Abstract

Background: Pregnancy-related cardiovascular (CV) conditions, including hypertensive disorders of pregnancy (HDP) and gestational diabetes (GDM), are associated with increased long-term CV risk.
Methods: This retrospective cohort study defined the prevalence of HDP and GDM within a large, academic health system in the southeast United States between 2012 and 2015 and described health care utilization and routine CV screening up to 1-year following delivery among those with pregnancy-related CV conditions. Rates of follow-up visits and blood pressure, hemoglobin A1c (HbA1c), and lipid screening in the first postpartum year were compared by provider type and pregnancy-related CV condition.
Results: Of the 6027 deliveries included, 20% were complicated by HDP and/or GDM. Rates of pre-pregnancy CV risk factors were high, with a significantly higher proportion of pre-pregnancy obesity among women with HDP than in normal pregnancies. Those with both HDP/GDM had the highest rates of follow-up by 1-year postpartum, yet only half of those with any pregnancy-related CV condition had any follow-up visit after 12 weeks. Although most (70%) of those with HDP had postpartum blood pressure screening, less than one-third of those with GDM had a repeat HbA1c by 12 months. Overall, postpartum lipid screening was rare (<20%).
Conclusion: There is a high burden of pregnancy-related CV conditions in a large U.S. academic health system. Although overall rates of follow-up in the early postpartum period were high, gaps in longitudinal follow-up exist. Low rates of CV risk factor follow-up at 1 year indicate a missed opportunity for early CV prevention.

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cover image Journal of Women's Health
Journal of Women's Health
Volume 33Issue Number 7July 2024
Pages: 853 - 862
PubMed: 38533846

History

Published online: 4 July 2024
Published in print: July 2024
Published ahead of print: 27 March 2024

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Department of Medicine (General Internal Medicine), Duke University School of Medicine, Durham, North Carolina, USA.
Courtney B. Page
Duke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina, USA.
Matthew Phelan
Target RWE, Durham, North Carolina, USA.
Department of Obstetrics and Gynecology (Maternal Fetal Medicine), Duke University School of Medicine, Durham, North Carolina, USA.
Neha Pagidipati
Department of Medicine (Cardiology), Duke University School of Medicine, Durham, North Carolina, USA.

Notes

Address correspondence to: Rebecca Lumsden, MD, MS, Department of Medicine (General Internal Medicine), Duke University School of Medicine, 40 Medicine Circle, Box 3534, Durham, NC 27720, USA [email protected]

Authors’ Contributions

R.L.: conceptualization; methodology; writing—original draft; visualization; project administration; funding acquisition. C.B.P.: formal analysis; data curation; writing—review and editing; visualization. M.P.: methodology; software; formal analysis; data curation; visualization. S.W.: conceptualization; writing—review and editing. N.P.: conceptualization; methodology; writing—review and editing; supervision; funding acquisition.

Author Disclosure Statement

Dr. Pagidipati reports: Research support from Alnylam, Amgen, Bayer, Boehringer Ingelheim, Eggland’s Best, Eli Lilly, Novartis, Novo Nordisk, Merck. Consultation/Advisory Panels for Bayer, Boehringer Ingelheim, CRISPR Therapeutics, Eli Lilly, Esperion, AstraZeneca, Merck, Novartis, and Novo Nordisk. Executive Committee member for trials sponsored by Novo Nordisk and Amgen. Drug-safety monitoring board for trials sponsored by J + J and Novartis. Medical advisory board for Miga Health. The remaining authors have no disclosures to report.

Funding Information

This project was internally funded; no external funding sources to report.

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