Infection in cystic fibrosis: impact of the environment and climate.

scientific article published on 7 March 2016

Infection in cystic fibrosis: impact of the environment and climate. is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1586/17476348.2016.1162715
P8608Fatcat IDrelease_e42v2eiivnhaja7pnzmhvxld4m
P698PubMed publication ID26949990

P50authorRebecca E StockwellQ57052741
Timothy J. KiddQ42831844
Scott BellQ43545877
P2093author name stringK A Ramsay
P2860cites workLongevity of Patients With Cystic Fibrosis in 2000 to 2010 and Beyond: Survival Analysis of the Cystic Fibrosis Foundation Patient RegistryQ22305306
Identification of airborne dissemination of epidemic multiresistant strains of Pseudomonas aeruginosa at a CF centre during a cross infection outbreakQ22306482
Infections caused by Scedosporium spp.Q24657691
Stenotrophomonas maltophilia: an emerging global opportunistic pathogenQ26995336
Complex molecular epidemiology of methicillin-resistant staphylococcus aureus isolates from children with cystic fibrosis in the era of epidemic community-associated methicillin-resistant S aureusQ45411110
A steady increase in nontuberculous mycobacteriosis mortality and estimated prevalence in JapanQ45786860
Emergence of community-acquired methicillin-resistant Staphylococcus aureus skin and soft tissue infections as a common cause of hospitalization in United States childrenQ45880975
Early aggressive eradication therapy for intermittent Pseudomonas aeruginosa airway colonization in cystic fibrosis patients: 15 years experienceQ46436058
Risk factors and causative organisms in microbial keratitisQ46774915
What is the importance of classifying Aspergillus disease in cystic fibrosis patients?Q46888963
Increased prevalence and altered species composition of filamentous fungi in respiratory specimens from cystic fibrosis patientsQ46910359
Epidemiological analysis of methicillin-resistant Staphylococcus aureus isolates from adult patients with cystic fibrosis.Q46933712
Stenotrophomonas maltophilia strains from cystic fibrosis patients: genomic variability and molecular characterization of some virulence determinantsQ48062294
Achromobacter xylosoxidans in cystic fibrosis: prevalence and clinical relevanceQ49081215
Marked increase in incidence of Achromobacter xylosoxidans infections caused by sporadic acquisition from the environment.Q51015868
Pseudomonas aeruginosa and other predictors of mortality and morbidity in young children with cystic fibrosis.Q51711090
Stenotrophomonas maltophilia in cystic fibrosis: serologic response and effect on lung disease.Q53297625
Effect of culture conditions on the resistance of Pseudomonas aeruginosa biofilms to disinfecting agents.Q53689318
Persistent colonization of nine cystic fibrosis patients with an Achromobacter (Alcaligenes) xylosoxidans clone.Q53900736
Burkholderia cepacia complex epidemiology in persons with cystic fibrosis from Australia and New Zealand.Q54541142
Cystic fibrosisQ55881299
Inflammation in Achromobacter xylosoxidans infected cystic fibrosis patientsQ59139106
Anonymous mycobacteria in pulmonary diseaseQ28184336
Burkholderia fungorum sp. nov. and Burkholderia caledonica sp. nov., two new species isolated from the environment, animals and human clinical samplesQ28202427
Seasonal variations of indoor microbial exposures and their relation to temperature, relative humidity, and air exchange rateQ28390961
Prevalence of nontuberculous mycobacterial lung disease in U.S. Medicare beneficiariesQ28729217
Invasive fungal infections after natural disastersQ30763683
Pseudomonas aeruginosa population structure revisitedQ30913394
Burkholderia stagnalis sp. nov. and Burkholderia territorii sp. nov., two novel Burkholderia cepacia complex species from environmental and human sourcesQ30931813
Burkholderia and emerging pathogens in cystic fibrosisQ30998871
Global Pseudomonas aeruginosa biodiversity as reflected in a Belgian riverQ33216771
Diversity and occurrence of Burkholderia spp. in the natural environment.Q33329214
A spatial epidemiological analysis of nontuberculous mycobacterial infections in Queensland, AustraliaQ33726691
Antibiotic management of lung infections in cystic fibrosis. II. Nontuberculous mycobacteria, anaerobic bacteria, and fungiQ33792765
The changing microbial epidemiology in cystic fibrosisQ33825634
Disseminated Scedosporium/Pseudallescheria infection after double-lung transplantation in patients with cystic fibrosisQ33827090
