Eculizumab for the treatment of preeclampsia/HELLP syndrome

被引:144
作者
Burwick, R. M. [1 ]
Feinberg, B. B. [1 ]
机构
[1] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Obstet & Gynecol,Div Maternal Fetal Med, Boston, MA 02115 USA
关键词
Complement; C5; Eculizumab; Preeclampsia; HELLP syndrome; Pregnancy; COMPLEMENT ACTIVATION; HELLP-SYNDROME; ANGIOGENIC FACTORS; MANAGEMENT; PREGNANCY;
D O I
10.1016/j.placenta.2012.11.014
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Severe preeclampsia with hemolysis, elevated liver enzymes and low platelets (HELLP) syndrome is a leading cause of maternal and neonatal morbidity and mortality worldwide. Occurrence at an extremely premature gestational age is most challenging as there are dichotomous imperatives: delivery as definitive therapy for maternal health vs. prolongation of pregnancy to avoid prematurity and associated morbidities. We describe a patient presenting with severe preeclampsia/HELLP syndrome at 26 weeks gestation that was treated with Eculizumab, a targeted inhibitor of complement protein C5, which resulted in marked clinical improvement and complete normalization of lab parameters. Pregnancy was prolonged 17 days, likely resulting in a reduction of neonatal morbidity with its associated short and long-term health care costs. Successful use of Eculizumab in this case suggests that complement inhibition may be an effective treatment strategy for severe preeclampsia/HELLP syndrome. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:201 / 203
页数:3
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