Evidence map›Paper›PMID 40920396›Full record

ArticleJAMA pediatrics2025

Cost-Effectiveness of Treatment for Opioid Use Disorder in Pregnancy and Its Impact on Birth Outcomes.

Ashley A Leech, Shawn Garbett, Hanxuan A Yu, Elizabeth McNeer, Rashmi Bharadwaj, Benjamin P Linas, John Graves, Jessica Young, Lisa Su, Peter R Martin and 6 more

Abstract read
In one paragraph

Article in JAMA pediatrics, 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

16 authors.

Ashley A LeechDepartment of Health Policy, Vanderbilt University School of Medicine, Nashville, Tennessee.
Shawn GarbettDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee.
Hanxuan A YuDepartment of Health Policy, Vanderbilt University School of Medicine, Nashville, Tennessee.
Elizabeth McNeerDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee.
Rashmi BharadwajCollege of Medicine, University of Kentucky, Lexington.
Benjamin P LinasSection of Infectious Disease, Boston Medical Center, Boston, Massachusetts.
John GravesDepartment of Health Policy, Vanderbilt University School of Medicine, Nashville, Tennessee.
Jessica YoungDepartment of Obstetrics and Gynecology, Vanderbilt University Medical Center, Nashville, Tennessee.
Lisa SuCollege of Medicine, The University of Tennessee Health Science Center, Memphis.
Peter R MartinDepartment of Psychiatry and Behavioral Sciences and Pharmacology, Vanderbilt University Medical Center, Nashville, Tennessee.
Michael J WardDepartment of Emergency Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Mark N EllinghamDepartment of Mathematics, Vanderbilt University, Nashville, Tennessee.
Katy B KozhimannilDivision of Health Policy and Management, Rural Health Research Center, University of Minnesota School of Public Health, Minneapolis.
Lauren R SamuelsDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee.
Jiayu ShiDepartment of Health Policy, Vanderbilt University School of Medicine, Nashville, Tennessee.
Stephen W PatrickDepartment of Health Policy and Management, Rollins School of Public Health, Emory University, Atlanta, Georgia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: For the first time in nearly 2 decades, the US infant mortality rate has increased, coinciding with a rise in overdose-related deaths as a leading cause of pregnancy-associated mortality in some states. Prematurity and low birth weight-often linked to opioid use in pregnancy-are major contributors. Objective: To assess the health and economic impact of perinatal opioid use disorder (OUD) treatment on maternal and postpartum health, infant health in the first year of life, and infant long-term health. Design, Setting, and Participants: This was a cost-effectiveness, population-based analysis using a stochastic time-to-event discrete-event simulation model to simulate the clinical progression and outcomes for hypothetical pregnant individuals with OUD who initiate treatment during pregnancy. In addition, a scenario analysis was conducted assuming that individuals were stable taking OUD treatment before pregnancy and continued treatment during pregnancy. Data were analyzed from May to September 2024. Exposures: Study exposures included outpatient methadone, buprenorphine monotherapy, and buprenorphine-naloxone; outpatient methadone, buprenorphine, and naltrexone after inpatient-managed withdrawal; and inpatient-managed withdrawal with and without an intensive behavioral component. Main Outcomes and Measures: Outcomes included return to illicit use; fatal and nonfatal overdose; incremental discounted costs; quality-adjusted life-years (QALYs), which are a combined measure of mortality and morbidity; net health benefit; infant mortality within the first year of life; preterm birth; low birth weight; and neonatal opioid withdrawal syndrome (NOWS). Results: In this economic evaluation of a hypothetical cohort of 100 000 pregnant individuals (mean [SD] starting age, 29 [5.6] years), in the pregnancy and postpartum simulation, buprenorphine dominated all strategies, yet methadone was a viable alternative. In the combined infant lifetime model, compared with methadone, buprenorphine showed an incremental effect of 0.262 QALYs per person, totaling 20 960 QALYs for 80 000 Medicaid-affected mother-infant dyads (IQR uncertainty interval [UI] 25th to 75th percentiles, 14 880-27 040 QALYs); mean cost savings of $21 512 per person, totaling $1.72 billion (IQR UI, $1.46-1.98 billion). Compared with naltrexone, buprenorphine showed an incremental effect ranging from 0.228 to 0.229 QALYs per person; 18 240 of 18 320 total QALYs for 80 000 mother-infant dyads (IQR UI, 13 840-22 720 QALYs; naltrexone-oral; IQR UI, 13 760-22 880 QALYs; naltrexone-extended release [XR]). Mean cost savings ranged from $25 316 per person ($2.03 billion; IQR UI, $1.83-$2.21 billion; naltrexone-oral) to $46 437 per person ($3.71 billion; IQR UI, $3.47-$3.96 billion; naltrexone-XR). Conclusions and Relevance: Results of this analysis suggest that both methadone and buprenorphine remained viable options for managing OUD during pregnancy and post partum; however, buprenorphine offered the greatest benefits in the lifetime models that account for infant outcomes.

Indexed as

Cost-Benefit AnalysisOpiate Substitution TreatmentOpioid-Related DisordersPregnancy ComplicationsAdultBuprenorphineFemaleHumansInfantInfant, NewbornMethadoneNaltrexoneNarcotic AntagonistsPregnancyPregnancy OutcomeQuality-Adjusted Life YearsBuprenorphineMethadoneNaltrexoneNarcotic Antagonists

Identifiers

PMID40920396
PMCPMC12418224

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.