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Tuberculosis in HIV-Associated Cryptococcal Meningitis is Associated with an Increased Risk of Death
Tuberculosis (TB) and cryptococcal meningitis are leading causes of morbidity and mortality in advanced HIV disease. Data are limited on TB co-infection among individuals with cryptococcal meningitis. We performed a retrospective analysis of HIV-infected participants with cryptococcal meningitis fro...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7141367/ https://www.ncbi.nlm.nih.gov/pubmed/32183112 http://dx.doi.org/10.3390/jcm9030781 |
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author | Rutakingirwa, Morris K. Cresswell, Fiona V. Kwizera, Richard Ssebambulidde, Kenneth Kagimu, Enock Nuwagira, Edwin Tugume, Lillian Mpoza, Edward Dobbin, Joanna Williams, Darlisha A. Muzoora, Conrad Meya, David B. Boulware, David R. Hullsiek, Kathy H. Rhein, Joshua |
author_facet | Rutakingirwa, Morris K. Cresswell, Fiona V. Kwizera, Richard Ssebambulidde, Kenneth Kagimu, Enock Nuwagira, Edwin Tugume, Lillian Mpoza, Edward Dobbin, Joanna Williams, Darlisha A. Muzoora, Conrad Meya, David B. Boulware, David R. Hullsiek, Kathy H. Rhein, Joshua |
author_sort | Rutakingirwa, Morris K. |
collection | PubMed |
description | Tuberculosis (TB) and cryptococcal meningitis are leading causes of morbidity and mortality in advanced HIV disease. Data are limited on TB co-infection among individuals with cryptococcal meningitis. We performed a retrospective analysis of HIV-infected participants with cryptococcal meningitis from 2010–2017. Baseline demographics were compared between three groups: ‘prevalent TB’ if TB treated >14 days prior to cryptococcal meningitis diagnosis, ‘concurrent TB’ if TB treated ± 14 days from diagnosis, or ‘No TB at baseline’. We used time-updated proportional-hazards regression models to assess TB diagnosis as a risk for death. Of 870 participants with cryptococcal meningitis, 50 (6%) had prevalent TB, 67 (8%) had concurrent TB, and 753 (86%) had no baseline TB. Among participants without baseline TB, 67 (9%) were diagnosed with incident TB (after >14 days), with a median time to TB incidence of 41 days (IQR, 22–69). The 18-week mortality was 50% (25/50) in prevalent TB, 46% (31/67) in concurrent TB, and 45% (341/753) in the no TB group (p = 0.81). However, TB co-infection was associated with an increased hazard of death (HR = 1.75; 95% CI, 1.33–2.32; p < 0.001) in a time-updated model. TB is commonly diagnosed in cryptococcal meningitis, and the increased mortality associated with co-infection is a public health concern. |
format | Online Article Text |
id | pubmed-7141367 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-71413672020-04-10 Tuberculosis in HIV-Associated Cryptococcal Meningitis is Associated with an Increased Risk of Death Rutakingirwa, Morris K. Cresswell, Fiona V. Kwizera, Richard Ssebambulidde, Kenneth Kagimu, Enock Nuwagira, Edwin Tugume, Lillian Mpoza, Edward Dobbin, Joanna Williams, Darlisha A. Muzoora, Conrad Meya, David B. Boulware, David R. Hullsiek, Kathy H. Rhein, Joshua J Clin Med Article Tuberculosis (TB) and cryptococcal meningitis are leading causes of morbidity and mortality in advanced HIV disease. Data are limited on TB co-infection among individuals with cryptococcal meningitis. We performed a retrospective analysis of HIV-infected participants with cryptococcal meningitis from 2010–2017. Baseline demographics were compared between three groups: ‘prevalent TB’ if TB treated >14 days prior to cryptococcal meningitis diagnosis, ‘concurrent TB’ if TB treated ± 14 days from diagnosis, or ‘No TB at baseline’. We used time-updated proportional-hazards regression models to assess TB diagnosis as a risk for death. Of 870 participants with cryptococcal meningitis, 50 (6%) had prevalent TB, 67 (8%) had concurrent TB, and 753 (86%) had no baseline TB. Among participants without baseline TB, 67 (9%) were diagnosed with incident TB (after >14 days), with a median time to TB incidence of 41 days (IQR, 22–69). The 18-week mortality was 50% (25/50) in prevalent TB, 46% (31/67) in concurrent TB, and 45% (341/753) in the no TB group (p = 0.81). However, TB co-infection was associated with an increased hazard of death (HR = 1.75; 95% CI, 1.33–2.32; p < 0.001) in a time-updated model. TB is commonly diagnosed in cryptococcal meningitis, and the increased mortality associated with co-infection is a public health concern. MDPI 2020-03-13 /pmc/articles/PMC7141367/ /pubmed/32183112 http://dx.doi.org/10.3390/jcm9030781 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Rutakingirwa, Morris K. Cresswell, Fiona V. Kwizera, Richard Ssebambulidde, Kenneth Kagimu, Enock Nuwagira, Edwin Tugume, Lillian Mpoza, Edward Dobbin, Joanna Williams, Darlisha A. Muzoora, Conrad Meya, David B. Boulware, David R. Hullsiek, Kathy H. Rhein, Joshua Tuberculosis in HIV-Associated Cryptococcal Meningitis is Associated with an Increased Risk of Death |
title | Tuberculosis in HIV-Associated Cryptococcal Meningitis is Associated with an Increased Risk of Death |
title_full | Tuberculosis in HIV-Associated Cryptococcal Meningitis is Associated with an Increased Risk of Death |
title_fullStr | Tuberculosis in HIV-Associated Cryptococcal Meningitis is Associated with an Increased Risk of Death |
title_full_unstemmed | Tuberculosis in HIV-Associated Cryptococcal Meningitis is Associated with an Increased Risk of Death |
title_short | Tuberculosis in HIV-Associated Cryptococcal Meningitis is Associated with an Increased Risk of Death |
title_sort | tuberculosis in hiv-associated cryptococcal meningitis is associated with an increased risk of death |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7141367/ https://www.ncbi.nlm.nih.gov/pubmed/32183112 http://dx.doi.org/10.3390/jcm9030781 |
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