Literature DB >> 28898610

[Visceral Leishmaniasis in HIV-Infected Patients: The Challenge of Relapse and Treatment Failure].

Patrícia Cipriano1, Ana Cláudia Miranda2, Isabel Antunes2, Kamal Mansinho2.   

Abstract

INTRODUCTION: Visceral leishmaniasis is an endemic disseminated infection, considered to be the third most frequent opportunistic parasitic infection in Europe. It is especially prevalent in patients co-infected with human immunodeficiency virus, in whom it poses a great therapeutic challenge due to increased risk of relapse. The goal of this study is to characterize a population of co-infected patients, as well as the efficiency of the adopted treatment strategies.
MATERIAL AND METHODS: Retrospective study with a sample composed of all patients with visceral leishmaniasis and human immunodeficiency virus admitted in an Infectious Diseases ward over a period of 10 years.
RESULTS: Of the 23 enrolled patients, two were female (8.7%). The mean TCD4+ cell count was 104.4 cells/uL (± 120.3cells/uL), only two patients had undetectable viral load (< 20 copies/mL) and 16 (69.6%) were not under antiretroviral therapy at the time of diagnosis. Treatment-wise, liposomal amphotericin B was used in 18 patients, meglumine antimoniate in four and miltefosine in one. Fourteen (60.9%) were adherent to secondary prophylaxis protocol. A relapse rate of 26.1% was observed (six patients). DISCUSSION: Co-infection is responsible for higher treatment failure rates and more relapses. TCD4+ cell count is the main predictive factor of relapse, and strict adherence to chemoprophylaxis protocols unequivocally results in a reduction of relapse rate. Combined treatment strategies using liposomal amphotericin B and miltefosine yield fewer therapeutic failures than the classic approach.
CONCLUSION: We therefore conclude that alternative, combined therapeutic protocols seem to be a viable solution for these patients.

Entities:  

Keywords:  HIV Infections; Leishmaniasis, Visceral; Recurrence; Treatment Failure

Mesh:

Year:  2017        PMID: 28898610     DOI: 10.20344/amp.8291

Source DB:  PubMed          Journal:  Acta Med Port        ISSN: 0870-399X


  3 in total

1.  Meglumine antimoniate combination treatment for relapsing Kala-azar after treatment and secondary prophylaxis failure with liposomal amphotericin B in two HIV-coinfected patients.

Authors:  Lara Camara; João Queirós; Rita Ribeiro; Eugénio Teófilo
Journal:  BMJ Case Rep       Date:  2019-12-16

2.  ChimLeish, a new recombinant chimeric protein evaluated as a diagnostic and prognostic marker for visceral leishmaniasis and human immunodeficiency virus coinfection.

Authors:  Nathalia C Galvani; Amanda S Machado; Daniela P Lage; Camila S Freitas; Danniele L Vale; Daysiane de Oliveira; Fernanda Ludolf; Fernanda F Ramos; Bruna B Fernandes; Gabriel P Luiz; Débora V C Mendonça; João A Oliveira-da-Silva; Thiago A R Reis; Grasiele S V Tavares; Ana T Chaves; Nathalia S Guimarães; Unaí Tupinambás; Gláucia F Cota; Maria V Humbert; Vívian T Martins; Myron Christodoulides; Eduardo A F Coelho; Ricardo A Machado-de-Ávila
Journal:  Parasitol Res       Date:  2021-10-19       Impact factor: 2.289

3.  Cinnamides Target Leishmania amazonensis Arginase Selectively.

Authors:  Edson Roberto da Silva; Júlio Abel Alfredo Dos Santos Simone Come; Simone Brogi; Vincenzo Calderone; Giulia Chemi; Giuseppe Campiani; Trícia Maria Ferrreira de Sousa Oliveira; Thanh-Nhat Pham; Marc Pudlo; Corine Girard; Claudia do Carmo Maquiaveli
Journal:  Molecules       Date:  2020-11-12       Impact factor: 4.411

  3 in total

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