal conditions captured.

4. The WHO application of ICD-10 to deaths during the perinatal period

4.1 Application of ICD-PM to the cause of perinatal death

Initially the timing of perinatal death is classified as antepartum (A), intrapartum (I) or neonatal (N). This information is part of the minimum set of perinatal indicators that need to be collected for all births and perinatal deaths. The timing may be the only piece of information captured in some settings; however, classifying death by timing still provides valuable information for analysis and targeting of programmes in these areas.

ICD-PM groups the main condition in the fetus or infant into a limited number of categories of cause of death under the three headings for timing of death (i.e. A, I or N; see Table 1). There are six groups of antepartum causes of death, designated by a leading “A”; seven groups of intrapartum causes of death, designated by a leading “I”; and 11 groups of neonatal causes of death, designated by a leading “N”. All of the ICD-10 codes that can be assigned to the perinatal cause of death on a death certificate are represented in these new groupings. The ICD-10 codes have been reordered and clarified to better represent the pathologies at different times of perinatal death. Codes that are not considered to be a cause of perinatal death in these sections have been excluded from the ICDPM groupings.

4.2 Application of ICD-PM to the maternal condition in perinatal death

The five existing ICD-10 groups of maternal conditions in perinatal death have been rearranged into four groups denoted with a leading “M” as follows: M1 – the complications of placenta, cord and membranes; M2 – maternal complications of pregnancy; M3 – complications related to labour and delivery; and M4 – the medical and surgical conditions which may or may not be related to the present pregnancy (e.g. pre-eclampsia or pre-existing hypertension). A fifth group has also been added: when no maternal condition that might have been on the causal pathway for the perinatal death was identified at the time of presentation of the perinatal death, it must be coded as M5 – “no

maternal condition”. The list of the main maternal ICD-10 conditions included in each of the ICD-PM maternal condition groups can be seen in Table 2.

The specific ICD-10 codes applying to each ICD-PM group within each of the groups of perinatal cause of death and the maternal conditions can be found in Annexes A–D.

Table 1. The ICD-PM system: perinatal causes of death and linked ICD-10 codes, separated by timing of death, and maternal condition at the time of perinatal death*

Main perinatal cause of death ICD-PM groups

Antepartum death (A) A1 Congenital malformations, deformations and chromosomal abnormalities Infection Antepartum hypoxia

Main maternal condition ICD-PM groups

ICD-10 codes Q00–Q99 P35, P37, P39, A50 P20 P50, P52, P55, P56, P60, P61, P70, P75, P77, P83, P96.4, Misc. P05, P08

Maternal condition Complications of M1 placenta, cord and membranes Maternal complications M2 of pregnancy Other complications of M3 labour and delivery

ICD-10 codes P02

A2 A3

P01 P03

Other specified antepartum disorder (including codes specific to the antepartum period from haemorrhagic and haematological disorders of fetus and newborn)

Maternal medical and surgical conditions

P00

Disorders related to fetal growth

Antepartum death of unspecified cause

P95

M5 No maternal condition * Miscellaneous: While a perinatal death is most often coded to P05–P96 or a Q code, there are cases where codes from several other sections of ICD-10 should be used. For an extensive list, see ICD-10

(4) and ICD-10 volume 2: instruction manual (5). Intrapartum death (I) Congenital malformations, deformations and chromosomal abnormalities Birth trauma Acute intrapartum event Infection

I1 I2 I3 I4

Q00–Q99 P10–P15 P20 P35, P37, P39, A50 P50, P52, P55, P56, P60, P61, P70, P96, Misc. P05, P07, P08 P95

Other specified intrapartum disorder (including codes specific to the intrapartum period from haemorrhagic and haematological disorders of fetus and newborn)

I6 I7

Disorders related to fetal growth Intrapartum death of unspecified cause Neonatal death (N) Congenital malformations, deformations and chromosomal abnormalities Disorders related to fetal growth Birth trauma Complications of intrapartum events Convulsions and disorders of cerebral status Infection

N1 N2 N3 N4 N5 N6

Q00–Q99 P05, P08 P10–P15 P20, P21, P90, P91 P23, P35– 17

Respiratory and cardiovascular disorders Other neonatal conditions (including codes specific to the neonatal period from haemorrhagic and haematological disorders of fetus and newborn, transitory endocrine and metabolic disorders specific to fetus and newborn, digestive system disorders of fetus and newborn, conditions involving the integument and temperature regulation of fetus and newborn, other disorders originating in the perinatal period) Low birth weight and prematurity Miscellaneous Neonatal death of unspecified cause

P39 P22, P24– P29 P50–P61, P70–P78, P80–P83, P92–P94 P07 * P96.4 P96

N9 N10 N11

* In order to group and tabulate a perinatal death, the user needs information on the timing of the perinatal death (antenatal/intrapartum/neonatal) as well as the ICD-10 cause of death code. The information provided about the cause of death and the maternal condition should meet the ICD-10 coding rules for assigning a specific code before any tabulation can be undertaken. The table above is indicative for tabulation of data; for coding deaths, ICD-10 (4) and ICD-10 volume 2 (5) should be utilized.

Table 2. Maternal conditions in ICD-PM and the main maternal conditions (defined by ICD-10) included in each group* ICD-PM maternal condition group 1. 2. 3. 4. 5. 6. 7. 1. 2. 3. 4. 5. 6. 7. 8. 1. 2. Main maternal conditions included in group*

placenta praevia other forms of placental separation and haemorrhage placental dysfunction, infarction, insufficiency M1: Complications of placenta, fetal-placental transfusion syndromes cord and membranes prolapsed cord, other compression of umbilical cord chorioamnionitis other complications of membranes incompetent cervix preterm rupture of membranes oligohydramnios/polyhydramnios M2: Maternal complications of ectopic pregnancy pregnancy multiple pregnancy maternal death malpresentation before labour other complications of pregnancy breech delivery and extraction other malpresentation, malposition and disproportion during labour and delivery 3. forceps delivery/vacuum extraction M3: Other complications of 4. caesarean delivery labour and delivery 5. precipitate delivery 6. preterm labour and delivery 7. other complications of labour and delivery, including termination of pregnancy 1. pre-eclampsia, eclampsia 2. gestational hypertension 3. other hypertensive disorders 4. renal and urinary tract diseases 5. infectious and parasitic disease 6. circulatory and respiratory disease 7. nutritional disorders 8. injury M4: Maternal medical and 9. surgical procedure surgical conditions 10. other medical procedures 11. maternal diabetes, including gestational diabetes 12. maternal anaesthesia and analgesia 13. maternal medication 14. tobacco/alcohol/drugs of addiction 15. nutritional chemical substances 16. environmental chemical substances 17. unspecified maternal condition M5: No maternal condition 1. no maternal condition identified (healthy mother) * For a full list, definitions and the other and unspecified conditions that are listed in each group, see the current version of ICD-10 (4) and ICD-10 volume 2: instruction manual (5).

4.3 Summary and tabulation of ICD-PM

In summary, perinatal deaths are classified in a three-step process: 1. Deaths are first grouped according to timing – whether the death occurred in the antepartum period (prior to the onset of labour), intrapartum or in the neonatal period (early neonatal: up to day 7 of postnatal life; or late neonatal: days 8–28 of postnatal life). 2. The main cause of perinatal death is assigned and grouped according to the new ICD-PM groupings. 3. The main maternal condition at the time of perinatal death is assigned and grouped according to the new ICD-PM groupings.

Following these steps, the perinatal cause of death and the maternal condition are tabulated in a way that highlights the linkages between the two (see Table 3).

Table 3. ICD-PM tabulation for perinatal cause of death and maternal condition separated by timing of death* M1: Complications of placenta, cord and membranes M2: Maternal complications of pregnancy

M3: Other complications of labour and delivery

M5: No maternal condition identified

M4: Maternal medical and surgical conditions

Maternal condition

Perinatal cause of death Antepartum death (A)

A1: Congenital malformations, deformations and chromosomal abnormalities A2: Infection A3: Antepartum hypoxia A4: Other specified antepartum disorder A5: Disorders related to fetal growth A6: Fetal death of unspecified cause Total (%) Intrapartum death (I)

I1: Congenital malformations, deformations and chromosomal abnormalities I2: Birth trauma I3: Acute intrapartum event I4: Infection I5: Other specified intrapartum disorder I6: Disorders related to fetal growth I7: Intrapartum death of unspecified cause Total (%) Neonatal death (N)

N1: Congenital malformations, deformations and chromosomal abnormalities 21

Total (%)

Other

N2: Disorders related to fetal growth N3: Birth trauma N4: Complications of intrapartum events N5: Convulsions and disorders of cerebral status N6: Infection N7: Respiratory and cardiovascular disorders N8: Other neonatal conditions N9: Low birth weight and prematurity N10: Miscellaneous N11: Neonatal death of unspecified cause Total (%)

* In order to group and tabulate a perinatal death, the user needs information on the timing of the perinatal death (antenatal/intrapartum/neonatal) as well as the ICD-10 cause of death code. The information provided about the cause of death and the maternal condition should meet the ICD-10 coding rules for assigning a specific code before any tabulation can be undertaken. The table above is indicative for tabulation of data; for coding deaths, the current version of ICD-10 (4) and ICD-10 volume 2: instruction manual (5) should be utilized.

