A contemporary investigation of burden and natural history of aspergillosis in people living with HIV/AIDS

Author:

Truda Vanessa Souza Santos1ORCID,Falci Diego Rodrigues2ORCID,Porfírio Fátima Maria Venancio3,de Santos Daniel Wagner de Castro Lima4ORCID,Junior Francisco Ivanildo Oliveira3ORCID,Pasqualotto Alessandro Comaru56ORCID,Puga Fernanda Guioti7ORCID,Bollela Valdes Roberto7ORCID,Junior João Nobrega Almeida1ORCID,Ferreira Paulo Roberto Abrão1ORCID,Colombo Arnaldo Lopes1ORCID

Affiliation:

1. Escola Paulista de Medicina Universidade Federal de São Paulo (UNIFESP) São Paulo Brazil

2. Infectious Disease Department, Hospital de Clínicas de Porto Alegre Porto Alegre Brazil

3. Instituto de Infectologia Emílio Ribas São Paulo Brazil

4. Instituto D'or de Pesquisa e Ensino (IDOR) Rio de Janeiro Brazil

5. Santa Casa de Misericórdia de Porto Alegre Porto Alegre Brazil

6. Universidade Federal de Ciências da Saúde de Porto Alegre Porto Alegre Brazil

7. Divisions of Clinical Immunology, Emergency, Infectious Diseases and Intensive Care Unit, Ribeirão Preto Medical School University of São Paulo São Paulo Brazil

Abstract

AbstractBackgroundUntreated HIV infection can lead to profound immunosuppression and increase susceptibility of people living with HIV/AIDS (PLHA) to aspergillosis.ObjectivesReporting the burden and natural history of aspergillosis documented in PLHA admitted in five medical centres in Brazil.Patients and MethodsClinical, epidemiological and laboratory data were collected in all sequential cases of proven or probable aspergillosis documented in PLHA hospitalised in five medical centres between 2012 and 2020.ResultsWe enrolled 25 patients ageing between 23 and 58 years (mean = 39) including 11 patients with invasive aspergillosis (IA) and 14 with chronic pulmonary aspergillosis (CPA). The prevalence rate of aspergillosis was 0.1% of 19.616 PLHA. Overall, 72.7% of patients with IA exhibited CD4 < 100 cells/mL and 42.8% of patients with CPA exhibited CD4 count >200 cells/mL. Most patients had a history of tuberculosis, especially those with CPA (85.7%). IA was documented after a mean of 16.5 days of hospitalisation, mainly in critically ill patients exposed to corticosteroids and broad‐spectrum antibiotics. In the CPA group, a positive culture (71.4%) and radiological alterations were the most frequent findings supporting their diagnosis. Episodes of IA were mostly documented by tissue biopsies. Crude mortality rates were 72.7% and 42.8% in patients with IA and CPA, respectively.ConclusionsDespite being considered an unusual complication in PLHA (0.1%), IA should be considered in patients with profound immunosuppression and pneumonia refractory to conventional therapy. CPA should be investigated in PLHA with chronic deterioration of pulmonary function and previous diagnosis of tuberculosis.

Publisher

Wiley

Subject

Infectious Diseases,Dermatology,General Medicine

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