Martha - Point-of-Care Patient Genetic Lab Test Reporting

Martha is a patient reporting and analytic suite with real-time data integration of cancer molecular and genetic testing data from external and internal lab partners with patient EMR data. Employing custom, complex multi-source data integration routines, Martha overcomes existing data accessibility limitations to centralize distributed and decentralized EMR and lab pdf source data. The resulting simplified and searchable data work flow enables quicker clinician decision making directly at the patient point-of-care in the clinic leading to increased physician and patient interaction time to discuss diagnosis and treatment planning.

Built upon our custom enterprise Hyperion Data Platform providing data interoperability and management, Martha utilizes our Hyperion Common Data Model to harmonize and standardize diverse vendor data schema and naming conventions ensuring accurate and reliable reporting. Hyperion architecture provides a scalable environment to easily incorporate more lab partners or additional EMR data.

Martha, an acronym for Molecular As say Repository for Tumor Heterogeneity Aassessment, is named after the pioneering geneticist Martha Chase who, with Alfred Hershey, conducted the ground-breaking Hershey-Chase experiments confirming DNA carried genetic material. Hershey received a Nobel Prize for this discovery, while Martha Chase’s contribution went largely unrecognized. Martha is named to honor Martha Chase’s legacy.

Features:

• Reporting Characteristics:
  • Reporting is real-time, discrete, and sortable.
  • Rapid identification of patient biomarker and gene alteration profiles supporting patient care, clinical trials, and health population research planning.
• Search Options:
  • Genes and gene alterations.
  • Patient name and EMR number.
  • Physician name.
  • Testing lab partner and Report date.
  • Multi-term search.
• Reporting Elements:
  • Biomarker findings (TMB total mutation burden status and score, MSI/MMR, ctDNA).
  • Genes and gene alterations.
  • Ordering physician and individual patient or complete clinician caseload.
  • Patient name and EMR number.
  • Testing lab data source and report date.
  • One-click access to original detailed PDF lab report.
  • Unique patient counts and total report count.
• Gene Reference Library: Integrated Gene Search reference library with point and click access to gene alteration interpretations of biological mechanisms and clinical significance.
• Lab Partner Integrations: Custom interface library enables fast data integration of lab partner data currently including FoundationOne, Guardant, and Caris with plans for more lab integrations.