Characteristics and Outcomes of COVID-19-Related Hospitalization among PLWH
- PMID: 35329872
- PMCID: PMC8953934
- DOI: 10.3390/jcm11061546
Characteristics and Outcomes of COVID-19-Related Hospitalization among PLWH
Abstract
Background: There is conflicting evidence for how HIV influences COVID-19 infection. The aim of this study was to compare characteristics at presentation and the clinical outcomes of people living with HIV (PLWH) versus HIV-negative patients (non-PLWH) hospitalized with COVID-19. Methods: Primary endpoint: time until invasive ventilation/death. Secondary endpoints: time until ventilation/death, time until symptoms resolution. Results: A total of 1647 hospitalized patients were included (43 (2.6%) PLWH, 1604 non-PLWH). PLWH were younger (55 vs. 61 years) and less likely to be with PaO2/FiO2 < 300 mmHg compared with non-PLWH. Among PLWH, nadir of CD4 was 185 (75−322) cells/μL; CD4 at COVID-19 diagnosis was 272 cells/μL (127−468) and 77% of these were virologically suppressed. The cumulative probability of invasive mechanical ventilation/death at day 15 was 4.7% (95%CI 1.2−17.3) in PLWH versus 18.9% (16.9−21.1) in non-PLWH (p = 0.023). The cumulative probability of non-invasive/invasive ventilation/death at day 15 was 20.9% (11.5−36.4) in PLWH versus 37.6% (35.1−40.2) in non-PLWH (p = 0.044). The adjusted hazard ratio (aHR) of invasive mechanical ventilation/death of PLWH was 0.49 (95% CI 0.12−1.96, p = 0.310) versus non-PLWH; similarly, aHR of non-invasive/invasive ventilation/death of PLWH was 1.03 (95% CI 0.53−2.00, p = 0.926). Conclusion: A less-severe presentation of COVID-19 at hospitalization was observed in PLWH compared to non-PLWH; no difference in clinical outcomes could be detected.
Keywords: COVID-19; HIV; SARS-CoV-2.
Conflict of interest statement
R.G. received institutional grant from Gilead Sciences, personal fees for consultancy from Janssen-Cilag, M.S.D., Gilead, Viiv and Theratechnologies; A.V. received institutional grant from Gilead Sciences, personal fees for consultancy and travel grant from Janssen-Cilag, speaker’s fee from M.S.D.; S.C. received personal fees for consultancy from Janssen-Cilag, M.S.D., Gilead and Viiv; C.P. received travel grants and honoraria from Gilead and Janssen-Cilag; A.M. received honoraria from Gilead Sciences and Viiv Healthcare; E.N. received training fee and medical board from Gilead Science, S.O.B.I., Eli Lilly and Roche; EG received grants from Gilead e Mylan, speakers fee from Gilead; A.A. received personal fees for consultancy from Janssen-Cilag, M.S.D., Gilead, GlaxoSmithKline, Theratechnologies, Roche and Viiv. The other authors have nothing to declare.
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