Staying smoke free: An intervention to prevent postpartum relapse

This pilot study evaluated the effectiveness of a nurse-delivered home-visiting program during the postpartum period that included a low-intensity smoking relapse–prevention intervention. A prospective two-group design was used. Participants were women who had quit smoking during their pregnancy. Th...

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Veröffentlicht in:Nicotine & tobacco research 2007-06, Vol.9 (6), p.663-670
Hauptverfasser: French, Gina M., Groner, Judith A., Wewers, Mary Ellen, Ahijevych, Karen
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Sprache:eng
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Zusammenfassung:This pilot study evaluated the effectiveness of a nurse-delivered home-visiting program during the postpartum period that included a low-intensity smoking relapse–prevention intervention. A prospective two-group design was used. Participants were women who had quit smoking during their pregnancy. They were invited to participate during postpartum hospitalization on a university hospital postpartum ward. A brief intervention during postpartum hospitalization, a home visit, and two follow-up phone calls over a 1- to 2-month period were compared with a routine home visit without any prescribed focus on tobacco use. The main outcome was biochemically verified smoking abstinence at 3 and 6 months postenrollment. Abstinence was defined as a salivary cotinine level of 14 ng/ml or less. At 3 months postenrollment, 26.4% of the intervention group were classified as abstinent, compared with 12.4% of the comparison group (OR=2.4, 95% CI=1.16–4.98). At 6 months, the proportion of the intervention group categorized as abstinent was 21.5%, compared with 10.2% of comparison group participants (OR=2.5, 95% CI=1.13–5.71). Greater than three times as many in the intervention group remained abstinent at both times (18.2%), compared with the comparison group (5.2%; OR=2.4, 95% CI=1.16–4.93). The effectiveness of this brief, low-cost, and potentially replicable intervention in improving the rate of persistent postpartum smoke-free status for women who quit smoking during pregnancy is encouraging. A randomized trial of the approach is warranted.
ISSN:1462-2203
1469-994X
DOI:10.1080/14622200701365277