Do health outcomes following pain service utilization vary for young people experiencing chronic pain according to pain phenotype? An exploratory analysis using the electronic Persistent Pain Outcomes Collaboration database.

IF 4 2区 医学 Q1 CLINICAL NEUROLOGY
Robert Waller, Helen Slater, Andrew M Briggs, Susan M Lord, Anne J Smith
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引用次数: 0

Abstract

The prevalence of chronic pain in young people increases with age, approaching rates observed in adults. Utilizing Australiasian electronic Persistent Pain Outcomes Collaboration (ePPOC) data for young people, we previously derived three phenotypes ("low", "moderate", "high") characterized by an increasing symptom-severity gradient in multi-dimensional pain-related variables measured at referral to pain service. In this study, we explored whether health outcomes varied by phenotypes at the end of care episode. We included young people captured in the Australian adult ePPOC data registry representing 80 tertiary and private pain services, within a 5-year period (2018 to 2022) if previously phenotyped and had episode end patient reported outcome measures. Self-reported global rating of change was measured at episode end, while pain severity and interference, pain-related worry (quasisurrogate 'catastrophizing'), emotional functioning and pain self-efficacy were measured at referral and episode end. Differences in outcomes across phenotypes were estimated using logistic regression for binary indicators and clinically significant improvements, and linear regression for mean change. Of 3518 young people initially phenotyped from adult service data, 477 (13.6%) aged 15-25 years had episode end outcomes. The proportion of participants reporting meaningful improvement in outcomes ranged from 24.0%-74.2%, with differences observed across phenotypes. Although the limited proportion of participants with episode end data may have introduced bias, those with and without end episode outcomes were broadly comparable on baseline demographics. Results suggests tailoring care to symptom-severity may be important for optimising outcomes, particularly for young people with "high" symptom-severity whose care needs are more complex. PERSPECTIVE: This study reports unique exploration of whether the outcomes following specialized pain service care supporting young people living with chronic pain varied according to their symptom-severity phenotype. This evidence provides impetus for system and service improvements to more equitably and efficiently meet young people's needs by providing timely, differential care.

疼痛服务使用后的健康结果在经历慢性疼痛的年轻人中根据疼痛表型有所不同吗?使用电子持续性疼痛结果协作数据库进行探索性分析。
慢性疼痛在年轻人中的患病率随着年龄的增长而增加,接近于在成年人中观察到的比率。利用澳大利亚电子持续性疼痛结果协作(ePPOC)的年轻人数据,我们之前导出了三种表型(“低”,“中等”,“高”),其特征是在转诊到疼痛服务时测量的多维疼痛相关变量的症状-严重程度梯度增加。在这项研究中,我们探讨了在护理结束时,健康结果是否因表型而变化。我们纳入了澳大利亚成人ePPOC数据注册表中捕获的年轻人,这些年轻人代表了5年(2018年至2022年)期间80个三级和私人疼痛服务机构,如果之前有表型,并且有发作末期患者报告的结果测量。在发作结束时测量自我报告的整体变化评分,而在转诊和发作结束时测量疼痛严重程度和干扰、疼痛相关担忧(准替代“灾难化”)、情绪功能和疼痛自我效能。使用二元指标和临床显著改善的逻辑回归和平均变化的线性回归来估计不同表型结果的差异。在3518名从成人服务数据中初始表型的年轻人中,477名(13.6%)年龄在15-25岁的人有发作性结局。报告结果有意义改善的参与者比例在24.0%-74.2%之间,在不同表型之间观察到差异。虽然具有发作结束数据的参与者比例有限,可能会引入偏倚,但有和没有发作结束结果的参与者在基线人口统计学上具有广泛的可比性。结果表明,根据症状严重程度量身定制护理可能对优化结果很重要,特别是对那些护理需求更为复杂的“高”症状严重的年轻人。观点:这项研究报告了一项独特的探索,即支持患有慢性疼痛的年轻人的专业疼痛服务护理的结果是否会根据他们的症状-严重程度表型而变化。这一证据为改进系统和服务提供了动力,通过提供及时、有区别的护理,更公平、更有效地满足年轻人的需求。
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
Journal of Pain
Journal of Pain 医学-临床神经学
CiteScore
6.30
自引率
7.50%
发文量
441
审稿时长
42 days
期刊介绍: The Journal of Pain publishes original articles related to all aspects of pain, including clinical and basic research, patient care, education, and health policy. Articles selected for publication in the Journal are most commonly reports of original clinical research or reports of original basic research. In addition, invited critical reviews, including meta analyses of drugs for pain management, invited commentaries on reviews, and exceptional case studies are published in the Journal. The mission of the Journal is to improve the care of patients in pain by providing a forum for clinical researchers, basic scientists, clinicians, and other health professionals to publish original research.
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