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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
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.
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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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