Duration of medical home participation and quality of care for patients with chronic conditions

Karen E. Swietek, Marisa Elena Domino, Lexie R. Grove, Chris Beadles, Alan R. Ellis, Joel F. Farley, Carlos Jackson, Jesse C. Lichstein, C. Annette DuBard

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

Objective: To examine whether the length of participation in a patient-centered medical home (PCMH), an evidence-based practice, leads to higher quality care for Medicaid enrollees with multiple co-morbid chronic conditions and major depressive disorder (MDD). Data Sources: This analysis uses a unique data source that links North Carolina Medicaid claims and enrollment data with other administrative data including electronic records of state-funded mental health services, a state psychiatric hospital utilization database, and electronic records from a five-county behavioral health carve-out program. Study Design: This retrospective cohort study uses generalized estimating equations (GEEs) on person-year-level observations to examine the association between the duration of PCMH participation and measures of guideline-concordant care, including the receipt of minimally adequate care for MDD, defined as 6 months of antidepressant use or eight psychotherapy visits each year. Data Collection/Extraction Methods: Adults with two or more chronic conditions reflected in administrative data, including MDD. Principal Findings: We found a 1.7 percentage point increase in the likelihood of receiving guideline-concordant care at 4 months of PCMH participation, as compared to newly enrolled individuals with a single month of participation (p < 0.05). This effect increased with each additional month of PCMH participation; 12 months of participation was associated with a 19.1 percentage point increase in the likelihood of receiving guideline-concordant care over a single month of participation (p < 0.01). Conclusions: The PCMH model is associated with higher quality of care for patients with multiple chronic conditions and MDD over time, and these benefits increase the longer a patient is enrolled. Providers and policy makers should consider the positive effect of increased contact with PCMHs when designing and evaluating initiatives to improve care for this population.

Original languageEnglish (US)
Pages (from-to)1069-1079
Number of pages11
JournalHealth services research
Volume56
Issue numberS1
DOIs
StatePublished - Oct 2021

Bibliographical note

Funding Information:
Funding informationThis work was funded by the Agency for Healthcare Research and Quality (Grant No. R24 HS019659‐01). This research was partially supported by a National Research Service Award Pre‐Doctoral Traineeship from the Agency for Healthcare Research and Quality sponsored by The Cecil G. Sheps Center for Health Services Research, The University of North Carolina at Chapel Hill (Grant No. T32‐HS000032). Dr. DuBard and Dr. Jackson were employed by Community Care of North Carolina (CCNC) during the conduct of this research. CCNC operates the medical home program that is the subject of this analysis. The authors report no other relevant financial interests pertaining to this manuscript.

Publisher Copyright:
© 2021 Health Research and Educational Trust

Keywords

  • depression
  • medical homes
  • multiple chronic conditions
  • quality of care

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