IJC:他汀类强化治疗益处仅限于非致死性事件

2012-01-01 MedSci原创 MedSci原创

12月23日,巴西学者在Int J Cardiol杂志上发表的一项荟萃分析"Impact of statin dose on major cardiovascular events: A mixed treatment comparison meta-analysis involving more than 175,000 patients"显示,他汀类强化治疗的益处仅限于非致死性心血管事件。

12月23日,巴西学者在Int J Cardiol杂志上发表的一项荟萃分析"Impact of statin dose on major cardiovascular events: A mixed treatment comparison meta-analysis involving more than 175,000 patients"显示,他汀类强化治疗的益处仅限于非致死性心血管事件。

数项安慰剂对照试验显示他汀类在减少心血管事件方面可产生益处。更为强化的治疗似乎与更大的获益相关。研究者对Medline和Cochrane CENTRAL数据库进行了系统检索,并利用随机效应贝叶斯混合治疗比较(MTC)模型综合安慰剂对照和他汀类直接比较试验。依据预期的低密度脂蛋白(LDL)胆固醇降低对他汀类剂量强度进行分类:≤30%为低,30~40%为中等,≥40%为高。转归指标为非致死性心肌梗死(MI)、卒中、冠脉血运重建以及冠脉、心血管和全因死亡。

结果显示,共有47项试验符合纳入标准。与中、小剂量相比,大剂量分别使非致死性MI减少28%和14%。大剂量同样减少了血运重建和卒中。强化治疗方案未使死亡率发生变化;与中、小剂量相比,大剂量的全因死亡率危险比分别为0.93和0.98。在分析中未发现统计学不一致性。(生物谷Bioon.com)

Impact of statin dose on major cardiovascular events: A mixed treatment comparison meta-analysis involving more than 175,000 patients

Rodrigo Antonini Ribeiro,Patricia Klarmann Ziegelmann,Bruce Bartholow Duncan,Steffan Frosi Stella,José Luiz da Costa Vieira,Luciane Maria Fabian Restelatto,Emílio Hideyuki Moriguchi,Carisi Anne Polanczyk

Background
The benefit of statins in the reduction of cardiovascular events was demonstrated in several placebo-controlled trials. More intensive therapy seems to be associated with greater benefit. Our objective was to compare different statin doses in the reduction of cardiovascular events and deaths, combining direct and indirect evidence, through mixed treatment comparisons (MTC).
Methods
We conducted a systematic review in MEDLINE and Cochrane CENTRAL. A random-effects Bayesian MTC model was used to combine placebo-controlled and direct statin comparison trials. Intensity of statin doses was classified according to expected LDL-cholesterol reduction effect: ≤30% as low; 30–40%, intermediate, and ≥40%, high. Outcomes evaluated were non-fatal myocardial infarction (MI), stroke, coronary revascularization and coronary, cardiovascular and all-cause death. Inconsistency was assessed with split-node methodology.
Results
47 trials (11 with direct statin comparisons) were included. High doses reduced non-fatal MI by 28% (95% CI: 18%–36%) and by 14% (7%–21%) when compared to low and intermediate doses, respectively. High doses also diminished revascularization [RR versus low and intermediate doses of 0.81 (0.69–0.95) and 0.88 (0.77–0.99), respectively] and stroke [RR of 0.83 (0.68–0.99) against low doses]. Regimen intensity did not change death rates (e.g., for all-cause mortality, RRs of 0.93 (0.80–1.06) and 0.98 (0.87–1.08) for high vs. low and intermediate doses, respectively). No statistical inconsistencies were found in the analyses.
Conclusions
In this study, in which all available evidence from statin trials was simultaneously analyzed, the benefit of more intensive therapy was restricted to non-fatal events.

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