Ibrahim Homam, Rao Sunil V
New York University Langone Medical Center, 530 1st Ave skirball 9V, New York, NY, 10016, USA.
Duke University Medical Center and Duke Clinical Research Institute, Durham, NC, USA.
J Thromb Thrombolysis. 2017 May;43(4):519-527. doi: 10.1007/s11239-017-1483-3.
Oral Antiplatelet Drugs (OAD) have a proven track record in the risk reduction of major cardiovascular events in patients with cardiovascular disease and normal kidney function. However, major gaps exist in our understanding of their effects on thrombosis and bleeding in chronic kidney disease (CKD). Clinical practice guidelines are ambiguous about use of such drugs in CKD patients, because patients with moderate to severe CKD were systematically excluded from clinical trials evaluating the efficacy and safety of OAD. Paradoxically, CKD patients are at high risk of thrombosis and major bleeding events. Thus, choosing the right combination of OAD for cardiovascular protection in these patients is challenging. Patients with CKD exhibit high rates of OAD hyporesponsiveness. It is, therefore, imperative to explore the mechanisms responsible for poor response to OAD in CKD patients in order to use these drugs more safely and effectively. This review explores suggested mechanisms of platelet dysfucntion in CKD patients and the available evidence on the efficacy and safety of oral antiplatelet drugs in patients with renal dysfunction.
口服抗血小板药物(OAD)在降低心血管疾病且肾功能正常患者的主要心血管事件风险方面有着已被证实的良好记录。然而,我们对其在慢性肾脏病(CKD)患者中对血栓形成和出血影响的了解存在重大差距。临床实践指南对于在CKD患者中使用此类药物含糊不清,因为中重度CKD患者被系统性地排除在评估OAD疗效和安全性的临床试验之外。矛盾的是,CKD患者发生血栓形成和重大出血事件的风险很高。因此,为这些患者选择合适的OAD组合以进行心血管保护具有挑战性。CKD患者中OAD低反应率很高。因此,必须探究CKD患者对OAD反应不佳的机制,以便更安全有效地使用这些药物。本综述探讨了CKD患者血小板功能障碍的潜在机制以及关于口服抗血小板药物在肾功能不全患者中疗效和安全性的现有证据。