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首页> 外文期刊>International Journal of Cardiology >Real-life effectiveness of statins in the prevention of first acute coronary syndrome in France: A prospective observational study
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Real-life effectiveness of statins in the prevention of first acute coronary syndrome in France: A prospective observational study

机译:他汀类药物在法国预防第一例急性冠状动脉综合症的现实效果:一项前瞻性观察研究

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摘要

Background Evidence on the real effectiveness of statins on acute coronary syndrome (ACS) incidence is scarce. We assessed the effectiveness of real-life statins on the risk of first non-fatal ACS in a low-cardiovascular-risk country. Methods Systematic case-control study was conducted in 60 cardiology centres and 371 general practices from across France. A total of 2238 cases with first ACS within 1 month from recruitment and 2238 controls without history of ACS were included; controls were matched to ACS cases on sex, age, frequency of visits to GPs, date of recruitment and personal history of chronic diseases. Statin exposure and risk factors were documented through patient telephone interviews and validated against medical records. The index date was the date of ACS for cases. Adjusted odds ratios (OR) of first ACS and statin use were estimated by multiple conditional logistic regression models controlled for risk factors and propensity score for statin exposure. Results Statin use was associated with lower ACS risk, with an adjusted matched OR of 0.67; 95% confidence interval (CI): 0.56 to 0.79 for current use (within 2 months) and 0.73; 95% CI: 0.62 to 0.86 for any use within 24 months [atorvastatin: 0.83 (0.63-1.10), fluvastatin: 0.75 (0.43-1.30), pravastatin: 0.98 (0.72-1.34), rosuvastatin: 0.49 (0.35-0.68) and simvastatin: 0.62 (0.46-0.84)]. The preventive effect of statins on non-fatal ACS reached its maximum after one to four years of use. Conclusion A similar magnitude of effect for statin use was observed in real life, as compared to randomised clinical trials in France.
机译:背景他汀类药物对急性冠状动脉综合征(ACS)发病率的实际有效性的证据很少。我们评估了在低心血管疾病风险国家中,他汀类药物对首次非致命ACS风险的有效性。方法在法国的60个心脏病学中心和371个一般实践中进行了系统的病例对照研究。总共包括2238例自招募后1个月内首次发生ACS的病例和2238例无ACS病史的对照组;对照与ACS病例相匹配,包括性别,年龄,全科医生就诊频率,招募日期和慢性病的个人病史。通过患者电话采访记录了他汀类药物的暴露和危险因素,并根据病历进行了验证。索引日期是案例的ACS日期。首次使用ACS和他汀类药物的调整后优势比(OR)是通过多个条件Logistic回归模型估算的,这些模型控制了危险因素和他汀类药物暴露倾向得分。结果使用他汀类药物可降低ACS风险,匹配OR调整后为0.67; 95%置信区间(CI):当前使用(2个月内)为0.56至0.79,为0.73; 95%CI:0.62至0.86(24个月内使用)[阿托伐他汀:0.83(0.63-1.10),氟伐他汀:0.75(0.43-1.30),普伐他汀:0.98(0.72-1.34),瑞舒伐他汀:0.49(0.35-0.68)和辛伐他汀:0.62(0.46-0.84)]。他汀类药物对非致命性ACS的预防作用在使用一到四年后达到了最大。结论与法国的随机临床试验相比,在现实生活中观察到他汀类药物的使用效果相似。

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