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Meeting ReportDiabetes and endocrine disease

Factors Associated with Accumulating Diabetes Complications in a Medicare Advantage Cohort to Inform a Prediction Tool

Winston Liaw, Omolola Adepoju, Pete Womack, Ben King, Todd Prewitt, Jessica Dobbins, William Glasheen, LeChauncy Woodard and Ioannis Kakadiaris
The Annals of Family Medicine November 2024, 22 (Supplement 1) 5940; DOI: https://doi.org/10.1370/afm.22.s1.5940
Winston Liaw
MD, MPH, MD, MPH
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Omolola Adepoju
PhD, MPH
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Pete Womack
MS, MT(ASCP)
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Ben King
PhD, MPH
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Todd Prewitt
MD
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Jessica Dobbins
DrPH, MA
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William Glasheen
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LeChauncy Woodard
MD, MPH
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Ioannis Kakadiaris
PhD
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Abstract

Context: Complications contribute to significant type 2 diabetes mellitus (T2DM) morbidity. While preventable, many fail to receive timely treatment in primary care, leading the most vulnerable to accumulate complications.

Objective: To identify the factors associated with the accumulation of T2DM complications

Study Design and Analysis: In this cohort study, we assessed the factors associated with the Diabetes Complications Severity Index (DCSI; which captures the number and severity of complications).

Population Studied: Adults aged 65 years and older with T2DM enrolled in a national Medicare Advantage plan

Setting or Dataset: Enrollment and claims data (2016-2020)

Measures: The dependent variable was DCSI. Independent variables included year, demographics (age, sex, race/ethnicity, language, dual eligibility), geography (rural vs. non-rural), comorbidities (Charlson Comorbidity Index (CCI) and Functional Comorbidity Index (FCI)), utilization, and quality measures. We used multilevel mixed effects models with a progressively expanding set of variables, including demographics (model 1), comorbidities (model 2), utilization (model 3), and quality measures (model 4).

Results: We included 49,843 individuals in model 1. All four models showed a consistent relationship between year (incidence rate ratio (IRR)=1.30, p<0.001, 2020 vs. 2016, model 1), sex (IRR=0.85, p<0.001, female vs. male, model 1), race / ethnicity (IRR=1.05, p<0.001, Black vs. white, model 1), dual eligibility (IRR=1.26, p<0.001 yes vs. no), and rurality (IRR=0.90, p<0.001, yes vs. no, model 1). In model 2, CCI (IRR=1.18, p<0.001) and FCI (IRR=1.08, p<0.001) were associated with higher DCSI. In model 3, emergency department visits (IRR=1.002, p=0.01) were associated with higher DCSI while physician visits (IRR=0.998, p<0.001) were associated with lower DCSI. In model 4, not meeting the quality measure for blood pressure (a target blood pressure that is less than 140/90) was associated with higher DCSI (IRR=1.08, p<0.001), while meeting the quality measures for LDL cholesterol and hemoglobin A1c were not associated with DCSI.

Conclusions: Year, male sex, race / ethnicity, non-rural status, comorbidities, emergency department visits, and not meeting the quality measure for blood pressure were associated with higher DCSI. These results will inform a primary care tool that uses artificial intelligence/machine learning to predict those individuals at high risk for diabetes progression.

  • © 2024 Annals of Family Medicine, Inc. For the private, noncommercial use of one individual user of the Web site. All other rights reserved.
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The Annals of Family Medicine: 22 (Supplement 1)
The Annals of Family Medicine: 22 (Supplement 1)
Vol. 22, Issue Supplement 1
20 Nov 2024
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Factors Associated with Accumulating Diabetes Complications in a Medicare Advantage Cohort to Inform a Prediction Tool
Winston Liaw, Omolola Adepoju, Pete Womack, Ben King, Todd Prewitt, Jessica Dobbins, William Glasheen, LeChauncy Woodard, Ioannis Kakadiaris
The Annals of Family Medicine Nov 2024, 22 (Supplement 1) 5940; DOI: 10.1370/afm.22.s1.5940

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Factors Associated with Accumulating Diabetes Complications in a Medicare Advantage Cohort to Inform a Prediction Tool
Winston Liaw, Omolola Adepoju, Pete Womack, Ben King, Todd Prewitt, Jessica Dobbins, William Glasheen, LeChauncy Woodard, Ioannis Kakadiaris
The Annals of Family Medicine Nov 2024, 22 (Supplement 1) 5940; DOI: 10.1370/afm.22.s1.5940
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