铜绿假单胞菌合并曲霉菌感染患者的临床特征及危险因素分析
Clinical Characteristics and Risk Factors Analysis of Patients with Co-Infection of Pseudomonas aeruginosa and Aspergillus
DOI: 10.12677/acm.2025.152522, PDF,   
作者: 朱玉成, 赵京明*:青岛大学附属医院呼吸与危重症医学科,山东 青岛
关键词: 铜绿假单胞菌曲霉菌合并感染危险因素Pseudomonas aeruginosa Aspergillus Co-Infection Risk Factor
摘要: 目的:通过对铜绿假单胞菌合并曲霉菌感染的患者进行分析,了解铜绿假单胞菌合并曲霉菌感染在临床患者中的流行情况及患者的临床特征,了解铜绿假单胞菌合并曲霉菌感染的临床现状,并且通过对合并感染的患者进行预后不佳危险因素的单因素、多因素分析,为铜绿假单胞菌合并曲霉菌感染的临床治疗提供参考,以期制定合理的诊疗策略,改善患者预后。方法:回顾性收集2013年2月至2022年10月青岛大学附属医院铜绿假单胞菌及曲霉菌培养阳性标本60例,总结临床特征,筛选出单因素危险因素,分析预后良好组和预后不佳组的临床资料,再对单因素危险因素中有统计学意义的因素采用Logistic多因素回归分析,导致预后不良的影响因素,按检验水准P < 0.05表示差异具有统计学意义,得出独立危险因素和独立保护因素。结果:应用抗真菌药物、中性粒细胞百分比、血小板、C反应蛋白(CRP)水平是铜绿假单胞菌合并曲霉菌感染导致预后不佳的单因素危险因素;应用抗真菌药物、血小板水平是铜绿假单胞菌合并曲霉菌感染预后的独立保护因素;C反应蛋白(CRP)水平为独立危险因素,中性粒细胞百分比是非独立危险因素。
Abstract: Objective: This study aims to analyze patients with Pseudomonas aeruginosa co-infected with Aspergillus to understand the epidemiological characteristics and clinical features of such infections. By investigating the clinical status of co-infections and conducting univariate and multivariate analyses of risk factors associated with poor prognosis, the study seeks to provide clinical insights for the treatment of Pseudomonas aeruginosa and Aspergillus co-infections. The ultimate goal is to formulate rational diagnostic and therapeutic strategies to improve patient outcomes. Methods: A retrospective analysis was conducted on 60 cases of Pseudomonas aeruginosa and Aspergillus co-infection at the Affiliated Hospital of Qingdao University between February 2013 and October 2022. Clinical characteristics were summarized. Univariate analysis was used to identify risk factors for poor prognosis, and clinical data of the good prognosis group and the poor prognosis group were compared. Factors with statistical significance in univariate analysis were further analyzed using multivariate logistic regression to determine independent risk and protective factors associated with poor prognosis. Statistical significance was set at P < 0.05. Results: The use of antifungal drugs, neutrophil percentage, platelet count, and C-reactive protein (CRP) levels were identified as univariate risk factors for poor prognosis in patients with Pseudomonas aeruginosa co-infected with Aspergillus. The administration of antifungal drugs and platelet count emerged as independent protective factors for prognosis in these co-infected cases. Specifically, C-reactive protein (CRP) levels were determined to be an independent risk factor, while neutrophil percentage was identified as a non-independent risk factor for clinical outcomes.
文章引用:朱玉成, 赵京明. 铜绿假单胞菌合并曲霉菌感染患者的临床特征及危险因素分析[J]. 临床医学进展, 2025, 15(2): 1654-1665. https://doi.org/10.12677/acm.2025.152522

参考文献

[1] Sass, G., Shrestha, P. and Stevens, D.A. (2021) Pseudomonas aeruginosa Virulence Factors Support Voriconazole Effects on Aspergillus fumigatus. Pathogens, 10, Article No. 519. [Google Scholar] [CrossRef] [PubMed]
[2] Sass, G., Nazik, H., Penner, J., Shah, H., Ansari, S.R., Clemons, K.V., et al. (2018) Studies of Pseudomonas aeruginosa Mutants Indicate Pyoverdine as the Central Factor in Inhibition of Aspergillus fumigatus Biofilm. Journal of Bacteriology, 200, e00345-17. [Google Scholar] [CrossRef] [PubMed]
[3] Mowat, E., Rajendran, R., Williams, C., McCulloch, E., Jones, B., Lang, S., et al. (2010) Pseudomonas aeruginosa and Their Small Diffusible Extracellular Molecules Inhibit Aspergillus fumigatus Biofilm Formation. FEMS Microbiology Letters, 313, 96-102. [Google Scholar] [CrossRef] [PubMed]
[4] Jensen, B.G., Jelsbak, L., Søndergaard, I., et al. (2011) Aspergillus Triggers Phenazine Production in Pseudomonas aeruginosa. 2nd European Congress on Microbial Biofilms: Basic and Clinical Aspects, Copenhagen, 6-8 July 2011.
