Evidence map›Paper›PMID 39342492›Full record

ArticleThe American journal on addictions2025

Is buprenorphine maternal dose associated with neonatal opioid withdrawal syndrome severity?

Besnier Marc, Delouche Marion, Birault François, Lebonheur Lakshmipriya

Abstract read
In one paragraph

Article in The American journal on addictions, 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

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Besnier MarcUniversity of Poitiers, Poitiers, France.ORCID 0000-0002-1912-2580
Delouche MarionUniversity of Poitiers, Poitiers, France.
Birault FrançoisUniversity of Poitiers, Poitiers, France.
Lebonheur LakshmipriyaUniversity of Poitiers, Poitiers, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNeonatal opioid withdrawal syndrome (NOWS) is a drug withdrawal syndrome occurring mainly after in utero opioid exposure. Buprenorphine is commonly used for opioid withdrawal. Studies are conflicted about a potential dose effect

objectiveThe aim of our study was to investigate the impact of buprenorphine maternal maintenance therapy on the NOWS based on NOWS duration, birth weight and therapy. STUDY

designWe conducted a retrospective study analysing data from infants admitted for NOWS in two Neonatal Intensive Care Unit between January 2010 and December 2020. INCLUSION CRITERIA: Nonpreterm infants born to mothers who were treated with buprenorphine or therapy during pregnancy and who had a Lipsitz score of 4 or higher.

resultsA total of 75 term newborns were hospitalized for the treatment of NOWS from mother substituted with buprenorphine during the study inclusion period. The duration of NOWS differed significantly between all dose cohorts, with higher doses of maternal buprenorphine maintenance correlating with longer length of NOWS duration. Infants exposed to high doses required 17 days [10; 23], while infants exposed to intermediate doses required 7 days [2; 16] and infants exposed to low doses required 3 days [2; 5], with p-values < .003. Infants exposed to high doses required a longer time to regain their birth weight and higher morphine doses as therapy compared to others. Infants exposed to low doses, intermediate doses, and high doses of buprenorphine demonstrated dose-dependent increases in the durations of hospitalization, respectively. CONCLUSION AND SCIENTIFIC SIGNIFICANCE: Increased doses of maternal buprenorphine during pregnancy are correlated with NOWS severity. Our study shows that increased doses of maternal buprenorphine during pregnancy are correlated with NOWS severity. Exploring low doses and having different ranges are a new argument to define the impact of maternal buprenorphine consumption.

Indexed as

BuprenorphineNeonatal Abstinence SyndromeOpiate Substitution TreatmentAdultAnalgesics, OpioidDose-Response Relationship, DrugFemaleHumansInfant, NewbornMaleOpioid-Related DisordersPregnancyPregnancy ComplicationsPrenatal Exposure Delayed EffectsRetrospective StudiesSeverity of Illness IndexAnalgesics, OpioidBuprenorphine

Identifiers

PMID39342492
PMCPMC11673401

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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.