Lipid-lowering therapy with PCSK9-inhibitors in the real-world setting: Two-year experience of a regional lipid clinic

被引:28
作者
Zafrir, Barak [1 ,2 ]
Jubran, Ayman [1 ,2 ]
机构
[1] Lady Davis Carmel Med Ctr, Cardiovasc Dept, Haifa, Israel
[2] Clalit Hlth Serv, Haifa, Israel
关键词
adherence; familial hypercholesterolemia; low-density lipoproteins; PCSK9; inhibitors; side effects; HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA; STATIN THERAPY; PCSK9; INHIBITORS; REDUCING LIPIDS; SAFETY; EFFICACY; ALIROCUMAB; GUIDELINES; MANAGEMENT; EZETIMIBE;
D O I
10.1111/1755-5922.12439
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
AimPCSK9 inhibitors (PCSK9i) effectively lower cholesterol levels in randomized trials with reduction in cardiovascular outcomes and favorable safety profile. However, the access to PCSK9i is limited due to high cost and data regarding the use of PCSK9i in real-world practice is limited. MethodsData on all patients submitted for approval of PCSK9i at a regional lipid clinic, outside of clinical trials. Patients' profile, approval rates, low-density lipoprotein cholesterol (LDL-C) reduction rates, and adverse events were evaluated. ResultsRecommendation for PCSK9i was given to 133 patients; 16 did not receive insurance approval and additional 16 were approved but did not initiate therapy. Of the 101 treated patients (47% females; mean age 6111years), 52 had probable/definite familial hypercholesterolemia (FH) (peak LDL-C level 305 +/- 87mg/dL vs non-FH 204 +/- 39mg/dL) and 62% had an established cardiovascular disease. Statin intolerance was reported by 77%. Follow-up lipid panel was available in 66/101 patients: mean LDL-C reduction was 59%+/- 19. Subjects with heterozygous FH had similar LDL-C decrease than those with non-FH (59%+/- 22 vs 60%+/- 14, P=.792). LDL-C <100mg/dL was achieved by 76%, LDL-C<70mg/dL by 58% and LDL-C<40mg/dL by 18% of those with follow-up data. Side effects were reported by 10%, mainly musculoskeletal complaints and flu-like symptoms, and 15% have discontinued treatment. ConclusionsPatient selection by a regional lipid clinic resulted in a high real-world PCSK9i insurance approval, with efficacy and safety comparable to randomized clinical trials. Cost and medication nonadherence are potential barriers to successful implementation of therapy in routine clinical care.
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