Skip to main content
Download PDF

A scoping review of severe maternal morbidity: describing risk factors and methodological approaches to inform population-based surveillance

Maternal Health, Neonatology and Perinatology volume 7, Article number: 3 (2021) Cite this article

Abstract

Background

Current interest in using severe maternal morbidity (SMM) as a quality indicator for maternal healthcare will require the development of a standardized method for estimating hospital or regional SMM rates that includes adjustment and/or stratification for risk factors.

Objective

To perform a scoping review to identify methodological considerations and potential covariates for risk adjustment for delivery-associated SMM.

Search methods

Following the guidelines for Preferred Reporting Items for Systematic Reviews and Meta-analyses Extension for Scoping Reviews, systematic searches were conducted with the entire PubMed and EMBASE electronic databases to identify publications using the key term “severe maternal morbidity.”

Selection criteria

Included studies required population-based cohort data and testing or adjustment of risk factors for SMM occurring during the delivery admission. Descriptive studies and those using surveillance-based data collection methods were excluded.

Data collection and analysis

Information was extracted into a pre-defined database. Study design and eligibility, overall quality and results, SMM definitions, and patient-, hospital-, and community-level risk factors and their definitions were assessed.

Main results

Eligibility criteria were met by 81 studies. Methodological approaches were heterogeneous and study results could not be combined quantitatively because of wide variability in data sources, study designs, eligibility criteria, definitions of SMM, and risk-factor selection and definitions. Of the 180 potential risk factors identified, 41 were categorized as pre-existing conditions (e.g., chronic hypertension), 22 as obstetrical conditions (e.g., multiple gestation), 22 as intrapartum conditions (e.g., delivery route), 15 as non-clinical variables (e.g., insurance type), 58 as hospital-level variables (e.g., delivery volume), and 22 as community-level variables (e.g., neighborhood poverty).

Conclusions

The development of a risk adjustment strategy that will allow for SMM comparisons across hospitals or regions will require harmonization regarding: a) the standardization of the SMM definition; b) the data sources and population used; and c) the selection and definition of risk factors of interest.

Introduction

The tracking of severe maternal morbidity (SMM) has continued to evolve since it was first initiated by the World Health Organization (WHO) in 2004 as an alternative to maternal mortality surveillance for identifying failures and priorities in maternal health care [1]. By 2009, the WHO adopted a definition for a maternal near-miss (i.e., “a woman who nearly died but survived a complication that occurred during pregnancy, childbirth or within 42 days of termination of pregnancy”) and presented a list of identification criteria [2]. Using this approach, cases are first identified as having “potentially life-threatening conditions” associated with organ system dysfunction or failure. Surveillance relies on medical record review to document clinical, laboratory-based, or management-based SMM criteria. Case identification can occur retrospectively by identifying those who met criteria or prospectively by using a list of potentially life-threatening conditions.

A population-based approach to tracking SMM began in parallel to the WHO approach in 2005, when Wen et al. proposed a definition of SMM using population-based Canadian administrative data [3], which, although less specific compared to medical record data, was more feasible for routine monitoring. In 2008, Callaghan et al. at the United States (US) Centers for Disease Control and Prevention (CDC) published a definition using 15 conditions [4]. The CDC definition was expanded to 25 conditions in 2012 [5], and in 2015 when International Classification of Diseases, Clinical Modification, Version 9 (ICD-9) coding was upgraded to ICD-10, the SMM definition was reduced and consolidated to 21 and then to 18 conditions [6]. Roberts et al. in Australia contributed substantially to these efforts [7], and this work was further adapted in Canada by Joseph et al. [8]. Canadian and Australian SMM definitions were developed in ICD-10.

In the US, in addition to the CDC calculations of national, population-based trends for SMM using administrative data, facility-based SMM case audit (here referred to as “facility-based surveillance”) has been encouraged by both the CDC and the American College of Obstetricians and Gynecologists [9, 10]. In a recent review, Kuklina and Goodman promoted these complementary approaches, asserting that while case audits can go into depth to identify the causes of SMM and suggest avenues for prevention, population-based administrative data can be used not only to examine trends, but also to compare “hospitals, cities, or states” and to develop priorities for research and practice [11]. With funding from the Centers for Medicare and Medicaid services, the National Quality Forum, which provides standards for healthcare quality measurement in the US, has begun to explore the use of maternal morbidity and mortality measures to improve outcomes [12].

To make comparisons (e.g., by region or hospital) interpretable and amenable to policy directives and interventions, it will be necessary to develop a standardized method for adjusting for the most relevant risk factors. To address the research question of how an SMM measure might be adjusted for such comparisons, the objective of this scoping review was to describe what is currently known regarding the risk factors and methodological approaches for studying SMM using routinely collected population-based data.

Materials and methods

Data sources and search strategy

We performed a scoping literature review for predictors of delivery-admission SMM, using the definition provided by Anderson et al. [13]: “Scoping studies are concerned with contextualizing knowledge in terms of identifying the current state of understanding; identifying the sorts of things we know and do not know; and then setting this within policy and practice contexts.” This review conformed to guidelines for Preferred Reporting Items for Systematic Reviews and Meta-analyses Extension for Scoping Reviews (PRISMA-ScR) [14]. The PRISMA-ScR checklist is available in Additional file 1. Using the search term “severe maternal morbidity,” the search was conducted in PubMed and Embase, (both initiated in the late 1940’s), and included the entire databases through June 9, 2019. Since SMM is a composite measure that may include as few as one (e.g., intensive care unit admission) or more than 25 indicators, we used only this term (SMM) to narrow our search and retrieve articles using SMM definitions that were most relevant to population-based SMM tracking.

Inclusion and exclusion criteria

The inclusion criteria were that each study examined SMM as an outcome occurring during the delivery admission and that SMM was presented with risk factor adjustment or stratification. The exclusion criteria were the following: 1) case reports; 2) reviews, letters, or editorials; 3) errata; 4) methodological studies; 5) protocol only studies; 6) descriptive only studies; 7) quality improvement studies; 8) limited outcome studies (i.e., those that did not include a comprehensive SMM composite); 9) studies using SMM as a risk factor/predictor for further complications; 10) qualitative studies; 11) readmission SMM studies; 12) studies focused on SMM due to gynecological conditions (e.g., ectopic pregnancy or spontaneous abortion); 13) studies that relied predominantly on risk factors that were not routinely available in administrative data (e.g., clinical data, laboratory test results); 14) studies that relied on surveillance-based data collection methods (e.g., WHO-based methods); and 15) studies that were not in English. Citations identified through the searches were assessed by one reviewer and verified by another based on title and abstract using these pre-defined criteria. Duplicates were removed. Full text publications of potentially relevant citations were then examined by the same reviewers to assure that eligibility criteria were met.

Data extraction

Reviewer disagreements about study selection in the full text review and extraction phases were resolved by jointly re-examining studies and reaching mutual agreement. Information regarding each study was then extracted into a pre-defined database. Variables extracted included: study design and eligibility criteria; datasets used; SMM definition used; and risk factors used, including all patient-, hospital-, and community-level risk factors as reported.

