Clinical OMICs - Issue 8 - (Page 21)
Identifying the right kidney cancer subtype
is key to determining the right treatment.
UroGenRA®, CGI's Array-CGH test for urogenital cancer, detects genomic copy
number alterations with diagnostic and prognostic value. UroGenRA®-Kidney
can predicts benign vs. malignant tumors, and is the only CGH array for the
subtyping of renal masses.
Learn more at www.cancergenetics.com
MAXIMIZING EFFICACY (continued from p. 5)
testing, while avoiding unnecessary,
wasteful testing.
"Genetic counseling provided by
trained specialists can bridge the gap
between patients and the appropriate
use of genetic testing. It provides an
evidence-based solution that allows
specialists to ensure the right patient
gets the right test," said Dr. Sutphen,
president and chief medical officer
of InformedDNA. "The results of a
genetic test can also have an enormous impact on future healthcarerelated choices. Genetics specialists
help patients evaluate their results
and make more informed choices
based on the best and most current
information available."
While genetic testing can provide a
www.clinicalomics.com
life-saving service, it only paints a partial picture of a patient's health risks.
To accurately determine a patient's
risk-profile, the following steps are
taken by genetic specialists:
*
Conduct a complete personal and
family history risk assessment.
*
Determine whether a patient is
appropriate for genetic testing and,
if so, which test is right for them.
*
If a test is ordered, interpret the
results in the context of the patient's
family history and help them
develop a personalized care plan in
coordination with their
physicians.
However, there are gaps in physician
knowledge of genetics and with more
than 10,000 genetic tests available,
it's not surprising that as many as half
of tests are ordered inappropriately.
Misuse of genetic testing can carry a
number of unintended consequences.
In 2010, annual spending on genetic
testing eclipsed $5 billion and could
reach $25 billion within a decade.
As payers continue to look for
ways to reduce costs, consulting with
genetic specialists can safeguard
insurers against paying for diagnostics that are not medically useful,
while also improving quality of care.
"Inappropriate testing can have
unintended consequences for
patients, even beyond their individual
health," noted Steenblock, InformedDNA's senior vp for clinical services.
"Genetic counselors help patients
navigate these difficult issues."
August 13, 2014 Clinical OMICs
21
http://www.cancergenetics.com
http://ir.cancergenetics.com/
https://www.facebook.com/CancerGenetics
https://twitter.com/Cancer_Genetics
https://www.linkedin.com/company/cancer-genetics-inc.
https://www.pinterest.com/cancergenetics/
http://www.cancergenetics.com
http://www.clinicalomics.com
Table of Contents for the Digital Edition of Clinical OMICs - Issue 8
Contents
Clinical OMICs - Issue 8
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol3iss9
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol3iss8
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol3iss7
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol3iss6
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol3iss5
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol3iss4
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol3iss3
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol3iss2
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol3iss1
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss12
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss11
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss10
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss9
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss8
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss7
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss6
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss5
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss4
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss3
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss2
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss1
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue15
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue14
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue13
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue12
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue11
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue10
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue9
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue8
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue7
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue6
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue5
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue4
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue3
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue2
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue1
https://www.nxtbookmedia.com