2021
DOI: 10.1016/j.atherosclerosis.2021.09.022
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Lipid-lowering and anti-thrombotic therapy in patients with peripheral arterial disease

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Cited by 11 publications
(5 citation statements)
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“…Statins are recommended as first-line therapy in the treatment of patients with PAD to decrease the lipid plaque burden and reduce the risk of adverse CV events [6,7]. Statins competitively inhibit 3-β-Hydroxy β-methylglutaryl-CoA reductase, which is an enzyme responsible for the synthesis of mevalonic acid.…”
Section: Role Of Statins In Pad 41 Mechanism Of Action Of Statinsmentioning
confidence: 99%
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“…Statins are recommended as first-line therapy in the treatment of patients with PAD to decrease the lipid plaque burden and reduce the risk of adverse CV events [6,7]. Statins competitively inhibit 3-β-Hydroxy β-methylglutaryl-CoA reductase, which is an enzyme responsible for the synthesis of mevalonic acid.…”
Section: Role Of Statins In Pad 41 Mechanism Of Action Of Statinsmentioning
confidence: 99%
“…A high-intensity statin, at the highest tolerated dose, should be prescribed as first-line therapy given the evidence showing reductions in MALE and MACE. Addition of ezetimibe or proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors is recommended if the LDL-C remains above goal (based on the degree of risk, ESC guidelines give a goal of either <55 or <40 mg/dL in those with recurrent ASCVD events) [7]. The multi-society guidelines for management of patients in 2018 classified PAD as an ASCVD equivalent alongside MI, stroke, and CAD [50].…”
Section: Current Guidelinesmentioning
confidence: 99%
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“…Further, statin treatment has been reported to reduce all-cause mortality by 39 %, CV death by 41 %, CV outcomes by 34 % and ischaemic stroke by 28 %, but also reduced acute limb ischaemia by 30 % and amputations by 35 %. 16 …”
Section: Introductionmentioning
confidence: 99%
“… 30 Thus the FOURIER was the first randomized trial to demonstrate that intensive LDL-C lowering was safe and effective in decreasing the risk of acute limb ischaemia. 16 Similarly, in Alirucumab and cardiovascular outcome after acute coronary syndrome (ODYSSEY) trial wherein primary endpoint was composite death with a median follow up of 2.8 years. In this study, patients on high intensity statins were randomized to receive alirocumab or placebo with dose adjustment every 2 weeks.…”
Section: Introductionmentioning
confidence: 99%