Abdollahpour, 2019
Abdollahpour, 2019
Systematic Review
Citation: Abdollahpour S, Heidarian Miri H, Khadivzadeh T. The global prevalence of maternal near miss: a systematic review and meta-
analysis. Health Promot Perspect. 2019;9(4):255-262. doi: 10.15171/hpp.2019.35.
© 2019 The Author(s). This is an open access article distributed under the terms of the Creative Commons Attribution License
(http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the
original work is properly cited.
Abdollahpour et al
ratio (MNMR) mentions to the number of maternal near- adequacy of the sample size, the objectivity and standard
miss cases per 1000 live births (LB).3 This criterion is of the criteria used for measurement of the condition, the
being reviewed to improve the quality of care, because a detailed description of the participants and the setting, the
large number of MNM cases will experience long-term reliability of the condition measurement, the adequacy
physical and psychological effects.3 That due to the lack of the response rate the appropriateness of the statistical
of accurate statistics of psychological complications and analysis, and the appropriate coping with the low response
burden of disease, implementation of supportive care, rate, in case it existed. All the article met the high-quality
screening of traumatic childbirth, and early counseling standard. When the indicators were not mentioned, but
prior to the beginning of post-traumatic stress or contained the necessary information for its calculation,
depression was suggested.4,5 But at present, studies that it was assessed and added to the results in the review.
have examined the global MNM rate are very low or old6,7 Among the results, the following quantitative indicators
and according to WHO criteria, accurate statistics are not were extracted.
available from these mothers. Considering this gap and To explore MNM ratio with WHO approach, the
need for aggregated information for policy and decision number of cases in a thousand LB was considered.3 We
making on reducing maternal morbidity and mortalities, applied a random effects meta-analysis to obtain the
the purpose of this study is to systematically review weighted average prevalence with 95% CIs for studies.
worldwide prevalence of MNM. Heterogeneity was estimated using the Cochran I2 statistic
and its P value.59 Subgroup analysis was accomplished to
Material and Methods analyze MNM as WHO criteria. All statistical analyses
Based on the Preferred Reporting Items for Systematic were conducted using Stata version 14.1(Stata Corp,
Reviews and Meta-analyses (PRISMA) checklist,8 this College Station, TX).
study was designed to review the body of the available
literature on MNM published until March 2019. We have Results
searched the electronic databases including PubMed, The primary search recognized 300 published papers,
Scopus and Web of Science and manually checked including 86 in PubMed, 89 in Web of Science and 104
references of the identified relevant papers. Regarding in Scopus. From those, 164 articles were elimi nated
eligibility criteria and regardless of the type of study, we after removal of duplicates. Nearly 135 articles were
include articles that have identified mothers according initially screened by abstract. After excluding those who
to WHO criteria (Including renal, cardiovascular, had inclusion criteria, 67 articles remained for full-text
respiratory, hepatic, coagulation/hematological, uterine screening. Out of these 67 articles, in the next step 18
dysfunction and neurological) 3 as well as articles that were excluded either because they had not followed the
extract the number of MD and the number of live births. WHO definition criteria. Data have been extracted from
We excluded studies targeted certain groups or conditions 49 articles (Figure 1). There was well agreement (88.37%)
such as some ethnic groups, twin pregnancy, post-partum between reviewers on the terminal articles eligible for
hemorrhage, preeclampsia, ectopic pregnancy etc because inclusion.
of lack of generalizability. Depending on the study design, the selected papers
We restricted the search to published articles in English were cross-sectional (n = 34), cohorts (n = 12), case control
language. The search strategy focused on three key words (n = 3). In almost all continents, the prevalence of MNM
or phrases: (“maternal near miss” AND (prevalence or was investigated. No studies were conducted in North
incidence)). The full-text articles were read to confirm America and Australia. The number of articles conducted
eligibility and to collect relevant information from the in Asia, South America, Africa, Europe and Oceania was
selected abstracts. Each article was read by at least two 20, 9, 16, 2, and 2, respectively. Most of these studies were
authors independently for the reading and synthesis conducted in Brazil (n = 7) and India (n = 9). Of the 34
stages. The disagreements between them were solved by articles, both MNM and MD were extracted; out of 15,
consensus. The reasons for exclusion criteria were listed only the prevalence of MNM was extracted. All articles
in the PRISMA flowchart. were conducted since 2012, because the WHO criteria for
The information of studies include author, year, identifying MNM was announced this year. Prevalence
country, continent , design of study, sample size, MNM, of MNM is reported by all the studies ranged from 2.2 to
MD, MNMR and quality score were collected in prepared 287.7 /1000 LB.