Quality assessment

Risk of bias assessment is not a mandatory part of this review; however, for informative purposes, risk of bias was assessed using a version of the Newcastle-Ottawa Scale (NOS) [15] that was modified to evaluate observational cross-sectional studies relevant to the research question (Additional file 2). Risk of bias was assessed for a single outcome (SMM) within a study. Two reviewers assessed the articles for NOS criteria. Any discrepancy in scoring was resolved by joint re-examination to arrive at consensus. NOS scores were subdivided into those indicating high- (7–10), moderate- (5–6), and low-quality (1–4) of the publication with respect to the research question. Quality scores were used as part of the general assessment of the literature and did not affect the synthesis of results.

Synthesis of results

Risk factors were categorized into patient-, hospital-, and community-level groups. The patient-level risk factors were classified as pre-existing conditions (e.g., medical or behavioral risk factors), obstetrical conditions (e.g., multiple gestation), and non-clinical conditions (e.g., insurance type). The obstetrical conditions were further divided into those known to exist in the antepartum period (e.g., prior cesarean birth) versus those occurring in the intrapartum or postpartum periods of the delivery admission (e.g., dystocia, delivery mode).

The heterogeneity of the studies included in this review precluded any quantitative synthesis of the effect sizes (odds ratios or relative risks) of the identified risk factors. However, we present a comprehensive list of the risk factors for SMM that were reported in these publications and summarize: 1) the number of studies that used each risk factor; 2) the number of studies for which the effect size for a risk factor was reported to be statistically significant; and 3) the number of studies that did not report an effect size for the risk factor but did one of the following: a) included it in a risk adjustment model, b) stratified analyses by the risk factor, or c) excluded subsets of the population based on the risk factor. This information is presented with the understanding that it was not meaningful to compare or aggregate effect sizes across studies because of the wide heterogeneity of the study designs and covariates in the models.

The synthesis of results was organized by placing the 81 studies in the following categories defined by study approach: 1) Testing of multiple conditions for association with SMM without invoking a specific hypothesis; 2) Hypothesis testing of specific patient-level risk factors; 3) Hypothesis testing of hospital-level risk factors; and 4) Risk-adjusted SMM rates and trends. For purposes of this review, both maternal age and race/ethnicity were treated as pre-existing clinical risk factors.

Results

Study selection and characteristics

Results of the literature search are described in Fig. 1. A total of 1489 publications were identified by the original searches, and, of 861 unique titles, 81 (9.4%) met all inclusion and exclusion criteria after thorough review of the full text [3, 8, 16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,84,85,86,87,88,89,90,91,92,93,94]. Table 1 summarizes selected study characteristics and Table 2 presents the risk factors used in the models. Most of the studies (n = 71, 87.7%) relied on hospital claims data, medical records, or discharge/birth certificate data from US hospitals. Although some studies sought to examine and identify general clinical risk factors as defined above (n = 16, 19.8%), most (n = 57, 70.4%) hypothesized an association of SMM with a specific risk factor, such as maternal age or race/ethnicity, or other pre-existing clinical condition; eight studies (9.9%) examined hospital-level risk factors, such as delivery volume. Over one-quarter of the studies (n = 22, 27.2%) limited the study population by patient characteristics (e.g., women at low risk) or hospital type (e.g., community hospitals).

Fig. 1
figure 1

Number of included publications by scoping review step

Full size image
Table 1 Summary of included studies with reference numbers. N = 81 [3, 8, 16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,84,85,86,87,88,89,90,91,92,93,94]
Full size table
Table 2 Risk factors tested for association with severe maternal morbidity
Full size table

Risk of bias of included studies

Quality scoring is presented in Table 3. Of 10 potential points per study, the median score was 6 (range 3–10). There were 37 high-quality, 39 moderate-quality, and 5 low-quality studies.

Table 3 Quality scoring of included studies (n = 81)
Full size table

Synthesis of results by study approach

Testing of multiple conditions for association with SMM

The 16 publications in this category are described in Table 2. Four of these publications attempted to describe the accuracy of the models using various statistical techniques [22, 43, 44, 83]. All studies used maternal age and 11 used race/ethnicity. In several studies, maternal age [3, 27, 33, 47, 69, 81, 82] and parity [3, 42, 53, 82] appeared to have a U- or J-shaped relationship with SMM, requiring categorization into three or more groups or appropriate selection of the functional form (e.g., polynomial or logistic) for the association of these covariates with SMM. Two studies used no pre-existing risk factors [3, 90] and one used no obstetrical risk factors [60]. Of the 15 studies that did use obstetrical risk factors, four included intrapartum risk factors [3, 38, 44, 53].

Hypothesis testing of specific risk factors for SMM

There were 57 studies in this category, and the key risk factors used in modelling are listed in Table 2. As with the studies that tested multiple conditions, maternal age and race/ethnicity were common covariates, as was body mass index (BMI). Where BMI was treated as an independent risk factor, it appeared to have a U-shape. Patients who were underweight and those who were obese had increased risk [42, 53, 55, 62, 63].

There were 10 publications that focused specifically on race [18, 26, 33, 46,47,48, 50, 57, 58, 72]. SMM rates of Black women have been found to be higher than those of White women, even among those with no comorbidities. In a study by Admon et al., among women with no physical or behavioral health conditions, the SMM rate of non-Hispanic Black women was nearly twice that of non-Hispanic White women [18]. Among women with two or more chronic health conditions, non-Hispanic Black women again had an SMM rate that was nearly twice the rate of non-Hispanic White women. Viewed another way, over time, Metcalfe et al. examined trends of SMM rates by race/ethnicity and found that adjustment for race did not change the SMM trends for 5-year periods between 1993 and 2012, over and above adjustment for comorbidity [72]. Similarly, Leonard et al., in a California study [26], and Booker et al., in a study of older women [57], examined SMM rates over time and found that all racial groups experienced rising SMM; SMM was strongly affected by the presence of comorbidities; and the SMM increases for Black and White women were proportionate. Furthermore, Howland et al. demonstrated that Black-White disparities persisted in the highest income and educational groups [50]. Taken together, these studies suggest that there is a baseline difference in SMM between Black and White women that has not been explained.

Several studies [23, 34, 54, 67, 70, 93] tested whether infertile women were at increased risk of SMM. All found an increased risk for SMM among those receiving infertility treatments, cautioning that this increased risk may be attributable to multiple gestation; however, one publication found SMM risk to be elevated among singleton gestations [70].

There have been separate approaches to including drug, alcohol, and/or tobacco use as covariates in SMM models using administrative data. Some studies incorporated these conditions within a risk factor category labelled mental health while others treated these as separate risk factors. However, the sensitivity of administrative data for this information has been reported to be low [96, 97].

Fifteen studies examined specific intrapartum risk factors for their contribution to SMM: induction of labor [40, 65, 82], off-hours delivery [69, 75], route of delivery [20, 24, 41, 56, 66, 74, 77, 84, 94], and anesthesia type for cesarean delivery [16]. Others included intrapartum risk factors as covariates in the context of other hypotheses or in trying to explain the variation in SMM [21, 25, 37, 41, 46,47,48, 61, 63, 67, 76, 79]. Multiple investigators specifically used risk-adjustment models that only included antepartum risk factors for SMM to avoid adjustment for differences in patient management.

Hypothesis testing of hospital-level risk factors for SMM

Eight studies focused on hospital-level risk factors [19, 27, 29, 32, 36, 39, 49, 91]. There were few consistent findings. Three studies focused on annual hospital delivery volume and had mixed results [27, 29, 39]. Three other investigations tested various hypotheses regarding an association between the following specific hospital characteristics and SMM and found no association: the use of laborists in community hospitals [36], hospital quality indicators [49], and the percent of practitioners doing deliveries at the hospital that were midwives [19].

