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Cigarette Smoking Cessation Intervention for Buprenorphine Treatment Patients

INTRODUCTION: Patients receiving medication assisted therapy (MAT) for opioid use disorder have high cigarette smoking rates. Cigarette smoking interventions have had limited success. We evaluated an intervention to increase cigarette abstinence rates in patients receiving buprenorphine-assisted the...

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Autores principales: Hall, Sharon M, Humfleet, Gary L, Gasper, James J, Delucchi, Kevin L, Hersh, David F, Guydish, Joseph R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7207071/
https://www.ncbi.nlm.nih.gov/pubmed/28549161
http://dx.doi.org/10.1093/ntr/ntx113
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author Hall, Sharon M
Humfleet, Gary L
Gasper, James J
Delucchi, Kevin L
Hersh, David F
Guydish, Joseph R
author_facet Hall, Sharon M
Humfleet, Gary L
Gasper, James J
Delucchi, Kevin L
Hersh, David F
Guydish, Joseph R
author_sort Hall, Sharon M
collection PubMed
description INTRODUCTION: Patients receiving medication assisted therapy (MAT) for opioid use disorder have high cigarette smoking rates. Cigarette smoking interventions have had limited success. We evaluated an intervention to increase cigarette abstinence rates in patients receiving buprenorphine-assisted therapy. METHODS: Cigarette smokers (N = 175; 78% male; 69% Caucasian; 20% Hispanic), recruited from a buprenorphine clinic were randomly assigned to either an extended innovative system intervention (E-ISI) or to Standard Treatment Control (STC). The E-ISI combined motivational intervention with extended treatment (long-term nicotine replacement therapy , varenicline, and extended cognitive behavioral therapy). STC received written information about quit-lines, medication, and resources. Assessments were held at baseline and 3, 6, 12, and 18 months. Seven-day biochemically verified point-prevalence cigarette abstinence was the primary outcome measure. RESULTS: Fifty-four percent of E-ISI participants entered the extended treatment intervention; E-ISI and STC differed at 3 months on abstinence status but not at months 6, 12, and 18. E-ISI participants were more likely to attempt to quit, to have a goal of complete abstinence, and to be in a more advanced stage of change than STC participants. A higher number of cigarettes smoked and the use of cannabis in the previous 30 days predicted continued smoking CONCLUSIONS: The E-ISI was successful in increasing motivation to quit smoking but did not result in long-term abstinence. The failure of treatments that have been efficacious in the general population to produce abstinence in patients receiving MAT of opioid use disorder suggests that harm reduction and other innovative interventions should be explored. IMPLICATIONS: This study demonstrates that an intervention combining motivational interviewing with an extended treatment protocol can increase cigarette quit attempts, enhance cigarette abstinence goals, and further movement through stages of change about quitting smoking in patients receiving MAT for opioid use disorder who smoke cigarettes. The intervention did not increase abstinence rates over those observed in a standard treatment control, however. The latter finding supports those of earlier investigators who also failed to find efficacy for smoking cessation in this population and who also used interventions effective in the general population. This pattern of findings suggests that patients with opioid use disorder can be motivated to change smoking behavior, but alternative and innovative approaches to cigarette smoking treatment should be studied.
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spelling pubmed-72070712020-05-13 Cigarette Smoking Cessation Intervention for Buprenorphine Treatment Patients Hall, Sharon M Humfleet, Gary L Gasper, James J Delucchi, Kevin L Hersh, David F Guydish, Joseph R Nicotine Tob Res Original Investigations INTRODUCTION: Patients receiving medication assisted therapy (MAT) for opioid use disorder have high cigarette smoking rates. Cigarette smoking interventions have had limited success. We evaluated an intervention to increase cigarette abstinence rates in patients receiving buprenorphine-assisted therapy. METHODS: Cigarette smokers (N = 175; 78% male; 69% Caucasian; 20% Hispanic), recruited from a buprenorphine clinic were randomly assigned to either an extended innovative system intervention (E-ISI) or to Standard Treatment Control (STC). The E-ISI combined motivational intervention with extended treatment (long-term nicotine replacement therapy , varenicline, and extended cognitive behavioral therapy). STC received written information about quit-lines, medication, and resources. Assessments were held at baseline and 3, 6, 12, and 18 months. Seven-day biochemically verified point-prevalence cigarette abstinence was the primary outcome measure. RESULTS: Fifty-four percent of E-ISI participants entered the extended treatment intervention; E-ISI and STC differed at 3 months on abstinence status but not at months 6, 12, and 18. E-ISI participants were more likely to attempt to quit, to have a goal of complete abstinence, and to be in a more advanced stage of change than STC participants. A higher number of cigarettes smoked and the use of cannabis in the previous 30 days predicted continued smoking CONCLUSIONS: The E-ISI was successful in increasing motivation to quit smoking but did not result in long-term abstinence. The failure of treatments that have been efficacious in the general population to produce abstinence in patients receiving MAT of opioid use disorder suggests that harm reduction and other innovative interventions should be explored. IMPLICATIONS: This study demonstrates that an intervention combining motivational interviewing with an extended treatment protocol can increase cigarette quit attempts, enhance cigarette abstinence goals, and further movement through stages of change about quitting smoking in patients receiving MAT for opioid use disorder who smoke cigarettes. The intervention did not increase abstinence rates over those observed in a standard treatment control, however. The latter finding supports those of earlier investigators who also failed to find efficacy for smoking cessation in this population and who also used interventions effective in the general population. This pattern of findings suggests that patients with opioid use disorder can be motivated to change smoking behavior, but alternative and innovative approaches to cigarette smoking treatment should be studied. Oxford University Press 2018-05 2017-05-26 /pmc/articles/PMC7207071/ /pubmed/28549161 http://dx.doi.org/10.1093/ntr/ntx113 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of the Society for Research on Nicotine and Tobacco. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial reuse, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Investigations
Hall, Sharon M
Humfleet, Gary L
Gasper, James J
Delucchi, Kevin L
Hersh, David F
Guydish, Joseph R
Cigarette Smoking Cessation Intervention for Buprenorphine Treatment Patients
title Cigarette Smoking Cessation Intervention for Buprenorphine Treatment Patients
title_full Cigarette Smoking Cessation Intervention for Buprenorphine Treatment Patients
title_fullStr Cigarette Smoking Cessation Intervention for Buprenorphine Treatment Patients
title_full_unstemmed Cigarette Smoking Cessation Intervention for Buprenorphine Treatment Patients
title_short Cigarette Smoking Cessation Intervention for Buprenorphine Treatment Patients
title_sort cigarette smoking cessation intervention for buprenorphine treatment patients
topic Original Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7207071/
https://www.ncbi.nlm.nih.gov/pubmed/28549161
http://dx.doi.org/10.1093/ntr/ntx113
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