A programme for reducing smoking in pre-operative surgical patients: randomised controlled trial

Anaesthesia. 2005 Feb;60(2):172-9. doi: 10.1111/j.1365-2044.2004.04070.x.

Abstract

We assessed the efficacy of a comprehensive programme for stopping smoking in 210 smokers scheduled for surgery, before admission and 3 months after attending a pre-operative clinic. Participants were randomly allocated to receive an intervention incorporating nicotine replacement therapy for patients smoking more than 10 cigarettes per day ("dependent smokers"), or to a control group to receive usual care. Dependent smokers allocated to the intervention group were more likely to report abstinence before surgery than those allocated to receive usual-care (63 (73%) vs. 29 (56%), respectively; OR 2.2 (95% CI 1.0-4.8)), and 3 months after attendance (16 (18%) vs. 3 (5%), respectively; OR = 3.9 (95% CI 1.0-21.7).

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Female
  • Health Care Costs
  • Humans
  • Male
  • Middle Aged
  • Nicotine / therapeutic use
  • Nicotinic Agonists / therapeutic use
  • Preoperative Care / economics
  • Preoperative Care / methods*
  • Program Evaluation
  • Smoking Cessation / economics
  • Smoking Cessation / methods*
  • Smoking Prevention*
  • Tobacco Use Disorder / rehabilitation
  • Treatment Outcome

Substances

  • Nicotinic Agonists
  • Nicotine