a separate page and are summarized in Table 1.9-57 Quality The weighted pooled worldwide prevalence of MNM,
of the studies was evaluated according to the set of was 18.67/1000 (95% CI: 16.28-21.06). There was a large
criteria based on Joanna Briggs Institute (JBI) guidance volume of heterogeneity in the prevalence of MNM (I2
on conducting prevalence and incidence reviews.58 The = 99.8%; Cochran Q-statistic P < 0.0001; Figure 2). The
quality of a paper was assessed based on criteria such subgroup analysis will help to explore heterogeneity in
as the appropriate recruitment of the participants, the the MNM prevalence. Subgroup analysis was conducted
representativeness of the sample, the sufficiency of the based on the continent and the country. Because maternal
coverage of the identified sample by the data analysis, the health indicators are very diverse in countries and
Table 1. Specifications of studies about prevalence Maternal Near Miss based on the WHO approach in world
Author Year Country Continent Design Sample (LB) MNM MD MNM/1000 JBI Score
Souza9 2012 Brazil South America Cross-sectional 82 388 770 140 9/34 17
Jabir 10
2013 Iraq Asia Cross-sectional 25 472 129 16 5/06 16
Nelissen11 2013 Tanzania Africa Cross-sectional 9152 216 32 23/6 17
Ps12 2013 India Asia Cross-sectional 7390 131 17/80 18
Rana 13
2013 Nepal Asia Cohort 41 676 157 3/80 15
Tunçalp14 2013 Ghana Africa Cohort 3438 94 37 28/60 17
Setia 15
2013 Indonesia Asia Cross-sectional 14 559 341 23/42 16
Dias16 2014 Brazil South America Cross-sectional 2 300 000 10/21 16
Galvão17 2014 Brazil South America Cross-sectional 16243 77 17 5/80 15
Luexay 18
2014 Laos Asia Cohort 1215 11 2 9/80 15
Pandey19 2014 India Asia Case-control 5273 633 247 120/04 14
Tahira 20
2014 Pakistan Asia Cross-sectional 1000 67 67 17
Bakshi21 2015 India Asia Cross-sectional 688 51 10 5/12 18
Bashour22 2015 Egypt* Africa Cross-sectional 9063 71 6 7/83 17
Madeiro 23
2015 Brazil South America Cohort 5841 56 10 9/60 18
Mazhar24 2015 Pakistan Asia Cross-sectional 13 175 94 38 7/13 15
Menezes 25
2015 Brazil South America Cross-sectional 20 435 77 17 3/76 16
Oliveira26 2015 Brazil South America Cross-sectional 2055 . 12/8 17
Rulisa27 2015 Rwanda Africa Cross-sectional 1739 13 8 14
Tan 28
2015 China Asia Cross-sectional 34 547 8 5 2/3 15
Abha29 2016 India Asia Cohort 13 895 211 102 15/18 17
Cecatti 20
2016 Brazil South America Cross-sectional 82 388 770 140 9/34 17
De Mucio31 2016 Latin America South America Cross-sectional 3196 37 12/3 16
Ghazivakili32 2016 Iran Asia Cross-sectional 38 663 192 7 4/97 16
Kalisa 33
2016 Rwanda Africa Cohort 3994 86 13 21/51 16
Mohammadi34 2016 Iran Asia Case-control 12 965 82 12 6/30 15
Nakimuli 35
2016 Uganda Africa Cohort 25 840 695 130 8/42 15
Nansubuga36 2016 Uganda Africa Cross-sectional 1557 434 287/70 18
Norhayati37 2016 Malaysia Asia Cross-sectional 21 579 395 2 2/20 15
Oladapo 38
2016 Nigeria Africa Cross-sectional 91 724 1451 998 15/81 16
O'Malley39 2016 Ireland Europe Cross-sectional 4502 16 0 3/55 17
Parmar 40
2016 India Asia Cross-sectional 1929 46 18 23/85 18
Rathod41 2016 India Asia Cohort 21 992 161 66 7/56 17
Ray42 2016 India Asia Cross-sectional 4800 220 17 45/83 16
Papua New
Tanimia 43
2016 Oceania Cross-sectional 13 338 122 9 9/1 16
Guinea
Witteveen44 2016 Netherlands Europe Cross-sectional 371 623 1179 3/17 15
Papua New
Bolnga 45
