Literature DB >> 27147766

Reclassifying causes of obstetric death in Mexico: a repeated cross-sectional study.

Margaret C Hogan1, Biani Saavedra-Avendano2, Blair G Darney2, Luis M Torres-Palacios3, Ana L Rhenals-Osorio3, Bertha L Vázquez Sierra3, Patricia N Soliz-Sánchez4, Emmanuela Gakidou1, Rafael Lozano2.   

Abstract

OBJECTIVE: To describe causes of maternal mortality in Mexico over eight years, with particular attention to indirect obstetric deaths and socioeconomic disparities.
METHODS: We conducted a repeated cross-sectional study using the 2006-2013 Búsqueda intencionada y reclasificación de muertes maternas (BIRMM) data set. We used frequencies to describe new cases, cause distributions and the reclassification of maternal mortality cases by the BIRMM process. We used statistical tests to analyse differences in sociodemographic characteristics between direct and indirect deaths and differences in the proportion of overall direct and indirect deaths, by year and by municipality poverty level.
FINDINGS: A total of 9043 maternal deaths were subjected to the review process. There was a 13% increase (from 7829 to 9043) in overall identified maternal deaths and a threefold increase in the proportion of maternal deaths classified as late maternal deaths (from 2.1% to 6.9%). Over the study period direct obstetric deaths declined, while there was no change in deaths from indirect obstetric causes. Direct deaths were concentrated in women who lived in the poorest municipalities. When compared to those dying of direct causes, women dying of indirect causes had fewer pregnancies and were slightly younger, better educated and more likely to live in wealthier municipalities.
CONCLUSION: The BIRMM is one approach to correct maternal death statistics in settings with poor resources. The approach could help the health system to rethink its strategy to reduce maternal deaths from indirect obstetric causes, including prevention of unwanted pregnancies and improvement of antenatal and post-obstetric care.

Entities:  

Mesh:

Year:  2016        PMID: 27147766      PMCID: PMC4850531          DOI: 10.2471/BLT.15.163360

Source DB:  PubMed          Journal:  Bull World Health Organ        ISSN: 0042-9686            Impact factor:   9.408


Introduction

Maternal mortality – defined as the death of a woman during pregnancy, childbirth or in the 42 days after delivery – is used as an outcome measure for any health system. The indicator of maternal mortality is the maternal mortality ratio (MMR), which is defined as the number of maternal deaths per 100 000 live births. MMR is a problematic indicator to measure, due to the relative few maternal deaths.– It is even more challenging to measure cause-specific maternal mortality, since available methods have either low sensitivity or specificity. Therefore, accurate estimates of cause-specific maternal mortality are often not available in many countries. The International statistical classification of diseases and related health problems, 10th revision (ICD-10) manual divides the causes of maternal mortality into three broad categories: direct obstetric deaths (resulting from obstetric complications of the pregnant state); indirect obstetric deaths (resulting from a disease, often pre-existing and aggravated by the physiologic effects of the pregnancy); and late maternal death (death between 42 days and one year post-obstetric event)., Sequelae, which is maternal deaths that occur one year or more after delivery, is included in the late maternal death category. Indirect maternal deaths represent on average 20% of a country’s overall maternal mortality,– but this proportion varies considerably across settings. Particularly indirect and late maternal causes are likely to be misclassified as non-maternal deaths.,, Even within countries with a very high quality vital registration system, there is a wide variation in the fraction of maternal deaths attributable to indirect causes; estimates range from zero to more than half of all reported maternal deaths.– In recent decades, Mexico has improved its measurement of maternal mortality, but problems of underreporting and misreporting in its vital statistics systems still exist., In response, a new strategy was undertaken by the government in 2002 that aimed to identify all maternal deaths in Mexico using an approach of intentional search, review and reclassification of maternal deaths. A new procedure, referred to as Búsqueda intencionada y reclasificación de muertes maternas (BIRMM) was put in place,, which provides a mechanism for a comprehensive examination of maternal deaths in Mexico. There has been a rapid increase in obesity,, diabetes, hypertension, and hypercholesterolaemia in Mexico,, which puts women of reproductive age at higher risk for pre-existing hypertensive disorders and diabetes mellitus. The epidemiologic transition from communicable to noncommunicable diseases has implications for maternal health. The purpose of this study is to describe the reclassified and newly identified maternal deaths – especially indirect obstetric deaths – identified through the BIRMM process. We also compared sociodemographic characteristics at individual and municipality level of the women who died from direct and indirect causes.

