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静脉注射糖蛋白IIb/IIIa受体抑制剂治疗并发血小板减少症:一项汇总分析。

Thrombocytopenia complicating treatment with intravenous glycoprotein IIb/IIIa receptor inhibitors: a pooled analysis.

作者信息

Dasgupta H, Blankenship J C, Wood G C, Frey C M, Demko S L, Menapace F J

机构信息

Geisinger Medical Center, Penn State Geisinger Health System, and The Janet Weis Research Center, Danville, PA 17822, USA.

出版信息

Am Heart J. 2000 Aug;140(2):206-11. doi: 10.1067/mhj.2000.107554.

DOI:10.1067/mhj.2000.107554
PMID:10925331
Abstract

BACKGROUND

Despite the increasingly prevalent role of platelet glycoprotein (GP) IIb/IIIa receptor inhibitors in acute coronary syndromes and percutaneous coronary interventions, the incidence and clinical relevance of thrombocytopenia occurring with their use remain unclear.

METHODS

We identified 8 placebo-controlled, randomized, large trials of GP IIb/IIIa receptor inhibitors reporting the incidence of thrombocytopenia, grouped by severity. The clinical courses of 42 patients with GP IIb/IIIa-related thrombocytopenia in these studies and other case reports were reviewed for bleeding complications.

RESULTS

Abciximab increased mild thrombocytopenia compared with placebo (4.2% vs 2.0%; P <.001; odds ratio 2.14) and increased severe thrombocytopenia compared with placebo (1.0% vs 0.4%; P =.01; odds ratio 2.48). Small-molecule IIb/IIIa inhibitors did not significantly increase mild or severe thrombocytopenia compared with placebo. Mild thrombocytopenia occurred more frequently in acute coronary syndrome trials than in coronary intervention trials, even in patients not receiving any IIb/IIIa inhibitors. No major bleeding sequelae were reported in 23 patients with severe thrombocytopenia or in 19 patients with profound thrombocytopenia.

CONCLUSIONS

Abciximab, but not eptifibatide or tirofiban, increases the incidence of thrombocytopenia compared with placebo in patients also treated with heparin. Thrombocytopenia associated with GP IIb/IIIa inhibition does not routinely lead to severe bleeding complications.

摘要

背景

尽管血小板糖蛋白(GP)IIb/IIIa受体抑制剂在急性冠脉综合征和经皮冠状动脉介入治疗中的作用日益普遍,但其使用时发生血小板减少症的发生率及临床相关性仍不明确。

方法

我们确定了8项关于GP IIb/IIIa受体抑制剂的安慰剂对照、随机、大型试验,这些试验报告了按严重程度分组的血小板减少症发生率。对这些研究及其他病例报告中42例与GP IIb/IIIa相关血小板减少症患者的临床病程进行回顾,以了解出血并发症情况。

结果

与安慰剂相比,阿昔单抗增加了轻度血小板减少症的发生率(4.2%对2.0%;P<.001;比值比2.14),且与安慰剂相比增加了严重血小板减少症的发生率(1.0%对0.4%;P =.01;比值比2.48)。与安慰剂相比,小分子IIb/IIIa抑制剂未显著增加轻度或严重血小板减少症的发生率。轻度血小板减少症在急性冠脉综合征试验中比在冠状动脉介入试验中更常见,即使在未接受任何IIb/IIIa抑制剂的患者中也是如此。23例严重血小板减少症患者和19例极重度血小板减少症患者均未报告有严重出血后遗症。

结论

与安慰剂相比,在同时接受肝素治疗的患者中,阿昔单抗而非依替巴肽或替罗非班增加了血小板减少症的发生率。与GP IIb/IIIa抑制相关的血小板减少症通常不会导致严重出血并发症。

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