2017 Oceania Cohort 6019 153 10 25/4 16
Guinea
Chandak46 2017 India Asia Cross-sectional 13 186 137 10/38 16
Goldenberg 47
2017 Zambia** Africa Cross-sectional 122 707 4866 39/65 15
Liyew48 2017 Ethiopia Africa Cross-sectional 29 697 238 8/01 15
Mbachu 49
2017 Nigeria Africa Cross-sectional 262 52 5 198 15
Serruya50 2017 Latin America South America Cross-sectional 712 081 21985 1028 31/50 16
Awowole51 2018 Nigeria Africa Case-control 11 242 . 3/8 15
Chikadaya 52
2018 Zimbabwe Africa Cohort 11 871 110 13 9/3 16
Iwuh53 2018 South Africa Africa Case-control 19 222 112 13 5/83 17
Oppong 54
2018 Ghana Africa Cross-sectional 8433 288 62 34/2 17
Woldeyes55 2018 Ethiopia Africa Cross-sectional 2737 138 24 50/42 16
Yang56 2018 China Asia Cohort 14 014 265 18/90 17
Deepti Gupta 57
2018 India Asia Cohort 4533 74 15 16/32 16
Identification
Records identified through database Additional records identified through
searching (ISI=89, PubMed=86, Scholar
Scopus=104) (n = 1)
(n = 279)
Screening
EP= 4
Twin=7
ICU=4
Records screened Infection=3
Neonatal=11
(n =136)
Abortion=3)
RCT study=2
Qualitative study=2
Review=3
Full-text articles (n =69 )
assessed for eligibility
Eligibility
(n =67)
Full-text articles
excluded: Not having the
WHO definition criteria
Studies included in (n =18)
qualitative synthesis
(n =49)
Included
Studies included in
quantitative synthesis
(meta-analysis)
(n =49)
continents. By continents, MNM prevalence ranged from the studies that had been conducted in South America,
3.10/1000 in the Europe to 31.88/1000 LB in the Africa. weighted pooled prevalence of MNM was 11.57 (95%
Among the studies that had been conducted in Asia, CI: 4.68-18.47) with significant heterogeneity between
weighted pooled prevalence of MNM was 16.92 (95% studies (I2 = 99.9%; Cochran Q-statistic P < 0.001).Among
CI: 14.21-19.64) with significant heterogeneity between the studies that had been conducted in Africa, weighted
studies (I2 = 98.9%; Cochran Q-statistic P < 0.001).Among pooled prevalence of MNM was 31.88 [95% CI: 25.14-
38.61] with significant heterogeneity between studies
(I2 = 99.6%; Cochran Q-statistic P = 0.00). Among the
studies that had been conducted in Europe, weighted
pooled prevalence of MNM was 3.10 (95% CI: 2.93-3.28)
with non-significant little heterogeneity between studies
(I2 = 0.0%; Cochran Q-statistic P = 0.61). Among the
studies that had been conducted in Oceania, weighted
pooled prevalence of MNM was 17.14 (95% CI: 1.17-
33.12) with significant heterogeneity between studies
(I2 = 98.2%; Cochran Q-statistic P < 0.001; Figure 3). For
heterogeneous justification, a subgroup analysis was
also conducted based on the country; for example, the
prevalence of MNM in Brazil was 8.36 (95% CI: 6.50-
10.21) with significant heterogeneity between studies
(I2 = 97.9%; Cochran Q-statistic P < 0.001). Among the
studies that had been conducted in India, weighted pooled
prevalence of MNM was 28.22 [95% CI: 19.21-37.22]
with significant heterogeneity between studies (I2 = 99
%; Cochran Q-statistic P < 0.001) and in the Nigeria was
20.87 [95% CI: 8.37-33.37] with significant heterogeneity
between studies (I2 = 99.4 %; Cochran Q-statistic P < 0.001;
Figure 4). The results indicate that the heterogeneity
between studies is significant in a country (Including
Figure 2. Forest plot of the pooling of overall worldwide prevalence Brazil, India and Nigeria).
