Kerkhoffs Jean-Louis H, Eikenboom Jeroen C J, van de Watering Leo M G, van Wordragen-Vlaswinkel Rinie J, Wijermans Pierre W, Brand Anneke
Sanquin Blood Bank, South West Region, Leiden, The Netherlands.
Transfusion. 2008 Sep;48(9):1959-65. doi: 10.1111/j.1537-2995.2008.01799.x. Epub 2008 Jun 28.
Despite supportive care with platelet (PLT) transfusions, bleeding complications occur in a substantial number of patients with thrombocytopenia due to cytotoxic therapy. Moreover, refractoriness to PLT transfusions remains a frequently encountered problem. The clinical impact of PLT transfusion failure was investigated in 117 patients, part of a randomized PLT transfusion trial, which excluded patients with HLA and/or HPA alloantibodies.
Between October 2003 and April 2005, a multicenter randomized controlled trial, testing the clinical efficacy of PLTs stored in plasma compared to PLT additive solution (PAS II), was performed. Using multiple regression analysis of observational data of patients randomized in one of the participating centers, the occurrence of PLT transfusion refractoriness was analyzed for a relation with bleeding complications and patient survival.
PLT transfusion failure occurred at least once in 49.6 percent of the patients. Mild to moderate bleeding complications occurred in 19 percent of the patients. PLT transfusion failure was, independently from thrombocytopenia, positively associated with bleeding complications (odds ratio, 3.4; 95% confidence interval, 1.1-11). Moreover, patients experiencing one or more 24-hour PLT transfusion failures had, compared to patients always showing a sufficient 24-hour increment, a significantly reduced median survival of 491 days (interquartile range [IQR], 156-858 days) versus 825 days (IQR, 355-996 days), respectively. In a Cox regression model, the effect on survival was independent of therapy, diagnosis, and age.
Our results suggest that PLT transfusion failure might be a sensitive clinical marker for the occurrence of bleeding and impaired patient survival. PLT transfusion failure, bleeding complications, and decreased survival could be manifestations of a more severe degree of endothelial damage.
尽管采用血小板(PLT)输注进行支持性治疗,但由于细胞毒性疗法导致血小板减少的大量患者仍会出现出血并发症。此外,对PLT输注的难治性仍然是一个常见问题。在一项随机PLT输注试验的117例患者中研究了PLT输注失败的临床影响,该试验排除了患有HLA和/或HPA同种抗体的患者。
2003年10月至2005年4月期间,进行了一项多中心随机对照试验,比较了储存在血浆中的PLT与PLT添加剂溶液(PAS II)的临床疗效。通过对参与中心之一随机分组患者的观察数据进行多元回归分析,分析PLT输注难治性的发生与出血并发症和患者生存的关系。
49.6%的患者至少发生过一次PLT输注失败。19%的患者出现轻度至中度出血并发症。PLT输注失败与血小板减少无关,与出血并发症呈正相关(优势比,3.4;95%置信区间,1.1-11)。此外,与始终显示足够24小时增量的患者相比,经历一次或多次24小时PLT输注失败的患者中位生存期显著缩短,分别为491天(四分位间距[IQR],156-858天)和825天(IQR,355-996天)。在Cox回归模型中,对生存的影响独立于治疗、诊断和年龄。
我们的结果表明,PLT输注失败可能是出血发生和患者生存受损的敏感临床标志物。PLT输注失败、出血并发症和生存期缩短可能是更严重程度内皮损伤的表现。