Table 4
Author, date and countryPatient groupStudy type (level of evidence)OutcomesKey resultsStudy weaknesses
Short JA et al, 2000, UK70 children aged 6–15 years with a diagnosis of asthma, recruited from a hospital respiratory clinic or at presentation for day case surgery.Clinical trialChange in PEFR or FEV1 at 10, 20, and 30 minutes after diclofenacNo patient showed decrease >15% in PEFR or FEV1Uncontrolled, no healthy volunteers to compare with specific population. No sample size analysis; sample size of 70 seems small.
All patients given 1–1.5 mg/kg orally diclofenac after baseline spirometry and after filling a questionnaire detailing the severity of their asthma15% reduction in PEFR or FEV1 considered significant but no explanation offered as to why this figure was chosen
Lesko SM et al, 2002, UK1879 febrile children (aged 6 months to 12 years) receiving asthma medications randomised to receive either paracetamol 12 mg/kg, ibuprofen 5 mg/kg or ibuprofen 10 mg/kgProspective randomised double-blind controlled trialHospitalisation rates for asthma over four weeks. Outpatient visits for asthma over four weeksRelative risk for hospitilisation in ibuprofen group of 0.63 (95% confidence intervals 0.25 to 1.6) 18 admitted.Original study was not designed to look at these outcomes. No objective measure of pulmonary function—follow up by case note review and parental questionnaire. Wide confidence intervals for first outcome. No power calculations. No details of randomisation process
Relative risk in ibuprofen group 0.56 (95% confidence intervals 0.34 to 0.95) 69 patients