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Dr. Ahmed Mahmoud Bendary :: Publications:

Title:
Egyptian association for vascular biology and atherosclerosis (EAVA) consensus on the use of inclisiran in clinical practice
Authors: A. Reda , A. Shawky , A. Elkersh , A. Elbahry , E. Farag , M. Ashraf , A. Bendary
Year: 2022
Keywords: Inclisiran; EAVA; Egypt
Journal: Atherosclerosis
Volume: 355
Issue: Not Available
Pages: 83
Publisher: Elsevier
Local/International: International
Paper Link:
Full paper Ahmed Mahmoud Bendary_Atherosclerosis abstract.pdf
Supplementary materials Not Available
Abstract:

Background and Aims : Small interfering RNA molecules (siRNA) e.g., Inclisiran represent an attractive alternative to monoclonal antibodies for Proprotein convertase subtilisin/kexin type 9 (PCSK9) lowering. These molecules offer profound lowering of (intra- and extracellular) PCSK9 at a lower-dose frequency and potentially at a lower cost. Inclisiran has undergone phase 1, 2, and 3 evaluation all within the context of the ORION trials, with good efficacy and safety. Considering that Egypt is a middleincome country with a burdened economy, concerns are raised on which patients would benefit from this expensive medication. Therefore, the Egyptian Association for Vascular biology and Atherosclerosis (EAVA) took the responsibility of providing the 1st Egyptian consensus on the use of Inclisiran in clinical practice. Methods: EAVA analyzed the data that would enable us to obtain clear indications for the use of Inclisiran. Results: Dyslipidemia represents a major atherosclerotic risk factor in Egypt. Among Egyptian patients with acute coronary syndromes, it has been estimated that the prevalence of dyslipidemia is 48%, and that of ‘atleast- possible’ FH is 17%. Reaching low-density lipoprotein cholesterol (LDL-C) goals is difficult as well. Conclusions: We recommend the use of Inclisiran in addition to statins ± ezetimibe in patients with either [1]. established ASCVD or [2]. FH with one of the following: another major risk factor, eGFR < 30 ml/min,or veryhigh risk DM, who didn’t reach LDL-C goals and/or with true statin intolerance.

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