Challenges of Engaging Primary Care Providers in Specialized Telementoring Education About Sickle Cell Disease for Sickle Cell Specialists: Results from the Sickle Cell Disease Training and Mentoring Program for Primary Care Providers (STAMP) Project ECHO

Lisa M. Shook DHPE, MA, MCHES , Bailey House MPH , Christina Bennett Farrell MPH , Rosalyn Stewart MD , Sophie Lanzkron MD, MHS , Allison A. King MD, MPH, PhD , Taniya Varughese MSOT , J.J. Strouse MD, PhD , Marsha Treadwell PhD , Julie Kanter MD
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Abstract

Introduction

Sickle cell disease (SCD) is an inherited blood disorder affecting approximately 100,000 individuals in the U.S. A lack of knowledgeable providers, particularly for adult patients, has led to a significant number of adults without access to high-quality care. Several federal partners collaborated with the Sickle Cell Disease Treatment Demonstration Program (SCDTDP) grantees to develop and test a national Project ECHO telementoring program targeting primary care providers (PCPs).

Methods

Federal partners developed an extensive recruitment and outreach strategy to engage PCPs in the Sickle Cell Disease Training and Mentoring (STAMP) virtual educational (telementoring) program using a multi-pronged recruitment strategy. The SCDTDP grantees created a tailored curriculum of didactic presentations about the management of SCD, especially for PCPs.

Results

STAMP hosted 12 sessions over 6 months. Despite the multi-pronged recruitment strategy and tailored curriculum, there were very few PCPs among the 763 attendees. The majority of attendees were hematologists and other community-based advocates with a vested interest in SCD.

Conclusions

Despite a federal partnership, the STAMP outreach strategy was unsuccessful in recruiting PCPs to participate in a virtual telementoring education program designed to increase access to care for adults with SCD. STAMP's attendee participation and the lack of engagement by PCPs were unable to significantly show an increase in interest or willingness by PCPs to learn to co-manage SCD care with specialists.
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导言:镰状细胞病(SCD)是一种遗传性血液疾病,在美国约有 10 万人患病。由于缺乏知识丰富的医疗服务提供者,尤其是成年患者,导致大量成年人无法获得高质量的医疗服务。几个联邦合作伙伴与镰状细胞疾病治疗示范计划(SCDTDP)受赠方合作,开发并测试了一项针对初级保健提供者(PCPs)的全国性 ECHO 项目辅导计划:方法:联邦合作伙伴制定了广泛的招募和推广策略,通过多管齐下的招募策略让初级保健提供者参与镰状细胞疾病培训和指导(STAMP)虚拟教育(telementoring)计划。SCDTDP 受赠方特别为初级保健医生量身定制了有关 SCD 管理的说教课程:结果:STAMP 在 6 个月内举办了 12 场讲座。尽管采取了多管齐下的招募策略和量身定制的课程,但在 763 名与会者中,初级保健医生寥寥无几。大多数与会者是血液科医生和其他对 SCD 有既得利益的社区倡导者:结论:尽管与联邦政府建立了合作关系,但 STAMP 外联策略在招募初级保健医生参与旨在增加成人 SCD 患者获得护理机会的虚拟辅导教育计划方面并不成功。STAMP 的参与者参与度以及初级保健医生参与度的缺乏无法显著提高初级保健医生学习与专科医生共同管理 SCD 护理的兴趣或意愿。
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AJPM focus
AJPM focus Health, Public Health and Health Policy
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