Synthetic data only. Never enter patient information; nothing is sent or stored. For clinicians. Not FDA cleared.

CPE-003 · synthetic case CKD-FX-018

Transient UACR confounder

Transient UACR confounder

Synthetic · no real patientReviewed acceptance scenarioKidney engine v1.2.0

Purpose: Prevent albuminuria diagnosis during active UTI

Inputs the engine received

Patient

Age
49 years

Context

Sex for equation
female
Urinary tract infection
active
Urine collection type
random untimed

Laboratory

Serum creatinine
0.82 mg/dL
UACR
95 mg/g

What the engine reports

Detected clinical pattern

Kidney Abnormality Detected — CKD Not Confirmed

A single abnormal result does not establish CKD. Persistence over at least three months and exclusion of acute or transient causes are needed.

  • Chronicity: Chronicity unconfirmed
  • CGA: Indicative G2A2 (not a classification)

Clinical summary

A kidney abnormality was detected (eGFR 87.6 and UACR 95 mg/g), but chronicity is not established; CKD is not confirmed. Priority: confirm persistence and exclude acute or transient causes.

Why this pattern was identified

  • Estimated GFR. 87.6 mL/min/1.73 m² (eGFRcr 2021, race-free), category G2 (60–89).
  • Albuminuria. UACR 95 mg/g, category A2 (30–300 mg/g).

Calculations

eGFRcr (CKD-EPI 2021, race-free)
87.6 mL/min/1.73 m²

Creatinine-based.

Recommended next steps

For physician consideration. Urgent review always comes first.

  1. 1Confirm persistence (repeat testing at ≥3 months) and evaluate acute or transient causes before labeling CKD.A single abnormal eGFR or UACR does not establish CKD.
  2. 2Obtain a subsequent first-morning-void midstream UACR to confirm an abnormal random ACR.Random-sample ACR is confirmed on first-morning void (KDIGO).
  3. 3Repeat UACR after the confounder resolves unless urgent clinical context requires immediate action.

Differentials, pitfalls and contradicting signals

  • UACR may be transiently elevated (active urinary tract infection).

Why it matters

Isolated abnormal eGFR or UACR values are common and often transient. Labeling CKD early can misclassify patients, while missing persistent disease delays care. Confirmation at three months balances both.

Evidence and rule trace · 6 rules

DQ-004eGFR calculation assay provenance

Inputs: creatinine assay IDMS traceability not confirmed

eGFR computed with unknown/non-confirmed standardized assay; interpret with assay provenance visible.

GFR-001Compute initial adult race-free creatinine eGFR

Inputs: creatinine 0.82 mg/dL · age 49 · sex female

eGFRcr 2021 = 87.6 mL/min/1.73 m²

DET-001Kidney abnormality detected

Inputs: UACR 95 mg/g (≥30)

kidney_abnormality_detected: determine chronicity and evaluate acute causes before confirming CKD

CHR-003Single abnormal result does not confirm CKD

Inputs: abnormality without dated evidence of ≥3 months

kidney_abnormality_unconfirmed: CKD is not confirmed

ACR-001Confirm abnormal random ACR using first morning void

Inputs: UACR 95 mg/g · random untimed specimen

abnormal_unconfirmed_specimen: obtain a subsequent first-morning-void midstream UACR to confirm

ACR-002Transient albuminuria confounder warning

Inputs: UACR 95 mg/g · active urinary tract infection

possible_transient_elevation: confirm after the confounder resolves

Evidence

  • R1 · KDIGO 2024 Clinical Practice Guideline for the Evaluation and Management of Chronic Kidney Disease. Kidney Disease: Improving Global Outcomes (KDIGO), 2024.
  • R3 · eGFR Equations for Adults: 2021 CKD-EPI creatinine and creatinine-cystatin C race-free equations. National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) / NIH, 2026.
  • R4 · NKF/ASN recommendations implementing race-free CKD-EPI equations. National Kidney Foundation / American Society of Nephrology, 2021.

Physician adjudication required. Clinical decision support for physician review. Criteria-based status is not a probability. Findings require physician adjudication and correlation with the complete clinical context. Validation-only release: not for production clinical use.

