Want to Quit Smoking?
Study Says Success Can Improve Significantly When Drug Therapy is Combined
with Behavioral Counseling
MENLO
PARK, California – October 28, 2003 – Smokers who want to quit by taking
the drug bupropion SR (marketed by GlaxoSmithKline as Zyban®) could
see a substantial increase in their chances for quitting when the drug
is taken in combination with a moderate level of behavioral modification
counseling, according to a new study led by researchers at independent
research institute SRI International.
The
study shows that a combination of bupropion SR with minimal or moderate
behavioral counseling results in a “quit rate” of 24% to 33% after one
year, compared to a CDC-reported 5% quit rate for “self-quitters” after
a three-month period (those who quit “cold turkey” without some form of
assistance).
The
study evaluated the effectiveness of different doses of the bupropion
SR in combination with behavioral counseling support, which was provided
through the Center for Health Promotion at the Group Health Cooperative
(GHC) health care system in the State of Washington. For this open-label
trial, a total of 1,524 adult smokers interested in quitting were randomly
assigned to receive one of four combinations of bupropion SR (150 mg or
300 mg) and behavioral counseling (minimal or moderate intensity), and
queried about their smoking status at three and 12 months.
The
findings indicate that at three months, more people on the 300-mg dose
than those on the 150-mg dose reported not smoking (30.9% versus 24.2%).
After one year's time, however, quit rates were not significantly better
at the higher dosage (a result similar to one of the drug's clinical efficacy
trials).
While
after one year the drug dosage was no longer related to the number of
people reporting not smoking, the type of behavioral treatment was significantly
related to reports of nonsmoking. Those participants who were assigned
to moderate-intensity behavioral intervention via the CHP Free & Clear
smoking cessation program had a 21% greater chance of quitting than those
who received minimal-intensity behavioral intervention. The group that
combined the 300-mg dose and the moderate-intensity behavioral counseling
achieved a 33.2% nonsmoking rate, higher than the other three groups.
This was possibly due to the increased use of behavioral skills, a feature
of the yearlong Free & Clear counseling program.
Moderate-intensity
behavioral intervention included a mailing of self-help materials, an
in-depth phone assessment and counseling intervention, four brief pre-scheduled
follow-up calls, and access to a toll-free “Quitline” for a full year,
where counselors provided individualized counseling for participants on
motivation, quitting and avoiding the return to smoking. Minimal-intensity
behavioral intervention included a mailing of tailored self-help materials
and a quit-day phone call.
The
results suggest that health care systems can decrease tobacco use rates
among their enrollees if they provide modest interventions such as those
described above.
Other
results of the study indicate that at three months, the 300-mg dose was
associated with a significantly increased frequency of self-reported symptoms
such as difficulty sleeping and concentrating, shakiness/tremor, and gastrointestinal
problems. The proportion of those who indicated that they deliberately
took less bupropion SR than prescribed was significantly greater among
those prescribed 300 mg as compared to those assigned to receive 150 mg.
“Even
with a combination of treatments, quitting smoking remains a difficult
achievement for many people. The toll of smoking on our health and health
care system is very high. SRI has a long-standing commitment to addressing
the important field of nicotine addiction and will continue its research
in not only improving the effectiveness of existing smoking cessation
therapies, but in developing entirely new treatments as well,” said Gary
Swan, Ph.D., director of SRI's Center for Health Studies and the report's
lead author.
SRI
designed and led the National Cancer Institute-funded study. A research
article describing the outcomes of the study titled “Effectiveness of
Bupropion SR for Smoking Cessation in a Health Care Setting: A Randomized
Trial” has been published in the October 27 edition of Archives of
Internal Medicine.
The
paper's authors also include Tim McAfee, M.D., M.PH. (Chief Medical
Officer of the GHC Center for Health Promotion), Susan J. Curry,
Ph.D. (formerly with GHC and now affiliated with the School of Public
Health, University of Illinois at Chicago), Lisa M. Jack (SRI),
Harold Javitz, Ph.D. (SRI), Sara Dacey, M.D. (GHC), and Katherine
Bergman, R.Ph. (GHC).
About
SRI International
Silicon
Valley-based SRI International
is one of the world's leading independent research and technology
development organizations. Founded as Stanford Research Institute
in 1946, SRI has been meeting the strategic needs of clients for
more than 55 years. The nonprofit research institute performs contract research and development for government agencies, commercial businesses and private foundations. In addition to conducting contract R&D,
SRI licenses its technologies, forms strategic partnerships and
creates spin-off companies.
SRI's
Center for Health
Sciences uses a multidisciplinary research approach to address
complex challenges that arise at the interface of the basic sciences,
clinical medicine, health care economics, and the regulatory and
legal environments. Capabilities include clinical trials design,
management, and analysis; health surveys; disease follow-ups; long-term
tracking of study populations; and disease-related psychological
and behavioral assessments. The Center also provides education on
behavioral risk factors and offers cost-effectiveness analyses and
litigation support.
About
the Group Health Cooperative
Founded
in 1947, Group Health is a consumer-governed,
nonprofit health care system that coordinates care and coverage. Based
in Seattle, Group Health and Group Health Options, Inc., serve 562,000
members in Washington and Idaho.
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