CLINICAL STUDIES
Effectiveness of a Pregnancy Smoking Cessation Program

https://doi.org/10.1111/j.1552-6909.1992.tb01755.xGet rights and content

Objective

To evaluate two nursing approaches to promoting smoking cessation during initial antenatal visits.

Design

Experimental, with assignment to interventions using a random, alternate‐day strategy and blind assessment of smoking at baseline, 1 month postintervention, 36 weeks' gestation, and 6 weeks postpartum.

Setting/Participants:

224 daily smokers, fewer than 31 weeks' gestation, during first prenatal visit, at a teaching hospital antenatal clinic.

Interventions:

An evening class providing guidance on a self‐help program for 2 hours on a group basis or 20 minutes on an individual basis during the prenatal appointment.

Main outcome measure:

Smoking cessation, confirmed by urinary cotinine levels.

Results:

All women assigned to the referral intervention received a referral, but none attended the classes. In contrast, 93% assigned to the immediate intervention received the intervention. The group receiving immediate intervention had two to three times higher rates of cessation at all follow‐up periods, with significant differences at the 1‐month follow‐up. There were certain similarities between the groups.

Conclusion:

Cessation interventions should be administered during the first prenatal visit.

Section snippets

Design and sample

All new referrals to an antenatal clinic were screened for eligibility. The eligibility criteria were confirmed pregnancy, smoked at least one cigarette daily at the time of first visit to the clinic, and less than 31 weeks’ gestation. Self-reported cigarette smoking and urinary cotinine levels were monitored before intervention, 1 month postintervention, at 36 weeks’ gestation, and at 6 weeks postpartum.

The usual care control interventionvris provided to all subjects by a research nurse. This

Patient accrual and follow-up

The numbers of women screened and recruited over time are provided in Table 1. Of the 267 daily smokers identified, 39 were ineligible because of the following reasons: less than 31 weeks’ gestation (n = 21), missed abortions (n = 4), consultations for therapeutic abortion (n = 3), congenital anomaly (n = 1), participated in study during previous pregnancy (n = 3), severe retardation, psychiatric illness, or only 1-day consultation (n = 7).

Of the participating women, 76.3% provided complete data over all

Discussion

The immediate administration of a smoking cessation program at the first antenatal visit produced cessation rates comparable to the rates achieved in the experimental group (14%) in the study by Windsor et al. (1985). These results are encouraging, given that our control subjects had higher cessation rates than Windsor’s control subjects (5-6% versus 2%) and that our refusal rates were much lower (2% versus 19%) • Moreover, although Windsor’s study was terminated at delivery, the current study

Acknowledgments

This study was funded by the Ontario Ministry of Health and the Ontario Thoracic Society.

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