通过 JUMP 计划为脊柱裂患者提供过渡指导:一项试点研究。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Pedram D Maleknia, Logan Hopson, Jeffrey P Blount, Brandon G Rocque, Anastasia Arynchyna-Smith, Betsy D Hopson
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引用次数: 0

摘要

目的:对于脊柱裂(SB)患者和家属来说,从儿科护理过渡到成人护理是一项挑战。终生的护理关系会转变为新的护理环境,而新的护理环境通常较大、较少个性化、较少涉及脊柱裂护理的细微差别。青春期和青年期通常会因疾病或慢性医疗复杂性以外的因素而产生个人和心理压力。调查显示,对于许多 SB 患者来说,过渡时期与不确定性、焦虑和不良事件风险升高有关。为了缓解这一问题,作者开发了一项青少年 SB 患者与本科生/医学生之间的试验性导师计划。本研究分析并介绍了该项目取得的初步成果:作者制定了 "加入、团结、激励和准备"(JUMP)计划,以提高过渡过程的准备程度。被指导者的目标人群是在作者的 SB 诊所接受治疗的 13-19 岁患者。导师是经过筛选/批准的本科生/医学生,他们自愿参加并成功完成了导师在线培训。入院后,每位患者都会根据个性化过渡计划设定临床、自我和家长/监护人的综合目标。这些目标将与导师、被指导者、家长/监护人和医生共享。为了监控成功,SB 项目主任定期与每位导师会面,讨论取得的进展和需要改进的地方。这包括持续的定量和定性目标设定,以及每个议程需要解决的失败问题:结果:在 9 个月的时间里,建立了 13 个导师与被指导者的匹配关系。在这 13 个配对中,有 6 个在初次见面后进行了 5 次以上的交流,有 1 个配对至今仍保持联系。该计划的成功之处在于受指导者获得了工作、申请到了奖学金、开始上大学以及与其他经历相似的人建立了联系。面临的挑战包括:初次诊疗后未能进行后续跟踪、使用虚拟平台存在风险,以及作者所在州的指导者和被指导者地域分散:结论:事实证明,患有 SB 的青少年从儿科治疗向成人治疗的过渡是一个巨大的障碍。通过深思熟虑的互动过程来缓解这一过程,有可能改善准备情况、提高患者的自主性,并让他们接触到成人医疗保健社区。然而,事实证明,在 SB 环境中,导师模式并不能解决这一问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transition mentorship for spina bifida patients with the JUMP program: a pilot study.

Objective: The transition from pediatric to adult care is challenging for patients and families with spina bifida (SB). Lifelong care relationships yield to new care environments that are typically larger, less personal, and less engaged with the nuances of SB care. Adolescence and young adulthood are often characterized by personal and psychological stresses due to factors independent of illness or chronic medical complexity. Surveys have demonstrated that transition is associated with uncertainty, anxiety, and elevated risk of adverse events for many SB patients. To help mitigate this, the authors developed a trial mentorship program between teen patients with SB and undergraduate/medical students. This study analyzes and presents the initial outcomes from this program.

Methods: The authors created the Join, Unite, Motivate, and Prepare (JUMP) program to improve readiness for the transition process. The mentee target population was patients aged 13-19 years receiving care at the authors' SB clinic. Mentors were screened/approved undergraduate/medical students who volunteered to participate and successfully completed online training in mentorship. Upon enrollment, each patient set a combination of clinical, self, and parent/guardian goals using the individualized transition plan. These goals were shared with the mentor, mentee, parent/guardian, and physician. To monitor success, the SB program director routinely met with each mentor to discuss progress made and areas of growth. These included continuous quantitative and qualitative goal setting and failures that needed to be addressed for each agenda.

Results: Thirteen mentor-mentee matches were created over 9 months. Of the 13 matches, 6 had more than 5 communications after the initial meeting, and 1 mentor-mentee match is still in contact today. Noted success in the program has been through mentees gaining employment, applying for scholarships, starting college, and connecting with others who are going through similar circumstances. Challenges have arisen through failure to follow-up after the initial office visit, risk with using the virtual platform, and wide geographic dispersion of both mentors and mentees across the authors' state.

Conclusions: Transition from pediatric to adult care for adolescents with SB has proven to be a large hurdle. Easing this process through well-thought-out, interactive processes has the potential to improve readiness, increase patient autonomy, and provide exposure to the adult healthcare community. However, the mentorship model, in the SB setting, has not proven to be the remedy.

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CiteScore
7.20
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