Abstract | OBJECTIVE: METHODS: RESULTS: In women randomized to receive atosiban (n=295) or usual care (n=290), significantly more women receiving atosiban remained undelivered at 48 h with no alternative tocolytic compared with usual care (77.6% vs. 56.6%; P<0.001). The proportion of women remaining undelivered after 48 h was comparable between the treatment groups. However, more women in the atosiban group required no additional tocolytics (85.1% vs. 62.8%; P<0.001). Maternal and fetal safety was significantly superior with atosiban. Neonatal safety was comparable. CONCLUSIONS: These findings support the use of atosiban to delay preterm birth and are consistent with previously conducted, randomized, controlled trials. Atosiban was associated with fewer maternal and fetal adverse events compared with other tocolytics, and presented no safety concerns for either the mother or the unborn baby.
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Authors | Peter Husslein, Luis Cabero Roura, Joachim W Dudenhausen, Hanns Helmer, René Frydman, Nicola Rizzo, Dirk Schneider |
Journal | Journal of perinatal medicine
(J Perinat Med)
Vol. 35
Issue 4
Pg. 305-13
( 2007)
ISSN: 0300-5577 [Print] Germany |
PMID | 17614750
(Publication Type: Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
- Tocolytic Agents
- atosiban
- Vasotocin
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Topics |
- Adolescent
- Adult
- Endpoint Determination
- Female
- Humans
- Infant, Newborn
- Obstetric Labor, Premature
(drug therapy)
- Pregnancy
- Prospective Studies
- Safety
- Tocolysis
(adverse effects)
- Tocolytic Agents
(adverse effects, therapeutic use)
- Vasotocin
(adverse effects, analogs & derivatives, therapeutic use)
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