Journal of Fungi (Apr 2022)

Severe Sporotrichosis Treated with Amphotericin B: A 20-Year Cohort Study in an Endemic Area of Zoonotic Transmission

  • Vivian Fichman,
  • Dayvison Francis Saraiva Freitas,
  • Antonio Carlos Francesconi do Valle,
  • Rogerio Valls de Souza,
  • André Luiz Land Curi,
  • Cláudia Maria Valete-Rosalino,
  • Priscila Marques de Macedo,
  • Andréa Gina Varon,
  • Maria Helena Galdino Figueiredo-Carvalho,
  • Fernando Almeida-Silva,
  • Rosely Maria Zancopé-Oliveira,
  • Raquel de Vasconcelos Carvalhaes Oliveira,
  • Rodrigo Almeida-Paes,
  • Maria Clara Gutierrez-Galhardo

DOI
https://doi.org/10.3390/jof8050469
Journal volume & issue
Vol. 8, no. 5
p. 469

Abstract

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Although rare, disseminated sporotrichosis is increasing in several countries. Despite its limiting toxic potential, amphotericin B is the only intravenous antifungal available to treat severe sporotrichosis. We aimed to describe the effectiveness and safety of amphotericin B treatment for severe sporotrichosis. Clinical records of patients with disseminated sporotrichosis at a reference center were reviewed. This study included 73 patients. Most (53.4%) were men and non-white. HIV coinfection was the main comorbidity (52.1%). Most reported contact with cats (76.7%). Sporothrix brasiliensis was the causative species. Affected sites were skin (98.6%), osteoarticular system (64.4%), upper airway (42.5%), central nervous system (20.5%), eyes (12.3%), and lungs (8.2%). Median doses of amphotericin B used were 750 mg and 4500 mg for deoxycholate and lipid complex formulations, respectively. Amphotericin B discontinuation occurred in 20.5% due to adverse events, mainly azotemia. The outcomes included cure (52.1%), death due to sporotrichosis (21.9%), death due to other causes (9.6%), and loss to follow-up (8.2%). Survival analysis showed an association between cure and the absence of bone, upper airway, and central nervous system involvement. Amphotericin B is the first-choice treatment for disseminated sporotrichosis; however, the severity of systemic dissemination might predict its response. Favorable clinical results depend on prompt diagnosis, investigation of fungal dissemination, and early therapy initiation.

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