St Luke's Roosevelt Hospital, Columbia University College of Physicians and Surgeons, New York, NY 10019, USA.
Am J Med. 2011 Feb;124(2):128-35. doi: 10.1016/j.amjmed.2010.08.007.
Peripheral edema is a common adverse effect of calcium channel blockers. The addition of a renin-angiotensin system blocker, either an angiotensin-converting enzyme inhibitor or an ARB, has been shown to reduce peripheral edema in a dose-dependent way.
We performed a MEDLINE/COCHRANE search for all prospective randomized controlled trials in patients with hypertension, comparing calcium channel blocker monotherapy with calcium channel blocker/renin-angiotensin system blocker combination from 1980 to the present. Trials reporting the incidence of peripheral edema or withdrawal of patients because of edema and total sample size more than 100 were included in this analysis.
We analyzed 25 randomized controlled trials with 17,206 patients (mean age 56 years, 55% were men) and a mean duration of 9.2 weeks. The incidence of peripheral edema with calcium channel blocker/renin-angiotensin system blocker combination was 38% lower than that with calcium channel blocker monotherapy (P<.00001) (relative risk [RR] 0.62; 95% confidence interval [CI], 0.53-0.74). Similarly, the risk of withdrawal due to peripheral edema was 62% lower with calcium channel blocker/renin-angiotensin system blocker combination compared with calcium channel blocker monotherapy (P=.002) (RR 0.38; 95% CI, 0.22-0.66). ACE inhibitors were significantly more efficacious than ARBs in reducing the incidence of peripheral edema (P<.0001) (ratio of RR 0.74; 95% CI, 0.64-0.84) (indirect comparison).
In patients with hypertension, the calcium channel blocker/renin-angiotensin system blocker combination reduces the risk of calcium channel blocker-associated peripheral edema when compared with calcium channel blocker monotherapy. ACE inhibitor seems to be more efficacious than ARB in reducing calcium channel blocker-associated peripheral edema, but head-to-head comparison studies are needed to prove this.
外周水肿是钙通道阻滞剂的常见不良反应。添加肾素-血管紧张素系统阻滞剂(ACEI 或 ARB)已被证明可呈剂量依赖性减少外周水肿。
我们对 1980 年至今所有比较高血压患者中钙通道阻滞剂单药治疗与钙通道阻滞剂/肾素-血管紧张素系统阻滞剂联合治疗的前瞻性随机对照试验进行了 MEDLINE/COCHRANE 检索。纳入了分析报告外周水肿发生率或因水肿而停药以及总样本量超过 100 例的试验。
我们分析了 25 项随机对照试验,共纳入 17206 例患者(平均年龄 56 岁,55%为男性),平均随访时间为 9.2 周。与钙通道阻滞剂单药治疗相比,钙通道阻滞剂/肾素-血管紧张素系统阻滞剂联合治疗的外周水肿发生率低 38%(P<.00001)(相对风险 [RR] 0.62;95%置信区间 [CI],0.53-0.74)。同样,与钙通道阻滞剂单药治疗相比,钙通道阻滞剂/肾素-血管紧张素系统阻滞剂联合治疗因外周水肿而停药的风险低 62%(P=.002)(RR 0.38;95% CI,0.22-0.66)。与 ARB 相比,ACEI 降低外周水肿发生率的疗效更显著(P<.0001)(RR 0.74;95% CI,0.64-0.84)(间接比较)。
在高血压患者中,与钙通道阻滞剂单药治疗相比,钙通道阻滞剂/肾素-血管紧张素系统阻滞剂联合治疗可降低钙通道阻滞剂相关的外周水肿风险。与 ARB 相比,ACEI 似乎更能降低钙通道阻滞剂相关的外周水肿,但仍需进行头对头比较研究来证实这一点。