author_facet Barakat, LA
Juthani‐Mehta, M
Allore, H
Trentalange, M
Tate, J
Rimland, D
Pisani, M
Akgün, KM
Goetz, MB
Butt, AA
Rodriguez‐Barradas, M
Duggal, M
Crothers, K
Justice, AC
Quagliarello, VJ
Barakat, LA
Juthani‐Mehta, M
Allore, H
Trentalange, M
Tate, J
Rimland, D
Pisani, M
Akgün, KM
Goetz, MB
Butt, AA
Rodriguez‐Barradas, M
Duggal, M
Crothers, K
Justice, AC
Quagliarello, VJ
author Barakat, LA
Juthani‐Mehta, M
Allore, H
Trentalange, M
Tate, J
Rimland, D
Pisani, M
Akgün, KM
Goetz, MB
Butt, AA
Rodriguez‐Barradas, M
Duggal, M
Crothers, K
Justice, AC
Quagliarello, VJ
spellingShingle Barakat, LA
Juthani‐Mehta, M
Allore, H
Trentalange, M
Tate, J
Rimland, D
Pisani, M
Akgün, KM
Goetz, MB
Butt, AA
Rodriguez‐Barradas, M
Duggal, M
Crothers, K
Justice, AC
Quagliarello, VJ
HIV Medicine
Comparing clinical outcomes in HIV‐infected and uninfected older men hospitalized with community‐acquired pneumonia
Pharmacology (medical)
Infectious Diseases
Health Policy
author_sort barakat, la
spelling Barakat, LA Juthani‐Mehta, M Allore, H Trentalange, M Tate, J Rimland, D Pisani, M Akgün, KM Goetz, MB Butt, AA Rodriguez‐Barradas, M Duggal, M Crothers, K Justice, AC Quagliarello, VJ 1464-2662 1468-1293 Wiley Pharmacology (medical) Infectious Diseases Health Policy http://dx.doi.org/10.1111/hiv.12244 <jats:sec><jats:title>Objectives</jats:title><jats:p>Outcomes of community–acquired pneumonia (<jats:styled-content style="fixed-case">CAP</jats:styled-content>) among <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐infected older adults are unclear.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>Associations between <jats:styled-content style="fixed-case">HIV</jats:styled-content> infection and three <jats:styled-content style="fixed-case">CAP</jats:styled-content> outcomes (30‐day mortality, readmission within 30 days post‐discharge, and hospital length of stay [<jats:styled-content style="fixed-case">LOS</jats:styled-content>]) were examined in the <jats:styled-content style="fixed-case">V</jats:styled-content>eterans <jats:styled-content style="fixed-case">A</jats:styled-content>ging <jats:styled-content style="fixed-case">C</jats:styled-content>ohort <jats:styled-content style="fixed-case">S</jats:styled-content>tudy (<jats:styled-content style="fixed-case">VACS</jats:styled-content>) of male Veterans, age ≥ 50 years, hospitalized for <jats:styled-content style="fixed-case">CAP</jats:styled-content> from 10/1/2002 through 08/31/2010. Associations between the <jats:styled-content style="fixed-case">VACS</jats:styled-content> Index and <jats:styled-content style="fixed-case">CAP</jats:styled-content> outcomes were assessed in multivariable models.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>Among 117 557 <jats:styled-content style="fixed-case">V</jats:styled-content>eterans (36 922 <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐infected and 80 635 uninfected), 1203 met our eligibility criteria. The 30‐day mortality rate was 5.3%, the mean <jats:styled-content style="fixed-case">LOS</jats:styled-content> was 7.3 days, and 13.2% were readmitted within 30 days of discharge. In unadjusted analyses, there were no significant differences between <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐infected and uninfected participants regarding the three <jats:styled-content style="fixed-case">CAP</jats:styled-content> outcomes (<jats:italic>P</jats:italic> &gt; 0.2). A higher <jats:styled-content style="fixed-case">VACS</jats:styled-content> Index was associated with increased 30‐day mortality, readmission, and <jats:styled-content style="fixed-case">LOS</jats:styled-content> in both <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐infected and uninfected groups. Generic organ system components of the <jats:styled-content style="fixed-case">VACS</jats:styled-content> Index were associated with adverse <jats:styled-content style="fixed-case">CAP</jats:styled-content> outcomes; <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐specific components were not. Among <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐infected participants, those not on antiretroviral therapy (<jats:styled-content style="fixed-case">ART</jats:styled-content>) had a higher 30‐day mortality (<jats:styled-content style="fixed-case">HR</jats:styled-content> 2.94 [95% <jats:styled-content style="fixed-case">CI</jats:styled-content> 1.51, 5.72]; <jats:italic>P</jats:italic> = 0.002) and a longer <jats:styled-content style="fixed-case">LOS</jats:styled-content> (slope 2.69 days [95% <jats:styled-content style="fixed-case">CI</jats:styled-content> 0.65, 4.73]; <jats:italic>P</jats:italic> = 0.008), after accounting for <jats:styled-content style="fixed-case">VACS</jats:styled-content> Index. Readmission was not associated with <jats:styled-content style="fixed-case">ART</jats:styled-content> use (<jats:styled-content style="fixed-case">OR</jats:styled-content> 1.12 [95% <jats:styled-content style="fixed-case">CI</jats:styled-content> 0.62, 2.00] <jats:italic>P</jats:italic> = 0.714).</jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p>Among <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐infected and uninfected older adults hospitalized for <jats:styled-content style="fixed-case">CAP</jats:styled-content>, organ system components of the <jats:styled-content style="fixed-case">VACS</jats:styled-content> Index were associated with adverse <jats:styled-content style="fixed-case">CAP</jats:styled-content> outcomes. Among <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐infected individuals, <jats:styled-content style="fixed-case">ART</jats:styled-content> was associated with decreased 30‐day mortality and <jats:styled-content style="fixed-case">LOS</jats:styled-content>.</jats:p></jats:sec> Comparing clinical outcomes in <scp>HIV</scp>‐infected and uninfected older men hospitalized with community‐acquired pneumonia HIV Medicine
doi_str_mv 10.1111/hiv.12244
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Medizin
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imprint Wiley, 2015
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1468-1293
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match_str barakat2015comparingclinicaloutcomesinhivinfectedanduninfectedoldermenhospitalizedwithcommunityacquiredpneumonia
publishDateSort 2015
publisher Wiley
recordtype ai
record_format ai
series HIV Medicine
source_id 49
title Comparing clinical outcomes in HIV‐infected and uninfected older men hospitalized with community‐acquired pneumonia
title_unstemmed Comparing clinical outcomes in HIV‐infected and uninfected older men hospitalized with community‐acquired pneumonia
title_full Comparing clinical outcomes in HIV‐infected and uninfected older men hospitalized with community‐acquired pneumonia
title_fullStr Comparing clinical outcomes in HIV‐infected and uninfected older men hospitalized with community‐acquired pneumonia
title_full_unstemmed Comparing clinical outcomes in HIV‐infected and uninfected older men hospitalized with community‐acquired pneumonia
title_short Comparing clinical outcomes in HIV‐infected and uninfected older men hospitalized with community‐acquired pneumonia
title_sort comparing clinical outcomes in <scp>hiv</scp>‐infected and uninfected older men hospitalized with community‐acquired pneumonia
topic Pharmacology (medical)
Infectious Diseases
Health Policy
url http://dx.doi.org/10.1111/hiv.12244
publishDate 2015
physical 421-430
description <jats:sec><jats:title>Objectives</jats:title><jats:p>Outcomes of community–acquired pneumonia (<jats:styled-content style="fixed-case">CAP</jats:styled-content>) among <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐infected older adults are unclear.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>Associations between <jats:styled-content style="fixed-case">HIV</jats:styled-content> infection and three <jats:styled-content style="fixed-case">CAP</jats:styled-content> outcomes (30‐day mortality, readmission within 30 days post‐discharge, and hospital length of stay [<jats:styled-content style="fixed-case">LOS</jats:styled-content>]) were examined in the <jats:styled-content style="fixed-case">V</jats:styled-content>eterans <jats:styled-content style="fixed-case">A</jats:styled-content>ging <jats:styled-content style="fixed-case">C</jats:styled-content>ohort <jats:styled-content style="fixed-case">S</jats:styled-content>tudy (<jats:styled-content style="fixed-case">VACS</jats:styled-content>) of male Veterans, age ≥ 50 years, hospitalized for <jats:styled-content style="fixed-case">CAP</jats:styled-content> from 10/1/2002 through 08/31/2010. Associations between the <jats:styled-content style="fixed-case">VACS</jats:styled-content> Index and <jats:styled-content style="fixed-case">CAP</jats:styled-content> outcomes were assessed in multivariable models.