Murphy Michael F, Bussel James B
National Blood Service, Department of Haematology, John Radcliffe Hospital, University of Oxford, Oxford, UK.
Br J Haematol. 2007 Feb;136(3):366-78. doi: 10.1111/j.1365-2141.2006.06418.x.
There have been considerable advances in the clinical and laboratory diagnosis of alloimmune thrombocytopenia (AIT), and its postnatal and antenatal management. The antenatal management of AIT has been particularly problematic, because severe haemorrhage occurs as early as 16 weeks gestation and there is no non-invasive investigation that reliably predicts the severity of AIT in utero. The strategies for antenatal treatment have included the use of serial platelet transfusions that, while effective, are invasive and associated with significant morbidity and mortality. Maternal therapy involving the administration of intravenous immunoglobulin and/or steroids is also effective and associated with fewer risks to the fetus. Significant recent progress has involved refinement of maternal treatment, stratifying it according to the likely severity of AIT based on the history in previous pregnancies. However, the ideal antenatal treatment, which is effective without causing significant side-effects to the mother or fetus, has yet to be determined, and further clinical trials are needed.
在同种免疫性血小板减少症(AIT)的临床和实验室诊断以及产后和产前管理方面已经取得了相当大的进展。AIT的产前管理一直特别棘手,因为早在妊娠16周时就会发生严重出血,而且没有可靠的非侵入性检查能预测子宫内AIT的严重程度。产前治疗策略包括多次输注血小板,虽然有效,但具有侵入性,且伴有显著的发病率和死亡率。涉及静脉注射免疫球蛋白和/或类固醇的母体治疗也有效,且对胎儿的风险较小。最近的重大进展包括改进母体治疗,根据既往妊娠史对AIT的可能严重程度进行分层。然而,理想的产前治疗方法,即有效且不会对母亲或胎儿造成重大副作用的方法,尚未确定,还需要进一步的临床试验。