Change the values

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Live eGFR and CGA map

eGFR (mL/min/1.73 m²)

87.6

CKD-EPI 2021 creatinine, race-free

GFR \ ALBA1<30A230–300A3>300
G1≥90
G260–89◌
G3a45–59
G3b30–44
G415–29
G5<15

Indicative cell G2A2 only: CKD is not confirmed, so this is not a classification. Colors follow the KDIGO risk heat map: green low, yellow moderately increased, orange high, red very high.

Kidney functionAdd a prior result with dates to test chronicity
Sex for the equation

Switches the engine to the combined eGFRcr-cys equation.

Albuminuria
Chemistry
Kidney findings and red flags
Context
Transient albuminuria confounders
Creatinine may be unreliable
Complications (persistent)
Therapy
Documented history and special populations

Live result · computed in your browser

Detected clinical pattern

Kidney Abnormality Detected — CKD Not Confirmed

A single abnormal result does not establish CKD. Persistence over at least three months and exclusion of acute or transient causes are needed.

  • Chronicity: Chronicity unconfirmed
  • CGA: Indicative G2A2 (not a classification)

Clinical summary

A kidney abnormality was detected (eGFR 87.6 and UACR 95 mg/g), but chronicity is not established; CKD is not confirmed. Priority: confirm persistence and exclude acute or transient causes.

Why this pattern was identified

  • Estimated GFR. 87.6 mL/min/1.73 m² (eGFRcr 2021, race-free), category G2 (60–89).
  • Albuminuria. UACR 95 mg/g, category A2 (30–300 mg/g).

Calculations

eGFRcr (CKD-EPI 2021, race-free)
87.6 mL/min/1.73 m²

Creatinine-based.

Recommended next steps

For physician consideration. Urgent review always comes first.

  1. 1Confirm persistence (repeat testing at ≥3 months) and evaluate acute or transient causes before labeling CKD.A single abnormal eGFR or UACR does not establish CKD.
  2. 2Obtain a subsequent first-morning-void midstream UACR to confirm an abnormal random ACR.Random-sample ACR is confirmed on first-morning void (KDIGO).
  3. 3Repeat UACR after the confounder resolves unless urgent clinical context requires immediate action.

Differentials, pitfalls and contradicting signals

  • UACR may be transiently elevated (active urinary tract infection).

Why it matters

Isolated abnormal eGFR or UACR values are common and often transient. Labeling CKD early can misclassify patients, while missing persistent disease delays care. Confirmation at three months balances both.

Evidence and rule trace · 6 rules

DQ-004eGFR calculation assay provenance

Inputs: creatinine assay IDMS traceability not confirmed

eGFR computed with unknown/non-confirmed standardized assay; interpret with assay provenance visible.

GFR-001Compute initial adult race-free creatinine eGFR

Inputs: creatinine 0.82 mg/dL · age 49 · sex female

eGFRcr 2021 = 87.6 mL/min/1.73 m²

DET-001Kidney abnormality detected

Inputs: UACR 95 mg/g (≥30)

kidney_abnormality_detected: determine chronicity and evaluate acute causes before confirming CKD

CHR-003Single abnormal result does not confirm CKD

Inputs: abnormality without dated evidence of ≥3 months

kidney_abnormality_unconfirmed: CKD is not confirmed

ACR-001Confirm abnormal random ACR using first morning void

Inputs: UACR 95 mg/g · random untimed specimen

abnormal_unconfirmed_specimen: obtain a subsequent first-morning-void midstream UACR to confirm

ACR-002Transient albuminuria confounder warning

Inputs: UACR 95 mg/g · active urinary tract infection

possible_transient_elevation: confirm after the confounder resolves

Evidence

  • R1 · KDIGO 2024 Clinical Practice Guideline for the Evaluation and Management of Chronic Kidney Disease. Kidney Disease: Improving Global Outcomes (KDIGO), 2024.
  • R3 · eGFR Equations for Adults: 2021 CKD-EPI creatinine and creatinine-cystatin C race-free equations. National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) / NIH, 2026.
  • R4 · NKF/ASN recommendations implementing race-free CKD-EPI equations. National Kidney Foundation / American Society of Nephrology, 2021.

Physician adjudication required. Clinical decision support for physician review. Criteria-based status is not a probability. Findings require physician adjudication and correlation with the complete clinical context. Validation-only release: not for production clinical use.

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