| Literature DB >> 34621087 |
Anke Heitkamp1, Anne Meulenbroek2, Jos van Roosmalen3, Stefan Gebhardt1, Linda Vollmer1, Johanna I de Vries4, Gerhard Theron1, Thomas van den Akker3.
Abstract
OBJECTIVE: To describe the incidence and main causes of maternal near-miss events in middle-income countries using the World Health Organization's (WHO) maternal near-miss tool and to evaluate its applicability in these settings.Entities:
Mesh:
Year: 2021 PMID: 34621087 PMCID: PMC8477432 DOI: 10.2471/BLT.21.285945
Source DB: PubMed Journal: Bull World Health Organ ISSN: 0042-9686 Impact factor: 9.408
Fig. 1Flowchart of studies included in the systematic review of maternal near miss in middle-income countries
Characteristics of studies included in the review on maternal near miss in middle-income countries
| Author | Setting | Study period | Study type | Medical care setting | Primary objective | Data source | Identification of cases of maternal near miss done by | Training of staff | Follow-up of the patient after end of pregnancy |
|---|---|---|---|---|---|---|---|---|---|
|
| |||||||||
| Ps et al., 2013 | India, Karnataka | 2011–2012 | Audit | 1 tertiary referral hospital with 6 primary health centres attached | To determine incidence of maternal near miss | NR | NR | NR | 42 days |
| Tunçalp et al., 2013 | Ghana | 2010–2011 | Prospective descriptive | 1 tertiary referral centre | To assess incidence of maternal near miss and related indicators | Medical records | NR | NR | 42 days |
| Kaur et al., 2014 | India, Himachal Pradesh | 2012–2013 | Prospective observational | 1 tertiary care hospital | To assess the causes and incidence of maternal near miss | NR | NR | NR | 42 days |
| Kushwah et al., 2014 | India, Madhya Pradesh | 2012–2013 | Prospective cross-sectional | 1 government tertiary care referral centre | To describe profile and outcomes of maternal near miss | Daily identification of women with maternal near miss in wards | Investigator | NR | 42 days |
| Luexay et al., 2014 | Lao People's Democratic Republic | 2011 | Descriptive prospective | 243 villages (community and local hospitals) | To determine incidence and causes of maternal near miss and maternal death in Lao People's Democratic Republic | Daily home visits | Health volunteers and health-centre staff | Yes | 42 days |
| Nacharajuh et al., 2014 | India | 2012–2014 | NR | 1 rural medical college | To assess number of maternal near misses and maternal near miss ratio | NR | NR | NR | 42 days |
| Pandey et al., 2014 | India | 2011–2012 | Retrospective | 1 tertiary hospital | To assess frequency and nature of maternal near miss | Medical records | NR | NR | 42 days |
| Bakshi et al., 2015 | India | NR | Cross-sectional epidemiological | 2 primary, 1 community and 1 tertiary facility | To determine prevalence and indicators of maternal near miss | Medical records | NR | NR | 42 days |
| Mazhar et al., 2015 | Pakistan | 2011 | Cross-sectional | 16 government facilities | To determine incidence and causes of severe maternal outcome | Medical records | Coordinators and data collector | Yes | 7 days |
| Sangeeta et al., 2015 | India | 2012–2013 | Prospective | 1 tertiary referral centre | To determine frequency and analyse causes of complications of maternal near miss and deaths | Medical records | NR | NR | 42 days |
| Abha et al., 2016 | India, Raipur | 2013–2015 | Prospective observational | 1 medical college hospital | To audit maternal near miss and to review substandard care | Clinical examinations; laboratory results and criteria meeting the WHO maternal near-miss criteria | NR | NR | 42 days |
| Ansari et al., 2016 | Pakistan | 2013 | Cross-sectional descriptive | Obstetric unit of 1 tertiary referral centre | To determine frequency and nature of maternal near miss | NR | NR | NR | 42 days |
| Kulkarni et al., 2016 | India, Maharashtra | 2012–2014 | Prospective observational | 2 tertiary centres | To investigate incidence and patterns of maternal near miss and to study classification criteria | Hospital registers; patient interviews | Research officers | No | 42 days |
| Oladapo et al., 2016 | Nigeria | 2012–2013 | Cross-sectional | 42 tertiary hospitals | To investigate burden and causes of life-threatening maternal complications and quality of obstetric care | Medical records collected during daily ward rounds | Trained data collector | Yes | 42 days |
| Parmar et al., 2016 | India | 2012 | Cross-sectional | 1 tertiary referral hospital | To describe incidence of maternal near miss | In-depth patient interviews | Investigators | NR | 42 days |
