Evidence map›Paper›PMID 39424123›Full record

Trial reportContraception2025

Potential effect of immediate postpartum use of injectable contraception on lactogenesis.

Maria F Gallo, Fernanda L Schumacher, Megan Lawley, Sarah A Keim, Amy C Dupper, Lisa Keder

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Contraception, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Maria F GalloThe Ohio State University, College of Public Health, Columbus, OH, USA. Electronic address: gallo.86@osu.edu.
Fernanda L SchumacherThe Ohio State University, College of Public Health, Columbus, OH, USA.
Megan LawleyEmory University School of Medicine, Department of Gynecology and Obstetrics, Division of Family Planning, Atlanta, GA, USA.
Sarah A KeimThe Ohio State University, College of Public Health, Columbus, OH, USA; Nationwide Children's Hospital, Abigail Wexner Research Institute, Center for Biobehavioral Health, Columbus, OH, USA; The Ohio State University, College of Medicine, Columbus, OH, USA.
Amy C DupperThe Ohio State University, College of Public Health, Columbus, OH, USA.
Lisa KederThe Ohio State University, College of Medicine, Columbus, OH, USA.

Funding

The Ohio State University Center for clinical and Translational ScienceUL1TR001070 · NCATS · OHIO STATE UNIVERSITY · PI JACKSON, REBECCA D · 2013 to 2017
$22.6M
Institute for Population ResearchP2CHD058484 · NICHD · OHIO STATE UNIVERSITY · PI HAYFORD, SARAH R · 2014 to 2023
$5.0M
Postpartum Family PlanningR01HD091274 · NICHD · OHIO STATE UNIVERSITY · PI GALLO, MARIA F, SCHUMACHER, FERNANDA · 2018 to 2023
$1.9M
NCATS NIH HHS UL1 TR001070NICHD NIH HHS P2C HD058484NICHD NIH HHS R01 HD091274
6 · The paper itself

Abstract

objectivesWe evaluated the effect of immediate postpartum use of depot medroxyprogesterone acetate (DMPA) on the timing of lactogenesis stage II (LS-II). STUDY

designThe initial design randomly assigned adults who delivered a full-term infant in 2019-2021 to receive within 48 hours of delivery: (1) DMPA, (2) placebo injection, or (3) no injection. Due to low enrollment, we changed in 2021-2023 to a nonrandomized design using matching at recruitment for obesity and delivery method and propensity score weighting for analysis. We combined data from both designs to compare immediate postpartum DMPA use (N = 55) vs control (placebo or no injection) group (N = 95). We defined noninferiority a priori as being met if the upper bound of a two-sided 95% CI for mean difference in time to LS-II between groups was <6 hours.

resultsThe unweighted mean time to LS-II was 57.8 hours in the DMPA group (SD, 29.4) and 64.1 hours in the control group (SD, 36.1). Using propensity score weighting to make the groups comparable with respect to age, race, delivery method, and previous live births, the mean time to LS-II was 5.5 hours shorter (95% CI, -16.4, 5.5) for women in the DMPA relative to control group.

conclusionsWe found no evidence that DMPA use inhibits the onset of LS-II. Findings support immediate postpartum DMPA initiation among those intending to engage in human milk feeding. IMPLICATIONS: A controlled trial (N = 150) did not detect any difference in time to lactogenesis stage II ("milk let-down") between injectable contraception use within the first 48 hours postpartum and those without this exposure.

Indexed as

Contraceptive Agents, FemaleLactationMedroxyprogesterone AcetatePostpartum PeriodAdultFemaleHumansTime FactorsYoung AdultContraceptive Agents, FemaleMedroxyprogesterone AcetateHuman milkLactogenesis stage IIMedroxyprogesterone acetateProgestinsPropensity scoreRandomized controlled trial

Identifiers

PMID39424123
PMCPMC11725434

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.