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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...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2010
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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. |
format | Text |
id | pubmed-2799667 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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