Effects of Sustained-Release Bupropion and Supportive Group Therapy on Cigarette Consumption in Patients With Schizophrenia

Nine medically stable outpatients from the Maryland Psychiatric Research Center volunteered for the study. Patients had stable cigarette smoking habits and expressed interest in decreasing their smoking. Patients with neurologic illnesses, a current depressive episode, or active substance abuse and those receiving bupropion were excluded from participation. All patients had a DSM-IV diagnosis of either schizophrenia or schizoaffective disorder and were judged to be clinically stable by their treatment team. All patients provided written informed consent before study entry.

The study design included a 2-week stabilization period to obtain baseline measures and a 14-week treatment phase. During the treatment phase, patients participated in nine sessions of weekly group therapy led by clinic nurses trained in the educational model of the American Cancer Society Fresh Start Program, modified for patients with schizophrenia (2). Subjects were told that the goal was to stop smoking, but they were encouraged to continue to participate even if they were not successful in complete cessation. Adjunctive sustained-release bupropion was started at the third group session, initially 150 mg once a day for 3 days and then 150 mg twice a day for the remainder of the study. Adjunctive nicotine replacement was not prescribed.

The primary measure of cigarette consumption was end expired breath carbon monoxide level (7), since patients’ self-reports of the number of cigarettes smoked per day were suspected to be unreliable. A EC 50 Micro III Smokerlyzer breath carbon monoxide monitor (Bedfont Scientific, Kent, U.K.) was used to measure patients’ end expired breath carbon monoxide weekly throughout the study, immediately before or immediately after each support group, which met at 2:00 p.m. Clinical assessments were obtained during the first week of stabilization, at the beginning of treatment with sustained-release bupropion (week 2), on the smoking quit day (week 4), at the end of the support group (week 8), and at study completion (week 14). Clinical assessments were done with the Brief Psychiatric Rating Scale (BPRS), the Scale for the Assessment of Negative Symptoms (SANS) (8), and the Fagerstrom Test for Nicotine Dependence (9). During the second week of the stabilization period and at study completion (week 14), the patients received a brief neuropsychological test battery consisting of the Rey Auditory Verbal Learning Test (10) and the Brief Visuospatial Memory Test (11) to measure auditory and visual-spatial memory, the Gordon Diagnostic System Continuous Performance Task (12) to measure attention, and the Grooved Pegboard test (13) to measure manual dexterity. Measures of P50 suppression (ratio of response to successive auditory clicks [S2/S1]) (14) were also obtained during the second week of stabilization and at study completion.

T tests were used to assess baseline and end-of-study differences in end expired breath carbon monoxide level, symptom ratings, neuropsychological test performance, and P50 suppression.

Nine subjects entered the study, and eight completed the study. One subject dropped out in the first week of sustained-release bupropion treatment owing to a rash thought to be secondary to the study medication. Two patients complained of orthostatic dizziness, and one of them required a decrease in the sustained-release bupropion dose. One patient complained of an initial feeling of agitation that resolved without intervention.

Of the subjects who completed the study, five were Caucasian, three were African American, and seven were male. The mean age of the eight subjects who completed the study was 48.05 years (SD=9.29), and their mean duration of illness was 29.68 years (SD=10.95). Their mean baseline score on the Fagerstrom Test for Nicotine Dependence was 6.13 (SD=2.10), which represents a high level of dependency.

Subjects’ mean end expired breath carbon monoxide level decreased over the treatment phase (Figure 1). The mean carbon monoxide level was 39.44 ppm (SD=21.30) at baseline (the average of the two measures during the stabilization period) and 18.38 (SD=11.96) at week 14, for a mean change of 21.06 (SD=22.25) (t=–2.68, df=7, p≤0.05). The decrease in carbon monoxide level between baseline and treatment week 2 was not significant (p=0.07).

Between baseline and week 14, there were no significant changes (all p>0.20) in the BPRS positive symptom score (mean=10.63, SD=4.53, versus mean=10.63, SD=3.81), the BPRS anxiety item (mean=2.63, SD=1.19, versus mean=1.88, SD=0.83), or the BPRS depression item (mean=1.63, SD=1.19, versus mean=1.75, SD=1.16). There were no significant changes from baseline to week 14 on any of the cognitive measures (all p>0.05) or on the measure of P50 suppression (p=0.80). Mean scores on these measures at baseline and week 14 were as follows: Rey Auditory Verbal Learning Test, mean=37.63 (SD=6.21) versus 35.63 (SD=9.65); Brief Visuospatial Memory Test, mean=18.38 (SD=7.11) versus 20.25 (SD=9.24); Continuous Performance Task total correct, mean=35.75 (SD=8.14) versus 31.25 (SD=9.38); and P50 S2/S1 ratio, mean=0.56 (SD=0.34) versus 0.57 (SD=0.34). Treatment with sustained-release bupropion was associated with an 18% decrease in the mean SANS total score from 29.38 (SD=5.53) at baseline to 24.13 (SD=7.61) at week 14, but the difference was not significant (t=–1.78, df=7, p=0.12). There was a significant reduction in the mean SANS alogia factor score over the course of the study from 3.00 (SD=2.98) to 1.13 (SD=1.25), for a mean change of 1.88 (SD=1.89) (t=2.18, df=7, p≤0.05).

Four of eight patients chose to continue treatment with sustained-release bupropion for an additional 12 weeks after the conclusion of the open-label study. One of those patients subsequently stopped smoking completely. Two of the remaining three had further decreases in their expired breath carbon monoxide levels, and the third patient maintained the decrease he had achieved at study completion.

Although none of the subjects quit smoking during the study, adjunctive use of sustained-release bupropion in combination with supportive group therapy seemed to help patients with schizophrenia decrease their cigarette consumption, as measured by the change in their expired breath carbon monoxide levels. The decrease in cigarette consumption began before the initiation of sustained-release bupropion and before the designated quit day and then stabilized after treatment week 4. The early reduction in cigarette consumption may have been due to the group therapy itself and/or to the subjects’ heightened attention to smoking cessation.

Similarly positive findings have been seen with group therapy and adjunctive use of the nicotine patch (15) and in studies of smoking behavior before and after treatment with clozapine (16). It is difficult to compare these findings with those of the current study, since the primary outcome measures and treatment settings were different.

Patients generally tolerated sustained-release bupropion well. There was no associated worsening of positive symptoms or anxiety. There was no evidence of cognitive worsening or of change in suppression of the P50 event-related potential, which might have been expected with loss of nicotine stimulation. These findings are difficult to interpret, as no patients stopped smoking completely during the study, and it is not known how much nicotine stimulation is required to enhance these cognitive processes. The finding of a potential benefit of sustained-release bupropion in improving negative symptoms is of clinical interest but would need to be evaluated with a more rigorous study design.

Although the current study is limited by the small sample size, the open-label design, and the lack of strict inclusion criteria regarding cigarette consumption, it provides preliminary support for the use of a combination of group therapy and adjunctive sustained-release bupropion for the treatment of nicotine addiction in schizophrenia. Further double-blind placebo-controlled studies of this combination of interventions are warranted.

Received June 13, 2000; revision received Sept. 29, 2000; accepted Oct. 9, 2000. From the Maryland Psychiatric Research Center, Department of Psychiatry, University of Maryland at Baltimore. Address reprint requests to Dr. Weiner, Maryland Psychiatric Research Center, P.O. Box 21247, Baltimore, MD 21228; [email protected] (e-mail). Supported in part by NIMH grant MH-40279.