| Rathod et al., 2016 | India, Maharashtra | 2011–2013 | Retrospective cohort | 1 tertiary referral centre | To determine incidence of maternal near miss | Medical records | NR | NR | 42 days |
| Ray et al., 2016 | India, Maharashtra | 2014–2015 | Cross-sectional observational | 1 tertiary referral centre | To determine prevalence of maternal near miss | NR | NR | NR | 42 days |
| Tanimia et al., 2016 | Papua New Guinea | 2012–2013 | Prospective observational | 1 teaching referral hospital | To assess routinely collected data and determine rates of maternal near miss | Identification of women with maternal near miss in daily ward rounds and discussions in unit meetings | House officers | NR | NR |
| Bolnga et al., 2017 | Papua New Guinea | 2014–2016 | Prospective observational | 1 provincial hospital | To determine maternal near-miss ratio, mortality index and associated indices | Identification of women with maternal near miss in wards | Obstetric team | NR | NR |
| Chandak & Kedar, 2017 | India, Maharashtra | 2013–2015 | Cross-sectional observational | 1 tertiary care institute | To determine frequency and nature of maternal near miss | NR | NR | NR | 42 days |
| Mbachu et al., 2017 | Nigeria | 2014–2015 | Cross-sectional | 1 tertiary centre | To evaluate maternal near miss and maternal deaths | Medical records by daily rounds | Medical officer and interns | NR | 42 days |
| Tallapureddy et al., 2017 | India | 2014 | Retrospective cohort | 1 tertiary care hospital | To study severe maternal outcome and use WHO maternal near-miss tool | Admissions and medical records | NR | NR | 42 days |
| Panda et al., 2018 | India, Odisha | 2017 | Cross-sectional | 1 tertiary care hospital | To estimate burden of maternal near miss | Medical records | NR | NR | 42 days |
| Reena & Radha, 2018 | India, Kerala | 2011–2012 | Cross-sectional | 1 government medical college | To determine frequency, nature and timing of delays in cases of maternal near miss | Medical records; patient interviews | Obstetrician | NR | NR |
| Chaudhuri & Nath, 2019 | India, Kolkata | 2013–2014 | Prospective observational | 1 tertiary care hospital | To test application of clinical definition of life-threatening complications in pregnancy and to determine the level of near-miss maternal morbidity and mortality due to life-threatening obstetric complications | Medical records | Doctors, nurses and investigator | No | 42 days |
| Chhabra et al., 2019 | India, Delhi | 2013–2014 | Case–control | 1 tertiary level | To study incidence of severe maternal morbidity and maternal near miss, to assess feasibility of application of criteria and to assess causes and associated factors | Daily ward visits; medical records | Investigator | No | 42 days |
| El Agwany, 2019 | Egypt, Alexandria | 2015–2016 | Retrospective cohort | 1 tertiary level | To assess characteristics of maternal near miss by applying WHO approach | Intensive care unit medical records | Investigators | NR | 42 days |
| Gabbur et al., 2019 | India, Karnataka | 2015–2017 | Case series | 1 tertiary level | To assess maternal near miss and responsible factors | Medical records | NR | NR | 42 days |
| Herklots et al., 2019 | United Republic of Tanzania, Zanzibar | 2017–2018 | Prospective cohort | 1 main referral hospital | To determine correlation between number of organ dysfunctions and risk of mortality and to calculate sensitivity and specificity | Medical records | Junior investigators and research assistants | Yes | 42 days |
| Jayaratnam et al., 2019 | Timor-Leste | 2015–2016 | Prospective observational | Main referral hospital (only tertiary hospital in country) | To determine rate of severe maternal outcomes and most common etiologies | Daily ward rounds; medical records | Investigator and assistant investigators | NR | 42 days |
| Mansuri & Mall, 2019 | India, Ahmedabad City | 2015–2016 | Cross-sectional study, facility-based retrospective | 4 tertiary care centres | To describe the demographic characteristics of near miss patients and to determine the indicators of severe maternal morbidity and mortality | Second-day ward rounds; medical records | NR | NR | NR |
| Oppong et al., 2019 | Ghana | 2015 | Cross-sectional and case–control | 3 tertiary referral hospitals | To explore incidence and factors associated with maternal near miss | Medical records | Research assistants | Yes | 42 days |
