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http://dx.doi.org/10.1016/j.jmii.2020.05.010DOI Listing

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Background: The World Health Organization (WHO) recommended cryptococcal antigen (CrAg) screening for people presenting with advanced HIV disease (AHD) and for those with positive CrAg without evidence of meningitis to initiate preemptive antifungal medication. Data on the implementation of WHO recommendations regarding CrAg screening is limited. We estimated pooled prevalence of CrAg screening uptake, cryptococcal antigenemia, lumbar puncture, cryptococcal meningitis and initiation of preemptive antifungal medication from available eligible published studies conducted in Africa.

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We evaluated the prevalence of serum and meningeal cryptococcosis in asymptomatic outpatients with advanced HIV disease (CD4 < 200 cells/mm3) in a cross-sectional screening context in Kinshasa clinics (DRC). Lumbar puncture (LP) was performed in patients with positive serum cryptococcal antigen (CrAg) test, and Cryptococcus spp. isolated from cerebrospinal fluid (CSF) were identified by MALDI-TOF-MS, and characterized using serotyping-PCR, ITS-sequencing and multilocus sequence typing (MLST).

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Cryptococcosis is the third most common invasive fungal infection in solid-organ transplant (SOT) recipients after candidiasis and aspergillosis. These patients are at risk of disseminated cryptococcosis because of immuosuppressive therapy. The median time to disease onset after kidney transplantation is approximately 35 months and it rarely occurs more than 10 years after transplantation.

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Article Synopsis
  • The study investigated how common cryptococcal antigenemia is in AIDS patients using a lateral flow assay (LFA) and its effectiveness in diagnosing cryptococcosis.
  • Conducted in Brazil from March 2015 to July 2017, the study included 230 AIDS patients with low CD4+ counts and found a 13.0% prevalence of cryptococcal antigen detected by LFA.
  • The LFA demonstrated high accuracy, with a sensitivity of 83.9% and specificity of 98.0%, making it a reliable diagnostic tool for detecting cryptococcal antigenemia in severely immunocompromised individuals.
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