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A Parental Smoking Cessation Intervention in the Pediatric Emergency Setting: A Randomized Trial

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  • E. Melinda Mahabee-Gittens

    (Division of Emergency Medicine, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH 45229–3026, USA
    College of Medicine, University of Cincinnati, Cincinnati, OH 45267, USA)

  • Robert T. Ammerman

    (College of Medicine, University of Cincinnati, Cincinnati, OH 45267, USA
    Division of Behavioral Medicine and Clinical Psychology, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH 45229–3026, USA)

  • Jane C. Khoury

    (College of Medicine, University of Cincinnati, Cincinnati, OH 45267, USA
    Division of Biostatistics and Epidemiology, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH 45229–3026, USA)

  • Meredith E. Tabangin

    (College of Medicine, University of Cincinnati, Cincinnati, OH 45267, USA
    Division of Biostatistics and Epidemiology, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH 45229–3026, USA)

  • Lili Ding

    (College of Medicine, University of Cincinnati, Cincinnati, OH 45267, USA
    Division of Biostatistics and Epidemiology, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH 45229–3026, USA)

  • Ashley L. Merianos

    (School of Human Services, University of Cincinnati, Cincinnati, OH 45221, USA)

  • Lara Stone

    (Division of Emergency Medicine, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH 45229–3026, USA)

  • Judith S. Gordon

    (College of Nursing, University of Arizona, Tucson, AZ 85721, USA)

Abstract

We examined the efficacy of a pediatric emergency visit-based screening, brief intervention, and referral to treatment (SBIRT) condition compared to a control condition (Healthy Habits Control, HHC) to help parental smokers quit smoking. We enrolled 750 parental smokers who presented to the pediatric emergency setting with their child into a two-group randomized controlled clinical trial. SBIRT participants received brief cessation coaching, quitting resources, and up to 12-weeks of nicotine replacement therapy (NRT). HHC participants received healthy lifestyle coaching and resources. The primary outcome was point-prevalence tobacco abstinence at six weeks (T1) and six months (T2). The mean (SD) age of parents was 31.8 (7.7) years, and 86.8% were female, 52.7% were Black, and 64.6% had an income of ≤$15,000. Overall abstinence rates were not statistically significant with 4.2% in both groups at T1 and 12.9% and 8.3% in the SBIRT and HHC groups, respectively, at T2. There were statistically significant differences in SBIRT versus HHC participants on the median (IQR) reduction of daily cigarettes smoked at T1 from baseline (−2 [−5, 0] versus 0 [−4, 0], p = 0.0008),at T2 from baseline (−4 [−9, −1] vs. −2 [−5, 0], p = 0.0006), and on the mean (SD) number of quit attempts at T2 from baseline (1.25 (6.5) vs. 0.02 (4.71), p = 0.02). Self-reported quitting rates were higher in SBIRT parents who received NRT (83.3% vs. 50.9%, p = 0.04). The novel use of the pediatric emergency visit to conduct cessation interventions helped parents quit smoking. The near equivalent abstinence rates in both the SBIRT and HHC groups may be due to underlying parental concern about their child’s health. Cessation interventions in this setting may result in adult and pediatric public health benefits.

Suggested Citation

  • E. Melinda Mahabee-Gittens & Robert T. Ammerman & Jane C. Khoury & Meredith E. Tabangin & Lili Ding & Ashley L. Merianos & Lara Stone & Judith S. Gordon, 2020. "A Parental Smoking Cessation Intervention in the Pediatric Emergency Setting: A Randomized Trial," IJERPH, MDPI, vol. 17(21), pages 1-14, November.
  • Handle: RePEc:gam:jijerp:v:17:y:2020:i:21:p:8151-:d:440013
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    References listed on IDEAS

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    1. E. Melinda Mahabee-Gittens & Matthew J. Mazzella & John T. Doucette & Ashley L. Merianos & Lara Stone & Chase A. Wullenweber & Stefanie A. Busgang & Georg E. Matt, 2020. "Comparison of Liquid Chromatography Mass Spectrometry and Enzyme-Linked Immunosorbent Assay Methods to Measure Salivary Cotinine Levels in Ill Children," IJERPH, MDPI, vol. 17(4), pages 1-12, February.
    2. Kenneth F Schulz & Douglas G Altman & David Moher & for the CONSORT Group, 2010. "CONSORT 2010 Statement: Updated Guidelines for Reporting Parallel Group Randomised Trials," PLOS Medicine, Public Library of Science, vol. 7(3), pages 1-7, March.
    3. Gordon, J.S. & Andrews, J.A. & Albert, D.A. & Crews, K.M. & Payne, T.J. & Severson, H.H., 2010. "Tobacco Cessation via public dental clinics: Results of a randomized trial," American Journal of Public Health, American Public Health Association, vol. 100(7), pages 1307-1312.
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    Cited by:

    1. E. Melinda Mahabee-Gittens & Georg E. Matt & Roman A. Jandarov & Ashley L. Merianos, 2023. "The Associations of Trans -3′-Hydroxy Cotinine, Cotinine, and the Nicotine Metabolite Ratio in Pediatric Patients with Tobacco Smoke Exposure," IJERPH, MDPI, vol. 20(9), pages 1-12, April.

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