98%
921
2 minutes
20
Post-kala-azar dermal leishmaniasis (PKDL) is widely prevalent in the endemic regions of India, but its treatment remains unsatisfactory. The WHO recommends a 12-week treatment with oral miltefosine, but its ocular toxicities are a serious concern. The late 1980s and early 1990s saw the use of sodium stibogluconate and amphotericin B (AmB) for a brief period. Both drugs had frequent adverse events and were expensive, and the duration of treatments was unacceptably long. This retrospective study evaluated, analyzed, and reported the outcomes of PKDL patients treated with a shorter course of AmB, the most effective antileishmanial drug. The hospital records of PKDL patients treated with AmB by 30 alternate-day infusions over 60 days (instead of conventional 60-80 infusions over 100-120 days) between September 2010 and August 2016 were reviewed. Only patients with confirmed parasitological diagnosis were included. Their records were studied for treatment-related adverse events, end-of-treatment parasitological status, and 12-month follow-up results. One hundred two patients were eligible for this study between September 2010 and August 2016. After therapy, 92/102 (90.2%) patients improved; 3 (2.9%) had to cease treatment owing to severe adverse effects, and one died of severe diarrhea unrelated to AmB. Six (5.9%) patients withdrew consent before the treatment was complete. At the 12-month evaluation, 89/102 (87.3%) patients attained a final cure. A 30-infusion regimen of AmB remains highly effective in PKDL. Without a shorter, safer, and more economical regimen for the treatment of PKDL, it should be used until a better regimen is available.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11229639 | PMC |
http://dx.doi.org/10.4269/ajtmh.23-0738 | DOI Listing |
PLoS Negl Trop Dis
August 2025
Department of General Medicine, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India.
The earliest record of visceral leishmaniasis (kala-azar, KA, VL) dates back two centuries from Jessore (now in Bangladesh), with 0.75 million deaths in 3 years. In the 1950s, there was extensive insecticide dichlorodiphenyltrichloroethane (DDT) spray under the aegis of the National Malaria Eradication Program.
View Article and Find Full Text PDFFront Cell Infect Microbiol
July 2025
Immunology & Infection Laboratory, QIMR Berghofer Medical Research Institute, Herston, QLD, Australia.
Sci Rep
July 2025
Laboratory of Molecular Biochemistry and Cell Biology, Department of Biochemistry, ICMR-Rajendra Memorial Research Institute of Medical Sciences (RMRIMS), Agam Kuan, Patna, India.
Post Kala-azar Dermal Leishmaniasis (PKDL) is a complication of Visceral Leishmaniasis (VL) and acts as a reservoir for Leishmania parasites. With climatic changes and ozone depletion increasing ultraviolet radiation (UVR), we investigated the connection between UVR and PKDL development. We have measured sun-light UVR intensities by UV light meters and satellite-based methods.
View Article and Find Full Text PDFBMC Infect Dis
July 2025
ICMR-Rajendra Memorial Research Institute of Medical Sciences, Agamkuan, Patna, Bihar, 800007, India.
Background: Visceral leishmaniasis-human immunodeficiency virus (VL-HIV) co-infection has emerged as a serious concern, which could adversely affect the VL elimination efforts of the country. These patients have a poor VL therapeutic success rate, more drug-related toxicity, and relapses resulting in high mortality. Despite the emerging pattern of VL-HIV co-infection, there have been limited studies analyzing the presentation of VL-HIV co-infection in Bihar, India.
View Article and Find Full Text PDFBMJ Open
June 2025
Department of General Internal Medicine, University of Washington, Seattle, Washington, USA.
Objectives: With recent efforts to eliminate visceral leishmaniasis in East Africa, we aimed to map the breadth of research on leishmaniases in Ethiopia, one of the high-endemic countries in the region, to help understand the current literature landscape and highlight priority areas for future research.
Design: The scoping review was conducted in accordance with the JBI Scoping Review Methodology Group's guidance and reported following Preferred Reporting Items for Systematic Reviews and Meta-Analyses-Extension for Scoping Reviews guidelines.
Data Sources: We searched the following databases and sources: PubMed, Embase, Web of Science, Cochrane Library, Global Medicus Index, PROSPERO, ClinicalTrials.