TY - JOUR
T1 - Overview of the current status of familial hypercholesterolaemia care in over 60 countries - The EAS Familial Hypercholesterolaemia Studies Collaboration (FHSC)
AU - Vallejo-Vaz, Antonio J.
AU - Marco, Martina De
AU - Stevens, Christophe A.T.
AU - Akram, Asif
AU - Freiberger, Tomas
AU - Hovingh, G. Kees
AU - Kastelein, John J.P.
AU - Mata, Pedro
AU - Raal, Frederick J.
AU - Santos, Raul D.
AU - Soran, Handrean
AU - Watts, Gerald F.
AU - Abifadel, Marianne
AU - Aguilar-Salinas, Carlos A.
AU - Al-Khnifsawi, Mutaz
AU - Alkindi, Fahad A.
AU - Alnouri, Fahad
AU - Alonso, Rodrigo
AU - Al-Rasadi, Khalid
AU - Al-Sarraf, Ahmad
AU - Ashavaid, Tester F.
AU - Binder, Christoph J.
AU - Bogsrud, Martin P.
AU - Bourbon, Mafalda
AU - Bruckert, Eric
AU - Chlebus, Krzysztof
AU - Corral, Pablo
AU - Descamps, Olivier
AU - Durst, Ronen
AU - Ezhov, Marat
AU - Fras, Zlatko
AU - Genest, Jacques
AU - Groselj, Urh
AU - Harada-Shiba, Mariko
AU - Kayikcioglu, Meral
AU - Lalic, Katarina
AU - Lam, Carolyn S.P.
AU - Latkovskis, Gustavs
AU - Laufs, Ulrich
AU - Liberopoulos, Evangelos
AU - Lin, Jie
AU - Maher, Vincent
AU - Majano, Nelson
AU - Marais, A. David
AU - Nordestgaard, Børge G.
AU - Tybjærg-Hansen, Anne
AU - Benn, Marianne
AU - Schmidt, Nina
AU - The EAS Familial Hypercholeserolaemia Studies Collaboration (FHSC)
PY - 2018/10/10
Y1 - 2018/10/10
N2 - Background and aims: Management of familial hypercholesterolaemia (FH) may vary across different settings due to factors related to population characteristics, practice, resources and/or policies. We conducted a survey among the worldwide network of EAS FHSC Lead Investigators to provide an overview of FH status in different countries. Methods: Lead Investigators from countries formally involved in the EAS FHSC by mid-May 2018 were invited to provide a brief report on FH status in their countries, including available information, programmes, initiatives, and management. Results: 63 countries provided reports. Data on FH prevalence are lacking in most countries. Where available, data tend to align with recent estimates, suggesting a higher frequency than that traditionally considered. Low rates of FH detection are reported across all regions. National registries and education programmes to improve FH awareness/knowledge are a recognised priority, but funding is often lacking. In most countries, diagnosis primarily relies on the Dutch Lipid Clinics Network criteria. Although available in many countries, genetic testing is not widely implemented (frequent cost issues). There are only a few national official government programmes for FH. Under-treatment is an issue. FH therapy is not universally reimbursed. PCSK9-inhibitors are available in ∼2/3 countries. Lipoprotein-apheresis is offered in ∼60% countries, although access is limited. Conclusions: FH is a recognised public health concern. Management varies widely across countries, with overall suboptimal identification and under-treatment. Efforts and initiatives to improve FH knowledge and management are underway, including development of national registries, but support, particularly from health authorities, and better funding are greatly needed.
AB - Background and aims: Management of familial hypercholesterolaemia (FH) may vary across different settings due to factors related to population characteristics, practice, resources and/or policies. We conducted a survey among the worldwide network of EAS FHSC Lead Investigators to provide an overview of FH status in different countries. Methods: Lead Investigators from countries formally involved in the EAS FHSC by mid-May 2018 were invited to provide a brief report on FH status in their countries, including available information, programmes, initiatives, and management. Results: 63 countries provided reports. Data on FH prevalence are lacking in most countries. Where available, data tend to align with recent estimates, suggesting a higher frequency than that traditionally considered. Low rates of FH detection are reported across all regions. National registries and education programmes to improve FH awareness/knowledge are a recognised priority, but funding is often lacking. In most countries, diagnosis primarily relies on the Dutch Lipid Clinics Network criteria. Although available in many countries, genetic testing is not widely implemented (frequent cost issues). There are only a few national official government programmes for FH. Under-treatment is an issue. FH therapy is not universally reimbursed. PCSK9-inhibitors are available in ∼2/3 countries. Lipoprotein-apheresis is offered in ∼60% countries, although access is limited. Conclusions: FH is a recognised public health concern. Management varies widely across countries, with overall suboptimal identification and under-treatment. Efforts and initiatives to improve FH knowledge and management are underway, including development of national registries, but support, particularly from health authorities, and better funding are greatly needed.
KW - Familial hypercholesterolaemia
KW - FHSC
KW - Primary dyslipidaemia
UR - http://www.scopus.com/inward/record.url?scp=85053666909&partnerID=8YFLogxK
U2 - 10.1016/j.atherosclerosis.2018.08.051
DO - 10.1016/j.atherosclerosis.2018.08.051
M3 - Journal article
C2 - 30270054
AN - SCOPUS:85053666909
VL - 277
SP - 234
EP - 255
JO - Atherosclerosis
JF - Atherosclerosis
SN - 0021-9150
ER -