Department of General Internal Medicine, Akashi Medical Center, 743-33, Ohkubo-Cho Yagi, Akashi, Hyogo, 674-0063, Japan.
Department of General Medicine, Tone Chuo Hospital, Numata, Gunma, Japan.
Intern Emerg Med. 2021 Nov;16(8):2129-2137. doi: 10.1007/s11739-021-02744-6. Epub 2021 May 13.
Community-acquired pneumonia (CAP) is a common illness that can lead to mortality. β-lactams are ineffective against atypical pathogen including Mycoplasma pneumoniae. We used molecular examinations to develop a decision tree to predict atypical pathogens with CAP and to examine the prevalence of macrolide resistance in Mycoplasma pneumoniae. We conducted a prospective observational study of patients aged ≥ 18 years who had fever and respiratory symptoms and were diagnosed with CAP in one of two community hospitals between December 2016 and October 2018. We assessed combinations of clinical variables that best predicted atypical pathogens with CAP by classification and regression tree (CART) analysis. Pneumonia was defined as respiratory symptoms and new infiltration recognized on chest X-ray or chest computed tomography. We analyzed 47 patients (21 females, 44.7%, mean age: 47.6 years). Atypical pathogens were detected in 15 patients (31.9%; 12 Mycoplasma pneumoniae, 3 Chlamydophila pneumoniae). Ten patients carried macrolide resistant Mycoplasma pneumoniae (macrolide resistant rate 83.3%). CART analysis suggested that factors associated with presence of atypical pathogens were absence of crackles, age < 45 years, and LD ≥ 183 U/L (sensitivity 86.7% [59.5, 98.3], specificity 96.9% [83.8, 99.9]). ur simple clinical decision rules can be used to identify primary care patients with CAP that are at risk for atypical pathogens. Further research is needed to validate its usefulness in various populations.Trial registration Clinical Trial (UMIN trial ID: UMIN000035346).
社区获得性肺炎(CAP)是一种常见的疾病,可导致死亡。β-内酰胺类药物对包括肺炎支原体在内的非典型病原体无效。我们使用分子检测方法制定了一个决策树,以预测 CAP 中的非典型病原体,并检查肺炎支原体中大环内酯类药物耐药的流行情况。我们对 2016 年 12 月至 2018 年 10 月期间在两家社区医院中诊断为 CAP 的年龄≥18 岁的发热和呼吸道症状患者进行了前瞻性观察性研究。我们通过分类和回归树(CART)分析评估了预测 CAP 中非典型病原体的最佳临床变量组合。肺炎定义为胸部 X 线或胸部计算机断层扫描上出现新的浸润和呼吸道症状。我们分析了 47 例患者(21 例女性,44.7%,平均年龄:47.6 岁)。15 例患者(31.9%;12 例肺炎支原体,3 例肺炎衣原体)检测到非典型病原体。10 例患者携带大环内酯类耐药肺炎支原体(大环内酯类耐药率 83.3%)。CART 分析表明,与非典型病原体存在相关的因素是无爆裂声、年龄<45 岁和 LD≥183U/L(敏感性 86.7%[59.5,98.3],特异性 96.9%[83.8,99.9])。简单的临床决策规则可用于识别有发生 CAP 风险的非典型病原体的初级保健患者。需要进一步的研究来验证其在不同人群中的有效性。试验注册 临床研究(UMIN 试验 ID:UMIN000035346)。