EFFECTIVENESS OF THE 4-MG DOSE OF NICOTINE POLACRILEX FOR THE INITIAL TREATMENT OF HIGH-DEPENDENT SMOKERS

被引:47
作者
SACHS, DPL [1 ]
机构
[1] STANFORD UNIV,SCH MED,DIV PULM & CRIT CARE MED,STANFORD,CA 94305
关键词
D O I
10.1001/archinte.155.18.1973
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose: To determine the effectiveness of the 4-mg and 2-mg dosages of nicotine polacrilex vs placebo through the first 6 weeks of treatment (during which 75% of relapse occurs when there is no treatment) in assisting high-dependent smokers to stop smoking when instructed to use a fixed number (12 pieces) of medication daily. Subjects and Methods: Ninety high-dependent (Fagerstrom Tolerance Questionnaire score greater than or equal to 7 plus baseline carbon monoxide level > 15 ppm) healthy male and female smokers, highly motivated to quit smoking, were enrolled in a 6-week, randomized, double-blind, placebo-controlled trial in which they were instructed to use 12 pieces per day of their assigned dosage formulation: 4 mg, 2 mg, or 0.5 mg (placebo) of nicotine polacrilex. The behavioral intervention did not depend on providing any special psychological training, skills, or services but rather employed a standard medical practice model that could easily be implemented by any primary care physician. Results: Sustained abstinence from weeks 2 through 6, determined at each visit by absolutely no cigarette use plus a carbon monoxide level of 8 ppm or lower was 59% (4-mg group), 30% (2-mg group), and 39% (placebo group) (P<.02). For the 55 of the 90 smokers who met the originally planned definition of high dependence (Fagerstrom Tolerance Questionnaire score greater than or equal to 7 plus baseline smoking serum cotinine level >250 ng/ml plus baseline carbon monoxide level >15 ppm), results were 63% (4-mg group), 25% (2-mg group), and 25% (placebo group) (P<.02). In addition, the 4-mg dose produced statistically significantly higher abstinence rates in compliant subjects (P<.02) and also in subjects with high baseline serum cotinine levels who were compliant (P<.01) than did either the 2-mg dose or placebo. Conclusions: It appears that the 4-mg dose of nicotine polacrilex is the drug and dose of choice for the initial phase of tobacco dependence treatment in high-dependent smokers; the 2-mg dose of nicotine polacrilex is no better than placebo during the first 6 weeks of treatment for high-dependent cigarette smokers, and thus should not be used for these patients during the initial treatment phase.
引用
收藏
页码:1973 / 1980
页数:8
相关论文
共 33 条
[1]  
BENOWITZ NL, 1993, NIDA RES MONOGR, V48, P6
[2]   CONTROLLED TRIAL OF NICOTINE POLACRILEX GUM WITH SUPPORTIVE MEASURES [J].
BLONDAL, T .
ARCHIVES OF INTERNAL MEDICINE, 1989, 149 (08) :1818-1821
[3]   SMOKING CESSATION IN HOSPITAL PATIENTS GIVEN REPEATED ADVICE PLUS NICOTINE OR PLACEBO CHEWING GUM [J].
CAMPBELL, IA ;
PRESCOTT, RJ ;
TJEDERBURTON, SM .
RESPIRATORY MEDICINE, 1991, 85 (02) :155-157
[4]   MEASURING NICOTINE DEPENDENCE - A REVIEW OF THE FAGERSTROM TOLERANCE QUESTIONNAIRE [J].
FAGERSTROM, KO ;
SCHNEIDER, NG .
JOURNAL OF BEHAVIORAL MEDICINE, 1989, 12 (02) :159-182
[6]   EFFECTIVENESS OF NICOTINE PATCH AND NICOTINE GUM AS INDIVIDUAL VERSUS COMBINED TREATMENTS FOR TOBACCO WITHDRAWAL SYMPTOMS [J].
FAGERSTROM, KO ;
SCHNEIDER, NG ;
LUNELL, E .
PSYCHOPHARMACOLOGY, 1993, 111 (03) :271-277
[7]   EFFECTS OF NICOTINE CHEWING GUM AND FOLLOW-UP APPOINTMENTS IN PHYSICIAN-BASED SMOKING CESSATION [J].
FAGERSTROM, KO .
PREVENTIVE MEDICINE, 1984, 13 (05) :517-527
[8]  
FORTMANN SP, 1988, JAMA-J AM MED ASSOC, V260, P1575
[9]   PREDICTORS OF SMOKING RELAPSE AMONG SELF-QUITTERS - A REPORT FROM THE NORMATIVE AGING STUDY [J].
GARVEY, AJ ;
BLISS, RE ;
HITCHCOCK, JL ;
HEINOLD, JW ;
ROSNER, B .
ADDICTIVE BEHAVIORS, 1992, 17 (04) :367-377
[10]   LONG-TERM USE OF NICOTINE CHEWING GUM - OCCURRENCE, DETERMINANTS, AND EFFECT ON WEIGHT-GAIN [J].
HAJEK, P ;
JACKSON, P ;
BELCHER, M .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1988, 260 (11) :1593-1596