Furuuchi Koji, Ito Akihiro, Hashimoto Toru, Kumagai Shogo, Ishida Tadashi
Department of Respiratory Medicine, Ohara Healthcare Foundation, Kurashiki Central Hospital, Kurashiki, Japan.
Department of Respiratory Medicine, Ohara Healthcare Foundation, Kurashiki Central Hospital, Kurashiki, Japan.
J Infect Chemother. 2018 Aug;24(8):654-659. doi: 10.1016/j.jiac.2018.04.002. Epub 2018 Apr 26.
The number of patients with pulmonary nontuberculous mycobacterial disease complicated by chronic pulmonary aspergillosis (CPA) has been increasing. Additionally, CPA is reportedly associated with mortality in patients with Mycobacterium avium complex lung disease (MAC-LD). In the present study, we aimed to identify risk factors for developing CPA and stratify the risk for CPA development in patients with MAC-LD.
We retrospectively examined 361 patients newly diagnosed with MAC-LD. Risk factors for CPA development were examined using multivariate Cox proportional hazards regression analyses. A risk stratification system was established using the risk factors and receiver operating characteristic curve analyses.
CPA developed in 20 (5.5%) of the 361 patients. Independent risk factors for CPA development included the presence of pulmonary emphysema, baseline steroid use, a serum albumin level <3.5 g/dL, and the presence of MAC-LD cavities. A 4-point scoring system was established to stratify patients into low-risk (0-1 point) and high-risk (2-4 points) groups. The 5-year incidence rates of CPA were 2.2% and 31% in the low- and high-risk groups, respectively (P < 0.001).
We identified independent predictors of CPA development and established a simple risk stratification system for identifying patients with MAC-LD who were at a high risk of developing CPA.
肺部非结核分枝杆菌病合并慢性肺曲霉病(CPA)的患者数量一直在增加。此外,据报道CPA与鸟分枝杆菌复合群肺病(MAC-LD)患者的死亡率相关。在本研究中,我们旨在确定CPA发生的危险因素,并对MAC-LD患者发生CPA的风险进行分层。
我们回顾性研究了361例新诊断为MAC-LD的患者。使用多变量Cox比例风险回归分析来研究CPA发生的危险因素。利用危险因素和受试者工作特征曲线分析建立了风险分层系统。
361例患者中有20例(5.5%)发生了CPA。CPA发生的独立危险因素包括存在肺气肿、基线使用类固醇、血清白蛋白水平<3.5 g/dL以及存在MAC-LD空洞。建立了一个4分评分系统,将患者分为低风险(0-1分)和高风险(2-4分)组。低风险组和高风险组CPA的5年发病率分别为2.2%和31%(P<0.001)。
我们确定了CPA发生的独立预测因素,并建立了一个简单的风险分层系统,用于识别有发生CPA高风险的MAC-LD患者。