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Association Between Recommended Preconception Health Behaviors and Screenings and Improvements in Cardiometabolic Outcomes of Pregnancy

Kaitlyn K. Stanhope, PhD, MPH1; Michael R. Kramer, PhD, MMSc2 (View author affiliations)

Suggested citation for this article: Stanhope KK, Kramer MR. Association Between Recommended Preconception Health Behaviors and Screenings and Improvements in Cardiometabolic Outcomes of Pregnancy. Prev Chronic Dis 2021;18:200481. DOI: http://dx.doi.org/10.5888/pcd18.200481.

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Summary

What is known on this topic?

Risk of gestational diabetes and hypertensive disorders of pregnancy vary by maternal race/ethnicity, family history, and body mass index.

What is added by this report?

Women’s behaviors in the year before pregnancy were not predictive of gestational diabetes or hypertensive disorders of pregnancy in the 2016–2017 Pregnancy Risk Assessment Monitoring System. However, chronic disease status (obesity, diabetes, or hypertensive diagnosis) was associated with increased risk.

What are the implications for public health practice?

Efforts to improve preconception health may be best directed broadly to expand access to primary care for all women.

Abstract

Introduction

Gestational diabetes (GDM) and hypertensive disorders of pregnancy (HDP) are associated with increased risk of maternal and infant illness and long-term elevated cardiometabolic risk. Little information exists on the prevention of either disorder before pregnancy. Our goal was to describe the association between preconception indicators and risk of gestational diabetes and hypertensive disorders of pregnancy.

Methods

We used logistic regression to analyze cross-sectional data from the 2016–2017 Pregnancy Risk Assessment Monitoring System (N = 68,493) to quantify the association between 14 preconception health indicators (across domains of health care, nutrition and physical activity, tobacco and alcohol, chronic conditions, mental health, and emotional and social support) and, separately, GDM and HDP. We accounted for sampling weights and controlled for maternal age, race/ethnicity, prepregnancy insurance, prepregnancy body mass index, and report of a check-up in the year before pregnancy.

Results

Prepregnancy obesity was the strongest predictor of both HDP (adjusted odds ratio [aOR], 3.1; 95% CI, 2.8–3.5) and GDM (aOR, 3.1; 95% CI, 2.7–3.5). Individual behaviors (eg, exercise, attending a check-up) were not associated with either HDP or GDM. A diagnosis of diabetes before pregnancy predicted HDP (aOR, 2.3; 95% CI, 1.7–3.0).

Conclusion

Prepregnancy chronic disease and obesity predicted pregnancy complications (ie, GDM and HDP). Given the challenges in reversing these conditions in the year before pregnancy, efforts to improve preconception health may be best directed broadly to expand access to primary care for all women.

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Introduction

Since the early 1990s, pediatricians, obstetricians, and public health practitioners have focused on promoting preconception health to improve pregnancy outcomes (1,2). Preconception health encompasses physical, mental, and social health indicators and allows for assessing population-level well-being among individuals of reproductive age (3). For individuals, preconception health is often operationalized as recommended behavior changes in the year before pregnancy (4). For example, the Centers for Disease Control and Prevention (CDC) recommends that women attend preventive health visits, achieve a healthy weight, maintain control of chronic diseases, meet recommended levels of exercise, and avoid drinking or smoking (2). Evidence about how women’s individual behaviors in the year before pregnancy contribute to maternal outcomes is limited (5).

Rates of hypertensive disorders of pregnancy (HDP) and gestational diabetes (GDM) have increased over the past 2 decades, particularly among women of racial and ethnic minorities. In this population, rates of HDP increased from 3.8% in 2001 to 8.0% in 2019, and rates of GDM increased from 3.7% in 2000 to 6.9% in 2019 (6–8). GDM and HDP are associated with increased risk of maternal illness and death (9,10) and increased risk of cardiovascular disease (11–13). Evidence for the effectiveness of preconception behavior changes for preventing GDM or HDP is sparse (14,15). The only behavior with strong evidence of effectiveness is control of preexisting diabetes to reduce risk of HDP, which applies only to the small number of women with chronic diabetes (16,17). Although preconception obesity is associated with increased risk of both GDM and HDP (18,19), no evidence indicates that weight loss interventions in the year before pregnancy (eg, diet, exercise) reduce risk of either HDP or GDM (14,15,20).

Identifying risk factors for GDM and HDP modifiable in the year before pregnancy would provide individuals planning their pregnancies with a way to prevent adverse maternal and cardiovascular outcomes. The goal of this article is to describe the association between preconception health indicators and risk of GDM and HDP.

