Tanabe Paula, Blewer Audrey L, Bonnabeau Emily, Bosworth Hayden B, Clayton Denise H, Crego Nancy, Earls Marian F, Eason Kern, Forlines Grayson, Rains Gary, Young Matthew, Shah Nirmish
School of Nursing, Duke University, Durham, NC, USA; Duke University School of Medicine, Durham, NC, USA.
Department of Family Medicine and Community Health, School of Medicine, Duke University, Durham, NC, USA; Department of Population Health Sciences, School of Medicine, Duke University, Durham, NC, USA.
J Health Econ Outcomes Res. 2021 Apr 1;8(1):18-28. doi: 10.36469/jheor.2021.21535.
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. 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. 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. 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. Although we did not find the expected shift to increased PCP visits and decreased ED visits and hospitalizations, there were many lessons learned.
镰状细胞病(SCD)是一种主要影响非洲裔个体的遗传疾病,这些个体恰好受到贫困的影响尤为严重,且缺乏医疗保健服务。患有SCD的个体极有可能频繁使用急性护理并经历慢性疼痛发作。SCD中出现的多种并发症导致了严重的发病率和过早死亡,同时也给医疗系统带来了巨大成本。SCD是一种复杂的慢性疾病,需要初级、专科和急诊护理。尽管有循证指南,但许多医疗服务提供者觉得没有准备好为患有SCD的个体提供护理。我们报告了一个SCD工具箱的开发以及向北卡罗来纳州(NC)的初级保健和急诊科(ED)提供者的传播过程。我们报告了这种传播对医疗保健利用、护理成本和总体成本效益的影响。SCD工具箱是根据美国国立心肺血液研究所的建议改编的。向质量改进专家提供了工具箱培训,这些专家随后将工具箱分发给与NC唯一的管理式医疗协调系统相关联的初级保健提供者(PCP)和ED提供者。工具以纸质、在线和应用程序格式提供给参与的管理式医疗网络机构(n = 1800)。对医疗补助索赔数据进行了分析,以了解在干预前24个月和干预后18个月期间工具箱传播的总成本和效益。门诊专科就诊、ED就诊或住院次数没有统计学上的显著变化。实施后PCP就诊次数略有减少。传播带来了361,414美元(平均每位参保人每月14.03美元)的净成本节约。然而,与SCD工具箱传播相关的估计财务效益在统计学上并不显著。尽管我们没有发现预期的PCP就诊增加以及ED就诊和住院减少的转变,但还是吸取了许多经验教训。