This chapter describes the current landscape of clinical preventive services that relate to cardiovascular risk in and around pregnancy and where important gaps remain. Building on the background Chapter 1 provided, this chapter focuses on preventive services that are relevant across the reproductive life course—from prepregnancy and pregnancy through the postpartum and interpregnancy periods—and have implications for cardiovascular health.
This chapter has three main goals. First, it briefly outlines the guideline and coverage infrastructure that shapes which clinical preventive services are routinely offered to women who are of reproductive age, pregnant, or postpartum. Second, it highlights selected services that are especially important for cardiovascular risk around pregnancy, such as hypertension (HTN) screening and treatment; diabetes, lifestyle, and behavioral counseling; lipid management; contraception; and lactation support, and summarizes how current guidelines and coverage policies address these services, along with remaining gaps and opportunities to strengthen practice and coverage. Third, it identifies crosscutting gaps in preventive services guidance and explains how the committee used those gaps, together with its guiding principles in Chapter 1, to identify priority clinical services and associated research questions for formal evidence review.
The examples in this chapter are not intended as a comprehensive catalog of all existing guidelines or preventive services that might influence cardiovascular risk around pregnancy. Rather, they illustrate the kinds of
services that matter most for this report’s charge and show how guidance and coverage align—or fail to align—with women’s needs across the reproductive life course.
As Chapter 1 described, several national guideline bodies play key roles in determining which preventive services are recommended and often which services are covered without cost-sharing. The U.S. Preventive Services Task Force (USPSTF) issues recommendations on clinical preventive services for asymptomatic adults and children, including screening, counseling, and preventive medications (USPSTF, n.d.). The Women’s Preventive Services Initiative (WPSI) develops recommendations on preventive services for women’s health (WPSI, n.d.-a), and Bright Futures provides guidance on pediatric and adolescent preventive care (AAP, 2024). Under the Affordable Care Act (ACA), most private health plans and Medicaid expansion programs are required to cover, without patient cost-sharing, services that receive an A or B grade from USPSTF, are WPSI recommended, or are endorsed by Bright Futures.
Other professional societies also issue guidelines that strongly influence clinical practice but do not directly determine coverage requirements. For pregnancy and cardiovascular disease (CVD), these include the American College of Cardiology and American Heart Association (ACC/AHA), American Heart Association/American Stroke Association (AHA/ASA), American College of Obstetricians and Gynecologists (ACOG), Society for Maternal-Fetal Medicine (SMFM), American College of Nurse Midwives, American Academy of Family Physicians (AAFP), American Academy of Pediatrics (AAP), American Diabetes Association (ADA), and Endocrine Society. These organizations provide detailed recommendations on topics such as managing hypertensive disorders of pregnancy (HDPs), diabetes care before and during pregnancy, lipid management, and lifestyle counseling. Their guidance frequently but not always aligns with USPSTF, WPSI, or Bright Futures recommendations. Therefore, how well these organizations’ recommendations have translated into coverage can vary across payers and states.
A patchwork of payers and programs shapes coverage. Coverage for preventive or primary care before and after pregnancy may change or even be nonexistent for some women, compared to the source or extent during pregnancy. For many women of reproductive age, preventive services are financed through employer-sponsored or marketplace plans that are subject to the ACA’s coverage requirements (CMS, 2025). In contrast, Medicaid plays a central role for pregnant and postpartum women, particularly in states that have expanded eligibility and adopted extended postpartum coverage. Chapter 6 describes these coverage arrangements. In this chapter,
the committee focuses on how these coverage frameworks interact with specific preventive services, such as whether a service is tied to a USPSTF A or B grade or WPSI recommendation, and whether postpartum women retain coverage long enough to receive recommended follow-up services months or even years after.
Consistent with its guiding principles in Chapter 1—including taking a life-course perspective, emphasizing the postpartum period, focusing on services with the potential to reduce severe maternal morbidity (SMM) and mortality, and attending to women who face the greatest barriers to care—the committee systematically reviewed preventive services guidance relevant to cardiovascular risk in and around pregnancy. This review centered on USPSTF, WPSI, and Bright Futures recommendations, given their direct connection to coverage, and also drew on guidelines from professional societies, such as ACC/AHA, ACOG, SMFM, AAFP, ADA, Endocrine, and AHA/ASA, and international guidance from government-affiliated bodies, such as the U.K. National Institute for Health and Care Excellence (NICE).
For each guideline source, the committee examined how recommendations addressed women who are of reproductive age, pregnant, or postpartum; whether adverse pregnancy outcomes (APOs) were explicitly recognized as indicators of elevated cardiovascular risk; and how timing, frequency, and setting of services were specified across the prepregnancy, prenatal, and postpartum periods. The committee also considered how recommendations aligned with or diverged from each other and with the coverage frameworks described.
In addition to formal guideline documents, the committee drew on its clinical and research expertise, information from stakeholder input and public comment, and the epidemiologic patterns summarized in Chapters 1 and 2. These inputs helped the committee identify where clear, actionable preventive services guidance already exists and where gaps or inconsistencies limit the ability of clinicians and health systems to deliver coordinated, evidence-informed care for cardiovascular risk around pregnancy. This review revealed that while many preventive services relevant to cardiovascular risk are addressed in existing guidelines, they are often fragmented across disciplines, inconsistently incorporate pregnancy-related risk enhancers, or lack clarity regarding timing and coordination across the reproductive life course. These observations provide the foundation for the focused discussion that follows.
The sections that follow use selected clinical preventive services to illustrate this landscape, highlighting both alignment and gaps. The chapter
then synthesizes what is known about crosscutting limitations and time period–specific gaps in preventive services guidance and describes how these findings informed the committee’s identification of potential research topics and, ultimately, nine priority clinical services for formal evidence review in Chapter 4.
As noted in the introduction, this section does not catalog every preventive service relevant to pregnancy-related cardiovascular risk. Instead, it highlights selected services that are central to this report’s charge and illustrates how guidelines and coverage do—or do not—support coordinated cardiovascular risk prevention around pregnancy. For each topic—cardiometabolic risk, medications and services, lifestyle and behavior services, substance use disorders, and reproductive planning—the committee considered why the service matters for CVD risk, what guidelines and coverage frameworks provide, how the service is used, the main implementation barriers, and where gaps remain in guidance in that area. See Appendix A for a table summarizing relevant USPSTF, WPSI, and Bright Futures covered services and Appendix B for a table on recommendations/clinical care guidelines from relevant professional societies.
Chronic HTN that begins before pregnancy increases the risk of maternal death, stroke, myocardial infarction, pulmonary edema, renal insufficiency, preeclampsia, placental abruption, postpartum hemorrhage, cesarean delivery, and gestational diabetes mellitus (GDM) (diabetes that develops during pregnancy) and fetal stillbirth, growth restriction, preterm birth, and congenital abnormalities (ACOG, 2019b). HDPs are blood pressure–related conditions that occur before, during, or after pregnancy, including chronic HTN, gestational HTN, preeclampsia, and chronic HTN with superimposed preeclampsia. They are common, increasing in prevalence, and a leading cause of U.S. maternal morbidity and mortality (CDC, 2025b). Women diagnosed with HDP are at increased risk of chronic HTN and CVD postpartum and later in life (Honigberg et al., 2019; Melamed et al., 2014).
USPSTF recommends screening all asymptomatic adults 18+ years for HTN and universal
screening for HDP via blood pressure measurement throughout pregnancy (USPSTF, 2021d, 2023c). As long as women have insurance and access to primary care, these services are generally covered and available.