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Methods

Study population

We used data from all sites participating in phase 8 of the Pregnancy Risk Assessment Monitoring System (PRAMS), comprising a cross-sectional, representative sample of births for each included site (state or US territory) for years 2016–2017. CDC releases sites with at least 55% response rates; 39 sites during 2016–2017 had a sufficient response rate. Each site participating in PRAMS randomly selects women who have had a live birth in the past year to complete a survey about their preconception, prenatal, and postpartum behaviors, health outcomes, and experiences (21). PRAMS is weighted to give a representative sample of all women who gave birth in participating sites in those years. For this analysis, we included all women who had complete information on gestational diabetes, gestational hypertension, or both, as well as all included covariates In total, 8.1% of observations were excluded because of missing data (n = 1,105 excluded for missing information on GDM or HDP; n = 4,945 excluded for missing race/ethnicity or insurance). The final analytic sample of unweighted observations was 68,493. Compared with women who were included in the analysis, women who were excluded were more likely to have public insurance before their pregnancy (39.1% [SE, 0.26] vs 29.1% [SE, 1.84]) and less likely to report non-Hispanic white race/ethnicity (42.7% [SE, 1.32] vs 56.9% [SE, 0.27]). For analyses of GDM, we excluded an additional 2,617 participants who reported pregestational diabetes (analytic data set: n = 65,876 unweighted observations). For analyses of associations with HDP, we exclude an additional 4,350 participants reporting pregestational hypertension (analytic data set: n = 64,143 unweighted observations).

Measures

Our outcomes were 1) whether a woman had experienced GDM during this pregnancy and 2) whether a woman had experienced HDP during this pregnancy. Previous research has shown low positive predictive value (~50%) for self-report of pregnancy complications on PRAMS (22). Thus, for GDM and HDP, we used data from the birth certificate, which is linked to PRAMS survey responses for all participants. Both GDM and HDP have acceptable (>80%) positive predictive values on the birth certificate when compared with medical record diagnoses (23).

CDC considers 38 preconception health indicators, 23 of which are measured on PRAMS (3). Of these, we excluded 8 indicators that applied only to multiparous women or reflected postpartum recommendations and 2 for which we did not have data (ie, emotional abuse and use of assisted reproductive technology) resulting in 13 indicators across 7 domains: health care (health-care coverage in the month before pregnancy; and routine check-up, teeth cleaning, and advice to improve health before pregnancy in 12 months before pregnancy); pregnancy intention; tobacco and alcohol use (any smoking or drinking in 3 months before pregnancy); nutrition and physical activity, including prepregnancy body mass index (BMI: underweight [<18.5 kg/m2], normal weight [18.5–24.9 kg/m2], overweight [25.0–29.9 kg/m2], or obese [≥30.0 kg/m2]), folic acid supplementation, and exercising at least 3 times per week in 3 months before pregnancy); mental health (clinical care for depression or anxiety in 12 months before pregnancy); emotional and social support (physical abuse in 12 months before pregnancy); and chronic conditions (diabetes or hypertension diagnosis at any time before pregnancy).

Analysis

All analyses were conducted using SAS survey procedures version 9.4 (SAS Institute) or SUDAAN (RTI International) to account for survey weights. To understand sources of variation in the prevalence of GDM and HDP, we first calculated the prevalence of GDM and HDP across maternal demographic and socioeconomic characteristics and the prevalence of each preconception recommendation across maternal race/ethnicity. Because of the small number of Hawaiian/Pacific Islander women who met inclusion criteria, we do not present estimates on them, although they are included in the total number of women in the final sample. For multivariable analyses, we grouped American Indian/Alaska Native women, Hawaiian/Pacific Island women, Asian women, and Other/Mixed women.

To estimate associations between recommended preconception indicators and GDM/HDP, we fit logistic models between each indicator and each outcome (GDM/HDP) separately. We present adjusted odds ratios (ORs) and 95% CIs. For GDM, we excluded women who reported a diagnosis of diabetes before pregnancy. For HDP, we excluded women who reported a diagnosis of hypertension before pregnancy. Because maternal preconception health indicators and perinatal risk are correlated with women’s socioeconomic status, including demographics and access to care, we selected certain variables a priori for adjustment. In each model, we adjusted for maternal age (≤17, 18–19, 20–24, 25–29, 30–34, 35–39, ≥40), race/ethnicity (non-Hispanic white, non-Hispanic black, Hispanic, non-Hispanic other), prepregnancy insurance (private, public, or none), prepregnancy BMI, and whether the woman reported attending a check-up with an obstetrician/gynecologist (OB/GYN) or primary care physician before pregnancy.

