Cardiovascular Division, Brigham and Women's Hospital, Boston, MA, USA.
Eur J Heart Fail. 2010 Sep;12(9):936-42. doi: 10.1093/eurjhf/hfq094. Epub 2010 Jun 5.
Randomized clinical trials have suggested that treatment of anaemia with erythropoiesis-stimulating agents (ESAs) in patients with cancer or chronic kidney disease may increase cardiovascular risk. We therefore examined the effect of treating anaemia with an ESA in patients with heart failure in a meta-analysis of randomized clinical trials, including the recently reported TREAT study.
We performed a systematic review and meta-analysis of all prospective, randomized, controlled studies of ESAs enrolling patients with heart failure and reporting data on mortality or non-fatal heart failure events. Of 10 trials initially identified by our search strategy, we pooled data from 9 placebo-controlled studies enrolling a total of 2039 patients, of whom 1023 (50.2%) were allocated to ESA treatment. The pooled risk ratio for ESA treatment relative to placebo was 1.03 [95% confidence interval (CI): 0.89-1.21, P = 0.68] for overall mortality and 0.95 (95% CI: 0.82-1.10, P = 0.46) for worsening heart failure.
The use of ESAs to manage anaemia in patients with heart failure was associated with a neutral effect on both mortality and non-fatal heart failure events. Definitive assessment of the balance of risk and benefit in this population awaits the completion of a randomized clinical trial adequately powered to assess clinical outcomes.
随机临床试验表明,在癌症或慢性肾脏病患者中使用促红细胞生成素刺激剂(ESA)治疗贫血可能会增加心血管风险。因此,我们在一项随机临床试验的荟萃分析中检查了在心力衰竭患者中使用 ESA 治疗贫血的效果,包括最近报告的 TREAT 研究。
我们对所有纳入心力衰竭患者并报告死亡率或非致命性心力衰竭事件数据的前瞻性、随机、对照 ESA 研究进行了系统评价和荟萃分析。通过我们的搜索策略最初确定的 10 项试验中,我们汇总了来自 9 项安慰剂对照研究的数据,这些研究共纳入了 2039 名患者,其中 1023 名(50.2%)被分配到 ESA 治疗组。ESA 治疗与安慰剂相比的总体死亡率的合并风险比为 1.03(95%可信区间:0.89-1.21,P = 0.68),心力衰竭恶化的风险比为 0.95(95%可信区间:0.82-1.10,P = 0.46)。
在心力衰竭患者中使用 ESA 治疗贫血对死亡率和非致命性心力衰竭事件的影响均为中性。在这个人群中,风险和获益的平衡的明确评估需要等待一项充分评估临床结局的随机临床试验完成。