Given patients with the same high-risk conditions, it has been assumed that delivery at higher level hospitals will lead to less SMM. However, evidence for this supposition is limited. Two studies attempted to find an association between hospital resources and SMM. In both cases, hospital resource levels were studied as proxies for levels of maternal care, which are proposed designations for hospitals based on their resources and staffing [98]. Vanderlaan et al. used American Hospital Association data indicating the risk level of patients cared for by the hospital [91], and Clapp et al. assigned risk levels to patients based on Bateman’s Obstetrical Comorbidity Index and then rated hospitals as high versus low acuity based on their percentages of high-risk patients [32]. In spite of extensive sensitivity analyses, Vanderlaan et al. found no relationship between these proxy resource levels and SMM [91]. Clapp et al. found that high-risk patients had a higher absolute risk of SMM at low-acuity hospitals when compared with high-risk patients at high-acuity centers; however, 95% confidence intervals overlapped and no p-value for the comparison was reported [32].

SMM rates and trends

Twenty-seven of the included studies presented SMM rates. Several examined trends of SMM rates over the years [17, 26, 38, 45, 72], reporting rising rates of both SMM and associated comorbidities. Some investigators disaggregated SMM rates and reported rates of the various indicators [18, 89]. SMM rates were highly dependent on the SMM definitions, study populations, and adjustment models. For example, some investigators built on the CDC definitions [52, 61,62,63,64]; others used broad definitions that included maternal intensive care unit admission [21, 25, 28, 40, 53, 65, 67, 71, 73]. A number of studies extended SMM case finding to 42 days postpartum or readmission with SMM.

In the last 5 years, and particularly with the use of administrative data wherein the number of units of packed red blood cells cannot be reliably ascertained, investigators have recognized that blood transfusion accounts for a large proportion of the SMM cases, and, consequently, whether or not it is included in the SMM definition substantially affects the SMM rate and its interpretability [7]. Fifteen studies did sensitivity analyses to display trends or determine if the effect sizes of risk factors were confirmed when transfusion was eliminated from the SMM definition. Trends from year to year were less likely to show statistical differences, and most studies (with some exceptions [50, 55, 78, 94] showed minimal to no changes in the magnitude of risk factors when excluding transfusion. Another 10 did not include transfusion in their SMM definition, nine studies using a maternal ICU admission did not separate transfusion out, and six used medical chart review to assure that at least 4 units of packed red blood cells were used to qualify as meeting the SMM definition (Table 1).

From the seven studies using administrative data with unrestricted delivery populations and including transfusion in the SMM definition [3, 8, 38, 44, 53, 60, 81], SMM rates varied from 0.44% [3] to 2.55% [53]. Using the US National Inpatient Sample [99], the CDC reported the most recent SMM rates from 2014 as 1.44% with transfusions and 0.35% when using the definition excluding transfusions [7]. The overall rate of SMM increased 200% from 1993 to 2014 when transfusion was included and 20% in the same time period when transfusion was excluded.

Maternal death is not an exclusion criterion for the CDC definition of SMM [7]. Some studies specifically included maternal death whether or not SMM was reported. One posited that the coding of death without SMM must be erroneous, and, therefore, excluded such cases [70]. Friedman et al. studied both SMM and death, finding that: 1) 78.7% of deaths in the dataset had been identified as having SMM (these deaths were referred to as “failure to rescue”); and 2) 1.0% of patients with SMM died [39]. This study did not extend the SMM definition to include post-discharge follow-up. In a study by Ray et al., 68.0% of deaths in a population-based delivery cohort had been identified as having SMM [80].

Discussion

Principal findings

This review identified 81 studies of SMM that relied on risk adjustment of routinely collected population-based data. Although the key search term was deliberately chosen to be “severe maternal morbidity” in an attempt to identify studies that incorporated similar outcomes, only 37 (45.7%) used an SMM definition with a CDC basis; the SMM definitions used in the remaining studies varied to a much larger extent. The inclusion of blood transfusions (yes/no) in the SMM definition added a layer of complexity to the comparability of these analyses, given that, in various studies, more than half of the SMM cases had this single indicator of SMM. Such heterogeneity was also evident in the principal datasets used (e.g., claims data, electronic medical record or medical record data, administrative data in both ICD-9 and ICD-10), which may have included linkages to other datasets (e.g., infertility, birth certificate, hospital surveys, census data). Study populations also differed with respect to the definition of a delivery admission and, depending on the purpose of the study, the inclusion and exclusion criteria.

The covariates used for risk adjustment also varied extensively (n = 180, Table 2), not only with respect to the choice of covariates, but also with respect to their definitions (e.g., BMI as a continuous, ordinal, or binary variable). Interpretation of the results also depends on the study design (e.g., subset of deliveries included) and model specification (e.g., other covariates included). Some studies attempted to limit the types of covariates to patient-level conditions that would be apparent prior to the childbirth admission, while others attempted to develop more explanatory models for SMM and included intrapartum variables such as dystocia and delivery mode. Several studies used hospital characteristics (e.g., delivery volume, ownership, or teaching status) or community-level variables (e.g., median household income, percent foreign-born by zip code or county) to make comparisons more interpretable or models more explanatory. Consequently, effect sizes (odds ratios and relative risks) could not be synthesized in a meaningful way.

Interpretation

The call for facility-based surveillance of SMM through case review [10, 11] remains critical for identifying SMM causes, so that prevention strategies and interventions can be developed, implemented, and tested prospectively. In addition, there remains a role for population-based administrative data to describe and monitor the SMM burden [12]. The use of administrative data enables the development of standard SMM rates that can be used to describe trends and disparities and, potentially, to make comparisons across regions and hospitals. Such comparisons can highlight regions or hospitals with disproportionate burdens and can potentially provide insight regarding the quality of pregnancy care for those with SMM and/or the resources needed to address SMM. This use of administrative data at the population level can also inform decisions regarding the potential for public health interventions, such as improving the availability of preconception care [100], and can be used to track their success. Demonstrated success could mean more resources can be deployed to scale-up effective interventions and attenuate the SMM burden.

The results of this review point to several areas that are in need of development for the continued evolution of SMM tracking using population-based data. First is the standardization of the SMM definition. In the US, this definition has been gravitating toward that used by the CDC. However, differences remain across recent US studies, particularly with respect to the inclusion of blood transfusion. The role of transfusions in the administrative definition of SMM needs further evaluation and standardization because the rise in transfusions is due largely to quality improvement efforts to decrease mortality from postpartum hemorrhage [101]. It is apparent that blood products are increasingly being used as part of a secondary prevention effort and that such usage in practice (which is life-saving) conflicts with the interpretation of the SMM measure as a poor outcome.

The second area in need of development is the standardization of the content and size of datasets used for hospital or regional comparisons. Hospital discharge datasets appear to be the best choice because they are relatively similar and nearly universally available. The marginal benefit for the addition of linked patient-level datasets, such as the birth certificate data, may be too resource-intensive for some states. The linkage of a basic subset of hospital variables such as ownership, delivery volume, and teaching status, could be gleaned from a variety of sources and maintained in a central location for consistent use. The importance of community-level variables (e.g., by census tract, zip code, county) has not been well-explored in the literature and needs further evaluation, especially as it relates to the potential for public health intervention and ability to impact SMM rates. Community-level summary measures (e.g., median income, rural status) were frequently used as proxies for patient- or hospital-level comparisons and were relatively infrequently reported as contributing to risk adjustment models.