5. Specific conditions 5.1 Growth restriction

It can be challenging to detect growth restriction in low- and middle-income countries. This is due to the frequent lack of early, accurate dating of pregnancy and the limitations of examination to detect growth restriction, in combination with the lack of resources – namely, ultrasound – to support or refute any clinical suspicion. Moreover, in high-income settings, the identification of growth restriction may be a consequence of an underlying pathology and, therefore, not the main cause of perinatal death. The line between causality and consequence is often unclear. One of the challenges of identifying growth restriction relates to the resources available in many settings to do this. There is no clear evidence that measurement of symphysis fundal height is able to identify growth restriction (14); however, options for investigation other than this may be limited or non-existent. Moreover, there are obvious limitations to using the definition of the 10th centile based on a single plot of birth weight and gestational age at the time of perinatal death, and it may be difficult to distinguish the constitutionally small fetus or the fetus above the 10th centile that has had a significant drop in weight velocity (15). Despite all of this, it is clear that growth-restricted fetuses remain a high-risk group for many adverse outcomes, including perinatal mortality, and are potentially under-recognized as contributing to the burden of global perinatal mortality.

[START SHADED BOX] It is preferable to consider an assessment of growth for gestational age (with the best assessed method available) for all fetuses. This information can be recorded in the minimum set of perinatal indicators (Box 3). Classifying each and every case in terms of fetal growth will give a clearer picture of the role of growth restriction in perinatal deaths. [END SHADED BOX]

5.2 Preterm labour

The contribution of prematurity to perinatal mortality is of great interest to clinicians and researchers alike. It is helpful to be able to distinguish those mothers with apparently idiopathic preterm labour from those with pathology or provider-initiated delivery. Those who review perinatal deaths and complete death certificates should remain mindful of this.

[START SHADED BOX] Preterm labour as a maternal condition applies to those mothers who present prior to 37 completed weeks of gestation with spontaneous onset of contractions and cervical change in the absence of any apparent underlying pathology (e.g. chorioamnionitis or urinary tract infection). [START SHADED BOX]

5.3 Prematurity

Volume 2 of ICD-10 requests that clinicians do not enter prematurity as the main disease or condition in the fetus or infant unless it was the only fetal or infant condition known (5). There is a tendency in many settings to assign prematurity as a cause of death when further evidence to suggest a more definitive cause of death has not been actively sought.

As it stands, low birth weight and prematurity are coded together in ICD-10 (with the qualifying note that when both birth weight and gestational age are available, priority of assignment should be given to birth weight), yet while prematurity may be a cause of low birth weight, the inverse is not necessarily true. More importantly, the outcomes for babies born preterm and appropriately small are different from those for babies of the same weight yet small for gestational age (16).

[START SHADED BOX] It is preferable to only accept the diagnosis of prematurity as the main disease or condition in the infant if further evidence supports this notion, such as if a gestational age of less than 28 weeks was specified. Further to this, as per ICD-10 coding rules, if the only other cause of perinatal

mortality reported is respiratory failure of the newborn, then the diagnosis of prematurity can be the main disease or condition in the infant. [END SHADED BOX]

5.4 Obstructed labour

Obstructed labour is addressed comprehensively in The WHO application of ICD-10 to deaths during pregnancy, childbirth and the puerperium: ICD-maternal mortality (ICD-MM) in relation to when this condition can be considered the underlying cause of maternal mortality and when it merely contributes to the outcome of maternal mortality (17). As outlined in ICD-MM, “obstructed labour may be the start of a sequence leading to death, or may itself be due to some preceding condition such as contracted maternal pelvis or transverse lie”. A similar logic applies when considering the role of obstructed labour in perinatal death. The programmatic aim is to prevent its occurrence in the first place or, in the absence of this, to be able to initiate prompt access to safe emergency obstetric care to the benefit of both mother and baby.

[START SHADED BOX] Where the obstructed labour is the start of a sequence leading to perinatal death, this should be recorded as the main maternal condition. Where the obstructed labour is the consequence of another condition (e.g. malpresentation of the fetus), then this other condition should be recorded as the main maternal condition. [END SHADED BOX]

5.5 HIV and AIDS

There is a tendency in many parts of the world to attribute all deaths in people known to have HIV or AIDS to HIV or AIDS as the cause of death. However, such patients may die “from AIDS” (i.e. as the cause of death) or “with HIV” (i.e. not the cause of death). There is a concern that this tendency will

translate into assigning the cause of death as HIV or AIDS in all perinatal deaths where there is maternal HIV or AIDS, regardless of the lack of evidence to support this as the cause of death.

While maternal HIV may increase the risk of perinatal death (4), the causal relationship may be difficult to establish, and it is useful to distinguish those perinatal deaths in the context of other maternal conditions where the maternal HIV is incidental.

[START SHADED BOX] It is preferable to classify each and every case in terms of maternal HIV status. This will give a clearer picture of the role of maternal HIV and AIDS in perinatal deaths. [END SHADED BOX]

5.6 Termination of pregnancy

Termination of pregnancy (TOP) will result in perinatal mortality and, depending on the gestational age, may be suitable for classification in ICD-PM.

Several situations may lead to TOP: (i) severe (life-threatening) maternal disease; (ii) fetal congenital malformations; (iii) multiple pregnancy; and (iv) psychosocial reasons. Globally, legal and social situations differ with regard to TOP in different settings; the local situation in a particular setting may influence the will and possibilities for proper recording and classification.

Nevertheless, starting from 22 weeks of gestational age, registration of all deaths is warranted and needed for proper comparison of causes of perinatal mortality. This will also influence stillbirth rates, since these stillbirths (i.e. related to TOP) may also not be registered in the national vital statistics or they may be registered but with the wrong cause of death listed (i.e. TOP not listed as the cause of death). It is important to count all perinatal deaths and to assign the cause of death as accurately as possible. 26

The timing of perinatal death following a TOP may be antepartum, intrapartum or neonatal. For gestational ages beyond 22 weeks, it is most likely that either the fetus or the mother has a pathology (e.g. congenital anomaly or severe maternal pre-eclampsia) that can be recorded and grouped according to ICD-PM as the main cause of death or maternal condition.

Where the reason for the TOP is a maternal pathology, then the maternal condition can be recorded as this pathology (e.g. severe pre-eclampsia), with the maternal TOP recorded as another condition. In this case the timing of perinatal death and its grouping can be A4 (Other specified antepartum disorder), I5 (Other specified intrapartum disorder) or N10 (Miscellaneous). The ICD-10 code that corresponds to all of these is P96.4: Termination of pregnancy, affecting fetus and newborn.

Where the reason for the TOP is a fetal pathology (e.g. chromosomal anomaly), then the main condition in the fetus or neonate can be recorded as this pathology under the appropriate time of death (A, I or N), with the TOP affecting the fetus or newborn being captured as another condition. The main maternal condition will be the TOP, which is captured in ICD-PM under M3 (Other complications of labour and delivery) and coded with the ICD-10 code P03.8: Fetus and newborn affected by other specified complications of labour and delivery.

6. Case examples

6.1 Case 1

A 19-year-old para 1, with a certain gestation of 38 weeks based on early clinical examination, presented in a healthy condition during labour with no significant history. A 2450 g baby was delivered after an 8-hour labour. An early neonatal death on day 2 of life from meconium aspiration syndrome of a 2450 g baby occurred. Factors that are potentially modifiable identified by clinical review of the case were fetal distress not detected in labour and personnel too junior to manage the patient.

The neonatal cause of death is meconium aspiration syndrome. The maternal condition is no maternal condition identified at the time of perinatal death. The time of the death is neonatal.

The death certificate was completed by the clinicians, and subsequently coded as follows: Clinical details ICD-10 code Meconium aspiration syndrome Small for gestational age No maternal condition P24.0 P05.1

Causes of death (a) Main disease or condition in fetus or infant (b) Other diseases of conditions in fetus or infant (c) Main maternal disease or condition affecting fetus or infant (d) Other maternal diseases or conditions affecting fetus or infant

The final ICD-PM groups would be: N7; M5 This case highlights the need for having “no maternal condition” identified as the maternal code at the time of perinatal death, as the ability to predict this death antenatally is limited. It also highlights the need for personnel to continue to be trained in intrapartum care and obstetric emergencies.

6.2 Case 2

A 30-year-old para 1 presented in labour at 39 weeks of gestation, based on a certain last menstrual period, with the fetus alive at admission. The woman was HIV-positive and on long-term antiretroviral therapy. There was poor progress in labour, with incorrect interpretation of the partograph. An acute intrapartum event occurred with a hypoxic intrapartum stillbirth. The fetus was delivered via caesarean section.

The intrapartum cause of death is intrapartum hypoxia, with the maternal condition of obstructed labour.

The death certificate was completed by the clinicians, and subsequently coded as follows: Causes of death (a) Main disease or condition in fetus or infant (b) Other diseases of conditions in fetus or infant (c) Main maternal disease or condition affecting fetus or infant (d) Other maternal diseases or conditions affecting fetus or infant HIV Obstructed labour P03.8 P00.2 Clinical details Intrapartum hypoxia ICD-10 code P20.1

The final ICD-PM groups would be: I3; M3 This case highlights the need to capture maternal conditions other than HIV.

6.3 Case 3

A 16-year-old para 0 with no medical history presented in spontaneous labour at 29 certain weeks of gestation and subsequently had a forceps delivery of a liveborn baby weighing 1100 g. The baby died on day 2 of life from hyaline membrane disease. The neonatal cause of death is hyaline membrane disease, with the maternal condition of spontaneous preterm labour.

The death certificate was completed by the clinicians, and subsequently coded as follows: Causes of death (a) Main disease or condition in fetus or infant (b) Other diseases of conditions in fetus or infant (c) Main maternal disease or condition affecting fetus or infant (d) Other maternal diseases or conditions affecting fetus or infant Forceps delivery P03.2 Spontaneous preterm labour P03.8 Clinical details Hyaline membrane disease Prematurity ICD-10 code P22.0 P07.1

The final ICD-PM groups would be: N7; M3 This case highlights the need to identify a specific cause of neonatal premature death other than prematurity. In addition, although the mother had no medical history, the occurrence of spontaneous preterm labour is abnormal and so should be recorded as the main maternal condition contributing to the perinatal death.

