Management of disseminated histoplasmosis in a high-complexity clinic in Cali, Colombia.

IF 2.7 3区 医学 Q3 INFECTIOUS DISEASES Medical mycology Pub Date : 2024-07-04 DOI:10.1093/mmy/myae058
Natalia Ramos-Ospina, Indira Carolina Lambertinez-Álvarez, Leidy Johanna Hurtado-Bermúdez, Jenny Patricia Muñoz-Lombo, Juan Diego Vélez-Londoño, Jorge Andrés Valencia-Montagut, Pablo Andrés Moncada-Vallejo
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Abstract

Histoplasmosis presents a substantial clinical challenge globally, with a particular prevalence in South America, especially among patients with concurrent Human Immunodeficiency Virus (HIV) infection. Despite itraconazole's established efficacy, investigating alternative therapeutic approaches remains imperative. This is the largest study in our region to date, assessing the effectiveness of the less explored posaconazole treatment. This observational study, conducted at Fundación Valle del Lili (FVL) from 2016 to 2022, encompassed adults with disseminated histoplasmosis. Patients (n = 31) were treated with liposomal amphotericin B as an initial treatment, followed by consolidation treatment with posaconazole or itraconazole. Patients with single-organ cases, those lacking microbiological diagnosis, those who received initial treatment with antifungals other than liposomal Amphotericin B and those with < 6 months follow-up were excluded (Figure 1). Analyses considered population characteristics, treatments, and outcomes. Patients (average age: 45.6; 58.1% female) had common comorbidities (HIV 38.7%, solid organ transplantation 29% and oncologic disease 12.9%). Lungs (48.4%) and lymph nodes (16.1%) were commonly affected. Biopsy (64.5%) was the primary diagnostic method. Initial treatment with liposomal amphotericin B (100%) was given for 14 days on average. Follow-up indicated 71% completion with 19.4% requiring treatment modifications. Notably, 70.9% completed a posaconazole consolidation regimen over 350 days on average. Drug interactions during consolidation (80.6%) were common. No relapses occurred, and three deaths unrelated to histoplasmosis were reported. Traditionally, itraconazole has been the prevalent initial treatment; however, in our cohort, 55.9% of patients received posaconazole as the primary option. Encouragingly, posaconazole showed favorable tolerance and infection resolution, suggesting its potential as an effective and well-tolerated alternative for consolidation treatment. This finding prompts further exploration of posaconazole, potentially leading to more effective patient care and better outcomes.

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哥伦比亚卡利一家高难度诊所对播散性组织胞浆菌病的管理。
组织胞浆菌病是全球面临的一项重大临床挑战,在南美洲尤为流行,特别是在同时感染人类免疫缺陷病毒(HIV)的患者中。尽管伊曲康唑具有公认的疗效,但研究替代治疗方法仍然势在必行。这是迄今为止本地区规模最大的一项研究,旨在评估探索较少的泊沙康唑治疗方法的有效性。这项观察性研究于2016年至2022年在Fundación Valle del Lili(FVL)进行,涵盖了患有播散性组织胞浆菌病的成人患者。患者(n = 31)在接受脂质体两性霉素B的初始治疗后,再接受泊沙康唑或伊曲康唑的巩固治疗。单器官病例患者、缺乏微生物学诊断的患者、接受过两性霉素 B 脂质体以外的其他抗真菌药物初始治疗的患者,以及有下列情况之一的患者,均被排除在外
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来源期刊
Medical mycology
Medical mycology 医学-兽医学
CiteScore
5.70
自引率
3.40%
发文量
632
审稿时长
12 months
期刊介绍: Medical Mycology is a peer-reviewed international journal that focuses on original and innovative basic and applied studies, as well as learned reviews on all aspects of medical, veterinary and environmental mycology as related to disease. The objective is to present the highest quality scientific reports from throughout the world on divergent topics. These topics include the phylogeny of fungal pathogens, epidemiology and public health mycology themes, new approaches in the diagnosis and treatment of mycoses including clinical trials and guidelines, pharmacology and antifungal susceptibilities, changes in taxonomy, description of new or unusual fungi associated with human or animal disease, immunology of fungal infections, vaccinology for prevention of fungal infections, pathogenesis and virulence, and the molecular biology of pathogenic fungi in vitro and in vivo, including genomics, transcriptomics, metabolomics, and proteomics. Case reports are no longer accepted. In addition, studies of natural products showing inhibitory activity against pathogenic fungi are not accepted without chemical characterization and identification of the compounds responsible for the inhibitory activity.
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