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      Lipid goal attainment in post‐acute coronary syndrome patients in China: Results from the 6‐month real‐world dyslipidemia international study II

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          Abstract

          Background

          Dyslipidemia International Study II (DYSIS II)‐China was conducted to determine the low‐density lipoprotein cholesterol (LDL‐C) goal (<1.8 mmol/L) attainment rate in patients with post‐acute coronary syndrome (ACS).

          Hypothesis

          Compliance with treatment guideline recommendations improves the LDL‐C goal attainment rate in post‐ACS patients.

          Methods

          This multicenter prospective observational study conducted at 28 tertiary hospitals determined the LDL‐C goal attainment rates at admission and 6‐month follow‐up in patients on lipid‐lowering treatment (LLT) for ≥3 months and those not on LLT (LLT‐naive or off LLT for ≥3 months) at admission. Predictors of goal attainment at 6 months were identified using multivariate logistic regression.

          Results

          The LDL‐C goal attainment rate at admission in 1102/1103 enrolled patients was 17.1%; it was 41.2% among 752 patients with available lipid results at 6 months. The distance to goal was 0.7 mmol/L at 6 months. Statin monotherapy was the most prescribed LLT. Only 7.7% of patients were receiving statin + ezetimibe and 8.4% of patients were receiving an atorvastatin‐equivalent dose of ≥40 mg/day at 6 months. Being male (odds ratio [OR] 1.7, 95% confidence interval [CI] 1.1–2.6) and undergoing percutaneous coronary intervention during index hospitalization (OR 1.5, 95% CI 1.1 to 2.1) were the independent predictors for LDL‐C goal attainment.

          Conclusions

          This real‐world DYSIS II study in China reports a low LDL‐C goal attainment rate in post‐ACS patients even after 6 months of LLT. Lack of intensification of statin therapy and underutilization of combinations suggest gaps between real‐world treatment practices and guideline recommendations.

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          Most cited references34

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          2019 ESC/EAS Guidelines for the management of dyslipidaemias: lipid modification to reduce cardiovascular risk

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            Efficacy and safety of more intensive lowering of LDL cholesterol: a meta-analysis of data from 170 000 participants in 26 randomised trials

            Summary Background Lowering of LDL cholesterol with standard statin regimens reduces the risk of occlusive vascular events in a wide range of individuals. We aimed to assess the safety and efficacy of more intensive lowering of LDL cholesterol with statin therapy. Methods We undertook meta-analyses of individual participant data from randomised trials involving at least 1000 participants and at least 2 years' treatment duration of more versus less intensive statin regimens (five trials; 39 612 individuals; median follow-up 5·1 years) and of statin versus control (21 trials; 129 526 individuals; median follow-up 4·8 years). For each type of trial, we calculated not only the average risk reduction, but also the average risk reduction per 1·0 mmol/L LDL cholesterol reduction at 1 year after randomisation. Findings In the trials of more versus less intensive statin therapy, the weighted mean further reduction in LDL cholesterol at 1 year was 0·51 mmol/L. Compared with less intensive regimens, more intensive regimens produced a highly significant 15% (95% CI 11–18; p<0·0001) further reduction in major vascular events, consisting of separately significant reductions in coronary death or non-fatal myocardial infarction of 13% (95% CI 7–19; p<0·0001), in coronary revascularisation of 19% (95% CI 15–24; p<0·0001), and in ischaemic stroke of 16% (95% CI 5–26; p=0·005). Per 1·0 mmol/L reduction in LDL cholesterol, these further reductions in risk were similar to the proportional reductions in the trials of statin versus control. When both types of trial were combined, similar proportional reductions in major vascular events per 1·0 mmol/L LDL cholesterol reduction were found in all types of patient studied (rate ratio [RR] 0·78, 95% CI 0·76–0·80; p<0·0001), including those with LDL cholesterol lower than 2 mmol/L on the less intensive or control regimen. Across all 26 trials, all-cause mortality was reduced by 10% per 1·0 mmol/L LDL reduction (RR 0·90, 95% CI 0·87–0·93; p<0·0001), largely reflecting significant reductions in deaths due to coronary heart disease (RR 0·80, 99% CI 0·74–0·87; p<0·0001) and other cardiac causes (RR 0·89, 99% CI 0·81–0·98; p=0·002), with no significant effect on deaths due to stroke (RR 0·96, 95% CI 0·84–1·09; p=0·5) or other vascular causes (RR 0·98, 99% CI 0·81–1·18; p=0·8). No significant effects were observed on deaths due to cancer or other non-vascular causes (RR 0·97, 95% CI 0·92–1·03; p=0·3) or on cancer incidence (RR 1·00, 95% CI 0·96–1·04; p=0·9), even at low LDL cholesterol concentrations. Interpretation Further reductions in LDL cholesterol safely produce definite further reductions in the incidence of heart attack, of revascularisation, and of ischaemic stroke, with each 1·0 mmol/L reduction reducing the annual rate of these major vascular events by just over a fifth. There was no evidence of any threshold within the cholesterol range studied, suggesting that reduction of LDL cholesterol by 2–3 mmol/L would reduce risk by about 40–50%. Funding UK Medical Research Council, British Heart Foundation, European Community Biomed Programme, Australian National Health and Medical Research Council, and National Heart Foundation.
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              Ezetimibe Added to Statin Therapy after Acute Coronary Syndromes.