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Results

Overall, 8.4 of women reported an HDP and 6.2% reported GDM (Table 1). The prevalence of both conditions varied most by race/ethnicity, age, and educational level, and both conditions were more common among older women. HDP were most common among non-Hispanic Black women (12.6%), whereas GDM was most common among American Indian/Alaska Native women (13.1%). No clear pattern was found for HDP by maternal education. However, women with the least education (<8th grade) were the most likely to report a diagnosis of GDM (8.5% compared with 6.4% among women with a college degree or higher).

Preconception indicators across all domains varied by maternal race/ethnicity (Table 2). Most women did not receive advice about improving their health before pregnancy (70.7%). Asian and non-Hispanic White women were the most likely to have insurance 1 month before conception and non-Hispanic White women were more likely to attend a check-up or have a teeth cleaning 1 year before conception. Hispanic women were the least likely to have insurance (35.4% uninsured). Non-Hispanic Black women (38.7%) were the most likely to report the pregnancy as unintended, followed by American Indian/Alaska Native women (27.2%). Non-Hispanic White women were more likely to report drinking prior to conception and engaging in protective behaviors (vitamin use or exercise) compared with any other racial/ethnic group. American Indian/Alaska Native women were the most likely to report a diagnosis of depression in the year before pregnancy (18.7% compared with 12.6% overall). Non-Hispanic Black women were more likely to report a prepregnancy diagnosis of hypertension compared with all other groups (8.6% compared with 5.2% overall).

Adjusting for all covariates (age, race/ethnicity, insurance, BMI, prepregnancy check-up), the strongest preconception predictor of GDM was prepregnancy obesity (aOR, 3.1; 95% CI, 2.7–3.5) followed by receiving prepregnancy advice to improve health compared with not receiving advice (aOR, 1.4; 95% CI, 1.2–1.5), and lack of insurance (aOR, 1.2; 95% CI, 1.0–1.4) (Table 3). In adjusted models, other individual behaviors (exercising before pregnancy, drinking before pregnancy, a prepregnancy check-up, or taking folic acid) were not associated with decreased risk of GDM.

Similarly, prepregnancy obesity was the strongest preconception predictor of HDP across all models (aOR, 3.1; 95% CI, 2.8–3.5, adjusted model) (Table 3). Maternal report of a prepregnancy diagnosis of diabetes (aOR 2.3; 95% CI, 1.7–3.0) was also associated with elevated risk of HDP. Reported prepregnancy advice about improving health was associated with increased risk of HDP (aOR, 1.1; 95% CI, 1.0–1.3). The only maternal behavior associated with decreased risk of HDP was teeth cleaning in the year before pregnancy (aOR, 0.8; 95% CI, 0.7–0.9).

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Discussion

Women’s health status in the year before conception (women’s prepregnancy BMI and prepregnancy diabetes for HDP) were associated with elevated risk of GDM and HDP. However, maternal behaviors in the year before pregnancy did not predict GDM or HDP. This finding suggests that improving perinatal health may require interventions more than a year before conception, with an emphasis on cardiometabolic and mental health. For example, evidence exists that bariatric surgery reduces risk of gestational diabetes; however, women are recommended to wait at least 12 months before conceiving following surgery (24). Thus, bariatric surgery is not a viable intervention for women seeking to conceive within a year, but it may be for women seeking to conceive in 2 or more years. Alternatively, the set of commonly measured preconception behaviors may be insufficient to capture interventions that would improve preconception health and subsequent maternal outcomes. Receiving prepregnancy advice about improving health was associated with increased risk, suggesting that primary care and OB/GYN providers accurately target high-risk women for advice. However, although providers may accurately identify women for advice in the year before pregnancy, it may be unrealistic for women to make sufficient changes in the year before conception to reduce risk. Given the socioeconomic and racial and ethnic disparities in GDM and HDP diagnoses, structural and social interventions more than 1 year before pregnancy may be necessary for prevention.

As previous authors have reported, racial/ethnic and socioeconomic disparities exist in experiences of GDM or HDP and in preconception health indicators (25). Disparities in preconception indicators were minor for health behaviors and greatest for indicators of health care access (eg, insurance, check-up) and prepregnancy health status (eg, obesity, diabetes, hypertension), and non-White women were less likely to have optimal preconception health. Our results regarding the prevalence of GDM and HDP are consistent with other estimates based on older data (26).

