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Precision population analytics: population management at the point-of-care

OBJECTIVE: To present clinicians at the point-of-care with real-world data on the effectiveness of various treatment options in a precision cohort of patients closely matched to the index patient. MATERIALS AND METHODS: We developed disease-specific, machine-learning, patient-similarity models for h...

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Autores principales: Tang, Paul C, Miller, Sarah, Stavropoulos, Harry, Kartoun, Uri, Zambrano, John, Ng, Kenney
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7936526/
https://www.ncbi.nlm.nih.gov/pubmed/33180897
http://dx.doi.org/10.1093/jamia/ocaa247
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author Tang, Paul C
Miller, Sarah
Stavropoulos, Harry
Kartoun, Uri
Zambrano, John
Ng, Kenney
author_facet Tang, Paul C
Miller, Sarah
Stavropoulos, Harry
Kartoun, Uri
Zambrano, John
Ng, Kenney
author_sort Tang, Paul C
collection PubMed
description OBJECTIVE: To present clinicians at the point-of-care with real-world data on the effectiveness of various treatment options in a precision cohort of patients closely matched to the index patient. MATERIALS AND METHODS: We developed disease-specific, machine-learning, patient-similarity models for hypertension (HTN), type II diabetes mellitus (T2DM), and hyperlipidemia (HL) using data on approximately 2.5 million patients in a large medical group practice. For each identified decision point, an encounter during which the patient’s condition was not controlled, we compared the actual outcome of the treatment decision administered to that of the best-achieved outcome for similar patients in similar clinical situations. RESULTS: For the majority of decision points (66.8%, 59.0%, and 83.5% for HTN, T2DM, and HL, respectively), there were alternative treatment options administered to patients in the precision cohort that resulted in a significantly increased proportion of patients under control than the treatment option chosen for the index patient. The expected percentage of patients whose condition would have been controlled if the best-practice treatment option had been chosen would have been better than the actual percentage by: 36% (65.1% vs 48.0%, HTN), 68% (37.7% vs 22.5%, T2DM), and 138% (75.3% vs 31.7%, HL). CONCLUSION: Clinical guidelines are primarily based on the results of randomized controlled trials, which apply to a homogeneous subject population. Providing the effectiveness of various treatment options used in a precision cohort of patients similar to the index patient can provide complementary information to tailor guideline recommendations for individual patients and potentially improve outcomes.
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spelling pubmed-79365262021-03-10 Precision population analytics: population management at the point-of-care Tang, Paul C Miller, Sarah Stavropoulos, Harry Kartoun, Uri Zambrano, John Ng, Kenney J Am Med Inform Assoc Research and Applications OBJECTIVE: To present clinicians at the point-of-care with real-world data on the effectiveness of various treatment options in a precision cohort of patients closely matched to the index patient. MATERIALS AND METHODS: We developed disease-specific, machine-learning, patient-similarity models for hypertension (HTN), type II diabetes mellitus (T2DM), and hyperlipidemia (HL) using data on approximately 2.5 million patients in a large medical group practice. For each identified decision point, an encounter during which the patient’s condition was not controlled, we compared the actual outcome of the treatment decision administered to that of the best-achieved outcome for similar patients in similar clinical situations. RESULTS: For the majority of decision points (66.8%, 59.0%, and 83.5% for HTN, T2DM, and HL, respectively), there were alternative treatment options administered to patients in the precision cohort that resulted in a significantly increased proportion of patients under control than the treatment option chosen for the index patient. The expected percentage of patients whose condition would have been controlled if the best-practice treatment option had been chosen would have been better than the actual percentage by: 36% (65.1% vs 48.0%, HTN), 68% (37.7% vs 22.5%, T2DM), and 138% (75.3% vs 31.7%, HL). CONCLUSION: Clinical guidelines are primarily based on the results of randomized controlled trials, which apply to a homogeneous subject population. Providing the effectiveness of various treatment options used in a precision cohort of patients similar to the index patient can provide complementary information to tailor guideline recommendations for individual patients and potentially improve outcomes. Oxford University Press 2020-11-12 /pmc/articles/PMC7936526/ /pubmed/33180897 http://dx.doi.org/10.1093/jamia/ocaa247 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the American Medical Informatics Association. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research and Applications
Tang, Paul C
Miller, Sarah
Stavropoulos, Harry
Kartoun, Uri
Zambrano, John
Ng, Kenney
Precision population analytics: population management at the point-of-care
title Precision population analytics: population management at the point-of-care
title_full Precision population analytics: population management at the point-of-care
title_fullStr Precision population analytics: population management at the point-of-care
title_full_unstemmed Precision population analytics: population management at the point-of-care
title_short Precision population analytics: population management at the point-of-care
title_sort precision population analytics: population management at the point-of-care
topic Research and Applications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7936526/
https://www.ncbi.nlm.nih.gov/pubmed/33180897
http://dx.doi.org/10.1093/jamia/ocaa247
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