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  5. Evaluation of new semi-quantitative cryptococcal antigen Immy (immunochromatographic) SQ (semi-quantitative) and Biosynex tests in plasma for detection of subclinical cryptococcal meningitis in HIV positive patients with CD4 <100
 
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Evaluation of new semi-quantitative cryptococcal antigen Immy (immunochromatographic) SQ (semi-quantitative) and Biosynex tests in plasma for detection of subclinical cryptococcal meningitis in HIV positive patients with CD4 <100

Author(s)
Blasich, Nozuko Precious
Date Issued
2021
Type
Thesis
Publisher
Cape Peninsula University of Technology
DOI
https://doi.org/10.25381/cput.19575790.v1
Abstract
Introduction: Blood cryptococcal antigen (CrAg) titres >160 are associated with concurrent subclinical cryptococcal meningitis (CM). When lumbar puncture (LP) is not immediately available in a CrAg screening programme, semi-quantitative CrAg assays may provide risk stratification for CM.
Materials and methods: Two semi-quantitative assays (SQ [Immuno-Mycologics, Norman, OK, USA] and CryptoPS [Biosynex, Strasbourg, France]) were evaluated against a qualitative lateral flow assay (LFA) using 194 plasma samples from a cohort of HIV-seropositive individuals with CD4 counts <100 cells/μL. We compared SQ and CryptoPS results to titres for LFA-positive samples. Among patients with LP, we examined the association between semi-quantitative CrAg results and CM. We used a Cox proportional hazards model to determine the association between SQ score and mortality.
Results: Of 194 participants, 60 (31%) had positive LFA results, of whom 41 (68%) had a titre of ≤160 and 19 (32%) a titre >160. Fifty individuals with antigenaemia had an LP; a clinically-useful SQ score that identified all ten cases of subclinical CM was ≥3 (100% sensitivity, 55% specificity). Patients with an SQ score of 3 or 4 also had a 2.2-fold increased adjusted hazards of 6-month mortality (95% CI, 0.79-6.34; p=0.13) versus those with score of <3. Nine of ten patients with subclinical CM had a strong-positive CryptoPS result versus 10/40 without subclinical CM (p<0.001).
Conclusions: Semi-quantitative assays offered a sensitive though not specific means of gauging the risk of concurrent CM in this patient population.
Additional information
Thesis (MSc (Biomedical Technology))--Cape Peninsula University of Technology, 2021
Subjects

Cryptococcus

HIV (Viruses)

HIV infections

Meningitis

Medical screening

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Nozuko_Blasich_211267961.pdf

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581.31 KB

Format

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Checksum

(MD5):b4669d34570bf937057d666dc4438a63

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