化脓性汗腺炎管理的患者偏好:欧洲多国离散选择实验的结果。

IF 3.4 3区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Patient-Patient Centered Outcomes Research Pub Date : 2023-03-01 DOI:10.1007/s40271-022-00614-7
Damon Willems, Eva-Lotta Hinzpeter, Hessel H Van der Zee, Christopher J Sayed, John R Ingram, Charlotte Beaudart, Silvia M A A Evers, Mickael Hiligsmann
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引用次数: 2

摘要

背景和目的:化脓性汗腺炎是一种慢性炎症性皮肤病,可导致生活质量的大幅下降。最近的研究表明,化脓性汗腺炎患者的护理需求未得到满足的程度很高,但他们在治疗决策方面的偏好很少被调查。本研究旨在揭示欧洲成年HS患者在治疗决策中最重要的治疗属性。方法:对欧洲成年化脓性汗腺炎患者进行离散选择实验,揭示治疗决策时最重要的治疗属性。参与者有15组两种治疗方案,并要求每个人选择他们喜欢的治疗方案。根据先前的文献回顾和定性研究,这些治疗方法有六个特征:有效性、疼痛减轻、治疗获益持续时间、轻度不良事件风险、严重感染风险和给药方式。使用随机参数logit模型来估计患者的偏好,并使用额外的亚组和潜在类别模型来探索患者组间偏好的差异。结果:219例成人化脓性汗腺炎纳入分析(90%为女性,平均年龄38岁)。对于所有六个治疗属性,在水平之间观察到显着差异。考虑到每个属性的水平范围,最重要的治疗属性是有效性(47.9%),其次是疼痛减轻(17.3%),轻度不良事件年风险(14.4%),严重感染年风险(10.3%),给药方式(5.3%)和治疗获益持续时间(4.8%)。较高水平的有效性,即脓肿和炎性结节计数减少75%或100%,优先于在化脓性汗腺炎随机临床试验中主要研究的有效性水平(减少50%)。结果在亚组之间基本一致,并确定了三个潜在类别组。结论:本研究揭示了化脓性汗腺炎患者最重要的治疗特征,可以帮助告知化脓性汗腺炎管理的患者-医生联合决策。根据患者的偏好设计未来的化脓性汗腺炎治疗方案,即在不发生较高不良事件风险的情况下提供更高水平的疗效和疼痛改善,这可能会增加患者的治疗一致性,并改善疾病管理结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Patient Preferences in the Management of Hidradenitis Suppurativa: Results of a Multinational Discrete Choice Experiment in Europe.

Background and objective: Hidradenitis suppurativa is a chronic inflammatory skin disease that can lead to a substantial reduction in quality of life. Recent studies revealed high levels of unmet care needs of patients with hidradenitis suppurativa, but their preferences in treatment decision making have scarcely been investigated. This study aimed to reveal which treatment attributes adult patients with HS in Europe consider most important in treatment decision-making.

Methods: A discrete choice experiment was conducted with adult patients with hidradenitis suppurativa in Europe to reveal which treatment attributes are most important when making treatment decisions. Participants were presented with 15 sets of two treatment options and asked for each to choose the treatment they preferred. The treatments were characterized by six attributes informed by a prior literature review and qualitative research: effectiveness, pain reduction, duration of treatment benefit, risk of mild adverse event, risk of serious infection, and mode of administration. A random parameter logit model was used to estimate patients' preferences with additional subgroup and latent class models used to explore any differences in preferences across patient groups.

Results: Two hundred and nineteen adult patients with hidradenitis suppurativa were included in the analysis (90% women, mean age 38 years). For all six treatment attributes, significant differences were observed between levels. Given the range of levels of each attribute, the most important treatment attributes were effectiveness (47.9%), followed by pain reduction (17.3%), annual risk of a mild adverse event (14.4%), annual risk of a serious infection (10.3%), mode of administration (5.3%), and duration of treatment benefit (4.8%). Higher levels of effectiveness, namely a 75% or 100% reduction in the abscess and inflammatory nodule count, were preferred over levels of effectiveness primarily investigated in randomized clinical trials of hidradenitis suppurativa (a 50% reduction). Results were largely consistent across subgroups and three latent class groups were identified.

Conclusions: This study revealed the most important treatment characteristics for patients with hidradenitis suppurativa that can help inform joint patient-physician decision making in the management of hidradenitis suppurativa. Designing future hidradenitis suppurativa treatments according to stated preferences, namely, to offer higher levels of effectiveness and pain improvement without higher risks of adverse events, may increase patients' treatment concordance and lead to improved disease management outcomes.

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来源期刊
Patient-Patient Centered Outcomes Research
Patient-Patient Centered Outcomes Research HEALTH CARE SCIENCES & SERVICES-
CiteScore
6.60
自引率
8.30%
发文量
44
审稿时长
>12 weeks
期刊介绍: The Patient provides a venue for scientifically rigorous, timely, and relevant research to promote the development, evaluation and implementation of therapies, technologies, and innovations that will enhance the patient experience. It is an international forum for research that advances and/or applies qualitative or quantitative methods to promote the generation, synthesis, or interpretation of evidence. The journal has specific interest in receiving original research, reviews and commentaries related to qualitative and mixed methods research, stated-preference methods, patient reported outcomes, and shared decision making. Advances in regulatory science, patient-focused drug development, patient-centered benefit-risk and health technology assessment will also be considered. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in The Patient may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances. All manuscripts are subject to peer review by international experts.
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