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

BACKGROUND: Electronic medical records (EMRs) offer the promise of computationally identifying sarcoidosis cases. However, the accuracy of identifying these cases in the EMR is unknown. OBJECTIVE: The aim of this study is to determine the statistical performance of using the International Classifica...

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Autores principales: Seedahmed, Mohamed I, Mogilnicka, Izabella, Zeng, Siyang, Luo, Gang, Whooley, Mary A, McCulloch, Charles E, Koth, Laura, Arjomandi, Mehrdad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: JMIR Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8928044/
https://www.ncbi.nlm.nih.gov/pubmed/35081036
http://dx.doi.org/10.2196/31615
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author Seedahmed, Mohamed I
Mogilnicka, Izabella
Zeng, Siyang
Luo, Gang
Whooley, Mary A
McCulloch, Charles E
Koth, Laura
Arjomandi, Mehrdad
author_facet Seedahmed, Mohamed I
Mogilnicka, Izabella
Zeng, Siyang
Luo, Gang
Whooley, Mary A
McCulloch, Charles E
Koth, Laura
Arjomandi, Mehrdad
author_sort Seedahmed, Mohamed I
collection PubMed
description BACKGROUND: Electronic medical records (EMRs) offer the promise of computationally identifying sarcoidosis cases. However, the accuracy of identifying these cases in the EMR is unknown. OBJECTIVE: 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. METHODS: 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. RESULTS: 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. CONCLUSIONS: 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.
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spelling pubmed-89280442022-03-18 Performance of a Computational Phenotyping Algorithm for Sarcoidosis Using Diagnostic Codes in Electronic Medical Records: Case Validation Study From 2 Veterans Affairs Medical Centers Seedahmed, Mohamed I Mogilnicka, Izabella Zeng, Siyang Luo, Gang Whooley, Mary A McCulloch, Charles E Koth, Laura Arjomandi, Mehrdad JMIR Form Res Original Paper BACKGROUND: Electronic medical records (EMRs) offer the promise of computationally identifying sarcoidosis cases. However, the accuracy of identifying these cases in the EMR is unknown. OBJECTIVE: 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. METHODS: 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. RESULTS: 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. CONCLUSIONS: 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. JMIR Publications 2022-03-02 /pmc/articles/PMC8928044/ /pubmed/35081036 http://dx.doi.org/10.2196/31615 Text en ©Mohamed I Seedahmed, Izabella Mogilnicka, Siyang Zeng, Gang Luo, Mary A Whooley, Charles E McCulloch, Laura Koth, Mehrdad Arjomandi. Originally published in JMIR Formative Research (https://formative.jmir.org), 02.03.2022. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in JMIR Formative Research, is properly cited. The complete bibliographic information, a link to the original publication on https://formative.jmir.org, as well as this copyright and license information must be included.
spellingShingle Original Paper
Seedahmed, Mohamed I
Mogilnicka, Izabella
Zeng, Siyang
Luo, Gang
Whooley, Mary A
McCulloch, Charles E
Koth, Laura
Arjomandi, Mehrdad
Performance of a Computational Phenotyping Algorithm for Sarcoidosis Using Diagnostic Codes in Electronic Medical Records: Case Validation Study From 2 Veterans Affairs Medical Centers
title Performance of a Computational Phenotyping Algorithm for Sarcoidosis Using Diagnostic Codes in Electronic Medical Records: Case Validation Study From 2 Veterans Affairs Medical Centers
title_full Performance of a Computational Phenotyping Algorithm for Sarcoidosis Using Diagnostic Codes in Electronic Medical Records: Case Validation Study From 2 Veterans Affairs Medical Centers
title_fullStr Performance of a Computational Phenotyping Algorithm for Sarcoidosis Using Diagnostic Codes in Electronic Medical Records: Case Validation Study From 2 Veterans Affairs Medical Centers
title_full_unstemmed Performance of a Computational Phenotyping Algorithm for Sarcoidosis Using Diagnostic Codes in Electronic Medical Records: Case Validation Study From 2 Veterans Affairs Medical Centers
title_short Performance of a Computational Phenotyping Algorithm for Sarcoidosis Using Diagnostic Codes in Electronic Medical Records: Case Validation Study From 2 Veterans Affairs Medical Centers
title_sort performance of a computational phenotyping algorithm for sarcoidosis using diagnostic codes in electronic medical records: case validation study from 2 veterans affairs medical centers
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8928044/
https://www.ncbi.nlm.nih.gov/pubmed/35081036
http://dx.doi.org/10.2196/31615
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