Clinically validated genetic screening and family health history tracking in one platform. INHERET screens for risk factors associated with all hereditary cancers not just the more common hereditary diseases like breast and colon cancers. INHERET utilizes, and continuously updates, the most comprehensive set of guidelines, including NCCN Guidelines®, to ensure you don't miss a patient at risk.
INHERET doesn't stop at year one - we will annually rerun patient records against the most current guidelines and notify if their risk changes to avoid patients being left behind as science advances.
Via text or email, patients receive a link to INHERET's user-friendly screening tool. A pedigree is automatically generated and a family ID is assigned, allowing patients to share with relatives. Patients and family members are left with a comprehensive risk profile that facilitates cascade counseling and testing.
We keep patients engaged and involved in building their own pedigree. 98% of patients found INHERET easy to use and with an 86% completion rate for genetics clinic (compared to 60% using paper forms), which reduced the average submission time to just 72 hours (compared to 4 weeks using paper forms).
INHERET makes prior authorization a breeze and provides robust decision support to guide providers of the appropriate genes to consider for testing. INHERET automatically generates medical necessity documentation (including evidence-based publications) to streamline reimbursement.
After conducting 3 pilot studies on over two-thousand patients, we documented a dramatic increase in histories completed from less than 60% before INHERET to 86% using it. We detected the 1 in 5 individuals at increased risk. At-risk individuals require follow-up imaging, testing, and treatments. In fact, our study analysis showed that one genetic counselor using INHERET was able to counsel an additional 144 patients, many of whom may then receive laboratory and imaging tests, and some may pursue prophylaxis and therapeutic treatments. These services could generate an additional $809,000 in preventive-care billable revenues today while improving patient outcomes and reducing future cancer-care burdens.
Additional High-risk Patients Screened by One Genetic Counselor
Additional Revenue from Preventive Laboratory and Imaging Tests
Additional Annual New Billable Revenue
Written for 4th-grade literacy, patients easily complete INHERET on their device, at their convenience; allowing more flexibility, improving data accuracy, while saving precious in-clinic time.
Harnessing the power of NCCN Guidelines® and other best-practice guidelines, patient personal and family health information runs through our proprietary algorithms to identify risk levels.
Patient health history is summarized in easy-to-read reports, complete with health history summary, pedigree, and clear indications of next-steps recommendations. HL7 and FIHR ready for EHR integration.
Comprehensive pedigrees are provided - with up to 7 generations - in INHERET reports, saving clinics valuable time
INHERET saves precious clinic in-office time, provides a better understanding of the patient health history, utilizes the most current guidelines, supplies tailored educational resources, and helps billable revenue.
Contact us with questions or schedule a demo to learn how INHERET identifies your high-risk patients and provides you with robust clinical decision support.
P: 866-464-3738