Premium
Screening for invasive fungal disease using non‐culture‐based assays among inpatients with advanced HIV disease at a large academic hospital in South Africa
Author(s) -
van Schalkwyk Erika,
Mhlanga Mabatho,
Maphanga Tsidiso G.,
Mpembe Ruth S.,
Shillubane Amanda,
Iyaloo Samantha,
Tsotetsi Ernest,
Pieton Kim,
Karstaedt Alan S.,
Sahid Faieza,
Menezes Colin N.,
Tsitsi Merika,
Motau Ayanda,
Wadula Jeannette,
Seetharam Sharona,
van den Berg Eunice,
Sriruttan Charlotte,
Govender Nelesh P.
Publication year - 2020
Publication title -
mycoses
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.13
H-Index - 69
eISSN - 1439-0507
pISSN - 0933-7407
DOI - 10.1111/myc.13071
Subject(s) - medicine , tuberculosis , histoplasmosis , disease , mycosis , cryptococcosis , immunology , pathology
Summary Introduction Despite widespread access to antiretroviral therapy (ART), the burden of advanced HIV disease in South Africa is high. This translates into an increased risk of AIDS‐related opportunistic infections, including invasive mycoses. Methods Using a limited number of non‐culture‐based diagnostic assays, we aimed to determine the prevalence of invasive mycoses and tuberculosis among hospitalised adults with very advanced HIV (CD4 counts < 100 cells/µL) at a large academic hospital. We conducted interviews and prospective medical chart reviews. We performed point‐of‐care finger stick and serum cryptococcal antigen lateral flow assays; serum (1 → 3) ß‐D‐glucan assays; urine Histoplasma galactomannan antigen enzyme immunoassays and TB lipoarabinomannan assays. Results We enrolled 189 participants from 5280 screened inpatients. Fifty‐eight per cent were female, with median age 37 years (IQR: 30‐43) and median CD4 count 32 cells/µL (IQR: 13‐63). At enrolment, 60% (109/181) were receiving ART. Twenty‐one participants (11%) had a diagnosis of an invasive mycosis, of whom 53% (11/21) had cryptococcal disease. Thirteen participants (7%) had tuberculosis and a concurrent invasive mycosis. ART‐experienced participants were 60% less likely to have an invasive mycosis than those ART‐naïve (adjusted OR: 0.4; 95% CI 0.15‐1.0; P = .03). Overall in‐hospital mortality was 13% (invasive mycosis: 10% [95% CI 1.2‐30.7] versus other diagnoses: 13% (95% CI 8.4‐19.3)). Conclusions One in ten participants had evidence of an invasive mycosis. Diagnosis of proven invasive fungal disease and differentiation from other opportunistic infections was challenging. More fungal‐specific screening and diagnostic tests should be applied to inpatients with advanced HIV disease.