6.4 Case 4

A 36-year-old para 5 presented at 35 weeks of gestation determined by clinical palpation, complaining of a headache and decreased fetal movements. A fetal death in utero was diagnosed. Clinical and biochemical investigation revealed maternal proteinuric hypertension. Spontaneous vaginal delivery of a macerated 2100 g stillborn followed induction of labour. The proteinuric hypertension subsequently resolved.

The antepartum cause of death is intrauterine hypoxia, and the maternal condition is pre-eclampsia.

The death certificate was completed by the clinicians, and subsequently coded as follows: Causes of death (a) Main disease or condition in fetus or infant (b) Other diseases of conditions in fetus or infant (c) Main maternal disease or condition affecting fetus or infant (d) Other maternal diseases or conditions affecting fetus or infant Pre-eclampsia P00.0 Clinical details Intrauterine hypoxia Prematurity ICD-10 code P20.0 P07.3

The final ICD-PM groups would be: A3; M4 This case highlights the need to always capture the maternal condition, as the fetal cause of death of intrauterine hypoxia provides less specific information than the maternal condition of pre-eclampsia.

7. Implications for practice and research

It is envisaged that ICD-PM will lead to better classification of perinatal deaths, as well as clearer linkage to the maternal condition in these deaths.

8. Perinatal audit Consistent information about the nature and cause of death is needed for planning health systems and distributing resources, as well as for improving quality of care at the point of service delivery. These data are necessary for recommendations to be made, so that actions can be taken to prevent similar deaths in the future. Mortality audit is an established mechanism to examine the circumstances surrounding a death and the breakdowns in care that may be preventable. WHO has developed the Making every baby count: audit and review of stillbirths and neonatal deaths guide and tools (8). Embedded within the data collection tools in that publication (i.e. in particular, the Stillbirth and Neonatal Death Case Review Form, and the Births and Deaths Summary Form), and addressed in the training and education being done in the dissemination of the guide, is a simplified version of ICD-PM which can be used to classify the stillbirths and neonatal deaths as part of audit and response.

The ICD-PM classification is useful for mortality audit because the focus on the mother–baby dyad highlights areas requiring programmatic intervention that will benefit maternal and perinatal outcomes. It simplifies the certification of perinatal deaths, but it also offers programme officers and public health workers a means to identify solutions that meet the needs of both mother and baby concurrently. The categories on the data collection forms have been collapsed to facilitate ease of data entry and analysis, but they can also be expanded to include more specific causes and categories, depending on the capacity and interest of the facility staff and the perinatal mortality audit team.

9. Conclusion

The WHO application of ICD-10 to deaths during the perinatal period: ICD-PM uses the existing ICD10 as a framework for a system that both separates out the timing of perinatal deaths and links perinatal deaths to maternal conditions (or lack thereof). It not only allows health workers clarity in certifying perinatal deaths but also enables programme officers and public health workers to drive interventions that meet the needs of both mother and baby concurrently.

ICD-PM builds on ICD-10 and is modelled on ICD-MM, so much will be familiar to users. The new concepts of timing of perinatal death and compulsory linkage to maternal condition will need to be monitored, and further research on the application of ICD-PM will be necessary.

References 1. Blencowe H, Cousens S, Bianchi Jassir F, Say L, Chou D, Mathers C et al.; for The Lancet Stillbirth Epidemiology Investigator Group. National, regional, and worldwide estimates of stillbirth rates in 2015 with trends from 2000: a systematic analysis. Lancet. 2016;4:e98–e108. doi:10.17037/DATA.25. Liu L, Oza S, Hogan D, Perin J, Rudan I, Lawn JE et al. Global, regional, and national causes of child mortality in 2000–13, with projections to inform post-2015 priorities: an updated systematic analysis. Lancet. 2015;385(9966):430–40. doi:10.1016/S0140-6736(14)61698-6. Every newborn: an action plan to end preventable deaths. Geneva: World Health Organization; 2014 (http://apps.who.int/iris/bitstream/10665/127938/1/9789241507448_eng.pdf, accessed 26 July 2016). International Statistical Classification of Diseases and Related Health Problems 10th revision. In: ICD version:2016 [website]. Geneva: World Health Organization; 2016 (http://apps.who.int/classifications/icd10/browse/2016/en, accessed 26 July 2016). International statistical classification of diseases and related health problems, 10th revision. Volume 2: Instruction manual, 2010 edition. Geneva: World Health Organization; 2011 (http://www.who.int/classifications/icd/ICD10Volume2_en_2010.pdf, accessed 26 July 2016). Aminu M, Unkels R, Mdegela M, Utz B, Adaji S, van den Broek N. Causes of and factors associated with stillbirth in low- and middle-income countries: a systematic literature review. BJOG. 2014;121(Suppl 4):141–53. doi:10.1111/1471-0528.12995. Flenady V, Wojcieszek AM, Middleton P, Ellwood E, Erwich JJ, Coory M et al. Stillbirths: recall to action in high-income countries? Lancet. 2016;387(10019):691–702. doi:10.1016/S01406736(15)01020-X. Making every baby count: audit and review of stillbirths and neonatal deaths at facility. Geneva: World Health Organization; 2016 (INSERT URL WHEN AVAILABLE). Hopkins Leisher S, Reinebrant H, Wojcieszek AM, Korteweg F, Blencowe H, Erwich JJ et al. Seeking order amidst chaos: a systematic review of classification systems for causes of stillbirth and neonatal death, 2009–2014. BMC Pregnancy Childbirth. 2016 (in press). Wojcieszek AM, Hopkins Leisher S, Allanson E, Coory M, Erwich JJ, Frøen JF et al. Characteristics of a global classification system for perinatal deaths: a Delphi consensus study. BMC Pregnancy Childbirth. 2016 (in press). Hopkins Leisher S, Reinebrant H, Wojcieszek AM, Korteweg F, Blencowe H, Erwich JJ et al. Classification systems for causes of stillbirth and neonatal death, 2009–2014: an assessment of alignment 2 with characteristics for an effective global system. BMC Pregnancy Childbirth. 2016 (in press). Allanson E, Tunçalp Ö, Gardosi J, Pattinson RC, Erwich JJ, Flenady VJ et al. Classifying the causes of perinatal death. Bull World Health Organ. 2016;94(2):79-79A. doi:10.2471/BLT.15.168047. Chou D, Tunçalp Ö, Hotamisligil S, Norman J, Say L, Volkmer B et al. Steps through the revision process of reproductive health sections of ICD-11. Gynecol Obstet Invest. 2012;74(3):228–32. doi:10.1159/000343062. Peter JR, Ho JJ, Valliapan J, Sivasangari S. Symphysial fundal height (SFH) measurement in pregnancy for detecting abnormal fetal growth. Cochrane Database Syst Rev. 2015;(9):CD008136. Zhang J, Merialdi M, Platt LD, Kramer MS. Defining normal and abnormal fetal growth: promises and challenges. Am J Obstet Gynecol. 2010;202(6):522–8. doi:10.1016/j.ajog.2009.10.889. Tsai LY, Chen YL, Tsou KI, Mu SC; Taiwan Premature Infant Developmental Collaborative Study Group. The impact of small-for-gestational-age on neonatal outcome among very-low-birthweight infants. Pediatr Neonatol. 2015;56(2):101–7. doi:10.1016/j.pedneo.2014.07.007.

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17. The WHO application of ICD-10 to deaths during pregnancy, childbirth and the puerperium: ICDMM. Geneva: World Health Organization; 2012 (http://apps.who.int/iris/bitstream/10665/70929/1/9789241548458_eng.pdf, accessed 26 July 2016).

Annex A: ICD-PM groups and ICD-10 codes for antepartum deaths In order to group and tabulate a perinatal death, the user needs information on the timing of the perinatal death (antenatal/intrapartum/neonatal) as well as the ICD-10 cause of death code. The information provided about the cause of death and the maternal condition should meet the ICD-10 coding rules for assigning a specific code before any tabulation can be undertaken. The codes included below are indicative for tabulation of data; for coding deaths, ICD-10 version:2016 and ICD10 volume 2: instruction manual (2010) should be utilized.4

A1 Congenital malformations, deformations and chromosomal abnormalities Q00 Anencephaly and similar malformations Q01 Encephalocele Q02 Microcephaly Q03 Congenital hydrocephalus Q04 Other congenital malformations of brain Q05 Spina bifida Q06 Other congenital malformations of spinal cord Q07 Other congenital malformations of nervous system Q10 Congenital malformations of eyelid, lacrimal apparatus and orbit Q11 Anophthalmos, microphthalmos and macrophthalmos Q12 Congenital lens malformations Q13 Congenital malformations of anterior segment of eye Q14 Congenital malformations of posterior segment of eye Q15 Other congenital malformations of eye Q16 Congenital malformations of ear causing impairment of hearing Q17 Other congenital malformations of ear Q18 Other congenital malformations of face and neck Q20 Congenital malformations of cardiac chambers and connections 4

