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Treatment of Cryptococcal Meningitis in KwaZulu-Natal, South Africa

BACKGROUND: Cryptococcal meningitis (CM) remains a leading cause of death for HIV-infected individuals in sub-Saharan Africa. Improved treatment strategies are needed if individuals are to benefit from the increasing availability of antiretroviral therapy. We investigated the factors associated with...

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Autores principales: Lightowler, Josephine V. J., Cooke, Graham S., Mutevedzi, Portia, Lessells, Richard J., Newell, Marie-Louise, Dedicoat, Martin
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2799667/
https://www.ncbi.nlm.nih.gov/pubmed/20062814
http://dx.doi.org/10.1371/journal.pone.0008630
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author Lightowler, Josephine V. J.
Cooke, Graham S.
Mutevedzi, Portia
Lessells, Richard J.
Newell, Marie-Louise
Dedicoat, Martin
author_facet Lightowler, Josephine V. J.
Cooke, Graham S.
Mutevedzi, Portia
Lessells, Richard J.
Newell, Marie-Louise
Dedicoat, Martin
author_sort Lightowler, Josephine V. J.
collection PubMed
description BACKGROUND: Cryptococcal meningitis (CM) remains a leading cause of death for HIV-infected individuals in sub-Saharan Africa. Improved treatment strategies are needed if individuals are to benefit from the increasing availability of antiretroviral therapy. We investigated the factors associated with mortality in routine care in KwaZulu-Natal, South Africa. METHODOLOGY/PRINCIPAL FINDINGS: A prospective year long, single-center, consecutive case series of individuals diagnosed with cryptococcal meningitis 190 patients were diagnosed with culture positive cryptococcal meningitis, of whom 186 were included in the study. 52/186 (28.0%) patients died within 14 days of diagnosis and 60/186 (32.3%) had died by day 28. In multivariable cox regression analysis, focal neurology (aHR 11 95%C.I. 3.08–39.3, P<0.001), diastolic blood pressure <60 mmHg (aHR 2.37 95%C.I. 1.11–5.04, P = 0.025), concurrent treatment for tuberculosis (aHR 2.11 95%C.I. 1.02–4.35, P = 0.044) and use of fluconazole monotherapy (aHR 3.69 95% C.I. 1.74–7.85, P<0.001) were associated with increased mortality at 14 and 28 days. CONCLUSIONS: Even in a setting where amphotericin B is available, mortality from cryptococcal meningitis in this setting is high, particularly in the immediate period after diagnosis. This highlights the still unmet need not only for earlier diagnosis of HIV and timely access to treatment of opportunistic infections, but for better treatment strategies of cryptococcal meningitis.
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spelling pubmed-27996672010-01-09 Treatment of Cryptococcal Meningitis in KwaZulu-Natal, South Africa Lightowler, Josephine V. J. Cooke, Graham S. Mutevedzi, Portia Lessells, Richard J. Newell, Marie-Louise Dedicoat, Martin PLoS One Research Article BACKGROUND: Cryptococcal meningitis (CM) remains a leading cause of death for HIV-infected individuals in sub-Saharan Africa. Improved treatment strategies are needed if individuals are to benefit from the increasing availability of antiretroviral therapy. We investigated the factors associated with mortality in routine care in KwaZulu-Natal, South Africa. METHODOLOGY/PRINCIPAL FINDINGS: A prospective year long, single-center, consecutive case series of individuals diagnosed with cryptococcal meningitis 190 patients were diagnosed with culture positive cryptococcal meningitis, of whom 186 were included in the study. 52/186 (28.0%) patients died within 14 days of diagnosis and 60/186 (32.3%) had died by day 28. In multivariable cox regression analysis, focal neurology (aHR 11 95%C.I. 3.08–39.3, P<0.001), diastolic blood pressure <60 mmHg (aHR 2.37 95%C.I. 1.11–5.04, P = 0.025), concurrent treatment for tuberculosis (aHR 2.11 95%C.I. 1.02–4.35, P = 0.044) and use of fluconazole monotherapy (aHR 3.69 95% C.I. 1.74–7.85, P<0.001) were associated with increased mortality at 14 and 28 days. CONCLUSIONS: Even in a setting where amphotericin B is available, mortality from cryptococcal meningitis in this setting is high, particularly in the immediate period after diagnosis. This highlights the still unmet need not only for earlier diagnosis of HIV and timely access to treatment of opportunistic infections, but for better treatment strategies of cryptococcal meningitis. Public Library of Science 2010-01-07 /pmc/articles/PMC2799667/ /pubmed/20062814 http://dx.doi.org/10.1371/journal.pone.0008630 Text en Lightowler et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Lightowler, Josephine V. J.
Cooke, Graham S.
Mutevedzi, Portia
Lessells, Richard J.
Newell, Marie-Louise
Dedicoat, Martin
Treatment of Cryptococcal Meningitis in KwaZulu-Natal, South Africa
title Treatment of Cryptococcal Meningitis in KwaZulu-Natal, South Africa
title_full Treatment of Cryptococcal Meningitis in KwaZulu-Natal, South Africa
title_fullStr Treatment of Cryptococcal Meningitis in KwaZulu-Natal, South Africa
title_full_unstemmed Treatment of Cryptococcal Meningitis in KwaZulu-Natal, South Africa
title_short Treatment of Cryptococcal Meningitis in KwaZulu-Natal, South Africa
title_sort treatment of cryptococcal meningitis in kwazulu-natal, south africa
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2799667/
https://www.ncbi.nlm.nih.gov/pubmed/20062814
http://dx.doi.org/10.1371/journal.pone.0008630
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