Third is the selection and definition of risk factors of interest. This will depend on the purpose of the risk adjustment. For the purpose of comparing hospital SMM rates, we suggest that models should adjust for case-mix using the risk factors known upon admission but without including those variables describing intrapartum management (e.g., route of delivery) because these variables are under the control of a given hospital and there is no need to keep them balanced across hospitals. Hospital-level factors, such as resources or staffing characteristics, should also be excluded if hospitals are being ranked. The “within” hospital correlation in SMM can be addressed using clustered standard errors. A more serviceable comparison can be achieved by comparing only hospitals of the same type (e.g., teaching hospitals or community hospitals). By confining hospital comparisons to a group with a similar type, the average hospital for that type yields a better representation of the group compared with an average hospital in a group composed of diverse hospital types. On the other hand, if the purpose is to predict the SMM risk, it is reasonable for these models to include intrapartum-, hospital-, and community-level risk factors to increase explanatory power.

Furthermore, the inclusion of patient-level non-clinical variables (e.g., insurance type, educational level) in SMM risk adjustment models deserves reflection. Such variables may be potential proxies for unmeasured clinical risk factors (e.g., malnutrition), measures of access to higher quality of care, or sources of variation due to discrimination. The risk adjustment purpose and the hypothesized source for the variation in SMM risk due to such variables should determine their use in modelling. For example, for hospital comparisons, use of these covariates would not be appropriate given that they would credit hospitals for poor care given to disadvantaged patients.

Limitations of the review

As discussed in depth above, a limitation of this review is the study heterogeneity, which prevents meaningful synthesis of effect sizes. More narrow inclusion criteria may have allowed for increased detail regarding the relative importance of specific risk factors, such as race/ethnicity and prematurity.

Conclusions

This review identified multiple potential risk factors associated with SMM. The heterogeneity of the studies precluded any quantitative synthesis of the effect sizes (odds ratios or relative risks) of the identified risk factors. The development of a risk adjustment strategy that will allow for SMM comparisons across hospitals or regions will require harmonization regarding the standardization of the SMM definition, the datasets and population used, and the selection and definition of risk factors of interest. The ability to perform such comparisons would contribute to the capacity of public health systems to monitor SMM trends and disparities and to develop strategies to decrease the SMM burden. Administrative data comparisons also allow for evaluating the potential for interventions, tracking their success, and estimating the resources needed to scale-up effective interventions.

Availability of data and materials

No data or materials were used for the publication of this article beyond the review of those articles referenced.

Abbreviations

AIDS:

Acquired immune deficiency syndrome

ART:

Assisted reproductive technology

BMI:

Body mass index

CDC:

Centers for Disease Control and Prevention

CHF:

Congestive heart failure

CHD:

Congenital heart disease

CNS:

Central nervous system

CMS:

Centers for Medicare and Medicaid Services

D&C:

Dilatation and curettage

FHR:

Fetal heart rate

IBD:

Inflammatory bowel disease

ICD-9,10:

International Classification of Diseases, Clinical Modification, versions 9,10

ICSI:

Intracytoplasmic sperm injection

IUI:

Intrauterine insemination

IVF:

In vitro fertilization

L&D:

Labor and delivery area

LGA:

Large for gestational age

MFM:

Maternal fetal medicine specialist

MS:

Multiple sclerosis

MVA:

Motor vehicle accident

NICU:

Neonatal intensive care unit

NOS:

Newcastle-Ottawa Scale

NTSV:

Nulliparous term singleton vertex

PCOS:

Polycystic ovary syndrome

PNC:

Prenatal care

PRISMA-ScR:

Preferred Reporting Items for Systematic Reviews and Meta-analyses extension for scoping reviews

PROM:

Premature rupture of membranes

PPROM:

Preterm premature rupture of membranes

SART:

Society for Assisted Reproductive Technology

SES:

Socioeconomic status

SGA:

Small for gestational age

SLE:

Systemic lupus erythematosus

SMM:

Severe maternal morbidity

TOLAC :

Trial of labor after cesarean

VD:

Vaginal delivery

VTE:

Venous thromboembolism

US:

United States

WHO:

World Health Organization

References

  1. World Health Organization. Beyond the numbers: reviewing maternal deaths and complications to make pregnancy safer. Geneva: World Health Organization; 2004. Available from: https://apps.who.int/iris/handle/10665/42984. Accessed 1 Sept 2020.

    Google Scholar 

  2. Say L, Souza JP, Pattinson RC, for the WHO working group on Maternal Mortality and Morbidity classifications. Maternal near miss – towards a standard tool for monitoring quality of maternal health care. Best Pract Res Clin Obstet Gynaecol. 2009;23:287–96.

    Article  PubMed  Google Scholar 

  3. Wen SW, Huang L, Liston R, Heaman M, Baskett T, Rusen ID, et al. Severe maternal morbidity in Canada, 1991-2001. CMAJ. 2005;173(7):759–64.

    Article  PubMed  PubMed Central  Google Scholar 

  4. Callaghan WM, MacKay AP, Berg CY. Identification of severe maternal morbidity during delivery hospitalizations, United States, 1991–2003. Am J Obstet Gynecol. 2008;199:133.e1–8.

    Article  Google Scholar 

  5. Callaghan WM, Creanga AA, Kuklina EV. Severe maternal morbidity among delivery and postpartum hospitalizations in the United States. Obstet Gynecol. 2012;120:1029–36.

    Article  PubMed  Google Scholar 

  6. Centers for Disease Control and Prevention. How does CDC identify severe maternal morbidity. Available from: https://www.cdc.gov/reproductivehealth/maternalinfanthealth/smm/severe-morbidity-ICD.htm. Accessed 1 Sept 2020.

  7. Roberts CL, Cameron CA, Bell JC, Algert CS, Morris JM. Measuring maternal morbidity in routinely collected health data: development and validation of a maternal morbidity outcome indicator. Med Care. 2008;46(8):786–94.

    Article  PubMed  Google Scholar 

  8. Joseph KS, Liu S, Rouleau J, Kirby RS, Dramer MS, Sauve R, et al. Severe maternal morbidity in Canada, 2003 to 2007: surveillance using routine hospitalization data and ICD-10ca codes. J Obstet Gynaecol Can. 2010;32(9):837–46.

    Article  CAS  PubMed  Google Scholar 

  9. Callaghan WM, Grobman WA, Kilpatrick SJ, Main EK, D’Alton M. Facility-based identification of women with severe maternal morbidity: it is time to start. Obstet Gynecol. 2014;123:978–81.

    Article  PubMed  PubMed Central  Google Scholar 

  10. Kilpatrick SJ, Berg C, Bernstein P, Bingham D, Delgado A, Callaghan WM, et al. Standardized severe maternal morbidity review: rationale and process. Obstet Gynecol. 2014;124:361–6.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Kuklina EV, Goodman DA. Severe maternal or near miss morbidity: implications for public health surveillance and clinical audit. Clin Obstet Gynecol. 2018;61(2):307–18.