| Karim et al., 2020 | Pakistan | 2016−2017 | Descriptive | Tertiary hospital | To describe types and frequencies of maternal near miss | Identification of cases during admission | NR | NR | 42 days |
| Lilungulu et al., 2020 | United Republic of Tanzania, Dodoma | 2015–2016 | Retrospective | 1 regional referral hospital | To identify magnitude and predictors of maternal and perinatal mortality among women with severe maternal outcome | Identification of cases during admission and in the wards | Three investigators | NR | NR |
| Owolabi et al., 2020 | Kenya | 2018 | Cross-sectional | 16 county hospitals, 2 national level hospitals and 46 subcounty hospitals | To determine incidence and causes of maternal near miss | Identification of cases in wards; medical records; patient interviews in case of missing data | Identified ”study clinician” such as Medical officers and nurses | Yes | 42 days |
| Samuels & Ocheke, 2020 | Nigeria | 2012–2013 | Cross-sectional | 1 university hospital | To determine frequency of maternal near miss and maternal deaths to identify common causes | Identification of cases during admission and in the wards; medical records | NR | NR | 42 days |
| Ugwu et al., 2020 | Nigeria | 2013–2016 | Prospective | 1 hospital | To determine frequency of maternal near miss and maternal deaths, to document primary causative factor and to compare maternal near miss and maternal deaths | Medical records | Research assistants (residents in internal medicine) | Yes | 42 days |
|
| |||||||||
| Cecatti et al., 2011 | Brazil, São Paulo State | 2002–2007 | Retrospective | Intensive care unit of 1 tertiary referral centre | To evaluate WHO maternal near-miss criteria | Medical records | Investigators and research assistants | NR | 42 days |
| Morse et al., 2011 | Brazil, Rio de Janeiro | 2009 | Cross-sectional prospective | 1 regional public referral hospital | To investigate severe maternal morbidity and maternal near miss using different identification criteria | Medical records; identification of cases during daily ward rounds | Principal investigator and trained students | Yes | 42 days |
| Lotufo et al., 2012 | Brazil, São Paulo State | 2004–2007 | Cross-sectional retrospective | Intensive care unit of 1 university referral hospital | To study maternal morbidity and mortality among women in intensive care | Medical records | Investigator | No | 42 days |
| Jabir et al., 2013 | Iraq | 2010 | Cross-sectional | 6 public hospitals | To use WHO maternal near-miss tool to assess characteristics and quality of care in women with severe complications | Medical records; daily staff interviews | Coordinators | Yes | 7 days |
| Shen et al., 2013 | China | 2008–2012 | Retrospective | 1 private tertiary hospital | To investigate factors associated with maternal near miss and mortality | Medical records | Audit committee of obstetricians and specialist registrars | Yes | 42 days |
| Dias et al., 2014 | Brazil, nationwide | 2011 – 2012 | National, hospital-based study of women who have recently given birth and their newborns | 1043 hospitals | To estimate incidence of maternal near miss in hospitals | Medical records; patient interviews | Students and health-care workers, coordinators from different health facilities and specialists | Yes | 42 days |
| Galvão et al., 2014 | Brazil, Sergipe | 2011–2012 | Cross-sectional and case–control | 2 reference maternity hospitals | To determine prevalence of severe acute maternal morbidity and maternal near miss and to identify risk factors | Identification of cases in wards; medical records; patient interviews | Obstetrician and trained staff | Yes | 42 days |
| Madeiro et al., 2015 | Brazil, Piaui | 2012–2013 | Prospective | 1 public tertiary referral hospital | To investigate incidence and determinants of severe maternal morbidity and maternal near miss | Medical records | Trained investigators | Yes | 42 days |
| Naderi et al., 2015 | Islamic Republic of Iran | 2013 | Prospective | 8 hospitals | To estimate incidence and identify underlying factors of severe maternal morbidity | Identification of cases during admission and in the wards | Midwife and gynaecologist | NR | 42 days |
| Oliveira & Da Costa, 2015 | Brazil, Pernambuco | 2007–2010 | Descriptive cross-sectional | Obstetric intensive care unit of 1 tertiary hospital | To analyse epidemiological and clinical profile of maternal near miss | Medical records | Investigator and research assistants | Yes | 42 days |
