Literature DB >> 21706927

Glucantime efficacy in the treatment of zoonotic cutaneous leishmaniasis.

B Pourmohammadi1, M H Motazedian, F Handjani, G H R Hatam, S Habibi, B Sarkari.   

Abstract

Pentavalent antimony (SbV) compounds are still considered the first line of treatment for all forms of leishmaniasis. There have been reports of drug resistance and unresponsiveness to treatment with these drugs. We investigated the clinical response to treatment of cutaneous leishmaniasis with glucantime, the drug of choice for all forms of leishmaniasis in Iran. All individuals suspected of cutaneous leishmaniasis from October 2007 to March 2008 were included in the study if met specific criteria. After laboratory diagnosis and parasite identification by PCR, 43 patients agreed to participate and complete the protocol for treatment. Meglumine antimoniate (glucantime) was given at a dose of 20 mg/kg/day for 20 days (two 10-day periods) according to a World Health Organization (WHO) recommended protocol. Response to treatment was evaluated 6 weeks after initiation of treatment. Fifteen patients (34.9%) were clinically unresponsive to glucantime treatment while the remaining 28 patients (65.1%) responded to treatment. There were no statistically significant differences by occupation, gender, chronicity of the disease before starting treatment, number of lesions, or age between the glucantime sensitive and resistant patients. Our study showed a significant level of unresponsiveness to glucantime among patients with cutaneous leishmaniasis caused by Leishmania major in Iran. These findings highlight the need for new treatment regimens.

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Year:  2011        PMID: 21706927

Source DB:  PubMed          Journal:  Southeast Asian J Trop Med Public Health        ISSN: 0125-1562            Impact factor:   0.267


  15 in total

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Authors:  Afsaneh Vazin; Mohammad Saleh Heidaripour; Mohsen Kalantari; Gholamreza Hatam
Journal:  J Parasit Dis       Date:  2022-02-11

3.  Effects of topical gel formulation of Ficus carica latex on cutaneous leishmaniasis induced by Leishmania major in BALB/c mice.

Authors:  Ali Pouryousef; Erfan Eslami; Sepehr Shahriarirad; Sina Zoghi; Mehdi Emami; Mohammad Reza Cheraghi; Bardia Zamiri; Soliman Mohammadi-Samanii; Bahador Sarkari
Journal:  BMC Res Notes       Date:  2021-05-22

4.  P-glycoprotein A Gene Expression in Glucantime-Resistant and Sensitive Leishmania major (MRHO/IR/75/ER).

Authors:  Simindokht Soleimanifard; Reza Arjmand; Sedighe Saberi; Ali Khamesipour; Mohammad Kazemi; Mansoor Salehi; Mojtaba Akbari; SeyedHossein Hejazi
Journal:  Iran J Parasitol       Date:  2014-09       Impact factor: 1.012

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Journal:  PLoS Negl Trop Dis       Date:  2018-03-21

6.  Effect of hydroalcoholic extract of Echinacea purpurea in combination with meglumine antimoniate on treatment of Leishmania major-induced cutaneous leishmaniasis in BALB/c mice.

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Review 7.  Determinants of Unresponsiveness to Treatment in Cutaneous Leishmaniasis: A Focus on Anthroponotic Form Due to Leishmania tropica.

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8.  Comparison of Agar Dilution, Broth Dilution, Cylinder Plate and Disk Diffusion Methods for Evaluation of Anti-leishmanial Drugs on Leishmania promastigotes.

Authors:  T Mohammadzadeh; Sm Sadjjadi; P Habibi; B Sarkari
Journal:  Iran J Parasitol       Date:  2012       Impact factor: 1.012

9.  The activity of ozonated olive oil against Leishmania major promastigotes.

Authors:  Omid Rajabi; Ameneh Sazgarnia; Fatemeh Abbasi; Pouran Layegh
Journal:  Iran J Basic Med Sci       Date:  2015-09       Impact factor: 2.699

10.  Visceral Leishmaniasis in Southwestern Iran: A Retrospective Clinico-Hematological Analysis of 380 Consecutive Hospitalized Cases (1999-2014).

Authors:  Bahador Sarkari; Tahereh Naraki; Mohammad Amin Ghatee; Samaneh Abdolahi Khabisi; Mohammad Hassan Davami
Journal:  PLoS One       Date:  2016-03-04       Impact factor: 3.240

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