    PubMed  PubMed Central  Google Scholar 

  12. National Quality Forum. National Quality Forum launches new project to improve maternal morbidity and mortality outcomes. 2019. Available from: https://www.pressreleasepoint.com/national-quality-forum-launches-new-project-improve-maternal-morbidity-and-mortality-outcomes. Accessed 1 Sept 2020.

    Google Scholar 

  13. Anderson S, Allen P, Peckham S, Goodwin N. Asking the right questions: scoping studies in the commissioning of research on the organization and delivery of health services. Health Res Policy Sys. 2008;6:7.

    Article  Google Scholar 

  14. Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) website. Available from: http://www.prisma-statement.org/Extensions/ScopingReviews. Accessed 1 Sept 2020.

  15. Wells GA, Shea B, O'Connell D, Robertson J, Peterson J, Welch V et al. The Newcastle-Ottawa scale (NOS) for assessing the quality of nonrandomised studies in meta-analyses. Available from: http://www.ohri.ca/programs/clinical_epidemiology/oxford.asp. Accessed 1 Sept 2020.

  16. Abe H, Sumitani M, Uchida K, Ikeda T, Matsui H, Fushimi K, et al. Association between mode of anaesthesia and severe maternal morbidity during admission for scheduled caesarean delivery: a nationwide population-based study in Japan, 2010-2013. Br J Anaesth. 2018;120(4):779–89.

    Article  CAS  PubMed  Google Scholar 

  17. Admon LK, Bart G, Kozhimannil KB, Richardson CR, Dalton VK, Winkelman TNA. Amphetamine- and opioid-affected births: incidence, outcomes, and costs, United States, 2004-2015. Am J Public Health. 2018;109(1):148–54.

    Article  PubMed  Google Scholar 

  18. Admon LK, Winkelman TNA, Zivin K, Terplan M, Mhyre JM, Dalton VK. Racial and ethnic disparities in the incidence of severe maternal morbidity in the United States, 2012-2015. Obstet Gynecol. 2018;132(5):1158–66.

    Article  PubMed  Google Scholar 

  19. Attanasio L, Kozhimannil KB. Relationship between hospital-level percentage of midwife-attended births and obstetric procedure utilization. J Midwifery Womens Health. 2018;63(1):14–22.

    Article  PubMed  Google Scholar 

  20. Bannister-Tyrrell M, Patterson JA, Ford JB, Morris JM, Nicholl MC, Roberts CL. Variation in hospital caesarean section rates for preterm births. Aust N Z J Obstet Gynaecol. 2015;55(4):350–6.

    Article  PubMed  Google Scholar 

  21. Barger MK, Nannini A, DeJoy S, Wisner K, Markenson G. Maternal and newborn outcomes following uterine rupture among women without versus those with a prior cesarean. J Matern Fetal Neonatal Med. 2013;26(2):183–7.

    Article  PubMed  Google Scholar 

  22. Bateman BT, Mhyre JM, Hernandez-Diaz S, Huybrechts KF, Fischer MA, Creanga AA, et al. Development of a comorbidity index for use in obstetric patients. Obstet Gynecol. 2013;122(5):957–65.

    Article  PubMed  Google Scholar 

  23. Belanoff C, Declercq ER, Diop H, Gopal D, Kotelchuck M, Luke B, et al. Severe maternal morbidity and the use of assisted reproductive technology in Massachusetts. Obstet Gynecol. 2016;127(3):527–34.

    Article  PubMed  PubMed Central  Google Scholar 

  24. Bin YS, Roberts CL, Ford JB, Nicholl MC. Outcomes of breech birth by mode of delivery: a population linkage study. Aust N Z J Obstet Gynaecol. 2016;56(5):453–9.

    Article  PubMed  Google Scholar 

  25. Blanc JN, Resseguier JN, Goffinet F, Lorthe E, Kayem G, Delorme P, et al. Association between gestational age and severe maternal morbidity and mortality of preterm cesarean delivery: a population-based cohort study. Am J Obstet Gynecol. 2019;220(4):399.e1–9.

    Article  Google Scholar 

  26. Booker WA, Gyamfi-Bannerman C, Sheen JJ, Wright JD, Siddiq Z, D’Alton ME, et al. Maternal outcomes by race for women aged 40 years or older. Obstet Gynecol. 2018;132(2):404–13.

    Article  PubMed  PubMed Central  Google Scholar 

  27. Booker WA, Ananth CV, Wright JD, Siddiq A, D’Alton ME, Cleary KL, et al. Trends in comorbidity, acuity, and maternal risk associated with preeclampsia across obstetric volume settings. J Matern Fetal Neonatal Med. 2018;32(16):2680–7.

    Article  PubMed  PubMed Central  Google Scholar 

  28. Bourjeily G, Danilack VA, Bublitz MH, Lipkind H, Muri J, Caldwell D, et al. Obstructive sleep apnea in pregnancy is associated with adverse maternal outcomes: a national cohort. Sleep Med. 2017;38:50–7.

    Article  PubMed  PubMed Central  Google Scholar 

  29. Bozzuto L, Passarella M, Lorch S, Srinivas S. Effects of delivery volume and high-risk condition volume on maternal morbidity among high-risk obstetric patients. Obstet Gynecol. 2019;133(2):261–8.

    Article  PubMed  Google Scholar 

  30. Chen JS, Roberts CL, Simpson JM, March LM. Pregnancy outcomes in women with rare autoimmune diseases. Arthritis Rheumatol. 2015;67(12):3314–23.

    Article  PubMed  Google Scholar 

  31. Chen JS, Ford JB, Roberts CL, Simpson JM, March LM. Pregnancy outcomes in women with juvenile idiopathic arthritis: a population-based study. Rheumatology. 2013;52(6):1119–25.

    Article  CAS  PubMed  Google Scholar 

  32. Clapp MA, James KE, Kaimal AJ. The effect of hospital acuity on severe maternal morbidity in high-risk patients. Am J Obstet Gynecol. 2018;219(1):111.e1–7.

    Article  Google Scholar 

  33. Creanga AA, Bateman BT, Kuklina EV, Callaghan WM. Racial and ethnic disparities in severe maternal morbidity: a multistate analysis, 2008–2010. Am J Obstet Gynecol. 2014;210(5):435.e1–8.

    Article  Google Scholar 

  34. Dayan N, Joseph KS, Fell DB, Laskin CA, Basso O, Park AL, et al. Infertility treatment and risk of severe maternal morbidity: a propensity score-matched cohort study. CMAJ. 2019;191(5):e118–27.

    Article  PubMed  PubMed Central  Google Scholar 

  35. Dayan N, Fell DB, Guo Y, Wang H, Velez MP, Spitzer K, et al. Severe maternal morbidity in women with high BMI in IVF and unassisted singleton pregnancies. Hum Reprod. 2018;33(8):1548–56.

    Article  CAS  PubMed  Google Scholar 

  36. Feldman DS, Bollman DL, Fridman M, Korst LM, El Haj IS, Fink A, et al. Do laborists improve delivery outcomes for laboring women in California community hospitals? Am J Obstet Gynecol. 2015;213(4):587.e581–7.

