Yu Qing, Jia Peng, Su Li, Zhao Hong, Que Chengli
Department of Respiratory and Critical Care Medicine, Peking University First Hospital, Beijing, 100034, China.
Department of Infectious Disease, Peking University First Hospital, Beijing, 100034, China.
BMC Infect Dis. 2017 Jun 5;17(1):392. doi: 10.1186/s12879-017-2492-8.
Pneumocystis jirovecii pneumonia (PJP) and pulmonary cytomegalovirus (CMV) infection are common opportunistic infections among immunocompromised patients. However, few studies have evaluated their co-infection, especially among non-HIV patients. Therefore, we aimed to evaluate the outcomes and prognostic factors among non-HIV patients with PJP according to their CMV infection status.
This retrospective study evaluated non-HIV patients who were diagnosed with PJP between January 2009 and January2016.The patients were classified and compared according to their pulmonary CMV infection status (positive infection: bronchoalveolar lavage fluid [BALF] CMV DNA loads of >500copies/mL).
Among 70 non-HIV patients with PJP, we identified 38 patients (54.3%) with pulmonary CMV infection. There was no significant difference in the mortality rates for the two groups (p = 0.15). Pulmonary CMV infection was significantly more common among patients who were receiving glucocorticoids and immunosuppressants, compared to corticosteroids only (p = 0.02). Pulmonary CMV infection was also significantly associated with severe dyspnea, a lower PaO/FiO, and the presence of centrilobular nodules (p = 0.008). Higher CMV DNA loads in the BALF were positively associated with mortality (p = 0.012).
Combined therapy using corticosteroids and other immunosuppressants may be a risk factor for pulmonary CMV co-infection among patients with PJP. In addition, CMV pneumonia should be considered when centrilobular nodules and/or severe hypoxemia are observed in non-HIV patients with PJP. Furthermore, antiviral treatment should be promptly initiated for patients with a high CMV DNA load in BALF, based on their poor prognosis.
耶氏肺孢子菌肺炎(PJP)和肺巨细胞病毒(CMV)感染是免疫功能低下患者常见的机会性感染。然而,很少有研究评估它们的合并感染情况,尤其是在非HIV患者中。因此,我们旨在根据CMV感染状况评估非HIV患者PJP的结局和预后因素。
这项回顾性研究评估了2009年1月至2016年1月期间被诊断为PJP的非HIV患者。根据其肺部CMV感染状况(阳性感染:支气管肺泡灌洗液[BALF]中CMV DNA载量>500拷贝/mL)对患者进行分类和比较。
在70例非HIV患者PJP中,我们确定了38例(54.3%)有肺部CMV感染。两组的死亡率无显著差异(p = 0.15)。与仅接受糖皮质激素治疗的患者相比,接受糖皮质激素和免疫抑制剂治疗的患者肺部CMV感染明显更常见(p = 0.02)。肺部CMV感染也与严重呼吸困难、较低的PaO/FiO以及小叶中心结节的存在显著相关(p = 0.008)。BALF中较高的CMV DNA载量与死亡率呈正相关(p = 0.012)。
使用糖皮质激素和其他免疫抑制剂的联合治疗可能是PJP患者肺部CMV合并感染的危险因素。此外,在非HIV患者PJP中观察到小叶中心结节和/或严重低氧血症时,应考虑CMV肺炎。此外,对于BALF中CMV DNA载量高的患者,鉴于其预后不良,应立即开始抗病毒治疗。