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从索赔数据库中识别获批用于治疗免疫介导性炎症疾病的生物药物使用指征的META算法的开发与验证:VALORE项目的见解

Development and Validation of a META-Algorithm to Identify the Indications of Use of Biological Drugs Approved for the Treatment of Immune-Mediated Inflammatory Diseases from Claims Databases: Insights from the VALORE Project.

作者信息

Spini Andrea, L'Abbate Luca, Ingrasciotta Ylenia, Pellegrini Giorgia, Carollo Massimo, Ientile Valentina, Leoni Olivia, Zanforlini Martina, Ancona Domenica, Stella Paolo, Cavazzana Anna, Scapin Angela, Lopes Sara, Belleudi Valeria, Trifirò Gianluca

机构信息

Department of Diagnostics and Public Health, University of Verona, Verona, Italy.

Department of Biomedical and Dental Sciences and Morphofunctional Imaging, University of Messina, Messina, Italy.

出版信息

Clin Epidemiol. 2024 Jun 4;16:395-407. doi: 10.2147/CLEP.S445120. eCollection 2024.

Abstract

PURPOSE

This research aimed to develop and validate a META-algorithm combining individual immune-mediated inflammatory disease (IMID)-specific algorithms to identify the exact IMID indications for incident biological drug users from claims data within the context of the Italian VALORE project.

METHODS AND PATIENTS

All subjects with at least one dispensing of TNF-alpha inhibitors, anti-interleukin agents, and selective immunosuppressants approved for IMIDs were identified from claims databases of Latium region in Italy (observation period: 2010-2020). Validated coding algorithms for identifying individual IMIDs from claims databases were found from published literature and combined into a META-algorithm. Positive predictive value (PPV), sensitivity (Se), negative predictive value (NPV), specificity (Sp), and accuracy (Acc) were estimated for each indication against the electronic therapeutic plans (ETPs) of the Latium region as the reference standard. Lastly, the frequency of the indication of use across individual biologic drugs was compared with that reported in three other Italian regions (Lombardy, Apulia, and the Veneto region).

RESULTS

In total, 9755 incident biological drug users with a single IMID indication were identified. Using the newly developed META-algorithm, an indication of use was detected in 95% (n=9255) of the total cohort. The estimated Acc, Se, Sp, PPV, and NPV, against the reference standard were as follows: 0.96, 0.86, 0.97, 0.82, and 0.98 for Crohn's disease, 0.96, 0.80, 0.98, 0.85, and 0.97 for ulcerative colitis, 0.93, 0.76, 0.99, 0.95, and 0.92 for rheumatoid arthritis, 0.97, 0.75, 0.99, 0.85, and 0.98 for spondylarthritis, and 0.91, 0.92, 0.91, 0.88, and 0.94 for psoriatic arthritis/psoriasis, respectively. Additionally, no substantial difference was observed in the frequency of indication of use by active ingredient among Latium and the other three Italian regions included in the study.

CONCLUSION

The newly developed META-algorithm demonstrated high validity estimates in the Italian claims data and was capable of discriminating with good performance among the most frequent IMID indications.

摘要

目的

本研究旨在开发并验证一种元算法,该算法结合个体免疫介导的炎症性疾病(IMID)特异性算法,以便在意大利VALORE项目背景下,从理赔数据中识别初用生物制剂患者的确切IMID适应症。

方法与患者

从意大利拉齐奥地区的理赔数据库中识别出所有至少有一次配用经批准用于IMID的肿瘤坏死因子-α抑制剂、抗白细胞介素药物和选择性免疫抑制剂的受试者(观察期:2010 - 2020年)。从已发表文献中找到用于从理赔数据库中识别个体IMID的经过验证的编码算法,并将其合并为一种元算法。以拉齐奥地区的电子治疗计划(ETP)作为参考标准,对每种适应症的阳性预测值(PPV)、敏感性(Se)、阴性预测值(NPV)、特异性(Sp)和准确性(Acc)进行估计。最后,将个体生物制剂的使用适应症频率与意大利其他三个地区(伦巴第、普利亚和威尼托地区)报告的频率进行比较。

结果

总共识别出9755名有单一IMID适应症的初用生物制剂患者。使用新开发的元算法,在整个队列的95%(n = 9255)中检测到了使用适应症。相对于参考标准,估计的Acc、Se、Sp、PPV和NPV如下:克罗恩病分别为0.96、0.86、0.97、0.82和0.98;溃疡性结肠炎分别为0.96、0.80、0.98、0.85和0.97;类风湿性关节炎分别为0.93、0.76、0.99、0.95和0.92;脊柱关节炎分别为0.97、0.75、0.99、0.85和0.98;银屑病关节炎/银屑病分别为0.91、0.92、0.91、0.88和0.94。此外,在研究纳入的拉齐奥地区和其他三个意大利地区之间,按活性成分划分的使用适应症频率未观察到实质性差异。

结论

新开发的元算法在意大利理赔数据中显示出较高的有效性估计,并且能够在最常见的IMID适应症之间进行良好区分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/505f/11162210/c916d80b8f92/CLEP-16-395-g0001.jpg

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