Abstract

BackgroundBangladesh is one of the endemic countries for Visceral Leishmaniasis (VL). Médecins Sans Frontières (MSF) ran a VL treatment clinic in the most endemic district (Fulbaria) between 2010 and 2013 using a semi-ambulatory regimen for primary VL of 15mg/kg Liposomal Amphotericin-B (AmBisome) in three equal doses of 5mg/kg. The main objective of this study was to analyze the effectiveness and safety of this regimen after a 12 month follow-up period by retrospective analysis of routinely collected program data. A secondary objective was to explore risk factors for relapse.Methods and Principal FindingsOur analysis included 1521 patients who were initially cured, of whom 1278 (84%) and 1179 (77.5%) were followed-up at 6 and 12 months, respectively. Cure rates at 6 and 12 months were 98.7% (1262/1278) and 96.4% (1137/1179), respectively. Most relapses (26/39) occurred between 6 and 12 months after treatment. Serious adverse events (SAE) were recorded for 7 patients (0.5%). Odds of relapse at 12 months were highest in the youngest and oldest age groups. There was some evidence that spleen size measured on discharge (one month after initiation of treatment) was associated with risk of relapse: OR=1.25 (95% CI 1.01 to 1.55) per cm below lower costal margin (P=0.04).ConclusionsOur study demonstrates that 15mg/kg AmBisome in three doses of 5mg/kg is an effective (>95% cure rate) and safe (<1% SAE) treatment for primary VL in Bangladesh. The majority of relapses occurred between 6 and 12 months, justifying the use of a longer follow-up period when feasible. Assessment of risk of relapse based on easily measured clinical parameters such as spleen size could be incorporated in VL treatment protocols in resource-poor settings where test-of-cure is not always feasible.

Highlights

  • Our study demonstrates that 15mg/kg AmBisome in three doses of 5mg/kg is an effective (>95% cure rate) and safe (

  • Visceral Leishmaniasis (VL), known as Kala Azar, is a vector borne disease caused by parasites of the genus Leishmania, L. donovani—L. infantum complex, which are transmitted through the bite of an infected sand fly, Leishmaniasis infection in humans presents as cutaneous, muco-cutaneous and visceral

  • Of the 1653 patients diagnosed with primary VL during this period, 40 complicated cases were transferred to tertiary care at Mymensingh Medical College

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Summary

Introduction

Visceral Leishmaniasis (VL), known as Kala Azar, is a vector borne disease caused by parasites of the genus Leishmania, L. donovani—L. infantum complex, which are transmitted through the bite of an infected sand fly (mainly genus Phlebotomus, old world, and Lutzomya, new world), Leishmaniasis infection in humans presents as cutaneous, muco-cutaneous and visceral. The Fulbaria district of Bangladesh reported an average annual VL incidence rate of 17.8 per 10,000 people between 2008 and 2013 [4]. This far exceeds the government’s goal of one reported case per 10,000 habitants by the year 2015, as set in the Bangladesh VL Elimination Program in 2005 [4]. SSG is given by intramuscular (IM) injections daily for 28 days This course of treatment is painful, toxic, cumbersome for patients, and costly for the health system. Médecins Sans Frontières (MSF) ran a VL treatment clinic in the most endemic district (Fulbaria) between 2010 and 2013 using a semi-ambulatory regimen for primary VL of 15mg/kg Liposomal Amphotericin-B (AmBisome) in three equal doses of 5mg/kg. A secondary objective was to explore risk factors for relapse

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