Methods

We conducted a repeated cross-sectional study using the 2006–2013 BIRMM data set, which includes all deaths in women of reproductive ages (10–54 years). The aim was to identify miscoded maternal deaths. We investigated the underlying cause of death for those who had been assigned to a subset of 46 ICD-10 codes that we suspected of being maternal deaths but did not have maternal codes from the ICD-10 O chapter. (The list of the 46 ICD codes are available from the corresponding author). In addition to these 46 codes, we also investigated: deaths that were assigned maternal codes found in the ICD-10 O chapter (Table 1); deaths with suspicious or incomplete codes; deaths with complications but without a valid underlying cause of death; and all death certificates where the pregnancy checkbox had been ticked.
Table 1

ICD-10 codes for indirect causes of maternal deaths

CategorySub-categoryTitle
O10O10.0–O10.9Pre-existing hypertension complicating pregnancy, childbirth and the puerperium
O24O24.0–O24.9Diabetes mellitus during pregnancy
O98O98.0–O98.9Maternal infectious and parasitic diseases classifiable elsewhere but complicating pregnancy, childbirth and the puerperium
O99O99.0–O99.8Other maternal diseases classifiable elsewhere but complicating pregnancy, childbirth and the puerperium

ICD: International classification of diseases and related health problems, 10.

ICD: International classification of diseases and related health problems, 10. The BIRMM review process collates maternal mortality and sociodemographic data from available mortality data sources including death certificates, medical records, verbal autopsy records and confidential enquiry or autopsy reports. (The distribution of information contributed by each data source is available from the corresponding author). The collated information was reviewed by two independent coders. In the event of a disagreement when assigning the appropriate code, a senior reviewer examined all documents and assigned the final cause. Full details of the BIRMM protocol have been published elsewhere. We extracted the following data from the BIRMM: individual-level sociodemographic data (age, marital status, education level, number of pregnancies and number of prenatal visits during the last pregnancy); care-related information on each maternal death (place of care where first complication was documented and where skilled birth attendant care was provided); and place of death. The proportions of missing data for each year for the care-related information are available from the corresponding author. We used cause-of-death data as reported before and after the intentional review process. In addition, we used the 2010 municipality-level development index as a measure of community level socioeconomic status. The development index data were grouped into quintiles and merged into the individual level BIRMM data record according to the residence municipality of the deceased. To calculate the MMR, live births data for 2006–2013 were obtained from the General Directorate of Health Information. This study was approved by the ethics committee of the National Institute of Public Health, Mexico.

Analysis

Table 1 presents the ICD-10 categories and associated sub-categories and titles for codes used for deaths identified as indirect obstetric deaths, as listed in the manual. The list includes all codes that constitute the internationally agreed definition of indirect maternal death. Maternal deaths related to human immunodeficiency virus (HIV) infections were treated as special cases due to evolving ICD-10 coding rules. HIV-related deaths coded to the specific HIV ICD codes (B20-B24) and the recently created HIV ICD code (O98.7) were included and recoded as indirect maternal deaths. New and recoded indirect maternal deaths, their cause distribution and reclassification by development index quintile were examined using tabulations. We used descriptive statistics to examine differences in direct and indirect cause, before and after the review process and across the eight years (2006–2013). Sociodemographic characteristics and health service use were examined and tested using t-test and χ tests for differences in the proportion and means of direct and indirect deaths. Maternal mortality cause was analysed by municipality-level development index. All analyses were done in Stata version 13.1 (StataCorp. LP, College Station, United States of America).

Results

The total number of deaths in women of reproductive age during the study period obtained from the BIRMM was 357 446, of which 9043 deaths (2.5%) were subjected to the maternal death cause review and reclassification process. Table 2 summarizes the findings from the reclassification process. Before the review 7829 deaths were classified as maternal deaths. Of the deaths coded as non-maternal, we reclassified 1214 (13.4%) to maternal deaths. The number of late maternal deaths increased from 192 (2.1%) before the review to 628 (6.9%) after the review, representing over threefold increase in the proportion of late maternal deaths. There was a 6.8% (from 2099 to 2243 deaths) and 11.4% (from 5538 to 6172 deaths) increase in deaths categorized as indirect and direct, respectively. Deaths that were categorized the same before and after the review were, 85.5% (5281/6172) of direct, 68.8% (1544/2243) of indirect and 28.3 (178/628) of late maternal deaths.
Table 2

Summary of the intentional search and review outcomes of maternal deaths, by municipality-level development index quintiles, Mexico, 2006–2013

