Suspected, but unfound
Your specialists know missed patients are in the population. Nobody can chart-review two hundred thousand records to find them.
For health systems
Find the patients your specialists are missing, without your data leaving home.
PathfindEHR™ runs governed, KOL-approved disease pathways across the FHIR and real-world data you already hold, in place, and hands your specialists a filtered, explainable list of candidates to review.
The problem
Why missed patients stay missed.
Tools that want your data
Many analytics vendors start by asking you to export clinical data. Your governance team is right to push back.
Alerts nobody reads
Single-signal rules over-fire until clinicians tune them out. Rare disease presents as combinations of evidence across years, which is exactly what simple alerts miss.
For a side-by-side look at chart review, alerts, predictive models, and governed phenotyping, see four ways to find rare disease patients.
The data foundation
FHIR-native analytics: runs where your data lives.
PathfindEHR™ is built on the data you already have. It reads standard FHIR and real-world clinical data and analyzes it in place. No migration, no copying PHI out of your environment.
FHIR & standards-based
Works with standard FHIR and real-world clinical data. No bespoke data model to build first.
Runs in your warehouse
Analytics execute where your data lives, so PHI stays inside your governed environment.
Deterministic & reproducible
Cohort logic compiles to governed SQL: the same inputs always produce the same patients.
Population-scale
Analyze whole populations at once, not one chart review at a time.
For your clinicians
A starting point, not another inbox.
The output is a filtered, explainable candidate list. A specialist opens it, sees the evidence that matched each patient against the governed pathway, and decides what happens next. No score to second-guess, no black box to trust.
It is decision support, not a diagnostic device: the software surfaces candidates and evidence, and your clinicians make every clinical decision.
Every pathway is versioned and reproducible: the same definition over the same data always surfaces the same patients. When your quality or compliance team asks why a patient appeared, the answer is in front of them.
FAQ
What health system teams ask us.
What does integration require?
PathfindEHR™ reads standard FHIR and real-world data where it already lives, and analysis runs inside your governed environment. There is no bespoke data model to build first and no migration project.
Who reviews the candidates PathfindEHR™ surfaces?
Your specialists. Each candidate comes with the specific evidence that matched the governed disease pathway, so the reviewing clinician can see why the patient surfaced. PathfindEHR™ is decision support, not a diagnostic device; your clinicians make every decision.
How much time does this ask of our clinicians?
The clinician’s job is reviewing a filtered candidate list, not running a search. Each candidate arrives with its matching evidence, and a plain-language guide walks the team through acting on a cohort without writing SQL.
Which diseases can we run?
Condition modules are curated per disease and signed off by key opinion leaders before use. A program starts with the conditions that matter most to your specialty services and adds governed pathways from there.
See it on a real cohort.
We’ll apply a governed disease pathway to your data, in your environment, and walk your team through the evidence behind every candidate.