Facilitating treatment initiation and reproductive care postpartum to prevent substance-exposed pregnancies: A randomized bayesian pilot trial.

Acceptance and Commitment Therapy Addiction Contraception Maternal substance use Motivational Interviewing SBIRT Treatment drug abuse perinatal postpartum

Journal

Drug and alcohol dependence
ISSN: 1879-0046
Titre abrégé: Drug Alcohol Depend
Pays: Ireland
ID NLM: 7513587

Informations de publication

Date de publication:
01 10 2022
Historique:
received: 13 05 2022
revised: 08 08 2022
accepted: 09 08 2022
pubmed: 21 8 2022
medline: 28 9 2022
entrez: 20 8 2022
Statut: ppublish

Résumé

For non-treatment-seeking women who use substances during pregnancy, immediately postpartum may be an optimum time for intervention. Our study tested a novel, brief, hospital-initiated, adaptive motivational interviewing plus acceptance and commitment therapy (MIACT) intervention to facilitate treatment initiation and reproductive planning postpartum among mothers who used substances during pregnancy. Mothers (N = 64) with an infant admitted to a neonatal intensive care unit were enrolled if they or their infant tested positive for an illicit substance at delivery or had a documented positive drug screen during pregnancy. A parallel group, randomized controlled design assigned participants to MIACT or conventional care (CC), with assessments at week 2 and 4 during treatment and follow-up at 2 and 6 months post treatment. Bayesian generalized linear modeling was used to evaluate outcomes as a function of treatment. Results indicated that during treatment the MIACT group demonstrated an 84% probability of benefit relative to CC with regard to initiating treatment (RR=1.5), however the effect was not seen at follow-up. MIACT was also associated with an increased probability of attending a postpartum obstetrics visit (RR=1.4), and receiving contraception during treatment and at both follow-ups, with posterior probabilities of 96% or higher and relative risks ranging from 1.5 to 5.1 at varying timepoints. Substance use rates for the MIACT versus CC were higher at follow-up. Brief, hospital-initiated interventions can assist postpartum mothers who use substances to enter treatment and obtain contraception in order to reduce future substance-exposed pregnancies.

Sections du résumé

BACKGROUND
For non-treatment-seeking women who use substances during pregnancy, immediately postpartum may be an optimum time for intervention. Our study tested a novel, brief, hospital-initiated, adaptive motivational interviewing plus acceptance and commitment therapy (MIACT) intervention to facilitate treatment initiation and reproductive planning postpartum among mothers who used substances during pregnancy.
METHODS
Mothers (N = 64) with an infant admitted to a neonatal intensive care unit were enrolled if they or their infant tested positive for an illicit substance at delivery or had a documented positive drug screen during pregnancy. A parallel group, randomized controlled design assigned participants to MIACT or conventional care (CC), with assessments at week 2 and 4 during treatment and follow-up at 2 and 6 months post treatment. Bayesian generalized linear modeling was used to evaluate outcomes as a function of treatment.
RESULTS
Results indicated that during treatment the MIACT group demonstrated an 84% probability of benefit relative to CC with regard to initiating treatment (RR=1.5), however the effect was not seen at follow-up. MIACT was also associated with an increased probability of attending a postpartum obstetrics visit (RR=1.4), and receiving contraception during treatment and at both follow-ups, with posterior probabilities of 96% or higher and relative risks ranging from 1.5 to 5.1 at varying timepoints. Substance use rates for the MIACT versus CC were higher at follow-up.
CONCLUSIONS
Brief, hospital-initiated interventions can assist postpartum mothers who use substances to enter treatment and obtain contraception in order to reduce future substance-exposed pregnancies.

Identifiants

pubmed: 35987083
pii: S0376-8716(22)00339-8
doi: 10.1016/j.drugalcdep.2022.109602
pii:
doi:

Types de publication

Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

109602

Subventions

Organisme : NIDA NIH HHS
ID : R34 DA041465
Pays : United States

Informations de copyright

Copyright © 2022 Elsevier B.V. All rights reserved.

Auteurs

Angela L Stotts (AL)

UTHealth McGovern Medical School, 6431 Fannin, Houston, TX 770030, USA. Electronic address: Angela.L.Stotts@uth.tmc.edu.

Yolanda R Villarreal (YR)

UTHealth McGovern Medical School, 6431 Fannin, Houston, TX 770030, USA.

Charles Green (C)

UTHealth McGovern Medical School, 6431 Fannin, Houston, TX 770030, USA.

Pamela Berens (P)

UTHealth McGovern Medical School, 6431 Fannin, Houston, TX 770030, USA.

Sean Blackwell (S)

UTHealth McGovern Medical School, 6431 Fannin, Houston, TX 770030, USA.

Amir Khan (A)

UTHealth McGovern Medical School, 6431 Fannin, Houston, TX 770030, USA.

Robert Suchting (R)

UTHealth McGovern Medical School, 6431 Fannin, Houston, TX 770030, USA.

Mary Velasquez (M)

The University of Texas at Austin, 1823 Red River St, Austin, TX 78712, USA.

Christine Markham (C)

UTHealth School of Public Health, 1200 Pressler, Houston, TX 77030, USA.

Michelle R Klawans (MR)

UTHealth McGovern Medical School, 6431 Fannin, Houston, TX 770030, USA.

Thomas F Northrup (TF)

UTHealth McGovern Medical School, 6431 Fannin, Houston, TX 770030, USA.

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