| Soma-Pillay et al., 2015 | South Africa | 2013–2014 | Descriptive population-based | 9 delivery facilities | To determine spectrum of maternal morbidity and mortality | Medical records; daily audit meetings | NR | No | 42 days |
| Cecatti et al., 2016 | Brazil, nationwide | 2009 – 2010 | Cross-sectional | 27 referral maternity hospitals | To identify severe maternal morbidity cases, study their characteristics and test WHO criteria | Medical records | Medical coordinators | Yes | 42 days |
| Ghazivakili et al., 2016 | Islamic Republic of Iran | 2012 | Cross-sectional | 13 public and private hospitals | To assess incidence of maternal near miss and audit quality of care | Medical records | Midwives with data collection form | Yes | 7 days |
| Mohammadi et al., 2016 | Islamic Republic of Iran | 2012–2014 | Incident case–control | 3 university hospitals; 1 secondary, 2 tertiary | To determine frequency, causes, risk factors and perinatal outcomes of maternal near miss | Medical records | Investigators | NR | 42 days |
| Norhayati et al., 2016 | Malaysia | 2014 | Cross-sectional | 2 referral and tertiary hospitals | To study severe maternal morbidity and maternal near miss and related indicators | Hospital and home-based medical records | Research assistant trained in nursing | No | 42 days |
| Akrawi et al., 2017 | Iraq | 2013 | Cross-sectional | 1 maternity teaching hospital | To determine major determinants of maternal near miss and maternal death | Medical records; interviews of women who experienced maternal near miss | NR | NR | 42 days |
| Iwuh et al., 2018 | South Africa | 2014 | Retrospective observational | 3 hospitals (secondary and tertiary) | To measure maternal near-miss ratio, maternal mortality ratio and mortality index | Medical records | Investigator and health-care providers, with identification confirmed by senior obstetric specialists | No | 42 days |
| Oliveira Neto et al., 2018 | Brazil, São Paulo State | 2013 – 2015 | Retrospective cross-sectional | Obstetric intensive care unit of 1 public teaching hospital | To explore indicators of WHO maternal near-miss criteria | Medical records | NR | NR | 42 days |
| De Lima et al., 2019 | Brazil, Alagoas | 2015–2016 | Prospective cohort observational | 1 tertiary | To collect data on maternal near miss | Patient interviews; medical records at admission and at day 42 | Principle investigator and research assistants | NR | 42 days |
| Mu et al., 2019 | China | 2012–2017 | Population-based surveillance system | 461 health facilities | To introduce maternal near miss into a national surveillance system and to report maternal near miss | Medical records, web-based online reporting system | Obstetrician and nurses responsible for patient care | Yes | 42 days |
| Heemelaar et al., 2020 | Namibia | 2018–2019 | Nationwide surveillance | All public hospitals (1 tertiary, 4 regional, 30 district) | To obtain data on pregnancy outcomes and assess benefits of such surveillance in comparison with surveillance of maternal deaths only | Medical records | Nominated staff | Yes | 42 days |
| Ma et al., 2020 | China | 2012–2018 | Cross-sectional | 18 hospitals in province | To explore prevalence of maternal near miss, risk factors for maternal near miss and relationship between maternal near miss and perinatal outcomes | Electronic medical record system | Nurses and doctors | Yes | 42 days |
| Verschueren et al., 2020 | Suriname | 2017–2018 | Prospective nationwide population-based cohort | All 5 hospitals and primary health-care centre | To find reason for high maternal mortality ratio and stillbirths and compare findings with other countries to improve quality of care | Identification of cases during daily ward rounds; medical records | Research coordinator (doctor) and investigator | Yes | 42 days |
|
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| Bashour et al., 2015 | Egypt, Lebanon | 2011 | Cross-sectional | Public maternity hospitals | To report on prevalence of maternal near miss | Medical records | Investigators | Yes | 7 days |
| De Mucio et al., 2016 | Colombia, Dominican Republic, Ecuador, Honduras, Nicaragua, Paraguay, Peru | 2013 | Cross-sectional | Hospitals multiple countries | To evaluate performance of a systematized form to detect severe maternal outcomes | Medical records | Health-care professionals | Yes | 42 days |
NR: data not reported; WHO: World Health Organization.
Incidence and causes of maternal near miss in middle-income countries
