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Breastfeeding patterns among parturients with diabetes: A secondary analysis of the MOMPOD randomized clinical trial

Minhazur R. Sarker, Marni B. Jacobs, Kim Boggess, A. Battarbee, J. Refuerzo, N. Zork, K. Eichelberger, C. Durnwald et al.

Pregnancy, 2025

794 participants · 1 citation

Abstract

Abstract Introduction Insulin resistance is associated with decreased milk supply in lactating people. Metformin is hypothesized to increase breast milk production by decreasing insulin resistance, suggesting use may increase breastfeeding success. We aimed to determine the association between metformin use during pregnancy and breastfeeding initiation and continuation. Methods This was a secondary analysis of the MOMPOD randomized controlled trial of metformin versus placebo in addition to insulin therapy among pregnant people with type 2 diabetes and early diabetes. We included parturients who delivered a living neonate, received at least one dose of study drug or placebo, endorsed an intention to breastfeed, and completed a breastfeeding survey. Breastfeeding intentions and breastfeeding outcomes were collected utilizing a breastfeeding questionnaire at 24–30 weeks and 30 days postpartum, respectively. The primary outcome was breastfeeding at 30 days postpartum defined by exclusive or partial breastfeeding. Secondary outcomes included immediate breastfeeding defined as any breastfeeding during the postpartum hospital admission until at least postpartum day 3, onset of lactogenesis (days), breast and bra size, and breastfeeding challenges. Baseline characteristics and outcomes were compared using chi‐square, t‐test, or Wilcoxon tests, as appropriate. Results Among the 794 women randomized and receiving either placebo or metformin in the primary trial, 378 (47.6%) met…

How strong is the evidence?

Evidence Hub reads this as a secondary / pooled analysis, done in people. Its evidence level is 3 of 5 (Moderate · trial / cohort / secondary analysis). Trials without a large randomized design, cohorts and secondary analyses give moderate evidence. Reported size: 794 participants or records.

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