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利用风险调整提高全球住院儿科抗生素处方解读。

Using risk adjustment to improve the interpretation of global inpatient pediatric antibiotic prescribing.

机构信息

Paediatric Infectious Diseases Research Group, Infection and Immunity, St George's University of London, London, United Kingdom.

Department of Health Services Research and Policy, London School of Hygiene and Tropical Medicine, London, United Kingdom.

出版信息

PLoS One. 2018 Jul 6;13(7):e0199878. doi: 10.1371/journal.pone.0199878. eCollection 2018.

Abstract

OBJECTIVES

Assessment of regional pediatric last-resort antibiotic utilization patterns is hampered by potential confounding from population differences. We developed a risk-adjustment model from readily available, internationally used survey data and a simple patient classification to aid such comparisons.

DESIGN

We investigated the association between pediatric conserve antibiotic (pCA) exposure and patient / treatment characteristics derived from global point prevalence surveys of antibiotic prescribing, and developed a risk-adjustment model using multivariable logistic regression. The performance of a simple patient classification of groups with different expected pCA exposure levels was compared to the risk model.

SETTING

226 centers in 41 countries across 5 continents.

PARTICIPANTS

Neonatal and pediatric inpatient antibiotic prescriptions for sepsis/bloodstream infection for 1281 patients.

RESULTS

Overall pCA exposure was high (35%), strongly associated with each variable (patient age, ward, underlying disease, community acquisition or nosocomial infection and empiric or targeted treatment), and all were included in the final risk-adjustment model. The model demonstrated good discrimination (c-statistic = 0.83) and calibration (p = 0.38). The simple classification model demonstrated similar discrimination and calibration to the risk model. The crude regional pCA exposure rates ranged from 10.3% (Africa) to 67.4% (Latin America). Risk adjustment substantially reduced the regional variation, the adjusted rates ranging from 17.1% (Africa) to 42.8% (Latin America).

CONCLUSIONS

Greater comparability of pCA exposure rates can be achieved by using a few easily collected variables to produce risk-adjusted rates.

摘要

目的

评估区域性儿科最后手段抗生素使用模式会受到人群差异的潜在混杂因素的影响。我们从现成的、国际上使用的抗生素处方调查数据和简单的患者分类中开发了一种风险调整模型,以帮助进行此类比较。

设计

我们调查了儿科保留抗生素(pCA)暴露与抗生素处方全球点患病率调查中得出的患者/治疗特征之间的关联,并使用多变量逻辑回归开发了风险调整模型。比较了具有不同预期 pCA 暴露水平的患者分类的简单分类与风险模型的性能。

地点

来自 5 大洲 41 个国家的 226 个中心。

参与者

1281 例败血症/血流感染的新生儿和儿科住院患者的抗生素处方。

结果

总体 pCA 暴露率较高(35%),与每个变量(患者年龄、病房、基础疾病、社区获得性或医院获得性感染以及经验性或靶向治疗)强烈相关,并且所有变量均包含在最终风险调整模型中。该模型表现出良好的区分度(c 统计量=0.83)和校准度(p=0.38)。简单分类模型与风险模型具有相似的区分度和校准度。未调整的区域 pCA 暴露率从 10.3%(非洲)到 67.4%(拉丁美洲)不等。风险调整大大降低了区域差异,调整后的比率从 17.1%(非洲)到 42.8%(拉丁美洲)不等。

结论

使用一些易于收集的变量来产生风险调整后的比率,可以实现 pCA 暴露率的更大可比性。

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