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Varying Nicotine Patch Dose and Type of Smoking Cessation Counseling
Douglas E. Jorenby, PhD;
Stevens S. Smith, PhD;
Michael C. Fiore, MD, MPH;
Richard D. Hurt, MD;
Kenneth P. Offord, MS;
Ivana T. Croghan, PhD;
J. Taylor Hays, MD;
Stephen F. Lewis, MD;
Timothy B. Baker, PhD
JAMA. 1995;274(17):1347-1352.
Abstract
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Objective.
—To compare the efficacy and safety of 22-mg and 44-mg doses of transdermal nicotine therapy when it is paired with minimal, individual, or group counseling to improve smoking cessation rates.
Design.
—An 8-week clinical trial (4 weeks double-blind followed by 4 weeks open label) using random assignment of participants to both dose (22 or 44 mg) and counseling (minimal, individual, or group) conditions.
Participants.
—Daily cigarette smokers ( 15 cigarettes per day for at least 1 year) who volunteered to participate in a study of smoking cessation treatment. A total of 504 participants were enrolled at two sites.
Intervention.
—Four weeks of 22- or 44-mg transdermal nicotine therapy followed by 4 weeks of dosage reduction (2 weeks of 22 mg followed by 2 weeks of 11 mg). Counseling consisted of a self-help pamphlet (minimal); a self-help pamphlet, a brief physician motivational message, and three brief (15 minutes) follow-up visits with a nurse (individual); or the pamphlet, the motivational message, and eight weekly 1-hour group smoking cessation counseling visits (group). All participants returned weekly to turn in questionnaires and for assessment of their smoking status.
Main Outcome Measures.
—Abstinence from smoking was based on selfreport, confirmed by an expired carbon monoxide concentration lower than 10 ppm. Withdrawal severity was assessed by means of an eight-item self-report questionnaire completed daily.
Results.
—Smoking cessation rates for the two nicotine patch doses and three levels of counseling did not differ significantly at either 8 weeks or 26 weeks following the quit date. Among those receiving minimal contact, the 44-mg dose produced greater abstinence at 4 weeks than did the 22-mg dose (68% vs 45%; P<.01). Participants receiving minimal-contact adjuvant treatment were less likely to be abstinent at the end of 4 weeks than those receiving individual or group counseling (56% vs 67%; P<.05). The 44-mg dose decreased desire to smoke more than the 22-mg dose, but this effect was not related to success in quitting smoking. Transdermal nicotine therapy at doses of 44 mg produced a significantly greater frequency of nausea (28%), vomiting (10%), and erythema with edema at the patch site (30%) than did a 22-mg dose (10%, 2%, and 13%, respectively; P<.01 for each adverse effect). Three serious adverse events occurred during use of the 44-mg patch dose.
Conclusions.
—There does not appear to be any general, sustained benefit of initiating transdermal nicotine therapy with a 44-mg patch dose or of providing intense adjuvant smoking cessation treatment. The two doses and all adjuvant treatments produced equivalent effects at the 26-week follow-up, and the higher patch dose produced more adverse effects. Higher-dose (44-mg) nicotine replacement does not appear to be indicated for general clinical populations, although it may provide short-term benefit to some smokers attempting to quit with minimal adjuvant treatment.
(JAMA. 1995;274:1347-1352)
Author Affiliations
From the Center for Tobacco Research and Intervention (Drs Jorenby, Smith, Fiore, Lewis, and Baker) and Department of Psychology (Drs Smith and Baker), University of Wisconsin-Madison; Division of General Internal Medicine, Department of Medicine, University of Wisconsin Medical School, Madison (Drs Jorenby, Fiore, and Lewis); and Nicotine Research Center (Drs Hurt, Croghan, and Hays and Mr Offord), Division of Community Internal Medicine (Dr Hurt), Section of Biostatistics (Mr Offord), and Division of General Internal Medicine (Dr Hays), Mayo Clinic, Rochester, Minn.
Footnotes
Drs Jorenby, Smith, Fiore, Lewis, and Baker have worked on clinical research studies funded in part by Alza Corporation; Ciba-Geigy Corporation; Elan Pharmaceutical Research Corporation; Lederle Laboratories; and Marion Merrell Dow, Inc. Drs Hurt, Croghan, and Hays and Mr Offord have worked on clinical research studies funded in part by Lederle Laboratories, Elan Pharmaceutical Research Corporation, BurroughsWellcome, and Kabi. Dr Fiore has received honoraria for educational activities from Ciba-Geigy Corporation; Elan Pharmaceutical Research Corporation, Lederle Laboratories Division; Marion Merrell Dow, Inc; and Parke-Davis. Dr Hurt has received honoraria for educational activities from Ciba-Geigy Corporation, Marion Merrell Dow, Inc, and McNeil Pharmaceuticals. Mr Offord has received honoraria for educational activities from Elan Pharmaceutical Research Corporation.
Reprint requests to Center for Tobacco Research and Intervention, University of Wisconsin Medical School, 1300 University Ave, 7275 MSC, Madison, WI 53706-1532 (Dr Jorenby).
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