The 2025 AHA/ACC/ACOG HTN guidelines include recommendations for management in pregnancy. To prevent maternal morbidity and mortality, the guidelines advise treating pregnant women with chronic HTN to achieve a goal blood pressure of <140/90 mmHg (ACOG Committee on Clinical Practice Guidelines et al., 2025; Jones et al., 2025; Tita et al., 2022). AHA/ACC and other sources recommend against atenolol, ACE inhibitors, angiotensin II receptor blockers, direct renin inhibitors, dual endothelin receptor antagonists, and mineralocorticoid receptor antagonists in women planning pregnancy or who are pregnant and switching to labetalol or extended-release nifedipine for blood pressure control if possible (Abalos et al., 2018; Bellos et al., 2020; Bennett et al., 2025; Easterling et al., 2001; Jones et al., 2025; Moretti et al., 2012; Park et al., 2021; Pucci et al., 2015).
Most pregnant women receive blood pressure checks during prenatal care, consistent with USPSTF recommendations. However, prepregnancy optimization of blood pressure and cardiovascular medications and structured postpartum follow-up are more variable. Many women with chronic HTN enter pregnancy without prepregnancy counseling, and treatment (Marshall et al., 2021) thresholds for women who develop gestational HTN and target blood pressures are not well defined (see Prenatal Blood Pressure Target section in Chapter 4). Additionally, women with HDP often do not receive systematic postpartum blood pressure monitoring or linkage to primary care and cardiology.
Lack of insurance access or coverage is a primary barrier to screening and optimizing blood pressure before, during, and after pregnancy. Attending multiple visits, obtaining laboratory testing, affording medications, and purchasing home blood pressure monitors all are facilitated by adequate insurance coverage. Transitions of care—from obstetric to primary care and cardiology—are another barrier, as patients’ long-term clinicians may not become aware of HDP diagnoses without effective communication between obstetric teams and primary care or cardiology (Bryant et al., 2010; Malhotra et al., 2025; Slater et al., 2025).
USPSTF recommendations clearly address screening before and during pregnancy. However, they do not have a recommendation on postpartum blood pressure monitoring or enhanced postpartum HTN management programs, even though HDPs are strongly associated with CVD later in life. Preventive services guidance does not specify the optimal timing, frequency, or modality (i.e., clinic visits, home
blood pressure monitoring, or telehealth) for postpartum surveillance or screening or explicitly integrate HDP history into long-term preventive services frameworks.
For women with preexisting type 1 or type 2 diabetes, prepregnancy counseling and optimizing blood sugar control are necessary to optimize maternal and fetal health. They are at increased risk for miscarriage, congenital malformations and heart defects, intrauterine fetal demise, HDP, macrosomia, cesarean delivery, and CVD later in life, regardless of glycemic control, although achieving strict glycemic targets before and during pregnancy can mitigate these risks (ACOG and ASRM, 2019; ADA Professional Practice Committee for Diabetes, 2026b; Holmes et al., 2011; Jovanovič et al., 2015; Wang et al., 2025). According to a systematic review, higher periconceptional hemoglobin A1c (HbA1c) levels are associated with an increased risk of a pregnancy affected by a congenital anomaly (Guerin et al., 2007).
GDM is common, affecting 5–9 percent of U.S. pregnancies (CDC, 2024b). It is associated with a substantially increased risk of future diabetes and CVD, with cumulative diabetes incidence approaching 50 percent within 5–10 years (Selen et al., 2023) and an approximately twofold increased risk of subsequent cardiovascular events (Bellamy et al., 2009; Selen et al., 2023; Yu et al., 2019).
Diabetes and obstetric societies recommend that clinicians routinely ask women of reproductive age with diabetes about pregnancy intentions during primary care, diabetes, and gynecologic visits and that those considering it receive prepregnancy counseling and care to achieve HbA1c targets (<6.5 percent per ADA; <6 percent per ACOG) (ACOG, 2018a; ADA Professional Practice Committee, 2025; Wyckoff et al., 2025). Such prepregnancy care improves maternal and fetal outcomes (ADA Professional Practice Committee for Diabetes, 2026b; Wahabi et al., 2020).
USPSTF recommends universal screening for GDM during pregnancy (USPSTF et al., 2021b) and screening adults aged 35–70 who are overweight or obese for diabetes or prediabetes (USPSTF et al., 2021a). Since women diagnosed with GDM are at an increased risk of future diabetes diagnosis, “WPSI recommends screening for type 2 diabetes in women with a history of GDM who are not currently pregnant and who have not previously been diagnosed with type 2 diabetes; initial testing is ideally within the first year postpartum and can be done as early as 4–6 weeks postpartum” (WPSI, 2022b). ACA-compliant plans generally cover these services without cost-sharing.
Despite clear recommendations for diabetes screening and treatment, uptake is incomplete. Postpartum diabetes screening with a 2-hour oral glucose tolerance is recommended, but completion is low (Kim et al., 2006; Shah et al., 2011; Smirnakis et al., 2005; Zera et al., 2015); in a large insured managed-care cohort, only about 23 percent completed postpartum glucose testing in the 6–12-week window, and oral glucose tolerance testing was uncommon relative to fasting glucose (Lawrence et al., 2010). ADA recommends that women diagnosed with GDM are aware of their future metabolic risk and that continued diabetes screening with an initial 2-hour oral glucose tolerance testing and then HbA1c at least every 3 years are necessary after pregnancy (ADA Professional Practice Committee for Diabetes, 2026b). Prepregnancy care for women with preexisting diabetes is also underused, with studies demonstrating low rates of documented preconception counseling and glycemic optimization prior to pregnancy despite clear guideline recommendations (ACOG, 2019b; Kachoria and Oza-Frank, 2014; Magdaleno et al., 2020; Roberts et al., 2023).
Key barriers to recommended screening, treatment, and postpartum follow-up include lack of insurance coverage before and after pregnancy; limited access to primary care and postpartum care; limited access to endocrinology, maternal-fetal medicine, and cardiology specialty care in some parts of the country; and residence in areas medically underserved for maternity care where specialists familiar with diabetes in pregnancy are scarce. Even when coverage exists, attending multiple visits, obtaining laboratory testing, and affording medications can be difficult. Telemedicine interventions have been shown to support glycemic management during pregnancy and may help expand access to clinicians experienced in diabetes care (ADA Professional Practice Committee for Diabetes, 2026a). Emerging technologies, such as continuous glucose monitoring, may support remote blood sugar monitoring but require smartphones, connectivity, and coverage for the device—which can be prohibitive (Polsky and Garcetti, 2017). Some insurers require patients to need intensive insulin regimens before they will cover continuous glucose monitoring (Oser and Oser, 2024), though this modality may be particularly useful for postpartum patients who have irregular sleeping and eating schedules.
Transitions of care are another barrier. Primary care clinicians may not always be aware that their patients had GDM during pregnancy, and women may not be counseled about the need for ongoing diabetes and cardiovascular screening postpartum. Proposed strategies include postpartum “passports” and explicit handoffs between obstetric and primary care clinicians (ACOG, 2018b; ADA Professional Practice Committee, 2024a).
On a patient level, competing demands, lack of time, child care issues, challenges with fasting while lactating and caring for an infant, and
inadequate knowledge about the risk for diabetes are also factors. These barriers and facilitators occur across individual, interpersonal, health system, and community levels and affect GDM testing, treatment, and postpartum follow-up (see Figure 3-1) (Simmons et al., 2024).
