Development of CARRA/PReS-endorsed consensus Core and Expanded Datasets in childhood-onset systemic lupus erythematosus for international registry-based research.

IF 20.3 1区 医学 Q1 RHEUMATOLOGY
Rebecca E Sadun, Jennifer C Cooper, Alexandre Belot, Tadej Avcin, Amita Aggarwal, Jenny Ainsworth, Alisha Akinsete, Stacy P Ardoin, Michael W Beresford, Lynette Bortey, Hermine I Brunner, Joyce C Chang, Coziana Ciurtin, Ashley Daftary, Barbara Eberhard, Candace H Feldman, Christian M Hedrich, Aimee O Hersh, Linda T Hiraki, David A Isenberg, Sylvia Kamphuis, Andrea M Knight, Lou Lambert, Deborah M Levy, Stephen D Marks, Naomi Maxwell, Angela Migowa, Katharine Moore, Seza Ozen, Rosalind Ramsey-Goldman, Angelo Ravelli, Bryce B Reeve, Tamar B Rubinstein, Claudia Saad-Magalhaes, Sujata Sawhney, Laura E Schanberg, Emily von Scheven, Christiaan Scott, Mary Beth Son, Gladys Tony, Elissa R Weitzman, Scott E Wenderfer, Alisha Woodside, Laura B Lewandowski, Eve Md Smith
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引用次数: 0

Abstract

Objectives: Childhood-onset systemic lupus erythematosus (cSLE), representing 15%-20% of individuals with SLE, has been difficult to study globally due to differences between registries. This initiative, supported by Childhood Arthritis Rheumatology Research Alliance (CARRA) and Paediatric Rheumatology European Society (PReS), aims to create Core and Expanded cSLE Datasets to standardise and enhance research worldwide.

Methods: 21 international cSLE experts and 4 patients participated in a Delphi process (questionnaires, 2 topic-specific focus groups and 3 virtual consensus meetings) to create 2 standardised cSLE datasets. The Core cSLE Dataset was designed to include data essential to meaningful clinical research across many settings. The Expanded cSLE Dataset was designed for centres able to consistently collect data to address broader research questions. Final data items for the Core and Expanded datasets were determined by consensus defined as >80% agreement) using an adapted nominal group technique and voting.

Results: The resulting Core cSLE Dataset contains 46 items, including demographics, clinical features, laboratory results, medications and significant adverse events. The Expanded cSLE Dataset adds 26 additional items and includes patient-reported outcomes. Consensus was also achieved regarding the frequency and time points for data collection: baseline, quarterly follow-up visits, annually and flare visits.

Conclusion: Standardised Core and Expanded cSLE Datasets for registry-based international cSLE research were defined through the consensus of global experts and patient/caregiver representatives, endorsed by CARRA and PReS. These datasets incorporate disease-specific and patient-specific features, optimised for diverse settings to facilitate international collaborative research for children and adolescents with SLE worldwide.

开发 CARRA/PReS 认可的儿童发病型系统性红斑狼疮共识核心数据集和扩展数据集,用于基于注册表的国际研究。
研究目的儿童期发病的系统性红斑狼疮(cSLE)患者占系统性红斑狼疮患者的 15%-20%,但由于各登记处之间存在差异,因此很难在全球范围内开展研究。该倡议得到了儿童关节炎风湿病学研究联盟(CARRA)和欧洲儿童风湿病学会(PReS)的支持,旨在创建核心和扩展的系统性红斑狼疮数据集,以规范和加强全球范围内的研究。方法:21 名国际系统性红斑狼疮专家和 4 名患者参与了德尔菲过程(问卷调查、2 个特定主题焦点小组和 3 个虚拟共识会议),以创建 2 个标准化的系统性红斑狼疮数据集。核心系统性红斑狼疮数据集的设计包括了在多种环境下进行有意义的临床研究所必需的数据。扩展的系统性红斑狼疮数据集是为能够持续收集数据以解决更广泛的研究问题的中心而设计的。核心数据集和扩展数据集的最终数据项是通过改编的名义小组技术和投票表决达成共识的,共识的定义是>80%的一致意见:结果:最终形成的核心系统性红斑狼疮数据集包含 46 个项目,包括人口统计学、临床特征、实验室结果、药物和重大不良事件。扩展的 cSLE 数据集增加了 26 个项目,并包括患者报告的结果。数据收集的频率和时间点也已达成共识:基线、季度随访、年度和复发随访:通过全球专家和患者/护理者代表的共识,并经 CARRA 和 PReS 认可,为基于登记的国际系统性红斑狼疮研究定义了标准化核心数据集和扩展数据集。这些数据集结合了疾病特异性和患者特异性特征,针对不同的环境进行了优化,以促进全球系统性红斑狼疮儿童和青少年患者的国际合作研究。
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来源期刊
Annals of the Rheumatic Diseases
Annals of the Rheumatic Diseases 医学-风湿病学
CiteScore
35.00
自引率
9.90%
发文量
3728
审稿时长
1.4 months
期刊介绍: Annals of the Rheumatic Diseases (ARD) is an international peer-reviewed journal covering all aspects of rheumatology, which includes the full spectrum of musculoskeletal conditions, arthritic disease, and connective tissue disorders. ARD publishes basic, clinical, and translational scientific research, including the most important recommendations for the management of various conditions.
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