Cause of death After review
Cause of death, no. (%)
Total, no. (%)
IndirectaDirectbLate maternalc
All quintiles
  Before review
  Non-maternald479 (21.3)365 (5.9)370 (58.9)1214 (13.4)
  Indirecta1544 (68.8)e514 (8.3)41 (6.5)2099 (23.2)
  Directb218 (9.7)5281 (85.5)e39 (6.2)5538 (61.2)
  Late maternalc2 (0.1)12 (0.2)178 (28.3)e192 (2.1)
  Total2243 (100.0)6172 (100.0)628 (100.0)9043 (100.0)
Quintile 1 (poorest)
  Before review
  Non-maternald280 (21.1)193 (6.4)221 (57.7)694 (14.7)
  Indirecta921 (69.4)e303 (10.1)22 (5.7)1246 (26.4)
  Directb124 (9.3)2507 (83.3)e23 (6.0)2654 (56.2)
  Late maternalc2 (0.2)5 (0.2)117 (30.5)e124 (2.6)
  Total1327 (100.0)3008 (100.0)382 (100.0)4718 (100.0)
Quintile 5 (wealthiest)
  Before review
  Non-maternald38 (18.8)36 (3.3)34 (64.1)108 (8.1)
  Indirecta134 (66.3)e48 (4.4)5 (9.4)187(13.9)
  Directb30 (14.8)1008 (92.1)e1 (1.9)1039 (77.0)
  Late maternalc0 (0.0)2 (0.2)13 (24.5)e15 (1.1)
  Total202 (100.0)1094 (100.0)53 (100.0)1350 (100.0)

a Indirect is defined as maternal deaths resulting from a disease, often pre-existing and aggravated by the physiologic effects of the pregnancy.

b Direct is defined as maternal deaths resulting from obstetric complications during pregnancy.

c Late maternal is defined as death between 42 days and one year post-obstetric event.

d All other maternal deaths not coded to direct, indirect or later maternal.

e Concordant pair before and after review.

a Indirect is defined as maternal deaths resulting from a disease, often pre-existing and aggravated by the physiologic effects of the pregnancy. b Direct is defined as maternal deaths resulting from obstetric complications during pregnancy. c Late maternal is defined as death between 42 days and one year post-obstetric event. d All other maternal deaths not coded to direct, indirect or later maternal. e Concordant pair before and after review. In the poorest municipalities, 14.7% (694) of maternal deaths were recoded from non-maternal to maternal, while in the wealthiest municipalities this figure was 8.1% (108). An additional 14.8% (30) of all direct deaths in the wealthiest quintile were reclassified to indirect deaths (Table 2). Table 3 (available at: http://www.who.int/bulletin/volumes/94/5/15-1633560) shows the original codes of the deaths recoded to indirect maternal deaths. Many indirect maternal deaths were originally misclassified as infectious and parasitic diseases (96), diseases of the circulatory system (94), diseases of the respiratory system (70) and neoplasms (56). In addition, there was miscoding within the maternal chapter of the ICD. For instance, 40 deaths were originally assigned to O10O16 (oedema, proteinuria and hypertensive disorders in pregnancy, childbirth and the puerperium); 46 deaths were assigned to O21, O23–O31, O34 (other complications of pregnancy) and 46 more maternal deaths were assigned with the codes O89–O92 (other complications during the puerperium). Two hundred and twenty indirect maternal deaths were coded as direct obstetric causes before the correction.
Table 3

Cause of death reclassified as indirect maternal deaths, Mexico, 2006–2013

ICD-10 block8TitleNo. of recorded cases (%) (n = 699)
Non-maternal
A15–B49Infectious and parasitic diseases96 (13.7)
C00–C14Malignant neoplasms of lip, oral cavity and pharynx1 (0.1)
C15–C96, D10–D48Other malignant, benign and uncertain or unknown behaviour neoplasms56 (8.0)
D00–D09In situ neoplasms (carcinoma)1 (0.1)
D55–D89Diseases of blood and blood-forming organs8 (1.1)
E00–E90Endocrine, nutritional and metabolic diseases32 (4.6)
F50–F59Behavioural syndromes associated with physiological disturbances and physical factors1 (0.1)
G00–G99Diseases of the nervous system21 (3.0)
I00–I99Diseases of the circulatory system94 (13.4)
J00–J99Diseases of the respiratory system70 (10.0)
K00–K93Diseases of the digestive system37 (5.3)
L00–L08Infections of the skin and subcutaneous tissue1 (0.1)
M00–M99Diseases of the musculoskeletal system and connective tissue7 (1.0)
N00–N99Diseases of the genitourinary system9 (1.3)
Q00–Q99Congenital malformations, deformations and chromosomal abnormalities20 (2.9)
R10–R19Symptoms and signs involving the digestive system and abdomen1 (0.1)
R50–R69General symptoms and signs7 (1.0)
R95–R99Ill-defined and unknown causes of mortality1 (0.1)
V01–Y98External causes16 (2.3)
Maternal
O01Hydatidiform mole1(0.1)
O02–O08Other pregnancy with abortive outcome9 (1.3)
O10–O16Oedema, proteinuria and hypertensive disorders in pregnancy, childbirth and the puerperium40 (5.7)
O20, O45–O46, O67Premature separation of placenta and other haemorrhage of pregnancy or birth12 (1.7)
O21, O23–O31, O34Other complications of pregnancy46 (6.6)
O22,O87Other maternal disorders predominantly related to pregnancy2 (0.3)
O35–O43, O68–O69Fetal distress and other complications of pregnancy or birth16 (2.3)
O47–O48, O60–O75Prolonged pregnancy, other complications of labour9 (1.3)
O72Postpartum haemorrhage6 (0.9)
O88Obstetric embolism12 (1.7)
O89–O92Other complications during the puerperium46 (6.6)
O96–O97Late and sequelae maternal death2 (0.3)
A34, O85–O86Obstetrical tetanus, complications predominantly related to the peurperium19 (2.7)
For maternal deaths categorized as direct, there was a declining trend in MMR between 2006 and 2013, from 46.4 to 32.1 deaths per 100 000 live births. There was no change for indirect maternal deaths. MMR for indirect deaths was 12.2 deaths per 100 000 live births in 2006 and 13.3 deaths per 100 000 live births in 2013. There was a peak in 2009, mainly due to the Influenza A (H1N1) epidemic, which is known to increase the risk of hospitalization, severe illness and death in pregnant women., The trends for both direct and indirect causes were similar before and after reclassifying the causes of deaths (Fig. 1).
Fig. 1