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>Among 117 557 <jats:styled-content style="fixed-case">V</jats:styled-content>eterans (36 922 <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐infected and 80 635 uninfected), 1203 met our eligibility criteria. The 30‐day mortality rate was 5.3%, the mean <jats:styled-content style="fixed-case">LOS</jats:styled-content> was 7.3 days, and 13.2% were readmitted within 30 days of discharge. In unadjusted analyses, there were no significant differences between <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐infected and uninfected participants regarding the three <jats:styled-content style="fixed-case">CAP</jats:styled-content> outcomes (<jats:italic>P</jats:italic> &gt; 0.2). A higher <jats:styled-content style="fixed-case">VACS</jats:styled-content> Index was associated with increased 30‐day mortality, readmission, and <jats:styled-content style="fixed-case">LOS</jats:styled-content> in both <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐infected and uninfected groups. Generic organ system components of the <jats:styled-content style="fixed-case">VACS</jats:styled-content> Index were associated with adverse <jats:styled-content style="fixed-case">CAP</jats:styled-content> outcomes; <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐specific components were not. Among <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐infected participants, those not on antiretroviral therapy (<jats:styled-content style="fixed-case">ART</jats:styled-content>) had a higher 30‐day mortality (<jats:styled-content style="fixed-case">HR</jats:styled-content> 2.94 [95% <jats:styled-content style="fixed-case">CI</jats:styled-content> 1.51, 5.72]; <jats:italic>P</jats:italic> = 0.002) and a longer <jats:styled-content style="fixed-case">LOS</jats:styled-content> (slope 2.69 days [95% <jats:styled-content style="fixed-case">CI</jats:styled-content> 0.65, 4.73]; <jats:italic>P</jats:italic> = 0.008), after accounting for <jats:styled-content style="fixed-case">VACS</jats:styled-content> Index. Readmission was not associated with <jats:styled-content style="fixed-case">ART</jats:styled-content> use (<jats:styled-content style="fixed-case">OR</jats:styled-content> 1.12 [95% <jats:styled-content style="fixed-case">CI</jats:styled-content> 0.62, 2.00] <jats:italic>P</jats:italic> = 0.714).</jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p>Among <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐infected and uninfected older adults hospitalized for <jats:styled-content style="fixed-case">CAP</jats:styled-content>, organ system components of the <jats:styled-content style="fixed-case">VACS</jats:styled-content> Index were associated with adverse <jats:styled-content style="fixed-case">CAP</jats:styled-content> outcomes. Among <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐infected individuals, <jats:styled-content style="fixed-case">ART</jats:styled-content> was associated with decreased 30‐day mortality and <jats:styled-content style="fixed-case">LOS</jats:styled-content>.</jats:p></jats:sec>
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author Barakat, LA, Juthani‐Mehta, M, Allore, H, Trentalange, M, Tate, J, Rimland, D, Pisani, M, Akgün, KM, Goetz, MB, Butt, AA, Rodriguez‐Barradas, M, Duggal, M, Crothers, K, Justice, AC, Quagliarello, VJ
author_facet Barakat, LA, Juthani‐Mehta, M, Allore, H, Trentalange, M, Tate, J, Rimland, D, Pisani, M, Akgün, KM, Goetz, MB, Butt, AA, Rodriguez‐Barradas, M, Duggal, M, Crothers, K, Justice, AC, Quagliarello, VJ, Barakat, LA, Juthani‐Mehta, M, Allore, H, Trentalange, M, Tate, J, Rimland, D, Pisani, M, Akgün, KM, Goetz, MB, Butt, AA, Rodriguez‐Barradas, M, Duggal, M, Crothers, K, Justice, AC, Quagliarello, VJ
author_sort barakat, la
container_issue 7
container_start_page 421
container_title HIV Medicine
container_volume 16
description <jats:sec><jats:title>Objectives</jats:title><jats:p>Outcomes of community–acquired pneumonia (<jats:styled-content style="fixed-case">CAP</jats:styled-content>) among <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐infected older adults are unclear.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>Associations between <jats:styled-content style="fixed-case">HIV</jats:styled-content> infection and three <jats:styled-content style="fixed-case">CAP</jats:styled-content> outcomes (30‐day mortality, readmission within 30 days post‐discharge, and hospital length of stay [<jats:styled-content style="fixed-case">LOS</jats:styled-content>]) were examined in the <jats:styled-content style="fixed-case">V</jats:styled-content>eterans <jats:styled-content style="fixed-case">A</jats:styled-content>ging <jats:styled-content style="fixed-case">C</jats:styled-content>ohort <jats:styled-content style="fixed-case">S</jats:styled-content>tudy (<jats:styled-content style="fixed-case">VACS</jats:styled-content>) of male Veterans, age ≥ 50 years, hospitalized for <jats:styled-content style="fixed-case">CAP</jats:styled-content> from 10/1/2002 through 08/31/2010. Associations between the <jats:styled-content style="fixed-case">VACS</jats:styled-content> Index and <jats:styled-content style="fixed-case">CAP</jats:styled-content> outcomes were assessed in multivariable models.