心脏康复的残留风险:我们能进一步降低吗?参加心脏康复治疗的患者是否有资格使用乙基戊二醇

S. Gaine, J. Coughlan, V. Maher, M. Waters
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Our aim was to assess the proportion of patients attending cardiac rehabilitation who may benefit from E-EPA therapy as per REDUCE-IT trial criteria and the 2019 ESC/EAS guidelines. Methods We prospectively collected data on all cardiac rehabilitation patients in our centre in 2018/2019. We then performed a hierarchal analysis of these patients to determine the percentage of patients post MI/CABG that would meet criteria for E-EPA as per REDUCE-IT trial criteria and ESC/EAS guidelines. = The REDUCE IT trial criteria were: ≥45 years and established ASCVD 50 years with DM and at least one other CV RF Fasting TG level of 1.69 to 5.63 mmol/L LDL–C level of 1.06 to 2.59 mmol/L Receiving a stable dose of a statin for at least 4 weeks The initial trial protocol enrolled patients with a TG level as low as 1.52 mmol/L to account for the ~10% variability in TG levels. This protocol was amended and changed the lower level for TG to 2.26 mmol/L. We analysed patients as per both protocols. As per ESC: E-EPA 2 × 2 g per day should be considered in combination with a statin for patients with: Persistently high TGs (1.5–5.6 mmol/L) Treatment with a statin Results 398 patients completed cardiac rehab during this study and were included in our database. Of these 275 (69%) had a 6 month TG and LDL recorded and were included. All patients in our cohort had been on a stable dose of statin for at least 4 weeks. Analysis as per initial REDUCE IT protocol: 14/275 patients (5%) were excluded as they were less than 45 years old. 63 patients (23%) had a TG level of 1.5–5.6 and 42 of these had an LDL-C level of 1.06–2.59 mmol/L (15.3%). This led to an overall eligibility of 15.3% for E-EPA. Analysis as per amended REDUCE-IT protocol: 14/275 patients (5%) were excluded as they were less than 45 years old. 30 patients had a TG level eligible as per the amended REDUCE-IT protocol (10.9%) and 20 of these patients had an LDL-C level of 1.06–2.59 mmol/L (7.3%) leading to an overall eligibility of 7.3% for E-EPA. Analysis as per the ESC/EAS guidelines: Notably the ESC guidelines do not specify an LDL level or age required for E-EPA to be considered. 64 patients had a TG level of 1.5–5.6 mmol/L despite statin therapy. As such, 64/275 patients (23.3%) of our cohort would be eligible for E-EPA. Conclusions E-EPA is a dominant cost-effective strategy to reduce CV risk in patients with elevated TG levels despite statin therapy. Nearly one quarter (23.3%) of patients in our cohort would be suitable for E-EPA treatment in order to further reduce their CV risk. 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引用次数: 0

