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Comparative Study
. 2016 Sep 20;6(9):e011520.
doi: 10.1136/bmjopen-2016-011520.

Uptake and efficacy of a systematic intensive smoking cessation intervention using motivational interviewing for smokers hospitalised for an acute coronary syndrome: a multicentre before-after study with parallel group comparisons

Affiliations
Comparative Study

Uptake and efficacy of a systematic intensive smoking cessation intervention using motivational interviewing for smokers hospitalised for an acute coronary syndrome: a multicentre before-after study with parallel group comparisons

Reto Auer et al. BMJ Open. .

Abstract

Objectives: To compare the efficacy of a proactive approach with a reactive approach to offer intensive smoking cessation intervention using motivational interviewing (MI).

Design: Before-after comparison in 2 academic hospitals with parallel comparisons in 2 control hospitals.

Setting: Academic hospitals in Switzerland.

Participants: Smokers hospitalised for an acute coronary syndrome (ACS).

Intervention: In the intervention hospitals during the intervention phase, a resident physician trained in MI systematically offered counselling to all smokers admitted for ACS, followed by 4 telephone counselling sessions over 2 months by a nurse trained in MI. In the observation phase, the in-hospital intervention was offered only to patients whose clinicians requested a smoking cessation intervention. In the control hospitals, no intensive smoking cessation intervention was offered.

Primary and secondary outcomes: The primary outcome was 1 week smoking abstinence (point prevalence) at 12 months. Secondary outcomes were the number of smokers who received the in-hospital smoking cessation intervention and the duration of the intervention.

Results: In the intervention centres during the intervention phase, 87% of smokers (N=193/225) received a smoking cessation intervention compared to 22% in the observational phase (p<0.001). Median duration of counselling was 50 min. During the intervention phase, 78% received a phone follow-up for a median total duration of 42 min in 4 sessions. Prescription of nicotine replacement therapy at discharge increased from 18% to 58% in the intervention phase (risk ratio (RR): 3.3 (95% CI 2.4 to 4.3; p≤0.001). Smoking cessation at 12-month increased from 43% to 51% comparing the observation and intervention phases (RR=1.20, 95% CI 0.98 to 1.46; p=0.08; 97% with outcome assessment). In the control hospitals, the RR for quitting was 1.02 (95% CI 0.84 to 1.25; p=0.8, 92% with outcome assessment).

Conclusions: A proactive strategy offering intensive smoking cessation intervention based on MI to all smokers hospitalised for ACS significantly increases the uptake of smoking cessation counselling and might increase smoking abstinence at 12 months.

Keywords: PREVENTIVE MEDICINE; Smoking; acute coronary syndrome; hospitalization; motivational interviewing.

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Figures

Figure 1
Figure 1
Study design. Before–after intervention with parallel group comparisons: we compared the 7 days point smoking prevalence at 12 months follow-up between participants included in the reactive versus the proactive intervention phases in intervention sites (A and B). We also compared the 7 days point smoking prevalence at 12 months follow-up between participants included during the same period in observation sites (C and D).
Figure 2
Figure 2
Flow chart of participants included in the intervention sites (A and B) and control sites (C and D) during observation phase (August 2009–October 2010) and intervention phase (November 2010–February 2012). Intensive smoking cessation counselling was offered during the observation phase in the observation on request and systematically during the intervention phase. Phone follow-up was only offered in the intervention phase in the intervention sites (see Materials and methods section).

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