Our study has limitations. First, PRAMS collects data on pregnancy outcomes and prepregnancy health retrospectively. We attempted to correct for this by using information from the birth certificate on GDM and HDP, which is more accurate (22). However, our study design precludes assessment of causality. Second, in addition to measuring behaviors retrospectively, information about prepregnancy behaviors is vague. For example, drinking once in the 3 months before pregnancy and drinking daily may represent different levels of risk, which we are unable to capture. Future studies should consider prospective measurement of behaviors of interest. Third, PRAMS is only able to capture whether women report a diagnosis of depression before pregnancy. Thus, women who experienced depression but did not seek care were not included. Prospective measurement of depressive symptoms would better characterize the relationship between preconception depression and HDP. Finally, PRAMS captures whether women had a prepregnancy diagnosis of hypertension, diabetes, or depression but not whether the disease was controlled (by medication, diet, or otherwise) or not. This information could be critical in understanding whether screening before pregnancy has the potential to reduce risk for women with chronic disease. Evidence for diabetes suggests that control of diabetes before pregnancy reduces risk of adverse outcomes, including preeclampsia (16). However, whether control of hypertension would prevent GDM is unknown.

Our study also has strengths. First, PRAMS was conducted on a representative sample of women who gave birth to live infants in participating states for 2016–2017, representing 83% of live births in the United States for included years (21). Second, use of PRAMS allows for comparison of preconception health indicators across a range of domains with existing recommendations for state monitoring of preconception health (3).

These results support previous calls to improve all women’s health across the life course in addition to the focus on the year before conception (1,5,27). Although some preconception health indicators identified women at higher risk, none were promising candidates for intervention in the year before pregnancy. For example, prepregnancy obesity was strongly associated with elevated risk of both HDP and GDM. However, interventions to promote weight loss through diet or exercise among women planning to conceive in the next year have been unsuccessful at preventing GDM or HDP (14,15), which suggests that intervening to prevent or reverse obesity more than a year before women intend to conceive may be necessary to reduce risk of HDP and GDM. Additionally, in the PRAMS sample, only 60% of women planned their pregnancy. Thus, broader structural interventions to improve women’s health may have a greater impact than targeted interventions for women who plan to conceive in the next year. Measuring these indicators in the year before pregnancy describes the status of preconception health in a population; however, to improve preconception health, we must act longer before pregnancy. Many policy models exist to improve overall health outcomes in all women of reproductive age (eg, Medicaid expansion under the Affordable Care Act, Federally Qualified Health Centers) (27). Structural interventions are known to decrease the number of maternal deaths and may similarly improve maternal outcomes such as GDM or HDP, although evidence is limited. For example, states that expanded Medicaid under the Affordable Care Act experienced declines in maternal mortality rates following expansion (28). Conversely, states with fewer Planned Parenthood clinics or more restrictive abortion policies have higher maternal mortality rates (29). Policies to improve access may also decrease racial and ethnic disparities in pregnancy outcomes, as one study of infant mortality showed (30). Our study did not identify behavior changes in the year before pregnancy associated with decreased risk of HDP or GDM. This finding suggests that, although focusing on the year before conception may be a useful motivator for some women to improve their health, expanding, effectively implementing, and evaluating interventions to improve access to and utilization of care across the life course will be necessary to improve maternal outcomes.

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Acknowledgments

Thank you to the CDC PRAMS Working Group and PRAMS participating states and respondents. This work was supported in part by Health Resources and Services Administration Maternal and Child Health Bureau, award no. T03MC07651. No copyrighted materials or tools were used in this research.

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Author Information

Corresponding Author: Kaitlyn Stanhope, PhD, MPH, Postdoctoral Fellow, Division of Research, Department of Gynecology and Obstetrics, 50 Jesse Hill Jr Dr, Atlanta, GA 30303. Telephone: 404-556-0169. Email: Kaitlyn.keirsey.stanhope@emory.edu.

Author Affiliations: 1Department of Gynecology and Obstetrics, Emory University School of Medicine, Atlanta, Georgia. 2Department of Epidemiology, Emory University, Atlanta, Georgia.