Direct and indirect maternal deaths before and after the review process, Mexico, 2006–2013

Direct and indirect maternal deaths before and after the review process, Mexico, 2006–2013 CI: confidence interval. Comparison of sociodemographic characteristics and health system use showed that women who died of indirect maternal causes had fewer pregnancies, were slightly younger and were better educated than women dying of direct causes. The deceased women were also more likely to have delivered, received care for their first complication and died in Instituto Mexicano del Seguro Social facilities, which are employment-based insurance-affiliated facilities. Skilled birth attendants were more likely to have been present for the mothers who died of direct causes, but this could be due to the fact that women who died of indirect causes died before delivery (Table 4; available at: http://www.who.int/bulletin/volumes/94/5/15-1633560).
Table 4

Characteristics of indirect and direct maternal deaths, Mexico, 2006–2013

CharacteristicsCause of death
IndirectDirect
Number of pregnancies (mean, SD)2.45 (0.04)3.03 (0.03)*,a
Age (mean, SD)27.40 (0.14)28.70 (0.09)*,a
Number of prenatal visits (mean, SD)3.26 (0.07)2.86 (0.04)*,a
Marital status, n22086022
Single, n (proportion)394 (0.18)900 (0.15)
Common law, divorced or widowed, n (proportion)869 (0.39)2415 (0.40)
Married, no. (%)945 (0.43)2707 (0.45)*,b
Education, n21315807
Primary, no. (%)849 (0.40)2660 (0.46)
Secondary, no. (%)726 (0.34)1851 (0.32)
High school or more, no. (%)557 (0.26)1296 (0.22)*,b
Place of death, n417324331
Secretaria de Salud, no. (%)903 (0.52)2143 (0.49)
IMSS/ISSSTE/SEDENA, no. (%)511 (0.30)1010 (0.23)
Private medical unit, no. (%)92 (0.05)410 (0.09)
Home, street, other, no. (%)226 (0.13)768 (0.18)*,b
Place of delivery, n16575329
Secretaria de Salud, no. (%)901 (0.54)2603 (0.49)
IMSS/ISSSTE/SEDENA, no. (%)491 (0.30)1048 (0.20)
Private medical unit, no. (%)150 (0.09)833 (0.16)
Home, street, other, no. (%)115 (0.07)845 (0.16)*,b
Place of care for first complication, n18755129
Secretaria de Salud, no. (%)1044 (0.56)2864 (0.56)
IMSS/ISSSTE/SEDENA, no. (%)533 (0.28)1069 (0.21)
Private medical unit, no. (%)285 (0.15)1104 (0.22)
Home, street, other, no. (%)13 (0.01)92 (0.02)*,b
Development index, (municipality), n22376145
Quintile 1 – Poorest, no. (%)202 (0.09)1094 (0.18)*,b
Quintile 2, no. (%)194 (0.09)666 (0.11)
Quintile 3, no. (%)197 (0.09)604 (0.10)
Quintile 4, no. (%)317 (0.14)773 (0.13)
Quintile 5 – Wealthiest, no. (%)1327 (0.5993008 (0.49)
Skilled birth attendant, n19105477
Doctor, no. (%)1361 (0.71)4267 (0.78)
Nurse/auxiliary/midwife, no. (%)43 (0.02)460 (0.08)
Relative/other, n (proportion)20 (0.01)231 (0.04)
No delivery, n (proportion)486 (0.25)519 (0.09)

IMSS: Instituto Mexicano del Seguro Social, ISSSTE: Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado, SEDENA: Secretaría de la Defensa Nacional, SD: standard deviation.

* P < 0.05; **P < 0.01.

a Tested using differences in mean

b Tested using an overall Pearson χ2.

