TY - JOUR
T1 - Integrated Guidance for Enhancing the Care of Familial Hypercholesterolaemia in Australia
AU - Watts, Gerald F.
AU - Sullivan, David R.
AU - Hare, David L.
AU - Kostner, Karam M.
AU - Horton, Ari E.
AU - Bell, Damon A.
AU - Brett, Tom
AU - Trent, Ronald J.
AU - Poplawski, Nicola K.
AU - Martin, Andrew C.
AU - Srinivasan, Shubha
AU - Justo, Robert N.
AU - Chow, Clara K.
AU - Pang, Jing
AU - Ademi, Zanfina
AU - Ardill, Justin J.
AU - Barnett, Wendy
AU - Bates, Timothy R.
AU - Beilin, Lawrence J.
AU - Bishop, Warrick
AU - Black, J. Andrew
AU - Brett, Peter
AU - Brown, Alex
AU - Burnett, John R.
AU - Bursill, Christina A.
AU - Colley, Alison
AU - Clifton, Peter M.
AU - Ekinci, Elif I.
AU - Elias, Luke
AU - Figtree, Gemma A.
AU - Forge, Brett H.
AU - Garton-Smith, Jacquie
AU - Graham, Dorothy F.
AU - Hamilton-Craig, Ian
AU - Hamilton-Craig, Christian R.
AU - Heal, Clare
AU - Hespe, Charlotte M.
AU - Hooper, Amanda J.
AU - Howes, Laurence G.
AU - Ingles, Jodie
AU - Irvin, John
AU - Janus, Edward D.
AU - Kangaharan, Nadarajah
AU - Keech, Anthony C.
AU - Kirke, Andrew B.
AU - Kritharides, Leonard
AU - Kyle, Campbell V.
AU - Lacaze, Paul
AU - Lambert, Kirsten
AU - Li, Stephen C.H.
AU - Malan, Wynand
AU - Maticevic, Stjepana
AU - McQuillan, Brendan M.
AU - Mirzaee, Sam
AU - Mori, Trevor A.
AU - Morton, Allison C.
AU - Colquhoun, David M.
AU - Moullin, Joanna C.
AU - Nestel, Paul J.
AU - Nowak, Kristen J.
AU - O'Brien, Richard C.
AU - Pachter, Nicholas
AU - Page, Michael M.
AU - Pedrotti, Annette
AU - Psaltis, Peter J.
AU - Radford, Jan
AU - Reid, Nicola J.
AU - Robertson, Elizabeth N.
AU - Ryan, Jacqueline D.M.
AU - Sarkies, Mitchell N.
AU - Schultz, Carl J.
AU - Scott, Russell S.
AU - Semsarian, Christopher
AU - Simons, Leon A.
AU - Spinks, Catherine
AU - Tonkin, Andrew M.
AU - van Bockxmeer, Frank
AU - Waddell-Smith, Kathryn E.
AU - Ward, Natalie C.
AU - White, Harvey D.
AU - Wilson, Andrew M.
AU - Winship, Ingrid
AU - Woodward, Ann Marie
AU - Nicholls, Stephen J.
AU - FH Australasia Network Consensus Working Group
PY - 2021/3/1
Y1 - 2021/3/1
N2 - Familial hypercholesterolaemia (FH) is a dominant and highly penetrant monogenic disorder present from birth that markedly elevates plasma low-density lipoprotein (LDL)-cholesterol concentration and, if untreated, leads to premature atherosclerosis and coronary artery disease (CAD). There are approximately 100,000 people with FH in Australia. However, an overwhelming majority of those affected remain undetected and inadequately treated, consistent with FH being a leading challenge for public health genomics. To further address the unmet need, we provide an updated guidance, presented as a series of systematically collated recommendations, on the care of patients and families with FH. These recommendations have been informed by an exponential growth in published works and new evidence over the last 5 years and are compatible with a contemporary global call to action on FH. Recommendations are given on the detection, diagnosis, assessment and management of FH in adults and children. Recommendations are also made on genetic testing and risk notification of biological relatives who should undergo cascade testing for FH. Guidance on management is based on the concepts of risk re-stratification, adherence to heart healthy lifestyles, treatment of non-cholesterol risk factors, and safe and appropriate use of LDL-cholesterol lowering therapies, including statins, ezetimibe, proprotein convertase subtilisin/kexin type 9 inhibitors and lipoprotein apheresis. Broad recommendations are also provided for the organisation and development of health care services. Recommendations on best practice need to be underpinned by good clinical judgment and shared decision making with patients and families. Models of care for FH need to be adapted to local and regional health care needs and available resources. A comprehensive and realistic implementation strategy, informed by further research, including assessments of cost-benefit, will be required to ensure that this new guidance benefits all Australian families with or at risk of FH.
AB - Familial hypercholesterolaemia (FH) is a dominant and highly penetrant monogenic disorder present from birth that markedly elevates plasma low-density lipoprotein (LDL)-cholesterol concentration and, if untreated, leads to premature atherosclerosis and coronary artery disease (CAD). There are approximately 100,000 people with FH in Australia. However, an overwhelming majority of those affected remain undetected and inadequately treated, consistent with FH being a leading challenge for public health genomics. To further address the unmet need, we provide an updated guidance, presented as a series of systematically collated recommendations, on the care of patients and families with FH. These recommendations have been informed by an exponential growth in published works and new evidence over the last 5 years and are compatible with a contemporary global call to action on FH. Recommendations are given on the detection, diagnosis, assessment and management of FH in adults and children. Recommendations are also made on genetic testing and risk notification of biological relatives who should undergo cascade testing for FH. Guidance on management is based on the concepts of risk re-stratification, adherence to heart healthy lifestyles, treatment of non-cholesterol risk factors, and safe and appropriate use of LDL-cholesterol lowering therapies, including statins, ezetimibe, proprotein convertase subtilisin/kexin type 9 inhibitors and lipoprotein apheresis. Broad recommendations are also provided for the organisation and development of health care services. Recommendations on best practice need to be underpinned by good clinical judgment and shared decision making with patients and families. Models of care for FH need to be adapted to local and regional health care needs and available resources. A comprehensive and realistic implementation strategy, informed by further research, including assessments of cost-benefit, will be required to ensure that this new guidance benefits all Australian families with or at risk of FH.
KW - Adults
KW - Assessment
KW - Cascade testing
KW - Children
KW - Diagnosis
KW - Familial hypercholesterolaemia
KW - Genetic testing
KW - Guidance
KW - Management
KW - Organisation of care
UR - http://www.scopus.com/inward/record.url?scp=85098527802&partnerID=8YFLogxK
U2 - 10.1016/j.hlc.2020.09.943
DO - 10.1016/j.hlc.2020.09.943
M3 - Letter
C2 - 33309206
AN - SCOPUS:85098527802
VL - 30
SP - P324-349
JO - Heart Lung and Circulation
JF - Heart Lung and Circulation
SN - 1443-9506
IS - 3
ER -