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References

  1. ACOG committee opinion No. 762: prepregnancy counseling. Obstet Gynecol 2019;133(1):e78–89. CrossRef PubMed
  2. Johnson K, Posner SF, Biermann J, Cordero JF, Atrash HK, Parker CS, et al. ; CDC/ATSDR Preconception Care Work Group; Select Panel on Preconception Care. Recommendations to improve preconception health and health care — United States. A report of the CDC/ATSDR Preconception Care Work Group and the Select Panel on Preconception Care. MMWR Recomm Rep 2006;55(RR-6):1–23. PubMed
  3. Robbins CL, Zapata LB, Farr SL, Kroelinger CD, Morrow B, Ahluwalia I, et al. ; Centers for Disease Control and Prevention. Core state preconception health indicators — pregnancy risk assessment monitoring system and behavioral risk factor surveillance system, 2009. MMWR Surveill Summ 2014;63(3):1–62. PubMed
  4. Thompson EL, Vázquez-Otero C, Vamos CA, Marhefka SL, Kline NS, Daley EM. Rethinking preconception care: a critical, women’s health perspective. Matern Child Health J 2017;21(5):1147–55. CrossRef PubMed
  5. Hemsing N, Greaves L, Poole N. Preconception health care interventions: a scoping review. Sex Reprod Healthc 2017;14:24–32. CrossRef PubMed
  6. Bardenheier BH, Imperatore G, Gilboa SM, Geiss LS, Saydah SH, Devlin HM, et al. Trends in gestational diabetes among hospital deliveries in 19 U.S. states, 2000–2010. Am J Prev Med 2015;49(1):12–9. CrossRef PubMed
  7. Martin JA, Hamilton BE, Ventura SJ, Menacker F, Park MM, Sutton PD. Births: final data for 2001. National Center for Health Statistics; 2002. https://data.nber.org/natality/2001/docs/nvsr51_02.pdf. Accessed January 4, 2021.
  8. United States Department of Health and Human Services, Centers for Disease Control and Prevention, National Center for Health Statistics, Division of Vital Statistics. Natality public-use data 2016–2019. CDC WONDER online database, October 2020. http://wonder.cdc.gov/natality-expanded-current.html. Accessed January 4, 2021.
  9. Hitti J, Sienas L, Walker S, Benedetti TJ, Easterling T. Contribution of hypertension to severe maternal morbidity. Am J Obstet Gynecol 2018;219(4):405.e1–7. CrossRef PubMed
  10. Hirshberg A, Srinivas SK. Epidemiology of maternal morbidity and mortality. Semin Perinatol 2017;41(6):332–7. CrossRef PubMed
  11. Smith GN, Louis JM, Saade GR. Pregnancy and the postpartum period as an opportunity for cardiovascular risk identification and management. Obstet Gynecol 2019;134(4):851–62. CrossRef PubMed
  12. Stuart JJ, Tanz LJ, Missmer SA, Rimm EB, Spiegelman D, James-Todd TM, et al. Hypertensive disorders of pregnancy and maternal cardiovascular disease risk factor development: an observational cohort study. Ann Intern Med 2018;169(4):224–32. CrossRef PubMed
  13. Benschop L, Duvekot JJ, Roeters van Lennep JE. Future risk of cardiovascular disease risk factors and events in women after a hypertensive disorder of pregnancy. Heart 2019;105(16):1273–8. CrossRef PubMed
  14. Chatzakis C, Goulis DG, Mareti E, Eleftheriades M, Zavlanos A, Dinas K, et al. Prevention of gestational diabetes mellitus in overweight or obese pregnant women: a network meta-analysis. Diabetes Res Clin Pract 2019;158:107924. CrossRef PubMed
  15. Nasiri-Amiri F, Sepidarkish M, Shirvani MA, Habibipour P, Tabari NSM. The effect of exercise on the prevention of gestational diabetes in obese and overweight pregnant women: a systematic review and meta-analysis. Diabetol Metab Syndr 2019;11(1):72. CrossRef PubMed
  16. Alexopoulos A-S, Blair R, Peters AL. Management of preexisting diabetes in pregnancy: a review. JAMA 2019;321(18):1811–9. CrossRef PubMed
  17. Battarbee AN, Sinkey RG, Harper LM, Oparil S, Tita ATN. Chronic hypertension in pregnancy. Am J Obstet Gynecol 2020;222(6):532–41. PubMed
  18. Giannakou K, Evangelou E, Yiallouros P, Christophi CA, Middleton N, Papatheodorou E, et al. Risk factors for gestational diabetes: An umbrella review of meta-analyses of observational studies. PLoS One 2019;14(4):e0215372. CrossRef PubMed
  19. Coroyannakis C, Khalil A. Management of hypertension in the obese pregnant patient. Curr Hypertens Rep 2019;21(3):24. CrossRef PubMed
  20. Bain E, Crane M, Tieu J, Han S, Crowther CA, Middleton P. Diet and exercise interventions for preventing gestational diabetes mellitus. Cochrane Database Syst Rev 2015;(4):CD010443. CrossRef PubMed
  21. Shulman HB, D’Angelo DV, Harrison L, Smith RA, Warner L. The Pregnancy Risk Assessment Monitoring System (PRAMS): overview of design and methodology. Am J Public Health 2018;108(10):1305–13. CrossRef PubMed
  22. Dietz P, Bombard J, Mulready-Ward C, Gauthier J, Sackoff J, Brozicevic P, et al. Validation of self-reported maternal and infant health indicators in the Pregnancy Risk Assessment Monitoring System. Matern Child Health J 2014;18(10):2489–98. CrossRef PubMed
  23. Dietz P, Bombard J, Mulready-Ward C, Gauthier J, Sackoff J, Brozicevic P, et al. Validation of selected items on the 2003 U.S. standard certificate of live birth: New York City and Vermont. Public Health Rep 2015;130(1):60–70. CrossRef PubMed
  24. Shawe J, Ceulemans D, Akhter Z, Neff K, Hart K, Heslehurst N, et al. Pregnancy after bariatric surgery: Consensus recommendations for periconception, antenatal and postnatal care. Obes Rev 2019;20(11):1507–22. CrossRef PubMed
  25. Robbins C, Boulet SL, Morgan I, D’Angelo DV, Zapata LB, Morrow B, et al. Disparities in preconception health indicators — Behavioral Risk Factor Surveillance System, 2013–2015 and Pregnancy Risk Assessment Monitoring System, 2013–2014. MMWR Surveill Summ 2018;67(1):1–16. CrossRef PubMed
  26. DeSisto CL, Kim SY, Sharma AJ. Prevalence estimates of gestational diabetes mellitus in the United States, Pregnancy Risk Assessment Monitoring System (PRAMS), 2007–2010. Prev Chronic Dis 2014;11:130415. CrossRef PubMed
  27. Dunlop AL, Everett DL. Forthcoming changes in healthcare financing and delivery offer opportunities for reducing racial disparities in risks to reproductive health. J Womens Health (Larchmt) 2012;21(7):717–9. CrossRef PubMed
  28. Eliason EL. Adoption of Medicaid expansion is associated with lower maternal mortality. Women Health Issues 2020;30(3):147–52. CrossRef
  29. Hawkins SS, Ghiani M, Harper S, Baum CF, Kaufman JS. Impact of state-level changes on maternal mortality: a population-based, quasi-experimental study. Am J Prev Med 2020;58(2):165–74. CrossRef PubMed
  30. Bhatt CB, Beck-Sagué CM. Medicaid expansion and infant mortality in the United States. Am J Public Health 2018;108(4):565–7. CrossRef PubMed