USPSTF and WPSI recommendations complement each other but leave gaps. USPSTF does not explicitly address postpartum diabetes screening or long-term follow-up after GDM, despite the elevated risk to future pregnancies and infants and the high long-term risk of diabetes. In addition, USPSTF guidance on screening for prediabetes and type 2 diabetes focuses on nonpregnant adults ages 35–70 with overweight or obesity (USPSTF, 2021e) and concludes that evidence is insufficient to assess the balance of benefits and harms of screening asymptomatic children and adolescents (USPSTF, 2022b)—leaving less clarity for many adolescents and younger adults of reproductive age and adults who may be at risk despite having normal body mass index (BMI). Preventive services guidance does not specify how best to bundle postpartum diabetes screening with other cardiometabolic assessments or integrate intensive lifestyle interventions and metformin—both of which reduce diabetes incidence after GDM by about 50 percent—into routine postpartum care (ADA Professional Practice Committee, 2025; Ratner et al., 2008). A life-course model of care for GDM illustrates how prevention, screening, treatment, and postpartum follow-up could be organized to improve both short-term pregnancy outcomes and long-term cardiometabolic health for women and their children (see Figure 3-2).
Dyslipidemia, or abnormal levels of lipids in the bloodstream, before or during pregnancy is associated with APOs, including preeclampsia, GDM, preterm birth, and fetal overgrowth (Agarwala et al., 2024). APOs and cardiometabolic conditions, such as polycystic ovary syndrome (PCOS), diabetes, and obesity, are associated with elevated lifetime atherosclerotic CVD (ASCVD) risk (Alvarez et al., 2023; Teede et al., 2023a). Women with PCOS frequently have atherogenic dyslipidemia, insulin resistance, HTN, and central obesity, contributing to higher risks of type 2 diabetes and ASCVD over time; these metabolic features also have implications for diabetes risk (Alvarez et al., 2023; Teede et al., 2023a).
For women with familial hypercholesterolemia, prior premature ASCVD, or other high-risk profiles, lipid assessment and management before and after pregnancy are important components of long-term cardiovascular prevention (Arnett et al., 2019; Grundy et al., 2019). They may
need ongoing low-density lipoprotein (LDL)-lowering therapy across the reproductive years, yet pregnancy and breastfeeding raise complex questions about when to stop, modify, or restart therapy. This underscores the critical need for shared decision-making and thorough risk–benefit discussions in this population, akin to those for women with established ASCVD.
USPSTF does not have an active stand-alone recommendation on lipid disorder screening; its prior screening statement is archived, and current guidance focuses on statin use for the primary prevention of CVD—an approach that assumes lipid measurement as part of CVD assessment (USPSTF, 2013, 2022c). USPSTF provides clearer direction on when to initiate statins than on screening intervals and related implementation questions (e.g., how often to rescreen), which may be particularly relevant for younger adults of reproductive age. It recommends statins for primary prevention in nonpregnant adults aged 40–75 with at least one cardiovascular risk factor and elevated estimated 10-year risk, but its recommendations do not address pregnancy or prior APOs (USPSTF, 2022c). Bright Futures recommends universal lipid screening during adolescence and again in young adulthood (AAP, 2025), and WPSI recommends an annual well-woman preventive visit to provide age- and risk-appropriate preventive services, which may include lipid screening when clinically indicated (WSPI, 2025).
ACC/AHA cholesterol guidelines and National Lipid Association consensus documents acknowledge pregnancy considerations, generally advising discontinuation of most systemic lipid-lowering agents before and during pregnancy, with bile acid sequestrants as a potential option when treatment is necessary (AHA, n.d.; National Lipid Association, n.d.). In 2021, the U.S. Food and Drug Administration (FDA) removed the contraindication against statins in pregnancy but continues to advise that most patients stop statins once they learn they are pregnant, with continuation considered only in select very high-risk cases (FDA, 2021). Breastfeeding is generally not recommended if statins are required.
These guidance documents recognize pregnancy and reproductive plans as important in lipid management (Kirkpatrick et al., n.d.). However, they do not provide detailed, pregnancy-specific drug algorithms or standardized approaches to lipid screening and counseling before, during, and after pregnancy.
In practice, general adult prevention guidelines rather than pregnancy-specific considerations often drive lipid assessment and management for women of reproductive age. Lipids may be checked as part of routine primary care, diabetes, or PCOS evaluation, but prepregnancy and infertility care pathways do not consistently include structured cardiovascular risk assessment or lipid counseling.
Women with familial hypercholesterolemia or other very high-risk phenotypes may be on statins, nonstatin therapies (i.e., ezetimibe, PCSK9 inhibitors, and bempedoic acid), or other agents when they decide to attempt pregnancy, and unplanned pregnancies while on lipid-lowering therapies can occur. Evolving guidance and limited pregnancy-specific safety data contribute to uncertainty regarding when to discontinue statins before pregnancy, whether continuation is appropriate in select high-risk cases, which non-statin options may be considered, and how to manage therapy in the postpartum period, particularly during breastfeeding (FDA, 2021; Henry et al., n.d.; National Lipid Association, n.d.). Hydrophilic statins, such as pravastatin, have been studied in pregnancy because their physicochemical properties and placental transport suggest more limited fetal exposure than some lipophilic statins, but evidence directly comparing placental transfer across agents remains limited (Chang et al., 2021; Fokina et al., 2022; Nanovskaya et al., 2013; Vahedian-Azimi et al., 2021). Recent meta-analyses found no significant association between first-trimester exposure to statins and congenital malformations (Christensen et al., 2025; Karadas et al., 2022).
Practical issues that preventive services guidance do not address adequately include:
These challenges are magnified because physiologic lipid levels rise substantially during pregnancy (Agarwala et al., 2024)—even in women without preexisting dyslipidemia—and evidence to guide interpretation and treatment thresholds in this setting is limited.
From a preventive services perspective, several gaps emerge:
Given the limited and evolving evidence on lipid-lowering therapy during pregnancy and lactation, that the mainstay method (statins) is generally not recommended during breastfeeding in the United States and the lack of trials that directly link lipid-focused interventions around pregnancy to maternal cardiovascular events or pregnancy outcomes, the committee judged that lipid assessment and management would be difficult to address as a discrete preventive clinical service within this report. Nevertheless, lipid disorders remain an important part of the cardiovascular risk profile for many women of reproductive age, particularly those with PCOS, diabetes, familial hypercholesterolemia, prior APOs, or established ASCVD. The committee therefore viewed lipid assessment and counseling—especially in the context of prepregnancy and postpartum care—as an area where future preventive services guidance could more explicitly incorporate pregnancy history and reproductive plans into cardiovascular risk management.
Recent data indicate that HDP, including preeclampsia, is becoming increasingly common, with prevalence among hospitalized deliveries increasing from 13.3 percent to 15.9 percent 2017–2019 (Ford et al., 2022). Nearly one-third (31.6 percent) of deaths during delivery hospitalization had a documented diagnosis code for HDP (Ford et al., 2022). Preeclampsia is associated with substantially elevated long-term ASCVD risk (Parikh et al., 2021). Prevention is critical because delivery of the placenta is the only definitive treatment for preeclampsia during pregnancy, although hypertensive complications may persist or emerge postpartum. Low-dose aspirin is an inexpensive, guideline-recommended preventive therapy that reduces preeclampsia and related adverse outcomes for women with known risk factors.
