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DOI 10.1086/510860

Медицинская библиотека · The Journal of infectious diseases · 2007

Pharmacokinetics of antimony in children treated for leishmaniasis with meglumine antimoniate.

Cruz Adriana, Rainey Petrie M, Herwaldt Barbara L, Stagni Grazia, Palacios Ricardo, Trujillo Rodolfo, Saravia Nancy G

Сравнительное исследованиеСтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

BACKGROUND

In some settings, the response to pentavalent antimonial therapy for leishmaniasis may be lower in children than in adults. We hypothesized that there are age-dependent pharmacokinetic differences of potential clinical relevance.

METHODS

We compared the pharmacokinetics of antimony (Sb) in adults and 2 groups of children 3-6 years old who had cutaneous leishmaniasis treated with intramuscular meglumine antimoniate. Adults (n=9) and the first group of children (n=9) received 20 mg Sb/kg/day for 20 days; the second group of children (n=6) received 20 mg Sb/kg for 19 days and 30 mg Sb/kg on day 20. Drug exposure was assessed by the area under the 24-h time-concentration curve (AUC(0-24)) in plasma.

RESULTS

Children (vs. adults) who received 20 mg/kg had a 42% lower AUC(0-24) (mean +/- SE, 111+/-7 vs. 190+/-10 mg x h/L, compared with adults; P<.001), a 16% lower peak concentration (32.7+/-0.9 vs. 38.8+/-2.1 mg/L; P=.04), and a 75% higher weight-adjusted clearance (0.185+/-0.013 vs. 0.106+/-0.006 L/h/kg; P<.001). The 30 mg/kg dose in children increased the AUC(0-24) to 164+/-10 mg x h/L and the peak concentration to 43.8+/-2.3 mg/L.

CONCLUSIONS

Drug exposure is significantly lower in children than in adults treated with the same weight-adjusted regimen of meglumine antimoniate, which primarily stems from a higher antimony clearance rate.

Для цитирования: Cruz Adriana, Rainey Petrie M, Herwaldt Barbara L, Stagni Grazia, Palacios Ricardo, Trujillo Rodolfo, Saravia Nancy G. Pharmacokinetics of antimony in children treated for leishmaniasis with meglumine antimoniate.. The Journal of infectious diseases. 2007. DOI: 10.1086/510860.

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