Applying Petitmengin’s Explicitation Interview Method to Elicit the Lived Experience of Breathing Upon Waking by an Individual With Cystic Fibrosis
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چکیده
منابع مشابه
Facilitators and Barriers to Adapting to the Disease: The Lived Experience of Patients with Multiple Sclerosis
Objective: Multiple sclerosis (MS) is a neurological disease in which the myelin lining the central nervous system is damaged. This study aimed to explore the experiences of facilitators and barriers adapting to MS. Material & Methods: This study was conducted using a qualitative phenomenological method. The participants were 14 (8 female and 6 male) referred to Rofideh Hospital in Tehran. Th...
متن کاملAssessment of tidal breathing parameters in infants with cystic fibrosis.
Simple methods are needed to assess lung function in infants with cystic fibrosis (CF). This study determined the relationship between simple measurements obtained from tidal breathing with those from more complicated forced expiratory manoeuvres. Healthy infants and infants with CF were recruited from two maternity units and five specialist CF hospitals, respectively. Respiratory rate, tidal v...
متن کاملSleep disordered breathing in cystic fibrosis.
Cough, sleep fragmentation and oxyhaemoglobin desaturation have all been documented during sleep in patients with cystic fibrosis (CF). It has been proposed that repeated episodes of nocturnal hypoxia act as a stimulus for the development of pulmonary hypertension and right ventricular failure, a complication that is associated with a poor prognosis. In addition, sleep disturbance from these ev...
متن کاملPredicting sleep-disordered breathing in patients with cystic fibrosis.
STUDY OBJECTIVES To examine predictors of sleep-disordered breathing in patients with cystic fibrosis (CF) and moderate-to-severe lung disease using a comprehensive evaluation of both sleep and daytime function. DESIGN Cross-sectional analysis of sleep studies, lung function, respiratory muscle strength, and evening and morning arterial blood gas measurements in patients with stable CF. A que...
متن کاملSleep-disordered breathing in patients with cystic fibrosis *
OBJECTIVE To test the hypothesis that disease severity in patients with cystic fibrosis (CF) is correlated with an increased risk of sleep apnea. METHODS A total of 34 CF patients underwent clinical and functional evaluation, as well as portable polysomnography, spirometry, and determination of IL-1β levels. RESULTS Mean apnea-hypopnea index (AHI), SpO2 on room air, and Epworth Sleepiness S...
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ژورنال
عنوان ژورنال: Journal of Patient Experience
سال: 2020
ISSN: 2374-3735,2374-3743
DOI: 10.1177/2374373520956740