In 2021, USPSTF assigned a grade B to prescribing low-dose aspirin (81 mg/day) after 12 weeks’ gestation in women at high risk for preeclampsia (USPSTF, 2021a), defined by the presence of at least one high risk factor (e.g., history of preeclampsia, multifetal gestation, chronic HTN, pregestational diabetes, kidney disease, and autoimmune disease) or two or more moderate risk factors (e.g., nulliparity, BMI ≥30, family history of preeclampsia, Black race [as a proxy for social factors], lower income, aged 35+, pregnancy via in vitro conception, and certain prior pregnancy outcomes) (see Box 3-1). Low-dose aspirin is also recommended to be considered for women with only one moderate risk factor. WPSI does not issue a separate recommendation but adopts the USPSTF guidance and includes aspirin for preeclampsia prevention in its women’s preventive health care recommendations. Under ACA, aspirin prophylaxis for eligible pregnant women is covered without cost-sharing when prescribed.
Despite clear recommendations, available data suggest that fewer than half of eligible women receive low-dose aspirin prophylaxis (Wheeler et al., 2022). Because moderate risk factors are common in the obstetric population, a substantial proportion of pregnant women meet criteria for consideration of aspirin therapy under current guidelines (McElrath et al., 2025; Wheeler et al., 2022). Use appears to vary by setting, clinician awareness, and clinician comfort with risk assessment. Aspirin is inexpensive and available over the counter, but the need for a prescription to ensure no-cost coverage can create practical barriers. Evidence from randomized trials and systematic reviews has not demonstrated statistically
SOURCES: ACOG, 2021; USPSTF, 2021a.
significant increases in placental abruption, postpartum hemorrhage, fetal intracranial bleeding, or congenital anomalies with daily low-dose aspirin. Overall maternal and fetal harms appear to be small, particularly when used in women at increased risk for preeclampsia (Henderson et al., 2014; USPSTF, 2021a). Questions remain about optimal dosing; relative benefits in different risk profiles, including women with obesity and different HDP phenotypes; and best strategies to systematically identify and offer low-dose aspirin to all eligible women.
In general, lactation benefits both maternal and infant health and may be particularly important for
women with cardiovascular risk factors or pregnancy complications. A meta-analysis of eight studies that included over 1 million women found that breastfeeding compared to no breastfeeding was associated with a 10–12 percent risk reduction for future CVD, coronary heart disease, stroke, and fatal CVD (Tschiderer et al., 2022). An immediate protective effect has also been shown for women with cardiometabolic pregnancy complications; during the postpartum period, those who breastfed ≥6 months had significantly lower triglycerides, fasting serum glucose, ratio of cholesterol to HDL-C, and higher HDL-C compared to those who did not (Yu et al., 2020). Thus, there is a growing body of evidence linking longer durations of breastfeeding (e.g., greater than 6 months) to improved maternal cardiometabolic health, potentially through hormonal effects of oxytocin and prolactin on vascular remodeling and metabolic profiles, suggesting the importance of breastfeeding for maternal health (Villarreal et al., 2025). Observational studies suggest that the potential benefits for maternal health span multiple systems, including metabolic, cardiovascular, endocrine, and hematologic domains, and may extend to long-term health outcomes (see Figure 3-3), although the strength of evidence varies and may be influenced by confounding factors.
Clinical guidelines based on numerous scientific reports encourage asking pregnant women about their intentions early in pregnancy and at delivery and providing counseling and support to initiate and continue breastfeeding. USPSTF recommends providing supportive interventions, and WPSI recommends comprehensive support services across the antenatal, perinatal, and postpartum periods, including counseling, peer support, and provision of equipment such as breast pumps (USPSTF, 2025a; WPSI, 2022a). In general, ACA-compliant plans cover these services.
While breastfeeding intention and initiation rates are approximately 85 percent, only about 25 percent of women continue exclusive breastfeeding through 6 months (CDC, 2025a). This is especially low among women who require increased medical attention or had pregnancy complications (Burgess et al., 2021; Collins et al., 2023) as well as women from disadvantaged backgrounds (Roess and Robert, 2025). Although all women who breastfeed can benefit, these subpopulations are particularly vulnerable and may need targeted support (Merewood et al., 2007). Barriers reported in the literature associated with no or short breastfeeding duration include latching problems and mastitis; concerns about infant growth; medication use after delivery; lack of support from family and clinicians; cultural norms; postpartum depression; and limited maternity leave, pay for pumping time during work, and access to equipment for pumping and storage (OTSG, 2011). Limited paid maternity leave and early return to work are among the most important workplace and policy barriers: national reports identify the former as significant, particularly for women with lower incomes (CDC, 2022), and observational studies show that women with shorter leave are less likely to continue breastfeeding, whereas paid family leave policies are associated with higher rates and longer duration (Kortsmit et al., 2021; Rosenberg et al., 2024). Increased clinical support in the postpartum period can help address these barriers and may be particularly important for women with cardiovascular risk.
These barriers occur at multiple levels—including the health system, workplace, community, and clinical training—and have potential strategies to address them (see Figure 3-4). Because these barriers are largely structural—encompassing workplace policies, insurance coverage, access to trained support, and health system practices—lactation continuation should not be framed solely as an individual choice or responsibility. Efforts to improve maternal cardiovascular outcomes through lactation support therefore require coordinated action across policy, health systems, and community settings rather than reliance on individual behavior change alone. In many clinical settings, nurses, midwives, and lactation consultants provide much of the hands-on breastfeeding education and support; therefore, gaps
in training, resources, and institutional support across the broader maternity care team—not only physicians—can affect lactation success.
A 2025 consensus report from the National Academies of Sciences, Engineering, and Medicine provides a comprehensive review of breastfeeding, and the policies, programs, and investments to better understand the landscape of breastfeeding promotion, initiation, and support across the United States (NASEM, 2025).
Existing preventive services guidance endorses lactation support. However, it does not specifically target women with pregnancy complications or explicitly address how support might be integrated with postpartum cardiometabolic care and medication management for women who need ongoing treatment for HTN, diabetes, or dyslipidemia.
Substantial evidence links lifestyle behaviors to CVD risk factors (Kaminsky et al., 2022; Rippe and Angelopoulos, 2019). Key elements include dietary quality, physical activity, sleep patterns, and stress and anxiety management. Diets rich in plant-based foods and diverse protein sources, such as fish, seafood, lean meats, beans, legumes, and low-fat dairy, and low in red and processed meats, saturated fats, refined sugars, and sodium are recommended to reduce cardiovascular risk (Lichtenstein et al., 2021). Similar principles apply during pregnancy, with additional guidance to avoid foods that increase risk of foodborne illness and substances harmful to fetal development, such as alcohol (Procter and Campbell, 2014). Sedentary behavior has been consistently associated with adverse cardiovascular outcomes, and maintaining appropriate physical activity during pregnancy is recommended (Gascoigne et al., 2023). Emerging evidence also links poor sleep quality and high stress or anxiety to increased cardiovascular risk (Eshera et al., 2024).
Clinical guidelines recommend screening for lifestyle behaviors and offering behavioral counseling to promote healthy diet and physical activity and prevent excess gestational weight gain. This is reflected in USPSTF recommendations on behavioral counseling to promote healthy weight gain in pregnancy and broader adult diet and physical activity counseling (Gascoigne et al., 2023; Meander et al., 2021; USPSTF, 2021c). WPSI and well-woman visit recommendations also provide a framework for delivering lifestyle counseling across the reproductive life course.