Differential habitat use and niche partitioning by Pseudomonas species in human homesQ33876648
Phenotypic and genotypic characterization of Stenotrophomonas maltophilia isolates from patients with cystic fibrosis: genome diversity, biofilm formation, and virulence.Q33950924
Viability of Pseudomonas aeruginosa in cough aerosols generated by persons with cystic fibrosis.Q33956730
Effect of temperature on cystic fibrosis lung disease and infections: a replicated cohort studyQ34085781
Characteristics of pathogenic fungi and antifungal therapy in cystic fibrosisQ34130445
Microbiology of acute otitis externaQ34143706
Factors influencing acquisition of Burkholderia cepacia complex organisms in patients with cystic fibrosisQ34372132
Pseudomonas aeruginosa exhibits frequent recombination, but only a limited association between genotype and ecological setting.Q34412265
Environmental risks for nontuberculous mycobacteria. Individual exposures and climatic factors in the cystic fibrosis populationQ34425638
Continental-scale distributions of dust-associated bacteria and fungi.Q34473185
Factors associated with the isolation of Nontuberculous mycobacteria (NTM) from a large municipal water system in Brisbane, AustraliaQ34678540
The hospital water supply as a source of nosocomial infections: a plea for actionQ34714383
Epidemiology of nontuberculous mycobacteria among patients with cystic fibrosis in ScandinaviaQ34982469
Achromobacter xylosoxidans respiratory tract infection in cystic fibrosis patientsQ35094033
Diversity and dynamics of airborne fungi in São Luis, State of Maranhão, Brazil.Q35113076
Pseudomonas aeruginosa in cystic fibrosis patients with G551D-CFTR treated with ivacaftorQ35127240
New pharmacological approaches for cystic fibrosis: promises, progress, pitfalls.Q35188869
Nontuberculous mycobacteria from household plumbing of patients with nontuberculous mycobacteria diseaseQ35193554
Diversity and significance of Burkholderia species occupying diverse ecological niches.Q35200150
Summer Peaks in the Incidences of Gram-Negative Bacterial Infection Among Hospitalized PatientsQ40025289
Association of meteorological and geographical factors and risk of initial Pseudomonas aeruginosa acquisition in young children with cystic fibrosisQ40960703
Geographic variations in cystic fibrosis: An analysis of the U.S. CF Foundation RegistryQ41137775
Seasonal onset of initial colonisation and chronic infection with Pseudomonas aeruginosa in patients with cystic fibrosis in DenmarkQ41145157
Proximity to blue spaces and risk of infection with Pseudomonas aeruginosa in cystic fibrosis: A case-control analysisQ41259608
Pseudomonas aeruginosa genotypes acquired by children with cystic fibrosis by age 5-yearsQ41560657
Pseudomonas aeruginosa in CF and non-CF homes is found predominantly in drainsQ41638640
Nontuberculous mycobacteria, fungi, and opportunistic pathogens in unchlorinated drinking water in The NetherlandsQ41854088
Isolation and characterization of numerous novel phages targeting diverse strains of the ubiquitous and opportunistic pathogen Achromobacter xylosoxidansQ41886330
Detection of Achromobacter xylosoxidans in hospital, domestic, and outdoor environmental samples and comparison with human clinical isolatesQ42089409
Shared genotypes of Achromobacter xylosoxidans strains isolated from patients at a cystic fibrosis rehabilitation centerQ42130118
Chronic Stenotrophomonas maltophilia infection and mortality or lung transplantation in cystic fibrosis patientsQ42279891
Haemophilus influenzae and the lung (Haemophilus and the lung).Q43212173
Shared Pseudomonas aeruginosa genotypes are common in Australian cystic fibrosis centresQ43644594
Season is associated with Pseudomonas aeruginosa acquisition in young children with cystic fibrosisQ43721825
Bacterial community of biofilms developed under different water supply conditions in a distribution system.Q43726391
Acceleration of lung disease in children with cystic fibrosis after Pseudomonas aeruginosa acquisitionQ43745855
Increasing nontuberculous mycobacteria infection in cystic fibrosisQ44189223
Achromobacter species in cystic fibrosis: cross-infection caused by indirect patient-to-patient contactQ44252772
Diversity of β-lactam resistance mechanisms in cystic fibrosis isolates of Pseudomonas aeruginosa: a French multicentre study.Q44477142
