نتایج جستجو برای: children cystic fibrosis
تعداد نتایج: 588220 فیلتر نتایج به سال:
Introduction: Patients with Cystic Fibrosis have increased risk of malnutrition. Early detection of nutritional deterioration enables prompt intervention and correction. The aims of this project were to: - Define the nutritional status of CF patients in Iran and New Zealand - Compare and contrast the MacDonald Nutritional Screening tool with the Australasian guidelines for Nutrition in Cyst...
Early detection of cystic fibrosis lung disease: multiple-breath washout versus raised volume tests.
BACKGROUND Lung clearance index (LCI), a measure of ventilation inhomogeneity derived from the multiple-breath inert gas washout (MBW) technique, has been shown to detect abnormal lung function more readily than spirometry in preschool children with cystic fibrosis, but whether this holds true during infancy is unknown. OBJECTIVES To compare the extent to which parameters derived from the MBW...
RATIONALE Pulmonary inflammation, infection, and structural lung disease occur early in life in children with cystic fibrosis. OBJECTIVES We hypothesized that the presence of these markers of cystic fibrosis lung disease in the first 2 years of life would be associated with reduced lung function in childhood. METHODS Lung function (forced expiratory volume in the first three-quarters of a s...
background and objectives: cystic fibrosis (cf) is an autosomal recessive genetic disease. infections in these patients gene.are mostly caused by three bacteria: staphylococcus aureus , haemophilus influenza and particularly pseudomonas aeruginosa . carbapenems including antibiotics are used to combat infections with pseudomonas aeruginosa . in recent years, carbapenems resistant s...
background cystic fibrosis is a complex progressive disease which assessing its progression and severity is essential. for this purpose there are scoring systems available to evaluate the disease severity. objectives the aim of the present study was to determine the clinical status of cf patients using shwachman score system in the pediatric pulmonary ward of masih daneshvari hospital. patients...
Impaired glucose tolerance was shown to be present in a proportion of children with cystic fibrosis more than 30 years ago (Andersen, 1938), though symptomatic diabetes mellitus was not recognized as a complication until 1955(Schwachman and Leubner, 1955). This paper presents the results of blood glucose and serum insulin levels after oral and intravenous glucose, and after intravenous glucagon...
From 39 normal children and 36 patients, suffering from cystic fibrosis (C/F), the copper content of finger nail clippings and toe nail clippings were determined. From this study it can be concluded that, although the patients with cystic fibrosis (C/F) have a higher copper content, the determination of copper in nail samples cannot be used in order to differentiate between normal children and ...
BACKGROUND Growth retardation, delayed puberty and malnutrition are frequently observed in children suffering from cystic fibrosis. AIM The aim of this study was to estimate growth and nutritional status in children with cystic fibrosis on the basis of body proportions and body mass index. SUBJECTS AND METHODS Anthropometric data were collected from the medical histories of 62 patients trea...
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