Performance of a Computational Phenotyping Algorithm for Sarcoidosis Using Diagnostic Codes in Electronic Medical Records: Case Validation Study From 2 Veterans Affairs Medical Centers

• Published in: JMIR formative research Vol. 6; no. 3; p. e31615
• Main Authors: Seedahmed, Mohamed I, Mogilnicka, Izabella, Zeng, Siyang, Luo, Gang, Whooley, Mary A, McCulloch, Charles E, Koth, Laura, Arjomandi, Mehrdad
• Format: Journal Article
• Language: English
• Published: Canada JMIR Publications 02.03.2022
• Subjects: Accuracy; Algorithms; Biopsy; Chronic obstructive pulmonary disease; Electronic health records; Erythema; Granulomas; Histopathology; Magnetic resonance imaging; Medical records; Neurological disorders; Original Paper; R&D; Research & development; Sarcoidosis; Tomography; Veterans; Palo Alto California; United States > US; San Francisco California; diagnostic codes; electronic medical records; computational phenotype; practice guidelines; Veterans Affairs; EMRs; sarcoidosis; VA
• ISSN: 2561-326X; 2561-326X
• DOI: 10.2196/31615

Electronic medical records (EMRs) offer the promise of computationally identifying sarcoidosis cases. However, the accuracy of identifying these cases in the EMR is unknown. The aim of this study is to determine the statistical performance of using the International Classification of Diseases (ICD) diagnostic codes to identify patients with sarcoidosis in the EMR. We used the ICD diagnostic codes to identify sarcoidosis cases by searching the EMRs of the San Francisco and Palo Alto Veterans Affairs medical centers and randomly selecting 200 patients. To improve the diagnostic accuracy of the computational algorithm in cases where histopathological data are unavailable, we developed an index of suspicion to identify cases with a high index of suspicion for sarcoidosis (confirmed and probable) based on clinical and radiographic features alone using the American Thoracic Society practice guideline. Through medical record review, we determined the positive predictive value (PPV) of diagnosing sarcoidosis by two computational methods: using ICD codes alone and using ICD codes plus the high index of suspicion. Among the 200 patients, 158 (79%) had a high index of suspicion for sarcoidosis. Of these 158 patients, 142 (89.9%) had documentation of nonnecrotizing granuloma, confirming biopsy-proven sarcoidosis. The PPV of using ICD codes alone was 79% (95% CI 78.6%-80.5%) for identifying sarcoidosis cases and 71% (95% CI 64.7%-77.3%) for identifying histopathologically confirmed sarcoidosis in the EMRs. The inclusion of the generated high index of suspicion to identify confirmed sarcoidosis cases increased the PPV significantly to 100% (95% CI 96.5%-100%). Histopathology documentation alone was 90% sensitive compared with high index of suspicion. ICD codes are reasonable classifiers for identifying sarcoidosis cases within EMRs with a PPV of 79%. Using a computational algorithm to capture index of suspicion data elements could significantly improve the case-identification accuracy.