Data Entry: Please note that the research database will be replaced by UNIverse by the end of October 2023. Please enter your data into the system https://universe-intern.unibas.ch. Thanks

Login for users with Unibas email account...

Login for registered users without Unibas email account...

 
Cryptococcal antigenemia in immunocompromised human immunodeficiency virus patients in rural Tanzania : a preventable cause of early mortality
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 3183410
Author(s) Letang, Emilio; Müller, Matthias C; Ntamatungiro, Alex J; Kimera, Namvua; Faini, Diana; Furrer, Hansjakob; Battegay, Manuel; Tanner, Marcel; Hatz, Christoph; Boulware, David R; Glass, Tracy R
Author(s) at UniBasel Tanner, Marcel
Hatz, Christoph
Glass, Tracy
Year 2015
Title Cryptococcal antigenemia in immunocompromised human immunodeficiency virus patients in rural Tanzania : a preventable cause of early mortality
Journal Open forum infectious diseases
Volume 2
Number 2
Pages / Article-Number ofv046
Keywords cryptococcal antigen, cryptococcal meningitis, diagnosis, mortality, prevention, retention in care, screening, sub-Saharan Africa
Abstract

Background.  Cryptococcal meningitis is a leading cause of death in people living with human immunodeficiency virus (HIV)/acquired immune deficiency syndrome. The World Health Organizations recommends pre-antiretroviral treatment (ART) cryptococcal antigen (CRAG) screening in persons with CD4 below 100 cells/µL. We assessed the prevalence and outcome of cryptococcal antigenemia in rural southern Tanzania. Methods.  We conducted a retrospective study including all ART-naive adults with CD4 <150 cells/µL prospectively enrolled in the Kilombero and Ulanga Antiretroviral Cohort between 2008 and 2012. Cryptococcal antigen was assessed in cryopreserved pre-ART plasma. Cox regression estimated the composite outcome of death or loss to follow-up (LFU) by CRAG status and fluconazole use. Results.  Of 750 ART-naive adults, 28 (3.7%) were CRAG-positive, corresponding to a prevalence of 4.4% (23 of 520) in CD4 <100 and 2.2% (5 of 230) in CD4 100-150 cells/µL. Within 1 year, 75% (21 of 28) of CRAG-positive and 42% (302 of 722) of CRAG-negative patients were dead or LFU (P<.001), with no differences across CD4 strata. Cryptococcal antigen positivity was an independent predictor of death or LFU after adjusting for relevant confounders (hazard ratio [HR], 2.50; 95% confidence interval [CI], 1.29-4.83; P = .006). Cryptococcal meningitis occurred in 39% (11 of 28) of CRAG-positive patients, with similar retention-in-care regardless of meningitis diagnosis (P = .8). Cryptococcal antigen titer >1:160 was associated with meningitis development (odds ratio, 4.83; 95% CI, 1.24-8.41; P = .008). Fluconazole receipt decreased death or LFU in CRAG-positive patients (HR, 0.18; 95% CI, .04-.78; P = .022). Conclusions.  Cryptococcal antigenemia predicted mortality or LFU among ART-naive HIV-infected persons with CD4 <150 cells/µL, and fluconazole increased survival or retention-in-care, suggesting that targeted pre-ART CRAG screening may decrease early mortality or LFU. A CRAG screening threshold of CD4 <100 cells/µL missed 18% of CRAG-positive patients, suggesting guidelines should consider a higher threshold.

Publisher Oxford University Press]
ISSN/ISBN 2328-8957
edoc-URL http://edoc.unibas.ch/dok/A6419766
Full Text on edoc No
Digital Object Identifier DOI 10.1093/ofid/ofv046
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/26213690
ISI-Number WOS:000365786200029
Document type (ISI) Journal Article
 
   

MCSS v5.8 PRO. 0.416 sec, queries - 0.000 sec ©Universität Basel  |  Impressum   |    
03/05/2024