Department of Community Health Sciences, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Department of Paediatrics, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Pediatr Rheumatol Online J. 2023 Apr 21;21(1):37. doi: 10.1186/s12969-023-00818-7.
To determine whether and how often the information to measure a set of key performance indicators (KPIs) in juvenile idiopathic arthritis (JIA) is found in data collected routinely in a Pediatric Rheumatology Clinic.
A retrospective electronic chart review and administrative data analysis was conducted for a cohort of 140 patients with JIA at a tertiary Pediatric Rheumatology Clinic between 2016-2020. The set of KPIs include measuring patient outcomes (joint assessment, physician's global assessment of disease activity, assessment of functional ability, composite disease activity measurement), access to care (waiting time between referral and first visit, visit with the rheumatologist within the first year of diagnosis, annual follow-up visits with the rheumatologist), and safety (tuberculosis screening, and laboratory monitoring). Documentation was assessed as a binary variable indicating whether the required information was ever found. Documentation frequency for each KPI was assessed with counts and percentages of the number of times the required information was documented for each clinic visit. Compliance with the safety KPI definitions was assessed using administrative databases.
Data for each KPI were found at least once in the cohort and documentation varied in frequency and consistency. Access to care and safety KPIs were documented more frequently than patient outcome KPIs. A joint assessment was documented at every visit for 95% of patients, 46% for an assessment of pain, and none for a physician's global assessment of disease activity, an assessment of functional ability, or a composite disease activity measurement.
Although feasible to measure, there is an opportunity for improving the consistency of documentation. Having an active system of monitoring KPIs and tools to simplify measurement is a key step in the process toward improved patient care outcomes. Streamlining the collection of KPI data can increase the likelihood of compliance. Next steps should involve replicating this study in various centres.
确定在儿科风湿病诊所常规收集的数据中,是否以及有多少次可以找到衡量一组关键绩效指标(KPI)的信息,这些信息用于评估幼年特发性关节炎(JIA)患者。
对 2016 年至 2020 年间在一家三级儿科风湿病诊所就诊的 140 例 JIA 患者进行回顾性电子病历审查和行政数据分析。该组 KPI 包括测量患者结局(关节评估、医生整体疾病活动评估、功能能力评估、综合疾病活动测量)、获得医疗服务的机会(从转诊到首次就诊的等待时间、确诊后第一年看风湿病医生的就诊次数、每年看风湿病医生的随访就诊次数)和安全性(结核病筛查和实验室监测)。文档记录评估为一个二进制变量,指示是否存在所需信息。通过计算每个就诊次数记录所需信息的次数,并以百分比的形式评估每个 KPI 的文档记录频率。使用行政数据库评估安全性 KPI 定义的遵守情况。
在队列中,每个 KPI 的数据至少出现过一次,文档记录的频率和一致性存在差异。获得医疗服务和安全性 KPI 的记录频率高于患者结局 KPI。95%的患者每次就诊都进行了关节评估,46%的患者进行了疼痛评估,没有患者进行医生整体疾病活动评估、功能能力评估或综合疾病活动测量。
尽管可以衡量,但在提高文档记录的一致性方面仍有改进的空间。建立一个主动监测 KPI 的系统和简化测量工具是改善患者护理结局的关键步骤。简化 KPI 数据的收集可以提高遵守率。下一步应该在各个中心复制这项研究。