External Validation of Clinical Prediction Models in Unilateral Primary Aldosteronism

Author:

Sam Davis1ORCID,Kline Gregory A2,So Benny3ORCID,Hundemer Gregory L4,Pasieka Janice L5,Harvey Adrian5,Chin Alex67,Przybojewski Stefan J3,Caughlin Cori E3,Leung Alexander A28ORCID

Affiliation:

1. Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada

2. Department of Medicine, University of Calgary, Calgary, Alberta, Canada

3. Department of Radiology, University of Calgary, Calgary, Alberta, Canada

4. Department of Medicine, University of Ottawa, Ottawa, Ontario, Canada

5. Department of Surgery, University of Calgary, Calgary, Alberta, Canada

6. Alberta Precision Laboratories, Alberta Health Services, Calgary, Alberta, Canada

7. Department of Pathology and Laboratory Medicine, University of Calgary, Calgary, Alberta, Canada

8. Department of Community Health Sciences, University of Calgary, Calgary, Alberta, Canada

Abstract

Abstract BACKGROUND Targeted treatment of primary aldosteronism (PA) is informed by adrenal vein sampling (AVS), which remains limited to specialized centers. Clinical prediction models have been developed to help select patients who would most likely benefit from AVS. Our aim was to assess the performance of these models for PA subtyping. METHODS This external validation study evaluated consecutive patients referred for PA who underwent AVS at a tertiary care referral center in Alberta, Canada during 2006–2018. In alignment with the original study designs and intended uses of the clinical prediction models, the primary outcome was the presence of lateralization on AVS. Model discrimination was evaluated using the C-statistic. Model calibration was assessed by comparing the observed vs. predicted probability of lateralization in the external validation cohort. RESULTS The validation cohort included 342 PA patients who underwent AVS (mean age, 52.1 years [SD, 11.5]; 201 [58.8%] male; 186 [54.4%] with lateralization). Six published models were assessed. All models demonstrated low-to-moderate discrimination in the validation set (C-statistics; range, 0.60–0.72), representing a marked decrease compared with the derivation sets (range, 0.80–0.87). Comparison of observed and predicted probabilities of unilateral PA revealed significant miscalibration. Calibration-in-the-large for every model was >0 (range, 0.35–1.67), signifying systematic underprediction of lateralizing disease. Calibration slopes were consistently <1 (range, 0.35–0.87), indicating poor performance at the extremes of risk. CONCLUSIONS Overall, clinical prediction models did not accurately predict AVS lateralization in this large cohort. These models cannot be reliably used to inform the decision to pursue AVS for most patients.

Funder

Canadian Institutes of Health Research

Heart and Stroke Foundation

Canada’s National New Investigator

Publisher

Oxford University Press (OUP)

Subject

Internal Medicine

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