Relationship Between Gout Flare States and Patient-Reported Outcomes After Allopurinol Initiation.

IF 3.7 2区 医学 Q1 RHEUMATOLOGY
Lisa K Stamp, Chris Frampton, Sarah Stewart, Keith J Petrie, N Lawrence Edwards, Angelo Gaffo, Nicola Dalbeth
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Abstract

Objective: Gout flares are the most important clinical feature of the disease. A hypothetical maximum flare occurrence in the preceding six months has been suggested to be no flares for a patient-acceptable symptom state (PASS) and only one flare for low disease activity (LDA). The aim of this analysis was to determine the relationship between gout flare states (PASS, LDA, and not in LDA or PASS [non-LDA/PASS]) and patient-reported outcomes.

Methods: Post hoc analyses of variance were undertaken using data from a 12-month randomized controlled trial involving 172 people with gout, which compared low-dose colchicine to placebo for the first 6 months while starting allopurinol with a further 6-month follow-up. Self-reported gout flares were collected monthly. Health Assessment Questionnaire (HAQ) and EuroQol 5-domain (EQ-5D-3L) were completed at 0, 3, 6 ,9, and 12 months, and the gout-specific brief illness perception questionnaire (BIPQ) was collected at months 0, 6, and 12.

Results: In the final six months of the study, 68 participants (38%) were classified as being in PASS, 34 (19%) as in LDA, and 77 (43%) as non-LDA/PASS. There was no association between gout flare states and EQ-5D-3L or HAQ. There was a statistically significant association between three of eight BIPQ items with increasing consequences, identity, and concern scores across the three states of PASS, LDA, and non-LDA/PASS.

Conclusion: The majority of people were able to achieve gout flare PASS or LDA in the second six months after commencing allopurinol. As flare burden increases, so does the impact of gout on the patient. These findings highlight the importance of flare prevention in the management of gout.

别嘌呤醇起始治疗后痛风发作状态与患者报告结果的关系。
目的:痛风耀斑是该病最重要的临床特征。假设前6个月最大发作次数为患者可接受症状状态(PASS)无发作,低疾病活动性(LDA)只有一次发作。该分析的目的是确定痛风发作状态(PASS, LDA,而不是LDA或PASS(非LDA/PASS))与患者报告的结果之间的关系。方法:采用一项涉及179名痛风患者的12个月随机对照试验的数据进行事后方差分析,该试验在开始使用别嘌呤醇的前6个月比较低剂量秋水仙碱和安慰剂,并进行了6个月的随访。每月收集自我报告的痛风耀斑。每3个月完成HAQ和EQ-5D-3L,于第0、6、12个月收集痛风特异性简短疾病感知问卷。结果:在研究的最后6个月,68名(38%)参与者被归类为PASS, 34名(19%)参与者被归类为LDA, 77名(43%)参与者被归类为非LDA/PASS。痛风耀斑状态与EQ-5D-3L或HAQ之间没有关联。3/8个BIPQ项目之间存在统计学上显著的关联,在PASS、LDA和非LDA/PASS三种状态下,后果、身份和关注得分都在增加。结论:大多数患者在开始使用别嘌呤醇后的第二个6个月内能够达到痛风发作PASS或LDA。随着耀斑负荷的增加,痛风对患者的影响也在增加。这些发现强调了预防耀斑在痛风管理中的重要性。
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
9.40
自引率
6.40%
发文量
368
审稿时长
3-6 weeks
期刊介绍: Arthritis Care & Research, an official journal of the American College of Rheumatology and the Association of Rheumatology Health Professionals (a division of the College), is a peer-reviewed publication that publishes original research, review articles, and editorials that promote excellence in the clinical practice of rheumatology. Relevant to the care of individuals with rheumatic diseases, major topics are evidence-based practice studies, clinical problems, practice guidelines, educational, social, and public health issues, health economics, health care policy, and future trends in rheumatology practice.
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