Detection of Familial Hypercholesterolaemia: A Major Treatment Gap in Preventative Cardiology

Timothy Bates, John Burnett, Frank Van Bockxmeer, Sandy Hamilton, Leonard Arnolda, Gerald Watts

Research output: Contribution to journalArticlepeer-review

40 Citations (Scopus)

Abstract

Familial hypercholesterolaemia (FH) is a common genetic disorder that untreated has an almost one hundredfold risk of coronary artery disease (CAD). In an audit of 334 patients with premature CAD admitted to a Department of Cardiology, only 60% of medical records had sufficient clinical information for identifying FH. Of those with sufficient information recorded, 54% of patients had possible to definite FH on recognised clinical criteria. Amongst those with FH, only 38%, were on statin therapy and only 22% were treated to National Heart Foundation targets. Detection and treatment of FH represents a major gap in coronary prevention.
Original languageEnglish
Pages (from-to)411-413
JournalHeart, Lung and Circulation
Volume17
Issue number5
DOIs
Publication statusPublished - 2008

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