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Tables

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Table 1. Prevalence of Hypertensive Disorders of Pregnancy and Gestational Diabetes, by Socioeconomic Status (N = 68,493), Pregnancy Risk Assessment Monitoring System, United States, 2016–2017
Variable Hypertensive Disorders of Pregnancy Gestational Diabetes
Prevalence, % (SE)
Total 8.4 (0.16) 6.2 (0.14)
Maternal education
<8th grade 6.3 (0.77) 8.5 (0.98)
Grades 9–12, no diploma 8.0 (0.50) 4.7 (0.38)
High school graduate 8.8 (0.36) 5.8 (0.31)
Some college 9.7 (0.32) 6.7 (0.28)
College degree and beyond 7.4 (0.24) 6.4 (0.23)
Marital status
Married 7.9 (0.19) 6.9 (0.19)
Unmarried 9.2 (0.28) 5.0 (0.22)
Maternal age, y
≤17 7.0 (1.40) 0.3 (0.16)
18–19 8.9 (0.97) 1.6 (0.31)
20–24 7.4 (0.37) 3.0 (0.24)
25–29 7.5 (0.27) 5.3 (0.24)
30–34 8.7 (0.30) 7.5 (0.29)
35–39 9.7 (0.41) 10.0 (0.45)
≥40 13.6 (1.04) 12.4 (1.12)
Maternal race/ethnicity
Non-Hispanic White 8.2 (0.20) 5.5 (0.18)
Non-Hispanic Black 12.6 (0.52) 5.5 (0.37)
Asian 11.4 (0.95) 8.7 (0.76)
American Indian/Alaska Native 5.0 (0.43) 13.1 (0.81)
Other/mixed 8.4 (0.80) 5.7 (0.70)
Hispanic/Latina 6.9 (0.36) 7.3 (0.84)
Birth year
2016 8.2 (0.23) 5.2 (0.19)
2017 8.7 (0.22) 5.9 (0.20)

