Dissemination of Evidence-Based Recommendations for Sickle Cell Disease to Primary Care and Emergency Department Providers in North Carolina: A Cost Benefit Analysis.

dc.contributor.author

Tanabe, Paula

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Blewer, Audrey L

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Bonnabeau, Emily

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Bosworth, Hayden B

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Clayton, Denise H

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Crego, Nancy

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Earls, Marian F

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Eason, Kern

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Forlines, Grayson

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Rains, Gary

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Young, Matthew

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Shah, Nirmish

dc.date.accessioned

2023-11-07T23:28:15Z

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2023-11-07T23:28:15Z

dc.date.issued

2021-04

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2023-11-07T23:28:14Z

dc.description.abstract

Background: Sickle cell disease (SCD) is a genetic condition affecting primarily individuals of African descent, who happen to be disproportionately impacted by poverty and who lack access to health care. Individuals with SCD are at high likelihood of high acute care utilization and chronic pain episodes. The multiple complications seen in SCD contribute to significant morbidity and premature mortality, as well as substantial costs to the healthcare system. Objectives: SCD is a complex chronic disease resulting in the need for primary, specialty and emergency care. Many providers do not feel prepared to care for individuals with SCD, despite the existence of evidence-based guidelines. We report the development of a SCD toolbox and the dissemination process to primary care and emergency department (ED) providers in North Carolina (NC). We report the effect of this dissemination on health-care utilization, cost of care, and overall cost-benefit. Methods: The SCD toolbox was adapted from the National Heart, Lung, and Blood Institute recommendations. Toolbox training was provided to quality improvement specialists who then disseminated the toolbox to primary care providers (PCPs) affiliated with the only NC managed care coordination system and ED providers. Tools were made available in paper, online, and in app formats to participating managed care network practices (n=1 800). Medicaid claims data were analyzed for total costs and benefits of the toolbox dissemination for a 24-month pre- and 18-month post-intervention period. Results: There was no statistically significant shift in the number of outpatient specialty visits, ED visits or hospitalizations. There was a small decrease in the number of PCP visits in the post-implementation period. The dissemination resulted in a net cost-savings of $361 414 ($14.03 per-enrollee per-month on average). However, the estimated financial benefit associated with the dissemination of the SCD toolbox was not statistically significant. Conclusions: Although we did not find the expected shift to increased PCP visits and decreased ED visits and hospitalizations, there were many lessons learned.

dc.identifier

21535

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2326-697X

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2327-2236

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https://hdl.handle.net/10161/29349

dc.language

eng

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The Journal of Health Economics and Outcomes Research

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Journal of health economics and outcomes research

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10.36469/jheor.2021.21535

dc.subject

cost benefit analysis

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dissemination

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sickle cell

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toolkit

dc.title

Dissemination of Evidence-Based Recommendations for Sickle Cell Disease to Primary Care and Emergency Department Providers in North Carolina: A Cost Benefit Analysis.

dc.type

Journal article

duke.contributor.orcid

Blewer, Audrey L|0000-0003-2830-5191

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Bosworth, Hayden B|0000-0001-6188-9825

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Crego, Nancy|0000-0002-6045-9337

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Shah, Nirmish|0000-0002-7506-0935

pubs.begin-page

18

pubs.end-page

28

pubs.issue

1

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Duke

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School of Medicine

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School of Nursing

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Nursing

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Basic Science Departments

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Clinical Science Departments

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Institutes and Centers

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Family Medicine and Community Health

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Medicine

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Pediatrics

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Psychiatry & Behavioral Sciences

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Medicine, General Internal Medicine

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Medicine, Hematology

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Pediatrics, Hematology-Oncology

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Duke Cancer Institute

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Duke Clinical Research Institute

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Institutes and Provost's Academic Units

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Center for the Study of Aging and Human Development

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Initiatives

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Duke Science & Society

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Population Health Sciences

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Duke Innovation & Entrepreneurship

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Psychiatry & Behavioral Sciences, Behavioral Medicine & Neurosciences

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Emergency Medicine

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Duke - Margolis Center For Health Policy

pubs.publication-status

Published

pubs.volume

8

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