Læknablaðið : fylgirit - 01.05.1978, Side 46

Læknablaðið : fylgirit - 01.05.1978, Side 46
J. Haapasaari, A-L. Makelá, M. Lempiáinen and T. Yrjana. Departments of Paediatrics and Clinical Chemistry, Turku University Hospital, Turku, Finland. The liquid form of benorylate makes it easy to dosage this drug accurately for children in milligrams per kg of body weight. A harmful handicap is, however, the taste of benorylate mixture, which by some children is considered to be bad and disgusting. This is, however, not a rule, in general children take the mixture quite readily. Conceming the dosage of benorylate to children, in an earlier report from 1974, doctors Powell and Ansell1) recommend benorylate to be started with a dosage of 200 mg/kg/day in cases of juvenile rheumatoid arthritis. According to Powell and Anseil, the blood salicylate level should be checked at seven days during the treat- ment, and the dosage of benorylate should be adjusted to give blood salicylate levels between 25 and 30 mg/100 ml corresponding values 1800- 2300 umol/1. Once a satisfactory blood salicylate level of between 25 and 30 mg/100 ml has been achieved, this dosage should be maintained with an occa- sional monitoring of the salicylate level. This recommended daily dosage of 200 mg/kg of body weight was used also in our study, the BENORYLATE IN THE TREATMENT OF JUVENILE RHEUMATOID ARTHRITIS total daily dose did not, however, exceed 8grams. The purpose of our study was concentrated on clarifying the serumlevels of salicylate and paracetamol achieved with a constant dosage of 200 mg/kg/day of benorylate to children with JRA. In addition, the clinical effect of this constant dosage of benorylate was registered in these children, as well as the possible side-effects. The duration of the test was two weeks. During this period, the serum levels of both salicylates and paracetamol were controlled frequently to investigate their connection to the possible side effects. Twenty-two inpatients, 10 boys and 12 girls, suffering from active juvenile rheumatoid arthri- tis were included this trial. The age of the children ranged between 18 months and 13years. Benorylate was administered twice daily, the total daily dose being 200 mg/kg of body weight. In two cases, in which the weight of the children was more than 40 kg, the total daily dose of benorylate was 8 grams. Salicylate serum levels were estimated spectrophotometrically by Trinder's method. Figure 1. With a constant dosage of benorylate SALICYLATE IN SERUM fjmol/l mg/IOOml 2000 IS00 '600 U.00 '200 '000 aoo 600 400 200 SALICYLATE SERUM CONCENTRATION (MEAN : DOSAGE OF BENORYLATE 200 mg/kg/day S 0) Fig. 1. Salicylate serum levels in children treated with benorylate with a constan daily dose 200 mg/kg during fourteen days. I 2 3 4 5 1 6 7 8 9 10 il 12 13 14 DAYS OF AÐMINISTRATION NUMBER OF 20,SAMPLES 1 ’ 6 ■ 7 ' 8 9 ’ 10 ii ' 12 ' 13 14 DAYS OF ADMINISTRATION 44
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