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临床试验/NCT03496831
NCT03496831已完成不适用

Development of a Prediction Model for the Risk of Hospitalized Infection in Patients With Chronic Inflammatory Arthritis Treated With Biological Drugs

Simon Krabbe0 个研究点目标入组 7,500 人开始时间: 2006年1月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
7,500
主要终点
Hospitalized infection or death

研究概览

简要总结

Background The risk for hospitalized infection (i.e. infection leading to hospitalization) in patients with inflammatory arthritis (rheumatoid arthritis (RA), psoriatic arthritis (PsA) or axial spondyloarthritis (axSpA) treated with biological drugs is known to be increased compared to the background population. In daily clinical practice, there is a need for a simple way to assess the absolute risk for hospitalized infection in individual patients based on easily available information such as age, diagnosis, functional status, comorbidities and medication. This risk estimate will be useful in clinical decision making e.g. when advising patients on whether or not to initiate biologic therapy or when advising patients on influenza or pneumococcal vaccination.

Objectives The objectives are 1) to assess the risk for hospitalized infection (infection leading to hospitalization) in patients with inflammatory arthritis during 12 months of follow-up after initiating treatment with their first biological drug (bDMARD) with the risk in the general population, and 2) to develop a simple, clinically useful algorithm that allows prediction of the risk of hospitalized infection in individual patients.

Methods Observational cohort study based on existing data in: The Danish Rheumatology Register (DANBIO), The Danish National Patient Register, The Danish National Prescription Register and The Danish Register of Causes of Death. All patients registered in DANBIO with RA, PsA or axSpA who initiated treatment with their first biological drug between January 1, 2006 and December 31, 2016 will be identified. Baseline predictors and outcomes (hospitalized infection or death) during 12 months of follow-up are obtained. Logistic regression analysis and 10-fold cross-validation will be used to develop and internally validate the prediction model.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Rheumatoid Arthritis

Registered in DANBIO with a diagnosis of M05.9, M06.0 or M06.9.

干预措施: Biologic Agents (Drug)

Spondyloarthritis

Registered in DANBIO with a diagnosis of M45.9, M46.1, M46.8+M02.9, M46.8+M07.4, M46.8+M07.5 or M46.9.

干预措施: Biologic Agents (Drug)

Psoriatic Arthritis

Registered in DANBIO with a diagnosis of M07.3 or M46.8+M07.2.

干预措施: Biologic Agents (Drug)

结局指标

主要结局

Hospitalized infection or death

时间窗: 12 months of follow-up

Hospitalization caused by infection or death

次要结局

未报告次要终点

研究者

发起方
Simon Krabbe
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Simon Krabbe

Principal Investigator

Rigshospitalet, Denmark

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