Real-world treatment patterns of PCSK9 inhibitors among patients with dyslipidemia in Germany, Spain, and the United Kingdom.

Cardiovascular disease Dyslipidemia Low-density lipoprotein cholesterol (LDL-C) Proprotein convertase subtilisin/kexin type 9 (PCSK9) Treatment

Journal

Current medical research and opinion
ISSN: 1473-4877
Titre abrégé: Curr Med Res Opin
Pays: England
ID NLM: 0351014

Informations de publication

Date de publication:
05 2019
Historique:
pubmed: 6 10 2018
medline: 25 3 2020
entrez: 6 10 2018
Statut: ppublish

Résumé

Proprotein convertase subtilisin/kexin type 9 antibody inhibitors (PCSK9i) are approved as adjuncts to maximal tolerated statin therapy to lower low-density lipoprotein cholesterol (LDL-C). This study describes real-world use, characteristics of PCSK9i users and non-users, and factors influencing treatment choice. A physician and patient survey was conducted in Germany, Spain, and the UK from December 2016 to April 2017 through the Adelphi Dyslipidemia Disease Specific Program. Physicians reported patients' lipid-lowering therapy (LLT) history and characteristics. PCSK9i users were systematically over-sampled. Results were summarized using frequencies and proportions. The study included 110, 123, and 117 physicians from Germany, Spain, and the UK, respectively, providing data on 3,073 patients (mean age = 62 years; 60% male). Most patients (63-73%) had prior statin and/or ezetimibe use. Compared to patients receiving other LLT (n = 2686), PCSK9i users (222 in Germany, 97 in Spain, 68 in the UK) were, on average, 5-7.5 years younger and had LDL-C at diagnosis averaging 23-53 mg/dl higher. Familial hypercholesterolemia (FH), coronary heart/artery disease, myocardial infarction, and acute coronary syndrome were more common among PCSK9i users than non-users. PCSK9i users were also more likely to use high-intensity statins in their current LLT regimen (64-89% vs 28-50%). Physicians commonly reported PCSK9i benefits on LDL-C and total cholesterol as reasons for initiating these agents, and PCSK9i users reported good knowledge of cardiovascular disease and treatment options. Results indicate that physicians are prescribing PCSK9i to patients with high cardiovascular risk in accordance with European guidelines and reimbursement requirements.

Identifiants

pubmed: 30289004
doi: 10.1080/03007995.2018.1532885
doi:

Substances chimiques

Cholesterol, LDL 0
PCSK9 Inhibitors 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

829-835

Auteurs

Ming-Hui Tai (MH)

a Amgen Inc , Thousand Oaks , CA , USA.

Jason Shepherd (J)

b Adelphi Real World , Macclesfield , UK.

Hollie Bailey (H)

b Adelphi Real World , Macclesfield , UK.

Nathan Williams (N)

b Adelphi Real World , Macclesfield , UK.

Maximilian Hatz (M)

c Amgen GmbH , Munich , Germany.

Ignasi Campos Tapias (I)

d Amgen SA , Barcelona , Spain.

David Catterick (D)

e Amgen UK , Uxbridge , UK.

Gavin Worth (G)

f Amgen (Europe) GmbH , Zug , Switzerland.

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Classifications MeSH