Bv. Parilla et al., THE EFFICACY OF ORAL TERBUTALINE AFTER INTRAVENOUS TOCOLYSIS, American journal of obstetrics and gynecology, 169(4), 1993, pp. 965-969
OBJECTIVE: Our purpose was to investigate in a prospective, randomized
study the efficacy of oral terbutaline after successful intravenous t
ocolysis in reducing preterm birth. STUDY DESIGN: Patients between 28
and 35 weeks' gestation with uterine contractions and change in cervic
al examination were treated with intravenous magnesium sulfate for 12
to 24 hours. After successful tocolysis patients were approached for s
tudy participation and randomized to receive either oral terbutaline o
r no therapy. The dose of terbutaline was individualized to achieve a
maternal pulse > 100 beats/min, and terbutaline was continued until 36
completed weeks of gestation. Recurrent preterm labor (contractions w
ith change in cervical examination) for either group was treated with
intravenous magnesium sulfate, and subsequent treatment was based on t
he previous randomization. RESULTS: Fifty-five patients were enrolled
(28 terbutaline, 27 no oral tocolytic). No difference was found betwee
n groups with respect to time gained (4.0 +/- 2.7 vs 4.6 +/- 3.1 weeks
, p = 0.412), gestational age at delivery (35.6 +/- 2.7 vs 36.1 +/- 2.
4 weeks p = 0.562), greater-than-or-equal-to 37 weeks at delivery (nin
e vs 13, p = 0.291), recurrent preterm labor (10 vs four, p = 0.104),
recurrent uterine contractions alone (five vs eight, p = 0.527), birth
weight (2616 +/- 633 gm vs 2645 +/- 599 gm, p = 0.785), special care
nursery admissions (eight vs six, p = 0.759), or neonatal respiratory
distress syndrome (three vs two, p 0.965). CONCLUSION: The use of oral
terbutaline after successful parenteral tocolysis failed to reduce th
e rate of preterm birth.