Chronic Infection With Pseudomonas aeruginosa in Cystic Fibrosis: A Risk Factor for Nasal Polyposis After Lung Transplantation

被引:3
|
作者
Vital, Domenic [1 ]
Holzmann, David [1 ]
Boehler, Annette [2 ]
Hofer, Markus [2 ]
机构
[1] Univ Zurich Hosp, Dept Otorhinolaryngol Head & Neck Surg, CH-8091 Zurich, Switzerland
[2] Univ Zurich Hosp, Dept Pulm Med, CH-8091 Zurich, Switzerland
关键词
Pseudomonas aeruginosa; Nasal polyposis; Cystic fibrosis; Lung transplantation; Chronic rhinosinusitis; SINUS SURGERY; CLINICAL CHARACTERISTICS; CHRONIC RHINOSINUSITIS; BACTERIAL BIOFILMS; GENOTYPE ANALYSIS; DISEASE; COMPLICATIONS; RECIPIENTS; SURVIVAL;
D O I
10.1097/TP.0b013e31829282cd
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Nasal polyposis (NP) is common in cystic fibrosis (CF) patients. The prevalence of the CF phenotype with NP after lung transplantation (LTx) is unknown. Risk factors for the development of NP after LTx are not well described. Methods. CF patients with LTx at our center between November 1992 and December 2009 were included. They were regularly investigated with nasal endoscopy and aspiration of sinus secretions with microbiological evaluation. Patients with and without development of NP were compared along the following parameters: gender, age, dF508, diabetes, acute rejection, NP at LTx, and microbiology of the sinuses before and after LTx. A multivariate Cox regression analysis was performed. Results. The study included 94 patients; 21 were excluded because of incomplete data. Thirty-five (48%) of the remaining 73 patients developed NP. Mean time to diagnosis of NP was 4.2 (2.9-5.6) years after LTx. Prevalence of NP was 11% after the first year and 18%, 33%, and 44% after the first 2, 5, and 10 years, respectively. Patients with posttransplantation NP were younger, had NP before LTx, and were chronically infected with Pseudomonas aeruginosa (PA) in the nose. Multivariate analysis demonstrated that chronic infection with PA was the only significant risk factor for the development of nasal polyps after LTx (hazards ratio, 7.2; 95% confidence interval, 2.1-24.2; P-0.001). Conclusions. In contrast to pretransplantation patients, NP is more common after LTx. Development of NP occurs throughout the whole observation time. Chronic sinonasal PA infection seems to be the only significant risk factor for NP after LTx.
引用
收藏
页码:1548 / 1553
页数:6
相关论文
共 50 条
  • [41] Association of Pseudomonas aeruginosa infection stage with lung function trajectory in children with cystic fibrosis
    Rosenfeld, Margaret
    Faino, Anna, V
    Qu, Pingping
    Onchiri, Frankline M.
    Blue, Elizabeth E.
    Collaco, Joseph M.
    Gordon, William W.
    Szczesniak, Rhonda
    Zhou, Yi-Hui
    Bamshad, Michael J.
    Gibson, Ronald L.
    JOURNAL OF CYSTIC FIBROSIS, 2023, 22 (05) : 857 - 863
  • [42] Delivery of CFTR by adenoviral vector to cystic fibrosis mouse lung in a model of chronic Pseudomonas aeruginosa lung infection
    van Heeckeren, AM
    Scaria, A
    Schluchter, MD
    Ferkol, TW
    Wadsworth, S
    Davis, PB
    AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2004, 286 (04) : L717 - L726
  • [43] Improvement of a mouse infection model to capture Pseudomonas aeruginosa chronic physiology in cystic fibrosis
    Duncan, Rebecca P.
    Moustafa, Dina A.
    Lewin, Gina R.
    Diggle, Frances L.
    Bomberger, Jennifer M.
    Whiteley, Marvin
    Goldberg, Joanna B.
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2024, 121 (33)
  • [44] Chronic inhaled antibiotic therapy in people with cystic fibrosis with Pseudomonas aeruginosa infection in Germany
    Naehrig, S.
    Schulte-Hubbert, B.
    Hafkemeyer, S.
    Hammermann, J.
    Dumke, M.
    Sieber, S.
    Naehrlich, L.
    PULMONARY PHARMACOLOGY & THERAPEUTICS, 2023, 80
  • [45] Challenges with current inhaled treatments for chronic Pseudomonas aeruginosa infection in patients with cystic fibrosis
    Greally, Peter
    Whitaker, Paul
    Peckham, Daniel
    CURRENT MEDICAL RESEARCH AND OPINION, 2012, 28 (06) : 1059 - 1067
  • [46] Increased airway iron as a potential factor in the persistence of Pseudomonas aeruginosa infection in cystic fibrosis
    Reid, D. W.
    Carroll, V.
    O'May, C.
    Champion, A.
    Kirov, S. M.
    EUROPEAN RESPIRATORY JOURNAL, 2007, 30 (02) : 286 - 292
  • [47] Sinonasal persistence of Pseudomonas aeruginosa after lung transplantation
    Mainz, J. G.
    Hentschel, J.
    Schien, C.
    Cramer, N.
    Pfister, W.
    Beck, J. F.
    Tuemmler, B.
    JOURNAL OF CYSTIC FIBROSIS, 2012, 11 (02) : 158 - 161
  • [48] The role of microRNAs in chronic pseudomonas lung infection in Cystic fibrosis
    Fesen, Katherine
    Silveyra, Patricia
    Fuentes, Nathalie
    Nicoleau, Marvin
    Rivera, Lidys
    Kitch, Diane
    Graff, Gavin R.
    Siddaiah, Roopa
    RESPIRATORY MEDICINE, 2019, 151 : 133 - 138
  • [49] Nitrous Oxide Production in Sputum from Cystic Fibrosis Patients with Chronic Pseudomonas aeruginosa Lung Infection
    Kolpen, Mette
    Kuhl, Michael
    Bjarnsholt, Thomas
    Moser, Claus
    Hansen, Christine Ronne
    Liengaard, Lars
    Kharazmi, Arsalan
    Pressler, Tanja
    Hoiby, Niels
    Jensen, Peter Ostrup
    PLOS ONE, 2014, 9 (01):
  • [50] The immune response to chronic Pseudomonas aeruginosa lung infection in cystic fibrosis patients is predominantly of the Th2 type
    Moser, C
    Kjaergaard, S
    Pressler, T
    Kharazmi, A
    Koch, C
    Hoiby, N
    APMIS, 2000, 108 (05) : 329 - 335