Maintenance treatment of preterm labor with the oxytocin antagonist atosiban. The Atosiban PTL-098 Study Group.

OBJECTIVES Patients admitted with an acute episode of preterm labor who respond to early intravenously administered tocolysis remain at risk of having subsequent episodes of preterm labor and preterm delivery. Several pharmacologic agents have been used in an attempt to reduce subsequent episodes of preterm labor, and all are associated with significant side effects. Atosiban, an oxytocin receptor antagonist, is effective in the treatment of an acute episode of preterm labor. This study was designed to compare the efficacy and safety of atosiban with those of placebo maintenance therapy in women with preterm labor who achieved uterine quiescence with intravenous atosiban. STUDY DESIGN A multicenter, double-blind, placebo-controlled trial was designed for patients in preterm labor who responded to early intravenous treatment with atosiban. Five hundred thirteen patients were randomly assigned to receive maintenance therapy, 252 to receive atosiban, and 251 to receive matching placebo. Maintenance therapy was administered as a continuous subcutaneous infusion, via pump, of 30 microg/min to the end of 36 weeks' gestation. The primary end point was the number of days from the start of maintenance therapy until the first recurrence of labor. A secondary end point was the percentage of patients receiving subsequent intravenous atosiban therapy. RESULTS The time (median) from the start of maintenance treatment to the first recurrence of labor was 32.6 days with atosiban and 27.6 days with placebo (P =.02). At least one subsequent intravenous atosiban treatment was needed by 61 atosiban patients (23%) and 77 placebo patients (31%). Except for injection site reactions, adverse event profiles of atosiban and placebo were comparable. There were 4 neonatal deaths reported in the atosiban group and 5 in the placebo group after the start of maintenance therapy. Infant outcomes (including birth weight) were comparable between maintenance and treatment groups. CONCLUSIONS Maintenance therapy with the oxytocin receptor antagonist atosiban can prolong uterine quiescence after successful treatment of an acute episode of preterm labor with atosiban. Treatment was well tolerated.

[1]  P. Husslein,et al.  Oxytocin receptors in the human uterus during pregnancy and parturition. , 1984, American journal of obstetrics and gynecology.

[2]  R. Liston,et al.  Double-blind, randomized, controlled trial of atosiban and ritodrine in the treatment of preterm labor: a multicenter effectiveness and safety study. , 2000, American journal of obstetrics and gynecology.

[3]  J. Minogue,et al.  The efficacy of oral terbutaline after intravenous tocolysis. , 1993, American journal of obstetrics and gynecology.

[4]  Brown Sm,et al.  Terbutaline sulfate in the prevention of recurrence of premature labor. , 1981 .

[5]  H. Zingg,et al.  Uterine oxytocin gene expression: a novel framework for oxytocin action , 1993, Regulatory Peptides.

[6]  R Lane,et al.  An oxytocin receptor antagonist (atosiban) in the treatment of preterm labor: a randomized, double-blind, placebo-controlled trial with tocolytic rescue. , 2000, American journal of obstetrics and gynecology.

[7]  N. Tejani,et al.  Terbutaline Sulfate in the Prevention of Recurrence of Premature Labor , 1981, Obstetrics and gynecology.

[8]  M. Escobedo Follow-up of prematurely born infants. , 1988, Clinical obstetrics and gynecology.

[9]  J. Morrison,et al.  The clinical efficacy of oral tocolytic therapy. , 1996, American journal of obstetrics and gynecology.

[10]  I. Chalmers,et al.  Beta‐mimetics in preterm labour: an overview of the randomized controlled trials , 1988, British journal of obstetrics and gynaecology.

[11]  J. Parer,et al.  Oral ritodrine maintenance in the treatment of preterm labor. , 1980, American journal of obstetrics and gynecology.

[12]  T. Goodwin,et al.  Dose Ranging Study of the Oxytocin Antagonist Atosiban in the Treatment of Preterm Labor , 1996 .

[13]  R. Hale,et al.  Long‐Term Tocolysis With Combined Intravenous Terbutaline and Magnesium Sulfate: A 10‐Year Study of 1000 Patients , 1994, Obstetrics and gynecology.

[14]  D. Schoenfeld The asymptotic properties of nonparametric tests for comparing survival distributions , 1981 .

[15]  C. Pauerstein,et al.  Do tocolytic agents stop preterm labor? A critical and comprehensive review of efficacy and safety. , 1993, American journal of obstetrics and gynecology.

[16]  B. Sibai,et al.  Oral terbutaline after parenteral tocolysis: a randomized, double-blind, placebo-controlled trial. , 1996, American journal of obstetrics and gynecology.

[17]  T. Goodwin,et al.  The effect of the oxytocin antagonist atosiban on preterm uterine activity in the human. , 1994, American journal of obstetrics and gynecology.

[18]  S. Hariharan,et al.  Oral tocolysis with magnesium chloride: a randomized controlled prospective clinical trial. , 1991, American journal of obstetrics and gynecology.

[19]  M. Keirse,et al.  Double‐blind evaluation of ritodrine sustained release for oral maintenance of tocolysis after active preterm labour , 1996, British journal of obstetrics and gynaecology.

[20]  R. Vogel,et al.  Oral terbutaline in the outpatient management of preterm labor. , 1995, American journal of obstetrics and gynecology.