Available at: http://www.who.int/classifications/icd/icdonlineversions/en/

Q21 Congenital malformations of cardiac septa Q22 Congenital malformations of pulmonary and tricuspid valves Q23 Congenital malformations of aortic and mitral valves Q24 Other congenital malformations of heart Q25 Congenital malformations of great arteries Q26 Congenital malformations of great veins Q27 Other congenital malformations of peripheral vascular system Q28 Other congenital malformations of circulatory system Q30 Congenital malformations of nose Q31 Congenital malformations of larynx Q32 Congenital malformations of trachea and bronchus Q33 Congenital malformations of lung Q34 Other congenital malformations of respiratory system Q36 Cleft lip Q37 Cleft palate with cleft lip Q38 Other congenital malformations of tongue, mouth and pharynx Q39 Congenital malformations of oesophagus Q40 Other congenital malformations of upper alimentary tract Q41 Congenital absence, atresia and stenosis of small intestine Q42 Congenital absence, atresia and stenosis of large intestine Q43 Other congenital malformations of intestine Q44 Congenital malformations of gallbladder, bile ducts and liver Q45 Other congenital malformations of digestive system Q50 Congenital malformations of ovaries, fallopian tubes and broad ligaments Q51 Congenital malformations of uterus and cervix Q52 Other congenital malformations of female genitalia Q53 Undescended testicle

Q54 Hypospadias Q55 Other congenital malformations of male genital organs Q56 Indeterminate sex and pseudohermaphroditism Q60 Renal agenesis and other reduction defects of kidney Q61 Cystic kidney disease Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter Q63 Other congenital malformations of kidney Q64 Other congenital malformations of urinary system Q65 Congenital deformities of hip Q66 Congenital deformities of feet Q67 Congenital musculoskeletal deformities of head, face, spine and chest Q68 Other congenital musculoskeletal deformities Q69 Polydactyly Q70 Syndactyly Q71 Reduction defects of upper limb Q72 Reduction defects of lower limb Q73 Reduction defects of unspecified limb Q74 Other congenital malformations of limb(s) Q75 Other congenital malformations of skull and face bones Q76 Congenital malformations of spine and bony thorax Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine Q78 Other osteochondrodysplasias Q79 Congenital malformations of the musculoskeletal system, not elsewhere classified Q80 Congenital ichthyosis Q81 Epidermolysis bullosa Q82 Other congenital malformations of skin Q83 Congenital malformations of breast

Q84 Other congenital malformations of integument Q85 Phakomatoses, not elsewhere classified Q86 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified Q87 Other specified congenital malformation syndromes affecting multiple systems Q89 Other congenital malformations, not elsewhere classified Q90 Down syndrome Q91 Edwards syndrome and Patau syndrome Q92 Other trisomies and partial trisomies of the autosomes, not elsewhere classified Q93 Monosomies and deletions from the autosomes, not elsewhere classified Q95 Balanced rearrangements and structural markers, not elsewhere classified Q96 Turner syndrome Q97 Other sex chromosome abnormalities, female phenotype, not elsewhere classified Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified Q99 Other chromosome abnormalities, not elsewhere classified

A2 Infection A50 Congenital syphilis A50.0 Early congenital syphilis, symptomatic A50.1 Early congenital syphilis, latent A50.2 Early congenital syphilis, unspecified A50.9 Congenital syphilis, unspecified

P35 Congenital viral diseases P35.0 Congenital rubella syndrome Congenital rubella pneumonitis P35.1 Congenital cytomegalovirus infection P35.2 Congenital herpesviral [herpes simplex] infection P35.3 Congenital viral hepatitis P35.8 Other congenital viral diseases Congenital varicella [chickenpox] P35.9 Congenital viral disease, unspecified

P37 Other congenital infectious and parasitic diseases P37.0 Congenital tuberculosis P37.1 Congenital toxoplasmosis Hydrocephalus due to congenital toxoplasmosis P37.3 Congenital falciparum malaria P37.4 Other congenital malaria P37.8 Other specified congenital infectious and parasitic diseases P37.9 Congenital infectious and parasitic disease, unspecified

P39 Other infections specific to the perinatal period P39.2 Intra-amniotic infection of fetus, not elsewhere classified

P39.8 Other specified infections specific to the perinatal period P39.9 Infection specific to the perinatal period, unspecified

A3 Acute antepartum event P20 Intrauterine hypoxia P20.0 Intrauterine hypoxia first noted before onset of labour P20.9 Intrauterine hypoxia, unspecified

A4 Other specified antepartum disorder P50 Fetal blood loss P50.0 Fetal blood loss from vasa praevia P50.1 Fetal blood loss from ruptured cord P50.2 Fetal blood loss from placenta P50.3 Haemorrhage into co-twin P50.4 Haemorrhage into maternal circulation P50.5 Fetal blood loss from cut end of co-twin’s cord P50.8 Other fetal blood loss P50.9 Fetal blood loss, unspecified Fetal haemorrhage NOS

P52 Intracranial nontraumatic haemorrhage of fetus and newborn P52.0 Intraventricular (nontraumatic) haemorrhage, grade 1, of fetus and newborn Subependymal haemorrhage (without intraventricular extension) P52.1 Intraventricular (nontraumatic) haemorrhage, grade 2, of fetus and newborn Subependymal haemorrhage with intraventricular extension P52.2 Intraventricular (nontraumatic) haemorrhage, grade 3 and grade 4, of fetus and newborn Subependymal haemorrhage with both intraventricular and intracerebral extension P52.3 Unspecified intraventricular (nontraumatic) haemorrhage of fetus and newborn P52.4 Intracerebral (nontraumatic) haemorrhage of fetus and newborn P52.5 Subarachnoid (nontraumatic) haemorrhage of fetus and newborn P52.6 Cerebellar (nontraumatic) and posterior fossa haemorrhage of fetus and newborn P52.8 Other intracranial (nontraumatic) haemorrhages of fetus and newborn P52.9 Intracranial (nontraumatic) haemorrhage of fetus and newborn, unspecified

P55 Haemolytic disease of fetus and newborn P55.0 Rhesus isoimmunization of fetus and newborn 43

P55.1 ABO isoimmunization of fetus and newborn P55.8 Other haemolytic diseases of fetus and newborn P55.9 Haemolytic disease of fetus and newborn, unspecified

P56 Hydrops fetalis due to haemolytic disease P56.0 Hydrops fetalis due to isoimmunization P56.9 Hydrops fetalis due to other and unspecified haemolytic disease

P60 Disseminated intravascular coagulation of fetus and newborn

P61 Other perinatal haematological disorders P61.3 Congenital anaemia from fetal blood loss P61.4 Other congenital anaemias, not elsewhere classified Congenital anaemia NOS P61.8 Other specified perinatal haematological disorders P61.9 Perinatal haematological disorder, unspecified

P75 Meconium ileus in cystic fibrosis

P77 Necrotizing enterocolitis of fetus and newborn

P83 Other conditions of integument specific to fetus and newborn P83.2 Hydrops fetalis not due to haemolytic disease Hydrops fetalis NOS P83.3 Other and unspecified oedema specific to fetus and newborn P83.8 Other specified conditions of integument specific to fetus and newborn Bronze baby syndrome Neonatal scleroderma Urticaria neonatorum P83.9 Condition of integument specific to fetus and newborn, unspecified 44

P96 Other conditions originating in the perinatal period P96.0 Congenital renal failure Uraemia of newborn P96.4 Termination of pregnancy, affecting fetus and newborn P96.5 Complications of intrauterine procedures, not elsewhere classified P96.8 Other specified conditions originating in the perinatal period P96.9 Condition originating in the perinatal period, unspecified Congenital debility NOS

A5 Disorders related to length of gestation and fetal growth P05 Slow fetal growth and fetal malnutrition P05.0 Light for gestational age Usually referred to as weight below but length above 10th centile for gestational age Light-for-dates P05.1 Small for gestational age Usually referred to as weight and length below 10th centile for gestational age Small-for-dates Small-and-light-for-dates P05.2 Fetal malnutrition without mention of light or small for gestational age Infant, not light or small for gestational age, showing signs of fetal malnutrition, such as dry, peeling skin and loss of subcutaneous tissue P05.9 Slow fetal growth, unspecified Fetal growth retardation NOS

P08 Disorders related to long gestation and high birth weight Note: When both birth weight and gestational age are available, priority of assignment should be given to birth weight. P08.0 Exceptionally large baby Usually implies a birth weight of 4500 g or more P08.1 Other heavy for gestational age infants Usually implies a birth weight > 90th percentile for gestational age or 4000 g or more at term Other fetus or infant heavy- or large-for-dates regardless of period of gestation P08.2 Post-term infant, not heavy for gestational age Fetus or infant with gestation period of 42 completed weeks or more (294 days or more), not heavy- or large-for-dates Postmaturity NOS

A6 Antepartum death of unspecified cause P95 Fetal death of unspecified cause Incl.: Deadborn fetus NOS Stillbirth NOS

Annex B: ICD-PM groups and ICD-10 codes for intrapartum deaths In order to group and tabulate a perinatal death, the user needs information on the timing of the perinatal death (antenatal/intrapartum/neonatal) as well as the ICD-10 cause of death code. The information provided about the cause of death and the maternal condition should meet the ICD-10 coding rules for assigning a specific code before any tabulation can be undertaken. The codes included below are indicative for tabulation of data; for coding deaths, ICD-10 version:2016 and ICD10 volume 2: instruction manual (2010) should be utilized.5

I1 Congenital malformations, deformations and chromosomal abnormalities Q00 Anencephaly and similar malformations Q01 Encephalocele Q02 Microcephaly Q03 Congenital hydrocephalus Q04 Other congenital malformations of brain Q05 Spina bifida Q06 Other congenital malformations of spinal cord Q07 Other congenital malformations of nervous system Q10 Congenital malformations of eyelid, lacrimal apparatus and orbit Q11 Anophthalmos, microphthalmos and macrophthalmos Q12 Congenital lens malformations Q13 Congenital malformations of anterior segment of eye Q14 Congenital malformations of posterior segment of eye Q15 Other congenital malformations of eye Q16 Congenital malformations of ear causing impairment of hearing Q17 Other congenital malformations of ear Q18 Other congenital malformations of face and neck Q20 Congenital malformations of cardiac chambers and connections 5

