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[Methylglucamine antimoniate and sodium stibogluconate in the treatment of leishmaniasis. Study of 16 cases].

Abstract
Treatment of visceral and cutaneous leishmaniasis rests on pentavalent antimonial drugs. However, side effects are often a problem and resistance may emerge. N-methyl-glucamine given for kala-azar induced hematologic or hepatic toxicity in three patients and failed in two. Four patients with cutaneous leishmaniasis recovered but two exhibited adverse side effects. Sodium stibo-gluconate failed in one of three kala-azar patients and in one of two patients with cutaneous leishmaniasis. The effects of these two drugs are discussed, as well as indications of pentamidine and splenectomy.
AuthorsP Bourée, M L Anciaux, P Taugourdeau
JournalPathologie-biologie (Pathol Biol (Paris)) Vol. 33 Issue 5 Pt 2 Pg. 607-10 (Jun 1985) ISSN: 0369-8114 [Print] France
Vernacular TitleAntimoniate de méthyl-glucamine et stibo-gluconate de sodium dans le traitement des leishmanioses. Etude de seize cas.
PMID3003657 (Publication Type: Journal Article)
Chemical References
  • Gluconates
  • Organometallic Compounds
  • Pentamidine
  • Meglumine
  • Meglumine Antimoniate
  • Antimony
  • Antimony Sodium Gluconate
Topics
  • Adolescent
  • Adult
  • Antimony (adverse effects, therapeutic use)
  • Antimony Sodium Gluconate (adverse effects, therapeutic use)
  • Child
  • Child, Preschool
  • Female
  • Gluconates (therapeutic use)
  • Humans
  • Infant
  • Leishmaniasis (drug therapy, therapy)
  • Leishmaniasis, Visceral (drug therapy, therapy)
  • Male
  • Meglumine
  • Meglumine Antimoniate
  • Organometallic Compounds
  • Pentamidine (therapeutic use)
  • Splenectomy

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