of MNM. To further assess the source of heterogeneity we used
Discussion
We found that more than 18.67/1000 LB of the general
population of the world suffered from MNM based on
WHO criteria. So far, two systematic review in 20046 and
20117 have been conducted to determine the prevalence
of maternal mortality globally. In recent years, a review
study conducted to determine the death of mothers based
on WHO criteria, has not been carried out. Therefore,
Figure 3. Forest plot of the pooling of overall continents prevalence
comparing the prevalence’s changes during the passage of
of MNM.
time is relatively difficult. In a review conducted by Say
et al, prevalence’s of MNM ranged from 0.80% to 8.23%
in studies which had disease-specific criteria while it was
from 0.38% to1.09% in studies which had organ-system
based criteria and it was from 0.01% to 2.99% in studies
which had management-based criteria.6
In another review conducted by Tunçalp et al, the
prevalence’s varied between 0.6 and 14.98% in studies
which had disease specific criteria while it varied between
0.14% and 0.92% in studies which had Mantel (organ
dysfunction) criteria and it varied between 0.04% and
4.54% in studies which had management-based criteria.
A meta-analysis in the aforementioned study, estimated
that MNM was 0.42% (95% CI 0.40-0.44%) for the Mantel
(organ dysfunction) criteria.7 In both of these studies, the
reported MNM prevalence is in 100 live birth, but in our
study, according to the WHO definition, the number of
MNM reported in 1000 live births, Which indicates that
the MNM rate has declined in general, and the WHO’s
unit case-identification criteria of MNM and its declare to
Figure 4. Forest plot of the pooling of overall countries prevalence all countries has played a major role in improving quality
of MNM.
care.
Other results of our study were exploring the MNM
meta-regression of MNM on MD which resulted in prevalence in countries. In our study the prevalence
adjusted R-squared as 78.88%. This means that much of the of MNM according to the WHO criteria in Brazil was
observed heterogeneity among studies could be explained 8.36/1000, which is consistent with the systematic review
by maternal death as Pearson correlation coefficient of da Silva et al in Brazil (the MNMR varied from 4.4/1000
between MNM and MD among included studies was also LB).60 The reason for the little statistical difference is the
70.16% (P < 0.001). The coefficient of meta-regression difference in the years of the study as well as various
shows that for each unit increase in MD (per 100 000) definitions in identifying the cases of maternal death. In
the average of MDM (per 1000) is expected to increase the present study the MNM prevalence in middle and low
income countries of Asia and Africa to compare to high- Mashhad University of Medical Sciences.
income countries, are higher; which is in line with the study
of Tunçalp et al.7 Of course, in these continents, countries References
such as Iran have a MNM prevalence (1/1000 LB) similar 1. World Health Organization (WHO). Maternal mortality
fact sheet No. 348. Geneva: WHO; 2014. Available from:
to that of European countries.61 The meta-regression
http://apps.who.int/iris/bitstream/10665/112318/1/WHO_
between MNM and MD justifies the heterogeneity of
RHR_14.06_eng.pdf?ua=1. Accessed 5 February 2018.
studies in countries, because even in one country, there 2. World Health Organization (WHO). Beyond the numbers:
is variation in the factors like the quality of care which Reviewing maternal deaths and complications to make
are major determinant for both MD and MNM. In fact, pregnancy safer. Geneva: WHO; 2004.
the high correlation between MNM and MD is because of 3. World Health Organization (WHO). Evaluating the quality
possible common risk factors. of care for severe pregnancy complications: the WHO near-
The limitation of this study is the selection of articles miss approach for maternal health. Geneva: WHO; 2011.
based on WHO criteria that led to automatically deletion 4. Abdollahpour S, Keramat A, Mousavi SA, Khosravi A,
of the articles published before 2012. Despite this Motaghi Z. The effect of debriefing and brief cognitive-
limitation, the study has a number of strengths. First, it behavioral therapy on postpartum depression in traumatic
is the first worldwide systematic review of the prevalence childbirth: a randomized clinical trial. J Midwifery
Reproductive Health. 2018;6(1):1122-31. doi: 10.22038/
of MNM conducted according to WHO criteria that we
jmrh.2017.10000.
examined study quality, publication bias and sensitivity
5. Abdollahpour S, Khosravi A, Motaghi Z, Keramat A,
analysis. Secondly, the number of articles that have been Mousavi SA. Effect of brief cognitive behavioral counseling
Meta-analyzes is high and reflects a comprehensive view and debriefing on the prevention of post-traumatic stress
of the health of mothers. disorder in traumatic birth: a randomized clinical trial.
Community Ment Health J. 2019;55(7):1173-8. doi:
Conclusion 10.1007/s10597-019-00424-6.
