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The Cardiac Genetics Clinic: a model for multidisciplinary genomic medicine.
Zentner, Dominica; Thompson, Tina N; James, Paul A; Trainer, Alison; Adès, Lesley C; Macciocca, Ivan; Taylor, Jessica A; Mann, Kirsty; Bogwitz, Michael; Lewis, Nigel; Morgan, Natalie; Vohra, Jitendra; Winship, Ingrid.
Affiliation
  • Zentner D; Royal Melbourne Hospital, Melbourne, VIC dominica.zentner@mh.org.au.
  • Thompson TN; Royal Melbourne Hospital, Melbourne, VIC.
  • James PA; Royal Melbourne Hospital, Melbourne, VIC.
  • Trainer A; Royal Melbourne Hospital, Melbourne, VIC.
  • Adès LC; Children's Hospital at Westmead, Sydney, NSW.
  • Macciocca I; Murdoch Childrens Research Institute, Melbourne, VIC.
  • Taylor JA; Royal Melbourne Hospital, Melbourne, VIC.
  • Mann K; Royal Melbourne Hospital, Melbourne, VIC.
  • Bogwitz M; Royal Melbourne Hospital, Melbourne, VIC.
  • Lewis N; Royal Melbourne Hospital, Melbourne, VIC.
  • Morgan N; Victorian Institute of Forensic Medicine, Melbourne, VIC.
  • Vohra J; Royal Melbourne Hospital, Melbourne, VIC.
  • Winship I; Melbourne Health, Melbourne, VIC.
Med J Aust ; 203(6): 261.e1-6, 2015 Sep 21.
Article in En | MEDLINE | ID: mdl-26377294
ABSTRACT

OBJECTIVES:

To describe patient characteristics, standard operating procedure, and uptake of genetic testing at the multidisciplinary Cardiac Genetics Clinic (CGC) at the Royal Melbourne Hospital during its first 6 years.

DESIGN:

Database exploration of referral diagnoses, sex, number of clinic visits and incidence of genetic testing in a population of individuals attending the CGC.

SETTING:

Tertiary referral hospital (Royal Melbourne Hospital) providing cardiac genetics services to the state of Victoria.

PARTICIPANTS:

All individuals initially attending the clinic between July 2007 and July 2013, either as the proband or as an at-risk family member. MAIN OUTCOME

MEASURES:

Classification of patients into diagnostic categories, number of probands and at-risk relatives assessed, incidence and outcomes of genetic testing.

RESULTS:

1170 individuals were seen for the first time over the 6-year period; 57.5% made only one visit. The median age was 39 years. Most were encompassed within four broad diagnostic categories cardiomyopathy (315 patients), aortopathy (303 patients), arrhythmia disorders (203 patients) and resuscitated cardiac arrest and/or family history of sudden cardiac death (341 patients); eight patients had "other" diagnoses. Genetic testing (mutation detection or predictive testing) was undertaken in 381 individuals (32.6%), and a pathogenic mutation was identified in 47.6% of tests, representing 15.3% of the total population.

CONCLUSION:

The CGC fulfils an important role in assisting clinicians and patients by reviewing genetic cardiac diagnoses. Clinical practice during the study period moved from a selected candidate gene approach to broader gene panel-based testing. This move to next-generation sequencing may increase the detection of mutations and variants of unknown significance. A major contribution by the clinic to the care of these individuals and their families is the provision (or negating) of a diagnosis, and of a plan for managing risks of predictable cardiac disease.
Subject(s)
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Database: MEDLINE Main subject: Cardiovascular Diseases / Genetic Testing Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Country/Region as subject: Oceania Language: En Journal: Med J Aust Year: 2015 Type: Article
Search on Google
Database: MEDLINE Main subject: Cardiovascular Diseases / Genetic Testing Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Country/Region as subject: Oceania Language: En Journal: Med J Aust Year: 2015 Type: Article