A National Measurement Framework to Assess and Improve Sickle Cell Care in 4 US Regions

Elissa Z. Faro, Lisa Shook, Marsha J. Treadwell, Allison A. King, Lauren N. Whiteman, E. Donnell Ivy, Mary Hulihan, Patricia L. Kavanagh, Sabrina Selk, Suzette Oyeku, Scott D. Berns

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

Objectives: Coordinated measurement strategies are needed to inform collaborative approaches to improve access to and quality of care for persons with sickle cell disease (SCD). The objective of our study was to develop a multilevel measurement strategy to assess improvements in access to and quality of care for persons with SCD in 4 US regions. Methods: From 2014 through 2017, regional grantees in the Sickle Cell Disease Treatment Demonstration Program collected administrative and patient-level electronic health record (EHR) data to assess quality improvement initiatives. Four grantees—covering 29 US states and territories and an SCD population of 56 720—used a collective impact model to organize their work. The grantees collected administrative data from state Medicaid and Medicaid managed care organizations (MCOs) at multiple points during 2014-2017 to assess improvements at the population level, and local patient-level data were abstracted from site-level EHRs at regular intervals to track improvements over time. Results: Administrative data were an important source of understanding population-level improvements but were delayed, whereas patient-level data were more sensitive to small-scale quality improvements. Conclusions: We established a shared measurement approach in partnership with Medicaid and Medicaid MCO stakeholders that can be leveraged to effectively support quality improvement initiatives for persons with SCD in the United States.

Original languageEnglish (US)
Pages (from-to)442-451
Number of pages10
JournalPublic Health Reports
Volume135
Issue number4
DOIs
StatePublished - Jul 1 2020

Keywords

  • administrative data
  • collective impact
  • measurement
  • quality improvement
  • sickle cell disease

ASJC Scopus subject areas

  • Public Health, Environmental and Occupational Health

Fingerprint Dive into the research topics of 'A National Measurement Framework to Assess and Improve Sickle Cell Care in 4 US Regions'. Together they form a unique fingerprint.

Cite this