The prevalence of MNM is considerable in many countries, 6. Say L, Pattinson RC, Gülmezoglu AM. WHO systematic
especially in low- and middle-income countries. An review of maternal morbidity and mortality: the prevalence
important finding of this study was, the significant and of severe acute maternal morbidity (near miss). Reprod
direct relationship between MNM and maternal death. Health. 2004;1(1):3. doi: 10.1186/1742-4755-1-3.
7. Tunçalp O, Hindin MJ, Souza JP, Chou D, Say L. The
This means that fluctuations in one lead to another change.
prevalence of maternal near miss: a systematic review.
Therefore, the maternal mortality index can be considered
BJOG. 2012;119(6):653-61. doi: 10.1111/j.1471-
as the most reliable indicator in the assessment of maternal 0528.2012.03294.x.
health. Based on this index, countries should establish a 8. Moher D, Liberati A, Tetzlaff J, Altman DG. Preferred
national health care system for increase standard and safety reporting items for systematic reviews and meta-analyses:
practices of health providers. It is recommended that, in the PRISMA statement. Ann Intern Med. 2009;151(4):264-
view of the fact that improving maternal health is one 9. doi: 10.7326/0003-4819-151-4-200908180-00135.
of the goals of sustainable development by 2030, similar 9. Souza JP, Cecatti JG, Haddad SM, Parpinelli MA, Costa ML,
studies will be undertaken in the future to investigate the Katz L, et al. The WHO maternal near-miss approach and
trend of MNM rate in order to plan the necessary program the maternal severity index model (MSI): tools for assessing
and make the appropriate policies. the management of severe maternal morbidity. PLoS One.
2012;7(8):e44129. doi: 10.1371/journal.pone.0044129.
10. Jabir M, Abdul-Salam I, Suheil DM, Al-Hilli W, Abul-
Ethical approval
Hassan S, Al-Zuheiri A, et al. Maternal near miss and quality
Not applicable.
of maternal health care in Baghdad, Iraq. BMC Pregnancy
Childbirth. 2013;13:11. doi: 10.1186/1471-2393-13-11.
Competing interests
11. Nelissen EJ, Mduma E, Ersdal HL, Evjen-Olsen B, van
The authors declare that they have no competing interests.
Roosmalen JJ, Stekelenburg J. Maternal near miss and
mortality in a rural referral hospital in northern Tanzania:
Funding
a cross-sectional study. BMC Pregnancy Childbirth.
This research received no grant from any funding agency in the
2013;13:141. doi: 10.1186/1471-2393-13-141.
public.
12. Ps R, Verma S, Rai L, Kumar P, Pai MV, Shetty J. “Near
miss” obstetric events and maternal deaths in a tertiary
Authors’ contributions
care hospital: an audit. J Pregnancy. 2013;2013:393758. doi:
TK and SA designed the research, conducted systematic research,
10.1155/2013/393758.
extracted data and wrote the manuscript. HHM and SA analyzed
13. Rana A, Baral G, Dangal G. Maternal near-miss: a
data. All authors had primary responsibility for the final content
multicenter surveillance in Kathmandu Valley. JNMA J
of the manuscript and all authors read and approved the final
Nepal Med Assoc. 2013;52(190):299-304.
manuscript.
14. Tunçalp O, Hindin MJ, Adu-Bonsaffoh K, Adanu RM.
Assessment of maternal near-miss and quality of care in
Acknowledgements
a hospital-based study in Accra, Ghana. Int J Gynaecol
The authors would like to extend their deepest thanks to all
Obstet. 2013;123(1):58-63. doi: 10.1016/j.ijgo.2013.06.003.
librarians who helped them to access information resources in
15. Setia S, Mutahar R, Destriatania S. Determinant of Maternal 29. Abha S, Chandrashekhar S, Sonal D. Maternal near miss: a
Near Miss Incidence in Indonesia (Analysis Ofsecondary valuable contribution in maternal care. J Obstet Gynaecol
Data Sdki 2007). J Ilmu Kesehat Masy. 2013;4(3):270-80. India. 2016;66(Suppl 1):217-22. doi: 10.1007/s13224-015-
16. Dias MA, Domingues RM, Schilithz AO, Nakamura- 0838-y.
Pereira M, Diniz CS, Brum IR, et al. Incidence of maternal 30. Cecatti JG, Costa ML, Haddad SM, Parpinelli MA, Souza
near miss in hospital childbirth and postpartum: data from JP, Sousa MH, et al. Network for Surveillance of Severe
the Birth in Brazil study. Cad Saude Publica. 2014;30 Suppl Maternal Morbidity: a powerful national collaboration
1:S1-12. doi: 10.1590/0102-311x00154213. generating data on maternal health outcomes and care.
