文章摘要
崔顺顺,段植.HIV阴性肺孢子菌肺炎 51例临床特征及预后因素分析[J].安徽医药,2025,29(3):519-523.
HIV阴性肺孢子菌肺炎 51例临床特征及预后因素分析
Clinical characteristics and prognostic factors of HIV negative pneumocystis jirovecii pneumonia: an analysis of 51 cases
  
DOI:10.3969/j.issn.1009-6469.2025.03.017
中文关键词: 肺孢子菌肺炎  人类免疫缺陷病毒阴性  肺部磨玻璃影  乳酸脱氢酶  C反应蛋白
英文关键词: Pneumocystis pseumonia  Human immunodeficiency virus negative  Ground-glass opacity  Lactate dehydroge-nase  C-reactive protein
基金项目:国家自然科学基金资助项目( 82102460)
作者单位
崔顺顺 阜阳市人民医院呼吸与危重症医学科安徽阜阳 236000 
段植 安徽医科大学第二附属医院检验科安徽合肥 230601 
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中文摘要:
      目的分析人类免疫缺陷病毒( HIV)阴性肺孢子菌肺炎( PJP)临床特征和影响预后危险因素,为临床诊疗提供参考。方法收集阜阳市人民医院 2021年 12月至 2023年 10月 51例成人 HIV阴性 PJP住院病人的病历资料和治疗转归。根据预后将病人分为存活组与死亡组,比较两组病人的一般资料、临床资料、治疗转归等,将变量纳入到单因素和多因素 logistic回归中筛选与预后相关的风险因素,并建立受试者操作特征曲线(ROC曲线)对预后模型进行评估。结果 51例 HIV阴性 PJP住院病人,多合并混合感染 84.31%(43/51)以曲霉菌 37.21%(16/43)最常见;间质性肺病 23.53%(12/51)、激素 52.94%(27/51)应用为主要危险因素;影像学表现以肺部磨玻,璃影 82.35%(42/51)为主;主要临床症状为呼吸困难 76.47%(39/51)、咳嗽 64.71%(33/ 51)、发热 60.78%(31/51)。 HIV阴性 PJP病人死亡组白细胞( 10.85±4.50)×109/L、中性粒细胞比( 88.20±4.74)%、C反应蛋白(CRP)139.45(95.37,263.17)mg/L、乳酸脱氢酶( LDH)600.15(469.90,771.65)U/L均高于存活组[( 6.97±3.00)×109/L、(70.93± 14.97)%、32.82(12.16,101.71)mg/L、301.0(234.8,398.7)U/L](P<0.05);死亡组淋巴细胞比 8.45(4.93,10.28)%、白蛋白( 30.88±4.16)g/L均低于存活组[15.80(9.00,27.00)%、(34.30±5.12)g/L](P<0.05)。多因素 logistic回归分析发现, HIV阴性 PJP病人死亡的独立危险因素为 CRP[OR=1.02,95%CI:(1.00,1.03)P=0.023]、 LDH[OR=1.01,95%CI:(1.00,1.02)P=0.009]。利用 LDH、 CRP和二者联合建立 ROC曲线,曲线下面积分别为 0.92、0.85和 0.95。结论 HIV阴性 PJP多为混合感染,主要表现为呼吸困难、咳嗽、发热,影像学以双肺磨玻璃影为主,白细胞、中性粒细胞比、淋巴细胞比、 CRP、白蛋白、 AST、LDH和 D-二聚体影响预后, LDH和 CRP是不良预后的独立危险因素。
英文摘要:
      Objective To analyze the clinical characteristics and prognostic risk factors of HIV negative Pneumocystis jirovecii pneu-monia (PJP), so as to provide reference for clinical diagnosis and treatment.Methods Medical records and treatment outcomes of 51 adult HIV negative PJP inpatients admitted to Fuyang People's Hospital from December 2021 to October 2023 were collected. Accord-ing to the prognosis, patients were assigned into a survival group and a death group, and their general information, clinical data, andtreatment outcomes were compared between the two groups. Variables were included in univariate and multivariate logistic regressionto screen for risk factors related to prognosis, and a receiver operating characteristic curve (ROC curve) was established to evaluate theprognosis model.Results Most of the 51 hospitalized HIV negative PJP patients (84.31%, 43/51) had mixed infections, with Aspergil-lus being the most common at 37.21% (16/43). The main risk factors were interstitial lung disease (23.53%, 12/51) and hormone use(52.94%, 27/51). The imaging findings mainly showed ground glass opacities on the lungs, accounting for 82.35% (42/51). The mainclinical symptoms were dyspnea (76.47%, 39/51), cough (64.71%, 33/51), and fever (60.78%, 31/51). The white blood cell count, neu-trophil ratio, C-reactive protein (CRP), and lactate dehydrogenase (LDH) in the death group of HIV negative PJP patients were all high-er than those in the survival group [(10.85±4.50) ×109/L vs. (6.97±3.00) ×109/L, (88.20±4.74)% vs. (70.93±14.97)% , 139.45 (95.37, 263.17) mg/L vs. 32.82 (12.16,101.71) mg/L, 600.15 (469.90,771.65) U/L vs. 301.0 (234.8,398.7) U/L] (P<0.05). The lymphocyte ratio and albumin in the death group were lower than those in the survival group [8.45 (4.93, 10.28)% vs. 15.80 (9.00, 27.00)%, (30.88±4.16) g/L vs. (34.30±5.12) g/L, respectively] (P<0.05). Multivariate logistic regression analysis found that the independent risk factors fordeath in HIV negative PJP patients were CRP [OR=1.02, 95%CI: (1.00, 1.03), P=0.023] and LDH [OR=1.01, 95%CI:(1.00, 1.02), P=0.009]. ROC curves were established using LDH, CRP, and their combination, with areas under the curves of 0.92, 0.85, and 0.95, re-spectively.Conclusions HIV negative PJP is mostly a mixed infection, mainly manifested as dyspnea, cough, and fever. Imaging find-ings mainly show ground glass opacities on both lungs. The white blood cell count, neutrophil ratio, lymphocyte ratio, CRP, albumin,AST, LDH, and D-dimer affect prognosis. LDH and CRP are independent risk factors for poor prognosis.
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