Available at: http://www.who.int/classifications/icd/icdonlineversions/en/

Q21 Congenital malformations of cardiac septa Q22 Congenital malformations of pulmonary and tricuspid valves Q23 Congenital malformations of aortic and mitral valves Q24 Other congenital malformations of heart Q25 Congenital malformations of great arteries Q 26 Congenital malformations of great veins Q27 Other congenital malformations of peripheral vascular system Q28 Other congenital malformations of circulatory system Q30 Congenital malformations of nose Q31 Congenital malformations of larynx Q32 Congenital malformations of trachea and bronchus Q33 Congenital malformations of lung Q34 Other congenital malformations of respiratory system Q36 Cleft lip Q37 Cleft palate with cleft lip Q38 Other congenital malformations of tongue, mouth and pharynx Q39 Congenital malformations of oesophagus Q40 Other congenital malformations of upper alimentary tract Q41 Congenital absence, atresia and stenosis of small intestine Q42 Congenital absence, atresia and stenosis of large intestine Q43 Other congenital malformations of intestine Q44 Congenital malformations of gallbladder, bile ducts and liver Q45 Other congenital malformations of digestive system Q50 Congenital malformations of ovaries, fallopian tubes and broad ligaments Q51 Congenital malformations of uterus and cervix Q52 Other congenital malformations of female genitalia Q53 Undescended testicle

I2 Birth trauma P10 Intracranial laceration and haemorrhage due to birth injury P10.0 Subdural haemorrhage due to birth injury Subdural haematoma (localized) due to birth injury P10.1 Cerebral haemorrhage due to birth injury P10.2 Intraventricular haemorrhage due to birth injury P10.3 Subarachnoid haemorrhage due to birth injury P10.4 Tentorial tear due to birth injury P10.8 Other intracranial lacerations and haemorrhages due to birth injury P10.9 Unspecified intracranial laceration and haemorrhage due to birth injury

P11 Other birth injuries to central nervous system P11.0 Cerebral oedema due to birth injury P11.1 Other specified brain damage due to birth injury P11.2 Unspecified brain damage due to birth injury P11.5 Birth injury to spine and spinal cord Fracture of spine due to birth injury P11.9 Birth injury to central nervous system, unspecified

P12 Birth injury to scalp P12.0 Cephalhaematoma due to birth injury P12.1 Chignon due to birth injury P12.2 Epicranial subaponeurotic haemorrhage due to birth injury P12.3 Bruising of scalp due to birth injury P12.4 Monitoring injury of scalp of newborn Sampling incision Scalp clip (electrode) injury P12.8 Other birth injuries to scalp 52

P12.9 Birth injury to scalp, unspecified

P13 Birth injury to skeleton P13.0 Fracture of skull due to birth injury P13.1 Other birth injuries to skull P13.2 Birth injury to femur P13.3 Birth injury to other long bones P13.4 Fracture of clavicle due to birth injury P13.8 Birth injuries to other parts of skeleton P13.9 Birth injury to skeleton, unspecified

P15 Other birth injuries P15.0 Birth injury to liver Rupture of liver due to birth injury P15.1 Birth injury to spleen Rupture of spleen due to birth injury P15.2 Sternomastoid injury due to birth injury P15.8 Other specified birth injuries P15.9 Birth injury, unspecified

I3 Acute intrapartum event P20 Intrauterine hypoxia P20.1 Intrauterine hypoxia first noted during labour and delivery P20.9 Intrauterine hypoxia, unspecified

I4 Infection P35 Congenital viral diseases P35.0 Congenital rubella syndrome Congenital rubella pneumonitis P35.1 Congenital cytomegalovirus infection P35.2 Congenital herpesviral [herpes simplex] infection P35.3 Congenital viral hepatitis P35.8 Other congenital viral diseases Congenital varicella [chickenpox] P35.9 Congenital viral disease, unspecified

P39 Other infections specific to the perinatal period P39.2 Intra-amniotic infection of fetus, not elsewhere classified P39.8 Other specified infections specific to the perinatal period P39.9 Infection specific to the perinatal period, unspecified

I5 Other specified intrapartum disorder P50 Fetal blood loss P50.0 Fetal blood loss from vasa praevia P50.1 Fetal blood loss from ruptured cord P50.2 Fetal blood loss from placenta P50.3 Haemorrhage into co-twin P50.4 Haemorrhage into maternal circulation P50.5 Fetal blood loss from cut end of co-twin’s cord P50.8 Other fetal blood loss P50.9 Fetal blood loss, unspecified Fetal haemorrhage NOS

P55 Haemolytic disease of fetus and newborn P55.0 Rhesus isoimmunization of fetus and newborn 56

P55.1 ABO isoimmunization of fetus and newborn P55.8 Other haemolytic diseases of fetus and newborn P55.9 Haemolytic disease of fetus and newborn, unspecified haemolytic disease

P56 Hydrops fetalis due to haemolytic disease P56.0 Hydrops fetalis due to isoimmunization P56.9 Hydrops fetalis due to other and unspecified haemolytic disease

P60 Disseminated intravascular coagulation of fetus and newborn

I6 Disorders related to fetal growth P05 Slow fetal growth and fetal malnutrition P05.0 Light for gestational age Usually referred to as weight below but length above 10th centile for gestational age Light-for-dates P05.1 Small for gestational age Usually referred to as weight and length below 10th centile for gestational age Small-for-dates Small-and-light-for-dates P05.2 Fetal malnutrition without mention of light or small for gestational age Infant, not light or small for gestational age, showing signs of fetal malnutrition, such as dry, peeling skin and loss of subcutaneous tissue P05.9 Slow fetal growth, unspecified Fetal growth retardation NOS

P07 Disorders related to short gestation and low birth weight, not elsewhere classified Note: When both birth weight and gestational age are available, priority of assignment should be given to birth weight. Incl.: the listed conditions, without further specification, as the cause of mortality, morbidity or additional care in newborn P07.0 Extremely low birth weight Birth weight 999 g or less P07.1 Other low birth weight Birth weight 1000–2499 g P07.2 Extreme immaturity Less than 28 completed weeks (less than 196 completed days) of gestation P07.3 Other preterm infants 28 completed weeks or more but less than 37 completed weeks (196 completed days but less than 259 completed days) of gestation 58

Prematurity NOS

P08.1 Other heavy for gestational age infants Usually implies a birth weight > 90th percentile for gestational age or 4000 g or more at term Other fetus or infant heavy- or large-for-dates regardless of period of gestation P08.2 Post-term infant, not heavy for gestational age Fetus or infant with gestation period of 42 completed weeks or more (294 days or more), not heavy- or large-for-dates Postmaturity NOS

I7 Intrapartum death of unspecified cause P95 Fetal death of unspecified cause Incl.: Deadborn fetus NOS Stillbirth NOS

Annex C: ICD-PM groups and ICD-10 codes for neonatal deaths In order to group and tabulate a perinatal death, the user needs information on the timing of the perinatal death (antenatal/intrapartum/neonatal) as well as the ICD-10 cause of death code. The information provided about the cause of death and the maternal condition should meet the ICD-10 coding rules for assigning a specific code before any tabulation can be undertaken. The codes included below are indicative for tabulation of data; for coding deaths, ICD-10 version:2016 and ICD10 volume 2: instruction manual (2010) should be utilized.6

N1 Congenital malformations, deformations and chromosomal abnormalities Q00 Anencephaly and similar malformations Q01 Encephalocele Q02 Microcephaly Q03 Congenital hydrocephalus Q04 Other congenital malformations of brain Q05 Spina bifida Q06 Other congenital malformations of spinal cord Q07 Other congenital malformations of nervous system Q10 Congenital malformations of eyelid, lacrimal apparatus and orbit Q11 Anophthalmos, microphthalmos and macrophthalmos Q12 Congenital lens malformations Q13 Congenital malformations of anterior segment of eye Q14 Congenital malformations of posterior segment of eye Q15 Other congenital malformations of eye Q16 Congenital malformations of ear causing impairment of hearing Q17 Other congenital malformations of ear Q18 Other congenital malformations of face and neck Q20 Congenital malformations of cardiac chambers and connections Q21 Congenital malformations of cardiac septa 6

Available at: http://www.who.int/classifications/icd/icdonlineversions/en/

Q22 Congenital malformations of pulmonary and tricuspid valves Q23 Congenital malformations of aortic and mitral valves Q24 Other congenital malformations of heart Q25 Congenital malformations of great arteries Q 26 Congenital malformations of great veins Q27 Other congenital malformations of peripheral vascular system Q28 Other congenital malformations of circulatory system Q30 Congenital malformations of nose Q31 Congenital malformations of larynx Q32 Congenital malformations of trachea and bronchus Q33 Congenital malformations of lung Q34 Other congenital malformations of respiratory system Q36 Cleft lip Q37 Cleft palate with cleft lip Q38 Other congenital malformations of tongue, mouth and pharynx Q39 Congenital malformations of oesophagus Q40 Other congenital malformations of upper alimentary tract Q41 Congenital absence, atresia and stenosis of small intestine Q42 Congenital absence, atresia and stenosis of large intestine Q43 Other congenital malformations of intestine Q44 Congenital malformations of gallbladder, bile ducts and liver Q45 Other congenital malformations of digestive system Q50 Congenital malformations of ovaries, fallopian tubes and broad ligaments Q51 Congenital malformations of uterus and cervix Q52 Other congenital malformations of female genitalia Q53 Undescended testicle Q54 Hypospadias

