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AWARE 研究:方法学和基线特征。

The AWARE study: methodology and baseline characteristics.

机构信息

Innovaderm Research Inc., Montreal, QC.

出版信息

J Cutan Med Surg. 2009 Dec;13 Suppl 3:S113-21. doi: 10.2310/7750.2009.00029.

Abstract

BACKGROUND

Alefacept was the first biologic therapy approved by Health Canada for the treatment of moderate to severe chronic plaque psoriasis and is used either alone or as part of combination therapy.

OBJECTIVE

AWARE (Amevive Wisdom Acquired from Real-World Evidence) is a multicenter, observational phase IV Canadian study of psoriasis patients treated with alefacept. This study's main goals were to develop a shared, real-time, national clinical database to support best practice and optimize the care of patients receiving alefacept and to gain an understanding of how alefacept is used in Canadian clinical practice. Baseline patient demographic data are described herein.

METHODS

Patients with chronic plaque psoriasis were enrolled from 37 clinics across Canada. Subjects received at least one course of alefacept treatment followed by a period of at least 12 weeks off treatment and were prospectively followed for at least 60 weeks. Baseline assessments included patient demographics, relevant medical history, psoriasis and treatment history, reasons for initiating alefacept, enrolling physician's initial alefacept treatment plan and strategy, percent body surface area (BSA) involvement with psoriasis, and physician's baseline assessment of disease control. Subsequent assessments at each follow-up visit included the patient's response and the physician's assessment.

RESULTS

A total of 426 adult patients with predominantly chronic plaque psoriasis, with or without other types of psoriasis, were enrolled into the AWARE registry. Patients generally had moderate to severe psoriasis, with more than half (55.8%) having little or no disease control at baseline as assessed by their clinician, and 77% had > 10% BSA involvement with psoriasis. All patients in the AWARE patient population were receiving one or more treatments for psoriasis prior to or at the time of enrolment, and the majority continued to receive concomitant treatments at the time of study enrolment.

CONCLUSION

The AWARE registry enrolled a broad group of real-world patients with chronic plaque psoriasis treated with alefacept in clinical practices across Canada.

摘要

背景

阿法赛普特是加拿大卫生部批准的第一种用于治疗中重度慢性斑块型银屑病的生物疗法,可单独使用或与联合疗法联合使用。

目的

AWARE(从真实世界证据中获得的 Amevive 智慧)是一项多中心、观察性的、针对接受阿法赛普特治疗的银屑病患者的加拿大第四阶段研究。该研究的主要目标是开发一个共享的、实时的、全国性的临床数据库,以支持最佳实践并优化接受阿法赛普特治疗的患者的护理,并了解阿法赛普特在加拿大临床实践中的使用情况。本文描述了基线患者的人口统计学数据。

方法

从加拿大的 37 个诊所招募了慢性斑块型银屑病患者。受试者至少接受了一个疗程的阿法赛普特治疗,然后至少停药 12 周,并进行了至少 60 周的前瞻性随访。基线评估包括患者的人口统计学数据、相关病史、银屑病和治疗史、启动阿法赛普特治疗的原因、参与医生的初始阿法赛普特治疗计划和策略、银屑病受累的体表面积百分比(BSA),以及医生对疾病控制的基线评估。每次随访时的后续评估包括患者的反应和医生的评估。

结果

共有 426 名成年慢性斑块型银屑病患者(包括单纯性和混合性银屑病)入组 AWARE 登记处。患者的银屑病一般为中重度,超过一半(55.8%)的患者在基线时,根据医生的评估,病情控制较差或没有控制,77%的患者银屑病 BSA 受累大于 10%。在 AWARE 患者人群中,所有患者在入组前或入组时正在接受一种或多种银屑病治疗,并且在入组时大多数患者仍在接受同时治疗。

结论

AWARE 登记处招募了来自加拿大各地临床实践中接受阿法赛普特治疗的广泛的慢性斑块型银屑病真实世界患者。

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