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多胎妊娠的延迟间隔分娩

Authors
Richard P Porreco, MD
Lisa J Farkouh, MD
Section Editor
Charles J Lockwood, MD, MHCM
Deputy Editor
Vanessa A Barss, MD, FACOG
Translators
孙瑜, 主任医师,副教授

引言

多胎妊娠通常会并发自发性早产,因此新生儿具有住院时间延长、发生严重并发症和死亡的风险。通常情况下,多胎妊娠的所有胎儿会在很短的间隔内全部分娩;但在特定情况下,多胎妊娠中的一胎早产时可能并不需要娩出其余胎儿。对于处于关键孕龄时的胎儿,延长同胞之间分娩的间隔时间或有可能改善新生儿的存活率,并降低早产引起的并发症的发病率。

本专题将讨论延迟间隔分娩适用人群的选择方法及对这类妊娠的处理。对现有信息的解读充满了挑战,因为其证据基础仅由一些病例报告、小规模的病例系列研究和文献回顾构成,而缺乏随机试验的支持。确认偏倚是一个重要的问题,因为被报道的往往是有成功结局的病例,而许多失败的病例却未被报道。

延迟间隔分娩的适用人群

当多胎妊娠者因为母体、产科或胎儿因素而需要娩出部分胎儿,并且同时娩出其他未受上述因素影响的胎儿会导致其死亡或发生严重并发症时,我们会与患者讨论选择延迟间隔分娩的问题。这是一种罕见的事件,同时也是一项复杂的临床决策,因为不同的利益相关者难以客观地对潜在的风险和收益进行量化和比较。关于如何选择或排除延迟间隔分娩的适用人群,目前尚没有高质量数据,并且对于如何选择适当的妊娠,目前也没有广泛接受的指南。

我们认为,最适合接受延迟间隔分娩的多胎妊娠女性需满足的条件包括:孕龄较小(<24周),并且仅第一胎(先娩出的胎儿)因早产、宫颈机能不全、胎膜早破或胎死宫内而自然分娩。

对于妊娠已满28周的女性,我们不予以延迟间隔分娩,因为在我们的机构中,此孕龄时娩出的新生儿一般结果较好。在继续进行的妊娠中,一些妊娠并发症会有很高的风险导致母体或胎儿发生严重的并发症/死亡,例如重度子痫前期、胎盘早剥和存留胎儿的羊膜腔感染。在这些情况下,我们也会避免进行延迟间隔分娩。在我们的实践中,发现羊膜腔感染累及首个娩出的胎儿或需要缩宫素催产来利于胎儿分娩,该妊娠女性仍可能适合延迟间隔分娩;然而,存留胎儿有羊膜腔感染的证据(通过羊膜穿刺术获得)是这种方法的禁忌证,将需要彻底终止妊娠。

                 

