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用于促进胎儿肺成熟的皮质类固醇:对先兆子痫和HELLP综合征孕妇的影响。

Corticosteroids for the enhancement of fetal lung maturity: impact on the gravida with preeclampsia and the HELLP syndrome.

作者信息

Magann E F, Martin R W, Isaacs J D, Blake P G, Morrison J C, Martin J N

机构信息

Department of Obstetrics and Gynecology, University of Mississippi Medical Center, Jackson 39216-4505.

出版信息

Aust N Z J Obstet Gynaecol. 1993 May;33(2):127-31. doi: 10.1111/j.1479-828x.1993.tb02374.x.

DOI:10.1111/j.1479-828x.1993.tb02374.x
PMID:8216107
Abstract

This study was undertaken to determine maternal impact of corticosteroids administered for the promotion of fetal lung maturity in mothers with the HELLP syndrome. Twenty-seven of 427 women with the HELLP syndrome treated between 1980-1991 received a full course of steroids prior to preterm delivery. This group was compared to 27 matched control patients with the HELLP syndrome who received no corticosteroids. Subjects were matched for maternal age, race, sex of the fetus, and severity of the HELLP syndrome. The antepartum platelet count stabilized or increased in 25 of 27 steroid-treated women in contrast to 0 of 15 control women (p < 0.00001). In comparison to control patients, LDH serum concentrations in steroid-treated patients stabilized or decreased and the SGOT/AST and SGPT/ALT stabilized or decreased during therapy (p < 0.005). The interval from delivery to platelet nadir in patients with Class III HELLP syndrome was shorter in the steroid-treated group (p < 0.008) than in untreated patients.

摘要

本研究旨在确定在患有HELLP综合征的母亲中使用皮质类固醇促进胎儿肺成熟对母亲的影响。1980年至1991年间接受治疗的427例HELLP综合征女性中,有27例在早产前接受了完整疗程的类固醇治疗。将该组与27例匹配的未接受皮质类固醇治疗的HELLP综合征对照患者进行比较。根据产妇年龄、种族、胎儿性别和HELLP综合征的严重程度对受试者进行匹配。27例接受类固醇治疗的女性中有25例产前血小板计数稳定或增加,而15例对照女性中无一例如此(p<0.00001)。与对照患者相比,接受类固醇治疗的患者血清乳酸脱氢酶(LDH)浓度稳定或降低,治疗期间谷草转氨酶/天冬氨酸转氨酶(SGOT/AST)和谷丙转氨酶/丙氨酸转氨酶(SGPT/ALT)稳定或降低(p<0.005)。在III级HELLP综合征患者中,类固醇治疗组从分娩到血小板最低点的间隔时间比未治疗患者短(p<0.008)。

相似文献

1
Corticosteroids for the enhancement of fetal lung maturity: impact on the gravida with preeclampsia and the HELLP syndrome.用于促进胎儿肺成熟的皮质类固醇:对先兆子痫和HELLP综合征孕妇的影响。
Aust N Z J Obstet Gynaecol. 1993 May;33(2):127-31. doi: 10.1111/j.1479-828x.1993.tb02374.x.
2
Corticosteroids for enhanced fetal lung maturation in patients with HELLP syndrome: impact on neonates.用于促进HELLP综合征患者胎儿肺成熟的皮质类固醇:对新生儿的影响。
Aust N Z J Obstet Gynaecol. 1993 May;33(2):131-5. doi: 10.1111/j.1479-828x.1993.tb02375.x.
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Antepartum corticosteroids: disease stabilization in patients with the syndrome of hemolysis, elevated liver enzymes, and low platelets (HELLP).产前使用糖皮质激素:溶血、肝酶升高和血小板减少综合征(HELLP)患者的病情稳定。
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Impact of high-dose corticosteroid therapy for patients with HELLP (hemolysis, elevated liver enzymes, and low platelet count) syndrome.大剂量皮质类固醇疗法对HELLP(溶血、肝酶升高和血小板计数降低)综合征患者的影响。
Am J Obstet Gynecol. 2000 Oct;183(4):921-4. doi: 10.1067/mob.2000.108869.
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Corticosteroid-induced arrest of HELLP syndrome progression in a marginally-viable pregnancy.皮质类固醇诱导边缘性存活妊娠中HELLP综合征病情进展的停滞。
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Corticosteroids for HELLP syndrome in pregnancy.孕期HELLP综合征的皮质类固醇治疗
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Addition of platelet transfusions to corticosteroids does not increase the recovery of severe HELLP syndrome.在皮质类固醇基础上加用血小板输注并不能增加重度HELLP综合征的恢复。
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The maternal benefits of corticosteroids with HELLP (hemolysis, elevated liver enzymes, low platelet count) syndrome.皮质类固醇对伴有HELLP(溶血、肝酶升高、血小板计数降低)综合征的孕产妇的益处。
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Effects of high-dose dexamethasone in postpartum women with class 1 haemolysis, elevated liver enzymes and low platelets (HELLP) syndrome.大剂量地塞米松对产后Ⅰ级溶血、肝酶升高及血小板减少(HELLP)综合征妇女的影响。
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Dexamethasone in the post-partum treatment of HELLP syndrome.地塞米松用于产后HELLP综合征的治疗。
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引用本文的文献

1
Prognostic Factors of the Efficacy of High-dose Corticosteroid Therapy in Hemolysis, Elevated Liver Enzymes, and Low Platelet Count Syndrome During Pregnancy: A Meta-analysis.孕期溶血、肝酶升高和血小板减少综合征大剂量皮质类固醇治疗疗效的预后因素:一项荟萃分析
Medicine (Baltimore). 2016 Mar;95(13):e3203. doi: 10.1097/MD.0000000000003203.
2
Corticosteroids for HELLP (hemolysis, elevated liver enzymes, low platelets) syndrome in pregnancy.妊娠期HELLP(溶血、肝酶升高、血小板减少)综合征的糖皮质激素治疗
Cochrane Database Syst Rev. 2010 Sep 8(9):CD008148. doi: 10.1002/14651858.CD008148.pub2.