Most women of reproductive age do not meet federal recommendations for diet or physical activity levels, and fewer than one in three meet both aerobic and muscle-strengthening activity guidelines (CDC, 2023; HHS, 2018; USDA, 2020). During pregnancy, counseling on gestational weight gain, physical activity, and diet is inconsistent, and postpartum lifestyle interventions are uncommon, in part because only about two-thirds of women attend a postpartum visit (Attanasio et al., 2022). Barriers include limited time during visits, variable coverage for intensive behavioral interventions, and access challenges, such as transportation, child care, and limited availability of affordable nutritious foods and safe settings for physical activity. These are particularly pronounced for women who live in areas with fewer resources or have pregnancy complications.
Preventive services guidance endorses lifestyle counseling but does not consistently specify how to tailor interventions for women who are pregnant and postpartum or have recent HDP or GDM. ADA recommends referral to intensive lifestyle intervention programs, such as the National Diabetes Prevention Program (DPP), for women with prior gestational diabetes. In DPP and its follow-up studies, intensive lifestyle intervention and metformin reduced progression to type 2 diabetes by approximately 50 percent among women with a history of GDM (ADA Professional Practice Committee, 2024b; Aroda et al., 2015; Ratner et al., 2008). Limited evidence guides the design and delivery of postpartum lifestyle programs that can be integrated with other cardiometabolic services. In addition, participation in DPP remains limited in many communities, and postpartum women may face logistical barriers, such as child care responsibilities, work demands, and limited availability of in-person programs (Ely et al., 2017; Ferrara et al., 2014). Strategies that prioritize scalability and reach—such as group-based or telehealth-enabled DPP models—may be particularly important for reaching women after GDM, including those facing logistical or geographic barriers; however, further research is needed to determine how best to integrate these approaches into routine postpartum care (Ritchie et al., 2023).
Tobacco and alcohol use are major modifiable risk factors for CVD and APOs. Tobacco use in any form during pregnancy is associated with increased risks of placenta previa, placental abruption, preterm and prelabor rupture of membranes, fetal growth restriction, low birth weight, preterm birth, stillbirth, perinatal mortality, and sudden infant death syndrome (ACOG, 2020b; Kipling et al., 2024; Wells and Lotfipour, 2023). Tobacco smoke exposure also contributes to
long-term cardiovascular risk through endothelial dysfunction, oxidative stress, and promotion of atherosclerosis (Gould et al., 2020; Messner and Bernhard, 2014).
Excessive alcohol use increases the risk of HTN, coronary artery disease, stroke, arrhythmias, cardiomyopathy, and heart failure (Georgescu et al., 2024; Piano et al., 2025). During pregnancy, any alcohol use is considered unsafe and is a leading preventable cause of miscarriage, stillbirth, and fetal alcohol spectrum disorders. Recent surveillance indicates that roughly 1 in 7 pregnant women report current alcohol use and about 1 in 20 report binge drinking in the last 30 days (CDC, n.d.; Green et al., 2023). These exposures can also complicate efforts to manage other cardiovascular risk factors, including blood pressure, weight, glucose, and mental health (Evans et al., 2023; Habersham et al., 2025).
USPSTF recommends that clinicians ask all adults, including pregnant women, about tobacco use, advise them to stop, and provide behavioral interventions to support cessation (Grade A) (USPSTF, 2021f). For nonpregnant adults, USPSTF also recommends FDA-approved pharmacotherapy. For pregnant women, the evidence is considered insufficient to determine the balance of benefits and harms of pharmacotherapy and e-cigarettes, so behavioral interventions are the main recommended approach. The 2021 USPSTF recommendation remains in effect while the Task Force conducts an updated review of this topic.
USPSTF recommends screening adults 18+ years, including pregnant women, for unhealthy alcohol use in primary care and providing brief behavioral counseling interventions to those engaged in risky or hazardous drinking (Grade B) (USPSTF, 2018). Professional societies and public health agencies similarly recommend routine use of validated alcohol screening tools (e.g., AUDITC and single-question screeners) and brief interventions for women of reproductive age and throughout pregnancy and the postpartum period (AWHONN, 2023; Graves et al., 2020; Green et al., 2023). USPSTF issued the current operative recommendation statement in 2018 and is updating this topic.
These recommendations are tied to coverage requirements in many ACA-compliant plans when delivered in eligible settings and can be incorporated into well-woman, prenatal, and postpartum visits.
Despite clear recommendations, tobacco and alcohol use remain common in and around pregnancy. Recent data from the Pregnancy Risk Assessment Monitoring System (PRAMS) indicate that in 2021, 12.1 percent of women reported smoking in the 3 months before pregnancy, 5.4 percent during the last 3 months of pregnancy, and 7.2 percent in the postpartum period, with substantial variation across
states and evidence of relapse after delivery (Kipling et al., 2024). Counseling and pregnancy-specific self-help materials can substantially increase cessation rates (ACOG, 2020b), but underreporting of tobacco use, limited time in visits, and competing priorities can impede consistent delivery of intensive behavioral support.
For alcohol, national surveys suggest that screening is performed for many pregnant women, but USPSTF-recommended validated tools and structured brief interventions are used less consistently (Green et al., 2023; Luong et al., 2023). Obstetric and primary care clinicians report variable training and confidence in addressing alcohol and other substance use, and screening rates are lower among women with less formal education, pointing to disparities in implementation (Luong et al., 2023; Thomson et al., 2024).
From a preventive services perspective, recommendations clearly endorse tobacco cessation counseling and alcohol screening and brief interventions, but they are not integrated consistently with broader cardiometabolic risk management around pregnancy. Clinicians may not be aware of the specific Current Procedural Terminology codes related to tobacco and alcohol cessation counseling and screening and brief interventions, which are reimbursed in addition to traditional Evaluation & Management visit codes. Tobacco and alcohol use are often addressed separately from blood pressure, lipids, weight, diabetes risk, and mental health, and postpartum visits may not systematically revisit tobacco and alcohol use even though relapse and ongoing use are common (Kipling et al., 2024). This fragmentation limits opportunities to deliver coordinated, life course–oriented cardiovascular prevention for women who use tobacco or alcohol before, during, and after pregnancy.
Women’s experiences with substance use disorders are shaped by interacting biological, psychological, and social factors (O’Hagan and Wilson, 2018). Women experience more acute and chronic pain than men and have been prescribed opioids in greater numbers (Darnall and Stacey, 2012), and prescribed opioids are a major pathway to misuse and addiction (Goetz et al., 2021). Sex hormones, such as estrogens and progestins, may modulate both endogenous and exogenous opioid systems—animal and human studies suggest they can enhance opioid-mediated pain relief and alter drug reward pathways—which may contribute to sex differences in analgesic response and vulnerability to misuse (O’Hagan and Wilson, 2018; Shimu and Islam, 2025). Biological
differences, including hormonal influences and sex-specific neurobiologic responses, have been associated with more rapid progression from initiation to dependence, greater withdrawal severity, and differential treatment response among women, particularly for nicotine and alcohol use disorders (Bawor et al., 2015; Greenfield et al., 2010; O’Hagan and Wilson, 2018; Perkins and Scott, 2008; Quigley et al., 2021).
