Postpartum home blood pressure monitoring and lifestyle intervention in overweight and obese individuals the first year after gestational hypertension or pre‐eclampsia: A pilot feasibility trial

Author:

Hauspurg Alisse12,Seely Ellen W.34,Rich‐Edwards Janet34,Hayduchok Christina1,Bryan Samantha1,Roche Andrea T.3,Jeyabalan Arun12,Davis Esa M.5,Hart Renee6,Shirriel Jada7,Catov Janet12

Affiliation:

1. Magee‐Womens Research Institute University of Pittsburgh School of Medicine Pittsburgh Pennsylvania USA

2. Department of Obstetrics, Gynecology and Reproductive Sciences, Magee‐Womens Hospital University of Pittsburgh School of Medicine Pittsburgh Pennsylvania USA

3. Department of Medicine Brigham and Women's Hospital Boston Massachusetts USA

4. Harvard Medical School Boston Massachusetts USA

5. Department of Medicine University of Pittsburgh School of Medicine Pittsburgh Pennsylvania USA

6. University of Pittsburgh School of Medicine Pittsburgh Pennsylvania USA

7. Healthy Start, Inc. Pittsburgh Pennsylvania USA

Abstract

AbstractObjectiveTo test the feasibility of a randomised trial of home blood pressure monitoring paired with a remote lifestyle intervention (Heart Health 4 New Moms) versus home blood pressure monitoring alone versus control in individuals with a hypertensive disorder of pregnancy in the first year postpartum.DesignSingle‐blinded three‐arm randomised clinical trial.SettingTwo tertiary care hospitals and a community organisation.PopulationPostpartum overweight and obese individuals with a hypertensive disorder of pregnancy and without pre‐pregnancy hypertension or diabetes.MethodsWe assessed the feasibility of recruitment and retention of 150 participants to study completion at 1‐year postpartum with randomisation 1:1:1 into each arm. Secondary aims were to test effects of the interventions on weight, blood pressure and self‐efficacy.ResultsOver 23 months, we enrolled 148 of 400 eligible, screened individuals (37%); 28% black or other race and mean pre‐pregnancy body mass index (BMI) of 33.4 ± 6.7 kg/m2. In total, 129 (87%) participants completed the 1‐year postpartum study visit. Overall, 22% of participants developed stage 2 hypertension (≥140/90 mmHg or on anti‐hypertensive medications) by 1 year postpartum. There were no differences in weight or self‐efficacy across the study arms.ConclusionIn this pilot, randomised trial, we demonstrate feasibility of HBPM paired with a lifestyle intervention in the first year postpartum. We detected high rates of ongoing hypertension, emphasising the need for the development of effective interventions in this population.

Funder

National Institutes of Health

Publisher

Wiley

Subject

Obstetrics and Gynecology

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