Q55 Other congenital malformations of male genital organs Q56 Indeterminate sex and pseudohermaphroditism Q60 Renal agenesis and other reduction defects of kidney Q61 Cystic kidney disease Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter Q63 Other congenital malformations of kidney Q64 Other congenital malformations of urinary system Q65 Congenital deformities of hip Q66 Congenital deformities of feet Q67 Congenital musculoskeletal deformities of head, face, spine and chest Q68 Other congenital musculoskeletal deformities Q69 Polydactyly Q70 Syndactyly Q71 Reduction defects of upper limb Q72 Reduction defects of lower limb Q73 Reduction defects of unspecified limb Q74 Other congenital malformations of limb(s) Q75 Other congenital malformations of skull and face bones Q76 Congenital malformations of spine and bony thorax Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine Q78 Other osteochondrodysplasias Q79 Congenital malformations of the musculoskeletal system, not elsewhere classified Q80 Congenital ichthyosis Q81 Epidermolysis bullosa Q82 Other congenital malformations of skin Q83 Congenital malformations of breast Q84 Other congenital malformations of integument

Q85 Phakomatoses, not elsewhere classified Q86 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified Q87 Other specified congenital malformation syndromes affecting multiple systems Q89 Other congenital malformations, not elsewhere classified Q90 Down syndrome

N2 Disorders related to fetal growth P05 Slow fetal growth and fetal malnutrition P05.0 Light for gestational age Usually referred to as weight below but length above 10th centile for gestational age Light-for-dates P05.1 Small for gestational age Usually referred to as weight and length below 10th centile for gestational age Small-for-dates Small-and-light-for-dates P05.2 Fetal malnutrition without mention of light or small for gestational age Infant, not light or small for gestational age, showing signs of fetal malnutrition, such as dry, peeling skin and loss of subcutaneous tissue P05.9 Slow fetal growth, unspecified Fetal growth retardation NOS

N3 Birth trauma P10 Intracranial laceration and haemorrhage due to birth injury P10.0 Subdural haemorrhage due to birth injury Subdural haematoma (localized) due to birth injury P10.1 Cerebral haemorrhage due to birth injury P10.2 Intraventricular haemorrhage due to birth injury P10.3 Subarachnoid haemorrhage due to birth injury P10.4 Tentorial tear due to birth injury P10.8 Other intracranial lacerations and haemorrhages due to birth injury P10.9 Unspecified intracranial laceration and haemorrhage due to birth injury

P11 Other birth injuries to central nervous system P11.0 Cerebral oedema due to birth injury P11.1 Other specified brain damage due to birth injury P11.2 Unspecified brain damage due to birth injury P11.3 Birth injury to facial nerve Facial palsy due to birth injury P11.4 Birth injury to other cranial nerves P11.5 Birth injury to spine and spinal cord Fracture of spine due to birth injury P11.9 Birth injury to central nervous system, unspecified

Sampling incision Scalp clip (electrode) injury P12.8 Other birth injuries to scalp P12.9 Birth injury to scalp, unspecified

P14 Birth injury to peripheral nervous system P14.0 Erb paralysis due to birth injury P14.1 Klumpke paralysis due to birth injury P14.2 Phrenic nerve paralysis due to birth injury P14.3 Other brachial plexus birth injuries P14.8 Birth injuries to other parts of peripheral nervous system P14.9 Birth injury to peripheral nervous system, unspecified

P15.3 Birth injury to eye Subconjunctival haemorrhage due to birth injury Traumatic glaucoma due to birth injury P15.4 Birth injury to face Facial congestion due to birth injury P15.5 Birth injury to external genitalia P15.6 Subcutaneous fat necrosis due to birth injury P15.8 Other specified birth injuries P15.9 Birth injury, unspecified

N4 Complications of intrapartum events P20 Intrauterine hypoxia P20.1 Intrauterine hypoxia first noted during labour and delivery P20.9 Intrauterine hypoxia, unspecified

P21 Birth asphyxia Note: This category is not to be used for low Apgar score without mention of asphyxia or other respiratory problems. P21.0 Severe birth asphyxia Pulse less than 100 per minute at birth and falling or steady, respiration absent or gasping, colour poor, tone absent Asphyxia with 1-minute Apgar score 0–3 White asphyxia P21.1 Mild and moderate birth asphyxia Normal respiration not established within 1 minute, but heart rate 100 or above, some muscle tone present, some response to stimulation Asphyxia with 1-minute Apgar score 4–7 Blue asphyxia P21.9 Birth asphyxia, unspecified Anoxia NOS Asphyxia NOS Hypoxia NOS

N5 Convulsions and disorders of cerebral status P90 Convulsions of newborn

P91 Other disturbances of cerebral status of newborn P91.0 Neonatal cerebral ischaemia P91.1 Acquired periventricular cysts of newborn P91.2 Neonatal cerebral leukomalacia P91.3 Neonatal cerebral irritability P91.4 Neonatal cerebral depression P91.5 Neonatal coma P91.6 Hypoxic ischaemic encephalopathy of newborn P91.8 Other specified disturbances of cerebral status of newborn P91.9 Disturbance of cerebral status of newborn, unspecified

N6 Infection A33 Tetanus neonatorum

A50 Congenital syphilis A50.0 Early congenital syphilis, symptomatic A50.1 Early congenital syphilis, latent A50.2 Early congenital syphilis, unspecified A50.9 Congenital syphilis, unspecified

G00 Bacterial meningitis, not elsewhere classified G00.0 Haemophilus meningitis Meningitis due to Haemophilus influenzae G00.1 Pneumococcal meningitis G00.2 Streptococcal meningitis G00.3 Staphylococcal meningitis G00.8 Other bacterial meningitis G00.9 Bacterial meningitis, unspecified

G01

Meningitis in bacterial diseases classified elsewhere

G02

Meningitis in other infectious and parasitic diseases classified elsewhere

G02.0 Meningitis in viral diseases classified elsewhere G02.1 Meningitis in mycoses G02.8 Meningitis in other specified infectious and parasitic diseases classified elsewhere

G03

Meningitis due to other and unspecified causes

G03.0 Nonpyogenic meningitis Nonbacterial meningitis G03.1 Chronic meningitis G03.2 Benign recurrent meningitis [Mollaret] G03.8 Meningitis due to other specified causes G03.9 Meningitis, unspecified

G04

Encephalitis, myelitis and encephalomyelitis

G04.0 Acute disseminated encephalitis G04.1 Tropical spastic paraplegia G04.2 Bacterial meningoencephalitis and meningomyelitis, not elsewhere classified G04.8 Other encephalitis, myelitis and encephalomyelitis G04.9 Encephalitis, myelitis and encephalomyelitis, unspecified

G05

Encephalitis, myelitis and encephalomyelitis in diseases classified elsewhere

G05.0 Encephalitis, myelitis and encephalomyelitis in bacterial diseases classified elsewhere G05.1 Encephalitis, myelitis and encephalomyelitis in viral diseases classified elsewhere G05.2 Encephalitis, myelitis and encephalomyelitis in other infectious and parasitic diseases classified elsewhere

G06

Intracranial and intraspinal abscess and granuloma

G06.0 Intracranial abscess and granuloma G06.1 Intraspinal abscess and granuloma G06.2 Extradural and subdural abscess, unspecified

G07

Intracranial and intraspinal abscess and granuloma in diseases classified elsewhere

G08

Intracranial and intraspinal phlebitis and thrombophlebitis

G09

Sequelae of inflammatory diseases of central nervous system

P23 Congenital pneumonia Incl.: infective pneumonia acquired in utero or during birth P23.0 Congenital pneumonia due to viral agent P23.1 Congenital pneumonia due to Chlamydia P23.2 Congenital pneumonia due to staphylococcus P23.3 Congenital pneumonia due to streptococcus, group B P23.4 Congenital pneumonia due to Escherichia coli P23.5 Congenital pneumonia due to Pseudomonas P23.6 Congenital pneumonia due to other bacterial agents Haemophilus influenzae Klebsiella pneumoniae Mycoplasma Streptococcus, except group B P23.8 Congenital pneumonia due to other organisms P23.9 Congenital pneumonia, unspecified

P35.8 Other congenital viral diseases Congenital varicella [chickenpox] P35.9 Congenital viral disease, unspecified

P36 Bacterial sepsis of newborn Incl.: congenital septicaemia P36.0 Sepsis of newborn due to streptococcus, group B P36.1 Sepsis of newborn due to other and unspecified streptococci P36.2 Sepsis of newborn due to Staphylococcus aureus P36.3 Sepsis of newborn due to other and unspecified staphylococci P36.4 Sepsis of newborn due to Escherichia coli P36.5 Sepsis of newborn due to anaerobes P36.8 Other bacterial sepsis of newborn P36.9 Bacterial sepsis of newborn, unspecified

P37 Other congenital infectious and parasitic diseases P37.0 Congenital tuberculosis P37.1 Congenital toxoplasmosis Hydrocephalus due to congenital toxoplasmosis P37.2 Neonatal (disseminated) listeriosis P37.3 Congenital falciparum malaria P37.4 Other congenital malaria P37.5 Neonatal candidiasis P37.8 Other specified congenital infectious and parasitic diseases P37.9 Congenital infectious and parasitic disease, unspecified

P38 Omphalitis of newborn with or without mild haemorrhage

P39 Other infections specific to the perinatal period P39.0 Neonatal infective mastitis P39.1 Neonatal conjunctivitis and dacryocystitis Neonatal chlamydial conjunctivitis Ophthalmia neonatorum NOS P39.2 Intra-amniotic infection of fetus, not elsewhere classified P39.3 Neonatal urinary tract infection P39.4 Neonatal skin infection Neonatal pyoderma P39.8 Other specified infections specific to the perinatal period P39.9 Infection specific to the perinatal period, unspecified