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Table 2. Prevalence of Self-Reported Preconception Health Indicators, by Race/Ethnicity (N = 68,493), Pregnancy Risk Assessment Monitoring System, United States, 2016–2017
Health Indicator Total AI/AN Asian Hispanic NHB NHW Other/Mixed
% (SE)
Health Care
Received advice about improving health (1 y before conception) 29.3 (0.32) 31.9 (1.95) 33.7 (1.40) 32.9 (0.92) 34.6 (0.97) 27.1 (0.39) 28.3 (1.72)
Check-up (OB/primary care) (1 y before conception) 62.9 (0.35) 59.0 (2.23) 56.7 (1.47) 55.0 (1.01) 51.1 (1.04) 67.9 (0.42) 56.1 (2.00)
Teeth cleaning (1 y before conception) 62.9 (0.35) 59.0 (2.23) 56.7 (1.47) 55.0 (1.01) 51.1 (1.04) 67.9 (0.42) 56.1 (2.00)
Health insurance (1 mo before conception)
Private 56.4 (0.29) 16.7 (1.61) 72.7 (1.04) 31.7 (0.68) 37.4 (0.80) 69.0 (0.37) 46.6 (1.58)
Medicaid/other public 29.1 (0.26) 76.4 (1.64) 18.5 (0.83) 32.9 (0.65) 50.1 (0.81) 22.3 (0.33) 42.4 (1.55)
None 14.5 (0.22) 6.9 (0.72) 8.8 (0.78) 35.4 (0.72) 12.6 (0.58) 8.7 (0.24) 11.0 (1.02)
Reproductive Health
Pregnancy intention
Intended 59.4 (0.29) 47.0 (1.56) 68.6 (1.09) 54.9 (0.74) 38.3 (0.80) 65.6 (0.38) 52.6 (1.59)
Ambivalent 15.1 (0.22) 25.8 (1.37) 12.5 (0.73) 13.8 (0.50) 23.0 (0.68) 13.7 (0.28) 17.7 (1.18)
Unintended 25.5 (0.27) 27.2 (1.34) 18.9 (0.94) 31.3 (0.69) 38.7 (0.80) 20.7 (0.33) 29.6 (1.45)
Nutrition and physical activity
Folic acid (1 mo before conception) 48.4 (0.30) 33.8 (1.40) 55.7 (1.17) 38.0 (0.72) 36.6 (0.79) 54.4 (0.39) 45.6 (1.59)
Exercise 3x weekly (1 y before conception) 42.9 (0.58) 34.9 (3.45) 37.0 (2.54) 45.2 (1.54) 32.3 (1.51) 45.9 (0.73) 38.5 (3.21)
Body mass index (kg/m2) 8.0 (0.17) 5.2 (0.57) 12.9 (0.78) 15.6 (0.53) 7.7 (0.45) 5.1 (0.17) 7.0 (0.86)
Underweight (<18.5) 44.6 (0.30) 33.5 (1.34) 59.3 (1.15) 35.0 (0.70) 33.8 (0.77) 49.3 (0.39) 41.5 (1.53)
Normal (18.5–24.9) 24.4 (0.26) 26.0 (1.36) 19.4 (0.91) 26.6 (0.67) 25.4 (0.70) 23.7 (0.33) 27.5 (1.47)
Overweight (25.0–29.9) 23.1 (0.25) 35.4 (1.61) 8.4 (0.67) 22.9 (0.61) 33.1 (0.77) 21.9 (0.32) 24.0 (1.35)
Obese (≥30.0) 23.1 (0.25) 35.4 (1.61) 8.4 (0.67) 22.9 (0.61) 33.1 (0.77) 21.9 (0.32) 24.0 (1.35)
Tobacco and alcohol use
Drinking (3 mo before conception) 57.3 (0.30) 48.9 (1.58) 33.3 (1.10) 40.8 (0.73) 46.4 (0.82) 68.2 (0.36) 57.0 (1.57)
Smoking (3 mo before conception) 17.4 (0.23) 37.6 (1.56) 4.3 (0.41) 9.5 (0.42) 16.9 (0.61) 21.1 (0.33) 23.2 (1.40)
Mental health status
Depression/anxiety diagnosis (1 y before conception) 12.6 (0.20) 18.7 (1.46) 4.9 (0.57) 8.6 (0.40) 11.2 (0.50) 14.9 (0.28) 14.8 (1.10)
Chronic conditions
Diabetes (3 mo before conception) 3.5 (0.11) 4.5 (0.60) 5.1 (0.58) 3.8 (0.28) 3.5 (0.27) 3.2 (0.14) 3.1 (0.52)
Hypertension (3 mo before conception) 5.2 (0.13) 8.3 (0.87) 4.3 (0.52) 4.2 (0.29) 8.6 (0.43) 4.8 (0.17) 5.5 (0.74)
Emotional and social support
Physical abuse (1 y before conception) 1.7 (0.08) 4.3 (0.76) 0.8 (0.20) 1.7 (0.18) 2.8 (0.29) 1.4 (0.09) 2.7 (0.48)

Abbreviations: AI/AN, American Indian/Alaska Native; NHB, non-Hispanic Black; NHW, non-Hispanic White; OB, obstetrician.

