TY - JOUR
T1 - Lipid-lowering and anti-thrombotic therapy in patients with peripheral arterial disease
T2 - European Atherosclerosis Society/European Society of Vascular Medicine Joint Statement
AU - Belch, Jill J. F.
AU - Brodmann, Marianne
AU - Baumgartner, Iris
AU - Binder, Christoph J.
AU - Casula, Manuela
AU - Heiss, Christian
AU - Kahan, Thomas
AU - Parini, Paolo
AU - Poredos, Pavel
AU - Catapano, Alberico L.
AU - Tokgözoğlu, Lale
N1 - Funding Information:
JJFB receives speaker honoraria from Amgen, receives speaker honoraria from Bayer, receives funding from Regeneron for the adjudication committee of a clinical trial, and as PI of a second clinical trial. She receives funding from Daiichi Sankyo and Astra Zeneca for advisory Boards. MB received a speaker honorarium from BD Brad, Phillips, Medtronic, Bayer. ALC receives research grant/research support from Sanofi, Sanofi Regeneron, Amgen, Mylan, Menarini, Eli Lilly. TK has research grants to the Karolinska Institute from Amgen, Medtronic, and ReCor Medical, all outside the area of the work presented here. PParini received research grants from Amgen AB and Akcea. LT received company speaker honorarium from Abbott, Actelion, Amgen, Bayer, Daiichi Sankyo, MSD, Mylan, Novartis, Novo Nordisk, Sanofi, Servier, Pfizer, Recordati Abdi-̇brahim.
Funding Information:
CB, IB, PPoredos none. JJFB sits on the PAD Advisory Board of Bayer. MB is a consultant for Biotronic, Cook Ltd and Boston cientific. ALC participates in the speaker bureau for Akcea, Amgen, Sanofi, Esperion, Kowa, Novartis, Ionis Pharmaceuticals, Mylan, Menarini, Merck, Recordati, Regeneron, Daiichi Sankyo, Astrazeneca, Aegerion, Amryt, Sandoz. He is a consultant on advisory boards for Akcea, Amgen, Sanofi, Esperion, Kowa, Novartis, Ionis Pharmaceuticals, Mylan, Menarini, Merck, Recordati, Regeneron Daiichi Sankyo, Genzyme, Aegerion, Sandoz. The work of ALC at MultiMedica been supported by Ministry of Health – Ricerca Corrente – IRCCS MultiMedica. CH has published with Mars, and the Cranberry Institute. PParini has equity interests in Galmed Pharmaceuticals; has ownership in Lipoprotein Research Stockholm AB; has ownership of patent Japanese Patent No. 2020-011068; is member of the Scientific Advisory Board of Ambys Medicine and of Diaccurate SAS. LT is Company consultant for Abbott, Amgen, Bayer, MSD, Mylan, Novartis, Sanofi and has participated in a study for Amgen.
Publisher Copyright:
© 2021 Hogrefe Verlag GmbH & Co. KG. All rights reserved.
PY - 2021/11
Y1 - 2021/11
N2 - Patients with peripheral arterial disease (PAD) are at very high risk of cardiovascular events, but risk factor management is usually suboptimal. This Joint Task Force from the European Atherosclerosis Society and the European Society of Vascular Medicine has updated evidence on the management on dyslipidaemia and thrombotic factors in patients with PAD. Guidelines recommend a low-density lipoprotein cholesterol (LDLC) goal of more than 50% reduction from baseline and <1.4 mmol/L (<55 mg/dL) in PAD patients. As demonstrated by randomized controlled trials, lowering LDL-C not only reduces cardiovascular events but also major adverse limb events (MALE), including amputations, of the order of 25%. Addition of ezetimibe or a PCSK9 inhibitor further decreases the risk of cardiovascular events, and PCSK9 inhibition has also been associated with reduction in the risk of MALE by up to 40%. Furthermore, statin- based treatment improved walking performance, including maximum walking distance, and pain-free walking distance and duration. This Task Force recommends strategies for managing statin-associated muscle symptoms to ensure that PAD patients benefit from lipid-lowering therapy. Antiplatelet therapy, either daily clopidogrel 75 mg or the combination of aspirin 100 mg and rivaroxaban (2×2.5 mg) is also indicated to prevent cardiovascular events. Dual pathway inhibition (aspirin and rivaroxaban) may be considered following revascularization, taking into account bleeding risk. This Joint Task Force believes that adherence with these recommendations for lipid-lowering and antithrombotic therapy will improve the morbidity and mortality in patients with PAD.
AB - Patients with peripheral arterial disease (PAD) are at very high risk of cardiovascular events, but risk factor management is usually suboptimal. This Joint Task Force from the European Atherosclerosis Society and the European Society of Vascular Medicine has updated evidence on the management on dyslipidaemia and thrombotic factors in patients with PAD. Guidelines recommend a low-density lipoprotein cholesterol (LDLC) goal of more than 50% reduction from baseline and <1.4 mmol/L (<55 mg/dL) in PAD patients. As demonstrated by randomized controlled trials, lowering LDL-C not only reduces cardiovascular events but also major adverse limb events (MALE), including amputations, of the order of 25%. Addition of ezetimibe or a PCSK9 inhibitor further decreases the risk of cardiovascular events, and PCSK9 inhibition has also been associated with reduction in the risk of MALE by up to 40%. Furthermore, statin- based treatment improved walking performance, including maximum walking distance, and pain-free walking distance and duration. This Task Force recommends strategies for managing statin-associated muscle symptoms to ensure that PAD patients benefit from lipid-lowering therapy. Antiplatelet therapy, either daily clopidogrel 75 mg or the combination of aspirin 100 mg and rivaroxaban (2×2.5 mg) is also indicated to prevent cardiovascular events. Dual pathway inhibition (aspirin and rivaroxaban) may be considered following revascularization, taking into account bleeding risk. This Joint Task Force believes that adherence with these recommendations for lipid-lowering and antithrombotic therapy will improve the morbidity and mortality in patients with PAD.
KW - Cholesterol, LDL
KW - Humans
KW - Hydroxymethylglutaryl-CoA Reductase Inhibitors/adverse effects
KW - Peripheral Arterial Disease/diagnosis
KW - Proprotein Convertase 9
KW - Treatment Outcome
KW - treatment targets
KW - Peripheral arterial disease
KW - lipid lowering
UR - http://www.scopus.com/inward/record.url?scp=85118919352&partnerID=8YFLogxK
U2 - 10.1024/0301-1526/a000969
DO - 10.1024/0301-1526/a000969
M3 - Review article
C2 - 34743585
SN - 0301-1526
VL - 50
SP - 401
EP - 411
JO - VASA
JF - VASA
IS - 6
ER -