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[PDF] Top 20 Lung function in infants with cystic fibrosis: Findings at diagnosis and changes with time

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Lung function in infants with cystic fibrosis: Findings at diagnosis and changes with time

Lung function in infants with cystic fibrosis: Findings at diagnosis and changes with time

... healthy infants, Tepper et ...their lung volumes at FRC than older children ...of lung emptying, is greatest in the newborn and decreases with age, declining from ...These findings are ... See full document

308

Lung function and energy expenditure in infants with cystic fibrosis

Lung function and energy expenditure in infants with cystic fibrosis

... and cystic fibrosis suggested if a known CF genotype is ...The diagnosis is confirmed by an elevated sweat chloride ( ) 60 mmol/ L) with the Gibson-Cooke ...these infants was studied aged 15 ... See full document

223

Effects of Viral Lower Respiratory Tract Infection on Lung Function in Infants With Cystic Fibrosis

Effects of Viral Lower Respiratory Tract Infection on Lung Function in Infants With Cystic Fibrosis

... a time. A total of 26 infants with CF, age 1 to 20 months, were enrolled; 4 failed to complete the study and 8 others were reenrolled for a second season, for a total of 30 CF ...The infants with CF ... See full document

10

No benefit of longer eradication therapy of Pseudomonas aeruginosa primoinfections in pediatric cystic fibrosis

No benefit of longer eradication therapy of Pseudomonas aeruginosa primoinfections in pediatric cystic fibrosis

... the time of the ...acute lung disease were excluded ...with cystic fibrosis was recently discussed [15– ...the lung func- tion (FEV1) before implementation of the eradication protocol ... See full document

6

Immunoreactive trypsinogen levels in newborn screened infants with an inconclusive diagnosis of cystic fibrosis

Immunoreactive trypsinogen levels in newborn screened infants with an inconclusive diagnosis of cystic fibrosis

... for cystic fibrosis (CF) not only identifies infants with a diagnosis of CF, but also those with an uncertain diagnosis of cystic fibrosis (CF), ...inconclusive ... See full document

7

Evolution of lung function during the first year of life in newborn screened cystic fibrosis infants.

Evolution of lung function during the first year of life in newborn screened cystic fibrosis infants.

... earlier diagnosis and implementa- tion of treatment within the narrow geographical area of southeast England that we recruited from, thereby halting progression of any early lung ...that infants ... See full document

9

Longitudinal Changes in Growth Parameters Are Correlated With Changes in Pulmonary Function in Children With Cystic Fibrosis

Longitudinal Changes in Growth Parameters Are Correlated With Changes in Pulmonary Function in Children With Cystic Fibrosis

... with time in CF, long-term studies are necessary to characterize better the association between nutri- tional status and pulmonary dysfunction and to identify which factors are most intimately involved in this ... See full document

7

Status of gene therapy for cystic fibrosis lung disease

Status of gene therapy for cystic fibrosis lung disease

... CF infants typical- ly present clinically with physical and roentgenographic findings of bronchiolitis, exhibit as their first pulmonary function abnormality small airways obstruction, and have ... See full document

6

Cystic fibrosis overview and update on infant care

Cystic fibrosis overview and update on infant care

... In 1976, Bedrossian et al. [22] reported a qualitative study of lower respiratory tracts in Human Pathology. The 82 patients were divided into five groups based on the age as follows: group one, 0 to 4 months, 16 ... See full document

10

Impact of pseudomonas aeruginosa Liverpool epidemic strain (LES) on cystic fibrosis patients

Impact of pseudomonas aeruginosa Liverpool epidemic strain (LES) on cystic fibrosis patients

... same time it would be interesting to study whether such an intervention may have any positive benefit to the lung function and to the overall outcomes of physical ... See full document

171

ECFS best practice guidelines: the 2018 revision

ECFS best practice guidelines: the 2018 revision

... Chest physiotherapy to achieve airway clearance is advo- cated in UK [36] and US [37] guidelines and should be available to all CF patients. A recent head-to-head trial [38] has shown that conventional positive ... See full document

26

Early Diagnosis of Cystic Fibrosis

Early Diagnosis of Cystic Fibrosis

... appeared in the April 2000 issue of Pediatrics. I agree with his well-founded concern regarding prolonged parenteral antibiotic therapy of Lyme disease based on empiric diagnosis and not based on serological ... See full document

9

DIAGNOSIS OF CYSTIC FIBROSIS OF THE PANCREAS

DIAGNOSIS OF CYSTIC FIBROSIS OF THE PANCREAS

... toms and are the major problem of cystic fibrosis. These children with advanced forms of cystic fibrosis are literally stmffo- cated by these secretions. Figure 1 shows.. how copioums th[r] ... See full document

10

Monitoring clinical and microbiological evolution of a cystic fibrosis patient over 26 years: experience of a Brazilian CF Centre

Monitoring clinical and microbiological evolution of a cystic fibrosis patient over 26 years: experience of a Brazilian CF Centre

... Microbiome analysis of sputum samples was performed by sequencing the V4 region of the 16S rRNA gene in an Illumina MiSeq instrument [9]. The following data was obtained from the three samples collected from June 2014 to ... See full document

5

Effect of ivacaftor on mucociliary clearance and clinical outcomes in cystic fibrosis patients with G551D-CFTR

Effect of ivacaftor on mucociliary clearance and clinical outcomes in cystic fibrosis patients with G551D-CFTR

... observed changes in MCC in response to ivacaftor correlated with clinical outcomes, including lung function (FEV 1 ...MCC changes was ... See full document

11

Heparin-binding protein in sputum as a marker of pulmonary inflammation, lung function, and bacterial load in children with cystic fibrosis

Heparin-binding protein in sputum as a marker of pulmonary inflammation, lung function, and bacterial load in children with cystic fibrosis

... Expectorated and induced sputum is a non-invasive method to obtain airway samples from CF-patients, as opposed to BAL which is still the gold standard for de- fining airway inflammation and microbiology in infants ... See full document

8

Myocardial infarction in an adult with cystic fibrosis and heart and lung transplant

Myocardial infarction in an adult with cystic fibrosis and heart and lung transplant

... The diagnosis of CTV is particularly challenging as it rarely presents with typical angina, despite 10-30% of pa- tients with heart transplants having partial reinnervation ...early diagnosis of CTV is ... See full document

5

Wheezing in Infants with Cystic Fibrosis: Clinical Course, Pulmonary Function, and Survival Analysis

Wheezing in Infants with Cystic Fibrosis: Clinical Course, Pulmonary Function, and Survival Analysis

... Association of respiratory viral infections with pulmonary deterioration in patients with cystic fibrosis. Ramsey BW, Gore EJ, Smith AL, Cooney MK, Redding GJ, Foy H[r] ... See full document

6

Inspiration for the Future: The Role of Inspiratory Muscle Training in Cystic Fibrosis

Inspiration for the Future: The Role of Inspiratory Muscle Training in Cystic Fibrosis

... Although IMT has the potential to be a useful rehabilita- tive and therapeutic tool for the management of CF lung disease, several crucial weaknesses in the current body of literature must be addressed in order to ... See full document

8

Outcomes of Infants With Indeterminate Diagnosis Detected by Cystic Fibrosis Newborn Screening

Outcomes of Infants With Indeterminate Diagnosis Detected by Cystic Fibrosis Newborn Screening

... in infants with a guideline diagnosis of CF compared with those with a guideline diagnosis of ...CRMS. Infants with CRMS were significantly more likely to be nonwhite (African American, Asian, ... See full document

9

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