|
|
||||||||
Pentavalent antimonial compounds have been the mainstay of the treatment of visceral, cutaneous, and mucosal leishmaniasis for approximately half a century. Pentostam (sodium stibogluconate) is the pentavalent antimonial compound available in the United States (through the Centers for Disease Control). As dosage regimens for treating leishmaniasis have evolved, the daily dose of antimony and the duration of therapy have been progressively increased to combat unresponsiveness to therapy. In the 1980s, the use of 20 mg/kg/day (instead of 10 mg/kg/day) of antimony was recommended, but only to a maximum daily dose of 850 mg. The authors have concluded on the basis of recent efficacy and toxicity data that this 850-mg restriction should be removed; the evidence to date, which is summarized here, suggests that a regimen of 20 mg/kg/day of pentavalent antimony, without an upper limit on the daily dose, is more efficacious and is not substantially more toxic than regimens with lower daily doses. We recommend treating all forms of leishmaniasis with a full 20 mg/kg/day of pentavalent antimony. We treat cutaneous leishmaniasis for 20 days and visceral and mucosal leishmaniasis for 28 days. Our judgment of cure is based on clinical criteria.
This article has been cited by other articles:
![]() |
A. J. Krolewiecki, H. D. Romero, S. P. Cajal, D. Abraham, T. Mimori, T. Matsumoto, M. Juarez, and N. J. Taranto A Randomized Clinical Trial Comparing Oral Azithromycin and Meglumine Antimoniate for the Treatment of American Cutaneous Leishmaniasis Caused by Leishmania (Viannia) braziliensis Am J Trop Med Hyg, October 1, 2007; 77(4): 640 - 646. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Foulet, F. Botterel, P. Buffet, G. Morizot, D. Rivollet, M. Deniau, F. Pratlong, J.-M. Costa, and S. Bretagne Detection and Identification of Leishmania Species from Clinical Specimens by Using a Real-Time PCR Assay and Sequencing of the Cytochrome b Gene J. Clin. Microbiol., July 1, 2007; 45(7): 2110 - 2115. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. MORIZOT, P. DELGIUDICE, E. CAUMES, E. LAFFITTE, P. MARTY, A. DUPUY, C. SARFATI, S. HADJ-RABIA, H. DARIE, A.-S. LE GUERN, et al. HEALING OF OLD WORLD CUTANEOUS LEISHMANIASIS IN TRAVELERS TREATED WITH FLUCONAZOLE: DRUG EFFECT OR SPONTANEOUS EVOLUTION? Am J Trop Med Hyg, January 1, 2007; 76(1): 48 - 52. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. St. George, J. V. Bishop, R. G. Titus, and C. P. Selitrennikoff Novel Compounds Active against Leishmania major Antimicrob. Agents Chemother., February 1, 2006; 50(2): 474 - 479. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Blum, P. Desjeux, E. Schwartz, B. Beck, and C. Hatz Treatment of cutaneous leishmaniasis among travellers J. Antimicrob. Chemother., February 1, 2004; 53(2): 158 - 166. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Laguna, S. Videla, M. E. Jimenez-Mejias, G. Sirera, J. Torre-Cisneros, E. Ribera, D. Prados, B. Clotet, M. Sust, R. Lopez-Velez, et al. Amphotericin B lipid complex versus meglumine antimoniate in the treatment of visceral leishmaniasis in patients infected with HIV: a randomized pilot study J. Antimicrob. Chemother., September 1, 2003; 52(3): 464 - 468. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Pagliano, M. Rossi, C. Rescigno, S. Altieri, M. G. Coppola, M. Gramiccia, A. Scalone, L. Gradoni, and F. Faella Mediterranean visceral leishmaniasis in HIV-negative adults: a retrospective analysis of 64 consecutive cases (1995-2001) J. Antimicrob. Chemother., August 1, 2003; 52(2): 264 - 268. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |