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Effects of angiotensin-converting enzyme inhibitors and angiotensin receptor blockers on cardiovascular events and residual renal function in dialysis patients: a meta-analysis of randomised controlled trials

机译:血管紧张素转化酶抑制剂和血管紧张素受体阻滞剂对透析患者心血管事件和残留肾功能的影响:随机对照试验的META分析

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Background The role of angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin receptor blockers (ARBs) reducing risk of cardiovascular events (CVEs) and preserving kidney function in patients with chronic kidney disease is well-documented. However, the efficacy and safety of these agents in dialysis patients is still a controversial issue. Methods We systematically searched MEDLINE, Embase, Cochrane Library and Wanfang for randomized trials. The relative risk (RR) reductions were calculated with a random-effects model. Major cardiovascular events, changes in GFR and drug-related adverse events were analyzed. Results Eleven trials included 1856 participants who were receiving dialysis therapy. Compared with placebo or other active agents groups, ARB therapy reduced the risk of heart failure events by 33% (RR 0.67, 95% CI 0.47 to 0.93) with similar decrement in blood pressure in dialysis patients. Indirect comparison suggested that fewer cardiovascular events happened during treatment with ARB (0.77, 0.63 to 0.94). The results indicated no significant differences between the two treatment regimens with regard to frequency of myocardial infarction (1.0, 0.45 to 2.22), stroke (1.16, 0.69 to 1.96), cardiovascular death (0.89, 0.64 to 1.26) and all-cause mortality (0.94, 0.75 to 1.17). Five studies reported the renoprotective effect and revealed that ACEI/ARB therapy significantly slowed the rate of decline in both residual renal function (MD 0.93?mL/min/1.73?m2, 0.38 to 1.47?mL/min/1.73?m2) and urine volume (MD 167?ml, 95% CI 21?ml to 357?ml). No difference in drug-related adverse events was observed in both treatment groups. Conclusions This study demonstrates that ACE-Is/ARBs therapy decreases the loss of residual renal function, mainly for patients with peritoneal dialysis. Overall, ACE-Is and ARBs do not reduce cardiovascular events in dialysis patients, however, treatment with ARB seems to reduce cardiovascular events including heart failure. ACE-Is and ARBs do not induce an extra risk of side effects.
机译:背景技术血管紧张素转换酶抑制剂(ACEIS)和血管紧张素受体阻滞剂(ARB)降低心血管事件(CVES)风险并在慢性肾疾病患者中保持肾功能的作用是良好的记录。然而,这些药剂在透析患者中​​的疗效和安全性仍然是一个有争议的问题。方法我们系统地搜索了Medline,Embase,Cochrane图书馆和Wanfang进行随机试验。用随机效应模型计算相对风险(RR)减少。分析了主要心血管事件,对GFR和药物相关不良事件的变化进行了分析。结果11项试验包括1856名接受透析治疗的参与者。与安慰剂或其他活性剂组相比,ARB疗法将心力衰竭事件的风险降低33%(RR 0.67,95%CI 0.47至0.93),透析患者血压同样下降。间接比较表明,在用arb(0.77,0.63至0.94)治疗过程中发生了更少的心血管事件。结果表明,在心肌梗死频率(1.0,0.45至2.22),中风(1.16,0.69至1.96),心血管死亡(0.89,0.64至1.26)和全导致死亡率( 0.94,0.75至1.17)。五项研究报告了一次逆保护作用,并揭示了Acei / Arb的治疗显着减缓了残留肾功能的下降率(MD 0.93?ml / min / 1.73?m 2 ,0.38至1.47?ml / min / 1.73?m 2 )和尿体积(MD 167?ml,95%CI 21-ml至357×ml)。在两种治疗组中观察到药物相关不良事件的差异。结论本研究表明,ACE-IS / ARBS治疗降低了残留肾功能的损失,主要针对腹膜透析的患者。总体而言,ACE-IS和ARB不会减少透析患者中​​的心血管事件,然而,ARB的治疗似乎减少了心血管事件,包括心力衰竭。 ACE-IS和ARB不会引起额外的副作用风险。

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