Cargando…

Bacterial Re-Colonization Occurs Early after Lung Transplantation in Cystic Fibrosis Patients

Most cystic fibrosis (CF) patients referred for lung transplantation are chronically infected with Gram-negative opportunistic pathogens. It is well known that chronic infections in CF patients have a significant impact on lung-function decline and survival before transplantation. The rate and timin...

Descripción completa

Detalles Bibliográficos
Autores principales:	Holm, Anna Engell, Schultz, Hans Henrik Lawaetz, Johansen, Helle Krogh, Pressler, Tania, Lund, Thomas Kromann, Iversen, Martin, Perch, Michael
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2021
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8003282/ https://www.ncbi.nlm.nih.gov/pubmed/33808547 http://dx.doi.org/10.3390/jcm10061275

Ejemplares similares

Achromobacter spp. in a Cohort of Non-Selected Pre- and Post-Lung Transplant Recipients
por: Crone, Cornelia Geisler, et al.
Publicado: (2022)

Omics-based tracking of Pseudomonas aeruginosa persistence in “eradicated” cystic fibrosis patients
por: Bartell, Jennifer A., et al.
Publicado: (2021)

Use of inhaled antibiotics among Danish patients with cystic fibrosis
por: Møller, Rikke, et al.
Publicado: (2022)

Can secretory immunoglobulin A in saliva predict a change in lung infection status in patients with cystic fibrosis? A prospective pilot study
por: Alanin, Mikkel Christian, et al.
Publicado: (2018)

Transmission and Antibiotic Resistance of Achromobacter in Cystic Fibrosis
por: Gabrielaite, Migle, et al.
Publicado: (2021)

Lung Ultrasound to Phenotype Chronic Lung Allograft Dysfunction in Lung Transplant Recipients. A Prospective Observational Study
por: Davidsen, Jesper Rømhild, et al.
Publicado: (2021)

Adapting to the Airways: Metabolic Requirements of Pseudomonas aeruginosa during the Infection of Cystic Fibrosis Patients
por: La Rosa, Ruggero, et al.
Publicado: (2019)

Shifting paradigms of nontuberculous mycobacteria in cystic fibrosis
por: Qvist, Tavs, et al.
Publicado: (2014)

Hypermutation as an Evolutionary Mechanism for Achromobacter xylosoxidans in Cystic Fibrosis Lung Infection
por: Veschetti, Laura, et al.
Publicado: (2020)

Is genotyping of single isolates sufficient for population structure analysis of Pseudomonas aeruginosa in cystic fibrosis airways?
por: Sommer, Lea M., et al.
Publicado: (2016)

High-resolution in situ transcriptomics of Pseudomonas aeruginosa unveils genotype independent patho-phenotypes in cystic fibrosis lungs
por: Rossi, Elio, et al.
Publicado: (2018)

Compensatory evolution of Pseudomonas aeruginosa’s slow growth phenotype suggests mechanisms of adaptation in cystic fibrosis
por: La Rosa, Ruggero, et al.
Publicado: (2021)

Pseudomonas aeruginosa Adaptation to Lungs of Cystic Fibrosis Patients Leads to Lowered Resistance to Phage and Protist Enemies
por: Friman, Ville-Petri, et al.
Publicado: (2013)

Azole-Resistant Aspergillus fumigatus Among Danish Cystic Fibrosis Patients: Increasing Prevalence and Dominance of TR(34)/L98H
por: Risum, Malene, et al.
Publicado: (2020)

Within-host microevolution of Pseudomonas aeruginosa in Italian cystic fibrosis patients
por: Marvig, Rasmus Lykke, et al.
Publicado: (2015)

Urine lipoarabinomannan point-of-care testing in patients affected by pulmonary nontuberculous mycobacteria – experiences from the Danish Cystic Fibrosis cohort study
por: Qvist, Tavs, et al.
Publicado: (2014)

Achromobacter spp. genetic adaptation in cystic fibrosis
por: Gabrielaite, Migle, et al.
Publicado: (2021)