| Author | Setting | No. of live births | No. of cases of maternal near miss | Maternal near misses per 1000 live birthsa | Most frequent organ dysfunction | Most frequent cause of maternal near missb | No. of maternal deaths | Maternal deaths per 100 000 live birthsc | Ratio of maternal near miss to maternal deathd | Mortality index, %e |
|---|---|---|---|---|---|---|---|---|---|---|
|
| ||||||||||
| Ps et al., 2013 | India | 7 330 | 131 | 17.9 | NR | Haemorrhage | 23 | 313 | 5.6 | 14.9 |
| Tunçalp et al., 2013 | Ghana | 3 206 | 94 | 28.6 | Coagulation or haematological dysfunction | Severe postpartum haemorrhage | 37 | 1 154 | 2.5 | 28.2 |
| Kaur et al., 2014 | India | 6 008 | 140 | 23.3 | NR | Hypertensive disorders | 16 | 266 | 8.8 | 10 |
| Kushwah et al., 2014 | India | 5 219 | 63 | 6.8 | NR | Hypertensive disorders | 47 | 901f | 1.3 | 42.9 |
| Luexay et al., 2014 | Lao People's Democratic Republic | 1 123 | 11 | 9.8 | Respiratory | Haemorrhage | 2 | 179 | 5.5 | 15.3 |
| Nacharajuh et al., 2014 | India | 2 385 | 22 | 9.2 | NR | Pre-eclampsia | 2 | 84f | 11.0 | 8.3 |
| Pandey et al., 2014 | India | 5 273 | 633 | 120.0 | NR | Haemorrhage | 247 | 45 | 2.6 | 27.2f |
| Bakshi et al., 2015 | India | 688 | 51 | 74.1f | NR | Sepsis | 10 | 1 | 5.1 | 16.4 |
| Bashour et al., 2015 | Egypt | 2641 | 32 | 12.1 | Coagulation or haematological dysfunction | Haemorrhage | 3 | 114 | 11.0 | 8.6 |
| Mazhar et al., 2015 | Pakistan | 12 729 | 94 | 7.0 | Cardiovascular | Postpartum haemorrhageg | 38 | 299 | 2.5 | 28.7 |
| Sangeeta et al., 2015 | India | 6 767 | 27 | 4.0 | Coagulation or haematological dysfunction | Haemorrhage | 13 | 188f | 3.4 | 22.8 |
| Abha et al., 2016 | India | 13 895 | 211 | 15.2 | Coagulation or haematological dysfunction | Hypertensive disorders | 102 | 734f | 2.1 | 32.9 |
| Ansari et al., 2016 | Pakistan | 1 035 | 76 | 73.4f | Cardiovascular | NR | 7 | 676 | 10.9f | 8.4f |
| De Mucio et al., 2016 | Honduras | 613 | 10 | 16.3f | NR | NR | 1 | 163 | 10.0 | 9.1f |
| De Mucio et al., 2016 | Nicaragua | 477 | 4 | 8.4f | NR | NR | 0 | 0 | 0 | 0 |
| Kulkarni et al., 2016 | India | 14 508 | 525 | 36.2 | Coagulation or haematological dysfunction | Hypertensive disorders | NR | 648f | 5.6 | 9.6 |
| Oladapo et al., 2016 | Nigeria | 91 724 | 1451 | 15.8 | NR | Obstetric haemorrhage | 998 | 1 088 | 2.5f | 40.8 |
| Parmar et al., 2016 | India | 1 929 | 40 | 20.7 | NR | NR | 2 | 933 | 2.2 | 31.0 |
| Rathod et al., 2016 | India | 22 092 | 167 | 7.6 | Coagulation or haematological dysfunction | Haemorrhage | 66 | 298 | 3.4 | 29.7 |
| Ray et al., 2016 | India | 4 038 | 218 | 54.0 | NR | Hypertensive disorders | 17 | 421 | 13.0 | 7.17 |
| Tanimia et al., 2016 | Papua New Guinea | 13 338 | 121 | 9.1 | NR | Obstetric haemorrhage | 9 | 67 | 13.5 | 6.8 |
| Bolnga et al., 2017 | Papua New Guinea | 6 019 | 153 | 25.4 | NR | Postpartum haemorrhage | 10 | 166 | 15.3 | 6.8 |
| Chandak & Kedar, 2017 | India | 12 757 | 137 | 10.7 | Cardiovascular | Eclampsia | NR | 243f | 10.5 | 18.5f |
| Mbachu et al., 2017 | Nigeria | 262 | 52 | 198.0 | NR | Hypertensive disorders | 5 | 1 908 | 11.4 | 8.8 |
| Tallapureddy et al., 2017 | India | 3 784 | 32 | 8.5 | Coagulation or haematological dysfunction | Haemorrhage | 6 | 159f | 5.3 | 15.8 |
| Oppong et al., 2019 | Ghana | 8 433 | 288 | 34.2 | Cardiovascular | Pre-eclampsia and eclampsiah | 62 | 735 | 4.6f | 21.7f |
| Panda et al., 2018 | India | 1 349 | 89 | 66.0 | NR | Severe pre-eclampsia | 8 | 593 | 11.1 | 8.2 |
| Reena & Radha, 2018 | India | 3 451 | 32 | 9.3 | Coagulation or haematological dysfunction | Severe pre-eclampsia | 5 | 145 | 6.4 | 13.5f |
| Chaudhuri & Nath, 2019 | India | 4 081 | 175 | 43.0 | Vascular dysfunction | Hypertensive disorder (eclampsia) | 23 | 564 | 7.7 | 11.5 |
| Chhabra et al., 2019 | India | 38 111 | 261 | 6.9 | Coagulation | Hypertensive disorder | 166 | 436 | 1.6 | 23 |
| El Agwany, 2019 | Egypt | 28 877 | 170 | 5.9 | Coagulation | Haemorrhage | 14 | 50f | 12.2 | 7.5 |
| Gabbur et al., 2019 | India | 6 053i | 100 | 16.4 | NR | Postpartum haemorrhage | 13 | 215f | 7.7 | 88.5f |
| Herklots et al., 2019 | United Republic of Tanzania | 22 011 | 256 | 11.6 | Coagulation or haematological dysfunction | NR | 79 | 359 | 3.2 | 24.0 |
| Jayaratnam et al., 2019 | Timor-Leste | 4 529 | 39 | 8.0 | NR | Eclampsia or postpartum haemorrhage | 30 | 662 | 1.3 | 43.0 |
| Mansuri & Mall, 2019 | India | 21 491 | 247 | 11.5 | NR | Eclampsia or pre-eclampsia | 79 | 367 | 3.1 | 24.2 |