Prevalence, persistence, and phenotypic variation of Aspergillus fumigatus in the outdoor environment in Manchester, UK, over a 2-year periodQ44567268
Differential geographical risk of initial Pseudomonas aeruginosa acquisition in young US children with cystic fibrosisQ44656924
Geographical differences in first acquisition of Pseudomonas aeruginosa in cystic fibrosis.Q45029608
Massive hemoptysis in cystic fibrosisQ45093448
Burkholderia pseudomallei: another emerging pathogen in cystic fibrosisQ35535652
Association between Stenotrophomonas maltophilia and lung function in cystic fibrosis.Q35536357
Pathophysiology and Management of Pulmonary Infections in Cystic FibrosisQ35557791
Emerging bacterial pathogens and changing concepts of bacterial pathogenesis in cystic fibrosisQ35604702
An international, multicentre evaluation and description of Burkholderia pseudomallei infection in cystic fibrosisQ35802333
Changing Epidemiology of Pulmonary Nontuberculous Mycobacteria InfectionsQ35804472
Increasing incidence of invasive Haemophilus influenzae disease in adults, Utah, USAQ35877520
Spatial clusters of nontuberculous mycobacterial lung disease in the United StatesQ36345297
Environmental factors that affect the survival and persistence of Burkholderia pseudomalleiQ36596229
Risk factors for age at initial Pseudomonas acquisition in the cystic fibrosis epic observational cohortQ36673569
The epidemiology, pathogenesis and treatment of Pseudomonas aeruginosa infectionsQ36750086
The effect of season and weather on physical activity: a systematic reviewQ36963251
Chronic Mycobacterium abscessus infection and lung function decline in cystic fibrosisQ37334924
Surrounded by mycobacteria: nontuberculous mycobacteria in the human environmentQ37396516
Staphylococcus aureus small-colony variants are independently associated with worse lung disease in children with cystic fibrosisQ37463364
Therapeutic drug monitoring (TDM) of antifungal agents: guidelines from the British Society for Medical MycologyQ37688257
Impact of human activities on the ecology of nontuberculous mycobacteriaQ37762557
Travelling with cystic fibrosis: Recommendations for patients and care team membersQ37789930
Link between CFTR mutations and ABPA: a systematic review and meta-analysisQ37945665
Staphylococcus aureus: determinants of human carriageQ38101786
Paediatric community-associated Staphylococcus aureus: a retrospective cohort studyQ38110584
Electrolyte abnormalities in cystic fibrosis: systematic review of the literatureQ38170270
Management of comorbidities in older patients with cystic fibrosis.Q38178773
Respiratory infections in travelers returning from the tropics.Q38266257
Burkholderia species infections in patients with cystic fibrosis in British Columbia, Canada. 30 years' experienceQ38283021
Melioidosis: evolving concepts in epidemiology, pathogenesis, and treatmentQ38341053
Review of fungal outbreaks and infection prevention in healthcare settings during construction and renovationQ38419604
The thymidine-dependent small-colony-variant phenotype is associated with hypermutability and antibiotic resistance in clinical Staphylococcus aureus isolatesQ38898519
Future trends in cystic fibrosis demography in 34 European countriesQ39027112
Human and planetary health: towards a common languageQ39279461
Cystic fibrosis detection in high-risk Egyptian children and CFTR mutation analysisQ39290648
Relationship between climate, disease severity, and causative organism for contact lens-associated microbial keratitis in Australia.Q39486666
Changes in concentration of Alternaria and Cladosporium spores during summer stormsQ39518334
Transmissible strains of Pseudomonas aeruginosa in cystic fibrosis lung infections.Q39653993
P433issue5
P921main subjectcystic fibrosisQ178194
P304page(s)505-519
P577publication date2016-03-28
P1433published inExpert Review of Respiratory MedicineQ15754583
P1476titleInfection in cystic fibrosis: impact of the environment and climate
P478volume10

Reverse relations

cites work (P2860)
Q40105439Air pollution exposure is associated with MRSA acquisition in young U.S. children with cystic fibrosis
Q38764394Household proximity to water and nontuberculous mycobacteria in children with cystic fibrosis
Q57812471Seasonal fluctuation of lung function in cystic fibrosis: A national register-based study in two northern European populations

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