Suppr超能文献

影响斑秃治疗决策的因素:一项定性评估。

Factors influencing alopecia areata treatment decisions: A qualitative assessment.

作者信息

Han Jane J, Faletsky Adam, Ghatnekar Shilpa, Lee Karen J, Pérez-Chada Lourdes M, Li Sara J, Manjaly Priya, Senna Maryanne M, Huang Kathie P, Mostaghimi Arash

机构信息

Department of Dermatology, Brigham and Women's Hospital, Boston, Massachusetts.

Stritch School of Medicine, Loyola University, Maywood, Illinois.

出版信息

JAAD Int. 2022 Nov 4;10:77-83. doi: 10.1016/j.jdin.2022.10.007. eCollection 2023 Mar.

Abstract

BACKGROUND

Alopecia areata (AA) is a disease of hair loss in which patients may benefit from comprehensive understanding of AA's disease process and therapeutic options during treatment decision-making.

OBJECTIVE

Determine factors influencing patients' AA treatment decision-making.

METHODS

Qualitative interviews were conducted using semi-structured interview guides. Interviews were coded using inductive thematic analysis.

RESULTS

Twenty-one participants with AA were interviewed. Coding interrater reliability was κ = 0.87-0.91, indicating strong-almost perfect agreement. Participants faced multiple barriers, including lack of access to health care ( = 10, 47.6%) and lack of transparency about their condition and treatment options ( = 9, 42.9%). Information about AA was sought from primarily the internet ( = 15, 71.4%) and physician recommendation ( = 15, 71.4%). When choosing AA treatments, patients often considered treatment efficacy ( = 21, 100%), safety ( = 21, 100%), and convenience of use ( = 20, 95.2%).

LIMITATIONS

Referral and regional biases may be present and limit generalizability.

CONCLUSIONS

Patients with AA face various challenges including medical uncertainty and lack of information. Patients need trustworthy and accessible sources of information regarding their treatment that also take into consideration their preferences and values.

摘要

背景

斑秃(AA)是一种脱发疾病,患者在治疗决策过程中若能全面了解斑秃的疾病进程和治疗选择,可能会从中受益。

目的

确定影响患者斑秃治疗决策的因素。

方法

使用半结构化访谈指南进行定性访谈。采用归纳主题分析法对访谈进行编码。

结果

对21名斑秃患者进行了访谈。编码者间信度κ = 0.87 - 0.91,表明一致性很强——几乎完全一致。参与者面临多种障碍,包括难以获得医疗服务(n = 10,47.6%)以及对自身病情和治疗选择缺乏透明度(n = 9,42.9%)。关于斑秃的信息主要来自互联网(n = 15,71.4%)和医生推荐(n = 15,71.4%)。在选择斑秃治疗方法时,患者通常会考虑治疗效果(n = 21,100%)、安全性(n = 21,100%)和使用便利性(n = 20,95.2%)。

局限性

可能存在转诊和地区偏差,限制了研究结果的普遍性。

结论

斑秃患者面临各种挑战,包括医疗不确定性和信息匮乏。患者需要关于其治疗的可靠且易于获取的信息来源,这些信息还应考虑到他们的偏好和价值观。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bdd/9850169/5c95c0c98cd2/gr1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验