IMSS: Instituto Mexicano del Seguro Social, ISSSTE: Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado, SEDENA: Secretaría de la Defensa Nacional, SD: standard deviation. * P < 0.05; **P < 0.01. a Tested using differences in mean b Tested using an overall Pearson χ2. For direct causes, poorer municipalities had a higher MMR, but also a slightly higher ratio of maternal indirect deaths (Fig. 2). Fig. 3 and Fig. 4 show the MMR by direct and indirect causes between the wealthiest and poorest quintiles by year. Between 2006 and 2013, direct causes of maternal deaths among women residing in the poorest municipalities have nearly halved, going down from 119.1 to 72.7 deaths per 100 000 live births (Fig. 3). The decline in MMR due to direct causes of maternal death in the wealthiest municipalities was 23.5%, going down from 35.2 to 26.9 deaths per 100 000 live births (Fig. 3). For each year and in both poorest and wealthiest quintiles, MMRs for indirect death causes were lower than the MMRs for direct causes. It is only in 2008 and 2010 that the poorest quintile had a statistically significant higher MMR due to indirect causes than the wealthiest quintile (Fig. 4). In 2009, there was a peak in indirect deaths among the wealthiest municipalities, presumably due to the H1N1 epidemic (Fig. 4).
Fig. 2

Direct and indirect maternal deaths by municipality-level development index, Mexico, 2006–2013

Fig. 3

Direct maternal deaths for the wealthiest and poorest quintile, Mexico, 2006–2013

Fig. 4

Indirect maternal deaths for the wealthiest and poorest quintile, Mexico, 2006–2013

Direct and indirect maternal deaths by municipality-level development index, Mexico, 2006–2013 CI: confidence interval. Note: Pooled number of indirect and direct deaths per 100 000 live births, by quintile of municipality-level development index, 2006–2013. Direct maternal deaths for the wealthiest and poorest quintile, Mexico, 2006–2013 CI: confidence interval; Q: quintile. Note: Number of direct deaths per 100 000 live births, by year, for the wealthiest and poorest quintile of the municipality-level development index. Indirect maternal deaths for the wealthiest and poorest quintile, Mexico, 2006–2013 CI: confidence interval; Q: quintile. Note: Number of indirect deaths per 100 000 live births, by year, for the wealthiest and poorest quintile of the municipality-level development index.

Discussion

This paper presents the results of a review and reclassification of causes of maternal death in Mexico, for the period 2006 to 2013. The identified 13% increase in the number of maternal deaths after the BIRMM review suggests that this type of exercise is one approach to correct misclassification of maternal cause-of-death data. There is progress in Mexico towards achieving a reliable assessment of the causes of death in women of reproductive age, with the aim of generating improved data on the causes of maternal mortality. Our findings show that MMR from direct maternal deaths has been declining between 2006 and 2013; it nearly halved among the poorest women. However, there was no such change in indirect deaths. Given the increase in the burden of noncommunicable diseases and associated risk factors, indirect deaths may continue to account for an increasing proportion of maternal deaths. Despite the overall decline in MMR from direct deaths, socioeconomic disparities among the poor persist. However, for indirect deaths, women residing in both poor and wealthy areas are affected. These findings are consistent with other studies that examined the obstetric death transition from direct to indirect causes. Similar projects to the BIRMM have been implemented in other settings as well; however there is a wide variation in the level of maternal death underreporting between settings. Correction factors for the number of maternal deaths range from 1.9 in north-east Brazil, to 3.2 in Menoufia, Egypt. In high-income countries the correction factor ranges between 0.9 and 2.2. This observed variation limits our ability to generalize the extent of underreporting or misclassification across settings. Our review also highlighted the importance of the maternal death review to explain an unusual disease pattern, such as the 2009 H1N1 epidemic in Mexico. This type of temporary change in the pattern of maternal deaths has also been observed in Rwanda and South Africa. Such increases should be anticipated during an epidemic. The feasibility of a project that focuses on reclassifying maternal death causes in a given country is dependent on the level of maternal death misclassification or under-coding. In countries with relatively few maternal deaths, extensive review of suspected cases may be feasible. For example, the reproductive age mortality study (RAMOS) investigates all reported deaths in women of reproductive age., In our study, we applied a cost-saving approach which uses expert opinion to identify a subset of maternal death cases. Our approach may be more appropriate for countries with poor resources. Most maternal health interventions are timed around the delivery period of the pregnancy and they focus mainly on skilled birth attendance or emergency obstetric care. These interventions have an impact on direct deaths and subsequently on the reduction of overall maternal mortality. However, except in cases where complications arise during labour, indirect deaths may not be averted through these delivery-focused interventions. To reduce indirect deaths, obstetricians and other health-care personnel interacting with pregnant women during the postpartum period need to be trained to treat the entire woman and not just her pregnancy., Planning for such training requires the development, dissemination and adoption of clinical guidelines. Effective implementation of such guidelines requires collaboration and the establishment of referral systems between specialities that deal with the major causes of indirect deaths. For example obstetricians need to be able to effectively communicate with chronic disease specialists regarding at-risk cases. There is a need for additional surveillance of pregnant women to identify at-risk pregnancies to respond to them appropriately. A health education programme focused on addressing indirect obstetric death risk factors, particularly for women with pre-existing conditions, is needed as well. Access to and use of effective contraception and safe abortion remains a key strategy to reduce maternal mortality worldwide. The Mexican Ministry of Health, recognizing the need for quality and state-level maternal mortality estimates, used its authority to ensure cooperation from states for the BIRMM project. While integration of the BIRMM as part of the vital statistics system treats the maternal mortality review as a core public health function, there is no separate specific budget for it from the ministry of health. The project is being implemented as a non-routine activity, subsidized by committed individuals and interested groups of public health practitioners. Annual results from the BIRMM are used to adjust official estimates of MMR. The adoption of electronic death registration would allow real-time reporting and validation of suspected maternal deaths. This study has several limitations. First, the review process did not target all deaths in women of reproductive age, but a subset identified based on the registered cause of death. While the codes used to identify cases capture most misclassified or miscoded maternal deaths, there may be some missed and not investigated., Second, the review process relies on the availability and quality of additional mortality data sources beyond the death certificate. For some deaths, the additional available information to make a reclassification decision was quite limited. Third, the role of improved ascertainment and categorization must not be overlooked when examining the trends in this analysis. Since the same search procedures have been used each year, it seems unlikely that the observed increase in indirect deaths would be solely due to improved ascertainment. Fourth, a few causes of death, considered to be indirect obstetric causes such as ICD-10 code O26.6 (liver disorders), are subsumed within chapters of the ICD broadly considered for direct maternal deaths. Full ICD-10 codes to the 4-digit level were not available for all deaths so the broader 3-digit categories were used and these cases were considered to be of questionable quality. This means that some rare causes of indirect deaths may have been grouped with direct causes, and if so, the analysis may have underestimated the contribution of indirect deaths. Fifth, missing data in the covariates is another limitation. Sixth, when examining socioeconomic disparities, the use of the municipality-level development index may hide within group differences. It is likely that the individual women dying of maternal deaths across all quintiles of the development index are the poorest women within those municipalities. The area-level nature of this component of the analysis does not allow for commentary about how an individual’s access to resources affects her risk of maternal death.

