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对患有慢性疼痛的年轻人的表型、临床及医疗利用关联进行特征分析:使用电子持续性疼痛结局协作数据库的潜在类别分析

Characterizing phenotypes and clinical and health utilization associations of young people with chronic pain: latent class analysis using the electronic Persistent Pain Outcomes Collaboration database.

作者信息

Slater Helen, Waller Robert, Briggs Andrew M, Lord Susan M, Smith Anne J

机构信息

School of Allied Health, Faculty of Health Sciences, Curtin University, Perth, Australia.

Children's Complex Pain Service, John Hunter Children's Hospital, Newcastle, Australia.

出版信息

Pain. 2025 Jan 1;166(1):67-86. doi: 10.1097/j.pain.0000000000003326. Epub 2024 Jul 9.

Abstract

Using the Australiasian electronic Persistent Pain Outcomes Collaboration, a binational pain registry collecting standardized clinical data from paediatric ePPOC (PaedsePPOC) and adult pain services (AdultePPOC), we explored and characterized nationally representative chronic pain phenotypes and associations with clinical and sociodemographic factors, health care utilization, and medicine use of young people. Young people ≥15.0 and <25.0 years captured in PaedePPOC and AdultePPOC Australian data registry were included. Data from 68 adult and 12 paediatric pain services for a 5-year period January 2018 to December 2022 (first episode, including treatment information) were analysed. Unsupervised latent class analysis was applied to explore the existence of distinct pain phenotypes, with separate models for both services. A 3-phenotype model was selected from both paediatric and adult ePPOC data, with 693 and 3518 young people included, respectively (at least one valid indicator variable). Indicator variables for paediatric models were as follows: pain severity, functional disability (quasisurrogate "pain interference"), pain count, pain duration, pain-related worry (quasisurrogate "catastrophizing"), and emotional functioning; and, for adult models: pain severity, pain interference, pain catastrophizing, emotional functioning, and pain self-efficacy. From both services, 3 similar phenotypes emerged ("low," "moderate," "high"), characterized by an increasing symptom-severity gradient in multidimensional pain-related variables, showing meaningful differences across clinical and sociodemographic factors, health service utilization, and medicines use. Derived phenotypes point to the need for novel care models that differentially respond to the needs of distinct groups of young people, providing timely, targeted, age-appropriate care. To effectively scale such care, digital technologies can be leveraged to augment phenotype-informed clinical care.

摘要

利用澳大利亚电子持续性疼痛结果协作组织(Australiasian electronic Persistent Pain Outcomes Collaboration),这是一个从儿科电子持续性疼痛结果协作项目(PaedsePPOC)和成人疼痛服务机构(AdultePPOC)收集标准化临床数据的双边疼痛登记处,我们探索并描述了具有全国代表性的慢性疼痛表型,以及与年轻人的临床和社会人口统计学因素、医疗保健利用情况和药物使用之间的关联。纳入了PaedePPOC和AdultePPOC澳大利亚数据登记处中年龄在15.0岁及以上且小于25.0岁的年轻人。分析了来自68个成人和12个儿科疼痛服务机构在2018年1月至2022年12月的5年期间(首次发作,包括治疗信息)的数据。应用无监督潜在类别分析来探索不同疼痛表型的存在,两个服务机构分别建立模型。从儿科和成人电子持续性疼痛结果协作项目数据中均选择了一个三表型模型,分别纳入了693名和3518名年轻人(至少有一个有效指标变量)。儿科模型的指标变量如下:疼痛严重程度、功能残疾(准替代指标“疼痛干扰”)、疼痛计数、疼痛持续时间、与疼痛相关的担忧(准替代指标“灾难化思维”)以及情绪功能;而成人模型的指标变量为:疼痛严重程度、疼痛干扰、疼痛灾难化思维、情绪功能以及疼痛自我效能感。两个服务机构都出现了3种相似的表型(“低”、“中”、“高”),其特征是多维疼痛相关变量的症状严重程度梯度逐渐增加,在临床和社会人口统计学因素、医疗服务利用情况和药物使用方面表现出有意义的差异。得出的表型表明需要新的护理模式,以不同方式应对不同年轻人群体的需求,提供及时、有针对性、适合年龄的护理。为了有效地推广这种护理,可以利用数字技术来加强基于表型的临床护理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68b3/11647817/9d55dfd6136e/jop-166-067-g001.jpg

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