| Karim et al., 2020 | Pakistan | 3 360 | 54 | 16.0 | NR | Adherent placenta | 8 | 238 | 6.8 | 12.9 |
| Lilungulu et al., 2020 | United Republic of Tanzania | 3 480 | 124 | 36.0 | NR | Haemorrhage | 16 | 460 | 7.8 | 11.4 |
| Owolabi et al., 2020 | Kenya | 36 162 | 260 | 7.2 | NR | Postpartum haemorrhage | 13 | 36 | 20.0 | 4.8 |
| Samuels & Ocheke, 2020 | Nigeria | 2 357 | 86 | 36.5f | NR | Hypertensive disorders | 19 | 806 | 4.5 | 81.9f |
| Ugwu et al., 2020 | Nigeria | 2 236k | 60 | 26.8f | Cardiovascular | Severe haemorrhage | 28 | 1251 | 2.1 | 31.8 |
|
| ||||||||||
| Cecatti et al., 2011 | Brazil | 14 418 | 194 | 13.5 | NR | NR | 18 | 125 | 10.7 | 8.5 |
| Morse et al., 2011 | Brazil | 1 069 | 10 | 9.4 | NR | Severe pre-eclampsiag | 3 | 280 | 3.3 | 23 |
| Lotufo et al., 2012 | Brazil | 9 683 | 43 | 4.4 | NR | Haemorrhage | 5 | 52 | 8.6 | 10.4 |
| Jabir et al., 2013 | Iraq | 25 472 | 129 | 5.1 | Cardiovascular | Obstetric haemorrhage | 16 | 63 | 9.0 | 11.0 |
| Shen et al., 2013 | China | 18 104 | 72 | 4.0 | NR | Postpartum haemorrhage | 3 | 16 | 23.0 | 4.2 |
| Dias et al., 2014 | Brazil | 23 894 | 243 | 10.2 | NR | NR | 7 | 29 | 34.7 | 2.8 |
| Galvão et al., 2014 | Brazil | 16 243 | 76 | 4.7 | NR | Hypertensive disordersj | 17 | 105 | 4.5 | 18 |
| Bashour et al., 2015 | Lebanon | 1 171 | 5 | 4.3 | Hepatic dysfunction | Multiple causesk | 0 | 0 | 0 | NR |
| Madeiro et al., 2015 | Brazil | 5 841 | 56 | 9.6 | NR | Hypertensive disorders | 10 | 171 | 5.6 | 15.2 |
| Naderi et al., 2015 | Islamic Republic of Iran | 19 908 | 501 | 25.2 | NR | Severe pre-eclampsia | 2 | 10f | 250.0 | NR |
| Oliveira & Da Costa, 2015 | Brazil | 19 940 | 255 | 12.8 | NR | Hypertensive disorders | NR | 280f | 4.5 | 18 |
| Soma-Pillay et al., 2015 | South Africa | 26 614i | 114 | 4.3f | Vascular | Obstetric haemorrhage | NR | 71f | 7.1f | 14 |
| Cecatti et al., 2016 | Brazil | 82 144 | 770 | 9.37 | NR | Hypertensive disorders | 140 | 170 | 5.5 | 15.4 |
| De Mucio et al., 2016 | Colombia | 334 | 3 | 9.0f | NR | NR | 0 | 0 | 0 | 0 |
| De Mucio et al., 2016 | Dominican Republic | 133 | 3 | 22.6f | NR | NR | 0 | 0 | 0 | 0 |
| De Mucio et al., 2016 | Ecuador | 228 | 2 | 8.9f | NR | NR | 0 | 0 | 0 | 0 |
| De Mucio et al., 2016 | Paraguay | 334 | 2 | 6.0f | NR | NR | 1 | 299f | 2.0f | 33.3f |
| De Mucio et al., 2016 | Peru | 315 | 11 | 35.0f | NR | NR | 0 | 0 | 0 | 0 |
| Ghazivakili et al., 2016 | Islamic Republic of Iran | 38 663 | 192 | 5.0 | Cardiovascular | Severe pre-eclampsia | NR | 18f | 2.4 | 3.5 |
| Mohammadi et al., 2016 | Islamic Republic of Iran | 12 965 | 82 | 6.3 | Coagulation or haematological dysfunction | Severe postpartum haemorrhage | NR | 93f | 6.9f | 13 |
| Norhayati et al., 2016 | Malaysia | 21 579 | 47 | 2.2 | Coagulation or haematological dysfunction | Postpartum haemorrhage | NR | 9f | 23.5 | 4.1 |
| Akrawi et al., 2017 | Iraq | 17 353 | 142 | 8.2f | Cardiovascular | Hypertensive disorders | 11 | 63 | 12.9 | 7.2 |
| Iwuh et al., 2018 | South Africa | 19 222 | 112 | 5.8 | NR | Hypertensive disorders | 13 | 68 | 8.6 | 10.4 |
| Oliveira Neto et al., 2018 | Brazil | 8 065 | 60 | 7.4 | Hepatic dysfunction | Pre-eclampsia | NR | 62f | 13.0 | 7.7f |
| De Lima et al., 2019 | Brazil | 1 002 | 55 | 54.8 | Respiratory | Hypertension | 1 | 99 | 11.0 | 8.3 |
| Mu et al., 2019 | China | 9 051 638l | 37 060 | 4.1f | Coagulation dysfunction | Hypertensive disorders | 380 | 4.1f | 97.5 | NR |
| Heemelaar et al., 2020 | Namibia | 37 106 | 298 | 8.0 | NR | Obstetric haemorrhage | 23 | 62 | 13.0 | 92.8f |
| Ma et al., 2020 | China | 542 109 | 3208 | 5.9 | Coagulation or haematological dysfunction | Postpartum haemorrhage | 34 | 6.3 | 94.4f | 1.1 |
| Verschueren et al., 2020 | Suriname | 9 114 | 71 | 7.8 | Coagulation or haematological dysfunction | Hypertensive disorders | 10 | 110 | 7.1f | 12.0 |
NR: not reported.
a Maternal near miss ratio.
b Most frequent causes of maternal near miss; terminology as used in the original article.
c Maternal mortality ratio.
d Ratio of number of maternal misses to the number of maternal deaths.
e Mortality index is: [number of maternal deaths / (number of cases of maternal near miss + number of maternal deaths) × 100].
f We calculated the value shown using formulae shown in the main text.
g Severe maternal outcome.
h Potentially life-threatening conditions.
i Per number of births.
j Severe acute maternal morbidity.
k Multiple causes: placenta praevia, placenta accreta, placenta increta, placenta percreta, hepatic disease.
l Number of pregnant women.
