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原发性胆汁性胆管炎长期管理中的患者自主性

Patient ownership of primary biliary cholangitis long-term management.

作者信息

Leighton Jessica, Thain Collette, Mitchell-Thain Robert, Dyson Jessica K, Jones David E

机构信息

ICM, Newcastle University, Newcastle upon Tyne, UK.

PBC Foundation, Edinburgh, Edinburgh, UK.

出版信息

Frontline Gastroenterol. 2020 Jun 1;12(5):370-373. doi: 10.1136/flgastro-2019-101324. eCollection 2021.

Abstract

OBJECTIVE

Patient ownership of disease is vital in rare diseases like primary biliary cholangitis (PBC). This survey of UK members of the PBC foundation aimed to assess patients' perception of their disease management, focusing on key biomarkers and problematic symptoms.

DESIGN

Registered PBC foundation members were surveyed on their experiences on their most recent clinic visit, covering the type of hospital and clinician and whether biochemical response and symptom burden were discussed, including who initiated these conversations. Respondents were also asked about their willingness to initiate these conversations.

RESULTS

Across 633 respondents, 42% remembered discussing alkaline phosphatase, the key biochemical response measure, and the majority of discussions were initiated by the healthcare provider. 56% of respondents remembered discussing itch, a key PBC symptom. There was no distinction between the grade of healthcare professional, but both patients and clinicians were significantly more likely to discuss symptoms over disease progression. Reassuringly, 84% of respondents felt willing to initiate conversations about their illness, regardless of the grade of managing clinician.

CONCLUSIONS

This work lays a positive foundation for patient education and empowerment projects, likely to improve clinical outcomes. Key aspects of management (biochemical response to treatment and symptom burden) should be emphasised as topics of discussion to both patients and clinicians managing PBC. We suggest a simple cue card to prompt patient-led discussion.

摘要

目的

在原发性胆汁性胆管炎(PBC)等罕见疾病中,患者对疾病的自主意识至关重要。这项针对英国PBC基金会成员的调查旨在评估患者对其疾病管理的认知,重点关注关键生物标志物和有问题的症状。

设计

对PBC基金会的注册成员就其最近一次门诊就诊经历进行调查,内容包括医院类型、临床医生类型,以及是否讨论了生化反应和症状负担,包括谁发起了这些讨论。还询问了受访者发起这些讨论的意愿。

结果

在633名受访者中,42%记得讨论过关键生化反应指标碱性磷酸酶,且大多数讨论由医疗服务提供者发起。56%的受访者记得讨论过PBC的关键症状瘙痒。医疗专业人员的级别之间没有差异,但患者和临床医生讨论症状的可能性明显高于疾病进展情况。令人欣慰的是,84%的受访者表示愿意发起关于其病情的讨论,无论主治临床医生的级别如何。

结论

这项工作为患者教育和赋权项目奠定了积极基础,可能会改善临床结果。应将管理的关键方面(对治疗的生化反应和症状负担)作为患者和治疗PBC的临床医生讨论的话题加以强调。我们建议使用一张简单的提示卡来促使由患者主导讨论。

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Patient ownership of primary biliary cholangitis long-term management.原发性胆汁性胆管炎长期管理中的患者自主性
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