# A Pilot Study of Opportunistic Chronic Kidney Disease Screening in Primary Care Using a Clinical Decision Support System

**Authors:** Maite López-Garrigós, Estanislao Puig, Selene Sánchez, Irene Gutiérrez, Maria Salinas, Alberto Ortiz, Emilio Flores

PMC · DOI: 10.3390/diagnostics16010008 · Diagnostics · 2025-12-19

## TL;DR

A pilot study shows that using a clinical decision support system in primary care can effectively detect chronic kidney disease at low cost.

## Contribution

The study demonstrates the feasibility and low cost of opportunistic CKD screening in primary care using a CDSS.

## Key findings

- 104 new CKD cases were identified in 1,774 patients screened.
- Most cases were early-stage and manageable in primary care.
- Reagent costs were EUR 0.51 per person and EUR 11.14 per CKD case detected.

## Abstract

Background/Objectives: CKD affects over 10% of adults and is often silent, delaying diagnosis. Opportunistic primary care screening supported by clinical decision support systems (CDSSs) may improve detection with minimal burden. We evaluated the feasibility, diagnostic yield, clinical actions, and reagent costs of a CDSS-enabled, albuminuria-first program using eGFR. Methods: This one-year cross-sectional intervention screened all patients receiving routine laboratory tests at a primary care center using a CDSS integrating prior labs, medical records, and guideline rules. Eligibility required patients age 60–85 (Group 1) or 18–59 with hypertension, diabetes, or cardiovascular disease (Group 2). Eligible patients received urine albumin and eGFR testing with standard phlebotomy; abnormal findings triggered confirmatory tests. Outcomes were diagnostic yield, KDIGO risk stratification, referral patterns, and reagent costs. The CDSS surfaced prompts and pre-populated orders in the laboratory interface. Results: Of 7722 targets, 1892 (24.5%) were flagged (34.2% of Group 2, 7.9% of Group 1), and 1774 (93.8%) completed screening. We identified 104 new CKD cases (5.9%): 75% KDIGO moderate risk, 19% high, and 6% very high. Twenty patients (1.1%) met criteria for nephrology referral. Guideline-directed therapy was started or optimized in 90%, and 62.5% received a new CKD diagnosis code. Reagent costs averaged EUR 0.51 per person screened and EUR 11.14 per CKD case detected. Most cases were early-stage and manageable in primary care. Conclusions: CDSS-enabled opportunistic screening in primary care is feasible, acceptable, and low-cost. It identifies previously unrecognized CKD at modest expense, enabling early interventions that may slow progression and reduce cardiovascular events. Scaling with follow-up should assess long-term outcomes.

## Linked entities

- **Diseases:** chronic kidney disease (MONDO:0005300), diabetes (MONDO:0005015), cardiovascular disease (MONDO:0004995)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** CKD (MESH:D012080), diabetes (MESH:D003920), cardiovascular disease (MESH:D002318), Chronic Kidney Disease (MESH:D051436), albuminuria (MESH:D000419), hypertension (MESH:D006973)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC12785800/full.md

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Source: https://tomesphere.com/paper/PMC12785800