Department of Medicine, Division of Cardiovascular Medicine, John Hopkins University School of Medicine, Baltimore, Maryland, USA.
Department of Medicine, Division of Cardiovascular Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Emerg Med J. 2018 Sep;35(9):559-563. doi: 10.1136/emermed-2017-207065. Epub 2018 Jun 19.
Beta blockers (β-blockers) remain a standard therapy in the early treatment of acute coronary syndromes. However, β-blocker therapy in patients with cocaine-associated chest pain (CACP) continues to be an area of debate due to the potential risk of unopposed α-adrenergic stimulation and coronary vasospasm. Therefore, we performed a systematic review and meta-analysis of available studies to compare outcomes of β-blocker versus no β-blocker use among patients with CACP.
We searched the MEDLINE and EMBASE databases through September 2016 using the keywords 'beta blocker', 'cocaine' and commonly used β-blockers ('atenolol', 'bisoprolol', 'carvedilol', 'esmolol', 'metoprolol' and 'propranolol') to identify studies evaluating β-blocker use among patients with CACP. We specifically focused on studies comparing outcomes between β-blocker versus no β-blocker usage in patients with CACP. Studies without a comparison between β-blocker and no β-blocker use were excluded. Outcomes of interest included non-fatal myocardial infarction (MI) and all-cause mortality. Quantitative data synthesis was performed using a random-effects model and heterogeneity was assessed using Q and Istatistics.
A total of five studies evaluating 1794 subjects were included. Overall, there was no significant difference on MI in patients with CACP on β-blocker versus no β-blocker (OR 1.36, 95% CI 0.68 to 2.75; p=0.39). Similarly, there was no significant difference in all-cause mortality in patients on β-blocker versus no β-blocker (OR 0.68, 95% CI 0.26 to 1.79; p=0.43).
In patients presenting with acute chest pain and underlying cocaine, β-blocker use does not appear to be associated with an increased risk of MI or all-cause mortality.
β受体阻滞剂(β-blockers)仍然是急性冠状动脉综合征早期治疗的标准疗法。然而,由于潜在的去甲肾上腺素能刺激和冠状动脉痉挛的风险,可卡因相关胸痛(CACP)患者的β受体阻滞剂治疗仍然存在争议。因此,我们对现有的研究进行了系统评价和荟萃分析,以比较 CACP 患者使用β受体阻滞剂与不使用β受体阻滞剂的结局。
我们通过关键词“β受体阻滞剂”、“可卡因”和常用的β受体阻滞剂(“阿替洛尔”、“比索洛尔”、“卡维地洛”、“艾司洛尔”、“美托洛尔”和“普萘洛尔”),在 MEDLINE 和 EMBASE 数据库中进行了截至 2016 年 9 月的检索,以确定评估 CACP 患者使用β受体阻滞剂的研究。我们特别关注比较 CACP 患者使用β受体阻滞剂与不使用β受体阻滞剂的结局的研究。未在β受体阻滞剂和不使用β受体阻滞剂之间进行比较的研究被排除在外。感兴趣的结局包括非致死性心肌梗死(MI)和全因死亡率。使用随机效应模型进行定量数据综合,并使用 Q 和 I 统计量评估异质性。
共有五项研究评估了 1794 名患者。总体而言,在 CACP 患者中,β受体阻滞剂与不使用β受体阻滞剂相比,MI 发生率没有显著差异(OR 1.36,95%置信区间 0.68 至 2.75;p=0.39)。同样,β受体阻滞剂与不使用β受体阻滞剂的患者的全因死亡率也没有显著差异(OR 0.68,95%置信区间 0.26 至 1.79;p=0.43)。
在出现急性胸痛和潜在可卡因的患者中,β受体阻滞剂的使用似乎不会增加 MI 或全因死亡率的风险。