N7 Respiratory and cardiovascular disorders P22 Respiratory distress of newborn P22.0 Respiratory distress syndrome of newborn Hyaline membrane disease P22.1 Transient tachypnoea of newborn P22.8 Other respiratory distress of newborn P22.9 Respiratory distress of newborn, unspecified

P24 Neonatal aspiration syndromes Incl.: neonatal pneumonia resulting from aspiration P24.0 Neonatal aspiration of meconium P24.1 Neonatal aspiration of amniotic fluid and mucus Aspiration of liquor (amnii) P24.2 Neonatal aspiration of blood P24.3 Neonatal aspiration of milk and regurgitated food P24.8 Other neonatal aspiration syndromes P24.9 Neonatal aspiration syndrome, unspecified Neonatal aspiration pneumonia NOS

P25 Interstitial emphysema and related conditions originating in the perinatal period P25.0 Interstitial emphysema originating in the perinatal period P25.1 Pneumothorax originating in the perinatal period P25.2 Pneumomediastinum originating in the perinatal period P25.3 Pneumopericardium originating in the perinatal period P25.8 Other conditions related to interstitial emphysema originating in the perinatal period

P26 Pulmonary haemorrhage originating in the perinatal period P26.0 Tracheobronchial haemorrhage originating in the perinatal period

P26.1 Massive pulmonary haemorrhage originating in the perinatal period P26.8 Other pulmonary haemorrhages originating in the perinatal period P26.9 Unspecified pulmonary haemorrhage originating in the perinatal period

P27 Chronic respiratory disease originating in the perinatal period P27.0 Wilson-Mikity syndrome Pulmonary dysmaturity P27.1 Bronchopulmonary dysplasia originating in the perinatal period P27.8 Other chronic respiratory diseases originating in the perinatal period Congenital pulmonary fibrosis Ventilator lung in newborn P27.9 Unspecified chronic respiratory disease originating in the perinatal period

P28 Other respiratory conditions originating in the perinatal period P28.0 Primary atelectasis of newborn Primary failure to expand terminal respiratory units Pulmonary: • • hypoplasia associated with short gestation immaturity NOS

P28.1 Other and unspecified atelectasis of newborn Atelectasis: • • • NOS partial secondary

Resorption atelectasis without respiratory distress syndrome P28.2 Cyanotic attacks of newborn P28.3 Primary sleep apnoea of newborn Sleep apnoea of newborn: 77

• • •

central NOS obstructive

P28.4 Other apnoea of newborn Apnoea (of): newborn, obstructive prematurity P28.5 Respiratory failure of newborn P28.8 Other specified respiratory conditions of newborn Congenital (laryngeal) stridor NOS Snuffles in newborn P28.9 Respiratory condition of newborn, unspecified

P29 Cardiovascular disorders originating in the perinatal period P29.0 Neonatal cardiac failure P29.1 Neonatal cardiac dysrhythmia P29.2 Neonatal hypertension P29.3 Persistent fetal circulation Delayed closure of ductus arteriosus Pulmonary hypertension of newborn (persistent) P29.4 Transient myocardial ischaemia of newborn P29.8 Other cardiovascular disorders originating in the perinatal period P29.9 Cardiovascular disorder originating in the perinatal period, unspecified

N8 Other neonatal conditions P50 Fetal blood loss P50.0 Fetal blood loss from vasa praevia P50.1 Fetal blood loss from ruptured cord P50.2 Fetal blood loss from placenta P50.3 Haemorrhage into co-twin P50.4 Haemorrhage into maternal circulation P50.5 Fetal blood loss from cut end of co-twin's cord P50.8 Other fetal blood loss P50.9 Fetal blood loss, unspecified Fetal haemorrhage NOS

P51 Umbilical haemorrhage of newborn P51.0 Massive umbilical haemorrhage of newborn P51.8 Other umbilical haemorrhages of newborn Slipped umbilical ligature NOS P51.9 Umbilical haemorrhage of newborn, unspecified

P52 Intracranial nontraumatic haemorrhage of fetus and newborn P52.0 Intraventricular (nontraumatic) haemorrhage, grade 1, of fetus and newborn Subependymal haemorrhage (without intraventricular extension) P52.1 Intraventricular (nontraumatic) haemorrhage, grade 2, of fetus and newborn Subependymal haemorrhage with intraventricular extension P52.2 Intraventricular (nontraumatic) haemorrhage, grade 3, and grade 4 of fetus and newborn Subependymal haemorrhage with both intraventricular and intracerebral extension P52.3 Unspecified intraventricular (nontraumatic) haemorrhage of fetus and newborn P52.4 Intracerebral (nontraumatic) haemorrhage of fetus and newborn P52.5 Subarachnoid (nontraumatic) haemorrhage of fetus and newborn 79

P52.6 Cerebellar (nontraumatic) and posterior fossa haemorrhage of fetus and newborn P52.8 Other intracranial (nontraumatic) haemorrhages of fetus and newborn P52.9 Intracranial (nontraumatic) haemorrhage of fetus and newborn, unspecified

P53 Haemorrhagic disease of fetus and newborn Incl.: Vitamin K deficiency of newborn

P54 Other neonatal haemorrhages P54.0 Neonatal haematemesis P54.1 Neonatal melaena P54.2 Neonatal rectal haemorrhage P54.3 Other neonatal gastrointestinal haemorrhage P54.4 Neonatal adrenal haemorrhage P54.5 Neonatal cutaneous haemorrhage P54.6 Neonatal vaginal haemorrhage Pseudomenses P54.8 Other specified neonatal haemorrhages P54.9 Neonatal haemorrhage, unspecified

P55 Haemolytic disease of fetus and newborn P55.0 Rhesus isoimmunization of fetus and newborn P55.1 ABO isoimmunization of fetus and newborn P55.8 Other haemolytic diseases of fetus and newborn P55.9 Haemolytic disease of fetus and newborn, unspecified P56 Hydrops fetalis due to haemolytic disease P56.0 Hydrops fetalis due to isoimmunization P56.9 Hydrops fetalis due to other and unspecified haemolytic disease

P57 Kernicterus P57.0 Kernicterus due to isoimmunization

P57.8 Other specified kernicterus P57.9 Kernicterus, unspecified

P58 Neonatal jaundice due to other excessive haemolysis P58.0 Neonatal jaundice due to bruising P58.1 Neonatal jaundice due to bleeding

P58.2 Neonatal jaundice due to infection P58.3 Neonatal jaundice due to polycythaemia P58.4 Neonatal jaundice due to drugs or toxins transmitted from mother or given to newborn P58.5 Neonatal jaundice due to swallowed maternal blood P58.8 Neonatal jaundice due to other specified excessive haemolysis P58.9 Neonatal jaundice due to excessive haemolysis, unspecified

P59 Neonatal jaundice from other and unspecified causes P59.0 Neonatal jaundice associated with preterm delivery Hyperbilirubinaemia of prematurity Jaundice due to delayed conjugation associated with preterm delivery P59.1 Inspissated bile syndrome P59.2 Neonatal jaundice from other and unspecified hepatocellular damage Fetal or neonatal giant cell hepatitis Fetal or neonatal (idiopathic) hepatitis P59.3 Neonatal jaundice from breast-milk inhibitor P59.8 Neonatal jaundice from other specified causes P59.9 Neonatal jaundice, unspecified Physiological jaundice (intense) (prolonged) NOS

P60 Disseminated intravascular coagulation of fetus and newborn

P61 Other perinatal haematological disorders P61.0 Transient neonatal thrombocytopenia Neonatal thrombocytopenia due to: • • • exchange transfusion idiopathic maternal thrombocytopenia isoimmunization

P61.1 Polycythaemia neonatorum P61.2 Anaemia of prematurity P61.3 Congenital anaemia from fetal blood loss P61.4 Other congenital anaemias, not elsewhere classified Congenital anaemia NOS P61.5 Transient neonatal neutropenia P61.6 Other transient neonatal disorders of coagulation P61.8 Other specified perinatal haematological disorders P61.9 Perinatal haematological disorder, unspecified

P75 Meconium ileus in cystic fibrosis

P76 Other intestinal obstruction of newborn P76.0 Meconium plug syndrome Meconium ileus in cases where cystic fibrosis is known not to be present P76.1 Transitory ileus of newborn P76.2 Intestinal obstruction due to inspissated milk P76.8 Other specified intestinal obstruction of newborn P76.9 Intestinal obstruction of newborn, unspecified

P77 Necrotizing enterocolitis of fetus and newborn

P78 Other perinatal digestive system disorders P78.0 Perinatal intestinal perforation Meconium peritonitis P78.1 Other neonatal peritonitis Neonatal peritonitis NOS P78.2 Neonatal haematemesis and melaena due to swallowed maternal blood P78.3 Noninfective neonatal diarrhoea P78.8 Other specified perinatal digestive system disorders Congenital cirrhosis (of liver) Neonatal oesophageal reflux Peptic ulcer of newborn P78.9 Perinatal digestive system disorder, unspecified

P80 Hypothermia of newborn P80.0 Cold injury syndrome Severe and usually chronic hypothermia associated with a pink flushed appearance, oedema, and neurological and biochemical abnormalities P80.8 Other hypothermia of newborn Mild hypothermia of newborn P80.9 Hypothermia of newborn, unspecified

