Adding a Second Drug for Febrile Children Treated With Acetaminophen

Methods:

Design: randomized double blind placebo controlled study. Setting: The ED and pediatric ward of a large University affiliated Hospital

Participants:

Inclusion criteria:

• Age: 6 mo- 4 years
• Rectal temperature > 38.5
• Received 10-15 mg/kg of acetaminophen or 5-10 mg/kg of ibuprofen 1.5 - 3.5 hours before admission to the ED.

Exclusion criteria:

• Received more than 75 mg acetaminophen in the last 24 hours
• Unable to take oral medications
• Hypersensitivity to acetaminophen or ibuprofen
• Varicella
• Renal failure
• Liver disease
• Rectal temperature can't be measured (due to anatomical or medical problem)
• Received both Ibuprofen and acetaminophen in the last 6 hours
• Informed consent could not be granted

Intervention:

Patients will be recruited in the ED and pediatric ward at Assaf Harofeh Medical Center. Legal guardians of eligible patients will be approached for consent. After obtaining informed consent a detailed history regarding the way fever was managed during the current illness will be collected (appendix 1). Patients will be randomized in a ratio of 2:1 (by a computer generated list of random numbers) into one of two groups. Group A will be treated with oral suspension of ibuprofen 10mg/kg (if the patient received acetaminophen at home) or oral suspension of acetaminophen 15 mg/kg (if treated previously with ibuprofen). The second group will be treated with the same amount of oral placebo suspension. The parents and the physician will be blinded to the treatment given. Body departure will be recoded at base line and at 15, 30, 60, 90, 120, 180 minutes after the drug administration. Blood sample for serum concentrations of acetaminophen or/and ibuprofen will be taken at the time of routine blood sampling according to the attending physician decision. Serum concentrations will not be measured if the attending physician decides that blood tests are not indicated.

Primary outcome:

· Maximal change in temperature during the 3-hour period after enrollment.

Secondary endpoints:

• Proportion of patients with a drop of at least 1°C and 2°C in mean temperature at the end of the study (3 hours).
• Decrement in fever at each time point, and the area under the temperature (versus time) curve for each group, calculated using the trapezoidal method. Continuous outcomes
• Proportion of patients with temperature < 38 at the end of the study (3 hours).