Literature DB >> 35339238

Considerations When Aggregating Data to Measure Performance Across Levels of the Health Care System.

Sarah L Reeves1, Kevin J Dombkowski2, Brian Madden2, Lindsay Cogan3, Shanshan Liu4, Paul B Kirby5, Sara L Toomey6.   

Abstract

BACKGROUND: Measuring quality at varying levels of the health care system requires attribution, a process of determining the patients and services for which each level is responsible. However, it is important to ensure that attribution approaches are equitable; otherwise, individuals may be assigned differentially based upon social determinants of health.
METHODS: First, we used Medicaid claims (2010-2018) from Michigan to assess the proportion of children with sickle cell anemia who had less than 12 months enrollment within a single Medicaid health plan and could therefore not be attributed to a specific health plan. Second, we used the Medicaid Analytic eXtract data (2008-2009) from 26 states to simulate adapting the 30-Day Pediatric All-Condition Readmission measure to the Accountable Care Organization (ACO) level and examined the proportion of readmissions that could not be attributed.
RESULTS: For the sickle cell measure, an average of 300 children with sickle cell anemia were enrolled in Michigan Medicaid each year. The proportion of children that could not be attributed to a Medicaid health plan ranged from 12.2% to 89.0% across years. For the readmissions measure, of the 1,051,365 index admissions, 22% were excluded in the ACO-level analysis because of being unable to attribute the patient to a health plan for the 30 days post discharge.
CONCLUSIONS: When applying attribution models, it is essential to consider the potential to induce health disparities. Differential attribution may have unintentional consequences that deepen health disparities, particularly when considering incentive programs for health plans to improve the quality of care.
Copyright © 2021 Academic Pediatric Association. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Attribution; Medicaid; health plans; readmission; sickle cell disease

Mesh:

Year:  2022        PMID: 35339238      PMCID: PMC9367211          DOI: 10.1016/j.acap.2021.11.013

Source DB:  PubMed          Journal:  Acad Pediatr        ISSN: 1876-2859            Impact factor:   2.993


  19 in total

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2.  Universal screening for social determinants of health in pediatric sickle cell disease: A quality-improvement initiative.

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4.  Insurance gaps among vulnerable children in the United States, 1999-2001.

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5.  Incorporating statistical uncertainty in the use of physician cost profiles.

Authors:  John L Adams; Elizabeth A McGlynn; J William Thomas; Ateev Mehrotra
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6.  Invasive pneumococcal disease among children with and without sickle cell disease in the United States, 1998 to 2009.

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7.  Healthcare utilization and expenditures for low income children with sickle cell disease.

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Review 8.  Continuity of public insurance coverage: a systematic review of the literature.

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9.  Transitions of care across hospital settings in patients with inflammatory bowel disease.

Authors:  Leigh R Warren; Jonathan M Clarke; Sonal Arora; Mauricio Barahona; Naila Arebi; Ara Darzi
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10.  GERD-related health care utilization, therapy, and reasons for transfer of GERD patients between primary care providers and gastroenterologists in a US managed care setting.

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  1 in total

1.  PQMP Phase 2: Implementation and Dissemination.

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