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改善儿童期起病的系统性红斑狼疮患者狼疮护理指数文档记录。

Improving lupus care index documentation in patients with childhood-onset systemic lupus erythematosus.

作者信息

Barbar-Smiley Fatima A, Yildirim-Toruner Cagri, Akoghlanian Shoghik, AlAhmed Ohoud, Ardoin Stacy P, Leone Ashlee, Oberle Edward, Sivaraman Vidya

机构信息

Research & Development, Amgen, Thousand Oaks, CA, United States.

Department of Pediatrics, Nationwide Children's Hospital, Columbus, OH, United States.

出版信息

Front Pediatr. 2024 Aug 27;12:1428644. doi: 10.3389/fped.2024.1428644. eCollection 2024.

Abstract

INTRODUCTION

Childhood-onset systemic lupus erythematosus (c-SLE) presents unique challenges due to increased risk for severe morbidity and mortality compared to adult-onset SLE. Effective disease management relies on accurate disease assessment and documentation. Our project aimed to improve the documentation of the Lupus Care Index (LCI), a disease assessment bundle, by implementing a quality improvement (QI) initiative.

METHODS

A QI project was conducted at Nationwide Children's Hospital (NCH), targeting patients with c-SLE. The LCI, comprising the Systemic Lupus Erythematosus Disease Activity Index (SLEDAI-2k) Physician Global Assessment (PGA) and patient-reported pain score, was introduced to capture comprehensive disease assessment. Interventions included provider education, standardization of documentation procedures, and electronic health record (EHR) modifications. Automated reports tracked documentation rates, and Pareto charts identified areas for targeted interventions.

RESULTS

Baseline analysis revealed incomplete documentation of LCI components in only one-third of c-SLE patients. Following interventions, documentation rates improved from 38% to 90%, with sustained improvement over at least a year.

DISCUSSION

Enhancing documentation of LCI in patients with c-SLE is crucial for optimizing disease management. Our quality improvement initiative demonstrated the feasibility of improving documentation practices through targeted interventions and system modifications. Future research should explore the impact of comprehensive documentation on clinical outcomes in pediatric lupus patients. Improving documentation of LCI in patients with c-SLE is essential for optimizing care delivery and clinical outcomes; our QI initiative highlights the effectiveness of systemic interventions in enhancing documentation practices and underscores the importance of continued efforts to improve pediatric lupus care.

摘要

引言

儿童期起病的系统性红斑狼疮(c-SLE)与成人期起病的系统性红斑狼疮相比,由于严重发病和死亡风险增加,带来了独特的挑战。有效的疾病管理依赖于准确的疾病评估和记录。我们的项目旨在通过实施质量改进(QI)计划来改善狼疮护理指数(LCI)(一种疾病评估组合)的记录情况。

方法

在全国儿童医院(NCH)开展了一项针对c-SLE患者的QI项目。引入了包括系统性红斑狼疮疾病活动指数(SLEDAI-2k)、医生整体评估(PGA)和患者报告的疼痛评分的LCI,以进行全面的疾病评估。干预措施包括对医疗服务提供者的教育、记录程序的标准化以及电子健康记录(EHR)的修改。自动报告跟踪记录率,帕累托图确定有针对性干预的领域。

结果

基线分析显示,只有三分之一的c-SLE患者的LCI组成部分记录不完整。干预后,记录率从38%提高到90%,并在至少一年的时间里持续改善。

讨论

加强c-SLE患者LCI的记录对于优化疾病管理至关重要。我们的质量改进计划证明了通过有针对性的干预和系统修改来改善记录做法的可行性。未来的研究应探讨全面记录对儿童狼疮患者临床结局的影响。改善c-SLE患者LCI的记录对于优化护理提供和临床结局至关重要;我们的QI计划突出了系统性干预在加强记录做法方面的有效性,并强调了持续努力改善儿童狼疮护理的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7d1/11385605/3da7ea6ab9bc/fped-12-1428644-g001.jpg

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