Nebulizer Care and Inhalation Technique in Children with Cystic Fibrosis
نویسندگان
چکیده
منابع مشابه
Prevalence of Cystic Fibrosis Trans-membrane Conductance Regulator Gene common mutations in children with cystic fibrosis in Isfahan, Iran
Background: Cystic fibrosis (CF) is the most common lethal genetic disorder of Cystic Fibrosis Trans-membrane Conductance (CFTR) Regulator gene mutations. We aimed to investigate common mutations in CF patients and to assess its possible relationship with clinical presentations. Materials and Methods: This cross sectional study was conducted on 36 CF patients who were referred to a tertiary ped...
متن کاملCYSTIC FIBROSIS Airway remodelling in children with cystic fibrosis
Background: The relationship between airway structural changes and inflammation is unclear in early cystic fibrosis (CF) lung disease. A study was undertaken to determine changes in airway remodelling in children with CF compared with appropriate disease and healthy controls. Methods: Bronchoalveolar lavage and endobronchial biopsy were performed in a cross-sectional study of 43 children with C...
متن کاملInhalation of antibiotics in cystic fibrosis.
Aerosol administration of antipseudomonal antibiotics is commonly used in cystic fibrosis. However, its contribution to the improvement of lung function, infection and quality of life is not well-established. All articles published from 1965 until the present time concerning the inhalation of antibiotics in cystic fibrosis were collected by computerized literature search and analysed. Effective...
متن کاملAllowances for care for children with cystic fibrosis.
Attendance allowance The attendance allowance was introduced in 1970 to provide financial assistance to those who require frequent or prolonged attention from others as a result of illness or a disabling condition. Assistance may be required because the person requires personal attention to help with bodily functions, mobility around the house, or medication or because the person requires super...
متن کاملAcute inhalation of hypertonic saline does not improve mucociliary clearance in all children with cystic fibrosis
BACKGROUND Little is known of how mucociliary clearance (MCC) in children with cystic fibrosis (CF) and normal pulmonary function compares with healthy adults, or how an acute inhalation of 7% hypertonic saline (HS) aerosol affects MCC in these same children. METHODS We compared MCC in 12 children with CF and normal pulmonary function after an acute inhalation of 0.12% saline (placebo), or HS...
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ژورنال
عنوان ژورنال: Children
سال: 2020
ISSN: 2227-9067
DOI: 10.3390/children7100153