Epidemiology Unit, German Rheumatism Research Centre (DRFZ), Charitéplatz 1, 10117, Berlin, Germany.
Rheumatology, Goethe University, Frankfurt, Germany.
Arthritis Res Ther. 2021 Jul 7;23(1):181. doi: 10.1186/s13075-021-02563-2.
Clinical data collection requires correct and complete data sets in order to perform correct statistical analysis and draw valid conclusions. While in randomized clinical trials much effort concentrates on data monitoring, this is rarely the case in observational studies- due to high numbers of cases and often-restricted resources. We have developed a valid and cost-effective monitoring tool, which can substantially contribute to an increased data quality in observational research.
An automated digital monitoring system for cohort studies developed by the German Rheumatism Research Centre (DRFZ) was tested within the disease register RABBIT-SpA, a longitudinal observational study including patients with axial spondyloarthritis and psoriatic arthritis. Physicians and patients complete electronic case report forms (eCRF) twice a year for up to 10 years. Automatic plausibility checks were implemented to verify all data after entry into the eCRF. To identify conflicts that cannot be found by this approach, all possible conflicts were compiled into a catalog. This "conflict catalog" was used to create queries, which are displayed as part of the eCRF. The proportion of queried eCRFs and responses were analyzed by descriptive methods. For the analysis of responses, the type of conflict was assigned to either a single conflict only (affecting individual items) or a conflict that required the entire eCRF to be queried.
Data from 1883 patients was analyzed. A total of n = 3145 eCRFs submitted between baseline (T0) and T3 (12 months) had conflicts (40-64%). Fifty-six to 100% of the queries regarding eCRFs that were completely missing were answered. A mean of 1.4 to 2.4 single conflicts occurred per eCRF, of which 59-69% were answered. The most common missing values were CRP, ESR, Schober's test, data on systemic glucocorticoid therapy, and presence of enthesitis.
Providing high data quality in large observational cohort studies is a major challenge, which requires careful monitoring. An automated monitoring process was successfully implemented and well accepted by the study centers. Two thirds of the queries were answered with new data. While conventional manual monitoring is resource-intensive and may itself create new sources of errors, automated processes are a convenient way to augment data quality.
临床数据收集需要正确和完整的数据集,以便进行正确的统计分析并得出有效的结论。虽然在随机临床试验中,大量的精力集中在数据监测上,但在观察性研究中却很少见,因为病例数量多且资源往往有限。我们开发了一种有效且具有成本效益的监测工具,可以大大提高观察性研究的数据质量。
德国风湿病研究中心 (DRFZ) 开发的用于队列研究的自动化数字监测系统在疾病登记处 RABBIT-SpA 中进行了测试,这是一项包括轴向脊柱关节炎和银屑病关节炎患者的纵向观察性研究。医生和患者每两年填写一次电子病例报告表 (eCRF),为期长达 10 年。在输入 eCRF 后,实施自动合理性检查以验证所有数据。为了识别无法通过这种方法找到的冲突,将所有可能的冲突都编入目录。这个“冲突目录”用于创建查询,这些查询作为 eCRF 的一部分显示。通过描述性方法分析查询的 eCRF 比例和响应比例。对于响应分析,将冲突类型分配给单个冲突(影响单个项目)或需要查询整个 eCRF 的冲突。
分析了 1883 名患者的数据。在基线 (T0) 和 T3(12 个月)之间提交的总共 n = 3145 份 eCRF 中存在冲突(40-64%)。完全缺失的 eCRF 查询中,有 56-100%得到了回答。每份 eCRF 平均出现 1.4 到 2.4 个单个冲突,其中 59-69%得到了回答。最常见的缺失值是 CRP、ESR、Schober 试验、全身糖皮质激素治疗数据和附着点炎的存在。
在大型观察性队列研究中提供高质量的数据是一项重大挑战,需要仔细监测。已成功实施自动化监测流程,并得到研究中心的广泛接受。三分之二的查询都得到了新数据的回答。虽然传统的手动监测资源密集且可能本身会产生新的错误源,但自动化流程是提高数据质量的一种便捷方式。