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

**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...

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Main Authors: Paula Tanabe, Audrey L. Blewer, Emily Bonnabeau, Hayden B. Bosworth, Denise H. Clayton, Nancy Crego, Marian F. Earls, Kern Eason, Grayson Forlines, Gary Rains, Matthew Young, Nirmish Shah
Format: Article
Language:English
Published: Columbia Data Analytics, LLC 2021-04-01
Series:Journal of Health Economics and Outcomes Research
Online Access:https://jheor.scholasticahq.com/article/21535-dissemination-of-evidence-based-recommendations-for-sickle-cell-disease-to-primary-care-and-emergency-department-providers-in-north-carolina-a-cost-b.pdf
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spelling doaj-e4e29c9876924490aa7287f0d9b7b71a2021-04-01T18:02:55ZengColumbia Data Analytics, LLCJournal of Health Economics and Outcomes Research2327-22362021-04-0181Dissemination of Evidence-Based Recommendations for Sickle Cell Disease to Primary Care and Emergency Department Providers in North Carolina: A Cost Benefit AnalysisPaula TanabeAudrey L. BlewerEmily BonnabeauHayden B. BosworthDenise H. ClaytonNancy CregoMarian F. EarlsKern EasonGrayson ForlinesGary RainsMatthew YoungNirmish Shah**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.https://jheor.scholasticahq.com/article/21535-dissemination-of-evidence-based-recommendations-for-sickle-cell-disease-to-primary-care-and-emergency-department-providers-in-north-carolina-a-cost-b.pdf
collection DOAJ
language English
format Article
sources DOAJ
author Paula Tanabe
Audrey L. Blewer
Emily Bonnabeau
Hayden B. Bosworth
Denise H. Clayton
Nancy Crego
Marian F. Earls
Kern Eason
Grayson Forlines
Gary Rains
Matthew Young
Nirmish Shah
spellingShingle Paula Tanabe
Audrey L. Blewer
Emily Bonnabeau
Hayden B. Bosworth
Denise H. Clayton
Nancy Crego
Marian F. Earls
Kern Eason
Grayson Forlines
Gary Rains
Matthew Young
Nirmish Shah
Dissemination of Evidence-Based Recommendations for Sickle Cell Disease to Primary Care and Emergency Department Providers in North Carolina: A Cost Benefit Analysis
Journal of Health Economics and Outcomes Research
author_facet Paula Tanabe
Audrey L. Blewer
Emily Bonnabeau
Hayden B. Bosworth
Denise H. Clayton
Nancy Crego
Marian F. Earls
Kern Eason
Grayson Forlines
Gary Rains
Matthew Young
Nirmish Shah
author_sort Paula Tanabe
title Dissemination of Evidence-Based Recommendations for Sickle Cell Disease to Primary Care and Emergency Department Providers in North Carolina: A Cost Benefit Analysis
title_short Dissemination of Evidence-Based Recommendations for Sickle Cell Disease to Primary Care and Emergency Department Providers in North Carolina: A Cost Benefit Analysis
title_full Dissemination of Evidence-Based Recommendations for Sickle Cell Disease to Primary Care and Emergency Department Providers in North Carolina: A Cost Benefit Analysis
title_fullStr Dissemination of Evidence-Based Recommendations for Sickle Cell Disease to Primary Care and Emergency Department Providers in North Carolina: A Cost Benefit Analysis
title_full_unstemmed Dissemination of Evidence-Based Recommendations for Sickle Cell Disease to Primary Care and Emergency Department Providers in North Carolina: A Cost Benefit Analysis
title_sort dissemination of evidence-based recommendations for sickle cell disease to primary care and emergency department providers in north carolina: a cost benefit analysis
publisher Columbia Data Analytics, LLC
series Journal of Health Economics and Outcomes Research
issn 2327-2236
publishDate 2021-04-01
description **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.
url https://jheor.scholasticahq.com/article/21535-dissemination-of-evidence-based-recommendations-for-sickle-cell-disease-to-primary-care-and-emergency-department-providers-in-north-carolina-a-cost-b.pdf
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