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Contemporary data on treatment practices for low-density lipoprotein cholesterol in 3867 patients who had suffered an acute coronary syndrome across the world

机译:关于全球3867例患有急性冠脉综合征的患者低密度脂蛋白胆固醇治疗实践的当代数据

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DYSIS II ACS was a longitudinal, observational study in 3867 patients from 18 countries. They were being hospitalized after suffering an acute coronary syndrome. Evaluations were performed at the time of admission and again 120±15 days following the date of admission (the follow-up time point). 2521 patients were on active lipid lowering treatment (LLT) at admission. Mean atorvastatin dose was 22mg per day and 2.7% received ezetimibe in combination with a statin. At discharge from hospital, 3767 patients received LLT expressed as a mean atorvastatin dose of 36mg per day with 4.8% receiving ezetimibe on top of a statin. After 120 days, intensity in lipid lowering treatment was reduced to 32mg per day with 4.9% of the patients receiving ezetimibe and a statin. Of note, during this 4-month follow up period, only 32% of all patients received laboratory lipid testing. 37% attained the low density lipoprotein cholesterol (LDL-C) target value of <70mg/dl after 120 days. There are differences in the therapy administered as well as in the switch strategies when comparing the data from the respective countries studied. Conclusions Only one in three patients achieved the LDL-C target value following only marginal improvements in atorvastatin dose or combination therapy after an ACS event.
机译:DYSIS II ACS是一项来自18个国家/地区的3867例患者的纵向观察性研究。他们患有急性冠状动脉综合症后正在住院。在入院时以及入院后120±15天(随访时间点)再次进行评估。 2521名患者在入院时接受了主动降脂治疗(LLT)。阿托伐他汀的平均剂量为每天22mg,2.7%的依泽替米贝联合他汀类药物。出院时,有3767名接受LLT的患者表示为阿托伐他汀的平均剂量,每天36毫克,其中4.8%的患者在他汀类药物的基础上接受依折麦布。 120天后,降脂治疗的强度降至每天32mg,其中4.9%的患者接受依泽替米贝和他汀类药物治疗。值得注意的是,在这4个月的随访期内,只有32%的患者接受了实验室脂质测试。 120天后,有37%的人达到了<70mg / dl的低密度脂蛋白胆固醇(LDL-C)目标值。比较所研究的各个国家的数据时,所用治疗方法和转换策略均存在差异。结论ACS事件发生后,仅在阿托伐他汀剂量或联合疗法的边缘改善后,只有三分之一的患者达到LDL-C目标值。

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