Epic Deterioration Index v2 AI
Epic Systems Corporation · epic.com ↗
Machine-learning score in the Epic EHR that estimates a hospitalized patient's risk of clinical deterioration (Deterioration Index Version 2).
AI status
AI product FDA 510(k) summary K260008: “The score is calculated by a static gradient boosted random forest (trained with LightGBM) algorithm” / “a machine-learning algorithm” · source
How Epic Deterioration Index v2 compares with its list-mates
Epic Deterioration Index v2 is ranked in one task list, Sepsis / deterioration early warning, at #5 of 5, behind eCART. Its evidence score there is 1005, against 1005 to 1215 for the other four. We found no vendor-stated HIPAA, BAA, SOC 2, HITRUST or Epic claim for Epic Deterioration Index v2; 1 of its 4 list-mates have at least one. It has an FDA record: 510(k) cleared, K260008. List-mates with an FDA record: eCART (K233253), Bayesian Health TREWS (K250680) and Prenosis Sepsis ImmunoScore (DEN230036), plus 1 more. We could not verify its pricing; 0 of its 4 list-mates publish a price.
Computed from our rankings and the sourced facts on each tool page. List-mates are the other tools in the same top-5 lists.
Compliance profile
| Field | Status | Detail | Source | Checked |
|---|---|---|---|---|
| FDA | Verified | 510(k) cleared · K260008 | accessdata.fda.gov | 2026-10-14 |
| HIPAA | Unverified | Not found on vendor pages we checked | — | 2026-10-14 |
| BAA | Unverified | Not found on vendor pages we checked | — | 2026-10-14 |
| SOC 2 | Unverified | Not found on vendor pages we checked | — | 2026-10-14 |
| HITRUST | Unverified | Not found on vendor pages we checked | — | 2026-10-14 |
| Epic integration | Unverified | Not found on vendor pages we checked | — | 2026-10-14 |
Vendor-stated means the claim appears on the vendor’s site; we have not audited it. Unverified means we found no source, which is not a negative finding. Vendors can request a correction.
FDA records
From the FDA AI-enabled medical devices list. Wording follows FDA: 510(k) “cleared”, De Novo “granted”. Clearance applies to the specific indication in the FDA record.
| Number | Device (as listed) | Pathway | Decision date | Panel |
|---|---|---|---|---|
| K260008 | Deterioration Index Version 2 | 510(k) cleared | 09/18/2026 | Cardiovascular |