ChallengeImpactSolutionEvidenceHow it works

Start with Certainty


TriVerity™ is the first and only FDA-cleared molecular blood test that simultaneously identifies infection type (bacterial vs. viral) and assesses illness severity in ED patients with suspected acute infection or sepsis — from a single blood draw, in ~30 minutes.

FDA Cleared

Results in ~30 Minutes

Published in Nature Medicine

1,222-Patient, 22-Site Study

The Challenge

Three questions every ED physician faces — with no good answer today

When a patient arrives with a possible infection, traditional biomarkers like WBC, lactate, and procalcitonin weren't designed to simultaneously tell you infection type (bacterial vs viral) and illness severity — leaving clinicians to guess at the most consequential decision point in care.

01

Is this actually an infection?

Non-infectious conditions — inflammation, autoimmune, metabolic — can mimic infection. Traditional biomarkers can't reliably distinguish between them, driving false sepsis alerts and unnecessary sepsis bundle activations.

02

Bacterial or viral?

The answer determines whether antibiotics are needed — but blood cultures take 12–72 hours and often return negative. Physicians are forced to default to broad-spectrum antibiotics "just in case," driving overuse and resistance.

03

How sick could this patient become?

Some patients appear stable at presentation while they've already begun decompensating.  Others aren't as sick as they appear. Without a severity signal, the safest decision defaults to admission — whether or not it's necessary.

Healthcare System Impact

Earlier, more confident decisions. Measurable outcomes

TriVerity enables clinicians to make admit vs. discharge, patient disposition, and treatment decisions earlier — at the front end of care, when clinical and financial impact is greatest.

Increase Effective Capacity

Deliver objective biological evidence that supports safe discharge decisions and reduces unnecessary admissions — without adding beds, staff, or infrastructure.

6–12% increase in direct discharges

30% decrease in ED length of stay

40% fewer transfers and diversions

Improve Patient Outcomes

TriVerity's Illness severity scoring enables earlier recognition of high-risk patients who may not yet appear critically ill — so escalation happens when it can still make a difference.

77% fewer missed high-risk patients

23% reduction in 28-day ED bounce backs

93% sensitivity for illness severity (vs. 66% for lactate)

Reduce Costs & Overuse

Identify patients who truly need aggressive diagnostics while avoiding unnecessary testing, antibiotic overuse, and costly SEP-1 variability — backed by defensible, biologically grounded documentation.

60% reduction in inappropriate antibiotics

$884 - $1,661 in cost savings per test

36% fewer false SIRS sepsis alerts

The Solution

One blood test. Three answers. ~30 minutes

Instead of looking for a specific pathogen or relying on traditional biomarkers, TriVerity reads the expression of 29 immune system mRNAs using AI/ML algorithms, giving clinicians a new capability to move from uncertainty-driven decisions to evidence-driven decisions at the very front end of care.

Bacterial Score

Likelihood of bacterial infection driving presentation. Supports earlier, targeted antibiotic decisions without waiting 12–72 hours for cultures.

Viral Score

Likelihood of viral etiology. Confidently identifies patients who don't need antibiotics — the backbone of a strong antimicrobial stewardship program.

Severity Score

Likelihood of requiring mechanical ventilation, vasopressors, or renal replacement therapy within 7 days. Identifies high-risk patients before they look critically ill.
Clinical lab researcher analyzing blood samples

Validated on 1,222 patients
at 22 leading hospitals.

Published in Nature Medicine — SEPSIS-SHIELD is one of the most rigorous prospective validation studies for any acute infection diagnostic.

ScoreSensitivitySpecificity
Bacterial97%95%
Viral95%98%
Severity93%99%

vs. PCT — Bacterial Infection

PCT <0.1 ng/ml71%
TriVerity Bacterial Score97%

vs. Lactate — Decompensation

Lactate <2 ng/ml66%
TriVerity Severity Score92%
Why It Works

How TriVerity Works

The body signals infection through immune-response changes long before inflammation via biomarkers or pathogens via cultures become detectable. TriVerity reads those signals first.

Infection Animation

TriVerity reads at the earliest signal

Infection
Begins

mRNA signals
in hours

PCT / CRP
Rise

Hours later,
non-specific

Lactate
Shifts

Later still,
imprecise

Culture
Result

12–72 hrs,
if bacteremic

Time from infection onset

For Every Stakeholder

The right signal for every stakeholder in your health system

TriVerity's three independent scores create value across clinical, operational, and financial priorities simultaneously — without adding complexity to existing workflows.

ED Directors & Medical Directors

Earlier, more confident admit vs. discharge and patient disposition decisions. TriVerity is the first FDA-cleared molecular diagnostic that provides both diagnosis and prognosis for suspected infection or sepsis patients — enabling clinicians to move beyond "is this sepsis?" to "what is driving this illness and what should we do next?"

Lab Directors & Chiefs of Pathology

A single, cost-effective, front-end test that changes patient disposition decisions early — reducing serial and redundant downstream testing while elevating the lab's role in acute infection and sepsis patient care. <1 min hands-on time, room-temperature storage, LIS connectivity.

Quality Officers & Sepsis Program Leads

Objective bacterial, viral, and severity scores that support SEP-1 compliance documentation and provide defensible, biologically grounded evidence for payer audit defense — including the ability to support stepping away from sepsis bundles when alerts are false alarms.

Hospital Executives

TriVerity represents a new capability, not a traditional diagnostic. It's a specialty diagnostic that aids decision-making at the very front end of care, supporting physician judgment rather than replacing it. Improvements in patient disposition and ED throughput flow directly to operational and financial performance.

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