    Article  Google Scholar 

  37. Ford JB, Patterson JA, Seeho SK, Roberts CL. Trends and outcomes of postpartum haemorrhage, 2003-2011. BMC Pregnancy Childbirth. 2015;15:334.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  38. Frederiksen BN, Lillehoj CJ, Kane DJ, Goodman D, Rankin K. Evaluating Iowa severe maternal morbidity trends and maternal risk factors: 2009-2014. Matern Child Health J. 2017;21(9):1834–44.

    Article  PubMed  Google Scholar 

  39. Friedman AM, Ananth CV, Huang Y, D'Alton ME, Wright JD. Hospital delivery volume, severe obstetrical morbidity, and failure to rescue. Am J Obstet Gynecol. 2016;215(6):795.e1–795.e714.

    Article  Google Scholar 

  40. Gibbs Pickens CM, Kramer MR, Howards PP, Badell ML, Caughey AB, Hogue CJ. Term elective induction of labor and pregnancy outcomes among obese women and their offspring. Obstet Gynecol. 2018;131(1):12–22.

    Article  PubMed  PubMed Central  Google Scholar 

  41. Grasch JL, Thompson JL, Newton JM, Zhai AW, Osmundson SS. Trial of labor compared with cesarean delivery in superobese women. Obstet Gynecol. 2017;130(5):994–1000.

    Article  PubMed  Google Scholar 

  42. Gray KE, Wallace ER, Nelson KR, Reed SD, Schiff MA. Population-based study of risk factors for severe maternal morbidity. Paediatr Perinat Epidemiol. 2012;26(6):506–14.

    Article  PubMed  PubMed Central  Google Scholar 

  43. Grobman WA, Bailit JL, Rice MM, Wapner RJ, Reddy UM, Varner MW, et al. Frequency of and factors associated with severe maternal morbidity. Obstet Gynecol. 2014;123(4):804–10.

    Article  PubMed  PubMed Central  Google Scholar 

  44. Guglielminotti J, Landau R, Wong CA, Li G. Patient-, hospital-, and neighborhood-level factors associated with severe maternal morbidity during childbirth: a cross-sectional study in New York state 2013-2014. Matern Child Health J. 2019;23(1):82–91.

    Article  PubMed  Google Scholar 

  45. Hehir MP, Ananth CV, Wright JD, Siddiq Z, D'Alton ME, Friedman AM. Severe maternal morbidity and comorbid risk in hospitals performing <1000 deliveries per year. Am J Obstet Gynecol. 2017;216(2):179.e1–179.e12.

    Article  Google Scholar 

  46. Howell EA, Egorova NN, Janevic T, Balbierz A, Zeitlin J, Hebert PL. Severe maternal morbidity among Hispanic women in New York City: investigation of health disparities. Obstet Gynecol. 2017;129(2):285–94.

    Article  PubMed  PubMed Central  Google Scholar 

  47. Howell EA, Egorova NN, Balbierz A, Zeitlin J, Hebert PL. Site of delivery contribution to black-white severe maternal morbidity disparity. Am J Obstet Gynecol. 2016;215(2):143–52.

    Article  PubMed  PubMed Central  Google Scholar 

  48. Howell EA, Egorova N, Balbierz A, Zeitlin J, Hebert PL. Black-white differences in severe maternal morbidity and site of care. Am J Obstet Gynecol. 2016;214(1):122.e1–7.

    Article  Google Scholar 

  49. Howell EA, Zeitlin J, Hebert PL, Balbierz A, Egorova N. Association between hospital-level obstetric quality indicators and maternal and neonatal morbidity. JAMA. 2014;312(15):1531–41.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  50. Howland RE, Angley M, Won SH, Wilcox W, Searing H, Liu SY, et al. Determinants of severe maternal morbidity and its racial/ethnic disparities in New York City, 2008-2012. Matern Child Health J. 2019;23(3):346–55.

    Article  PubMed  Google Scholar 

  51. Kilpatrick SJ, Abreo A, Gould J, Greene N, Main EK. Confirmed severe maternal morbidity is associated with high rate of preterm delivery. Am J Obstet Gynecol. 2016;215(2):233.e1–7.

    Article  Google Scholar 

  52. Korst LM, Fridman M, Lu MC, Mitchell C, Lawton E, Griffin F, et al. Monitoring childbirth morbidity using hospital discharge data: further development and application of a composite measure. Am J Obstet Gynecol. 2014;211(3):268.e1–268.e16.

    Article  Google Scholar 

  53. Lazariu V, Nguyen T, McNutt LA, Jeffrey J, Kacica M. Severe maternal morbidity: a population-based study of an expanded measure and associated factors. PLoS One. 2017;12(8):e0182343.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  54. Le Ray C, Pelage L, Seco A, Bouvier-Colle MH, Chantry AA, Deneux-Tharaux C, et al. Risk of severe maternal morbidity associated with in vitro fertilisation: a population-based study. BJOG. 2019;126(8):1033–41.

    PubMed  Google Scholar 

  55. Leonard SA, Carmichael SL, Main EK, Lyell DJ, Abrams B. Risk of severe maternal morbidity in relation to prepregnancy body mass index: roles of maternal co-morbidities and caesarean birth. Paediatr Perinat Epidemiol. 2020;34(4):460–8.

    Article  PubMed  Google Scholar 

  56. Leonard SA, Main EK, Carmichael SL. The contribution of maternal characteristics and cesarean delivery to an increasing trend of severe maternal morbidity. BMC Pregnancy Childbirth. 2019;19(1):16.

    Article  PubMed  PubMed Central  Google Scholar 

  57. Leonard SA, Main EK, Scott KA, Profit J, Carmichael SL. Racial and ethnic disparities in severe maternal morbidity prevalence and trends. Ann Epidemiol. 2019;33:30–6.

    Article  PubMed  PubMed Central  Google Scholar 

  58. Liese KL, Mogos M, Abboud S, Decocker K, Koch AR, Geller SE. Racial and ethnic disparities in severe maternal morbidity in the United States. J Racial Ethn Health Disparities. 2019;6(4):790–8.

    Article  PubMed  Google Scholar 

  59. Lindquist AC, Kurinczuk JJ, Wallace EM, Oats J, Knight M. Risk factors for maternal morbidity in Victoria, Australia: a population-based study. BMJ Open. 2015;5(8):e007903.

    Article  PubMed  PubMed Central  Google Scholar 

  60. Lipkind HS, Zuckerwise LC, Bragan Turner E, Collins JJ, Campbell KH, Reddy UM, et al. Severe maternal morbidity during delivery hospitalization in a large international administrative database, 2008-2013: a retrospective cohort. BJOG. 2019;126(10):1223–30.

    Article  CAS  PubMed  Google Scholar 

  61. Lisonkova S, Haslam MD, Dahlgren L, Chen I, Synnes AR, Lim KI. Maternal morbidity and perinatal outcomes among women in rural versus urban areas. CMAJ. 2016;188(17–18):e456–65.

    Article  PubMed  PubMed Central  Google Scholar 

  62. Lisonkova S, Muraca GM, Potts J, Liauw J, Chan WS, Skoll A, et al. Association between prepregnancy body mass index and severe maternal morbidity. JAMA. 2017;318(18):1777–86.

    Article  PubMed  PubMed Central  Google Scholar 

  63. Lisonkova S, Potts J, Muraca GM, Razaz N, Sabr Y, Chan WS, et al. Maternal age and severe maternal morbidity: a population-based retrospective cohort study. PLoS Med. 2017;14(5):e1002307.