P81 Other disturbances of temperature regulation of newborn P81.0 Environmental hyperthermia of newborn P81.8 Other specified disturbances of temperature regulation of newborn P81.9 Disturbance of temperature regulation of newborn, unspecified Fever of newborn NOS

P83 Other conditions of integument specific to fetus and newborn P83.0 Sclerema neonatorum

P83.1 Neonatal erythema toxicum P83.2 Hydrops fetalis not due to haemolytic disease Hydrops fetalis NOS P83.3 Other and unspecified oedema specific to fetus and newborn P83.8 Other specified conditions of integument specific to fetus and newborn Bronze baby syndrome Neonatal scleroderma Urticaria neonatorum P83.9 Condition of integument specific to fetus and newborn, unspecified

P92 Feeding problems of newborn P92.0 Vomiting in newborn P92.1 Regurgitation and rumination in newborn P92.2 Slow feeding of newborn P92.3 Underfeeding of newborn P92.4 Overfeeding of newborn P92.5 Neonatal difficulty in feeding at breast P92.8 Other feeding problems of newborn P92.9 Feeding problem of newborn, unspecified

P93 Reactions and intoxications due to drugs administered to fetus and newborn Incl.: Grey syndrome from chloramphenicol administration in newborn

P94 Disorders of muscle tone of newborn P94.0 Transient neonatal myasthenia gravis P94.1 Congenital hypertonia P94.2 Congenital hypotonia Nonspecific floppy baby syndrome

P94.8 Other disorders of muscle tone of newborn P94.9 Disorder of muscle tone of newborn, unspecified

N9 Low birth weight and prematurity P07 Disorders related to short gestation and low birth weight, not elsewhere classified Note: When both birth weight and gestational age are available, priority of assignment should be given to birth weight. Incl.: the listed conditions, without further specification, as the cause of mortality, morbidity or additional care in newborn P07.0 Extremely low birth weight Birth weight 999 g or less P07.1 Other low birth weight Birth weight 1000–2499 g P07.2 Extreme immaturity Less than 28 completed weeks (less than 196 completed days) of gestation P07.3 Other preterm infants 28 completed weeks or more but less than 37 completed weeks (196 completed days but less than 259 completed days) of gestation Prematurity NOS

N10 Miscellaneous While a perinatal death is most often coded to P05–P96 or a Q code, there are cases where codes from several other sections of ICD-10 should be used. For an extensive list see ICD-10 version:2016 and ICD-10 volume 2: instruction manual (2010).7

Available at: http://www.who.int/classifications/icd/icdonlineversions/en/

N11 Neonatal death of unspecified cause P96 Other conditions originating in the perinatal period P96.0 Congenital renal failure Uraemia of newborn P96.1 Neonatal withdrawal symptoms from maternal use of drugs of addiction Drug withdrawal syndrome in infant of dependent mother Neonatal abstinence syndrome P96.2 Withdrawal symptoms from therapeutic use of drugs in newborn P96.4 Termination of pregnancy, affecting fetus and newborn P96.5 Complications of intrauterine procedures, not elsewhere classified P96.8 Other specified conditions originating in the perinatal period P96.9 Condition originating in the perinatal period, unspecified Congenital debility NOS

Annex D: ICD-PM groups and ICD-10 codes for maternal conditions in perinatal death In order to group and tabulate a perinatal death, the user needs information on the timing of the perinatal death (antenatal/intrapartum/neonatal) as well as the ICD-10 cause of death code. The information provided about the cause of death and the maternal condition should meet the ICD-10 coding rules for assigning a specific code before any tabulation can be undertaken. The codes included below are indicative for tabulation of data; for coding deaths, ICD-10 version:2016 and ICD10 volume 2: instruction manual (2010) should be utilized.8

M1 Complications of placenta, cord and membranes P02 Fetus and newborn affected by complications of placenta, cord and membranes P02.0 Fetus and newborn affected by placenta praevia P02.1 Fetus and newborn affected by other forms of placental separation and haemorrhage Abruptio placentae Accidental haemorrhage Antepartum haemorrhage Damage to placenta from amniocentesis, caesarean section or surgical induction Maternal blood loss Premature separation of placenta P02.2 Fetus and newborn affected by other and unspecified morphological and functional abnormalities of placenta Placental: • • • dysfunction infarction insufficiency

P02.3 Fetus and newborn affected by placental transfusion syndromes Placental and cord abnormalities resulting in twin-to-twin or other transplacental transfusion 8

Available at: http://www.who.int/classifications/icd/icdonlineversions/en/

Use additional code, if desired, to indicate resultant condition in the fetus or newborn. P02.4 Fetus and newborn affected by prolapsed cord P02.5 Fetus and newborn affected by other compression of umbilical cord Cord (tightly) around neck Entanglement of cord Knot in cord P02.6 Fetus and newborn affected by other and unspecified conditions of umbilical cord Short cord Vasa praevia P02.7 Fetus and newborn affected by chorioamnionitis Amnionitis Membranitis Placentitis P02.8 Fetus and newborn affected by other abnormalities of membranes P02.9 Fetus and newborn affected by abnormality of membranes, unspecified

M2 Maternal complications of pregnancy P01 Fetus and newborn affected by maternal complications of pregnancy P01.0 Fetus and newborn affected by incompetent cervix P01.1 Fetus and newborn affected by premature rupture of membranes P01.2 Fetus and newborn affected by oligohydramnios P01.3 Fetus and newborn affected by polyhydramnios Hydramnios P01.4 Fetus and newborn affected by ectopic pregnancy Abdominal pregnancy P01.5 Fetus and newborn affected by multiple pregnancy Triplet (pregnancy) Twin (pregnancy) P01.6 Fetus and newborn affected by maternal death P01.7 Fetus and newborn affected by malpresentation before labour P01.8 Fetus and newborn affected by other maternal complications of pregnancy Spontaneous abortion, fetus P01.9 Fetus and newborn affected by maternal complication of pregnancy, unspecified

M3 Other complications of labour and delivery

P03 Fetus and newborn affected by other complications of labour and delivery P03.0 Fetus and newborn affected by breech delivery and extraction P03.1 Fetus and newborn affected by other malpresentation, malposition and disproportion during labour and delivery Contracted pelvis Fetus or newborn affected by conditions classifiable to O64–O66 Persistent occipitoposterior Transverse lie P03.2 Fetus and newborn affected by forceps delivery P03.3 Fetus and newborn affected by delivery by vacuum extractor [ventouse] P03.4 Fetus and newborn affected by caesarean delivery P03.5 Fetus and newborn affected by precipitate delivery Rapid second stage P03.6 Fetus and newborn affected by abnormal uterine contractions Fetus or newborn affected by conditions classifiable to O62.-, except O62.3 Hypertonic labour Uterine inertia P03.8 Fetus and newborn affected by other specified complications of labour and delivery Abnormality of maternal soft tissues Destructive operation to facilitate delivery Fetus or newborn affected by conditions classifiable to O60–O75 and by procedures used in labour and delivery not included in P02.– and P03.0–P03.6 Induction of labour P03.9 Fetus and newborn affected by complication of labour and delivery, unspecified

M4 Maternal medical and surgical conditions P00 Fetus and newborn affected by maternal conditions that may be unrelated to present pregnancy P00.0 Fetus and newborn affected by maternal hypertensive disorders Fetus or newborn affected by maternal conditions classifiable to O10–O11, O13–O16 P00.1 Fetus and newborn affected by maternal renal and urinary tract diseases Fetus or newborn affected by maternal conditions classifiable to N00–N39 P00.2 Fetus and newborn affected by maternal infectious and parasitic diseases Fetus or newborn affected by maternal infectious disease classifiable to A00–B99 and J09– J11, but not itself manifesting that disease P00.3 Fetus and newborn affected by other maternal circulatory and respiratory diseases Fetus or newborn affected by maternal conditions classifiable to I00–I99, J00–J99, Q20–Q34 and not included in P00.0, P00.2 P00.4 Fetus and newborn affected by maternal nutritional disorders Fetus or newborn affected by maternal disorders classifiable to E40–E64 Maternal malnutrition NOS P00.5 Fetus and newborn affected by maternal injury Fetus or newborn affected by maternal conditions classifiable to S00–T79 P00.6 Fetus and newborn affected by surgical procedure on mother P00.7 Fetus and newborn affected by other medical procedures on mother, not elsewhere classified Fetus or newborn affected by radiology on mother P00.8 Fetus and newborn affected by other maternal conditions Fetus or newborn affected by: • • • conditions classifiable to T80–T88 maternal genital tract and other localized infections maternal systemic lupus erythematosus

P00.9 Fetus and newborn affected by unspecified maternal condition

P04 Fetus and newborn affected by noxious influences transmitted via placenta or breast-milk Incl.: nonteratogenic effects of substances transmitted via placenta P04.0 Fetus and newborn affected by maternal anaesthesia and analgesia in pregnancy, labour and delivery Reactions and intoxications from maternal opiates and tranquillizers administered during labour and delivery P04.1 Fetus and newborn affected by other maternal medication Cancer chemotherapy Cytotoxic drugs P04.2 Fetus and newborn affected by maternal use of tobacco P04.3 Fetus and newborn affected by maternal use of alcohol P04.4 Fetus and newborn affected by maternal use of drugs of addiction P04.5 Fetus and newborn affected by maternal use of nutritional chemical substances P04.6 Fetus and newborn affected by maternal exposure to environmental chemical substances P04.8 Fetus and newborn affected by other maternal noxious influences P04.9 Fetus and newborn affected by maternal noxious influence, unspecified

M5 No maternal condition

Informations clés

Organisation Organisation mondiale de la santé (OMS)

Type de document Publications

Date d'adoption 11 août 2016

Source Organisation mondiale de la santé