Division of Newborn Medicine, Children's Hospital Boston and Harvard Medical School, 300 Longwood Avenue, Boston, MA 02115, USA.
J Perinatol. 2010 Dec;30(12):765-9. doi: 10.1038/jp.2010.50. Epub 2010 Apr 22.
The Food and Drug Administration recently approved two novel thrombopoiesis-stimulating agents, Romiplostim (AMG-531, Nplate) and Eltrombopag (Promacta), for the treatment of adults with immune thrombocytopenic purpura. For physicians taking care of critically ill neonates, this offers the opportunity of decreasing platelet transfusions and potentially improving the outcomes of neonates with severe and prolonged thrombocytopenia. However, several developmental factors need to be taken into consideration. First, the population of thrombocytopenic neonates likely to benefit from these agents needs to be carefully selected. Second, the mechanisms underlying neonatal and adult thrombocytopenia differ from each other and are incompletely understood, and pre-clinical evidence suggests that the response of neonates to thrombopoietic factors might be different from that of adults. Finally, the potential non-hematopoietic effects of thrombopoietin have not been well established. Here, we will discuss these issues in detail, and will highlight the critical developmental differences between neonates and adults that need to be considered as we think about introducing these agents into neonatal care.
美国食品和药物管理局最近批准了两种新型的促血小板生成素激动剂,罗米司亭(AMG-531,Nplate)和艾曲波帕(Promacta),用于治疗成人免疫性血小板减少性紫癜。对于照顾重症新生儿的医生来说,这为减少血小板输注和改善严重且持续血小板减少症新生儿的预后提供了机会。然而,有几个发育因素需要考虑。首先,需要仔细选择可能从这些药物中获益的血小板减少症新生儿人群。其次,新生儿和成人血小板减少症的发病机制不同,且尚未完全了解,临床前证据表明,新生儿对促血小板生成素的反应可能与成人不同。最后,血小板生成素的潜在非造血作用尚未得到很好的证实。在这里,我们将详细讨论这些问题,并强调新生儿和成人之间的关键发育差异,在考虑将这些药物引入新生儿护理时需要考虑这些差异。