Vasilakis-Scaramozza Catherine, Hagberg Katrina Wilcox, Persson Rebecca, Kafatos George, Maskell Joe, Neasham David, Jick Susan
Epidemiology, Boston Collaborative Drug Surveillance Program, Lexington, MA, USA.
Center for Observational Research, Amgen Ltd, Uxbridge, UK.
Clin Epidemiol. 2023 Dec 16;15:1207-1218. doi: 10.2147/CLEP.S434831. eCollection 2023.
To report distribution of codes associated with a rheumatoid arthritis (RA) diagnosis recorded in Clinical Practice Research Datalink (CPRD) Aurum compared to the previously validated CPRD GOLD database as a critical step toward making decisions about CPRD Aurum's suitability for medical research.
We analyzed the distribution of codes for RA diagnoses, labs, and treatments in the new CPRD Aurum database, compared to the CPRD GOLD database by selecting relevant indicators of RA diagnosis, treatment, and clinical care. We included all patients in England in CPRD Aurum and CPRD GOLD with an incident diagnosis code for RA on or after 1 January 2005 and at least two years recorded data before first RA diagnosis.
We found 53,083 and 18,167 patients with a new diagnosis code for RA in CPRD Aurum and CPRD GOLD, respectively. In both databases approximately 67% were female with similar mean ages at first diagnosis. There were few differences in RA-related recording patterns between the two data sources. Before first RA diagnosis, CPRD Aurum patients had more RA-specific labs and other supporting clinical codes. After diagnosis, CPRD Aurum patients had more RA diagnoses coded and more often had 10+ general RA labs than patients in CPRD GOLD. More CPRD GOLD patients had 10+ prescriptions for conventional disease-modifying antirheumatic drugs (cDMARD) compared to CPRD Aurum. Otherwise, the distribution of drugs used to treat RA was similar between databases. The standardized incidence of RA was similar between databases.
Overall, among patients with a diagnosis code for RA, recording of diagnoses, prescription drugs, and labs were similar between CPRD Aurum and CPRD GOLD. Slight differences were found for a few variables, but overall, we found consistency between the databases. In addition, standardized incidence of RA was similar between databases.
报告与类风湿性关节炎(RA)诊断相关的编码在临床实践研究数据链(CPRD)Aurum数据库中的分布情况,并与先前经验证的CPRD GOLD数据库进行比较,这是决定CPRD Aurum是否适合医学研究的关键一步。
通过选择RA诊断、治疗和临床护理的相关指标,我们分析了新的CPRD Aurum数据库中RA诊断、实验室检查和治疗编码的分布情况,并与CPRD GOLD数据库进行比较。我们纳入了CPRD Aurum和CPRD GOLD中所有在2005年1月1日或之后有RA确诊编码且在首次RA诊断前至少有两年记录数据的英格兰患者。
我们在CPRD Aurum和CPRD GOLD中分别发现了53083例和18167例有新RA诊断编码的患者。在两个数据库中,约67%为女性,首次诊断时平均年龄相似。两个数据源之间与RA相关的记录模式差异不大。在首次RA诊断前,CPRD Aurum的患者有更多的RA特异性实验室检查和其他支持性临床编码。诊断后,CPRD Aurum的患者有更多的RA诊断编码,且与CPRD GOLD中的患者相比,有10项以上常规抗风湿药物(cDMARD)实验室检查的情况更常见。与CPRD Aurum相比,更多的CPRD GOLD患者有10项以上传统改善病情抗风湿药物(cDMARD)的处方。否则,两个数据库中用于治疗RA的药物分布相似。两个数据库中RA的标准化发病率相似。
总体而言,在有RA诊断编码的患者中,CPRD Aurum和CPRD GOLD在诊断、处方药和实验室检查的记录方面相似。在一些变量上发现了细微差异,但总体而言,我们发现两个数据库之间具有一致性。此外,两个数据库中RA的标准化发病率相似。