Literature DB >> 29168543

Lipid-lowering therapy with PCSK9-inhibitors in the management of cardiovascular high-risk patients: Effectiveness, therapy adherence and safety in a real world cohort.

Michael Saborowski, Michael Dölle, Michael P Manns, Holger Leitolf, Steffen Zender1.   

Abstract

BACKGROUND: Proprotein convertase subtilisin/kexin type 9 (PCSK9)-inhibitors have shown great po-tential in efficient lipid lowering to achieve low-density lipoprotein-cholesterol (LDL-C) treatment goals. The aim of the study was too describe the clinical use of PCSK9-inhibitors and to investigate therapy adherence and safety outside of clinical trials.
METHODS: Thirty-eight patients were treated with PSCK9-inhibitors. Patients were eligible for this therapy based on their individual cardiovascular risk and when all other available lipid-lowering regi-men had failed. Every patient answered a questionnaire concerning medical history and relevant side effects and therapy adherence.
RESULTS: Conventional therapy reduced patient LDL-C levels by about 38%. However, in 26 of the 38 patients, LDL-C treatment goals were not fulfilled because patients did not tolerate further dose es-calation due to side effects. Using a PCSK9 inhibitor, LDL-C levels were reduced by another 54% and 42% of patients reaching treatment goals. The results show that most patients still require concomitant therapy to reach LDL-C target levels. Three patients required dose reduction or change of the PCSK9 inhibitor. 16% did not inject the PCSK9 inhibitor regularly.
CONCLUSIONS: Only a minority of patients reached the recommended LDL-C goals. PCSK9-inhibitors were generally well tolerated. Despite low rates of reported side effects, therapy adherence was incom-plete, with 6 patients not injecting PCSK9-inhibitors on a regular basis. In-depth information about the medication and close supervision is advisable. PCSK9 inhibitors have shown great potential in aggressive lipid lowering therapy, but basic therapy is still required in most cases. Close supervision is recommended to improve therapy adherence. (Cardiol J 2018; 25, 1: 32-41).

Entities:  

Keywords:  PCSK9-inhibitors; cardiovascular risk; lipid lowering therapy; prevention; therapy adherence

Mesh:

Substances:

Year:  2017        PMID: 29168543     DOI: 10.5603/CJ.a2017.0137

Source DB:  PubMed          Journal:  Cardiol J        ISSN: 1898-018X            Impact factor:   2.737


  10 in total

1.  Long-term lipoprotein apheresis in the treatment of severe familial hypercholesterolemia refractory to high intensity statin therapy: Three year experience at a lipoprotein apheresis centre.

Authors:  Agnieszka Mickiewicz; Justyna Borowiec-Wolna; Witold Bachorski; Natasza Gilis-Malinowska; Rafał Gałąska; Grzegorz Raczak; Magdalena Chmara; Bartosz Wasąg; Miłosz J Jaguszewski; Marcin Fijałkowski; Marcin Gruchała
Journal:  Cardiol J       Date:  2018-09-20       Impact factor: 2.737

Review 2.  Patient adherence, compliance, and perspectives on evolocumab for the management of resistant hypercholesterolemia.

Authors:  Constantine E Kosmas; Delia Silverio; Julio Ovalle; Peter D Montan; Eliscer Guzman
Journal:  Patient Prefer Adherence       Date:  2018-10-29       Impact factor: 2.711

3.  Treatment patterns and patient characteristics among early initiators of PCSK9 inhibitors.

Authors:  Dionne M Hines; Pallavi Rane; Jeetvan Patel; David J Harrison; Rolin L Wade
Journal:  Vasc Health Risk Manag       Date:  2018-12-10

4.  Adverse Events Associated With PCSK9 Inhibitors: A Real-World Experience.

Authors:  Muhammed T Gürgöze; Annemarie H G Muller-Hansma; Michelle M Schreuder; Annette M H Galema-Boers; Eric Boersma; Jeanine E Roeters van Lennep
Journal:  Clin Pharmacol Ther       Date:  2018-09-07       Impact factor: 6.875

5.  Real-world data on metabolic effects of PCSK9 inhibitors in a tertiary care center in patients with and without diabetes mellitus.

Authors:  Laurenz T Fischer; Daniel A Hochfellner; Lisa Knoll; Tina Pöttler; Julia K Mader; Felix Aberer
Journal:  Cardiovasc Diabetol       Date:  2021-04-24       Impact factor: 9.951

6.  Effectiveness and safety of PCSK9 inhibitor therapy in patients with familial hypercholesterolemia within a therapeutic program in Poland: Preliminary multicenter data.

Authors:  Krzysztof Chlebus; Barbara Cybulska; Piotr Dobrowolski; Marzena Romanowska-Kocejko; Marta Żarczyńska-Buchowiecka; Natasza Gilis-Malinowska; Aneta Stróżyk; Justyna Borowiec-Wolna; Marcin Pajkowski; Beata Bobrowska; Renata Rajtar-Salwa; Aleksandra Kwapiszewska; Małgorzata Waluś-Miarka; Magdalena Chmara; Rafał Gałąska; Maciej Małecki; Tomasz Zdrojewski; Marcin Gruchała
Journal:  Cardiol J       Date:  2022-02-11       Impact factor: 2.737

7.  Impact of PCSK9 Inhibition on Proinflammatory Cytokines and Matrix Metalloproteinases Release in Patients with Mixed Hyperlipidemia and Vulnerable Atherosclerotic Plaque.

Authors:  Marcin Basiak; Michal Kosowski; Marcin Hachula; Boguslaw Okopien
Journal:  Pharmaceuticals (Basel)       Date:  2022-06-27

Review 8.  PCSK9 Inhibitors in the Management of Cardiovascular Risk: A Practical Guidance.

Authors:  Xiaoming Jia; Mahmoud Al Rifai; Anum Saeed; Christie M Ballantyne; Salim S Virani
Journal:  Vasc Health Risk Manag       Date:  2022-07-20

9.  PCSK9 Inhibitors in a German Single-Center Clinical Practice: Real-World Treatment of Patients at High Cardiovascular Risk Over 68 Weeks.

Authors:  Tim Hollstein; Ursula Kassner; Thomas Grenkowitz; Friederike Schumann; Thomas Bobbert; Elisabeth Steinhagen-Thiessen
Journal:  Am J Cardiovasc Drugs       Date:  2021-01       Impact factor: 3.571

Review 10.  Treatment and prevention of lipoprotein(a)-mediated cardiovascular disease: the emerging potential of RNA interference therapeutics.

Authors:  Daniel I Swerdlow; David A Rider; Arash Yavari; Marie Wikström Lindholm; Giles V Campion; Steven E Nissen
Journal:  Cardiovasc Res       Date:  2022-03-25       Impact factor: 10.787

  10 in total

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