Opioid misuse has cardiovascular consequences, including increased risk of infective endocarditis, coronary heart disease, cardiac arrhythmias, and stroke (Evans et al., 2023). Nonacute opioid use is strongly associated with infective endocarditis and myocardial infarction (Singleton et al., 2021) and may contribute to cardiovascular aging through arterial stiffness and changes in heart rate variability (Toska and Mayrovitz, 2023). Opioid use disorder is associated with higher rates of preterm birth, low birth weight, and neonatal abstinence syndrome than in births to women without opioid use disorder. Women with opioid use disorder have high rates of co-occurring mental health conditions and frequently experience social vulnerabilities, including housing instability, intimate partner violence, and delayed or inadequate prenatal care (Barbosa-Leiker et al., 2021; Hahn et al., 2018; Haight et al., 2018; Khan et al., 2022).
ACOG recommends screening for substance use disorders as part of routine preventive care and at the first prenatal visit, with additional screening when clinically indicated (ACOG, 2017, 2019a). ACOG guidance also addresses the role of laboratory testing, brief intervention, and referral to treatment. USPSTF and WPSI recommend screening and brief intervention for substance use in adults, including women of reproductive age and pregnant women (USPSTF, 2018, 2020). However, these recommendations do not provide detailed pregnancy-specific implementation guidance for obstetric care settings.
Stigma, fear of legal or child welfare involvement, variable coverage for treatment, and scarcity of programs designed for pregnant women and new mothers limit screening and treatment for substance use disorders in pregnant and postpartum women. Preventive services guidance does not address integrated models that combine substance use treatment with cardiovascular risk management during pregnancy and postpartum or how to ensure that women with substance use disorders receive other preventive services discussed in this chapter.
Perinatal mental health conditions, particularly depression and anxiety, are among the most common
complications of pregnancy and the postpartum period. An estimated 10–20 percent of U.S. women experience perinatal depression (Van Niel and Payne, 2020), and a similar proportion have perinatal anxiety (Thornton and O’Conner, 2022). Maternal mental health conditions are now recognized as leading contributors to pregnancy-related morbidity and mortality (CDC, 2025c; Gimbel et al., 2024; Parekh et al., 2025). These conditions are also associated with adverse infant outcomes and impaired bonding and child development (O’Dea et al., 2023; Rogers et al., 2020). At delivery hospitalizations, a mental health diagnosis has also been associated with increased rates of cardiovascular SMM and other cardiovascular conditions and complications (Parekh et al., 2025). Recent expert reviews and AHA scientific statements further emphasize that perinatal mental health conditions are closely linked with maternal cardiovascular health across pregnancy and the postpartum period, including through shared risk factors, physiologic stress responses, and effects on engagement in preventive care (Jowell et al., 2022; Lewey et al., 2024; Sharma, 2025).
Depression and anxiety influence cardiovascular risk indirectly through behavioral pathways. They are associated with higher rates of tobacco and alcohol use, poorer diet and physical activity, sleep disturbance, reduced medication adherence, and lower engagement in preventive and chronic disease care, which collectively contribute to worse blood pressure, glycemic, and lipid control over time (Conner et al., 2009; Davidson, 2012; DiMatteo et al., 2000; Grenard et al., 2011). For women with pregnancy complications that signal elevated long-term cardiovascular risk, such as HDP or GDM, untreated perinatal depression or anxiety can further impede efforts to address cardiometabolic risk in the postpartum and interpregnancy periods.
USPSTF recommends screening all adults, including pregnant and postpartum women, for depression in settings where systems are in place to ensure accurate diagnosis, effective treatment, and appropriate follow-up (Grade B). In 2023, it issued an updated final recommendation on screening for depression and suicide risk in adults that continues to support routine depression screening for all adults, including in pregnancy and postpartum (USPSTF, 2023b). USPSTF also recommends screening for anxiety disorders in adults ages 19–64 (including pregnant and postpartum women) and in children and adolescents ages 8–18 (both Grade B) (USPSTF, 2022a, 2023a). USPSTF also recommends that clinicians provide or refer pregnant and postpartum women at increased risk of perinatal depression to counseling interventions, such as cognitive behavioral or interpersonal therapy (Grade B) (USPSTF, 2019). That 2019 recommendation remains in effect while USPSTF updates this topic, with it releasing a draft updated recommendation and evidence review for public comment.
Bright Futures guidelines recommend routine depression screening in adolescents and structured maternal depression screening at specific well-child visits (e.g., at 1, 2, 4, and 6 months postpartum), recognizing the close link between maternal mental health and child development (AAP, 2025).
WPSI includes depression and anxiety screening as part of its well-woman care framework and highlights perinatal depression preventive interventions in its Well-Woman Chart. These include counseling for women with risk factors, such as a history of depression, current subthreshold depressive symptoms, socioeconomic adversity, recent intimate partner violence, or elevated anxiety symptoms (WPSI, n.d.-b; WSPI, 2025). The WPSI resource guide on screening for anxiety and depression in women explicitly includes pregnancy and postpartum as periods when these conditions are more common. It emphasizes periodic universal screening with appropriate follow-up care (WPSI, n.d.-b; WSPI, 2025).
Despite professional recommendations for universal screening, implementation remains incomplete. Centers for Disease Control and Prevention (CDC) analyses of PRAMS data indicate that a substantial proportion of women with postpartum depressive symptoms report not being asked about depression during prenatal or postpartum visits (CDC, 2020; Ko et al., 2012). Screening practices and access to treatment vary by geography, insurance status, and race and ethnicity (CDC, 2020; HRSA, 2026; KFF, 2024; Olisaeloka et al., 2025).
From a cardiovascular prevention perspective, current guidelines clearly support screening and preventive counseling for perinatal depression and anxiety but do not explicitly integrate mental health conditions into risk follow-up pathways for women with pregnancy complications. Depression and anxiety are not incorporated systematically into protocols for postpartum HTN management, diabetes follow-up after GDM, or broader cardiometabolic risk assessment after APOs. As a result, women who are both at elevated cardiovascular risk and experiencing perinatal mental health conditions may be less likely to engage in the very preventive services, such as lifestyle interventions, medication management, and longitudinal primary care, needed to reduce their long-term risk. In addition, evidence remains limited on whether interventions to address stress, depression, or anxiety during the postpartum period reduce the development or progression of HTN or CVD or how best to design and integrate behavioral health services into postpartum and longer-term cardiovascular preventive care.
One of the most important strategies to prevent pregnancy-related morbidity and mortality is ensuring that women and families have the tools they need to achieve their reproductive goals and avoid unwanted or mistimed pregnancies (Askew et al., 2024). Globally, if everyone wanting to avoid pregnancy had access to modern contraception, maternal deaths would decrease by an estimated 23 percent annually (Sully et al., 2020). For women who desire pregnancy, improved access to contraception and family planning can allow them to delay it to optimize health and cardiovascular risk first. Among U.S. births covered by Medicaid, women who received contraceptive services in the year before pregnancy had lower rates of SMM, with even greater benefits among women with chronic conditions (Dude et al., 2022).
Since 2016, WPSI has recommended that adolescent and adult women be provided access to the full range of contraceptives and contraceptive care, including counseling, education, FDA-approved contraceptives, and follow-up care, to prevent unintended pregnancies and improve health outcomes (WPSI, 2016, 2024). This recommendation, which includes women with cardiovascular risk factors and conditions, is consistent with long-standing guidance from CDC, AAFP, ACOG, ADA, AAP, and the American Medical Association (AAFP, n.d.; ACOG, 2022; CDC, 2024d; Cleary, 2024; Ott et al., 2025). The Institute of Medicine committee on preventive services for women recommended coverage without copayments for the full range of FDA-approved contraceptives, sterilization procedures, and patient education and counseling, which was adopted under the ACA (IOM, 2011). The federal Title X program also provides contraceptive services for under- or uninsured women (HHS, n.d.).
