Abstract:
:Arrhythmogenic right ventricular dysplasia, also called right ventricular cardiomyopathy, is a genetically determined heart muscle disease, characterised by life-threatening ventricular arrhythmias in apparently healthy young people. The primary myocardial pathology is that the myocardium of the right ventricular free wall is replaced by fibrous or fibrofatty tissue, with scattered residual myocardial cells. Right ventricular function is abnormal and in severe cases is associated with global right ventricular dilation and overt biventricular heart failure. Although still relatively rare, arrhythmogenic right ventricular cardiomyopathy is a well recognised cause of sudden unexpected peri-operative death. In this review, we describe the basic characteristics of this disease, emphasising the diagnosis and we offer some suggestions for the anaesthetic management of these patients in the peri-operative period.
journal_name
Anaesthesiajournal_title
Anaesthesiaauthors
Alexoudis AK,Spyridonidou AG,Vogiatzaki TD,Iatrou CAdoi
10.1111/j.1365-2044.2008.05660.xsubject
Has Abstractpub_date
2009-01-01 00:00:00pages
73-8issue
1eissn
0003-2409issn
1365-2044pii
ANA5660journal_volume
64pub_type
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