Conclusion

This study presents a useful strategy towards achieving a relatively complete and accurate assessment of the causes of maternal mortality in a country with complete vital registration. It provides useful lessons for other countries looking to improve maternal mortality measurement and highlights the importance of developing an appropriate health system response to address indirect maternal deaths.
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4.  [Intentional search and reclassification of maternal deaths in Mexico: The effect on the distribution of causes].

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Journal:  Int J Epidemiol       Date:  1988-06       Impact factor: 7.196

10.  Global, regional, and national levels and causes of maternal mortality during 1990-2013: a systematic analysis for the Global Burden of Disease Study 2013.

Authors:  Nicholas J Kassebaum; Amelia Bertozzi-Villa; Megan S Coggeshall; Katya A Shackelford; Caitlyn Steiner; Kyle R Heuton; Diego Gonzalez-Medina; Ryan Barber; Chantal Huynh; Daniel Dicker; Tara Templin; Timothy M Wolock; Ayse Abbasoglu Ozgoren; Foad Abd-Allah; Semaw Ferede Abera; Ibrahim Abubakar; Tom Achoki; Ademola Adelekan; Zanfina Ademi; Arsène Kouablan Adou; José C Adsuar; Emilie E Agardh; Dickens Akena; Deena Alasfoor; Zewdie Aderaw Alemu; Rafael Alfonso-Cristancho; Samia Alhabib; Raghib Ali; Mazin J Al Kahbouri; François Alla; Peter J Allen; Mohammad A AlMazroa; Ubai Alsharif; Elena Alvarez; Nelson Alvis-Guzmán; Adansi A Amankwaa; Azmeraw T Amare; Hassan Amini; Walid Ammar; Carl A T Antonio; Palwasha Anwari; Johan Arnlöv; Valentina S Arsic Arsenijevic; Ali Artaman; Majed Masoud Asad; Rana J Asghar; Reza Assadi; Lydia S Atkins; Alaa Badawi; Kalpana Balakrishnan; Arindam Basu; Sanjay Basu; Justin Beardsley; Neeraj Bedi; Tolesa Bekele; Michelle L Bell; Eduardo Bernabe; Tariku J Beyene; Zulfiqar Bhutta; Aref Bin Abdulhak; Jed D Blore; Berrak Bora Basara; Dipan Bose; Nicholas Breitborde; Rosario Cárdenas; Carlos A Castañeda-Orjuela; Ruben Estanislao Castro; Ferrán Catalá-López; Alanur Cavlin; Jung-Chen Chang; Xuan Che; Costas A Christophi; Sumeet S Chugh; Massimo Cirillo; Samantha M Colquhoun; Leslie Trumbull Cooper; Cyrus Cooper; Iuri da Costa Leite; Lalit Dandona; Rakhi Dandona; Adrian Davis; Anand Dayama; Louisa Degenhardt; Diego De Leo; Borja del Pozo-Cruz; Kebede Deribe; Muluken Dessalegn; Gabrielle A deVeber; Samath D Dharmaratne; Uğur Dilmen; Eric L Ding; Rob E Dorrington; Tim R Driscoll; Sergei Petrovich Ermakov; Alireza Esteghamati; Emerito Jose A Faraon; Farshad Farzadfar; Manuela Mendonca Felicio; Seyed-Mohammad Fereshtehnejad; Graça Maria Ferreira de Lima; Mohammad H Forouzanfar; Elisabeth B França; Lynne Gaffikin; Ketevan Gambashidze; Fortuné Gbètoho Gankpé; Ana C Garcia; Johanna M Geleijnse; Katherine B Gibney; Maurice Giroud; Elizabeth L Glaser; Ketevan Goginashvili; Philimon Gona; Dinorah González-Castell; Atsushi Goto; Hebe N Gouda; Harish Chander Gugnani; Rahul Gupta; Rajeev Gupta; Nima Hafezi-Nejad; Randah Ribhi Hamadeh; Mouhanad Hammami; Graeme J Hankey; Hilda L Harb; Rasmus Havmoeller; Simon I Hay; Ileana B Heredia Pi; Hans W Hoek; H Dean Hosgood; Damian G Hoy; Abdullatif Husseini; Bulat T Idrisov; Kaire Innos; Manami Inoue; Kathryn H Jacobsen; Eiman Jahangir; Sun Ha Jee; Paul N Jensen; Vivekanand Jha; Guohong Jiang; Jost B Jonas; Knud Juel; Edmond Kato Kabagambe; Haidong Kan; Nadim E Karam; André Karch; Corine Kakizi Karema; Anil Kaul; Norito Kawakami; Konstantin Kazanjan; Dhruv S Kazi; Andrew H