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Evaluation of trypan blue stain in a haemocytometer for rapid detection of cerebrospinal fluid sterility in HIV patients with cryptococcal meningitis

Evaluation of trypan blue stain in a haemocytometer for rapid detection of cerebrospinal fluid sterility in HIV patients with cryptococcal meningitis

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dc.contributor.author Kwizera, Richard
dc.contributor.author Akampurira, Andrew
dc.contributor.author Kandole, Tadeo K.
dc.contributor.author Nielsen, Kirsten
dc.contributor.author Kambugu, Andrew
dc.contributor.author Meya, David B.
dc.contributor.author Boulware, David R.
dc.contributor.author Rhein, Joshua
dc.date.accessioned 2021-01-01T21:58:03Z
dc.date.available 2021-01-01T21:58:03Z
dc.date.issued 2017
dc.identifier.issn 1471-2180
dc.identifier.uri http://combine.alvar.ug/handle/1/48143
dc.description.abstract Background: Quantitative culture is the most common method to determine the fungal burden and sterility of cerebrospinal fluid (CSF) among persons with cryptococcal meningitis. A major drawback of cultures is a long turnaround-time. Recent evidence demonstrates that live and dead Cryptococcus yeasts can be distinguished using trypan blue staining. We hypothesized that trypan blue staining combined with haemocytometer counting may provide a rapid estimation of quantitative culture count and detection of CSF sterility. To test this, we evaluated 194 CSF specimens from 96 HIV-infected participants with cryptococcal meningitis in Kampala, Uganda. Cryptococcal meningitis was diagnosed by CSF cryptococcal antigen (CRAG). We stained CSF with trypan blue and quantified yeasts using a haemocytometer. We compared the haemocytometer readings versus quantitative Cryptococcus CSF cultures. Results: Haemocytometer counting with trypan blue staining had a sensitivity of 98% (64/65), while CSF cultures had a sensitivity of 95% (62/65) with reference to CSF CRAG for diagnostic CSF specimens. For samples that were positive in both tests, the haemocytometer had higher readings compared to culture. For diagnostic specimens, the median of log(10) transformed counts were 5.59 (n = 64, IQR = 5.09 to 6.05) for haemocytometer and 4.98 (n = 62, IQR = 3.75 to 5.79) for culture; while the overall median counts were 5.35 (n = 189, IQR = 4.78-5.84) for haemocytometer and 3.99 (n = 151, IQR = 2.59-5.14) for cultures. The percentage agreement with culture sterility was 2.4% (1/42). Counts among non-sterile follow-up specimens had a median of 5.38 (n = 86, IQR = 4.74 to 6.03) for haemocytometer and 2.89 (n = 89, IQR = 2.11 to 4.38) for culture. At diagnosis, CSF quantitative cultures correlated with haemocytometer counts (R-2 = 0.59, P < 0.001). At 7-14 days, quantitative cultures did not correlate with haemocytometer counts (R-2 = 0.43, P = 0.4). Conclusion: Despite a positive correlation, the haemocytometer counts with trypan blue staining did not predict the outcome of quantitative cultures in patients receiving antifungal therapy.
dc.description.sponsorship National Institutes of HealthUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USA [R01NS086312, T32AI055433 R25TW009345]
dc.description.sponsorship Grand Challenges CanadaCGIAR [S4 0296-01]
dc.description.sponsorship United Kingdom Medical Research CouncilMedical Research Council UK (MRC) [MR/M007413/1]
dc.description.sponsorship FOGARTY INTERNATIONAL CENTERUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USANIH Fogarty International Center (FIC) [K01TW010268, K01TW010268, K01TW010268, K01TW010268, K01TW010268] Funding Source: NIH RePORTER
dc.description.sponsorship Medical Research CouncilMedical Research Council UK (MRC) [MR/M007413/1] Funding Source: researchfish
dc.language English
dc.publisher BIOMED CENTRAL LTD
dc.relation.ispartof BMC Microbiology
dc.subject Trypan Blue
dc.subject Cryptococcal Meningitis
dc.subject Hiv
dc.subject Diagnostic Techniques And Procedures
dc.subject Point-Of-Care Systems
dc.title Evaluation of trypan blue stain in a haemocytometer for rapid detection of cerebrospinal fluid sterility in HIV patients with cryptococcal meningitis
dc.type Article
dc.identifier.isi 000408252200002
dc.identifier.doi 10.1186/s12866-017-1093-4
dc.identifier.pmid 288348
dc.publisher.city LONDON
dc.publisher.address 236 GRAYS INN RD, FLOOR 6, LONDON WC1X 8HL, ENGLAND
dc.identifier.volume 17
dc.subject.wc Microbiology
dc.subject.sc Microbiology
dc.description.oa DOAJ Gold
dc.description.oa Green Published
dc.description.pages 6
dc.contributor.group ASTRO-CM Study Team
dc.subject.kwp Global Burden
dc.subject.kwp Disease
dc.identifier.articleno 182
dc.description.affiliation Makerere Univ, Coll Hlth Sci, Infect Dis Inst, POB 22418, Kampala, Uganda
dc.description.affiliation Univ Minnesota, Minneapolis, MN USA
dc.description.affiliation Makerere Univ, Coll Hlth Sci, Sch Med, Dept Med, Kampala, Uganda
dc.description.email kwizerarichard@ymail.com
dc.description.corr Kwizera, R (corresponding author), Makerere Univ, Coll Hlth Sci, Infect Dis Inst, POB 22418, Kampala, Uganda.
dc.description.orcid Kwizera, Richard/0000-0002-5270-3539
dc.description.orcid Boulware, David/0000-0002-4715-0060


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