Lindmark G, Zador G, Nilsson B A
Acta Obstet Gynecol Scand Suppl. 1974;37:17-26.
Attempt to induce labour with PGF2alpha was made for various indications in 22 primiparous and 27 multiparous patients being between the 35th and 44th weeks of pregnancy. Intravenous infusion of PGF2alpha was started with 3 mug/min. and increased in steps of 3 mug/min. at intervals of about one hour until labour-like contractions were recorded. This dose level was then maintained until delivery. Uterine activity and fetal heart rate was monitored prior to and throughout the infusion. The clinical condition of the newborns was also assessed by Apgar score and by physical examination one and four days after delivery. Labour was successfully induced with total doses ranging between 0.4 and 8.4 mg. In 88 per cent of the cases this resulted in vaginal deliveries within 2 to 12 hours. The latter part of the first stage as well as the second stage were remarkably short. Uterine hypertonus was observed in five cases (10%). Other types of abnormal uterine contractility patterns were fairly common. These were, however, not associated with pathological FHR changes except in one case where severe late decelerations were observed following marked uterine hyperactivity. The condition of the newborns was generally good and maternal side effects were very rare. PGF2alpha seems particularly valuable in cases of pre-term inductions where low Bishop scores are present but the risk of overstimulation demands careful supervision, if possible with cardiotochographic monitoring.
对22例初产妇和27例经产妇进行了用前列腺素F2α引产的尝试,这些产妇妊娠周数在35至44周之间,引产指征各不相同。静脉输注前列腺素F2α起始剂量为3微克/分钟,每隔约1小时以3微克/分钟的幅度递增,直至记录到类似分娩的宫缩。然后维持该剂量水平直至分娩。在输注前及输注过程中监测子宫活动和胎儿心率。还通过阿普加评分以及产后1天和4天的体格检查评估新生儿的临床状况。引产成功,总剂量在0.4至8.4毫克之间。88%的病例在2至12小时内实现阴道分娩。第一产程的后半段以及第二产程明显缩短。5例(10%)出现子宫强直收缩。其他类型的异常子宫收缩模式相当常见。然而,除1例在明显子宫活动过度后观察到严重晚期减速外,这些均未伴有病理性胎心率变化。新生儿状况总体良好,母体副作用非常罕见。前列腺素F2α在宫颈成熟度评分低的早产引产病例中似乎特别有价值,但过度刺激的风险需要仔细监测,如有可能应进行胎心监护。