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Table 3. Associations Between Self-Reported Preconception Health Indicators and Gestational Diabetes or Hypertensive Disorders of Pregnancy, Pregnancy Risk Assessment Monitoring System, United States, 2016–2017a
Health Indicator Gestational Diabetes (N = 65,876) Hypertensive Disorders of Pregnancy (N = 67,950)
Crude OR (95% CI) Adjusted OR (95% CI) Crude OR (95% CI) Adjusted OR (95% CI)
Health Care
Received advice about improving health (1 y before conception) 1.5 (1.3–1.7) 1.4 (1.2–1.5) 1.2 (1.1–1.4) 1.1 (1.0–1.3)
Check-up (OB/primary care) (1 y before conception) 1.1 (1.0–1.2) 1.0 (0.9–1.1) 1.2 (1.1–1.3) 1.2 (1.1–1.3)
Teeth cleaning (1 y before conception) 0.9 (0.8–1.0) 1.0 (0.8–1.1) 0.8 (0.7–0.9) 0.8 (0.7–0.9)
Health insurance (1 mo before conception)
Private [1 Reference]
Medicaid or other public 0.9 (0.8–1.0) 1.1 (0.9–1.2) 1.0 (0.9–1.1) 0.9 (0.8–1.0)
None 1.1 (0.9–1.2) 1.2 (1.0–1.4) 0.8 (0.7–0.9) 0.9 (0.7–1.0)
Reproductive Health
Pregnancy intention
Intended 1 [Reference]
Ambivalent 0.8 (0.7–0.9) 0.8 (0.7–1.0) 1.0 (0.9–1.2) 1.0 (0.9–1.1)
Unintended 0.7 (0.6–0.8) 0.8 (0.7–1.0) 1.0 (0.9–1.1) 0.9 (0.8–1.0)
Nutrition and physical activity
Folic acid (1 mo before conception) 1.0 (0.9–1.1) 0.9 (0.8–1.0) 1.0 (0.9–1.1) 1.0 (0.9–1.1)
Exercise 3x weekly (1 y before conception) 1.1 (0.9–1.4) 1.1 (0.9–1.4) 0.9 (0.8–1.1) 0.9 (0.8–1.1)
Prepregnancy BMI (kg/m2)
Underweight (<18.5) 1.4 (1.1–1.7) 1.3 (1.1–1.6) 1.0 (0.8–1.3) 1.1 (0.9–1.4)
Normal (18.5–24.9) 1 [Reference]
Overweight (25.0–29.9) 1.7 (1.5–2.0) 1.7 (1.5–2.0) 1.8 (1.6–2.1) 1.8 (1.6–2.1)
Obese (≥30.0) 3.0 (2.6–3.3) 3.1 (2.7–3.5) 3.1 (2.8–3.5) 3.1 (2.8–3.5)
Tobacco and alcohol use
Drinking (3 mo before conception) 0.9 (0.8–1.0) 0.9 (0.8–1.0) 1.1 (1.0–1.2) 1.0 (0.9–1.1)
Smoking (3 mo before conception) 1.0 (0.8–1.1) 1.1 (0.9–1.2) 1.1 (1.0–1.2) 1.1 (0.9–1.2)
Mental health status
Depression/anxiety diagnosis (1 y before conception) 1.0 (0.9–1.2) 1.1 (0.9–1.3) 1.2 (1.0–1.4) 1.1 (0.9–1.2)
Chronic conditions
Hypertension diagnosis (3 mo before conception) 1.6 (1.3–2.0) 1.1 (0.9–1.4)
Diabetes diagnosis (3 mo before conception) 2.8 (2.1–3.7) 2.3 (1.7–3.0)
Emotional and social support
Physical abuse (1 year before conception) 0.9 (0.6–1.3) 0.9 (0.6–1.4) 1.2 (0.8–1.8) 1.2 (0.8–1.7)

Abbreviations: —, not applicable; BMI, body mass index; OB, obstetrician; OR, odds ratio.
a Adjusted for check-up in the year before pregnancy, race/ethnicity, age, BMI, and preconception insurance.

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