U.S. access to contraception is relatively high, and cost barriers decreased after implementing no-cost-sharing coverage. However, a 2022 nationally representative survey found ongoing barriers: 25 percent of privately insured respondents reported some out-of-pocket costs; 20 percent of uninsured respondents had stopped a method because of cost; 25 percent were not using their preferred method; and 70 percent reported not receiving all the information they needed to choose a method (Frederiksen et al., 2022). Geographic access varies widely. In some states, almost half the population lives in areas with minimal access, with poorer access more common among rural-dwelling, lower-income, and non-White populations (Kreitzer et al., 2021).
For women with cardiac disease, a systematic review estimated that only 63 percent reported receiving contraceptive counseling and 64 percent were using contraception (Feyissa et al., 2024). Many women were not using highly effective methods, and more than half misestimated their pregnancy-related CVD risk. Changes in access to contraception and family planning services may have important implications for cardiovascular risk among women of reproductive age, particularly for those with underlying cardiac conditions for whom pregnancy carries substantial health risks. Reduced access to effective contraception could increase rates of unintended and high-risk pregnancies; evidence suggests that family planning use is associated with fewer high-risk pregnancies overall (Jahanfar et al., 2024).
Women with chronic conditions report fragmented reproductive care that does not address chronic conditions and fragmented chronic disease care that does not incorporate reproductive goals (Verbiest et al., 2022). Clinician-related barriers include limited familiarity with evidence-based contraceptive eligibility guidelines and uncertainty in counseling patients with complex medical conditions such as HTN, cardiomyopathy, or prior thromboembolism (Lindley et al., 2021). CDC’s Medical Eligibility Criteria classifies adequately controlled HTN as Category 3 for combined hormonal contraceptives, indicating that risks usually outweigh benefits but that use may be considered in selected circumstances when other methods are not appropriate. In such cases, clinical decision-making may reasonably weigh contraceptive risks against the potential harms of an unintended high-risk pregnancy (CDC, 2024a). Competing priorities during visits and demands on patients’ time may also make it difficult to prioritize contraceptive counseling.
Women with CVD and CVD risk factors who take potentially teratogenic medications need access to contraceptive counseling that supports their preferences and reproductive goals. Because this includes some cardiovascular, HTN, lipid-lowering, and diabetes medications, contraceptive and family planning counseling is an essential component of care (ADA Professional Practice Committee, 2026; Lindley et al., 2021; Lindley and Teal, 2022; Minga and Dastmalchi, 2025). Ethical and clinical guidance on contraception emphasizes person-centered, noncoercive counseling (ACOG, 2022, 2024, 2025; CDC, 2024c), in recognition of a history of reproductive coercion in health care and evidence that some patients feel pressured by clinicians to start, continue, or stop specific methods (Scholars Strategy Network, 2024; Swan and Cannon, 2024). For women with conditions characterized as modified World Health Organization (mWHO) class IV, where pregnancy carries an unacceptably high risk of maternal mortality, the imperative for highly effective contraception is clear. Women classified as mWHO class III also face substantially elevated maternal cardiovascular
risk, often requiring expert multidisciplinary counseling and careful risk–benefit discussion regarding pregnancy; in these cases, shared decision-making and proactive reproductive planning are particularly important. However, the trade-offs between the risks and side effects need to be considered (see Figure 3-5), underscoring the need for careful shared decision-making in selecting the most appropriate method.
WPSI and other guidelines establish a strong foundation for contraceptive coverage. However, they do not fully address implementation challenges for women with cardiovascular conditions, such as how to integrate contraceptive counseling into chronic disease care or support shared decision-making in the face of complex risk–benefit tradeoffs. WPSI and other guideline bodies could explicitly highlight the need for coordinated, patient-centered contraceptive and family planning counseling in women with CVD and CVD risk factors and attention to reproductive goals when prescribing teratogenic cardiovascular medications.
In addition to the insurance and cost barriers noted in the previous section, the committee found that gaps and misalignments across clinical preventive service guidelines create added challenges for implementing evidence-based practices to reduce cardiovascular risk around pregnancy. For example, USPSTF offers separate recommendations on screening for HDP and low-dose aspirin for preeclampsia prevention in women at high risk, and most private health plans and Medicaid expansion programs are required to cover these services without cost-sharing. In contrast, guidelines such as those from NICE provide more detailed recommendations on exercise counseling and other behavioral strategies in pregnancy (National Institute for Health and Care Excellence, 2019), whereas USPSTF does not offer pregnancy-specific counseling recommendations for preventing or treating HDP. Similarly, WPSI recommends early GDM screening for pregnant women with risk factors and postpartum diabetes screening for women with a history of GDM (HRSA, 2025), whereas USPSTF concludes that evidence is insufficient to support universal early GDM screening before 24 weeks and does not address the postpartum period in its diabetes guidance (USPSTF, 2021b). In other areas, such as glycemic targets before pregnancy or lipid management in women of reproductive age, professional societies offer varying recommendations. Collectively, these gaps and misalignments contribute to uncertainty for clinicians and patients and can hinder coordinated prevention efforts.
The discussion in the earlier sections of this chapter illustrates these issues within specific clinical service areas. The committee’s review highlighted several crosscutting limitations and time period–specific gaps that shaped the long list of research topics and ultimately the priority clinical services selected for formal evidence review this report presents in subsequent chapters.
Across guideline sources, the committee identified three overarching limitations. First, pregnancy and the early postpartum period are not consistently framed as key opportunities for CVD prevention. Many recommendations are written for the general adult population, with pregnant and postpartum women either implicitly included, explicitly excluded, or not mentioned. For example, adult recommendations for blood pressure, diabetes, and lipid screening apply in principle to women of reproductive age but rarely address how to implement them before, during, and after complicated pregnancies or use pregnancy history to guide prevention across the life course.
Second, APOs, such as HDP, GDM, preterm birth, and placental disorders, are not incorporated consistently as risk-enhancing factors in preventive services guidance. Some cardiovascular and stroke guidelines recommend taking a history of APOs when assessing risk and managing HTN or stroke prevention, but this approach is not uniformly reflected in the recommendations that drive screening and counseling in primary care and obstetric settings. In addition, although APOs are associated with elevated long-term cardiovascular risk, incorporation of APO history into formal risk prediction models has not yet consistently demonstrated improved prediction of future cardiovascular events.
Third, guidelines offer limited direction on implementing and coordinating care across specialties and settings. Several professional societies encourage multidisciplinary cardio-obstetrics teams or enhanced postpartum follow-up for women with pregnancy complications, yet the guidance offers little detail on how to operationalize these models, which clinicians are responsible for specific services, and how to manage transitions between obstetrics, primary care, and cardiology or other specialists.
These crosscutting gaps highlight the need for the guiding principles developed by this committee. These principles emphasize a coordinated, longitudinal approach to cardiovascular risk related to pregnancy and the importance of addressing system barriers that contribute to differences in outcomes by geography, insurance coverage, and access to care. The following sections discuss several specific gaps the committee identified in the areas of prepregnancy and prenatal care and postpartum and interpregnancy care and several implementation and system-level areas where preventive services guidance is limited.