17. Galvão LP, Alvim-Pereira F, de Mendonça CM, Menezes BJOG. 2016;123(6):946-53. doi: 10.1111/1471-0528.13614.
FE, Góis KA, Ribeiro RF Jr, et al. The prevalence of severe 31. De Mucio B, Abalos E, Cuesta C, Carroli G, Serruya S,
maternal morbidity and near miss and associated factors Giordano D, et al. Maternal near miss and predictive
in Sergipe, Northeast Brazil. BMC Pregnancy Childbirth. ability of potentially life-threatening conditions at selected
2014;14:25. doi: 10.1186/1471-2393-14-25. maternity hospitals in Latin America. Reprod Health.
18. Luexay P, Malinee L, Pisake L, Marie-Hélène BC. Maternal 2016;13(1):134. doi: 10.1186/s12978-016-0250-9.
near-miss and mortality in Sayaboury Province, Lao PDR. 32. Ghazivakili Z, Lotfi R, Kabir K, Norouzi Nia R, Rajabi
BMC Public Health. 2014;14:945. doi: 10.1186/1471-2458- Naeeni M. Maternal near miss approach to evaluate quality
14-945. of care in Alborz province, Iran. Midwifery. 2016;41:118-
19. Pandey A, Das V, Agarwal A, Agrawal S, Misra D, Jaiswal 24. doi: 10.1016/j.midw.2016.08.009.
N. Evaluation of obstetric near miss and maternal deaths 33. Kalisa R, Rulisa S, van den Akker T, van Roosmalen J.
in a tertiary care hospital in north India: shifting focus Maternal Near Miss and quality of care in a rural Rwandan
from mortality to morbidity. J Obstet Gynaecol India. hospital. BMC Pregnancy Childbirth. 2016;16(1):324. doi:
2014;64(6):394-9. doi: 10.1007/s13224-014-0552-1. 10.1186/s12884-016-1119-1.
20. Tahira G, Sarfraz M. Cross-sectional retrospective study on 34. Mohammadi S, Essén B, Fallahian M, Taheripanah R, Saleh
prevalence of maternal near miss in mnch department of Gargari S, Källestål C. Maternal near-miss at university
Social Security Hospital, Islamabad. Paki J Public Health. hospitals with cesarean overuse: an incident case-control
2014;4(4):8-12. study. Acta Obstet Gynecol Scand. 2016;95(7):777-86. doi:
21. Bakshi RK, Aggarwal P, Roy D, Nautiyal R, Kakkar R. 10.1111/aogs.12881.
Indicators of maternal ‘near miss’ morbidity at different 35. Nakimuli A, Nakubulwa S, Kakaire O, Osinde MO,
levels of health care in North India: a pilot study. Bangladesh Mbalinda SN, Nabirye RC, et al. Maternal near misses from
J Med Sci. 2015;14(3):254-7. two referral hospitals in Uganda: a prospective cohort study
22. Bashour H, Saad-Haddad G, DeJong J, Ramadan MC, on incidence, determinants and prognostic factors. BMC
Hassan S, Breebaart M, et al. A cross sectional study of Pregnancy Childbirth. 2016;16:24. doi: 10.1186/s12884-
maternal ‘near-miss’ cases in major public hospitals in 016-0811-5.
Egypt, Lebanon, Palestine and Syria. BMC Pregnancy 36. Nansubuga E, Ayiga N, Moyer CA. Prevalence of maternal
Childbirth. 2015;15:296. doi: 10.1186/s12884-015-0733-7. near miss and community-based risk factors in Central
23. Madeiro AP, Rufino AC, Lacerda ÉZ, Brasil LG. Incidence Uganda. Int J Gynaecol Obstet. 2016;135(2):214-20. doi:
and determinants of severe maternal morbidity: a 10.1016/j.ijgo.2016.05.009.
transversal study in a referral hospital in Teresina, Piaui, 37. Norhayati MN, Nik Hazlina NH, Sulaiman Z, Azman MY.