    Article  PubMed  PubMed Central  Google Scholar 

  64. Lisonkova S, Sabr Y, Mayer C, Young C, Skoll A, Joseph KS. Maternal morbidity associated with early-onset and late-onset preeclampsia. Obstet Gynecol. 2014;124(4):771–81.

    Article  PubMed  Google Scholar 

  65. Liu S, Liston RM, Joseph KS, Heaman M, Sauve R, Kramer MS. Gestational age-specific severe maternal morbidity associated with labor induction. Am J Obstet Gynecol. 2013;209(3):209.e1–8.

    Article  Google Scholar 

  66. Liu S, Liston RM, Joseph KS, Heaman M, Sauve R, Kramer MS. Maternal mortality and severe morbidity associated with low-risk planned cesarean delivery versus planned vaginal delivery at term. CMAJ. 2007;176(4):455–60.

    Article  PubMed  PubMed Central  Google Scholar 

  67. Luke B, Baker VL, Doody KJ. Risk of severe maternal morbidity by maternal fertility status: a US study in 8 states. Am J Obstet Gynecol. 2019;220(2):195.e1–195.e12.

    Article  Google Scholar 

  68. Lyndon A, Baer RJ, Gay CL, El Ayadi AM, Lee HC, Jelliffe-Pawlowski L. A population-based study to identify the prevalence and correlates of the dual burden of severe maternal morbidity and preterm birth in California. J Matern Fetal Neonatal Med. 2019. https://doi.org/10.1080/14767058.2019.1628941.

  69. Lyndon A, Lee HC, Gay C, Gilbert WM, Gould JB, Lee KA. Effect of time of birth on maternal morbidity during childbirth hospitalization in California. Am J Obstet Gynecol. 2015;213(5):705.e1–11.

    Article  Google Scholar 

  70. Martin AS, Monsour M, Kissin DM, Jamieson DJ, Callaghan WM, Boulet SL. Trends in severe maternal morbidity after assisted reproductive technology in the United States, 2008-2012. Obstet Gynecol. 2016;127(1):59–66.

    Article  PubMed  Google Scholar 

  71. Masters HR, Housley E, van Hook JW, DeFranco E. Maternal obesity is an independent risk factor for intensive care unit admission during delivery hospitalization. Am J Perinatol. 2018;35(14):1423–8.

    Article  PubMed  Google Scholar 

  72. Metcalfe A, Wick J, Ronksley P. Racial disparities in comorbidity and severe maternal morbidity/mortality in the United States: an analysis of temporal trends. Acta Obstet Gynecol Scand. 2018;97(1):89–96.

    Article  PubMed  Google Scholar 

  73. Mourad M, Silverstein M, Bender S, Melka S, Klauser CK, Gupta S, et al. The effect of maternal obesity on outcomes in patients undergoing tertiary or higher cesarean delivery. J Matern Fetal Neonatal Med. 2015;28(9):989–93.

    Article  PubMed  Google Scholar 

  74. Muraca GM, Sabr Y, Lisonkova S, Skoll A, Brant R, Cundiff GW, et al. Morbidity and mortality associated with forceps and vacuum delivery at outlet, low, and midpelvic station. J Obstet Gynaecol Can. 2019;41(3):327–37.

    Article  PubMed  Google Scholar 

  75. Nam JY, Lee SG, Nam CM, Park S, Jang SI, Park EC. The effect of off-hour delivery on severe maternal morbidity: a population-based cohort study. Eur J Pub Health. 2019;29(6):1031–6.

    Article  Google Scholar 

  76. Osmundson SS, Gould JB, Butwick AJ, Yeaton-Massey A, El-Sayed YY. Labor outcome at extremely advanced maternal age. Am J Obstet Gynecol. 2016;214(3):362.e1–7.

    Article  Google Scholar 

  77. Pallasmaa N, Ekblad U, Gissler M, Alanen A. The impact of maternal obesity, age, pre-eclampsia and insulin dependent diabetes on severe maternal morbidity by mode of delivery-a register-based cohort study. Arch Gynecol Obstet. 2015;291(2):311–8.

    Article  CAS  PubMed  Google Scholar 

  78. Platner MH, Ackerman C, Howland RE, Xu X, Pettker CM, Illuzzi JL, et al. Gestational weight gain and severe maternal morbidity at delivery hospitalization. Obstet Gynecol. 2019;133(3):515–24.

    Article  PubMed  Google Scholar 

  79. Ramage K, Grabowska K, Silversides C, Quan H, Metcalfe A. Association of adult congenital heart disease with pregnancy, maternal, and neonatal outcomes. JAMA Netw Open. 2019;2(5):e193667.

    Article  PubMed  PubMed Central  Google Scholar 

  80. Ray JG, Park AL, Dzakpasu S, Dayan N, Deb-Rinker P, Luo W, et al. Prevalence of severe maternal morbidity and factors associated with maternal mortality in Ontario, Canada. JAMA Netw Open. 2018;1(7):e184571.

    Article  PubMed  PubMed Central  Google Scholar 

  81. Reid LD, Creanga AA. Severe maternal morbidity and related hospital quality measures in Maryland. J Perinatol. 2018;38(8):997–1008.

    Article  PubMed  Google Scholar 

  82. Roberts CL, Ford JB, Algert CS, Bell JC, Simpson JM, Morris JM. Trends in adverse maternal outcomes during childbirth: a population-based study of severe maternal morbidity. BMC Pregnancy Childbirth. 2009;9:7.

    Article  PubMed  PubMed Central  Google Scholar 

  83. Rosenbloom JI, Tuuli MG, Stout MJ, Young OM. Woolfolk, Macones GA, et al. a prediction model for severe maternal morbidity in laboring patients at term. Am J Perinatol. 2019;36(1):8–14.

    Article  PubMed  Google Scholar 

  84. Roy A, Peaceman A, Son M, Feinglass J. Maternal obstetric complication rates remain high in Illinois: a retrospective study, 2010–2015. Jt Comm J Qual Patient Saf. 2019;45(1):24–30.

    PubMed  Google Scholar 

  85. Schummers L, Hutcheon JA, Hacker MR, VanderWeele TJ, Williams PL, McElrath TF, et al. Absolute risks of obstetric outcomes risks by maternal age at first birth: a population-based cohort. Epidemiology. 2018;29(3):379–87.

    Article  PubMed  PubMed Central  Google Scholar 

  86. Schummers L, Hutcheon JA, Bodnar LM, Lieberman E, Himes KP. Risk of adverse pregnancy outcomes by prepregnancy body mass index: a population-based study to inform prepregnancy weight loss counseling. Obstet Gynecol. 2015;125(1):133–43.

    Article  PubMed  PubMed Central  Google Scholar 

  87. Shand AW, Chen JS, Selby W, Solomon M, Roberts CL. Inflammatory bowel disease in pregnancy: a population-based study of prevalence and pregnancy outcomes. BJOG. 2016;123(11):1862–70.

    Article  CAS  PubMed  Google Scholar 

  88. Siddiqui A, Azria E, Howell EA, Deneux-Tharaux C, Langer B, Dupont C, et al. Associations between maternal obesity and severe maternal morbidity: findings from the French EPIMOMS population-based study. Paediatr Perinat Epidemiol. 2019;33(1):7–16.

