Literature DB >> 29407882

The cost-effectiveness of screening strategies for familial hypercholesterolaemia in Poland.

Aleksandra Pelczarska1, Michał Jakubczyk2, Joanna Jakubiak-Lasocka1, Maciej Banach3, Małgorzata Myśliwiec4, Marcin Gruchała5, Maciej Niewada6.   

Abstract

BACKGROUND AND AIMS: Familial hypercholesterolaemia (FH) elevates the cholesterol level and increases the risk of coronary events and death. Early detection and treatment reduce this risk. We aimed to determine the cost-effectiveness of FH screening in Poland in children, first job takers, and after an acute coronary syndrome (ACS) event, each followed by a cascade screening in the relatives of the positively-diagnosed subjects.
METHODS: A decision tree was constructed to model the diagnosis process. We considered scenarios with and without genetic testing. A life-time Markov was built to investigate the effectiveness (life years gained, LYG; and quality-adjusted life years, QALY) and cost (public payer perspective) of treatment in FH-affected subjects. The clinical benefits result from early treatment reducing the risk of coronary heart disease (and death, in result). Model parameters were based on published data and experts' opinions. The costs (patients visits, tests, drugs) were estimated from the National Health Fund data and other publicly-available sources.
RESULTS: Screening ACS patients below 55/65 years of age in men/women is the most cost-effective strategy: the cost of one LYG (QALY) amounts to 100 EUR (110 EUR). Removing the age limit or using genetic tests reduced cost-effectiveness; nonetheless, all strategies remained cost effective: the cost of one LYG or QALY was <5040 EUR, much lower than the official threshold of ca. 29,800 EUR/QALY.
CONCLUSIONS: Screening for FH is highly cost-effective in Poland. The strategies are complementary, and using a combination thereof is recommended.
Copyright © 2018 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Cascade screening; Cost-effectiveness; Cost-utility; Familial hypercholesterolemia; Genetic test; Screening

Mesh:

Year:  2018        PMID: 29407882     DOI: 10.1016/j.atherosclerosis.2018.01.036

Source DB:  PubMed          Journal:  Atherosclerosis        ISSN: 0021-9150            Impact factor:   5.162


  4 in total

Review 1.  A systematic review of the methodological quality of economic evaluations in genetic screening and testing for monogenic disorders.

Authors:  Karl Johnson; Katherine W Saylor; Isabella Guynn; Karen Hicklin; Jonathan S Berg; Kristen Hassmiller Lich
Journal:  Genet Med       Date:  2021-12-07       Impact factor: 8.822

2.  Genetic Testing for Familial Hypercholesterolemia: Health Technology Assessment.

Authors: 
Journal:  Ont Health Technol Assess Ser       Date:  2022-08-23

Review 3.  Familial hypercholesterolaemia: evolving knowledge for designing adaptive models of care.

Authors:  Gerald F Watts; Samuel S Gidding; Pedro Mata; Jing Pang; David R Sullivan; Shizuya Yamashita; Frederick J Raal; Raul D Santos; Kausik K Ray
Journal:  Nat Rev Cardiol       Date:  2020-01-23       Impact factor: 32.419

4.  "Apple does not fall far from the tree" - subclinical atherosclerosis in children with familial hypercholesterolemia.

Authors:  Michał Podgórski; Katarzyna Szatko; Małgorzata Stańczyk; Monika Pawlak-Bratkowska; Agnieszka Konopka; Ewa Starostecka; Marcin Tkaczyk; Sebastian Góreczny; Lena Rutkowska; Agnieszka Gach; Maciej Łukaszewski; Piotr Grzelak; Maciej Banach
Journal:  Lipids Health Dis       Date:  2020-07-14       Impact factor: 3.876

  4 in total

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