Kemp; Andre Pascal Kengne; Maia Kereselidze; Yousef Saleh Khader; Shams Eldin Ali Hassan Khalifa; Ejaz Ahmed Khan; Young-Ho Khang; Luke Knibbs; Yoshihiro Kokubo; Soewarta Kosen; Barthelemy Kuate Defo; Chanda Kulkarni; Veena S Kulkarni; G Anil Kumar; Kaushalendra Kumar; Ravi B Kumar; Gene Kwan; Taavi Lai; Ratilal Lalloo; Hilton Lam; Van C Lansingh; Anders Larsson; Jong-Tae Lee; James Leigh; Mall Leinsalu; Ricky Leung; Xiaohong Li; Yichong Li; Yongmei Li; Juan Liang; Xiaofeng Liang; Stephen S Lim; Hsien-Ho Lin; Steven E Lipshultz; Shiwei Liu; Yang Liu; Belinda K Lloyd; Stephanie J London; Paulo A Lotufo; Jixiang Ma; Stefan Ma; Vasco Manuel Pedro Machado; Nana Kwaku Mainoo; Marek Majdan; Christopher Chabila Mapoma; Wagner Marcenes; Melvin Barrientos Marzan; Amanda J Mason-Jones; Man Mohan Mehndiratta; Fabiola Mejia-Rodriguez; Ziad A Memish; Walter Mendoza; Ted R Miller; Edward J Mills; Ali H Mokdad; Glen Liddell Mola; Lorenzo Monasta; Jonathan de la Cruz Monis; Julio Cesar Montañez Hernandez; Ami R Moore; Maziar Moradi-Lakeh; Rintaro Mori; Ulrich O Mueller; Mitsuru Mukaigawara; Aliya Naheed; Kovin S Naidoo; Devina Nand; Vinay Nangia; Denis Nash; Chakib Nejjari; Robert G Nelson; Sudan Prasad Neupane; Charles R Newton; Marie Ng; Mark J Nieuwenhuijsen; Muhammad Imran Nisar; Sandra Nolte; Ole F Norheim; Luke Nyakarahuka; In-Hwan Oh; Takayoshi Ohkubo; Bolajoko O Olusanya; Saad B Omer; John Nelson Opio; Orish Ebere Orisakwe; Jeyaraj D Pandian; Christina Papachristou; Jae-Hyun Park; Angel J Paternina Caicedo; Scott B Patten; Vinod K Paul; Boris Igor Pavlin; Neil Pearce; David M Pereira; Konrad Pesudovs; Max Petzold; Dan Poenaru; Guilherme V Polanczyk; Suzanne Polinder; Dan Pope; Farshad Pourmalek; Dima Qato; D Alex Quistberg; Anwar Rafay; Kazem Rahimi; Vafa Rahimi-Movaghar; Sajjad ur Rahman; Murugesan Raju; Saleem M Rana; Amany Refaat; Luca Ronfani; Nobhojit Roy; Tania Georgina Sánchez Pimienta; Mohammad Ali Sahraian; Joshua A Salomon; Uchechukwu Sampson; Itamar S Santos; Monika Sawhney; Felix Sayinzoga; Ione J C Schneider; Austin Schumacher; David C Schwebel; Soraya Seedat; Sadaf G Sepanlou; Edson E Servan-Mori; Marina Shakh-Nazarova; Sara Sheikhbahaei; Kenji Shibuya; Hwashin Hyun Shin; Ivy Shiue; Inga Dora Sigfusdottir; Donald H Silberberg; Andrea P Silva; Jasvinder A Singh; Vegard Skirbekk; Karen Sliwa; Sergey S Soshnikov; Luciano A Sposato; Chandrashekhar T Sreeramareddy; Konstantinos Stroumpoulis; Lela Sturua; Bryan L Sykes; Karen M Tabb; Roberto Tchio Talongwa; Feng Tan; Carolina Maria Teixeira; Eric Yeboah Tenkorang; Abdullah Sulieman Terkawi; Andrew L Thorne-Lyman; David L Tirschwell; Jeffrey A Towbin; Bach X Tran; Miltiadis Tsilimbaris; Uche S Uchendu; Kingsley N Ukwaja; Eduardo A Undurraga; Selen Begüm Uzun; Andrew J Vallely; Coen H van Gool; Tommi J Vasankari; Monica S Vavilala; N Venketasubramanian; Salvador Villalpando; Francesco S Violante; Vasiliy Victorovich Vlassov; Theo Vos; Stephen Waller; Haidong Wang; Linhong Wang; XiaoRong Wang; Yanping Wang; Scott Weichenthal; Elisabete Weiderpass; Robert G Weintraub; Ronny Westerman; James D Wilkinson; Solomon Meseret Woldeyohannes; John Q Wong; Muluemebet Abera Wordofa; Gelin Xu; Yang C Yang; Yuichiro Yano; Gokalp Kadri Yentur; Paul Yip; Naohiro Yonemoto; Seok-Jun Yoon; Mustafa Z Younis; Chuanhua Yu; Kim Yun Jin; Maysaa El Sayed Zaki; Yong Zhao; Yingfeng Zheng; Maigeng Zhou; Jun Zhu; Xiao Nong Zou; Alan D Lopez; Mohsen Naghavi; Christopher J L Murray; Rafael Lozano
Journal:  Lancet       Date:  2014-05-02       Impact factor: 79.321

