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Quitline usage does not improve rates of smoking cessation in orthopaedic trauma patients unless combined with nicotine replacement therapy

Producción científica: Articlerevisión exhaustiva

2 Citas (Scopus)

Resumen

Purpose: The negative effects of smoking following traumatic orthopaedic injury can lead to serious complications and decreased quality of life. The widely available quitline could be easily implemented in the orthopaedic postoperative period to improve outcome, but the effectiveness of this intervention in this population is unknown. The goal of this study was to determine if active referral to a quitline would improve rates of smoking cessation in this population. Methods: This is a secondary analysis of a randomized control trial assessing the effectiveness of an inpatient intervention with varying intensities to promote smoking cessation. Participants were actively referred to the quitline as part of their intervention. Participants were surveyed at 6 weeks, 3 months and 6 months following their injury for 7-day abstinence, chemically confirmed with exhaled carbon monoxide monitoring. Results: Smoking quitline use alone does not independently improve 7-day abstinence. Quitline and nicotine use are synergistic (OR, 5.6 vs. 2.3 at 3 months in patients who used nicotine patch and quitline vs. patch; OR, 7.8 vs. 2.1 at 3 months in patients who used any NRT and quitline vs. NRT alone). Conclusions: NRT use improves smoking cessation rates in orthopaedic trauma patients. Although smoking quitline use might not independently improve cessation rates in orthopaedic trauma patients postoperatively, concomitant use of NRT with quitline improves quit rates over NRT alone. Patients referred to quitline should be encouraged to use NRT.

Idioma originalEnglish
Páginas (desde-hasta)833-838
Número de páginas6
PublicaciónEuropean Journal of Orthopaedic Surgery and Traumatology
Volumen34
N.º2
DOI
EstadoPublished - feb 2024

Nota bibliográfica

Publisher Copyright:
© The Author(s), under exclusive licence to Springer-Verlag France SAS, part of Springer Nature 2023.

Financiación

The trial was funded by Maryland Department of Health, Center for Tobacco Prevention and Control (Contract ID: OPASS 17-17343 G). The sponsor had no role in design and conduct of the study or the decision to submit the manuscript for publication. Clinical Trial # NCT02428244.

FinanciadoresNúmero del financiador
Center for Tobacco Prevention and ControlOPASS 17-17343 G
Maryland Department of Health

    ASJC Scopus subject areas

    • Surgery
    • Orthopedics and Sports Medicine

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