Brazil. BMC Pregnancy Childbirth. 2015;15:210. doi: Severe maternal morbidity and near misses in tertiary
10.1186/s12884-015-0648-3. hospitals, Kelantan, Malaysia: a cross-sectional study. BMC
24. Mazhar SB, Batool A, Emanuel A, Khan AT, Bhutta S. Severe Public Health. 2016;16:229. doi: 10.1186/s12889-016-2895-
maternal outcomes and their predictors among Pakistani 2.
women in the WHO Multicountry Survey on Maternal and 38. Oladapo OT, Adetoro OO, Ekele BA, Chama C, Etuk SJ,
Newborn Health. Int J Gynaecol Obstet. 2015;129(1):30-3. Aboyeji AP, et al. When getting there is not enough: a
doi: 10.1016/j.ijgo.2014.10.017. nationwide cross-sectional study of 998 maternal deaths
25. Menezes FE, Galvão LP, de Mendonça CM, Góis KA, Ribeiro and 1451 near-misses in public tertiary hospitals in a
RF Jr, Santos VS, et al. Similarities and differences between low-income country. BJOG. 2016;123(6):928-38. doi:
WHO criteria and two other approaches for maternal near 10.1111/1471-0528.13450.
miss diagnosis. Trop Med Int Health. 2015;20(11):1501-6. 39. O’Malley EG, Popivanov P, Fergus A, Tan T, Byrne B.
doi: 10.1111/tmi.12568. Maternal near miss: what lies beneath? Eur J Obstet
26. Oliveira LC, da Costa AA. Maternal near miss in the Gynecol Reprod Biol. 2016;199:116-20. doi: 10.1016/j.
intensive care unit: clinical and epidemiological aspects. Rev ejogrb.2016.01.031.
Bras Ter Intensiva. 2015;27(3):220-7. doi: 10.5935/0103- 40. Parmar NT, Parmar AG, Mazumdar VS. Incidence of
507x.20150033. Maternal “Near-Miss” Events in a Tertiary Care Hospital
27. Rulisa S, Umuziranenge I, Small M, van Roosmalen J. of Central Gujarat, India. J Obstet Gynaecol India.
Maternal near miss and mortality in a tertiary care hospital 2016;66(Suppl 1):315-20. doi: 10.1007/s13224-016-0901-3.
in Rwanda. BMC Pregnancy Childbirth. 2015;15:203. doi: 41. Rathod AD, Chavan RP, Bhagat V, Pajai S, Padmawar A,
10.1186/s12884-015-0619-8. Thool P. Analysis of near-miss and maternal mortality at
28. Tan J, Liu XH, Yu C, Chen M, Chen XF, Sun X, et al. Effects tertiary referral centre of rural India. J Obstet Gynaecol
of medical co-morbidities on severe maternal morbidities India. 2016;66(Suppl 1):295-300. doi: 10.1007/s13224-016-
in China: a multicenter clinic register study. Acta Obstet 0902-2.
Gynecol Scand. 2015;94(8):861-8. doi: 10.1111/aogs.12657. 42. Ray N, Patil SK, Kshirsagar NS, Patil Y, Laddad M. Maternal
near miss in a tertiary care hospital: a cross sectional study. maternal near miss in the public health sector of Harare,
J Evol Med Dent Sci. 2016;5(51):3352-4. doi: 10.14260/ Zimbabwe: a prospective descriptive study. BMC Pregnancy
jemds/2016/755. Childbirth. 2018;18(1):458. doi: 10.1186/s12884-018-2092-
43. Tanimia H, Jayaratnam S, Mola GL, Amoa AB, de Costa 7.
C. Near-misses at the Port Moresby General Hospital: 53. Iwuh IA, Fawcus S, Schoeman L. Maternal near-miss audit
a descriptive study. Aust N Z J Obstet Gynaecol. in the Metro West maternity service, Cape Town, South
2016;56(2):148-53. doi: 10.1111/ajo.12430. Africa: a retrospective observational study. S Afr Med J.
44. Witteveen T, de Koning I, Bezstarosti H, van den Akker T, 2018;108(3):171-5. doi: 10.7196/SAMJ.2018.v108i3.12876.
van Roosmalen J, Bloemenkamp KW. Validating the WHO 54. Oppong SA, Bakari A, Bell AJ, Bockarie Y, Adu JA, Turpin
Maternal Near Miss Tool in a high-income country. Acta CA, et al. Incidence, causes and correlates of maternal near-
Obstet Gynecol Scand. 2016;95(1):106-11. doi: 10.1111/ miss morbidity: a multi-centre cross-sectional study. BJOG.
aogs.12793. 2019;126(6):755-62. doi: 10.1111/1471-0528.15578.
