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孕期原发性免疫性血小板减少症的母婴结局:一项回顾性研究。

Maternal and fetal outcomes of primary immune thrombocytopenia during pregnancy: A retrospective study.

作者信息

Gilmore K S, McLintock C

机构信息

National Women's Health, Auckland City Hospital, New Zealand.

出版信息

Obstet Med. 2018 Mar;11(1):12-16. doi: 10.1177/1753495X17727408. Epub 2017 Oct 25.

Abstract

OBJECTIVE

We reviewed outcomes of 52 pregnancies in 45 women with immune thrombocytopenic purpura who delivered at Auckland Hospital with an antenatal platelet count of <100 × 10/L.

OUTCOME MEASURES

Primary outcomes were maternal platelet count at delivery and treatment response. Secondary outcomes included post-partum haemorrhage (PPH).

RESULTS

Most women had thrombocytopenia at delivery. Treatment with prednisone was given in 14 (27%) pregnancies with responses considered safe for delivery in 11 pregnancies (79%). Women in eight pregnancies also received intravenous immunoglobulin; in five pregnancies (63%) a platelet response acceptable for delivery was achieved.Seventeen pregnancies (33%) were complicated by a PPH ≥500 mL. Ten pregnancies (19%) were complicated by a PPH ≥1000 mL. PPH was reported in all women with a platelet count <50 × 10/L at delivery.

CONCLUSIONS

There were no antenatal bleeding complications but PPH was common among women with platelet counts <50 × 10/L at the time of birth.

摘要

目的

我们回顾了45例免疫性血小板减少性紫癜女性的52次妊娠结局,这些女性在奥克兰医院分娩,产前血小板计数<100×10⁹/L。

结局指标

主要结局为分娩时的母体血小板计数和治疗反应。次要结局包括产后出血(PPH)。

结果

大多数女性在分娩时存在血小板减少。14例(27%)妊娠接受了泼尼松治疗,其中11例(79%)的治疗反应被认为对分娩安全。8例妊娠的女性还接受了静脉注射免疫球蛋白;5例(63%)妊娠实现了可接受的分娩血小板反应。17例(33%)妊娠并发PPH≥500 mL。10例(19%)妊娠并发PPH≥1000 mL。所有分娩时血小板计数<50×10⁹/L的女性均出现PPH。

结论

产前无出血并发症,但出生时血小板计数<50×10⁹/L的女性中PPH很常见。

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How I treat thrombocytopenia in pregnancy.我如何治疗妊娠期血小板减少症。
Blood. 2013 Jan 3;121(1):38-47. doi: 10.1182/blood-2012-08-448944. Epub 2012 Nov 13.
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Immune thrombocytopenia in pregnancy.妊娠合并免疫性血小板减少症。
Hematol Oncol Clin North Am. 2009 Dec;23(6):1299-316. doi: 10.1016/j.hoc.2009.08.005.
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Immune thrombocytopenic purpura in pregnancy.妊娠期免疫性血小板减少性紫癜
Curr Opin Hematol. 2007 Sep;14(5):574-80. doi: 10.1097/MOH.0b013e3282bf6dc2.

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