Difficulties reported and modifications applied to the World Health Organization maternal near-miss tool in middle-income countries
| Author | Setting | Modifications applied in study | Comments and problems reported by study researchers |
|---|---|---|---|
|
| |||
| Kaur et al., 2014 | India, Himachal Pradesh | Addition of items to clinical criteria (severe pre-eclampsia; eclampsia)a | NA |
| Kushwah et al., 2014 | India, Madhya Pradesh | NA | Maximum units of blood available in study institute were 3 units as blood bank was not well supplied. Researchers believed that WHO’s criterion of receiving 5 or more units of blood was less applicable in a resource-poor institute. |
| Luexay et al., 2014 | Lao People's Democratic Republic | Simplified modification of WHO tool for use in the communityc | Researchers concluded that maternal near misses could have been underestimated by application of the WHO definition of maternal near miss, which relies on good laboratory and management-based criteria. Adaptation of near-miss criteria for low-resource settings may benefit lower-middle-income countries where health services are also poorly resourced. |
| Pandey et al., 2014 | India | Omission of markers from laboratory criteria (pH; PaO2/FiO2) | NA |
| Sangeeta et al., 2015 | India | NA | Researchers concluded that in low-resource settings, interventions need to be developed with the local context in mind. |
| Kulkarni et al., 2016 | India, Maharashtra | Addition of item to clinical criteria (anaemia)d | NA |
| Parmar et al., 2016 | Papua New Guinea | Omission of markers from laboratory criteria (pH; lactate; glucose and keto-acids in urine; PaO2/FiO2) | Data collection in accordance with WHO maternal near-miss guidelines, adjusted for local factors, is possible in a busy maternity unit in a resource-poor setting. Researchers concluded that such data have the potential to improve early detection of life-threatening conditions and hence obstetric outcomes. |
| Parmar et al., 2016 | India | NA | Researchers noted that the WHO classification was remarkable for identifying the most serious cases with higher risk of death. However, the WHO classification showed a high threshold for detection of maternal near miss. Researchers therefore concluded that the method was missing a significant proportion of women with conditions such as pre-eclampsia and eclampsia. |
| Bolnga et al., 2017 | Papua New Guinea | NA | Papua New Guinea’s resource-poor setting lacks the capacity to perform some of the WHO-recommended laboratory investigations such as pH and lactate. Researchers noted that use of locally relevant criteria was also important to avoid underestimation of the true burden of maternal near miss as previously reported in other resource-poor settings. |
| Panda et al., 2018 | India, Odisha | Addition of items to clinical criteria (haemorrhage; hypertensive disorders; abortion; sepsis) | NA |
| El Agwany, 2019 | Egypt | NA | Researchers could not apply the criteria due to lack of resources. |
| Gabbur et al., 2019 | India, Karnataka | NA | Researchers concluded that modification of the WHO tool is required as currently it leads to underestimation of maternal near miss. |
| Herklots et al., 2019 | United Republic of Tanzania, Zanzibar | Not modified (researchers reported the tool was applicable in this setting) | Conclusions about maternal near miss are dependent on the quality of data and challenges to this should be acknowledged. Researchers recommended adhering to the WHO criteria (adjusted to specific settings as needed) to enable meaningful comparison between similar reference populations. |
| Jayaratnam et al., 2019 | Timor-Leste | Not modified | Determining a clear diagnosis in a woman with maternal near miss is difficult due to presence of multiple symptoms, lack of diagnostics due to fast deterioration of the woman and lack of laboratory-based markers. Researchers concluded that maternal near-miss criteria must be modified to the local context to enhance incorporation of cases (e.g. requiring lower transfusion requirements) in future studies. |
| Oppong et al., 2019 | Ghana | Addition to definition of coagulation in organ dysfunction criteria (bedside clotting time of > 7 mins) | Organ system-based criteria are regarded as the most specific means of identifying maternal near miss. However, researchers argued that these criteria require ready availability of laboratory tests and medical technologies, thus impeding their use in many low-resource local settings. |
| Owolabi et al., 2020 | Kenya | Adjustments were: lowering threshold for use of blood products to 2 units of blood (Kenyan method) | Kenyan method yielded 1.4 times the numbers of maternal near miss than the WHO method. Researchers concluded that there is under-reporting using the WHO maternal near-miss method. |
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| Morse et al., 2011 | Brazil, Rio de Janeiro | NA | As bed availability and intensive care unit admission criteria are not the same, researchers noted that use of intensive care unit admission as a marker is questionable because it is affected by level of complexity of care in a health setting and organization of obstetric care. |
| Lotufo et al., 2012 | Brazil, São Paulo State | NA | Researchers reported no difficulties in using and identifying the WHO criteria, with the exception of certain clinical criteria (e.g. gasping, cyanosis and bedside clotting tests) which generally occurred before starting complex care in the intensive care unit. |
| Shen et al., 2013 | China | NA | The study applied 16 of the 25 WHO criteria. Researchers noted that some women in their study received blood transfusion of < 5 units or intubation related to anaesthesia and therefore did not meet the WHO criteria. Women with pre-eclampsia without jaundice and loss of consciousness for < 12 hours were not included in the WHO clinical criteria group. In the laboratory-based group, women with maternal near miss were differentiated by oxygen saturation, blood creatinine level, platelet count and total bilirubin. Researchers reported it was impossible to always obtain blood pH or lactate level, because these parameters were not routinely checked in their institute. |
