Literature DB >> 30129484

Quality Metrics and Health Care Utilization for Adult Patients with Sickle Cell Disease.

Monica Ter-Minassian1, Sophie Lanzkron2, Alphonse Derus3, Elizabeth Brown2, Michael A Horberg3.   

Abstract

BACKGROUND: To date, there are no standardized, well-accepted, quality metrics that guide care for adults with sickle cell disease (SCD). The primary objective of this study was to evaluate the quality metrics that are in use at the Adult Sickle Cell Disease Program at Johns Hopkins Hospital (JHH) and the applicability of the metrics to Kaiser Permanente Mid-Atlantic States (KPMAS), an integrated healthcare system with a developing adult sickle cell disease program.
METHODS: We performed a retrospective cross-sectional study of 146 KPMAS and 308 JHH patients from January 1, 2014-December 31, 2015. Demographics, genotype and data on several key quality metrics (yearly screening labs, documented vaccinations and appropriate hydroxyurea prescriptions) were collected from electronic health records (EPIC Systems). We defined hydroxyurea adherence as having had at least 6 months of refills prescribed during the two years of study by either EHR or patient report.
RESULTS: Patients at KPMAS were older than those at JHH (median age 44 and 33 respectively) and less likely to have hemoglobin SS disease (29% and 66% respectively). Among KPMAS patients, 85% had documentation of any pneumococcal vaccination compared to 87% at JHH. 21 of 54 eligible patients at KPMAS and 95 of 165 eligible patients at JHH were prescribed hydroxyurea. At both institutions, 62% of patients were adherent to hydroxyurea. There were limitations to diagnosis coding and availability of vaccination and refill documentation.
CONCLUSIONS: Interventions to improve preventative care adherence are needed to improve outcomes in both academic medical centers and integrated health systems.
Copyright © 2019 National Medical Association. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Healthcare utilization; Hydroxyurea; Quality metrics; Quality of care; Sickle cell disease; Vaccinations

Year:  2018        PMID: 30129484     DOI: 10.1016/j.jnma.2018.05.003

Source DB:  PubMed          Journal:  J Natl Med Assoc        ISSN: 0027-9684            Impact factor:   1.798


  4 in total

1.  Patient-Reported Outcomes and Economic Burden of Adults with Sickle Cell Disease in the United States: A Systematic Review.

Authors:  Soyon Lee; Diana K Vania; Menaka Bhor; Dennis Revicki; Seye Abogunrin; Grammati Sarri
Journal:  Int J Gen Med       Date:  2020-07-07

2.  Sickle-Cell Disease Co-Management, Health Care Utilization, and Hydroxyurea Use.

Authors:  Nancy Crego; Christian Douglas; Emily Bonnabeau; Marian Earls; Kern Eason; Elizabeth Merwin; Gary Rains; Paula Tanabe; Nirmish Shah
Journal:  J Am Board Fam Med       Date:  2020 Jan-Feb       Impact factor: 2.657

3.  Building access to care in adult sickle cell disease: defining models of care, essential components, and economic aspects.

Authors:  Julie Kanter; Wally R Smith; Payal C Desai; Marsha Treadwell; Biree Andemariam; Jane Little; Diane Nugent; Susan Claster; Deepa G Manwani; Judith Baker; John J Strouse; Ifeyinwa Osunkwo; Rosalyn W Stewart; Allison King; Lisa M Shook; John D Roberts; Sophie Lanzkron
Journal:  Blood Adv       Date:  2020-08-25

4.  Patient Perspectives of Sickle Cell Management in the Emergency Department.

Authors:  Nancy Crego; Rita Masese; Emily Bonnabeau; Christian Douglas; Gary Rains; Nirmish Shah; Paula Tanabe
Journal:  Crit Care Nurs Q       Date:  2021 Apr-Jun 01
  4 in total

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