WPSI recommends annual well-woman visits to deliver preventive services based on age and risk, and ADA, Endocrine, and other societies provide guidance on prepregnancy counseling for women with diabetes. However, no dedicated preventive services recommendation focuses on comprehensive prepregnancy cardiovascular risk assessment for women who are planning pregnancy, particularly those with chronic conditions (e.g., HTN, diabetes, and kidney disease) or prior APOs. Questions remain regarding the optimal timing, content, and responsible clinician(s) for such visits and whether a structured prepregnancy cardiovascular assessment improves maternal or neonatal outcomes.
Existing guidelines address specific components of prenatal care, including screening for gestational diabetes at 24–28 weeks’ gestation (ADA Professional Practice Committee for Diabetes, 2026b) and recommending low-dose aspirin for women at increased risk of preeclampsia, initiated between 12 and 28 weeks and ideally before 16 weeks’ gestation (ACOG, 2021; USPSTF, 2021a). At the same time, evidence remains limited or insufficient to support improved maternal or neonatal outcomes from earlier gestational diabetes screening among high-risk women, more intensive blood pressure surveillance beyond routine office measurement in asymptomatic patients, or the routine use of angiogenic biomarker testing or Doppler ultrasound to refine risk stratification for preeclampsia (ACOG, 2020a; Burwick and Rodriguez, 2024; USPSTF, 2021b).
Group prenatal care, multidisciplinary care for pregnant women with cardiovascular risk factors, and telehealth-supported remote monitoring of blood pressure and glucose have been proposed or used in practice. However, these models are not the focus of preventive service recommendations, and their impact on cardiovascular and pregnancy outcomes remains uncertain. These gaps intersect with guiding principles related to aligning with existing preventive service frameworks while giving particular attention to women with higher baseline risk and interventions that could be integrated into routine prenatal care.
Despite the well-documented link between HDP and both short- and long-term cardiovascular risk, no USPSTF or WPSI recommendations or reviews of related evidence specifically address postpartum blood pressure monitoring—whether clinic based, home based, or telehealth supported—for women with HTN identified during pregnancy. Questions remain about the most effective frequency, modality, and duration of postpartum blood pressure surveillance and the impact of enhanced postpartum HTN programs on SMM, rehospitalization, and long-term cardiovascular outcomes.
WPSI and ADA provide guidance for diabetes screening after GDM, including early postpartum glucose testing and periodic screening thereafter,
but with less clarity on how to bundle postpartum cardiometabolic services—including blood pressure evaluation, lipid testing, and risk-based initiation of statins or antihypertensive therapy—and define the timing and frequency of such assessments for women with APOs. Guidance also provides limited direction on how clinicians can communicate the long-term cardiovascular implications of pregnancy complications and ensure linkage to ongoing primary care and cardiology or other specialists.
The committee noted a lack of preventive services guidance on structured approaches to identifying and responding to postpartum warning signs and symptoms of cardiovascular complications. Examples of such approaches include algorithms for emergency departments or urgent care settings and electronic health record (EHR) alerts for recently pregnant women presenting with chest pain, dyspnea, or neurologic symptoms. These approaches are not addressed by USPSTF, WPSI, or Bright Futures.
Transitions from delivery hospitalization to outpatient care and from obstetrics to primary care and cardiology or other specialists are only addressed sparsely in existing guidelines. The committee noted potential roles for discharge checklists, patient “passports” or action plans, structured referral pathways, and health information technology (e.g., patient portal tools or EHR-based prompts) to support safe transitions, but these strategies are not framed as preventive services with an evidence base for cardiovascular and pregnancy outcomes.
Nurse home visiting programs, doulas, community health workers, promotoras, and patient navigators are used in some settings to support postpartum women, particularly those facing social and economic barriers. However, major preventive service guideline bodies do not provide recommendations that link these services to cardiovascular outcomes in the context of pregnancy, and the evidence base for such linkages remains limited. WPSI recently issued its first recommendation related to patient navigation—focused on breast and cervical cancer screening—which is scheduled to take effect in 2026 (HRSA, 2025).
USPSTF has concluded that evidence is insufficient to determine the balance of benefits and harms of screening for food insecurity in primary care (USPSTF, 2025b), with similarly limited preventive service–oriented guidance on screening for other social needs in prenatal or postpartum care. However, ACOG recommends comprehensive assessments that include social and environmental factors. This disconnect highlights a gap between recognition of social barriers in clinical guidance and the evidence needed to support formal preventive service recommendations.
USPSTF and WPSI support screening for depression and anxiety in pregnant and postpartum women. However, existing recommendations do not explicitly address how mental health conditions intersect with cardiovascular risk after complicated pregnancies or integrated approaches to mental health and cardiovascular follow-up might influence outcomes.
The committee used its gap scan as a starting point to identify specific clinical services that could meaningfully reduce cardiovascular risk around pregnancy. Consistent with the guiding principles in Chapter 1, it focused on services that (1) address conditions that contribute substantially to pregnancy-related morbidity and mortality, (2) emphasize the postpartum and interpregnancy periods while maintaining a life-course perspective, (3) can be delivered as part of routine clinical care, and (4) could improve outcomes for women who face the greatest barriers to high-quality care.
Drawing on the guideline review summarized earlier in this chapter, the committee compiled an initial list of potential clinical services. Members considered services that directly target cardiovascular risk factors, such as blood pressure, glucose, and lipids; address pregnancy-related complications with long-term cardiovascular implications; or strengthen care coordination and follow-up after complicated pregnancies. To ensure this list reflected the real-world context in which pregnant and postpartum women receive care, the committee also drew on its own clinical and research experience, information from public comment and stakeholder input, and the epidemiologic patterns Chapters 1 and 2 describe.
The committee then organized potential research topics by period (e.g., prepregnancy, prenatal, postpartum, and interpregnancy) and type of service, including screening and management for specific risk factors, bundled
postpartum cardiometabolic care, models of integrated or multidisciplinary care, and approaches to improving transitions and follow-up. This resulted in a list of 20 potential research topics (see Box 3-2); for each, the committee noted whether components were already addressed by USPSTF, WPSI, or other guideline bodies and where important gaps remained, such as on the timing or intensity of services, use of pregnancy history to guide long-term prevention, or implementation models, such as telehealth and team-based care.
To narrow this list, the committee applied the guiding principles as explicit prioritization criteria. In particular, the committee considered the following:
Using these criteria and considering both the biological plausibility of benefit and likelihood of an actionable evidence base, the committee refined its long list into a set of 20 topics representing the most promising and policy-relevant opportunities to improve cardiovascular health around pregnancy (see Box 3-2). Committee members reviewed, discussed, and ranked these topics, with particular attention to how each one addressed the gaps identified in this chapter and aligned with the charge to focus on clinical preventive services.
Inclusion in this box indicates that a service was considered by the committee to be part of its evidence review, not that it is recommended. Research questions with an asterisk were chosen by the committee for its evidence review (see Chapters 4 and 5). Recommendations are presented separately in Chapter 7 and limited to areas where the committee determined that evidence was sufficient to support implementation guidance.
Through this iterative process, the committee identified nine priority clinical services and associated research questions for formal evidence review. These priority services span the prepregnancy, prenatal, postpartum, and interpregnancy periods and collectively address both individual risk-factor management and the organization of care. The next chapters (Chapters 4 and 5) describe the evidence review methods and present the committee’s findings and conclusions for each of these nine clinical services.
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