Abstract
Purpose
We aimed to evaluate the use and safety of double dose oseltamivir for patients manifesting severe respiratory symptoms or showing no improvement of clinical symptoms after 72 hours' treatment with the usual oseltamivir dosage.
Methods
We analyzed the clinical features of 2009 influenza A H1N1 inpatients who had been admitted to a university hospital's Department of Pediatrics between August 2009 and January 2010. The Influenza A H1N1 diagnoses were confirmed by real-time reverse transcriptase polymerase chain reaction.
Results
The study participants numbered 157 (mean age, 5.0 years; male-to-female ratio, 1.1:1). Among them, twenty (mean age, 5.2 years) were administered double dose oseltamivir. This double dose group showed higher peak body temperatures and more abnormal radiologic results than the other, usual-dose group. The mean time duration between high fever and afebrile status after initiation of double-dose oseltamivir administration was 2.1 days, whereas that within the usual-dose group was 1.7 days. There were no adverse effects in the patients treated with double-dose oseltamivir.
Figures and Tables
Table 2
Values are presented as mean (range).
GI, gastrointestinal; WBC, white blood cell; CRP, C-reactive protein.
*Other symptoms included arthralgia, skin lesion, and headache. The first patient complained of arthralgia and urticaria on the day of admittance; the second patient complained of macular rash, abdominal pain and the uttering of meaningless words, immediately upon taking the first double-dose of oseltamivir; the third patient complained of headache.
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