[5] Pattnaik, S., Ahmed, T., Ranganathan, S.K., Ampasala, D.R., Sarma, V.V. and Busi, S. (2018) Aspergillus ochraceopetaliformis SSP13 Modulates Quorum Sensing Regulated Virulence and Biofilm Formation in Pseudomonas aeruginosa PAO1. Biofouling, 34, 410-425. [Google Scholar] [CrossRef] [PubMed]
[6] Pressler, T., Frederiksen, B., Skov, M., Garred, P., Koch, C. and Høiby, N. (2006) Early Rise of Anti-Pseudomonas Antibodies and a Mucoid Phenotype of Pseudomonas aeruginosa Are Risk Factors for Development of Chronic Lung Infection—A Case Control Study. Journal of Cystic Fibrosis, 5, 9-15. [Google Scholar] [CrossRef] [PubMed]
[7] Briard, B., Heddergott, C. and Latgé, J. (2016) Volatile Compounds Emitted by Pseudomonas aeruginosa Stimulate Growth of the Fungal Pathogen Aspergillus fumigatus. mBio, 7, e00219. [Google Scholar] [CrossRef] [PubMed]
[8] Briard, B., Mislin, G.L.A., Latgé, J. and Beauvais, A. (2019) Interactions between Aspergillus fumigatus and Pulmonary Bacteria: Current State of the Field, New Data, and Future Perspective. Journal of Fungi, 5, Article No. 48. [Google Scholar] [CrossRef] [PubMed]
[9] Scott, J., Sueiro-Olivares, M., Ahmed, W., Heddergott, C., Zhao, C., Thomas, R., et al. (2019) Pseudomonas aeruginosa-Derived Volatile Sulfur Compounds Promote Distal Aspergillus fumigatus Growth and a Synergistic Pathogen-Pathogen Interaction That Increases Pathogenicity in Co-Infection. Frontiers in Microbiology, 10, Article No. 2311. [Google Scholar] [CrossRef] [PubMed]
[10] Briard, B., Bomme, P., Lechner, B.E., Mislin, G.L.A., Lair, V., Prévost, M., et al. (2015) Pseudomonas aeruginosa Manipulates Redox and Iron Homeostasis of Its Microbiota Partner Aspergillus fumigatus via Phenazines. Scientific Reports, 5, Article No. 8220. [Google Scholar] [CrossRef] [PubMed]
[11] Ostapska, H., Le Mauff, F., Gravelat, F.N., Snarr, B.D., Bamford, N.C., Van Loon, J.C., et al. (2022) Co-Operative Biofilm Interactions between Aspergillus fumigatus and Pseudomonas aeruginosa through Secreted Galactosaminogalactan Exopolysaccharide. Journal of Fungi, 8, Article No. 336. [Google Scholar] [CrossRef] [PubMed]
[12] Penner, J.C., Ferreira, J.A.G., Secor, P.R., Sweere, J.M., Birukova, M.K., Joubert, L., et al. (2016) Pf4 Bacteriophage Produced by Pseudomonas aeruginosa Inhibits Aspergillus fumigatus Metabolism via Iron Sequestration. Microbiology, 162, 1583-1594. [Google Scholar] [CrossRef] [PubMed]
[13] Margalit, A., Carolan, J.C. and Kavanagh, K. (2021) Bacterial Interactions with Aspergillus fumigatus in the Immunocompromised Lung. Microorganisms, 9, Article No. 435. [Google Scholar] [CrossRef] [PubMed]
[14] Semple, J.W., Italiano, J.E. and Freedman, J. (2011) Platelets and the Immune Continuum. Nature Reviews Immunology, 11, 264-274. [Google Scholar] [CrossRef] [PubMed]
[15] Ferrer, R. (2008) Improvement in Process of Care and Outcome after a Multicenter Severe Sepsis Educational Program in Spain. JAMA, 299, 2294-2303. [Google Scholar] [CrossRef] [PubMed]
[16] Kousha, M., Tadi, R. and Soubani, A.O. (2011) Pulmonary Aspergillosis: A Clinical Review. European Respiratory Review, 20, 156-174. [Google Scholar] [CrossRef] [PubMed]
[17] Ramirez-Garcia, A., Pellon, A., Buldain, I., Antoran, A., Arbizu-Delgado, A., Guruceaga, X., et al. (2017) Proteomics as a Tool to Identify New Targets against Aspergillus and Scedosporium in the Context of Cystic Fibrosis. Mycopathologia, 183, 273-289. [Google Scholar] [CrossRef] [PubMed]
[18] Lass‐Flörl, C. (2009) The Changing Face of Epidemiology of Invasive Fungal Disease in Europe. Mycoses, 52, 197-205. [Google Scholar] [CrossRef] [PubMed]
[19] Sproston, N.R. and Ashworth, J.J. (2018) Role of C-Reactive Protein at Sites of Inflammation and Infection. Frontiers in Immunology, 9, Article No. 754. [Google Scholar] [CrossRef] [PubMed]
[20] Taghizadeh-Armaki, M., Hedayati, M.T., Moqarabzadeh, V., Ansari, S., Mahdavi Omran, S., Zarrinfar, H., et al. (2017) Effect of Involved Aspergillus Species on Galactomannan in Bronchoalveolar Lavage of Patients with Invasive Aspergillosis. Journal of Medical Microbiology, 66, 898-904. [Google Scholar] [CrossRef] [PubMed]
[21] Kosmidis, C. and Denning, D.W. (2014) The Clinical Spectrum of Pulmonary Aspergillosis. Thorax, 70, 270-277. [Google Scholar] [CrossRef] [PubMed]
[22] Garcia‐Vidal, C., Upton, A., Kirby, K.A. and Marr, K.A. (2008) Epidemiology of Invasive Mold Infections in Allogeneic Stem Cell Transplant Recipients: Biological Risk Factors for Infection According to Time after Transplantation. Clinical Infectious Diseases, 47, 1041-1050. [Google Scholar] [CrossRef] [PubMed]
[23] Sharma, G., Rao, S., Bansal, A., Dang, S., Gupta, S. and Gabrani, R. (2014) Pseudomonas aeruginosa Biofilm: Potential Therapeutic Targets. Biologicals, 42, 1-7. [Google Scholar] [CrossRef] [PubMed]