Cost-free pharmacotherapy in smokers with TIA or stroke: QUIT-MED randomised controlled trial

Author:

Reid RobertORCID,Papadakis Sophia,Gocan Sophia,Bourgoin Aline,Laplante Mary Ann,Armstrong Ashley,Aitken Debbie,Sahlas Demetrios,Stotts Grant,Cotie Lisa,Mullen Kerri-Anne,Pipe Andrew,Mir HassanORCID,Sharma Mukul

Abstract

ObjectiveTo examine whether cost-free (CF) smoking cessation medication was more effective than a prescription for cessation medication in patients after transient ischaemic attack (TIA) or stroke.DesignTwo-site randomised trial.SettingStroke prevention clinics (SPCs) in Ontario, Canada.ParticipantsSmokers with TIA or stroke, willing to quit smoking.InterventionSmoking status was assessed in SPC attendees. Smokers were advised to quit smoking and received recommendations for cessation medication and counselling. Consenting participants were randomly assigned (1:1) to either a CF medication group or a prescription-only (Rx) group. CF participants immediately received a 12-week supply of cessation medication. Rx participants were given a prescription for 12 weeks of cessation medication. Follow-up counselling was provided for 26 weeks.Main outcomeThe primary outcome was 40-week continuous abstinence verified using a carbon monoxide breath test at 52-week follow-up. Secondary outcomes included abstinence at intermediate timepoints, medication adherence and serious adverse events.ResultsHundred and ninety-four participants were randomised and 131 (67.5%) completed the trial. The 40-week continuous abstinence rate at 52-week follow-up was 15.5% in the CF group versus 14.0% in the Rx group (OR=1.13; 95% CI 0.51 to 2.53). The 14-week continuous abstinence rate at 26-week follow-up was 18.6% in the CF group versus 16.8% in the Rx group (OR=1.20; 95% CI 0.56 to 2.55). Seven-day point-prevalence abstinence at 12 weeks was 38.1% in the CF group versus 26.9% in the Rx group (OR=1.76; 95% CI 0.94 to 3.28). Medication adherence was higher in the CF group versus the Rx group (47.4%±41.2% vs 25.5±36.8%, p<0.001). Serious adverse events occurred in 11.1% of participants and were unrelated to treatment.ConclusionsOur findings were inconclusive; we failed to meet our recruitment target and the effect size was smaller than anticipated. CF medication improved medication adherence.Trial registration numberNCT00962988; ClinicalTrials.gov Identifier.

Funder

Heart and Stroke Foundation of Canada

Publisher

BMJ

Subject

General Medicine

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