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Chris T Bolliger a Respiratory Division,
Department of Internal Medicine, University Hospital, 4031 Basle,
Switzerland, b University Medical Policlinic,
CHUV, 1000 Lausanne, Switzerland, c Pharmacia and Upjohn,
251 09 Helsingborg, Sweden
Correspondence
to: C T Bolliger ctb{at}gerga.sun.ac.za
Objectives:
To determine whether use of an oral
nicotine inhaler can result in long term reduction in smoking and
whether concomitant use of nicotine replacement and smoking is safe.
Design:
Double blind, randomised, placebo controlled trial. Four month trial with a two year follow up.
Setting:
Two university hospital pulmonary clinics in Switzerland.
Participants:
400 healthy volunteers, recruited
through newspaper advertisements, willing to reduce their smoking but unable or unwilling to stop smoking immediately.
Intervention:
Active or placebo inhaler as needed for
up to 18 months, with participants encouraged to limit their smoking as
much as possible.
Main outcome measures:
Number of cigarettes smoked per
day from week six to end point. Decrease verified by a measurement of
exhaled carbon monoxide at each time point compared with measurement at baseline.
Results:
At four months sustained reduction of smoking was achieved in 52 (26%) participants in the active group and 18 (9%)
in the placebo group (P<0.001; Fisher's test). Corresponding figures
after two years were 19 (9.5%) and 6 (3.0%) (P=0.012).
Conclusion:
Nicotine inhalers effectively and safely
achieved sustained reduction in smoking over 24 months. Reduction with or without nicotine substitution may be a feasible first step towards
smoking cessation in people not able or not willing to stop abruptly.
What can you learn from this BMJ paper? Read Leanne Tite's Paper+