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Efficacy of oral miltefosine in visceral leishmaniasis in rural West Bengal, India

CONTEXT: Visceral leishmaniasis (VL), also known as Kala-azar (KA) is a public health problem of tropical and subtropical countries, which infects about 12 million people annually, out of which about 1.5 million are new cases. India contributes a major share of the global burden of VL. For many year...

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Autores principales: Patra, Pradyumna, Guha, Subhasish K., Maji, Ardhendu Kumar, Saha, Pabitra, Ganguly, Swagata, Chakraborty, Abhiram, Kundu, Pratip K., Sarker, Sachchidananda, Ray, Krishnangshu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3469955/
https://www.ncbi.nlm.nih.gov/pubmed/23087513
http://dx.doi.org/10.4103/0253-7613.99326
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author Patra, Pradyumna
Guha, Subhasish K.
Maji, Ardhendu Kumar
Saha, Pabitra
Ganguly, Swagata
Chakraborty, Abhiram
Kundu, Pratip K.
Sarker, Sachchidananda
Ray, Krishnangshu
author_facet Patra, Pradyumna
Guha, Subhasish K.
Maji, Ardhendu Kumar
Saha, Pabitra
Ganguly, Swagata
Chakraborty, Abhiram
Kundu, Pratip K.
Sarker, Sachchidananda
Ray, Krishnangshu
author_sort Patra, Pradyumna
collection PubMed
description CONTEXT: Visceral leishmaniasis (VL), also known as Kala-azar (KA) is a public health problem of tropical and subtropical countries, which infects about 12 million people annually, out of which about 1.5 million are new cases. India contributes a major share of the global burden of VL. For many years leishmaniasis has been treated with pentavalent antimonials. Antimony resistance is a problem in India and in other different geographic areas of the world. Amphotericin B deoxycholate and pentamidine isethionate are effective by parenteral administration and associated with toxicities. The quest for an effective, orally administered, non-toxic and less expensive alternative resulted in the identification of miltefosine (hexadecylphosphocholine). In India, therapeutic efficacy of miltefosine in VL was assessed by many groups of scientists, mainly from Bihar and Uttar Pradesh. No such data is available from West Bengal. AIMS: The present study was designed to observe the efficacy of miltefosine in VL in rural West Bengal. MATERIALS AND METHODS: A total of 71 parasitologically proven VL patients participated in the study who received miltefosine in accordance with the National Vector Born Disease Control Programme (NVBDCP) of India and were followed up for the following one year. RESULTS: The overall efficacy of the drug was 93% and no significant adverse side effects were observed during the study period. CONCLUSIONS: The study concludes that miltefosine is effective, well tolerated, and easily administrable drug in the treatment of visceral leishmaniasis at the field levels.
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spelling pubmed-34699552012-10-19 Efficacy of oral miltefosine in visceral leishmaniasis in rural West Bengal, India Patra, Pradyumna Guha, Subhasish K. Maji, Ardhendu Kumar Saha, Pabitra Ganguly, Swagata Chakraborty, Abhiram Kundu, Pratip K. Sarker, Sachchidananda Ray, Krishnangshu Indian J Pharmacol Research Article CONTEXT: Visceral leishmaniasis (VL), also known as Kala-azar (KA) is a public health problem of tropical and subtropical countries, which infects about 12 million people annually, out of which about 1.5 million are new cases. India contributes a major share of the global burden of VL. For many years leishmaniasis has been treated with pentavalent antimonials. Antimony resistance is a problem in India and in other different geographic areas of the world. Amphotericin B deoxycholate and pentamidine isethionate are effective by parenteral administration and associated with toxicities. The quest for an effective, orally administered, non-toxic and less expensive alternative resulted in the identification of miltefosine (hexadecylphosphocholine). In India, therapeutic efficacy of miltefosine in VL was assessed by many groups of scientists, mainly from Bihar and Uttar Pradesh. No such data is available from West Bengal. AIMS: The present study was designed to observe the efficacy of miltefosine in VL in rural West Bengal. MATERIALS AND METHODS: A total of 71 parasitologically proven VL patients participated in the study who received miltefosine in accordance with the National Vector Born Disease Control Programme (NVBDCP) of India and were followed up for the following one year. RESULTS: The overall efficacy of the drug was 93% and no significant adverse side effects were observed during the study period. CONCLUSIONS: The study concludes that miltefosine is effective, well tolerated, and easily administrable drug in the treatment of visceral leishmaniasis at the field levels. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3469955/ /pubmed/23087513 http://dx.doi.org/10.4103/0253-7613.99326 Text en Copyright: © Indian Journal of Pharmacology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Patra, Pradyumna
Guha, Subhasish K.
Maji, Ardhendu Kumar
Saha, Pabitra
Ganguly, Swagata
Chakraborty, Abhiram
Kundu, Pratip K.
Sarker, Sachchidananda
Ray, Krishnangshu
Efficacy of oral miltefosine in visceral leishmaniasis in rural West Bengal, India
title Efficacy of oral miltefosine in visceral leishmaniasis in rural West Bengal, India
title_full Efficacy of oral miltefosine in visceral leishmaniasis in rural West Bengal, India
title_fullStr Efficacy of oral miltefosine in visceral leishmaniasis in rural West Bengal, India
title_full_unstemmed Efficacy of oral miltefosine in visceral leishmaniasis in rural West Bengal, India
title_short Efficacy of oral miltefosine in visceral leishmaniasis in rural West Bengal, India
title_sort efficacy of oral miltefosine in visceral leishmaniasis in rural west bengal, india
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3469955/
https://www.ncbi.nlm.nih.gov/pubmed/23087513
http://dx.doi.org/10.4103/0253-7613.99326
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