J 2022

Paediatric familial hypercholesterolaemia screening in Europe: public policy background and recommendations

GIDDING, Samuel S., Albert WIEGMAN, Urh GROSELJ, Tomáš FREIBERGER, Noel PERETTI et. al.

Basic information

Original name

Paediatric familial hypercholesterolaemia screening in Europe: public policy background and recommendations

Authors

GIDDING, Samuel S., Albert WIEGMAN, Urh GROSELJ, Tomáš FREIBERGER, Noel PERETTI, Kanika I DHARMAYAT, Magdalena DACCORD, Nicola BEDLINGTON, Jaka SIKONJA, Kausik K RAY, Raul D SANTOS, Martin HALLE, Lale TOKGOZOGLU, Inaki GUTIERREZ-IBARLUZEA, Fausto J PINTO and Marius GEANTA

Edition

EUROPEAN JOURNAL OF PREVENTIVE CARDIOLOGY, OXFORD, OXFORD UNIV PRESS, 2022, 2047-4873

Other information

Language

English

Type of outcome

Article in a journal

Country of publisher

United Kingdom of Great Britain and Northern Ireland

Confidentiality degree

is not subject to a state or trade secret

References:

Organization

Lékařská fakulta – Repository – Repository

UT WoS

000860847200001

EID Scopus

2-s2.0-85140631500

Keywords in English

Cholesterol; Familial hypercholesterolaemia; Myocardial infarction; Preventive cardiology; LDL cholesterol

Links

LX22NPO5104, research and development project.
Changed: 17/1/2023 03:52, RNDr. Daniel Jakubík

Abstract

V originále

Familial hypercholesterolaemia (FH) is under-recognized and under-treated in Europe leading to significantly higher risk for premature heart disease in those affected. As treatment beginning early in life is highly effective in preventing heart disease and cost-effective in these patients, screening for FH is crucial. It has therefore now been recognized by the European Commission Public Health Best Practice Portal as an effective strategy. Model programmes exist in Europe to identify young individuals with FH, which are based on cascade screening of first-degree relatives of affected individuals, universal screening for high cholesterol, opportunistic screening of high-risk individuals, or a combination of the above approaches. Recommendations presented herein to improve identification of FH emphasize that every country should have an FH screening programme. These programmes should be adapted from existing strategies to best fit the individual country's healthcare system, governments should provide financial support for these programmes and related care, and further research to optimize care and implementations should be conducted.

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