Varenicline and Nicotine Replacement Therapy for Smokers Admitted to Hospitals

Author:

Weeks Gregory R.12,Gobarani Rukshar K.1,Abramson Michael J.3,Bonevski Billie4,Webb Ashley5,Thomas Dennis6,Paul Eldho3,Sarwar Muhammad R.1,Smith Brian J.7,Perinpanathan Sharmilla2,Kirsa Sue18,Parkinson Jacqueline8,Meanger Darshana9,Coward Lisa5,Rofe Olivia9,Lee Paula9,van den Bosch Denise1,George Johnson1

Affiliation:

1. Centre for Medicine Use and Safety, Faculty of Pharmacy and Pharmaceutical Sciences, Monash University, Parkville, Victoria, Australia

2. Pharmacy Department, Barwon Health, Geelong, Victoria, Australia

3. School of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australia

4. Flinders Health and Medical Research Institute, College of Medicine and Public Health, Flinders University, Bedford Park, South Australia

5. Department of Anaesthesia and Pain Management, Peninsula Health, Frankston, Victoria, Australia

6. Centre of Excellence in Treatable Traits, College of Health, Medicine and Wellbeing, Hunter Medical Research Institute, University of Newcastle, Newcastle, New South Wales, Australia

7. General and Respiratory Medicine, Bendigo Hospital, Spring Gully, Victoria, Australia

8. Monash Health, Clayton, Victoria, Australia

9. Pharmacy Department, Eastern Health, Box Hill, Victoria, Australia

Abstract

ImportanceVarenicline is the most effective sole pharmacotherapy for smoking cessation. If used in combination with nicotine replacement therapy (NRT), cessation rates may be further improved, but the efficacy and safety of the combination need to be evaluated.ObjectiveTo examine whether hospitalized smokers treated with varenicline and NRT lozenges achieve higher prolonged smoking abstinence rates compared with those treated with varenicline alone.Design, Setting, and ParticipantsA double-blind, placebo-controlled randomized clinical trial was conducted in adult medical or surgical inpatients of 5 Australian public hospitals with a history of smoking 10 cigarettes or more per day, interested in quitting, and available for 12-month follow-up between May 1, 2019, and May 1, 2021 (final 12-month data collection in May 2022). Data analysis was performed from June 1 to August 30, 2023.InterventionsA 12-week varenicline regimen was initiated during hospitalization at standard doses in all participants. Participants were randomized to additionally use NRT (2 mg) or placebo lozenges if there was an urge to smoke. Behavioral support (Quitline) was offered to all participants.Main Outcomes and MeasuresThe primary outcome was biochemically verified sustained abstinence at 6 months. Secondary outcomes included self-reported prolonged abstinence, 7-day point prevalence abstinence (3, 6, and 12 months), and medicine-related adverse events.ResultsA total of 320 participants (mean [SD] age, 52.5 [12.1] years; 183 [57.2%] male) were randomized. The conduct of biochemical verification was affected by COVID-19 restrictions; consequently, the biochemically verified abstinence in the intervention vs control arms (18 [11.4%] vs 16 [10.1%]; odds ratio [OR], 1.14; 95% CI, 0.56-2.33) did not support the combination therapy. The secondary outcomes in the intervention vs control arms of 7-day point prevalence abstinence at 6 months (54 [34.2%] vs 37 [23.4%]; OR, 1.71; 95% CI, 1.04-2.80), prolonged abstinence at 12 months (47 [29.9%] vs 30 [19.1%]; OR, 1.77; 95% CI, 1.05-3.00), and 7-day point prevalence abstinence at 12-months (48 [30.6%] vs 31 [19.7%]; OR, 1.79; 95% CI, 1.07-2.99) significantly improved with the combination therapy. The self-reported 6-month prolonged abstinence (61 [38.6%] vs 47 [29.7%]; OR, 1.49; 95% CI, 0.93-2.39) favored the combination therapy but was not statistically significant. Medicine-related adverse events were similar in the 2 groups (102 [74.5%] in the intervention group vs 86 [68.3%] in the control group).Conclusions and RelevanceIn this randomized clinical trial of the combination of varenicline and NRT lozenges in hospitalized adult daily smokers, the combination treatment improved self-reported abstinence compared with varenicline alone, without compromising safety, but it did not improve biochemically validated abstinence.Trial Registrationanzctr.org.au Identifier: ACTRN12618001792213

Publisher

American Medical Association (AMA)

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