| Naderi et al., 2015 | Islamic Republic of Iran | Beside the collection of data on life-threatening disease, researchers added a form based on a published method. | NA |
| Oliveira & Da Costa, 2015 | Brazil, Pernambuco | NA | Mechanical ventilation was required in less than one quarter of cases of maternal near miss. Researchers noted that this finding may be attributed to local differences in accessibility of resources and interventions. It is one of the drawbacks of criteria based only on treatment because a more complex hospital and laboratory structure is required. |
| Soma-Pillay et al., 2015 | South Africa | NA | The WHO tool identified five potentially life-threatening conditions: severe postpartum haemorrhage; severe pre-eclampsia; eclampsia; sepsis or severe infection; and ruptured uterus. Researchers noted that conditions such as abruptio placentae, non-obstetric infections and medical and surgical disorders were also important causes of maternal morbidity. Researchers recommended that the WHO tool should expand the categories of potentially life-threatening conditions. |
| Ghazivakili et al., 2016 | Islamic Republic of Iran | NA | Researchers noted that a limitation of the WHO tool is that application of criteria based on organ failure requires relatively sophisticated laboratory and clinical monitoring. Underestimating occurrence of maternal near miss due to lack of equipment or unavailability of some tests is therefore possible. |
| Mohammadi et al., 2016 | Islamic Republic of Iran | Lowering threshold for use of blood products to 4 units of blood | NA |
| Norhayati et al., 2016 | Malaysia | NA | Researchers noted that use of the WHO criteria was limited in smaller health facilities. Laboratory-based markers (e.g. pH, PaO2, lactate) and management-based markers (e.g. vasoactive drugs and hysterectomy) were less likely to be applicable in these health facilities. |
| Akrawi et al., 2017 | Iraq | Lowering threshold for use of blood products to 3 units of blood | NA |
| Iwuh et al., 2018 | South Africa | Addition of items to definition of severe maternal complications (acute collapse or thromboembolism; non-pregnancy-related infections; medical or surgical disorders) | NA |
| Oliveira Neto et al., 2018 | Brazil, São Paulo State | NA | Researchers noted that arterial blood gas sampling was not routinely collected in all pregnant or postpartum patients admitted to the intensive care unit. PaO2 records were missing in some cases of maternal near miss. When evaluation of the level of consciousness by the Glasgow coma scale was compromised (due to residual effects of anaesthetics in the postoperative period, or by the use of continuous sedation), the Glasgow coma score of 15 was used as a criterion. |
| De Lima et al., 2019 | Brazil, Alagoas | Researchers noted that intensive care unit admission was not included in the WHO criteria but was an important marker of maternal severity in their study (identified in 94.5% of pregnant women) | Researchers noted that, in contrast to laboratory and management criteria, clinical criteria are important for low-income regions, because no complex laboratory and hospital infrastructures are required. Limitations of laboratory and management criteria are that most of these criteria require high-complexity units, wards, equipment or facilities for their use. Women experiencing near miss may therefore be missed. Lowering the numbers of packed red blood cell units or including disease-based criteria was necessary in low-resource settings to classify women as near miss. |
| Mu et al., 2019 | China | NA | Lack of high-quality medical institutions in rural areas is a problem for maternal health. In recent years, China has strengthened management of women with severe complications so that they must give birth in tertiary hospitals. The researchers argued that the lack of tertiary hospitals in rural areas will affect accessibility of pregnant women to high-quality health care. |
| Heemelaar et al., 2020 | Namibia | Adapted tool for middle-income countries | The researchers noted the limited availability of laboratory tests and management options resulting in under-reporting of maternal near miss. |
| Verschueren et al., 2020 | Suriname | Evaluation of the WHO maternal near-miss tool by comparing the Suriname obstetric surveillance system with WHO maternal near miss, Namibian and sub-Saharan African tools, to identify the most useful method | The researchers concluded that the WHO tool leads to underestimation of the prevalence of severe complications as the tool does not include certain disease-based conditions. |
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| De Mucio et al., 2016 | Colombia, Dominican Republic, Ecuador, Honduras, Nicaragua, Paraguay, Peru | Omission of items from laboratory criteria (glucose and keto-acids in urine) | NA |
NA: not applicable; PaO2: oxygen arterial pressure; PaO2/FiO2: ratio of arterial oxygen partial pressure to fractional inspired oxygen; WHO: World Health Organization.
a Severe pre-eclampsia (blood pressure of 170/110 mmHg measured twice); proteinuria of 5 g or more in 24 hours; and HELLP syndrome (haemolysis, elevated liver enzymes and low platelets) or pulmonary oedema or jaundice or eclampsia (generalized fits without previous history of epilepsy) or uncontrollable fits due to any other reason.
b Sepsis or severe systemic infection, fever (> 38 °C), confirmed or suspected infection (e.g. chorioamnionitis, septic abortion, endometritis, pneumonia), and at least one of the following: heart rate > 90 beats per minute, respiration rate > 20 breaths per minute, leukopenia (white blood cells < 4000/μL), leukocytosis (white blood cells > 12 000/μL).
c See the supplementary files of the original article for the complete list.
d Anaemia was defined by the researchers as haemoglobin level of < 60 g/L or clinical signs of severe anaemia without acute haemorrhage.
e Abnormal or difficult childbirth or labour for more than 24 hours.
f Low haemoglobin level (< 6 g/dL) or clinical signs of severe anaemia in women without severe haemorrhage.
Note: See Box 1 for the WHO inclusion criteria.