Department of Respiratory Medicine, Saiseikai Fukuoka General Hospital, 1-3-46 Tenjin, Chuo-ku, Fukuoka, 810-0001, Japan.
Department of Respiratory Medicine, Ohara Memorial Kurashiki Healthcare Foundation, Kurashiki Central Hospital, 1-1-1 miwa, Kurashiki, Okayama, 710-8602, Japan.
BMC Pulm Med. 2018 Jan 30;18(1):24. doi: 10.1186/s12890-018-0572-1.
Pneumococcal pneumonia causes high morbidity and mortality among adults. This study aimed to identify risk factors for bacteremic pneumococcal pneumonia, and to construct a prediction model for the development of bacteremia in patients with community-acquired pneumococcal pneumonia.
We retrospectively analyzed data from patients hospitalized with community-acquired pneumococcal pneumonia between April 2007 and August 2015. Logistic regression models were applied to detect risk factors for pneumococcal bacteremia, and a receiver operating characteristic curve was used to devise a prediction model.
Based on the results of sputum cultures, urine antigen tests, and/or blood cultures, 389 patients were diagnosed with pneumococcal pneumonia, 46 of whom had bacteremia. In the multivariate analysis, age < 65 years, serum albumin level < 3.0 g/dL, need for intensive respiratory or vasopressor support (IRVS), and C-reactive protein level > 20 mg/dL were identified as independent risk factors for the development of pneumococcal bacteremia. The bacteremia prediction score based on receiver operating characteristic curve analysis had a sensitivity of 0.74 and a specificity of 0.78 in patients with two risk factors. The area under the receiver operating characteristic curve was 0.77 (95% confidence interval (CI), 0.70-0.85).
Age < 65 years, hypoalbuminemia, IRVS, and high C-reactive protein level on admission are independent risk factors for the development of bacteremia in patients with community-acquired pneumococcal pneumonia. A prediction model based on these four risk factors could help to identify patients with community-acquired pneumococcal pneumonia at high risk of developing bacteremia; this can be used to guide antibiotic choices.
UMIN-CTR UMIN 000004353 . Registered 7 October 2010. Retrospectively registered.
肺炎球菌性肺炎可导致成人发病率和死亡率居高不下。本研究旨在确定细菌性肺炎球菌性肺炎的危险因素,并构建一个预测社区获得性肺炎球菌性肺炎患者发生菌血症的模型。
我们回顾性分析了 2007 年 4 月至 2015 年 8 月期间因社区获得性肺炎球菌性肺炎住院的患者的数据。应用 logistic 回归模型检测肺炎球菌菌血症的危险因素,并采用受试者工作特征曲线设计预测模型。
根据痰培养、尿抗原检测和/或血培养的结果,诊断 389 例肺炎球菌性肺炎患者,其中 46 例为菌血症。多因素分析显示,年龄<65 岁、血清白蛋白水平<3.0 g/dL、需要强化呼吸或血管加压支持(IRVS)以及 C 反应蛋白水平>20 mg/dL 是发生肺炎球菌菌血症的独立危险因素。基于受试者工作特征曲线分析的菌血症预测评分在具有两个危险因素的患者中具有 0.74 的敏感性和 0.78 的特异性。受试者工作特征曲线下面积为 0.77(95%置信区间为 0.70-0.85)。
年龄<65 岁、低白蛋白血症、IRVS 和入院时高 C 反应蛋白水平是社区获得性肺炎球菌性肺炎患者发生菌血症的独立危险因素。基于这四个危险因素的预测模型可以帮助识别发生菌血症风险较高的社区获得性肺炎球菌性肺炎患者;这可以用于指导抗生素的选择。
UMIN-CTR UMIN 000004353。注册于 2010 年 10 月 7 日。回顾性注册。