              Statin therapy reduces low-density lipoprotein (LDL) cholesterol levels and the risk of cardiovascular events, but whether the addition of ezetimibe, a nonstatin drug that reduces intestinal cholesterol absorption, can reduce the rate of cardiovascular events further is not known.
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                Author and article information

                Contributors
                huoyong@263.net.cn
                Journal
                Clin Cardiol
                Clin Cardiol
                10.1002/(ISSN)1932-8737
                CLC
                Clinical Cardiology
                Wiley Periodicals, Inc. (New York )
                0160-9289
                1932-8737
                15 October 2021
                November 2021
                : 44
                : 11 ( doiID: 10.1002/clc.v44.11 )
                : 1575-1585
                Affiliations
                [ 1 ] Department of Cardiology Peking University First Hospital Beijing China
                [ 2 ] Department of Cardiology Jinqiu Hospital of Liaoning Province Shenyang China
                [ 3 ] Department of Cardiology The First Affiliated Hospital of Xinjiang Medical University Urumqi China
                [ 4 ] Department of Cardiology Zhengzhou First People's Hospital Zhengzhou China
                [ 5 ] Department of Cardiology Shanghai East Hospital Shanghai China
                [ 6 ] Department of Cardiology Guangdong Provincial People's Hospital Guangzhou China
                [ 7 ] Department of Cardiology The Second Hospital of Harbin Harbin China
                [ 8 ] Department of Cardiology The First Affiliated Hospital of Shantou University Medical College Shantou China
                [ 9 ] Department of Cardiology Hebei General Hospital Shijiazhuang China
                [ 10 ] Department of Rehabilitation Shandong Provincial Third Hospital Jinan China
                [ 11 ] Department of Cardiology Traditional Chinese Medicine Hospital of Xinjiang Uygur Autonomous Region Urumqi China
                [ 12 ] Department of Cardiology The First Affiliated Hospital of Xi'an Jiaotong University Xi'an China
                [ 13 ] Department of Cardiology Shijiazhuang First Hospital Shijiazhuang China
                [ 14 ] Department of Cardiology Cardiovascular Hospital of Shanxi Province Taiyuan China
                [ 15 ] Department of Cardiology Shanghai General Hospital Shanghai China
                [ 16 ] Department of Cardiology The First Hospital of Hebei Medical University Shijiazhuang China
                [ 17 ] Department of Cardiology Wuxi People's Hospital Wuxi China
                [ 18 ] Department of Cardiology Beijing Anzhen Hospital, Capital Medical University Beijing China
                [ 19 ] Department of Cardiology Jiangsu Province Hospital Nanjing China
                [ 20 ] Department of Cardiology Jinzhong First People's Hospital Jinzhong China
                [ 21 ] Department of Cardiology The Ninth People's Hospital, Shanghai Jiaotong University School of Medicine Shanghai China
                [ 22 ] Department of Cardiology The Second Affiliated Hospital of Zhejiang University School of Medicine Hangzhou China
                [ 23 ] Department of Cardiology Shijiazhuang the Third Hospital Shijiazhuang China
                [ 24 ] Department of Cardiology Sir Run Shaw Hospital, Zhejiang University School of Medicine Hangzhou China
                [ 25 ] Department of Cardiology The First Hospital of Harbin Harbin China
                [ 26 ] Department of Cardiology The Second Xiangya Hospital of Central South University Changsha China
                [ 27 ] Department of Cardiology Peking Union Medical College Hospital Beijing China
                [ 28 ] Department of Cardiology Shanghai Chest Hospital Shanghai China
                [ 29 ] Global Medical and Scientific Affairs (GMSA) MSD China Shanghai China
                Author notes
                [*] [* ] Correspondence

                Yong Huo, Department of Cardiology, Peking University First Hospital, Xicheng District, Beijing 100034, China.

                Email: huoyong@ 123456263.net.cn

                Author information
                https://orcid.org/0000-0002-0335-3528
                https://orcid.org/0000-0002-9545-1984
                https://orcid.org/0000-0002-1532-0029
                https://orcid.org/0000-0002-5407-8773
                Article
                CLC23725
                10.1002/clc.23725
                8571548
                34651329
                87976775-13b5-4adb-97d1-17007dadefb0
                © 2021 The Authors. Clinical Cardiology published by Wiley Periodicals LLC.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 20 August 2021
                : 24 May 2021
                : 03 September 2021
                Page count
                Figures: 3, Tables: 2, Pages: 11, Words: 6320
                Funding
                Funded by: MSD China
                Categories
                Clinical Investigations
                Clinical Investigations
                Custom metadata
                2.0
                November 2021
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.0.8 mode:remove_FC converted:06.11.2021

                Cardiovascular Medicine
                acute coronary syndrome,dysis ii,ldl‐c goal,lipid‐lowering therapy,statin

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