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
  • [1] Nasal polyposis in lung transplant recipients with cystic fibrosis
    Vital, Domenic
    Holzmann, David
    Boehler, Annette
    Hofer, Markus
    JOURNAL OF CYSTIC FIBROSIS, 2013, 12 (03) : 266 - 270
  • [2] Pseudomonas aeruginosa endophthalmitis after lung transplantation for cystic fibrosis
    Sheares, BJ
    Prince, AS
    Quittell, LM
    Neu, NM
    Bye, MR
    PEDIATRIC INFECTIOUS DISEASE JOURNAL, 1997, 16 (08) : 820 - 821
  • [3] Epidemic Pseudomonas aeruginosa infection in patients with cystic fibrosis is not a risk factor for poor clinical Outcomes following lung transplantation
    Pritchard, Julia
    Thakrar, Mitesh V.
    Somayaji, Ranjani
    Surette, Michael G.
    Rabin, Harvey R.
    Helmersen, Doug
    Lien, Dale
    Purighalla, Swathi
    Waddell, Barbara
    Parkins, Michael D.
    JOURNAL OF CYSTIC FIBROSIS, 2016, 15 (03) : 392 - 399
  • [4] Effect of infection with transmissible strains of Pseudomonas aeruginosa on lung transplantation outcomes in patients with cystic fibrosis
    Srour, Nadim
    Chaparro, Cecilia
    Vandemheen, Katherine
    Singer, Lianne G.
    Keshavjee, Shaf
    Aaron, Shawn D.
    JOURNAL OF HEART AND LUNG TRANSPLANTATION, 2015, 34 (04) : 588 - 593
  • [5] Prevention of chronic infection with Pseudomonas aeruginosa infection in cystic fibrosis
    Zemanick, Edith T.
    Bell, Scott C.
    CURRENT OPINION IN PULMONARY MEDICINE, 2019, 25 (06) : 636 - 645
  • [6] Pseudomonas aeruginosa antibody response in cystic fibrosis decreases rapidly following lung transplantation
    Schwensen, Hanna Ferlov
    Moser, Claus
    Perch, Michael
    Pressler, Tacjana
    Hoiby, Niels
    JOURNAL OF CYSTIC FIBROSIS, 2020, 19 (04) : 587 - 594
  • [7] Small colony variants of Pseudomonas aeruginosa in chronic bacterial infection of the lung in cystic fibrosis
    Evans, Thomas J.
    FUTURE MICROBIOLOGY, 2015, 10 (02) : 231 - 239
  • [8] Chronic infection sustained by a Pseudomonas aeruginosa High-Risk clone producing the VIM-1 metallo-β-lactamase in a cystic fibrosis patient after lung transplantation
    Pollini, Simona
    Mugnaioli, Claudia
    Dolce, Daniela
    Campana, Silvia
    Neri, Anna Silvia
    Taccetti, Giovanni
    Rossolini, Gian Maria
    JOURNAL OF CYSTIC FIBROSIS, 2018, 17 (04) : 470 - 474
  • [9] Mouse models of chronic lung infection with Pseudomonas aeruginosa:: Models for the study of cystic fibrosis
    Stotland, PK
    Radzioch, D
    Stevenson, MM
    PEDIATRIC PULMONOLOGY, 2000, 30 (05) : 413 - 424
  • [10] Pseudomonas aeruginosa and cystic fibrosis:: first colonization to chronic infection
    Laurans, M.
    Arion, A.
    Fines-Guyon, M.
    Regeasse, A.
    Brouard, J.
    Leclercq, R.
    Duhamel, J. F.
    ARCHIVES DE PEDIATRIE, 2006, 13 : S22 - S29