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>Among 117 557 <jats:styled-content style="fixed-case">V</jats:styled-content>eterans (36 922 <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐infected and 80 635 uninfected), 1203 met our eligibility criteria. The 30‐day mortality rate was 5.3%, the mean <jats:styled-content style="fixed-case">LOS</jats:styled-content> was 7.3 days, and 13.2% were readmitted within 30 days of discharge. In unadjusted analyses, there were no significant differences between <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐infected and uninfected participants regarding the three <jats:styled-content style="fixed-case">CAP</jats:styled-content> outcomes (<jats:italic>P</jats:italic> &gt; 0.2). A higher <jats:styled-content style="fixed-case">VACS</jats:styled-content> Index was associated with increased 30‐day mortality, readmission, and <jats:styled-content style="fixed-case">LOS</jats:styled-content> in both <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐infected and uninfected groups. Generic organ system components of the <jats:styled-content style="fixed-case">VACS</jats:styled-content> Index were associated with adverse <jats:styled-content style="fixed-case">CAP</jats:styled-content> outcomes; <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐specific components were not. Among <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐infected participants, those not on antiretroviral therapy (<jats:styled-content style="fixed-case">ART</jats:styled-content>) had a higher 30‐day mortality (<jats:styled-content style="fixed-case">HR</jats:styled-content> 2.94 [95% <jats:styled-content style="fixed-case">CI</jats:styled-content> 1.51, 5.72]; <jats:italic>P</jats:italic> = 0.002) and a longer <jats:styled-content style="fixed-case">LOS</jats:styled-content> (slope 2.69 days [95% <jats:styled-content style="fixed-case">CI</jats:styled-content> 0.65, 4.73]; <jats:italic>P</jats:italic> = 0.008), after accounting for <jats:styled-content style="fixed-case">VACS</jats:styled-content> Index. Readmission was not associated with <jats:styled-content style="fixed-case">ART</jats:styled-content> use (<jats:styled-content style="fixed-case">OR</jats:styled-content> 1.12 [95% <jats:styled-content style="fixed-case">CI</jats:styled-content> 0.62, 2.00] <jats:italic>P</jats:italic> = 0.714).</jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p>Among <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐infected and uninfected older adults hospitalized for <jats:styled-content style="fixed-case">CAP</jats:styled-content>, organ system components of the <jats:styled-content style="fixed-case">VACS</jats:styled-content> Index were associated with adverse <jats:styled-content style="fixed-case">CAP</jats:styled-content> outcomes. Among <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐infected individuals, <jats:styled-content style="fixed-case">ART</jats:styled-content> was associated with decreased 30‐day mortality and <jats:styled-content style="fixed-case">LOS</jats:styled-content>.</jats:p></jats:sec>
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spelling Barakat, LA Juthani‐Mehta, M Allore, H Trentalange, M Tate, J Rimland, D Pisani, M Akgün, KM Goetz, MB Butt, AA Rodriguez‐Barradas, M Duggal, M Crothers, K Justice, AC Quagliarello, VJ 1464-2662 1468-1293 Wiley Pharmacology (medical) Infectious Diseases Health Policy http://dx.doi.org/10.1111/hiv.12244 <jats:sec><jats:title>Objectives</jats:title><jats:p>Outcomes of community–acquired pneumonia (<jats:styled-content style="fixed-case">CAP</jats:styled-content>) among <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐infected older adults are unclear.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>Associations between <jats:styled-content style="fixed-case">HIV</jats:styled-content> infection and three <jats:styled-content style="fixed-case">CAP</jats:styled-content> outcomes (30‐day mortality, readmission within 30 days post‐discharge, and hospital length of stay [<jats:styled-content style="fixed-case">LOS</jats:styled-content>]) were examined in the <jats:styled-content style="fixed-case">V</jats:styled-content>eterans <jats:styled-content style="fixed-case">A</jats:styled-content>ging <jats:styled-content style="fixed-case">C</jats:styled-content>ohort <jats:styled-content style="fixed-case">S</jats:styled-content>tudy (<jats:styled-content style="fixed-case">VACS</jats:styled-content>) of male Veterans, age ≥ 50 years, hospitalized for <jats:styled-content style="fixed-case">CAP</jats:styled-content> from 10/1/2002 through 08/31/2010. Associations between the <jats:styled-content style="fixed-case">VACS</jats:styled-content> Index and <jats:styled-content style="fixed-case">CAP</jats:styled-content> outcomes were assessed in multivariable models.