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B Bapat
a Familial GI Cancer
Registry, Mount Sinai Hospital, University of Toronto, Toronto, Canada, b Department of Pathology and
Laboratory Medicine, Mount Sinai Hospital, University of Toronto,
Toronto, Canada, c Department of Medicine, Mount Sinai
Hospital, University of Toronto, Toronto, Canada, d Molecular
and Medical Genetics, Department of Ophthalmology and Division of
Immunology and Cancer Research, The Hospital for Sick Children and Eye
Research Institute of Canada, University of Toronto, Toronto, Canada
Correspondence to: Dr B Bapat,
Department of Pathology and Laboratory Medicine, Mount Sinai Hospital,
600 University Avenue, Toronto, Ontario, M5G 1X5, Canada. Accepted for publication 4 November 1998
BACKGROUND Keywords:
familial adenomatous polyposis;
adenomatous
polyposis coli gene;
cost analysis;
genetic testing
Mutations of the
APC gene cause familial adenomatous polyposis (FAP), a hereditary colorectal cancer predisposition syndrome.
AIMS
To conduct a cost comparison
analysis of predictive genetic testing versus conventional clinical
screening for individuals at risk of inheriting FAP, using the
perspective of a third party payer.
METHODS
All direct health care
costs for both screening strategies were measured according to time and
motion, and the expected costs evaluated using a decision analysis model.
RESULTS
The baseline analysis
predicted that screening a prototype FAP family would cost $4975/£3109
by molecular testing and $8031/£5019 by clinical screening strategy,
when family members were monitored with the same frequency of clinical
surveillance (every two to three years). Sensitivity analyses revealed
that the genetic testing approach is cost saving for key variables including the kindred size, the age of screening onset, and the cost of
mutation identification in a proband. However, if the APC mutation carriers were monitored at an
increased (annual) frequency, the cost of the genetic screening
strategy increased to $7483/£4677 and was especially sensitive to
variability in age of onset of screening, family size, and cost of
genetic testing of at risk relatives.
CONCLUSIONS
In FAP kindreds, a
predictive genetic testing strategy costs less than conventional
clinical screening, provided that the frequency of surveillance is
identical using either strategy. An additional significant benefit is
the elimination of unnecessary colonic examinations for those family
members found to be non-carriers.
(Gut 1999;44:698-703)
This article has been cited by other articles:
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S. Morgan, J. Hurley, F. Miller, and M. Giacomini Predictive genetic tests and health system costs Can. Med. Assoc. J., April 15, 2003; 168(8): 989 - 991. [Full Text] [PDF] |
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