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Longer Opioid Addiction Medication Use Linked to Fewer Postpartum Deaths in 9,360 Pregnancies

A Tennessee Medicaid study found pregnant women who stayed on opioid addiction medication longer were far less likely to overdose or die in the year after delivery.

An orange plastic pill bottle tipped over with red and white tablets spilling out onto a grey surface, with a white cap nearby.
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A study of 9,360 pregnancies published October 2, 2026 in JAMA Network Open found that women who received 132 days of medication for opioid use disorder during pregnancy and early postpartum had a 48% lower risk of overdose or death in the year after delivery compared with women who received just 1 day.

9,360pregnancies tracked
132days vs 1 day
48%lower risk
1in 100 still at risk

Researchers followed 9,360 pregnancies among 7,776 individuals enrolled in Tennessee Medicaid between 2007 and 2020, tracking outcomes through 365 days postpartum using linked Medicaid claims, birth and death certificates, and hospital discharge data. All participants had received at least 1 day of medication for opioid use disorder, nearly all buprenorphine, during a window spanning 90 days before delivery through 41 days after. Median age at delivery was 27, and median medication supply during that 132-day window was 88 days. Over the following year, 1.58% of participants, 148 people, died or had a nonfatal overdose; 39 died and 109 overdosed. Women with 132 days of medication supply had a 48% lower risk of death or overdose than women with just 1 day (adjusted hazard ratio 0.52, 95% CI 0.31-0.88). Even among women who received medication in both pregnancy and postpartum, the best-protected group, 1.41% still died or overdosed within a year. Women who received medication only after delivery had a 71% higher risk than those treated in both periods. The study reported no data on side effects from the medications themselves, focusing only on overdose and death outcomes.

Buprenorphine and naltrexone act on the same brain receptors opioids target, easing withdrawal and cravings so a person can stay stable in daily life. The authors link longer, continuous use during pregnancy and early postpartum weeks to sustained treatment engagement, which they connect to lower overdose and death risk later in the first postpartum year.

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48% Lower Overdose-Death Risk With 132 Days vs 1 Day of Medication

48% Lower Overdose-Death Risk With 132 Days vs 1 Day of Medication9,360 pregnancies, Tennessee Medicaid. 1-day medication supply: 1 adjusted hazard ratio; 132-day medication supply: 0.52 adjusted hazard ratio9,360 pregnancies, Tennessee Medicaid
1 adjusted hazard ratio
1-DAY MEDICATION SUPPLY
0.52 adjusted hazard ratio
132-DAY MEDICATION SUPPLY
JAMA Network Open, 2026, Kim et al

This cohort study has no no-treatment comparison group, so it shows a link between longer medication use and lower risk rather than proof that one causes the other. Only 148 total outcomes occurred, limiting how finely researchers could adjust for other differences between women, and the study could not capture overdoses or deaths after someone left Tennessee or lost Medicaid coverage.

Dr. Axe’s Take

The postpartum period is where treatment gaps turn deadly, and this data shows it plainly: even women treated continuously in both pregnancy and postpartum still faced a 1.41% death-or-overdose rate, more than 1 in 100. Medication alone is not enough. I would pair any prescribed opioid use disorder medication with real postpartum infrastructure: home visits, lactation and mental health support, case management, and nutrition rebuilding, since pregnancy and recovery deplete B vitamins, magnesium and protein. If you are on buprenorphine or naltrexone postpartum, keep taking it as prescribed and never stop or lower it without your doctor. The weeks after 90 days postpartum need the system to show up loudest, not fade out.

Dr. Axe— Dr. Axe

Study summary

Who
9,360 pregnancies among 7,776 individuals aged 15 to 44 enrolled in Tennessee Medicaid, median age 27, deliveries 2007 to 2020
Design
Retrospective observational cohort study using linked Medicaid claims, birth/death certificates and hospital discharge data, followed through 365 days postpartum
Dose
Total nonoverlapping days of dispensed buprenorphine or naltrexone during a 132-day window spanning 90 days before to 41 days after delivery; median supply was 88 days (IQR 43-111)
Primary result
1-year risk of death or overdose was 1.58% (148 of 9,360); 132 days of medication supply was linked to a 48% lower risk of death or overdose versus 1 day (adjusted hazard ratio 0.52, 95% CI 0.31-0.88)
Secondary
Risk was 1.41% among those treated both before and after delivery, 1.89% treated only before delivery, and 2.58% treated only after delivery; postpartum-only treatment carried a 71% higher risk than treatment in both periods (HR 1.71, 95% CI 1.07-2.72)
Funding / conflicts
Funded by a grant from the National Institutes of Health (National Institute of Child Health and Human Development); the paper says the funder had no role in the study. Conflicts are declared in the PubMed record: three authors reported grants from the National Institutes of Health; one of them also reported personal fees from Merck and GlaxoSmithKline, a contract from the Centers for Disease Control and Prevention and SyneosHealth, and grants from the Agency for Healthcare Research and Quality; another reported personal fees as an expert consultant; a fourth author reported grants from Novocuff and fees for serving on a data safety monitoring board.
Date
Oct 2, 2026
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