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. 2019 Jan:147:e89.
doi: 10.1017/S0950268819000098.

Trends of hospitalisations rates in a cohort of HIV-infected persons followed in an Italian hospital from 1998 to 2016

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Trends of hospitalisations rates in a cohort of HIV-infected persons followed in an Italian hospital from 1998 to 2016

S Bellino et al. Epidemiol Infect. 2019 Jan.

Abstract

Here we evaluated hospitalisation rates and associated risk factors of human immunodeficiency virus (HIV)-infected individuals who were followed up in an Italian reference hospital from 1998 to 2016. Incidence rates (IR) of hospitalisations were calculated for five study periods from 1998 to 2016. The random-effects Poisson regression model was used to assess risk factors for hospitalisation including demographic and clinical characteristics. To consider that more events may occur for the same subject, multiple failure-time data analysis was also performed for selected causes using the Cox proportional hazards model. We evaluated 2031 patients. During 13 173 person-years (py) of follow-up, 3356 hospital admissions were carried out for 756 patients (IR: 255 per 1000 py). IR decreased significantly over the study period, from 634 in 1998-2000 to 126 per 1000 py in 2013-2016. Major declines were detected for AIDS-defining events, non-HIV/AIDS-related infections and neurological diseases. Older age, female sex, longer HIV duration and HCV coinfection were associated with a higher hospitalisation risk, whereas higher CD4 nadir and antiretroviral therapy were associated with a reduced risk. Influence of advanced HIV disease markers declined over time. Hospitalisation rates decreased during the study period in most causes. The relative weight of hospitalisations for non-AIDS-related tumours, cardiovascular, respiratory and kidney diseases increased during the study period, whereas those for AIDS-defining events declined.

Keywords: Causes for hospitalisation; HIV; Poisson regression model; cohort study; hospitalisation rates; multiple failure-time data analysis.

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Conflict of interest statement

I have read the journal's policy and the authors of this manuscript have the following competing interests: AB received non-financial support from Bristol-Myers Squibb and ViiV Healthcare, personal fees from Gilead Sciences. GB received travel grant from Bristol-Myers Squibb. RG received travel grant from Gilead, Mylan and Janssen-Cilag. ADL was a paid consultant or member of advisory boards for Gilead, ViiV Healthcare, AbbVie, Merck Sharp and Dohme, Roche, Bristol-Myers Squibb and Janssen-Cilag, and has received research grants and travel sponsorship from ViiV Healthcare and Merck Sharp & Dohme. SDG was a paid consultant or member of advisory boards for Gilead, ViiV Healthcare, Janssen-Cilag, Merck Sharp & Dohme and Bristol-Myers Squibb. The remaining authors have no funding or conflicts of interest to disclose.

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