Hiremath Swapnil, Holden Rachel M, Fergusson Dean, Zimmerman Deborah L
Division of Nephrology, University of Ottawa, Kidney Research Centre, Ottawa, Ontario, Canada.
Clin J Am Soc Nephrol. 2009 Aug;4(8):1347-55. doi: 10.2215/CJN.00810209. Epub 2009 Jul 2.
Patients with end stage renal disease (ESRD) are often prescribed antiplatelet medications. However, these patients are also at increased risk of bleeding compared with the general population, and an aim was made to quantify this risk with antiplatelet agents.
DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: A systematic review of the literature (Medline, EMBASE, Cochrane CENTRAL and Google Scholar databases) was done to determine the bleeding risk in ESRD patients prescribed antiplatelet therapy. The secondary outcome was the effect on access thrombosis. All case series, cohort studies and clinical trials were considered if they included ten or more ESRD patients, assessed bleeding risk with antiplatelet agents, and lasted for more than 3 mo.
Sixteen studies, including 40,676 patients, were identified that met predefined inclusion criteria. Due to study heterogeneity and weaknesses in methodology, bleeding rates were not pooled across studies. However, the bleeding risk appears to be increased for hemodialysis patients treated with combination antiplatelet therapy. The results are mixed for studies using a single antiplatelet agent. Antiplatelet agents appear to be effective in preventing shunt and central venous catheter thrombosis, but not for preventing thrombosis of arteriovenous grafts.
The risks and benefits of antiplatelet agents in ESRD patients remain poorly defined. Until a clinical trial addresses this in the dialysis population, individual risk stratification taking into account the increased risk of bleeding should be considered before initiating antiplatelet agents, especially in combination therapy.
终末期肾病(ESRD)患者常被开具抗血小板药物。然而,与普通人群相比,这些患者出血风险也更高,本研究旨在量化使用抗血小板药物时的这种风险。
设计、地点、参与者及测量方法:对文献(Medline、EMBASE、Cochrane CENTRAL和谷歌学术数据库)进行系统综述,以确定接受抗血小板治疗的ESRD患者的出血风险。次要结果是对血管通路血栓形成的影响。所有病例系列、队列研究和临床试验,只要纳入10名或更多ESRD患者、评估抗血小板药物的出血风险且持续时间超过3个月,均纳入考虑。
共识别出16项研究,包括40676名患者,符合预先设定的纳入标准。由于研究的异质性和方法学上的缺陷,未对各研究的出血率进行汇总。然而,接受联合抗血小板治疗的血液透析患者出血风险似乎有所增加。使用单一抗血小板药物的研究结果不一。抗血小板药物似乎对预防分流和中心静脉导管血栓形成有效,但对预防动静脉移植物血栓形成无效。
抗血小板药物在ESRD患者中的风险和益处仍不明确。在针对透析人群的临床试验解决这一问题之前,在开始使用抗血小板药物,尤其是联合治疗时,应考虑个体风险分层,同时考虑到出血风险增加的因素。