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基于电子健康记录的回顾性观察研究中,终身状况的无事件生存时间偏倚。

Immortal time bias for life-long conditions in retrospective observational studies using electronic health records.

机构信息

Department of Health Sciences (Biostatistics Research Group), University of Leicester, Leicester, UK.

Department of Non-communicable Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, UK.

出版信息

BMC Med Res Methodol. 2022 Mar 27;22(1):86. doi: 10.1186/s12874-022-01581-1.

Abstract

BACKGROUND

Immortal time bias is common in observational studies but is typically described for pharmacoepidemiology studies where there is a delay between cohort entry and treatment initiation.

METHODS

This study used the Clinical Practice Research Datalink (CPRD) and linked national mortality data in England from 2000 to 2019 to investigate immortal time bias for a specific life-long condition, intellectual disability. Life expectancy (Chiang's abridged life table approach) was compared for 33,867 exposed and 980,586 unexposed individuals aged 10+ years using five methods: (1) treating immortal time as observation time; (2) excluding time before date of first exposure diagnosis; (3) matching cohort entry to first exposure diagnosis; (4) excluding time before proxy date of inputting first exposure diagnosis (by the physician); and (5) treating exposure as a time-dependent measure.

RESULTS

When not considered in the design or analysis (Method 1), immortal time bias led to disproportionately high life expectancy for the exposed population during the first calendar period (additional years expected to live: 2000-2004: 65.6 [95% CI: 63.6,67.6]) compared to the later calendar periods (2005-2009: 59.9 [58.8,60.9]; 2010-2014: 58.0 [57.1,58.9]; 2015-2019: 58.2 [56.8,59.7]). Date of entry of diagnosis (Method 4) was unreliable in this CPRD cohort. The final methods (Method 2, 3 and 5) appeared to solve the main theoretical problem but residual bias may have remained.

CONCLUSIONS

We conclude that immortal time bias is a significant issue for studies of life-long conditions that use electronic health record data and requires careful consideration of how clinical diagnoses are entered onto electronic health record systems.

摘要

背景

在观察性研究中,永生时间偏倚很常见,但通常在药物流行病学研究中描述,因为在队列入组和治疗开始之间存在延迟。

方法

本研究使用了英格兰的临床实践研究数据链(CPRD)和链接的国家死亡率数据,从 2000 年到 2019 年,研究了一种特定的终身疾病——智力障碍的永生时间偏倚。使用五种方法比较了 33867 名暴露个体和 980586 名未暴露个体的预期寿命(Chiang 简化寿命表法):(1)将永生时间视为观察时间;(2)排除首次暴露诊断前的时间;(3)将队列入组与首次暴露诊断相匹配;(4)排除首次暴露诊断输入(由医生)的代理日期前的时间;(5)将暴露视为时间相关的测量。

结果

如果在设计或分析中未考虑(方法 1),则在第一个日历期间,暴露人群的预期寿命不成比例地较高(预期额外存活年数:2000-2004 年:65.6 [95%CI:63.6,67.6]),与以后的日历期间相比(2005-2009 年:59.9 [58.8,60.9];2010-2014 年:58.0 [57.1,58.9];2015-2019 年:58.2 [56.8,59.7])。在这个 CPRD 队列中,诊断进入日期(方法 4)不可靠。最终的方法(方法 2、3 和 5)似乎解决了主要的理论问题,但可能仍然存在残余偏倚。

结论

我们的结论是,对于使用电子健康记录数据的终身疾病研究,永生时间偏倚是一个重大问题,需要仔细考虑临床诊断是如何输入电子健康记录系统的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/342c/8962148/01df7986d6c9/12874_2022_1581_Fig1_HTML.jpg

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