Tapia Pérez J Humberto, Yildiz O Can, Schneider Thomas, Nimsky Christopher
Klinik für Neurochirurgie, Philipps-University Marburg, Marburg, Germany.
Klinik für Neurochirurgie, Universitätsklinik Otto von Guericke Magdeburg, Magdeburg, Germany.
J Stroke Cerebrovasc Dis. 2015 Nov;24(11):2521-6. doi: 10.1016/j.jstrokecerebrovasdis.2015.06.036. Epub 2015 Sep 18.
Growing evidence demonstrates the neuroprotective effects of statins, and the risk to develop an intracerebral hemorrhage (ICH) using statins has been refuted. However, some controversy remains regarding their role in the acute phase after ICH onset. Therefore, we performed a systematic review to investigate this issue.
We searched in MEDLINE, Web of Knowledge, and Scopus databases for studies examining the outcome in patients with spontaneous ICH and statin use. The analysis was performed for short-term (≤3 months) and long-term outcome (≥6 months) and a further subanalysis considered studies seeking for the effects of the discontinuation of statin after ICH onset. A random-effect model was applied, and country was used as a cofactor for meta-regression; odds ratios (ORs) with 95% confidence intervals (CIs) are offered.
A total of 17 studies were included, only 1 pseudo cohort trial assessed the new use of statin after ICH onset and 3 studies evaluated the suspension of statin after ICH onset, the rest of the studies focused on the effect of the regular use of statin before ICH onset. The number of patients with an ICH exposed and not exposed to statins were 3455 and 11,821, respectively. The absolute short-term mortality was 27.3% in statin users and 33% in nonusers that represented a significant risk reduction of mortality (OR, .73; 95% CI, .54-.97). For long-term mortality, the effect was less evident (OR, .71; 95% CI, .43-1.15). The analysis of the 3 studies assessing the discontinuation of statins suggested a reduction of mortality risk by continuing statin (OR, .14; 95% CI, .1-.20).
The current evidence suggests that continuing statin after ICH onset might be highly related to improvement of the outcome of patients with ICH. Despite this strong suggestion, randomized controlled trials should be performed to further investigate this association.
越来越多的证据表明他汀类药物具有神经保护作用,且使用他汀类药物引发脑出血(ICH)的风险已被否定。然而,关于其在ICH发病后急性期的作用仍存在一些争议。因此,我们进行了一项系统评价以研究此问题。
我们在MEDLINE、Web of Knowledge和Scopus数据库中检索了关于自发性ICH患者使用他汀类药物的研究结果。对短期(≤3个月)和长期结果(≥6个月)进行了分析,并进一步对研究ICH发病后停用他汀类药物效果的研究进行了亚分析。应用随机效应模型,并将国家作为元回归的协变量;给出了95%置信区间(CI)的比值比(OR)。
共纳入17项研究,只有1项伪队列试验评估了ICH发病后他汀类药物的新使用情况,3项研究评估了ICH发病后他汀类药物的停用情况,其余研究关注ICH发病前常规使用他汀类药物的效果。暴露于他汀类药物和未暴露于他汀类药物的ICH患者数量分别为3455例和11821例。他汀类药物使用者的绝对短期死亡率为27.3%,非使用者为33%,这表明死亡率显著降低(OR,0.73;95%CI,0.54 - 0.97)。对于长期死亡率,效果不太明显(OR,0.71;95%CI,0.43 - 1.15)。对3项评估他汀类药物停用情况的研究分析表明,继续使用他汀类药物可降低死亡风险(OR,0.14;95%CI,0.1 - 0.20)。
目前的证据表明,ICH发病后继续使用他汀类药物可能与改善ICH患者的预后高度相关。尽管有此强烈提示,但仍应进行随机对照试验以进一步研究这种关联。