Literature DB >> 21917530

Familial hypercholesterolaemia: a model of care for Australasia.

Gerald F Watts1, David R Sullivan, Nicola Poplawski, Frank van Bockxmeer, Ian Hamilton-Craig, Peter M Clifton, Richard O'Brien, Warrick Bishop, Peter George, Phillip J Barter, Timothy Bates, John R Burnett, John Coakley, Patricia Davidson, Jon Emery, Andrew Martin, Waleed Farid, Lucinda Freeman, Elizabeth Geelhoed, Amanda Juniper, Alexa Kidd, Karam Kostner, Ines Krass, Michael Livingston, Suzy Maxwell, Peter O'Leary, Amal Owaimrin, Trevor G Redgrave, Nicola Reid, Lynda Southwell, Graeme Suthers, Andrew Tonkin, Simon Towler, Ronald Trent.   

Abstract

Familial hypercholesterolaemia (FH) is a dominantly inherited disorder present from birth that causes marked elevation in plasma cholesterol and premature coronary heart disease. There are at least 45,000 people with FH in Australia and New Zealand, but the vast majority remains undetected and those diagnosed with the condition are inadequately treated. To bridge this major gap in coronary prevention the FH Australasia Network (Australian Atherosclerosis Society) has developed a consensus model of care (MoC) for FH. The MoC is based on clinical experience, expert opinion, published evidence and consultations with a wide spectrum of stakeholders, and has been developed for use primarily by specialist centres intending starting a clinical service for FH. This MoC aims to provide a standardised, high-quality and cost-effective system of care that is likely to have the highest impact on patient outcomes. The MoC for FH is presented as a series of recommendations and algorithms focusing on the standards required for the detection, diagnosis, assessment and management of FH in adults and children. The process involved in cascade screening and risk notification, the backbone for detecting new cases of FH, is detailed. Guidance on treatment is based on risk stratifying patients, management of non-cholesterol risk factors, safe and effective use of statins, and a rational approach to follow-up of patients. Clinical and laboratory recommendations are given for genetic testing. An integrative system for providing best clinical care is described. This MoC for FH is not prescriptive and needs to be complemented by good clinical judgment and adjusted for local needs and resources. After initial implementation, the MoC will require critical evaluation, development and appropriate modification.
Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21917530     DOI: 10.1016/j.atherosclerosissup.2011.06.001

Source DB:  PubMed          Journal:  Atheroscler Suppl        ISSN: 1567-5688            Impact factor:   3.235


  48 in total

Review 1.  Familial hypercholesterolemia.

Authors:  Victoria Enchia Bouhairie; Anne Carol Goldberg
Journal:  Cardiol Clin       Date:  2015-05       Impact factor: 2.213

2.  A model of care for familial hypercholesterolaemia: key role for clinical biochemistry.

Authors:  Gerald F Watts; David R Sullivan; Frank M van Bockxmeer; Nicola Poplawski; Ian Hamilton-Craig; Peter M Clifton; Richard C O'Brien; Peter M George; John R Burnett
Journal:  Clin Biochem Rev       Date:  2012-02

Review 3.  Detection and care of familial hypercholesterolaemia in the community: is there a role for the pharmacist?

Authors:  Ines Krass; Adrian T Walker; Gerald F Watts
Journal:  Int J Clin Pharm       Date:  2012-05-24

4.  New Treatments on the Horizon for Familial Hypercholesterolemia.

Authors:  Khalid Al-Rasadi; Khalid Al-Waili
Journal:  Oman Med J       Date:  2017-11

Review 5.  Familial Hypercholesterolaemia Diagnosis and Management.

Authors:  Rodrigo Alonso; Leopoldo Perez de Isla; Ovidio Muñiz-Grijalvo; Jose Luis Diaz-Diaz; Pedro Mata
Journal:  Eur Cardiol       Date:  2018-08

Review 6.  The panorama of familial hypercholesterolemia in Latin America: a systematic review.

Authors:  Roopa Mehta; Rafael Zubirán; Alexandro J Martagón; Alejandra Vazquez-Cárdenas; Yayoi Segura-Kato; María Teresa Tusié-Luna; Carlos A Aguilar-Salinas
Journal:  J Lipid Res       Date:  2016-10-24       Impact factor: 5.922

7.  Patients' perceptions and experiences of familial hypercholesterolemia, cascade genetic screening and treatment.

Authors:  Sarah J Hardcastle; Ellen Legge; Chris S Laundy; Sarah J Egan; Rosemary French; Gerald F Watts; Martin S Hagger
Journal:  Int J Behav Med       Date:  2015-02

8.  Predicting Self-Management Behaviors in Familial Hypercholesterolemia Using an Integrated Theoretical Model: the Impact of Beliefs About Illnesses and Beliefs About Behaviors.

Authors:  Martin S Hagger; Sarah J Hardcastle; Catherine Hingley; Ella Strickland; Jing Pang; Gerald F Watts
Journal:  Int J Behav Med       Date:  2016-06

9.  US physician practices for diagnosing familial hypercholesterolemia: data from the CASCADE-FH registry.

Authors:  Zahid S Ahmad; Rolf L Andersen; Lars H Andersen; Emily C O'Brien; Iris Kindt; Peter Shrader; Chandna Vasandani; Connie B Newman; Emil M deGoma; Seth J Baum; Linda C Hemphill; Lisa C Hudgins; Catherine D Ahmed; Iftikhar J Kullo; Samuel S Gidding; Danielle Duffy; William Neal; Katherine Wilemon; Matthew T Roe; Daniel J Rader; Christie M Ballantyne; MacRae F Linton; P Barton Duell; Michael D Shapiro; Patrick M Moriarty; Joshua W Knowles
Journal:  J Clin Lipidol       Date:  2016-08-06       Impact factor: 4.766

10.  Familial Hypercholesterolemia: Cascade Screening in Children and Relatives of the Affected.

Authors:  Nitika Setia; Renu Saxena; J P S Sawhney; Ishwar C Verma
Journal:  Indian J Pediatr       Date:  2018-02-15       Impact factor: 1.967

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.