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Clinical Decision Support

Kidney risk is hiding in data you already collect. NephroSense AI reads it.

Routine panels already drawn carry a signal the creatinine threshold cannot see. One platform surfaces it — prioritizing patients for confirmatory kidney testing in the clinic, and characterizing candidate populations for retrospective research.

Review queueIllustrative — synthetic data
Pt 04831routine visit
unremarkable · no flag raised
Pt 11274routine visit
unremarkable · no flag raised
Pt 02956routine visit
unremarkable · no flag raised
Pt 19408routine visit
unremarkable · no flag raisedPrioritize — confirmatory kidney evaluation
→ eGFR + urine albumin (uACR)
Pt 07362routine visit
unremarkable · no flag raisedPrioritize — confirmatory kidney evaluation
→ eGFR + urine albumin (uACR)
Pt 23517routine visit
unremarkable · no flag raised

Routine records. Nothing flagged.

Inputs
Values already present in a routine adult workup — standard blood work, vitals and basic history, drawn and recorded as part of ordinary care.
Evidence
Retrospective feasibility demonstrated on a US adult clinical cohort. Independent external validation is in progress and is not yet complete.
IP
Patent-pending technology. Provisional patent filed March 2026.

One Platform, Two Channels

One platform foundation. Separate models, workflows, and evidence paths.

Health systems ask who should be prioritized for confirmatory kidney testing. Research sponsors ask what routine records hold that a site query misses.

Biopharma Research · near-term focus

STRATA

Open for sponsor collaboration

Cohort construction for kidney and cardio-renal programs

Estimate the candidate population a site actually holds before you select it, rather than after.

For Clinical operations · Feasibility · Clinical development · Medical affairs

Explore the research platform4 further programs, each carrying its stage

Health Systems · clinical foundation

VANTAGE

Available today

CKD risk triage from the panel you already drew

Risk triage at the point of care.

For Clinicians, primary care groups, FQHCs

Problem → Solution Matrix

The Signal Is Already in Your Labs. We Surface It.

NephroSense AI connects unconnected routine lab results into actionable, explainable risk triage.

Global Scale850M+

People affected worldwide

Undiagnosed Rate87%

Silent until late stages

Trajectory2050

Projected 5th leading cause of death worldwide (ISN/WHO)

Sources: clinical references

01 · The Traditional Gap

Unconnected Routine Labs

Routine bloodwork and vitals are taken regularly, but early subtle trends across multiple biomarkers go unflagged until eGFR drops severely or symptoms emerge.

Consequence:

Late referrals, preventable disease progression, and costly emergency interventions.

02 · The Hidden Signal

Data Already Exists

The clinical signal to surface CKD risk is already present in standard adult primary care bloodwork, metabolic panels, and vitals. The bottleneck is synthesis, not testing.

Opportunity:

Extract earlier risk insights without requesting new tests or specialized equipment.

03 · The NephroSense Way

Automated AI Triage

NephroSense AI analyzes routine lab panels in seconds, surfacing explainable risk scores and KDIGO-aligned guidance for physician oversight.

Outcome:

Timely confirmatory testing follow-up and proactive primary care intervention.

3-Step Clinical Workflow

Three Steps. Ten Seconds. Zero New Hardware.

From routine adult lab panels to clinician-ready decision support in under 10 seconds. Built for primary care, FQHCs, and value-based care workflows.

  1. 01

    1. Ingest Routine Adult Bloodwork

    No new blood tests. No new hardware.

    Input routine adult patient biomarkers manually or upload a lab report (PDF/image). Operates directly on standard blood panels and vitals already present in patient records.

  2. 02

    2. Instant AI Risk Stratification

    KDIGO-aligned triage in under 10 seconds.

    NephroSense AI returns a CKD risk score from the routine adult panel already on file, with a confidence signal alongside it so the strength of the result is visible before you act on it.

  3. 03

    3. Clinician Review & Action

    Actionable guidance for physician oversight.