摘要

尽管他汀类药物治疗并控制低密度脂蛋白胆固醇(LDL-C),但甘油三酯(TG)升高的患者发生缺血性事件的风险增加。REDUCE IT试验表明,高度纯化的二十碳五烯酸(EPA)酯,二十碳五烯乙酯或二十碳五烯酸乙酯(E-EPA),可降低TG水平升高患者的缺血性事件和心血管(CV)死亡风险,尽管他汀类药物治疗。5点主要复合终点首次发生主要心脏不良事件的NNT为21。从成本效益的角度来看,E-EPA也是一种优势策略。因此,2019年ESC/EAS指南建议,尽管接受了他汀类药物治疗,但tg持续升高的患者仍可使用E-EPA。我们的目的是评估根据REDUCE-IT试验标准和2019年ESC/EAS指南接受E-EPA治疗的心脏康复患者的比例。方法前瞻性收集本中心2018/2019年度所有心脏康复患者的数据。然后,我们对这些患者进行了分层分析,以确定符合REDUCE-IT试验标准和ESC/EAS指南的E-EPA标准的MI/CABG后患者的百分比。= REDUCE IT试验标准为:≥45岁,ASCVD≥50岁,伴有糖尿病和至少一项其他CV RF,空腹TG水平为1.69至5.63 mmol/L LDL-C水平为1.06至2.59 mmol/L,接受至少4周稳定剂量的他汀类药物。初始试验方案纳入TG水平低至1.52 mmol/L的患者,以解释TG水平的~10%变异性。对该方案进行了修改,将TG的下限改为2.26 mmol/L。我们根据两种方案对患者进行分析。根据ESC: E-EPA 2 × 2 g /天应考虑与他汀类药物联合治疗:持续高TGs (1.5-5.6 mmol/L)患者使用他汀类药物治疗结果398例患者在本研究期间完成心脏康复,并被纳入我们的数据库。其中275人(69%)有6个月的TG和LDL记录并纳入研究。在我们的队列中,所有患者服用稳定剂量的他汀类药物至少4周。根据最初的REDUCE IT方案进行分析:14/275例患者(5%)因年龄小于45岁而被排除。63例患者(23%)的TG水平为1.5-5.6,42例患者的LDL-C水平为1.06-2.59 mmol/L(15.3%)。这使得E-EPA的总体合格率为15.3%。根据修订后的REDUCE-IT方案进行分析:14/275例患者(5%)因年龄小于45岁而被排除。30例患者的TG水平符合修订后的REDUCE-IT方案(10.9%),其中20例患者的LDL-C水平为1.06-2.59 mmol/L(7.3%),导致E-EPA的总体适格率为7.3%。根据ESC/EAS指南进行分析:值得注意的是,ESC指南没有规定考虑E-EPA所需的LDL水平或年龄。64例患者尽管接受他汀类药物治疗,但TG水平仍为1.5-5.6 mmol/L。因此,我们的队列中有64/275例患者(23.3%)符合E-EPA的条件。结论:E-EPA是降低TG升高患者心血管风险的主要策略,尽管他汀类药物治疗。在我们的队列中,近四分之一(23.3%)的患者适合E-EPA治疗,以进一步降低他们的CV风险。康复服务应制定筛选策略,以确定和治疗符合E-EPA治疗条件的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
54 Residual risk in cardiac rehab: can we reduce-it more? Eligibility for icosapent ethyl in patients attending cardiac rehabilitation
Introduction Patients with elevated triglycerides (TG) are at increased risk for ischemic events despite statin therapy and controlled low-density lipoprotein cholesterol (LDL-C). The REDUCE IT trial showed that a highly purified Eicosapentaenoic acid (EPA) ester, Icosapent Ethyl or Ethyl Eicosapentaenoic acid (E-EPA), reduces the risk of ischemic events and cardiovascular (CV) death in patients with elevated TG levels despite statin therapy. The NNT for the first occurrence of major adverse cardiac events for the five-point primary composite endpoint was 21. E-EPA is also a dominant strategy from a cost-effectiveness perspective in the study. Thus, the 2019 ESC/EAS guidelines recommend E-EPA for patients with persistently raised TGs despite treatment with a statin. Our aim was to assess the proportion of patients attending cardiac rehabilitation who may benefit from E-EPA therapy as per REDUCE-IT trial criteria and the 2019 ESC/EAS guidelines. Methods We prospectively collected data on all cardiac rehabilitation patients in our centre in 2018/2019. We then performed a hierarchal analysis of these patients to determine the percentage of patients post MI/CABG that would meet criteria for E-EPA as per REDUCE-IT trial criteria and ESC/EAS guidelines. = The REDUCE IT trial criteria were: ≥45 years and established ASCVD 50 years with DM and at least one other CV RF Fasting TG level of 1.69 to 5.63 mmol/L LDL–C level of 1.06 to 2.59 mmol/L Receiving a stable dose of a statin for at least 4 weeks The initial trial protocol enrolled patients with a TG level as low as 1.52 mmol/L to account for the ~10% variability in TG levels. This protocol was amended and changed the lower level for TG to 2.26 mmol/L. We analysed patients as per both protocols. As per ESC: E-EPA 2 × 2 g per day should be considered in combination with a statin for patients with: Persistently high TGs (1.5–5.6 mmol/L) Treatment with a statin Results 398 patients completed cardiac rehab during this study and were included in our database. Of these 275 (69%) had a 6 month TG and LDL recorded and were included. All patients in our cohort had been on a stable dose of statin for at least 4 weeks. Analysis as per initial REDUCE IT protocol: 14/275 patients (5%) were excluded as they were less than 45 years old. 63 patients (23%) had a TG level of 1.5–5.6 and 42 of these had an LDL-C level of 1.06–2.59 mmol/L (15.3%). This led to an overall eligibility of 15.3% for E-EPA. Analysis as per amended REDUCE-IT protocol: 14/275 patients (5%) were excluded as they were less than 45 years old. 30 patients had a TG level eligible as per the amended REDUCE-IT protocol (10.9%) and 20 of these patients had an LDL-C level of 1.06–2.59 mmol/L (7.3%) leading to an overall eligibility of 7.3% for E-EPA. Analysis as per the ESC/EAS guidelines: Notably the ESC guidelines do not specify an LDL level or age required for E-EPA to be considered. 64 patients had a TG level of 1.5–5.6 mmol/L despite statin therapy. As such, 64/275 patients (23.3%) of our cohort would be eligible for E-EPA. Conclusions E-EPA is a dominant cost-effective strategy to reduce CV risk in patients with elevated TG levels despite statin therapy. Nearly one quarter (23.3%) of patients in our cohort would be suitable for E-EPA treatment in order to further reduce their CV risk. Rehab services should develop screening strategies to identify and treat patients eligible for E-EPA therapy.
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