设计和实施遗传性癌症过渡诊所的临床医生观点。

IF 2 4区 医学 Q3 ONCOLOGY Hereditary Cancer in Clinical Practice Pub Date : 2025-01-11 DOI:10.1186/s13053-024-00304-5
Jazmine L Gabriel, Victoria Schlieder, Jessica M Goehringer, Tracey Leitzel, Emily Ann Sugrue, Sarah Zultevicz, Thomas W Davis, Gemme Campbell-Salome, Katrina Romagnoli
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引用次数: 0

摘要

在青少年和年轻人中早期发现遗传性癌症易感性是一个独特的机会,可以针对癌症预防和提高存在不良健康结果风险的人群的生存率。然而,青少年和年轻人面临着其生命阶段所特有的挑战,这些挑战可能会破坏他们从儿科向成人保健的过渡,并导致预防性保健的中断。本研究的目的是了解专家对设计和实施具有遗传性癌症易感性的青少年和年轻人过渡诊所的相关因素的看法。我们采用以人为中心的设计和实施科学的定性方法来确定根植于临床医生经验的实施考虑因素。为了了解Geisinger过渡诊所的临床设计和临床医生的经验,我们使用临床观察和临床医生的随访访谈进行了上下文调查。为了了解如何设计和实施过渡方案,我们还对美国各地积极参与发展、实施或参与过渡诊所的国家过渡专家进行了深入访谈。上下文调查得出了三个图表,描述了我们机构过渡诊所的以下共同要素:与患者建立关系,护理协调,逐步过渡教育,提供者之间的沟通,以及可持续的诊所之家。访谈采用主题分析进行演绎分析,以了解临床医生对RE-AIM理论框架中每个领域的项目实施的看法:覆盖范围、有效性、采用、实施和维护。
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Clinician perspectives on designing and implementing a hereditary cancer transition clinic.

Early identification of hereditary cancer predisposition in adolescents and young adults represents a unique opportunity to target cancer prevention and improve survival in a population at risk for adverse health outcomes. However, adolescents and young adults face challenges unique to their stage of life that can undermine their transition from pediatric to adult healthcare and lead to interruptions in preventative care. The purpose of this study was to understand expert perspectives on factors relevant to designing and implementing a transition clinic for adolescents and young adults with hereditary cancer predisposition. We used qualitative methods informed by human-centered design and implementation science to identify implementation considerations rooted in clinician experience. To understand clinic design and clinician experience at Geisinger transition clinics, we conducted a contextual inquiry using clinic observations and follow-up interviews of clinicians. To learn about designing and implementing a transition program, we also conducted in-depth interviews with national transition experts actively involved in developing, implementing, or participating in transition clinics around the United States. The contextual inquiry resulted in three diagrams depicting the following common elements of transition clinics at our institution: relationship building with patients, care coordination, stepwise transition education, communication between providers, and a sustainable clinic home. Interviews were analyzed deductively using thematic analysis to learn clinician perspectives about program implementation specific to each domain of the RE-AIM theoretical framework: reach, effectiveness, adoption, implementation, and maintenance.

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来源期刊
CiteScore
3.10
自引率
5.90%
发文量
38
审稿时长
>12 weeks
期刊介绍: Hereditary Cancer in Clinical Practice is an open access journal that publishes articles of interest for the cancer genetics community and serves as a discussion forum for the development appropriate healthcare strategies. Cancer genetics encompasses a wide variety of disciplines and knowledge in the field is rapidly growing, especially as the amount of information linking genetic differences to inherited cancer predispositions continues expanding. With the increased knowledge of genetic variability and how this relates to cancer risk there is a growing demand not only to disseminate this information into clinical practice but also to enable competent debate concerning how such information is managed and what it implies for patient care. Topics covered by the journal include but are not limited to: Original research articles on any aspect of inherited predispositions to cancer. Reviews of inherited cancer predispositions. Application of molecular and cytogenetic analysis to clinical decision making. Clinical aspects of the management of hereditary cancers. Genetic counselling issues associated with cancer genetics. The role of registries in improving health care of patients with an inherited predisposition to cancer.
期刊最新文献
Colorectal carcinogenesis in the Lynch syndromes and familial adenomatous polyposis: trigger events and downstream consequences. Clinician perspectives on designing and implementing a hereditary cancer transition clinic. Two independent families with de novo whole APC gene deletion and intellectual disability: a case report. BRCA2 germline mutation carrier with five malignancies: a case report. A genome-wide association study in Swedish colorectal cancer patients with gastric- and prostate cancer in relatives.
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