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.

Základní údaje

Originální název

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

Autoři

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 a Marius GEANTA

Vydání

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

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Stát vydavatele

Velká Británie a Severní Irsko

Utajení

není předmětem státního či obchodního tajemství

Odkazy

Organizace

Lékařská fakulta – Masarykova univerzita – Repozitář

UT WoS

000860847200001

EID Scopus

2-s2.0-85140631500

Klíčová slova anglicky

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

Návaznosti

LX22NPO5104, projekt VaV.
Změněno: 17. 1. 2023 03:52, RNDr. Daniel Jakubík

Anotace

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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