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Literature review current through: 2017-06 . | This topic last updated: 2017-06-01.
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References
Top
  1. Beinder E, Lang N. Delayed interval delivery in a twin pregnancy with monochorionic placenta. Am J Obstet Gynecol 1997; 176:254.
  2. Roman AS, Fishman S, Fox N, et al. Maternal and neonatal outcomes after delayed-interval delivery of multifetal pregnancies. Am J Perinatol 2011; 28:91.
  3. Berghella V, Davis GH, Macones GA, Wapner RJ. Prolongation of pregnancy and survival of remaining fetuses after operative evacuation of one triplet at 18 weeks' gestation. Obstet Gynecol 1996; 88:665.
  4. Porreco RP, Sabin ED, Heyborne KD, Lindsay LG. Delayed-interval delivery in multifetal pregnancy. Am J Obstet Gynecol 1998; 178:20.
  5. Farkouh LJ, Sabin ED, Heyborne KD, et al. Delayed-interval delivery: extended series from a single maternal-fetal medicine practice. Am J Obstet Gynecol 2000; 183:1499.
  6. Hamersley SL, Coleman SK, Bergauer NK, et al. Delayed-interval delivery in twin pregnancies. J Reprod Med 2002; 47:125.
  7. Cristinelli S, Fresson J, André M, Monnier-Barbarino P. Management of delayed-interval delivery in multiple gestations. Fetal Diagn Ther 2005; 20:285.
  8. Zhang J, Hamilton B, Martin J, Trumble A. Delayed interval delivery and infant survival: a population-based study. Am J Obstet Gynecol 2004; 191:470.
  9. Oyelese Y, Ananth CV, Smulian JC, Vintzileos AM. Delayed interval delivery in twin pregnancies in the United States: Impact on perinatal mortality and morbidity. Am J Obstet Gynecol 2005; 192:439.
  10. Arabin B, van Eyck J. Delayed-interval delivery in twin and triplet pregnancies: 17 years of experience in 1 perinatal center. Am J Obstet Gynecol 2009; 200:154.e1.
  11. Reinhard J, Reichenbach L, Ernst T, et al. Delayed interval delivery in twin and triplet pregnancies: 6 years of experience in one perinatal center. J Perinat Med 2012; 40:551.
  12. Kaneko M, Kawagoe Y, Oonishi J, et al. Case report and review of delayed-interval delivery for dichorionic, diamniotic twins with normal development. J Obstet Gynaecol Res 2012; 38:741.
  13. Rosbergen M, Vogt HP, Baerts W, et al. Long-term and short-term outcome after delayed-interval delivery in multi-fetal pregnancies. Eur J Obstet Gynecol Reprod Biol 2005; 122:66.
  14. Arias F. Delayed delivery of multifetal pregnancies with premature rupture of membranes in the second trimester. Am J Obstet Gynecol 1994; 170:1233.
  15. Kalchbrenner MA, Weisenborn EJ, Chyu JK, et al. Delayed delivery of multiple gestations: maternal and neonatal outcomes. Am J Obstet Gynecol 1998; 179:1145.
  16. Smith GN, Brien JF. Use of nitroglycerin for uterine relaxation. Obstet Gynecol Surv 1998; 53:559.
  17. Lavery JP, Austin RJ, Schaefer DS, Aladjem S. Asynchronous multiple birth. A report of five cases. J Reprod Med 1994; 39:55.
  18. Flynn A, Scott F, Birrell W, Evans N. Delayed-interval delivery in a quadruplet pregnancy: the use of transperineal ultrasound and cervical cerclage. Aust N Z J Obstet Gynaecol 1995; 35:280.
  19. Boehm FH, Lombardi SJ, Rosemond RL. Immediate cerclage following delivery of one nonviable twin. A report of three cases. J Reprod Med 1992; 37:986.
  20. Zhang J, Johnson CD, Hoffman M. Cervical cerclage in delayed interval delivery in a multifetal pregnancy: a review of seven case series. Eur J Obstet Gynecol Reprod Biol 2003; 108:126.
  21. Doger E, Cakiroglu Y, Ceylan Y, et al. Obstetric and neonatal outcomes of delayed interval delivery in cerclage and non-cerclage cases: an analysis of 20 multiple pregnancies. J Obstet Gynaecol Res 2014; 40:1853.
  22. Ziegler WF, Welgoss J. Delayed delivery of a triplet pregnancy without surgical intervention: a case report. Am J Perinatol 1996; 13:191.
  23. Porreco RP. World Symposium of Perinatal Medicine. Boston, 2004.
  24. Livingston JC, Livingston LW, Ramsey R, Sibai BM. Second-trimester asynchronous multifetal delivery results in poor perinatal outcome. Obstet Gynecol 2004; 103:77.
  25. Hoffman MK, Sciscione AC. Sepsis and multisystem organ failure in a woman attempting interval delivery in a triplet pregnancy: a case report. J Reprod Med 2004; 49:387.