Real-world evidence evaluation on consumer experience and prescription journey of diclofenac gel in Sweden.

IF 1.5 Q4 CLINICAL NEUROLOGY
Scandinavian Journal of Pain Pub Date : 2024-08-20 eCollection Date: 2024-01-01 DOI:10.1515/sjpain-2023-0147
Deepika Nair, Jan-Rickard Norrefalk, Emese Csoke, Teresa K Wilcox, Gilbert Shanga
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引用次数: 0

Abstract

Objectives: The aim of this study was to understand profiles of topical Voltaren gel diclofenac (VGD) 2.32 and 1.16% consumers through analyzing prescription patterns and to characterize treatment satisfaction, functional impairment, and pain relief after over-the-counter (OTC) VGD use in Sweden under real-world conditions.

Methods: This observational, real-world study conducted in Sweden had retrospective and prospective segments. The retrospective secondary data segment utilized 12-month diclofenac gel prescription data from the Swedish eHealth Agency (E-hälsomyndigheten). The prospective segment included electronic surveys completed at baseline and weeks 4 and 12 by adult consumers who purchased OTC VGD to treat their pain.

Results: Secondary data analyses (n = 12,145) showed that 56.7% of patients receiving diclofenac gel were females ≥70 years old. Most patients did not switch pain treatments; the mean time between diclofenac gel refills was about 2.5 months. From the surveys (n = 264), VGD provided pain relief, indicated by improvement in 11-point pain numeric rating scale scores. Average pain severity at baseline was 5.8 - improving by a mean of 1.3 and 1.9 points at weeks 4 and 12, respectively. The majority of consumers reported improvement in daily functioning (i.e., health-related quality of life [HRQoL]), and most were at least somewhat satisfied with VGD treatment results.

Conclusions: This real-world study provides important insights into the prescription patterns of diclofenac gel and the consumer experience with OTC VGD in Sweden. Patients rarely switched to other topical nonsteroidal anti-inflammatory drugs, and VGD consumers reported pain relief and improved HRQoL compared to baseline - resulting in treatment satisfaction.

瑞典消费者体验和双氯芬酸凝胶处方过程的真实世界证据评估。
研究目的本研究旨在通过分析处方模式,了解瑞典2.32%和1.16%伏他伦凝胶双氯芬酸外用药消费者的概况,并描述在真实世界条件下使用非处方(OTC)伏他伦凝胶双氯芬酸外用药后的治疗满意度、功能障碍和疼痛缓解情况:这项在瑞典进行的观察性真实世界研究分为回顾性和前瞻性两个部分。回顾性二级数据部分利用了瑞典电子卫生局(E-hälsomyndigheten)提供的 12 个月双氯芬酸凝胶处方数据。前瞻性数据包括购买非处方药VGD治疗疼痛的成年消费者在基线、第4周和第12周完成的电子调查:二次数据分析(n = 12,145)显示,接受双氯芬酸凝胶治疗的患者中有 56.7% 为年龄≥70 岁的女性。大多数患者没有更换止痛治疗方法;每次更换双氯芬酸凝胶的平均间隔时间约为 2.5 个月。调查显示(n = 264),VGD 可缓解疼痛,表现为 11 点疼痛数字评级量表评分有所改善。基线时的平均疼痛严重程度为 5.8,在第 4 周和第 12 周分别平均改善了 1.3 分和 1.9 分。大多数患者表示日常功能(即与健康相关的生活质量[HRQoL])有所改善,而且大多数人至少对VGD治疗结果感到有些满意:这项真实世界的研究为了解瑞典双氯芬酸凝胶的处方模式和消费者使用非处方药 VGD 的体验提供了重要依据。患者很少改用其他外用非甾体抗炎药,VGD 消费者报告疼痛得到缓解,HRQoL 与基线相比有所改善,因此对治疗感到满意。
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
Scandinavian Journal of Pain
Scandinavian Journal of Pain CLINICAL NEUROLOGY-
CiteScore
3.30
自引率
6.20%
发文量
73
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