Patient-Identified Treatment Goals for Psoriatic Disease: Results From a US Patient Survey.

Q3 Medicine
April Armstrong, Noah A Levit, Beth Schneider, Richard Seiden, Linyu Shi, Blair Kaplan, Jashin J Wu
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引用次数: 0

Abstract

Background: Despite advancements in the treatment landscape for psoriasis (PsO) and psoriatic arthritis (PsA), some patients may not achieve the desired disease improvement due to undertreatment. Understanding patient perspectives on treatment expectations can inform patient-centered decisions and enhance treatment satisfaction.

Objective: To describe patient-identified treatment goals and expectations for managing psoriatic disease.

Methods: A cross-sectional study was conducted using a survey through MyPsoriasisTeam, an online social community. The survey was available to its US-based patients aged ≥21 years with self-reported diagnoses of PsO and/or PsA. The study assessed patients' treatment goals, satisfaction with treatment outcomes, and satisfaction with health care providers (HCPs). Responses were summarized using descriptive statistics.

Results: This analysis included 386 patients (PsO, n = 130; PsA with/without PsO, n = 256). Treatment goals varied by psoriatic disease type. The top 3 treatment goals for PsO were reduce itching (73.1%), reduction in size/thickness (68.5%), and reduction in the number of plaques (63.1), and for PsA, were reducing joint pain (77.7%), lessening fatigue (64.8%), and reducing joint stiffness (62.1%). Patient satisfaction with treatment outcomes was low (extremely/very satisfied: PsO, 7.5%/8.5% and PsA, 9.2%/20.2%). Overall, 73.1% with PsO were treated by a dermatologist, and a dermatologist or rheumatologist treated 74.6% with PsA. Overall, patient satisfaction with HCPs who treated their disease was lacking (PsO, 19.3% and 19.3%; PsA, 27.3% and 33.6% were extremely and very satisfied, respectively).

Conclusion: These findings suggest the need for enhanced communication between patients and HCPs to align treatment goals and expectations and to improve treatment satisfaction and disease management.

患者确定的银屑病治疗目标:美国患者调查结果。
背景:尽管银屑病(PsO)和银屑病关节炎(PsA)的治疗取得了进展,但一些患者可能因治疗不当而无法实现预期的疾病改善。了解患者对治疗期望的看法可为以患者为中心的决策提供依据,并提高治疗满意度:描述患者确定的银屑病治疗目标和期望:通过在线社交社区 MyPsoriasisTeam 开展了一项横断面研究。调查对象为年龄≥21 岁、自述诊断为银屑病和/或 PsA 的美国患者。研究评估了患者的治疗目标、对治疗结果的满意度以及对医疗保健提供者(HCP)的满意度。研究采用描述性统计方法对患者的回答进行了总结:本分析包括 386 名患者(PsO,n = 130;有/无 PsO 的 PsA,n = 256)。不同类型银屑病的治疗目标各不相同。PsO的前三大治疗目标分别是减轻瘙痒(73.1%)、减小面积/厚度(68.5%)和减少斑块数量(63.1%);PsA的前三大治疗目标分别是减轻关节疼痛(77.7%)、减轻疲劳(64.8%)和减轻关节僵硬(62.1%)。患者对治疗结果的满意度较低(非常/非常满意:PsO,7.5%/8.5%;PsA,9.2%/20.2%)。总体而言,73.1% 的 PsO 患者接受了皮肤科医生的治疗,74.6% 的 PsA 患者接受了皮肤科医生或风湿免疫科医生的治疗。总体而言,患者对治疗其疾病的保健医生的满意度不高(PsO:19.3%和19.3%;PsA:27.3%和33.6%的患者分别表示非常满意和非常满意):这些研究结果表明,有必要加强患者与保健医生之间的沟通,以统一治疗目标和期望,提高治疗满意度和疾病管理水平。
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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来源期刊
CiteScore
1.30
自引率
0.00%
发文量
19
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