HIV disease metrics and COVID-19 infection severity and outcomes in people living with HIV in central and eastern Europe.

CD4 cell count COVID-19 HIV viral load strata PLWH outcomes

Journal

HIV medicine
ISSN: 1468-1293
Titre abrégé: HIV Med
Pays: England
ID NLM: 100897392

Informations de publication

Date de publication:
28 Nov 2023
Historique:
received: 20 04 2023
accepted: 27 10 2023
medline: 28 11 2023
pubmed: 28 11 2023
entrez: 28 11 2023
Statut: aheadofprint

Résumé

To date there remains much ambiguity in the literature regarding the immunological interplay between SARS-CoV-2 and HIV and the true risk posed to coinfected individuals. There has been little conclusive data regarding the use of CD4 cell count and HIV viral load stratification as predictors of COVID-19 severity in this cohort. We performed a retrospective, observational cohort study on people living with HIV (PLWH) who contracted COVID-19 in central and eastern Europe. We enrolled 536 patients from 16 countries using an online survey. We evaluated patient demographics, HIV characteristics and COVID-19 presentation and outcomes. Statistical analysis was performed using SPSS 20.1. The majority of the study cohort were male (76.4%) and 152 (28.3%) had a significant medical comorbidity. Median CD4 cell count at COVID-19 diagnosis was 605 cells/μL [interquartile range (IQR) 409-824]. The majority of patients on antiretroviral therapy (ART) were virally suppressed (92%). In univariate analysis, CD4 cell count <350 cells/μL was associated with higher rates of hospitalization (p < 0.0001) and respiratory failure (p < 0.0001). Univariate and multivariate analyses found that an undetectable HIV VL was associated with a lower rate of hospitalization (p < 0.0001), respiratory failure (p < 0.0001), ICU admission or death (p < 0.0001), and with a higher chance of full recovery (p < 0.0001). We can conclude that detectable HIV viral load was an independent risk factor for severe COVID-19 illness and can be used as a prognostic indicator in this cohort.

Sections du résumé

BACKGROUND BACKGROUND
To date there remains much ambiguity in the literature regarding the immunological interplay between SARS-CoV-2 and HIV and the true risk posed to coinfected individuals. There has been little conclusive data regarding the use of CD4 cell count and HIV viral load stratification as predictors of COVID-19 severity in this cohort.
METHODS METHODS
We performed a retrospective, observational cohort study on people living with HIV (PLWH) who contracted COVID-19 in central and eastern Europe. We enrolled 536 patients from 16 countries using an online survey. We evaluated patient demographics, HIV characteristics and COVID-19 presentation and outcomes. Statistical analysis was performed using SPSS 20.1.
RESULTS RESULTS
The majority of the study cohort were male (76.4%) and 152 (28.3%) had a significant medical comorbidity. Median CD4 cell count at COVID-19 diagnosis was 605 cells/μL [interquartile range (IQR) 409-824]. The majority of patients on antiretroviral therapy (ART) were virally suppressed (92%). In univariate analysis, CD4 cell count <350 cells/μL was associated with higher rates of hospitalization (p < 0.0001) and respiratory failure (p < 0.0001). Univariate and multivariate analyses found that an undetectable HIV VL was associated with a lower rate of hospitalization (p < 0.0001), respiratory failure (p < 0.0001), ICU admission or death (p < 0.0001), and with a higher chance of full recovery (p < 0.0001).
CONCLUSION CONCLUSIONS
We can conclude that detectable HIV viral load was an independent risk factor for severe COVID-19 illness and can be used as a prognostic indicator in this cohort.

Identifiants

pubmed: 38014768
doi: 10.1111/hiv.13578
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2023 British HIV Association.

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Auteurs

Cristiana Oprea (C)

Victor Babes Clinical Hospital for Infectious and Tropical Diseases, Bucharest, Romania.
Carol Davila University for Medicine and Pharmacy, Bucharest, Romania.

Siobhan Quirke (S)

Department of Medicine, Galway University Hospital, Galway, Ireland.

Irina Ianache (I)

Victor Babes Clinical Hospital for Infectious and Tropical Diseases, Bucharest, Romania.
Carol Davila University for Medicine and Pharmacy, Bucharest, Romania.

Dominik Bursa (D)

Department of Adults' Infectious Diseases, Medical University of Warsaw, Warsaw, Poland.

Sergii Antoniak (S)

Viral Hepatitis and AIDS Department, Gromashevsky Institute of Epidemiology and Infectious Diseases, Kyiv, Ukraine.

Nicolina Bogdanic (N)

University Hospital for Infectious Diseases, University of Zagreb, School of Medicine, Zagreb, Croatia.

Anne I Vassilenko (AI)

Global Fund Grant Management Department, Republican Scientific and Practical Center for Medical Technologies, Minsk, Belarus.

Kersti Aimla (K)

Tartu University Hospital, Tartu, Estonia.

Raimonda Matulionyte (R)

Vilnius University, Faculty of Medicine, Vilnius University Hospital Santaros Klinikos, Vilnius, Lithuania.

Nino Rukhadze (N)

Infectious Diseases, AIDS and Clinical Immunology Center, Tbilisi, Georgia.

Arjan Harxhi (A)

University Hospital Center of Tirana, Infectious Disease Service, Tirana, Albania.

Lukáš Fleischhans (L)

Department of Infectious Diseases, 1st Faculty of Medicine, Charles University in Prague and Faculty Hospital Bulovka Hospital, Prague, Czech Republic.

Botond Lakatos (B)

National Institute of Hematology and Infectious Diseases, South-Pest Central Hospital, National Center of HIV, Budapest, Hungary.

Dalibor Sedlacek (D)

Charles University, Faculty of Medicine in Plzeň, University Hospital Plzeň, Plzen, Czech Republic.

Gordana Dragovic (G)

Faculty of Medicine, University of Belgrade, Department of Pharmacology, Clinical Pharmacology and Toxicology, Belgrade, Serbia.

Antonija Verhaz (A)

Department for Infectious Diseases, Faculty of Medicine, University of Banja Luka, Banja Luka, Bosnia and Herzegovina.

Nina Yancheva (N)

Department for AIDS, Specialized Hospital for Active Treatment of Infectious and Parasitic Disease Sofia, Sofi, Bulgaria.

Oguzhan Acet (O)

Department of Infectious Diseases and Clinical Microbiology, Faculty of Medicine, Ege University, Izmir, Turkey.

Konstantinos Protopapas (K)

University General Hospital Attikon, Medical School, National and Kapodistrian University of Athens, Athens, Greece.

Justyna Dominika Kowalska (JD)

Department of Adults' Infectious Diseases, Medical University of Warsaw, Warsaw, Poland.

Classifications MeSH