Deetjen A, Heidland A, Pangerl A, Meyer-Sabellek W, Schaefer R M
Department of Nephrology, University of Würzburg, Germany.
Clin Nephrol. 1995 Jan;43(1):47-52.
Carvedilol is an antihypertensive agent which displays unselective beta-blocking, alpha 1-blocking and antioxidant properties. It is primarily metabolized by the liver and excreted via the biliary system. The compound is highly lipophilic and strongly bound to plasma proteins. Consequently, there is no elimination during hemodialysis. The efficacy, safety, and pharmacokinetic profile of carvedilol titrated to effect were investigated in an open clinical trial in 15 long-term hemodialysis patients with arterial hypertension over a period of 12 weeks. The drug was administered only on days without dialysis. After a wash-out phase of one week, carvedilol was started in a dose of 12.5 mg per day. All 15 patients were titrated according to the antihypertensive effect to a daily dose of 25 mg of carvedilol. Carvedilol was effective in lowering blood pressure in hemodialysis patients (RR systolic: 170 +/- 11 vs. 144 +/- 9 mmHg; RR diastolic: 98 +/- 10 vs. 85 +/- 10 mmHg). The pharmacokinetic parameters of carvedilol and its active metabolite M2, assessed in 12 of the 15 patients, were not influenced by the lack of renal function or intermittend haemodialysis. In particular, there was no accumulation of carvedilol or its metabolite M2. In terms of side effects, three patients had to be withdrawn from the trial, because of hypoglycemia (n = 1), insufficient blood pressure control (n = 1) and prolonged hypotension (n = 1). Taken together, these results indicate that carvedilol is a safe and efficacious antihypertensive agent which can be used in patients maintained by maintenance dialysis treatment.
卡维地洛是一种抗高血压药物,具有非选择性β受体阻断、α1受体阻断和抗氧化特性。它主要在肝脏代谢,并通过胆道系统排泄。该化合物具有高度脂溶性,与血浆蛋白紧密结合。因此,血液透析过程中不会有清除。在一项开放临床试验中,对15名患有动脉高血压的长期血液透析患者进行了为期12周的研究,以考察滴定至有效剂量的卡维地洛的疗效、安全性和药代动力学特征。该药物仅在非透析日给药。经过一周的洗脱期后,开始给予卡维地洛,剂量为每日12.5毫克。所有15名患者根据降压效果滴定至每日25毫克的卡维地洛剂量。卡维地洛对降低血液透析患者的血压有效(收缩压RR:170±11 vs. 144±9 mmHg;舒张压RR:98±10 vs. 85±10 mmHg)。在15名患者中的12名患者中评估的卡维地洛及其活性代谢物M2的药代动力学参数不受肾功能不全或间歇性血液透析的影响。特别是,卡维地洛及其代谢物M2没有蓄积。在副作用方面,三名患者因低血糖(n = 1)、血压控制不佳(n = 1)和低血压持续时间延长(n = 1)而不得不退出试验。综上所述,这些结果表明卡维地洛是一种安全有效的抗高血压药物,可用于维持性透析治疗的患者。