Literature DB >> 7519887

Pancreatitis induced by pentavalent antimonial agents during treatment of leishmaniasis.

R A Gasser1, A J Magill, C N Oster, E D Franke, M Grögl, J D Berman.   

Abstract

Pentavalent antimony (Sbv), formulated as sodium stibogluconate or meglumine antimoniate, is the standard treatment for the leishmaniases. In 16 of 17 consecutive, prospectively observed patients in Washington D.C., serum levels of amylase and lipase rose to abnormal values after therapy with sodium stibogluconate was started; 12 of 17 had symptoms of pancreatitis. Sbv therapy was continued to completion in 7 of 17 patients and interrupted in 10 of 17. Pancreatitis improved in every patient after Sbv therapy was stopped. Sbv treatment was resumed after brief interruptions in 6 of 10 patients. All six of these patients had flares of pancreatitis, but each completed therapy. Subsequently, we measured amylase and lipase levels in stored sera from 32 patients treated in Peru with either sodium stibogluconate or meglumine antimoniate for mucosal leishmaniasis. In all 32 Peruvian patients, serum amylase and lipase rose to abnormal levels during Sbv therapy; 11 of 32 had symptoms of pancreatitis. Standard Sbv regimens induce pancreatitis in almost all patients, but continued therapy is often tolerated; pancreatitis subsides when therapy is stopped, and rechallenge may be tolerated after a brief halt in treatment.

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Year:  1994        PMID: 7519887     DOI: 10.1093/clinids/18.1.83

Source DB:  PubMed          Journal:  Clin Infect Dis        ISSN: 1058-4838            Impact factor:   9.079


  24 in total

1.  Pancreatitis associated with N-methyl-glucamine therapy in a dog with leishmaniasis.

Authors:  G Aste; M Di Tommaso; J M Steiner; D A Williams; A Boari
Journal:  Vet Res Commun       Date:  2005-08       Impact factor: 2.459

2.  Acute pancreatitis due to zinc phosphide ingestion.

Authors:  P S Sarma; J Narula
Journal:  Postgrad Med J       Date:  1996-04       Impact factor: 2.401

3.  Efficacy and safety of liposomal amphotericin B (AmBisome) for visceral leishmaniasis in endemic developing countries.

Authors:  J D Berman; R Badaro; C P Thakur; K M Wasunna; K Behbehani; R Davidson; F Kuzoe; L Pang; K Weerasuriya; A D Bryceson
Journal:  Bull World Health Organ       Date:  1998       Impact factor: 9.408

Review 4.  Leishmania and human immunodeficiency virus coinfection: the first 10 years.

Authors:  J Alvar; C Cañavate; B Gutiérrez-Solar; M Jiménez; F Laguna; R López-Vélez; R Molina; J Moreno
Journal:  Clin Microbiol Rev       Date:  1997-04       Impact factor: 26.132

Review 5.  Potential of Piper spp. as a source of new compounds for the leishmaniases treatment.

Authors:  Juliana Figueiredo Peixoto; Ygor Jessé Ramos; Davyson de Lima Moreira; Carlos Roberto Alves; Luiz Filipe Gonçalves-Oliveira
Journal:  Parasitol Res       Date:  2021-07-10       Impact factor: 2.289

6.  Efficacy of the triazole SCH 56592 against Leishmania amazonensis and Leishmania donovani in experimental murine cutaneous and visceral leishmaniases.

Authors:  H M Al-Abdely; J R Graybill; D Loebenberg; P C Melby
Journal:  Antimicrob Agents Chemother       Date:  1999-12       Impact factor: 5.191

7.  Antimony and health.

Authors:  F A De Wolff
Journal:  BMJ       Date:  1995-05-13

Review 8.  Adverse effects of chemotherapeutic agents used in tropical medicine.

Authors:  G C Cook
Journal:  Drug Saf       Date:  1995-07       Impact factor: 5.606

Review 9.  Practical guide for the treatment of leishmaniasis.

Authors:  R N Davidson
Journal:  Drugs       Date:  1998-12       Impact factor: 9.546

10.  Bismuth(III) α-hydroxy carboxylates: highly selective toxicity of glycolates towards Leishmania major.

Authors:  Allan Loh; Yih Ching Ong; Victoria L Blair; Lukasz Kedzierski; Philip C Andrews
Journal:  J Biol Inorg Chem       Date:  2015-09-28       Impact factor: 3.358

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