At Mayo Clinic, the future of health care promises individual-driven innovation with patient care designed for your whole body. One way that we're fueling this innovation is through the Center for Individualized Medicine (IM Clinic) which offers genomic testing to patients in order to further personalize care. Health care providers use knowledge about a patient’s genome (or DNA) to diagnose, predict, treat and prevent disease — allowing medical care to be tailored to the patient’s genomic make-up.
Recently, researchers from the IM Clinic presented results of three different studies evaluating implications and feasibility of genome sequencing at the ACMG Annual Clinical Genetics Meeting in Nashville, Tenn. Here are the highlights from each presentation:
- Patients’ Views on Incidental Findings from Clinical Exome Sequencing: The IM Clinic offers whole-exome sequencing for patients with advanced cancers and difficult diagnoses. Among the difficult questions clinicians and patients wrestle with is, “How much information is too much?” Researchers interviewed 44 patients of the Individualized Medicine Clinic about what they would and wouldn’t want to know from next-generation sequencing. Findings demonstrate that patient perspectives of risks and benefits of knowing genomic information are personal and contextual. As one participant stated, “I think this is the Individual Medicine program for a reason. Everything has to be on a case-by-case basis.”
- Whole-Exome Sequencing of 10 Scientists: Evaluation of Process and Outcomes (poster presentation) — As genome sequencing technologies advance at a breakneck pace, patients will increasingly expect to have their whole exome — and eventually their whole genome — embedded in their records, just like family histories and medication lists. In an attempt to understand the difficulties and limitations of whole-exome sequencing in routine care, 10 genetics scientists underwent sequencing and genomic counseling.
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