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>Among 117 557 <jats:styled-content style="fixed-case">V</jats:styled-content>eterans (36 922 <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐infected and 80 635 uninfected), 1203 met our eligibility criteria. The 30‐day mortality rate was 5.3%, the mean <jats:styled-content style="fixed-case">LOS</jats:styled-content> was 7.3 days, and 13.2% were readmitted within 30 days of discharge. In unadjusted analyses, there were no significant differences between <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐infected and uninfected participants regarding the three <jats:styled-content style="fixed-case">CAP</jats:styled-content> outcomes (<jats:italic>P</jats:italic> &gt; 0.2). A higher <jats:styled-content style="fixed-case">VACS</jats:styled-content> Index was associated with increased 30‐day mortality, readmission, and <jats:styled-content style="fixed-case">LOS</jats:styled-content> in both <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐infected and uninfected groups. Generic organ system components of the <jats:styled-content style="fixed-case">VACS</jats:styled-content> Index were associated with adverse <jats:styled-content style="fixed-case">CAP</jats:styled-content> outcomes; <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐specific components were not. Among <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐infected participants, those not on antiretroviral therapy (<jats:styled-content style="fixed-case">ART</jats:styled-content>) had a higher 30‐day mortality (<jats:styled-content style="fixed-case">HR</jats:styled-content> 2.94 [95% <jats:styled-content style="fixed-case">CI</jats:styled-content> 1.51, 5.72]; <jats:italic>P</jats:italic> = 0.002) and a longer <jats:styled-content style="fixed-case">LOS</jats:styled-content> (slope 2.69 days [95% <jats:styled-content style="fixed-case">CI</jats:styled-content> 0.65, 4.73]; <jats:italic>P</jats:italic> = 0.008), after accounting for <jats:styled-content style="fixed-case">VACS</jats:styled-content> Index. Readmission was not associated with <jats:styled-content style="fixed-case">ART</jats:styled-content> use (<jats:styled-content style="fixed-case">OR</jats:styled-content> 1.12 [95% <jats:styled-content style="fixed-case">CI</jats:styled-content> 0.62, 2.00] <jats:italic>P</jats:italic> = 0.714).</jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p>Among <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐infected and uninfected older adults hospitalized for <jats:styled-content style="fixed-case">CAP</jats:styled-content>, organ system components of the <jats:styled-content style="fixed-case">VACS</jats:styled-content> Index were associated with adverse <jats:styled-content style="fixed-case">CAP</jats:styled-content> outcomes. Among <jats:styled-content style="fixed-case">HIV</jats:styled-content>‐infected individuals, <jats:styled-content style="fixed-case">ART</jats:styled-content> was associated with decreased 30‐day mortality and <jats:styled-content style="fixed-case">LOS</jats:styled-content>.</jats:p></jats:sec> Comparing clinical outcomes in <scp>HIV</scp>‐infected and uninfected older men hospitalized with community‐acquired pneumonia HIV Medicine
spellingShingle Barakat, LA, Juthani‐Mehta, M, Allore, H, Trentalange, M, Tate, J, Rimland, D, Pisani, M, Akgün, KM, Goetz, MB, Butt, AA, Rodriguez‐Barradas, M, Duggal, M, Crothers, K, Justice, AC, Quagliarello, VJ, HIV Medicine, Comparing clinical outcomes in HIV‐infected and uninfected older men hospitalized with community‐acquired pneumonia, Pharmacology (medical), Infectious Diseases, Health Policy
title Comparing clinical outcomes in HIV‐infected and uninfected older men hospitalized with community‐acquired pneumonia
title_full Comparing clinical outcomes in HIV‐infected and uninfected older men hospitalized with community‐acquired pneumonia
title_fullStr Comparing clinical outcomes in HIV‐infected and uninfected older men hospitalized with community‐acquired pneumonia
title_full_unstemmed Comparing clinical outcomes in HIV‐infected and uninfected older men hospitalized with community‐acquired pneumonia
title_short Comparing clinical outcomes in HIV‐infected and uninfected older men hospitalized with community‐acquired pneumonia
title_sort comparing clinical outcomes in <scp>hiv</scp>‐infected and uninfected older men hospitalized with community‐acquired pneumonia
title_unstemmed Comparing clinical outcomes in HIV‐infected and uninfected older men hospitalized with community‐acquired pneumonia
topic Pharmacology (medical), Infectious Diseases, Health Policy
url http://dx.doi.org/10.1111/hiv.12244