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      Lipid lowering therapy in primary and secondary prevention in Austria: are LDL-C goals achieved? : Results from the DA VINCI study

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          Abstract

          Background

          Cardiovascular disease (CVD) is the most frequent cause of death in Austria. The European Society of Cardiology (ESC)/European Atherosclerosis Society (EAS) guidelines recommend intensive lipid lowering therapy (LLT) in patients at high or very high CV risk. Lipid management and achievement of low-density lipoprotein cholesterol (LDL-C) goals in Austria have not recently been assessed.

          Methods

          Subgroup analysis for Austria of a European 18 country, cross-sectional, observational study. Patients received LLT for primary (PP) or secondary prevention (SP). Data including LLT in the preceding 12 months and most recent LDL‑C were collected during a single visit between June 2017 and November 2018. Achievement of the risk-based 2016 and 2019 ESC/EAS LDL‑C goal while receiving stabilized LLT was assessed.

          Results

          A total of 293 patients were enrolled from 8 Austrian sites, of which 200 (PP = 104, SP = 96) received stabilized LLT at the LDL‑C measurement date. Overall, 58% (71% PP, 43% SP) and 38% (52% PP, 23% SP) achieved the risk-based 2016 and 2019 goals, respectively. Most patients received moderate-intensity statin monotherapy (46%), while 34% used high-intensity statin monotherapy. Combination therapy of moderate/high-intensity statin with ezetimibe (12%), or proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors with statin ± ezetimibe (1%), was used infrequently.

          Conclusion

          The current Austrian routine lipid management using mainly moderate-intensity or high-intensity statin monotherapy is insufficient to attain ESC/EAS guideline goals, in particular the more stringent 2019 recommendations, a situation comparable to other participating European countries. In addition to switching to and optimizing doses of high-intensity statins, a combination with ezetimibe or PCSK9 inhibitors will be needed in many cases.

          Supplementary Information

          The online version of this article (10.1007/s00508-021-01978-w) contains supplementary material, which is available to authorized users.

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          Most cited references24

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

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            Evolocumab and Clinical Outcomes in Patients with Cardiovascular Disease

            Evolocumab is a monoclonal antibody that inhibits proprotein convertase subtilisin-kexin type 9 (PCSK9) and lowers low-density lipoprotein (LDL) cholesterol levels by approximately 60%. Whether it prevents cardiovascular events is uncertain.
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              Alirocumab and Cardiovascular Outcomes after Acute Coronary Syndrome

              Patients who have had an acute coronary syndrome are at high risk for recurrent ischemic cardiovascular events. We sought to determine whether alirocumab, a human monoclonal antibody to proprotein convertase subtilisin-kexin type 9 (PCSK9), would improve cardiovascular outcomes after an acute coronary syndrome in patients receiving high-intensity statin therapy.
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                Author and article information

                Contributors
                peter.siostrzonek@ordensklinikum.at
                Journal
                Wien Klin Wochenschr
                Wien Klin Wochenschr
                Wiener Klinische Wochenschrift
                Springer Vienna (Vienna )
                0043-5325
                1613-7671
                6 December 2021
                6 December 2021
                2022
                : 134
                : 7-8
                : 294-301
                Affiliations
                [1 ]Department of Internal Medicine 2, Cardiology, Ordensklinikum Linz, Barmherzige Schwestern, Seilerstätte 4, 4010 Linz, Austria
                [2 ]Diabetes & Metabolic Outpatient Clinic, Health Centre Favoriten, Vienna, Austria
                [3 ]GRID grid.11598.34, ISNI 0000 0000 8988 2476, Cardiology Department, , Medical University Graz, ; Graz, Austria
                [4 ]GRID grid.512665.3, Vorarlberg Institute for Vascular Investigation and Treatment (VIVIT), ; Feldkirch, Austria
                [5 ]Amgen GmbH, Vienna, Austria
                [6 ]hemetsberger medical services, Vienna, Austria
                [7 ]GRID grid.7445.2, ISNI 0000 0001 2113 8111, Imperial Centre for Cardiovascular Disease Prevention and Imperial Clinical Trials Unit, , Imperial College London, ; London, UK
                Author information
                http://orcid.org/0000-0002-4898-4606
                http://orcid.org/0000-0002-1601-4656
                http://orcid.org/0000-0001-5407-9832
                http://orcid.org/0000-0002-4677-9756
                http://orcid.org/0000-0001-7636-8002
                http://orcid.org/0000-0003-1877-6838
                http://orcid.org/0000-0003-0508-0954
                Article
                1978
                10.1007/s00508-021-01978-w
                9023395
                34870742
                512990f5-1bc2-4312-8015-534d10e4baf0
                © The Author(s) 2021

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 5 July 2021
                : 24 October 2021
                Funding
                Funded by: amgen (europe) gmbh
                Categories
                Original Article
                Custom metadata
                © Springer-Verlag GmbH Austria, part of Springer Nature 2022

                Medicine
                cross-sectional study,guideline,statin,pcsk9 inhibitor,dyslipidemia
                Medicine
                cross-sectional study, guideline, statin, pcsk9 inhibitor, dyslipidemia

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