Unresponsiveness to AmBisome in some Sudanese patients with kata-azar

被引:55
作者
Mueller, Marius [1 ]
Ritmeijer, Koert [1 ]
Balasegaram, Manica [1 ]
Koummuki, Youssif [1 ]
Santana, Muriel Ramirez [1 ]
Davidson, Robert [1 ]
机构
[1] Med Sans Frontieres, NL-1018 DD Amsterdam, Netherlands
关键词
visceral leishmaniasis; kala-azar; AmBisome; Sudan;
D O I
10.1016/j.trstmh.2006.02.005
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
In Sudan, two treatments are currently registered for visceral. leishmaniasis: sodium stibogluconate (SSG) as first line and liposomal amphotericin B (AmBisome) as second line. We present 64 patients (52 relapse cases to SSG, 12 new but complicated cases) treated with AmBisome in eastern Sudan. AmBisome was administered at 2.5-8.2 mg/kg (15-49 mg/kg in total) per dose six times (days 1, 2, 3, 5, 10, 15) as an intravenous infusion. We measured outcome according to clinical response and parasitological clearance (lymph node aspiration). Patient outcomes fell into three groups: group 1, clinical responders (cured) with a negative test of cure (n = 35); group 2, clinical responders with a positive test of cure (n = 19); group 3, clinical non-responders (failures) with a positive test of cure (n = 10). Of the 10 failures, six were already relapse cases. All of group 3, and 15 from group 2, were also treated with additional. SSG (20 mg/kg intramuscularly daily for 30-50 d) with resulting clinical and parasitological, improvement. Parasite persistence and clinical. failure were associated with a higher parasite density on admission (P< 0.002) and underlying immunosuppressive disease: tuberculosis (three cases) or HIV (two cases). Because AmBisome monotherapy may fail in Sudan, a combination of AmBisome and SSG is recommended for relapse cases. (C) 2006 Royal Society of Tropical, Medicine and Hygiene. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:19 / 24
页数:6
相关论文
共 13 条
[1]   AmBisome: liposomal formulation, structure, mechanism of action and pre-clinical experience [J].
Adler-Moore, J ;
Proffitt, RT .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2002, 49 :21-30
[2]   Current treatment approaches to leishmaniasis [J].
Berman, J .
CURRENT OPINION IN INFECTIOUS DISEASES, 2003, 16 (05) :397-401
[3]  
Berman JD, 1998, B WORLD HEALTH ORGAN, V76, P25
[4]   Recent developments in leishmaniasis: Epidemiology, diagnosis, and treatment [J].
Berman J. .
Current Infectious Disease Reports, 2005, 7 (1) :33-38
[5]  
CHULAY JD, 1983, AM J TROP MED HYG, V32, P475, DOI 10.4269/ajtmh.1983.32.475
[6]   RELAPSE OF VISCERAL LEISHMANIASIS IN PATIENTS WHO WERE COINFECTED WITH HUMAN-IMMUNODEFICIENCY-VIRUS AND WHO RECEIVED TREATMENT WITH LIPOSOMAL AMPHOTERICIN-B [J].
DAVIDSON, RN ;
RUSSO, R .
CLINICAL INFECTIOUS DISEASES, 1994, 19 (03) :560-560
[7]   In vitro reversion of amphotericin B resistance in Leishmania donovani by poloxamer 188 [J].
Espuelas, S ;
Legrand, P ;
Loiseau, PM ;
Bories, C ;
Barratt, C ;
Irache, JM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (08) :2190-2192
[8]  
FREIRE M, 1997, J INFECT DIS, V1, P230
[9]   Liposomal amphotericin B in secondary prophylaxis of visceral leishmaniasis in HIV-infected patients: report of five clinical cases [J].
Montana, M ;
Chochoi, N ;
Monges, P ;
Ravaux, I ;
Faraut, F ;
Gensollen, S ;
Bongrand, MC ;
Timon-David, R ;
Gallais, H .
PATHOLOGIE BIOLOGIE, 2004, 52 (02) :66-75
[10]  
*NMSLA SUD, 2004, MAN DIAGN TREATM LEI