45. Bolnga JW, Morris M, Totona C, Laman M. Maternal 55. Woldeyes WS, Asefa D, Muleta G. Incidence and
near-misses at a provincial hospital in Papua New Guinea: determinants of severe maternal outcome in Jimma
A prospective observational study. Aust N Z J Obstet University teaching hospital, south-West Ethiopia: a
Gynaecol. 2017;57(6):624-9. doi: 10.1111/ajo.12650. prospective cross-sectional study. BMC Pregnancy
46. Chandak PO, Kedar KV. Maternal near miss- a review from Childbirth. 2018;18(1):255. doi: 10.1186/s12884-018-
tertiary care hospital. J Evol Med Dent Sci. 2017;6(47):3633- 1879-x.
7. doi: 10.14260/Jemds/2017/783. 56. Yang YY, Fang YH, Wang X, Zhang Y, Liu XJ, Yin
47. Goldenberg RL, Saleem S, Ali S, Moore JL, Lokangako A, ZZ. A retrospective cohort study of risk factors and
Tshefu A, et al. Maternal near miss in low-resource areas. pregnancy outcomes in 14,014 Chinese pregnant women.
Int J Gynaecol Obstet. 2017;138(3):347-55. doi: 10.1002/ Medicine (Baltimore). 2018;97(33):e11748. doi: 10.1097/
ijgo.12219. md.0000000000011748.
48. Liyew EF, Yalew AW, Afework MF, Essén B. Incidence and 57. Deepti Gupta NA, Noor N, Joshi T, Bhargava M. Incidence
causes of maternal near-miss in selected hospitals of Addis of maternal near miss and mortality cases in central India
Ababa, Ethiopia. PLoS One. 2017;12(6):e0179013. doi: tertiary care centre and evaluation of various causes. The
10.1371/journal.pone.0179013. New Indian Journal of OBGYN. 2018;4(4):112-6.
49. Mbachu, II, Ezeama C, Osuagwu K, Umeononihu OS, 58. Munn Z, Moola S, Riitano D, Lisy K. The development
Obiannika C, Ezeama N. A cross sectional study of maternal of a critical appraisal tool for use in systematic reviews
near miss and mortality at a rural tertiary centre in southern addressing questions of prevalence. Int J Health Policy
Nigeria. BMC Pregnancy Childbirth. 2017;17(1):251. doi: Manag. 2014;3(3):123-8. doi: 10.15171/ijhpm.2014.71.
10.1186/s12884-017-1436-z. 59. Higgins JP, Thompson SG, Deeks JJ, Altman DG. Measuring
50. Serruya SJ, de Mucio B, Martinez G, Mainero L, de Francisco inconsistency in meta-analyses. BMJ. 2003;327(7414):557-
A, Say L, et al. Exploring the concept of degrees of maternal 60. doi: 10.1136/bmj.327.7414.557.
morbidity as a tool for surveillance of maternal health in 60. da Silva JM, Fonseca SC, Dias MAB, Izzo AS, Teixeira GP,
Latin American and Caribbean settings. Biomed Res Int. Belfort PP. Concepts, prevalence and characteristics of severe
2017;2017:8271042. doi: 10.1155/2017/8271042. maternal morbidity and near miss in Brazil: a systematic
51. Awowole IO, Omitinde OS, Arogundade FA, Bola- review. Rev Bras Saúde Mater Infant. 2018;18(1):7-35. doi:
Oyebamiji SB, Adeniyi OA. Pregnancy-related acute kidney 10.1590/1806-93042018000100002.
injury requiring dialysis as an indicator of severe adverse 61. Abdollahpour S, Miri HH, Khadivzadeh T. The maternal
maternal morbidity at a tertiary center in Southwest near miss incidence ratio with WHO approach in Iran: a
Nigeria. Eur J Obstet Gynecol Reprod Biol. 2018;225:205-9. systematic review and meta-analysis. Iran J Nurs Midwifery
doi: 10.1016/j.ejogrb.2018.04.041. Res. 2019;24(3):159-66. doi: 10.4103/ijnmr.IJNMR_165_18.
52. Chikadaya H, Madziyire MG, Munjanja SP. Incidence of