    Article  PubMed  Google Scholar 

  89. Urquia ML, Wanigaratne S, Ray JG, Joseph KS. Severe maternal morbidity associated with maternal birthplace: a population-based register study. J Obstet Gynaecol Can. 2017;39(11):978–87.

    Article  PubMed  Google Scholar 

  90. Urquia ML, Glazier RH, Mortensen L, Nybo-Andersen AM, Small R, Davey MA, et al. Severe maternal morbidity associated with maternal birthplace in three high-immigration settings. Eur J Pub Health. 2015;25(4):620–5.

    Article  Google Scholar 

  91. Vanderlaan J, Rochat R, Williams B, Dunlop A, Shapiro SE. Associations between hospital maternal service level and delivery outcomes. Womens Health Issues. 2019;29(3):252–8.

    Article  PubMed  Google Scholar 

  92. Wahlberg A, Roost M, Haglund B, Hogberg U, Essen B. Increased risk of severe maternal morbidity (near-miss) among immigrant women in Sweden: a population register-based study. BJOG. 2013;120(13):1605–11 discussion 1612.

    Article  CAS  PubMed  Google Scholar 

  93. Wang ET, Ozimek JA, Greene N, Ramos L, Vyas N, Kilpatrick SJ, et al. Impact of fertility treatment on severe maternal morbidity. Fertil Steril. 2016;106(2):423–6.

    Article  PubMed  PubMed Central  Google Scholar 

  94. Young CB, Liu S, Muraca GM, Sabr Y, Pressey T, Liston RM, et al. Mode of delivery after a previous cesarean birth, and associated maternal and neonatal morbidity. CMAJ. 2018;190(18):e556–64.

    Article  PubMed  PubMed Central  Google Scholar 

  95. Geller SE, Rosenberg D, Cox S, Brown M, Simonson L, Kilpatrick S. A scoring system identified near-miss maternal morbidity during pregnancy. J Clin Epidemiol. 2004;57:716–20.

    Article  PubMed  Google Scholar 

  96. Lain SJ, Hadfield RM, Raynes-Greenow CH, Ford JB, Mealing NM, Algert CS, et al. Quality of data in perinatal population health databases: a systematic review. Med Care. 2012;50(4):e7–e20.

    Article  PubMed  Google Scholar 

  97. Yasmeen S, Romano PS, Schembri ME, Keyzer JM, Gilbert WM. Accuracy of obstetric diagnoses and procedures in hospital discharge data. Am J Obstet Gynecol. 2006;194:992–1001.

    Article  PubMed  Google Scholar 

  98. American College of Obstetricians and Gynecologists (ACOG). Levels of maternal care. Obstetric Care Consensus No. 2. Obstet Gynecol. 2015;125(2):502–15.

    Article  Google Scholar 

  99. Agency for Healthcare Research and Quality. National Inpatient Sample Overview. Available from: https://www.hcup-us.ahrq.gov/nisoverview.jsp. Accessed 1 Sept 2020.

  100. Cauldwell M, Ghonim S, Uebing A, Swan L, Steer PJ, Gatzoulis M, et al. Preconception counseling, predicting risk and outcomes in women with mWHO 3 and 4 heart disease. Int J Cardiol. 2017;234:76–80.

    Article  PubMed  Google Scholar 

  101. California Maternal Quality Care Collaborative. OB Hemorrhage Toolkit v2.0. Available from: https://www.cmqcc.org/resources-tool-kits/toolkits/ob-hemorrhage-toolkit. Accessed 1 Sept 2020.

Download references

Acknowledgments

None.

Funding

Funding source: California Department of Public Health, Maternal, Child and Adolescent Health Division, contract number 18–10003. (LMK, KDG, LAN, and MF received the award.) role of the sponsor: DJR and JLT were involved in the study design, data collection and analysis, decision to publish, and preparation of the manuscript. The original funding source for this award is the Title V Maternal and Child Health Services Block Grant from the Maternal and Child Health Bureau/Health Resources & Services Administration.

Author information

Authors and Affiliations

  1. Childbirth Research Associates, LLC, North Hollywood, CA, USA

    Lisa M. Korst

  2. Department of Obstetrics and Gynecology, Cedars-Sinai Medical Center, Burns Allen Research Institute, Los Angeles, CA, USA

    Kimberly D. Gregory, Samia Saeb & Naomi Greene

  3. Department of Obstetrics and Gynecology, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA

    Kimberly D. Gregory & Lisa A. Nicholas

  4. Department of Community Health Sciences, Fielding School of Public Health at UCLA, Los Angeles, CA, USA

    Kimberly D. Gregory

  5. Maternal, Child and Adolescent Health Division, California Department of Public Health, Sacramento, CA, USA

    David J. Reynen & Jennifer L. Troyan

  6. AMF Consulting, Los Angeles, CA, USA

    Moshe Fridman

Authors
  1. Lisa M. Korst
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Kimberly D. Gregory
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Lisa A. Nicholas
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Samia Saeb
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. David J. Reynen
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Jennifer L. Troyan
    View author publications

    You can also search for this author in PubMed Google Scholar

  7. Naomi Greene
    View author publications

    You can also search for this author in PubMed Google Scholar

  8. Moshe Fridman
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

Conceptualization: LMK,KDG,LAN,SS,DJR,JLT,NG,MF; Data curation: LMK,MF; Formal analysis: LMK, MF; Funding acquisition: LMK,KDG,LAN,DJR,JLT,MF; Investigation: LMK,KDG,LAN,SS,DJR,JLT,NG,MF; Methodology: LMK,KDG,NG,MF; Project administration: LAN, KDG,SS,DJR,JLT; Resources: LMK,MF; Supervision: KDG,LAN,DJR,MF; Validation: LMK, MF; Visualization: LMK,KDG,LAN,DJR,JLT,MF; Writing-original draft preparation: LMK, MF; Writing-review and editing: LMK,KDG,LAN,SS,DJR,JLT,NG,MF. The authors read and approved the final manuscript.

Authors’ information

Dr. Kimberly Gregory is Helping Hand of Los Angeles Mariam Jacobs Chair in Maternal Fetal Medicine in the Department of Obstetrics and Gynecology at Cedars-Sinai Medical Center.

Corresponding author

Correspondence to Lisa M. Korst.

Ethics declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors report no conflicts of interest and the following disclosures. LMK and MF are shareholders in Maternal Metrics, Inc. LMK, MF, KDG, and LAN are recipients of federal and state grants for work regarding obstetrical outcomes. DJR and JLT are employees of the California Department of Public Health (CDPH). The remaining authors have nothing to disclose.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1.

Newcastle-Ottawa Quality Assessment Scale (adapted for cross sectional studies with healthcare data for research question: What are the risk factors for severe maternal morbidity associated with the delivery admission?

Additional file 2.

Preferred Reporting Items for Systematic reviews and Meta-Analyses Extension for Scoping Reviews (PRISMA-ScR) Checklist.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and Permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Korst, L.M., Gregory, K.D., Nicholas, L.A. et al. A scoping review of severe maternal morbidity: describing risk factors and methodological approaches to inform population-based surveillance. matern health, neonatol and perinatol 7, 3 (2021). https://doi.org/10.1186/s40748-020-00123-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s40748-020-00123-1

Keywords

Maternal Health, Neonatology and Perinatology

ISSN: 2054-958X

Contact us