Literature DB >> 12612746

Predictors of an unsatisfactory response to pentavalent antimony in the treatment of American visceral leishmaniasis.

Mácia A Santos1, Raynério C Marques, Carolinne A Farias, Danielle M Vasconcelos, Jay M Stewart, Dorcas L Costa, Carlos H N Costa.   

Abstract

Although treatment of visceral leishmaniasis with pentavalent antimony is usually successful, some patients require second-line drug therapy, most commonly with amphotericin B. To identify the clinical characteristics that predict an inadequate response to pentavalent antimony, a case-control study was undertaken in Teresina, Piaui, Brazil. Over a two-year period, there were 19 cases of VL in which the staff physicians of a hospital prescribed second-line therapy with amphotericin B after determining that treatment with pentavalent antimony had failed. The control group consisted of 97 patients that were successfully treated with pentavalent antimony. A chart review using univariate and multivariate analysis was performed. The cure rate was 90% with amphotericin B. The odds ratio for the prescription of amphotericin B was 10.2 for children less than one year old, compared with individuals aged over 10 years. Patients who presented coinfection had an OR of 7.1 while those on antibiotics had an OR of 2.8. These data support either undertaking a longer course of therapy with pentavalent antimony for children or using amphotericin B as a first-line agent for children and individuals with coinfections. It also suggests that chemoprophylaxis directed toward bacterial coinfection in small children with VL may be indicated.

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Year:  2003        PMID: 12612746     DOI: 10.1590/s0037-86822002000600014

Source DB:  PubMed          Journal:  Rev Soc Bras Med Trop        ISSN: 0037-8682            Impact factor:   1.581


  14 in total

1.  Treatment of visceral leishmaniasis in children in the Central-West Region of Brazil.

Authors:  Y M Brustoloni; R V Cunha; L Z Cônsolo; A L L Oliveira; M E C Dorval; E T Oshiro
Journal:  Infection       Date:  2010-05-28       Impact factor: 3.553

2.  Visceral leishmaniasis relapse in Southern Sudan (1999-2007): a retrospective study of risk factors and trends.

Authors:  Stanislaw Gorski; Simon M Collin; Koert Ritmeijer; Kees Keus; Francis Gatluak; Marius Mueller; Robert N Davidson
Journal:  PLoS Negl Trop Dis       Date:  2010-06-08

Review 3.  Therapeutic options for visceral leishmaniasis.

Authors:  Begoña Monge-Maillo; Rogelio López-Vélez
Journal:  Drugs       Date:  2013-11       Impact factor: 9.546

4.  Parasite load and risk factors for poor outcome among children with visceral leishmaniasis. A cohort study in Belo Horizonte, Brazil, 2010-2011.

Authors:  Maria Vitória Assumpção Mourão; Antonio Toledo; Luciana Inácia Gomes; Verônica Vieira Freire; Ana Rabello
Journal:  Mem Inst Oswaldo Cruz       Date:  2014-03-04       Impact factor: 2.743

5.  Visceral leishmaniasis treatment outcome and its determinants in northwest Ethiopia.

Authors:  Getachew Mebrahtu Welay; Kefyalew Addis Alene; Berihun Assefa Dachew
Journal:  Epidemiol Health       Date:  2016-12-28

Review 6.  Control of visceral leishmaniasis in latin america-a systematic review.

Authors:  Gustavo A S Romero; Marleen Boelaert
Journal:  PLoS Negl Trop Dis       Date:  2010-01-19

7.  Leishmania donovani infection induces anemia in hamsters by differentially altering erythropoiesis in bone marrow and spleen.

Authors:  William P Lafuse; Ryan Story; Jocelyn Mahylis; Gaurav Gupta; Sanjay Varikuti; Heidi Steinkamp; Steve Oghumu; Abhay R Satoskar
Journal:  PLoS One       Date:  2013-03-22       Impact factor: 3.240

8.  Zinc/copper imbalance reflects immune dysfunction in human leishmaniasis: an ex vivo and in vitro study.

Authors:  Johan Van Weyenbergh; Gisélia Santana; Argemiro D'Oliveira; Anibal F Santos; Carlos H Costa; Edgar M Carvalho; Aldina Barral; Manoel Barral-Netto
Journal:  BMC Infect Dis       Date:  2004-11-17       Impact factor: 3.090

Review 9.  Risk factors for adverse prognosis and death in American visceral leishmaniasis: a meta-analysis.

Authors:  Vinícius Silva Belo; Claudio José Struchiner; David Soeiro Barbosa; Bruno Warlley Leandro Nascimento; Marco Aurélio Pereira Horta; Eduardo Sérgio da Silva; Guilherme Loureiro Werneck
Journal:  PLoS Negl Trop Dis       Date:  2014-07-24

10.  TNF signalling drives expansion of bone marrow CD4+ T cells responsible for HSC exhaustion in experimental visceral leishmaniasis.

Authors:  Ana Isabel Pinto; Najmeeyah Brown; Olivier Preham; Johannes S P Doehl; Helen Ashwin; Paul M Kaye
Journal:  PLoS Pathog       Date:  2017-07-03       Impact factor: 6.823

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