Abstract Background While lung transplant (LTX) can be an effective therapy to provide the survival benefit in selected populations, post-transplant outcome in LTX recipients with bronchiectasis other than cystic fibrosis (CF) has been less studied. Pseudomonas aeruginosa, often associated with exacerbations in bronchiectasis, is the most common micro-organism isolated from LTX recipients. We aimed to see the outcomes of patients with bronchiectasis other than CF after LTX and seek the risk factors associated with pre- and post-transplant Pseudomonas status. Methods Patients who underwent LTX at Tohoku University Hospital between January 2000 and December 2020 were consecutively included into the retrospective cohort study. Pre- and post-tr...
OBJECTIVES: To evaluate the impact of Burkholderia cepacia complex colonization in cystic fibrosis p...
Objective. The aim of this study was to evaluate the epidemiology of bacterial and fungal pneumonia ...
Survival in patients with cystic fibrosis (CF) has improved dramatically over the past 30 to 40 year...
BACKGROUND: Lung transplantation is a well-established treatment for end-stage non-cystic fibrosis b...
SummaryBronchiolitis obliterans syndrome (BOS) represents the leading cause of late mortality after ...
Additional file 1. Risk factors for mortality, development of CLAD and Pseudomonas colonization from...
Abstract Background Chronic Lung Allograft Dysfunction (CLAD) is the main cause of morbidity and mor...
Long-term survival after lung transplantation (LTx) is hampered by development of chronic lung allog...
Lung transplantation is currently the most effective means of improving survival and quality of life...
BACKGROUND: The presence of pan-resistant organisms in patients with cystic fibrosis (CF) potenti...
Long-term survival after LTx is limited, mainly attributed to the development of chronic lung allogr...
Rationale: Lung transplantation offers the only survival option for patients with cystic fibrosis (C...
In cystic fibrosis (CF) patients, chronic airway infection by Pseudomonas leads to progressive lung ...
PURPOSE: Pseudomonas aeruginosa (PA) is an established risk factor for chronic lung allograft dysfun...
International audienceBackground: Fungus-positive respiratory samples (FPRS) are common in the inten...
OBJECTIVES: To evaluate the impact of Burkholderia cepacia complex colonization in cystic fibrosis p...
Objective. The aim of this study was to evaluate the epidemiology of bacterial and fungal pneumonia ...
Survival in patients with cystic fibrosis (CF) has improved dramatically over the past 30 to 40 year...
BACKGROUND: Lung transplantation is a well-established treatment for end-stage non-cystic fibrosis b...
SummaryBronchiolitis obliterans syndrome (BOS) represents the leading cause of late mortality after ...
Additional file 1. Risk factors for mortality, development of CLAD and Pseudomonas colonization from...
Abstract Background Chronic Lung Allograft Dysfunction (CLAD) is the main cause of morbidity and mor...
Long-term survival after lung transplantation (LTx) is hampered by development of chronic lung allog...
Lung transplantation is currently the most effective means of improving survival and quality of life...
BACKGROUND: The presence of pan-resistant organisms in patients with cystic fibrosis (CF) potenti...
Long-term survival after LTx is limited, mainly attributed to the development of chronic lung allogr...
Rationale: Lung transplantation offers the only survival option for patients with cystic fibrosis (C...
In cystic fibrosis (CF) patients, chronic airway infection by Pseudomonas leads to progressive lung ...
PURPOSE: Pseudomonas aeruginosa (PA) is an established risk factor for chronic lung allograft dysfun...
International audienceBackground: Fungus-positive respiratory samples (FPRS) are common in the inten...
OBJECTIVES: To evaluate the impact of Burkholderia cepacia complex colonization in cystic fibrosis p...
Objective. The aim of this study was to evaluate the epidemiology of bacterial and fungal pneumonia ...
Survival in patients with cystic fibrosis (CF) has improved dramatically over the past 30 to 40 year...