Review of recombinant human deoxyribonuclease (rhDNase) in the management of patients with cystic fibrosis
por: Pressler, Tacjana
Publicado: (2008)

Evolution of the Pseudomonas aeruginosa mutational resistome in an international Cystic Fibrosis clone
por: López-Causapé, Carla, et al.
Publicado: (2017)

Adaptive Interactions of Achromobacter spp. with Pseudomonas aeruginosa in Cystic Fibrosis Chronic Lung Co-Infection
por: Sandri, Angela, et al.
Publicado: (2021)

SERS detection of the biomarker hydrogen cyanide from Pseudomonas aeruginosa cultures isolated from cystic fibrosis patients
por: Lauridsen, Rikke Kragh, et al.
Publicado: (2017)

Loss of Social Behaviours in Populations of Pseudomonas aeruginosa Infecting Lungs of Patients with Cystic Fibrosis
por: Jiricny, Natalie, et al.
Publicado: (2014)

Understanding the natural progression in %FEV(1) decline in patients with cystic fibrosis: a longitudinal study
por: Taylor-Robinson, David, et al.
Publicado: (2012)

Draft Genome Sequences of Pseudomonas aeruginosa B3 Strains Isolated from a Cystic Fibrosis Patient Undergoing Antibiotic Chemotherapy
por: Marvig, Rasmus Lykke, et al.
Publicado: (2013)

Coexistence and Within-Host Evolution of Diversified Lineages of Hypermutable Pseudomonas aeruginosa in Long-term Cystic Fibrosis Infections
por: Feliziani, Sofía, et al.
Publicado: (2014)

Low socioeconomic status is associated with worse lung function in the Danish cystic fibrosis population
por: Taylor-Robinson, David C., et al.
Publicado: (2014)

Flying the nest: a challenge for young adults with cystic fibrosis and their parents
por: Bregnballe, Vibeke, et al.
Publicado: (2017)

Associations Between Glucose Tolerance, Insulin Secretion, Muscle and Fat Mass in Cystic Fibrosis
por: Nielsen, Bibi Uhre, et al.
Publicado: (2021)

Association between spirometry controlled chest CT scores using computer-animated biofeedback and clinical markers of lung disease in children with cystic fibrosis
por: Kongstad, Thomas, et al.
Publicado: (2017)

Gene Loss and Acquisition in Lineages of Pseudomonas aeruginosa Evolving in Cystic Fibrosis Patient Airways
por: Gabrielaite, Migle, et al.
Publicado: (2020)

Epidemiology of nontuberculous mycobacteria among patients with cystic fibrosis in Scandinavia
por: Qvist, Tavs, et al.
Publicado: (2015)

Osteoporosis Is Associated with Deteriorating Clinical Status in Adults with Cystic Fibrosis
por: Mathiesen, Inger Hee, et al.
Publicado: (2018)

Size matters in telomere biology disorders ‒ expanding phenotypic spectrum in patients with long or short telomeres
por: Byrjalsen, Anna, et al.
Publicado: (2023)

Seasonal fluctuation of lung function in cystic fibrosis: A national register-based study in two northern European populations
por: Qvist, Tavs, et al.
Publicado: (2019)

The effect of time-of-day and chest physiotherapy on multiple breath washout measures in children with clinically stable cystic fibrosis
por: Voldby, Christian, et al.
Publicado: (2018)

Impact of cystic fibrosis on birthweight: a population based study of children in Denmark and Wales
por: Schlüter, Daniela K, et al.
Publicado: (2019)

Increased sputum lactate during oral glucose tolerance test in cystic fibrosis
por: Jensen, Peter Østrup, et al.
Publicado: (2022)

Living with cystic fibrosis – a qualitative study of a life coaching intervention
por: Knudsen, Karin Bæk, et al.
Publicado: (2018)

Barriers to adherence in adolescents and young adults with cystic fibrosis: a questionnaire study in young patients and their parents
por: Bregnballe, Vibeke, et al.
Publicado: (2011)

Thoracic Ultrasound in Lung Transplantation—Insights in the Field
por: Schultz, Hans Henrik Lawaetz, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_08nss7p56it9q7s0koa20f8lui