Oxygen therapy for cystic fibrosis

Cochrane Database of Systematic Reviews

Volumn , Issue 1, 2009, Pages

  Elphick, Heather E ^a   Mallory, George ^b  

^a SHEFFIELD CHILDREN S HOSPITAL   (United Kingdom)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

*Oxygen inhalation therapy; Anoxia etiology; mortality; *therapy ; Cystic fibrosis *complications; mortality ; Exercise tolerance; Humans; Quality of life; Randomized controlled trials as topic; Sleep

Indexed keywords

OXYGEN;

BODY MASS; CLINICAL EVALUATION; CLINICAL FEATURE; CLINICAL TRIAL; COCHRANE LIBRARY; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; CYSTIC FIBROSIS; DATA BASE; EXERCISE; EXERCISE TOLERANCE; FORCED EXPIRATORY VOLUME; GAS EXCHANGE; HOSPITAL COST; HUMAN; HYPERCAPNIA; INFORMATION PROCESSING; LIFESTYLE; LONG TERM CARE; LONGEVITY; LUNG PRESSURE; NUTRITIONAL STATUS; OUTCOME ASSESSMENT; OXYGEN THERAPY; OXYGENATION; PATIENT CARE; POLYSOMNOGRAPHY; QUALITY OF LIFE; RANDOMIZED CONTROLLED TRIAL; REM SLEEP; REVIEW; RISK ASSESSMENT; SLEEP PARAMETERS; SLEEP TIME; SURVIVAL TIME; SYSTEMATIC REVIEW; TREATMENT DURATION; TREATMENT OUTCOME;

EID: 68849106997     PISSN: 1469493X     EISSN: None     Source Type: Journal    
DOI: 10.1002/14651858.CD003884.pub3     Document Type: Review

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