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dc.contributor.authorJarvis, Joseph N.
dc.contributor.authorBicanic, Tihana
dc.contributor.authorLoyse, Angela
dc.contributor.authorNamarika, Daniel
dc.contributor.authorJackson, Arthur
dc.contributor.authorNussbaum, Jesse C.
dc.contributor.authorLongley, Nicky
dc.contributor.authorMuzoora, Conrad
dc.contributor.authorPhulusa, Jacob
dc.contributor.authorTaseera, Kabanda
dc.contributor.authorKanyembe, Creto
dc.contributor.authorWilson, Douglas
dc.contributor.authorHosseinipour, Mina C.
dc.contributor.authorBrouwer, Annemarie E.
dc.contributor.authorLimmathurotsakul, Direk
dc.contributor.authorWhite, Nicholas
dc.contributor.authorder Horst, Charles van
dc.contributor.authorWood, Robin
dc.contributor.authorMeintjes, Graeme
dc.contributor.authorBradley, John
dc.contributor.authorJaffar, Shabbar
dc.contributor.authorHarrison, Thomas
dc.date.accessioned2022-02-03T09:33:01Z
dc.date.available2022-02-03T09:33:01Z
dc.date.issued2013-12-06
dc.identifier.citationJarvis, J. N., Bicanic, T., Loyse, A., Namarika, D., Jackson, A., Nussbaum, J. C., ... & Harrison, T. (2013). Determinants of Mortality in a Combined Cohort of 501 Patients With HIV-Associated Cryptococcal Meningitis.en_US
dc.identifier.urihttp://ir.must.ac.ug/xmlui/handle/123456789/1387
dc.description.abstractBackground: Cryptococcal meningitis (CM) is a leading cause of death in individuals infected with human immunodeficiency virus (HIV). Identifying factors associated with mortality informs strategies to improve outcomes. Methods: Five hundred one patients with HIV-associated CM were followed prospectively for 10 weeks during trials in Thailand, Uganda, Malawi, and South Africa. South African patients (n = 266) were followed for 1 year.Similar inclusion/exclusion criteria were applied at all sites. Logistic regression identified baseline variables independently associated with mortality. Results: Mortality was 17% at 2 weeks and 34% at 10 weeks. Altered mental status (odds ratio [OR], 3.1; 95% confidence interval [CI], 1.7–5.9), high cerebrospinal fluid (CSF) fungal burden (OR, 1.4 per log10 colony-forming units/mL increase; 95% CI, 1.0–1.8), older age (>50 years; OR, 3.9; 95% CI, 1.4–11.1), high peripheral white blood cell count (>10 × 109 cells/L; OR, 8.7; 95% CI, 2.5–30.2), fluconazole-based induction treatment, and slow clearance of CSF infection were independently associated with 2-week mortality. Low body weight, anemia (hemoglobin <7.5g/dL), and low CSF opening pressure were independently associated with mortality at 10 weeks in addition to altered mental status, high fungal burden, high peripheral white cell count, and older age. In those followed for 1 year, overall mortality was 41%. Immune reconstitution inflammatory syndrome occurred in 13% of patients and was associated with 2-week CSF fungal burden (P = .007), but not with time to initiation of antiretroviral therapy (ART). Conclusions: CSF fungal burden, altered mental status, and rate of clearance of infection predict acute mortality in HIV-associated CM. The results suggest that earlier diagnosis, more rapidly fungicidal amphotericin-based regimens, and prompt immune reconstitution with ART are priorities for improving outcomes.en_US
dc.description.sponsorshipWellcome Trust and Medical Research Council (UK), University of North Carolina Center for AIDS Research (P30-AI50410), and the National Institutes of Health Fogarty AIDS International Training and Research Program (DHHS/NIH/FIC 2-D43 TW01039).en_US
dc.language.isoen_USen_US
dc.publisherClinical Infectious Diseasesen_US
dc.subjectCryptococcal meningitisen_US
dc.subjectCryptococcus neoformansen_US
dc.subjectHIVen_US
dc.subjectAntiretroviral therapyen_US
dc.subjectMortality (determinants)en_US
dc.titleDeterminants of Mortality in a Combined Cohort of 501 PatientsWith HIV-Associated Cryptococcal Meningitis: Implications for Improving Outcomesen_US
dc.typeArticleen_US


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