Evidence map›Paper›PMID 42826020›Full record

ArticleJAMA network open2026

Duration of Medication Use for Opioid Use Disorder and Risk of Postpartum Overdose and Death.

Ahra Kim, Andrew D Wiese, Sarah Osmundson, Chad You, Carlos G Grijalva, Margaret A Adgent, Alexandra C Sundermann, Andrew J Spieker, Amelie Pham, Stephen W Patrick and 1 more

Abstract read
In one paragraph

Article in JAMA network open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Ahra KimDepartment of Health Policy, Vanderbilt University School of Medicine, Nashville, Tennessee.
Andrew D WieseDepartment of Health Policy, Vanderbilt University School of Medicine, Nashville, Tennessee.
Sarah OsmundsonDepartment of Obstetrics and Gynecology, Vanderbilt University Medical Center, Nashville, Tennessee.
Chad YouDepartment of Health Policy, Vanderbilt University School of Medicine, Nashville, Tennessee.
Carlos G GrijalvaDepartment of Health Policy, Vanderbilt University School of Medicine, Nashville, Tennessee.
Margaret A AdgentDepartment of Health Policy, Vanderbilt University School of Medicine, Nashville, Tennessee.
Alexandra C SundermannDepartment of Obstetrics and Gynecology, Vanderbilt University Medical Center, Nashville, Tennessee.
Andrew J SpiekerDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee.
Amelie PhamDepartment of Obstetrics and Gynecology, Vanderbilt University Medical Center, Nashville, Tennessee.
Stephen W PatrickDepartment of Health Policy and Management, Rollins School of Public Health, Emory University, Atlanta, Georgia.
Ashley A LeechDepartment of Health Policy, Vanderbilt University School of Medicine, Nashville, Tennessee.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Overdose is the leading cause of maternal mortality in the US, yet evidence on how medications for opioid use disorder (MOUD) affect postpartum overdose and mortality risk is limited. It is unclear whether cumulative MOUD exposure during this period reduces overdose or death beyond 90 days post partum. Objective: To examine whether longer duration of MOUD dispensed during pregnancy and early post partum is associated with reduced overdose or death through 365 days post partum. Design, Setting, and Participants: This is a retrospective cohort study of individuals delivering between 2007 and 2020, assessed through 1 year post partum or until the first outcome, through 2021. The study used Tennessee Medicaid (TennCare) data linked to vital records (birth and death certificates) and Tennessee Hospital Discharge Data. Participants were individuals aged 15 to 44 years with at least 1 day of dispensed MOUD during the exposure window (90 days before to 41 days after delivery), a delivery at least 20 weeks' gestation, and continuous TennCare enrollment during the exposure period. Data were analyzed from July 2024 to July 2026. Exposure: Total unique, nonoverlapping days of dispensed MOUD (buprenorphine and/or naltrexone) from 90 days before delivery through 41 days after delivery, with overlapping fills deduplicated so each calendar day was counted only once. Main Outcomes and Measures: The primary outcome was the first occurrence of all-cause death or overdose (opioid or nonopioid) from inpatient, outpatient, and emergency department claims 42 to 365 days post partum. Multivariable Cox proportional hazards models were used to estimate the association between MOUD days' supply and risk of death or overdose, adjusting for maternal and clinical characteristics. Results: The cohort included 9360 pregnancies among 7776 individuals (median [IQR] age at delivery, 27 [24-31] years). The 1-year postpartum risk of death or overdose was 1.58% (148 individuals), with a median (IQR) time to event of 186.5 (92.5-258.8) days. The median (IQR) MOUD duration during the 132-day exposure period was 88 (43-111) days. Longer MOUD duration was associated with lower risk of death or overdose, with the lowest hazard at 132 days' supply (adjusted hazard ratio for 132 vs 1 day, 0.52; 95% CI, 0.31-0.88). Conclusions and Relevance: Longer duration of MOUD receipt during pregnancy and early post partum was associated with lower risk of overdose or death in the first year post partum, underscoring the importance of supporting continuous MOUD treatment during this period.

Indexed as

Analgesics, OpioidDrug OverdoseOpioid-Related DisordersAdolescentAdultBuprenorphineFemaleHumansOpiate OverdosePostpartum PeriodPregnancyRetrospective StudiesTennesseeTime FactorsUnited StatesYoung AdultAnalgesics, OpioidBuprenorphine

Identifiers

PMID42826020
PMCPMC13633532

What OpenQuestion holds

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Registered trials

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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.