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基于用药史的综合合并症度量标准:在两个独立队列中的开发和评估。

An Aggregated Comorbidity Measure Based on History of Filled Drug Prescriptions: Development and Evaluation in Two Separate Cohorts.

机构信息

From the Department of Surgical Sciences, Uppsala University, Uppsala, Sweden.

Department of Surgery and Perioperative Sciences/Surgery, Umeå University, Umeå, Sweden.

出版信息

Epidemiology. 2021 Jul 1;32(4):607-615. doi: 10.1097/EDE.0000000000001358.

DOI:10.1097/EDE.0000000000001358
PMID:33935137
Abstract

BACKGROUND

The ability to account for comorbidity when estimating survival in a population diagnosed with cancer could be improved by using a drug comorbidity index based on filled drug prescriptions.

METHODS

We created a drug comorbidity index from age-stratified univariable associations between filled drug prescriptions and time to death in 326,450 control males randomly selected from the general population to men with prostate cancer. We also evaluated the index in 272,214 control females randomly selected from the general population to women with breast cancer.

RESULTS

The new drug comorbidity index predicted survival better than the Charlson Comorbidity Index (CCI) and a previously published prescription index during 11 years of follow-up. The concordance (C)-index for the new index was 0.73 in male and 0.76 in the female population, as compared with a C-index of 0.67 in men and 0.69 in women for the CCI. In men of age 75-84 years with CCI = 0, the median survival time was 7.1 years (95% confidence interval [CI] = 7.0, 7.3) in the highest index quartile. Comparing the highest to the lowest drug comorbidity index quartile resulted in a hazard ratio (HR) of 2.2 among men (95% CI = 2.1, 2.3) and 2.4 among women (95% CI = 2.3, 2.6).

CONCLUSIONS

A new drug comorbidity index based on filled drug prescriptions improved prediction of survival beyond age and the CCI alone. The index will allow a more accurate baseline estimation of expected survival for comparing treatment outcomes and evaluating treatment guidelines in populations of people with cancer.

摘要

背景

在评估诊断为癌症的人群的生存情况时,如果能够考虑到合并症,可以通过使用基于已用药物处方的药物合并症指数来提高预测能力。

方法

我们从年龄分层的单变量关联中创建了一个药物合并症指数,这些关联涉及随机选择的 326450 名普通男性人群中的男性前列腺癌患者与已用药物处方和死亡时间之间的关系,以及 272214 名随机选择的普通女性人群中的女性乳腺癌患者与已用药物处方和死亡时间之间的关系。

结果

在 11 年的随访期间,新的药物合并症指数比 Charlson 合并症指数(CCI)和之前发表的处方指数更好地预测了生存情况。新指数在男性和女性人群中的一致性(C)指数分别为 0.73 和 0.76,而 CCI 的 C 指数分别为 0.67 和 0.69。在年龄为 75-84 岁且 CCI = 0 的男性中,CCI 最高四分位数的中位生存时间为 7.1 年(95%置信区间 [CI] = 7.0,7.3)。将最高四分位数与最低四分位数的药物合并症指数进行比较,男性的风险比(HR)为 2.2(95% CI = 2.1,2.3),女性为 2.4(95% CI = 2.3,2.6)。

结论

基于已用药物处方的新药物合并症指数提高了对生存情况的预测能力,超越了年龄和 CCI 单独预测的能力。该指数将允许更准确地估计癌症人群的预期生存情况,以便比较治疗结果和评估治疗指南。

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