Department of Neurology, Universitair Ziekenhuis Brussel, Center for Neurosciences, Vrije Universiteit Brussel, Brussel, Belgium.
Acta Neurol Belg. 2011 Dec;111(4):261-7.
Animal pre-clinical studies suggest that statins may have neuroprotective effects in acute ischaemic stroke. Statins might also increase the risk of developing haemorrhagic transformation after thrombolytic treatment.
We performed a systematic review and included studies that compared good functional outcome, defined as a modified Rankin Scale (mRS) score < or = 2 at 3 months, in-hospital mortality and risk of symptomatic haemorrhagic transformation, between pre -stroke statin users and non users with acute ischaemic stroke.
Eleven studies met our predefined inclusion criteria. Statin therapy before stroke-onset was associated with a lower risk of in-hospital mortality (OR 0.56; 95% CI: 0.40 to 0.78, P < 0.0006). There was no difference between the two groups for good functional outcome at 3 months (OR 1.01; 95% CI: 0.64 to 1.61, P = 0.96). Statin use was associated with an increased risk of developing symptomatic haemorrhagic transformation after thrombolytic therapy (OR 2.34; 95% CI 1.31 to 4.17, P = 0.004).
Our meta-analysis suggests that pretreatment with statins does not improve 3 months functional outcome, defined as independence on mRS, but decreases in-hospital mortality and increases the risk of developing a symptomatic haemorrhagic transformation in patients treated with thrombolysis.
动物临床前研究表明他汀类药物可能对急性缺血性脑卒中具有神经保护作用。他汀类药物也可能增加溶栓治疗后发生出血性转化的风险。
我们进行了系统评价,纳入了比较急性缺血性脑卒中患者在发病前使用他汀类药物与未使用他汀类药物治疗后 3 个月时良好功能结局(改良 Rankin 量表评分<或=2)、住院死亡率和症状性出血性转化风险的研究。
11 项研究符合我们预先设定的纳入标准。发病前他汀类药物治疗与住院死亡率降低相关(OR 0.56;95%CI:0.40 至 0.78,P<0.0006)。两组在 3 个月时的良好功能结局(OR 1.01;95%CI:0.64 至 1.61,P=0.96)方面无差异。他汀类药物的使用与溶栓治疗后发生症状性出血性转化的风险增加相关(OR 2.34;95%CI 1.31 至 4.17,P=0.004)。
我们的荟萃分析表明,在溶栓治疗前使用他汀类药物并不能改善 3 个月的功能结局(定义为改良 Rankin 量表评分独立),但降低了住院死亡率,并增加了接受溶栓治疗的患者发生症状性出血性转化的风险。