LIPOSOMAL AMPHOTERICIN-B (AMBISOME) IN THE TREATMENT OF COMPLICATED KALA-AZAR UNDER FIELD CONDITIONS

被引:86
作者
SEAMAN, J
BOER, C
WILKINSON, R
DEJONG, J
DEWILDE, E
SONDORP, E
DAVIDSON, R
机构
[1] UNIV LONDON IMPERIAL COLL SCI TECHNOL & MED,NORTHWICK PK HOSP,ST MARYS HOSP MED SCH,HARROW HA1 3UJ,MIDDX,ENGLAND
[2] MEDECINS SANAS FRONTIERES HOLLAND,NAIROBI,KENYA
[3] MEDECINS SANAS FRONTIERES HOLLAND,AMSTERDAM,NETHERLANDS
关键词
D O I
10.1093/clinids/21.1.188
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
An open trial of liposomal amphotericin B (AmBisome [L-AmB]; Vestar, San Dimas, CA) for treatment of complicated visceral leishmaniasis was performed in Sudan. Forty-nine patients were treated, and there were six deaths (12% mortality); these were not attributed to therapy. Thirty-seven patients were selected for the trial because of (1) relapse after treatment with a combination of pentavalent antimony (Sb-V) and aminosidine, (2) incomplete parasitological response to Sb-V and aminosidine, or (3) severe illness. Drug regimen 1 (3 doses of 3-5 mg/kg, on days 0, 3, and 10) cured 8 (50%) of 16 patients; regimen 2 (6 doses of 3-5 mg/kg, on days 0, 3, 6, 8, 10, and 13) cured 14 (88%) of 16. For four of 10 partial responders, ''rescue'' therapy with L-AmB alone (3 mg!kg daily for 10 days) resulted in cure. Twelve less-unwell patients received regimen 3 (4 doses of 4-5 mg/kg, on days 0, 2, 5, and 7); seven of 11 patients evaluated (64%) were cured. The optimal regimen of L-AmB in these circumstances is administration of 4 mg/kg on days 0, 3, 6, 8, 10, and 13.
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页码:188 / 193
页数:6
相关论文
共 23 条
[21]  
Zijlstra E.E., Siddig Ali M., El-Hassan A.M., Et al., Kala-azar: A comparative study of parasitological methods and the direct agglutination test in diagnosis, Trans R Soc Trop Med Hyg, 86, pp. 505-507, (1992)
[22]  
Gradoni L., Davidson R.N., Orsini S., Betto P., Giambenedetti M., Activity of liposomal amphotericin B (AmBisome) against, J Drug Targeting, 1, pp. 311-316, (1993)
[23]  
Davidson R.N., Russo R., Relapse of visceral leishmaniasis in patients who were coinfectcd with human immunodeficiency virus and who received treatment with liposomal amphotericin B [letter], Clin Infect Dis, 19, (1994)