Barriers and facilitators to using aspirin for preventive therapy: a qualitative study exploring the views and experiences of people with Lynch syndrome and healthcare providers.

IF 2 4区 医学 Q3 ONCOLOGY
Kelly E Lloyd, Robbie Foy, Louise H Hall, Lucy Ziegler, Sophie M C Green, Zainab F Haider, David G Taylor, Mairead MacKenzie, Samuel G Smith
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引用次数: 0

Abstract

Background: The National Institute for Health and Care Excellence (NG151) recommends considering daily aspirin for people with Lynch syndrome to reduce colorectal cancer risk. However, deciding whether to initiate aspirin could be a complex decision for patients and their healthcare providers, as both the potential benefits and harms need to be considered.

Methods: We conducted semi-structured interviews to explore the barriers and facilitators to using aspirin for preventive therapy. We recruited 15 people with Lynch syndrome, and 23 healthcare providers across multiple professions in primary, and specialist care (e.g. clinical genetics) in the United Kingdom. Interview schedules were informed by the Theoretical Domains Framework.

Results: There were three themes: 1) Considering potential harms and benefits; 2) Healthcare pathway; 3) Patients' level of interest in aspirin. All healthcare providers, across primary and specialist care, viewed general practitioners (GPs) as being responsible for prescribing and overseeing the use of aspirin. However, GPs were unfamiliar with aspirin for preventive therapy, and concerned about prescribing at higher doses (300-600 mg). To support decision-making, GPs wanted clarification from specialist clinicians on the evidence and dose to prescribe. Not all participants with Lynch syndrome received information on aspirin from their healthcare provider, and several were unsure who to discuss aspirin with. GPs were more inclined to prescribe aspirin for patients with expressed preferences for the medication, however several patients were uncertain and wanted further guidance.

Conclusions: Coordinated and multilevel strategies are needed, addressing the needs of both GPs and people with Lynch syndrome, to ensure consistent implementation of national guidance on aspirin for preventive therapy.

使用阿司匹林进行预防性治疗的障碍和促进因素:探索林奇综合征患者和医疗服务提供者的观点和经验的定性研究。
背景:美国国家健康与护理优化研究所(NG151)建议考虑让林奇综合征患者每天服用阿司匹林,以降低患结直肠癌的风险。然而,对于患者及其医疗服务提供者来说,决定是否开始服用阿司匹林可能是一个复杂的决定,因为需要同时考虑潜在的益处和害处:我们进行了半结构式访谈,以探讨使用阿司匹林进行预防治疗的障碍和促进因素。我们在英国招募了 15 名林奇综合征患者和 23 名医疗服务提供者,他们来自基层医疗机构和专科医疗机构(如临床遗传学)的多个专业。访谈日程表参考了理论领域框架:有三个主题:1)考虑潜在的危害和益处;2)医疗保健途径;3)患者对阿司匹林的兴趣程度。所有医疗服务提供者(包括初级和专科医疗服务提供者)都认为全科医生(GPs)负责开具阿司匹林处方并监督其使用。然而,全科医生对阿司匹林的预防治疗并不熟悉,并对开具较大剂量(300-600 毫克)的处方表示担忧。为了支持决策,全科医生希望专科临床医生能够说明证据和处方剂量。并非所有患有林奇综合征的参与者都从其医疗保健提供者那里获得了阿司匹林的相关信息,有几位参与者不确定该与谁讨论阿司匹林。全科医生更倾向于为明确表示愿意服用阿司匹林的患者开阿司匹林处方,但也有一些患者不确定并希望得到进一步指导:结论:需要采取多层次的协调策略,满足全科医生和林奇综合征患者的需求,以确保一致执行阿司匹林预防治疗的国家指南。
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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.
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