Cai Xiao-Yu, Cheng Yi-Chun, Ge Shu-Wang, Xu Gang
Division of Internal Medicine, Department of Nephrology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, No. 1095 Jiefang Road, Wuhan, 430030, China.
Eur J Clin Microbiol Infect Dis. 2023 Mar;42(3):323-338. doi: 10.1007/s10096-023-04555-3. Epub 2023 Feb 1.
Patients with chronic kidney disease (CKD) who are being treated with immunosuppressive medications are at risk for developing Pneumocystis jirovecii pneumonia (PCP). We attempted to characterize the clinical aspects of PCP in CKD patients in order to alert high-risk patients with bad prognosis. A retrospective study of CKD patients was conducted from June 2018 to June 2022. Based on PCP diagnostic criteria, these patients were divided into PCP and non-PCP groups. Using univariate and multivariate logistic regression analysis, risk indicators were evaluated, and nomogram and decision tree were developed. Of the CKD patients screened for Pneumocystis carinii nucleic acid, 1512 were included. Two-hundred forty four (16.14%) were diagnosed with PCP. Of the PCP, 88.5% was receiving glucocorticoid (GC) therapy, of which 66.3% received more than 0.5 mg/kg GC. Multivariate analysis showed that membranous nephropathy (OR 2.35, 95% CI 1.45-3.80), immunosuppressive therapy (OR 1.94, 95% CI 1.06-3.69), and ground glass opacity of CT scanning (OR 1.71, 95% CI 1.10-2.65) were associated with increased risk of Pneumocystis carinii infection. The AUC of nomogram based on logistics regression was 0.78 (0.75-0.81). The mortality in patients with PCP was 32.40%. Univariate analysis and decision tree showed that pulmonary insufficiency (PO: OR 0.98, 95% CI 0.96-1.00), elevated APTT (OR 1.07, 95% CI 1.04-1.11), and reduced hemoglobin (OR 0.97, 95% CI 0.96-0.98) were associated with poor prognosis. PCP is not rare in CKD patients, particularly in those treated with immunosuppressive therapy. Considering the high mortality of the cases, further studies on the prevention and management of these patients are needed.
正在接受免疫抑制药物治疗的慢性肾脏病(CKD)患者有发生耶氏肺孢子菌肺炎(PCP)的风险。我们试图描述CKD患者中PCP的临床特征,以警示预后不良的高危患者。对2018年6月至2022年6月的CKD患者进行了一项回顾性研究。根据PCP诊断标准,将这些患者分为PCP组和非PCP组。采用单因素和多因素逻辑回归分析评估风险指标,并绘制列线图和决策树。在筛查卡氏肺孢子菌核酸的CKD患者中,纳入了1512例。244例(16.14%)被诊断为PCP。在PCP患者中,88.5%正在接受糖皮质激素(GC)治疗,其中66.3%接受的GC剂量超过0.5mg/kg。多因素分析显示,膜性肾病(OR 2.35,95%CI 1.45-3.80)、免疫抑制治疗(OR 1.94,95%CI 1.06-3.69)和CT扫描磨玻璃影(OR 1.71,95%CI 1.10-2.65)与卡氏肺孢子菌感染风险增加相关。基于逻辑回归的列线图的AUC为0.78(0.75-0.81)。PCP患者的死亡率为32.40%。单因素分析和决策树显示,肺功能不全(PO:OR 0.98,95%CI 0.96-1.00)、活化部分凝血活酶时间升高(OR 1.07,95%CI 1.04-1.11)和血红蛋白降低(OR 0.97,95%CI 0.96-0.98)与预后不良相关。PCP在CKD患者中并不罕见,尤其是在接受免疫抑制治疗的患者中。考虑到这些病例的高死亡率,需要对这些患者的预防和管理进行进一步研究。