Department of Internal Medicine, University of Utah School of Medicine.
Division of Infectious Diseases and Clinical Epidemiology, Intermountain Medical Center, Salt Lake City, Utah.
Curr Opin Pulm Med. 2020 May;26(3):249-259. doi: 10.1097/MCP.0000000000000670.
Although most patients with community-acquired pneumonia (CAP) are appropriately treated with narrow-spectrum antibiotics, predicting which patients require coverage of drug-resistant pathogens (DRP) remains a challenge. The 2019 American Thoracic Society/Infectious Diseases Society of America CAP guidelines endorse using locally validated prediction models for DRP. Here we review risk factors for DRP and provide a summary of available risk prediction models.
Both inadequate initial empiric spectrum as well as unnecessary broad-spectrum antibiotic use are associated with poor outcomes in CAP. Multiple prediction models for DRP-based patient-level risk factors have been published, with some variation in included predictor variables and test performance characteristics. Seven models have been robustly externally validated, and implementation data have been published for two of these models. All models demonstrated better performance than the healthcare-associated pneumonia criteria, with most favoring sensitivity over specificity. We also report validation of the novel, risk factor-based treatment algorithm proposed in the American Thoracic Society/Infectious Diseases Society of America guidelines which strongly favors specificity over sensitivity, especially in nonsevere pneumonia.
Using patient-level risk factors to guide the decision whether to prescribe broad-spectrum antibiotics is a rational approach to treatment. Several viable candidate prediction models are available. Hospitals should evaluate the local performance of existing scores before implementing in routine clinical practice.
尽管大多数社区获得性肺炎(CAP)患者经窄谱抗生素治疗即可,但预测哪些患者需要覆盖耐药病原体(DRP)仍然是一个挑战。2019 年美国胸科学会/传染病学会 CAP 指南支持使用经本地验证的 DRP 预测模型。本文我们将回顾 DRP 的危险因素,并对现有风险预测模型进行总结。
初始经验性治疗谱不足和不必要的广谱抗生素使用均与 CAP 预后不良有关。已经发表了多个基于 DRP 的患者水平危险因素预测模型,所包含的预测变量和测试性能特征存在差异。有 7 个模型已得到稳健的外部验证,其中 2 个模型已公布实施数据。所有模型的表现均优于医院获得性肺炎标准,大多数模型更倾向于敏感性而非特异性。我们还报告了美国胸科学会/传染病学会指南中提出的基于危险因素的新型治疗算法的验证结果,该算法强烈倾向于特异性而非敏感性,尤其是在非重症肺炎患者中。
使用患者水平的危险因素来指导是否开具广谱抗生素的决策是一种合理的治疗方法。目前有几种可行的候选预测模型。在常规临床实践中实施前,医院应评估现有评分的本地性能。