    Receive KDIGO 2024-aligned clinical considerations, referral urgency flags, and downloadable clinician-ready PDF summaries or FHIR R4 exports for early confirmatory testing follow-up.

nephrosenseai.com

Clinical Considerations

High

Nephrology Referral

High-risk CDS flag plus abnormal routine labs warrant expedited physician review

Moderate

Blood Pressure Optimization

Target < 130/80 mmHg per KDIGO guidelines

Routine

Lifestyle Modifications

Dietary sodium restriction and regular physical activity

Illustrative — synthetic data. Not a real patient or a performance claim.

See the walkthrough →

Who It's For

Built for the Clinicians Who Need It Most

NephroSense AI is designed for resource-constrained settings where the need is greatest and the impact highest.

FQHCs & Community Health Centers

Reach underserved populations with existing labs — no new laboratory tests required. Designed for the communities most affected by CKD disparities.

Primary Care Physicians

Surface at-risk patients early with risk scores whose basis is visible to the clinician and KDIGO-aligned clinical considerations, without needing nephrology expertise.

Value-Based Care Programs

Batch screen populations, visualize risk distributions, and prioritize interventions so at-risk patients get confirmatory testing sooner.

Across the CKD Ecosystem

Beyond the point of care, NephroSense AI becomes a risk-intelligence layer for the partners who shape how CKD is studied and surfaced.

Pharma & Life Sciences

Cohort construction for kidney and cardio-renal programs. Much of the recruitable population is invisible before it can be ranked. We surface a candidate population from routine panels already in a health system's data — including patients with no CKD diagnosis code and no urine albumin result on file.

Pathology & Diagnostic Labs

Routine results can carry a kidney-risk signal that a single-threshold review does not surface. NephroSense AI returns a risk score and confidence signal from values already present in a routine adult workup.

Clinical Foundation & Governance

Grounded in Evidence, Built for Interoperability

Designed to align with global nephrology guidelines, open EHR interoperability standards, and CDS regulatory pathways.

USA

Clinical Feasibility

Feasibility demonstrated on a US adult clinical cohort

KDIGO

Kidney Disease: Improving Global Outcomes

2024 Clinical Practice Guidelines for CKD

CDS

Routine-Lab Clinical Decision Support

Primary CDS workflow reads a routine adult lab workup. Confirmatory kidney testing follows after a patient is flagged.

FHIR R4

Fast Healthcare Interoperability Resources

HL7 standard for EHR data exchange

Founding Team

Built by Scientists, Physicians & AI Engineers

Deep expertise across clinical oversight, AI engineering, and healthtech scaling.

Dr. Poornima Dubey, PhD

Dr. Poornima Dubey, PhD

Co-Founder

MIT · HMS · IIT · AI/ML · Nanobiotech · HealthTech

Dew Prabhakar, MBA

Dew Prabhakar, MBA

Co-Founder

IIM · Ops · Strategy

Dr. Nisha, MBBS

Dr. Nisha, MBBS

Co-Founder

KGMU · Clinical Oversight

AJ

Dr. Amit Jain

Co-Founder

CS/AI Engineer

Institutional Ties & Background

Harvard Medical SchoolMassachusetts Institute of TechnologyIIT RoorkeeIIM RanchiKing George's Medical University, LucknowNSF I-CorpsPenn StateUniversity of Maryland, BaltimoreUniversity of CincinnatiUCL School of PharmacyBacked byC10 Labs accelerator
Regulatory Framework

21st Century Cures Act CDS Pathway

Physician Oversight Required

Regulatory Note: NephroSense AI is designed to qualify for the Clinical Decision Support exemption under the 21st Century Cures Act. We have not yet received FDA classification or clearance; regulatory status will evolve as the product advances through clinical validation. The tool provides risk scores and supporting explanations to assist qualified healthcare professionals. It does not provide diagnoses. All clinical decisions require physician review and independent clinical judgment.

Advised by clinical, commercial and regulatory veterans. Meet the advisory board →

Ready to see what your routine data holds?

Start a conversation about a retrospective look-back, or try the clinical demo with built-in scenarios.