Kobayashi Daisuke, Shindo Yuichiro, Ito Ryota, Iwaki Mai, Okumura Junya, Sakakibara Toshihiro, Yamaguchi Ikuo, Yagi Tetsuya, Ogasawara Tomohiko, Sugino Yasuteru, Taniguchi Hiroyuki, Saito Hiroshi, Saka Hideo, Kawamura Takashi, Hasegawa Yoshinori
Kyoto University Health Service, Kyoto, Japan.
Department of Respiratory Medicine, Nagoya University Graduate School of Medicine, Nagoya, Japan,
Infect Drug Resist. 2018 Oct 11;11:1703-1713. doi: 10.2147/IDR.S165669. eCollection 2018.
Appropriate initial antibiotic treatment and avoiding administration of unnecessary broad-spectrum antibiotics are important for the treatment of pneumonia. To achieve this, assessment of risk for drug-resistant pathogens (DRPs) at diagnosis is essential.
The aim of this study was to validate a predictive rule for DRPs that we previously proposed (the community-acquired pneumonia drug-resistant pathogen [CAP-DRP] rule), comparing several other predictive methods.
A prospective observational study was conducted in hospitalized patients with community-onset pneumonia at four institutions in Japan. Pathogens identified as not susceptible to ceftriaxone, ampicillin-sulbactam, macrolides, and respiratory fluoroquinolones were defined as CAP-DRPs.
CAP-DRPs were identified in 73 (10.1%) of 721 patients analyzed. The CAP-DRP rule differentiated low vs high risk of CAP-DRP at the threshold of ≥3 points or 2 points plus any of methicillin-resistant specific factors with a sensitivity of 0.45, specificity of 0.87, positive predictive value of 0.47, negative predictive value of 0.87, and accuracy of 0.79. Its discrimination performance, area under the receiver operating characteristic curve, was 0.73 (95% confidence interval 0.66-0.79). Specificity of the CAP-DRP rule against CAP-DRPs was the highest among the six predictive rules tested.
The performance of the predictive rules and criteria for CAP-DRPs was limited. However, the CAP-DRP rule yielded high specificity and could specify patients who should be treated with non-broad-spectrum antibiotics, eg, a non-pseudomonal β-lactam plus a macrolide, more precisely.
恰当的初始抗生素治疗以及避免使用不必要的广谱抗生素对于肺炎治疗至关重要。要做到这一点,在诊断时评估耐药病原体(DRP)的风险至关重要。
本研究的目的是验证我们之前提出的DRP预测规则(社区获得性肺炎耐药病原体[CAP-DRP]规则),并与其他几种预测方法进行比较。
在日本四家机构对社区起病的住院肺炎患者进行了一项前瞻性观察研究。被鉴定为对头孢曲松、氨苄西林舒巴坦、大环内酯类和呼吸喹诺酮类不敏感的病原体被定义为CAP-DRP。
在分析的721例患者中,有73例(10.1%)鉴定出CAP-DRP。CAP-DRP规则在阈值≥3分或2分加上任何耐甲氧西林特定因素时区分CAP-DRP的低风险与高风险,其灵敏度为0.45,特异度为0.87,阳性预测值为0.47,阴性预测值为0.87,准确度为0.79。其判别性能,即受试者操作特征曲线下面积为0.73(95%置信区间0.66 - 0.79)。在测试的六种预测规则中,CAP-DRP规则针对CAP-DRP的特异度最高。
CAP-DRP预测规则和标准的性能有限。然而,CAP-DRP规则具有高特异度,并且能够更准确地确定应使用非广谱抗生素治疗的患者,例如非假单胞菌β-内酰胺类加一种大环内酯类。