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  6 in total

1.  Indirect maternal deaths: UK and global perspectives.

Authors:  Manisha Nair; Catherine Nelson-Piercy; Marian Knight
Journal:  Obstet Med       Date:  2017-02-01

2.  Medical complications in pregnancy at Mulago Hospital, Uganda's national referral hospital.

Authors:  J M Milln; A Nakimuli
Journal:  Obstet Med       Date:  2018-11-26

3.  Contraceptive knowledge and use among women living in the poorest areas of five Mesoamerican countries.

Authors:  Diego Rios-Zertuche; Laura C Blanco; Paola Zúñiga-Brenes; Erin B Palmisano; Danny V Colombara; Ali H Mokdad; Emma Iriarte
Journal:  Contraception       Date:  2017-01-23       Impact factor: 3.375

4.  Hospitals by day, dispensaries by night: Hourly fluctuations of maternal mortality within Mexican health institutions, 2010-2014.

Authors:  Hector Lamadrid-Figueroa; Alejandra Montoya; Jimena Fritz; Eduardo Ortiz-Panozo; Dolores González-Hernández; Leticia Suárez-López; Rafael Lozano
Journal:  PLoS One       Date:  2018-05-31       Impact factor: 3.240

5.  Towards an Inclusive and Evidence-Based Definition of the Maternal Mortality Ratio: An Analysis of the Distribution of Time after Delivery of Maternal Deaths in Mexico, 2010-2013.

Authors:  Hector Lamadrid-Figueroa; Alejandra Montoya; Jimena Fritz; Marisela Olvera; Luis M Torres; Rafael Lozano
Journal:  PLoS One       Date:  2016-06-16       Impact factor: 3.240

6.  Maternal mortality audit in Suriname between 2010 and 2014, a reproductive age mortality survey.

Authors:  Lachmi R Kodan; Kim J C Verschueren; Jos van Roosmalen; Humphrey H H Kanhai; Kitty W M Bloemenkamp
Journal:  BMC Pregnancy Childbirth       Date:  2017-08-29       Impact factor: 3.007

  6 in total

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