Evidence map›Paper›PMID 40633180›Full record

ArticleDrug and alcohol dependence2025

Buprenorphine and norbuprenorphine concentrations associated with clinical withdrawal during pregnancy.

Steve N Caritis, Elizabeth E Krans, Raman Venkataramanan

Abstract read
In one paragraph

Article in Drug and alcohol dependence, 2025. 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

3 authors.

Steve N CaritisDepartments of Obstetrics and Gynecology and Reproductive Sciences, Pittsburgh, PA 15213, United States; University of Pittsburgh Schools of Medicine and Pharmacy, Magee-Womens Research Institute, Pittsburgh, PA 15213, United States. Electronic address: scaritis@mail.magee.edu.
Elizabeth E KransDepartments of Obstetrics and Gynecology and Reproductive Sciences, Pittsburgh, PA 15213, United States; University of Pittsburgh Schools of Medicine and Pharmacy, Magee-Womens Research Institute, Pittsburgh, PA 15213, United States.
Raman VenkataramananDepartments of Pathology and Pharmaceutical Sciences, Pittsburgh, PA 15213, United States.

Funding

Pharmacologically-based Strategies for Buprenorphine Treatment During PregnancyR01HD096796 · NICHD · MAGEE-WOMEN'S RES INST AND FOUNDATION · PI CARITIS, STEVE N · 2018 to 2022
$3.4M
NICHD NIH HHS R01 HD096796
6 · The paper itself

Abstract

backgroundDosing of buprenorphine during pregnancy is based on dosing recommendations for non-pregnant people. This approach is not appropriate as buprenorphine concentrations, for a given dose, are lower in pregnant than non-pregnant people. Furthermore, it is unclear if buprenorphine concentrations preventing withdrawal are similar in pregnant and non-pregnant people.

methodsWe sought to determine the plasma buprenorphine and norbuprenorphine concentrations at the time of withdrawal symptoms in 20 pregnant persons on a stable dose of sublingual buprenorphine. Previous evening and study day morning doses were withheld and at arrival to our research center, blood was obtained while pupillary diameter, COWS and craving scores were recorded frequently until withdrawal symptoms occurred and then the usual morning dose of buprenorphine was administered, and all measurements repeated 6 times over the ensuing 2h.

resultsAt withdrawal, the plasma concentration (mean ± SD) of buprenorphine was 0.79 ± 0.44ng/ml, range 0.3-1.7ng/ml and norbuprenorphine 1.54 ± 1.01ng/ml, range 0.3-4.7ng/ml. After dosing, these concentrations peaked after 30-45min while pupillary diameter, COWS and craving scores synchronously returned toward baseline but with maximal effects lagging the peak in plasma drug concentration by 45-60min.

conclusionsThe minimal concentration of buprenorphine required to suppress withdrawal symptoms is similar to that in non-pregnant people. The lag in the pharmacodynamic responses supports a central mu receptor effect of buprenorphine. The wide range of buprenorphine concentration at withdrawal suggests considerable variation in mu receptor responsiveness to buprenorphine and supports individualized dosing in pregnant people.

Indexed as

BuprenorphineOpioid-Related DisordersPregnancy ComplicationsSubstance Withdrawal SyndromeAdultCravingFemaleHumansOpiate Substitution TreatmentPregnancyPupilYoung AdultBuprenorphinenorbuprenorphineBuprenorphineCOWS scoresCraving scorePharmacologyPregnancyPupil diameterWithdrawal

Identifiers

PMID40633180
PMCPMC13293508

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.