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Vol. 30. Issue S1.
XXIV Brazilian Congress of Infectious Diseases 2025
(March 2026)
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Vol. 30. Issue S1.
XXIV Brazilian Congress of Infectious Diseases 2025
(March 2026)
156
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CYTOMEGALOVIRUS DNAEMIA AND TARGET ORGAN DISEASE IN PEOPLE LIVING WITH HIV AND SEVERE IMMUNOSUPPRESSION: FREQUENCIES, CHARACTERISTICS, AND PROGNOSTIC IMPACT IN A TERTIARY HOSPITAL IN SÃO PAULO

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José Ernesto Vidal
Corresponding author
josevibe@gmail.com

Corresponding author.
, Gustavo Arthur Reis Schneider, Giuliane Bogoni, Raphaela Ferrari, Rodovaldo Moraes Lucas Júnior, Nidyanara Francine Castanheira, Rosa Marcuso
Instituto de Infectologia Emílio Ribas (IIER), São Paulo, SP, Brazil
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Vol. 30. Issue S1

XXIV Brazilian Congress of Infectious Diseases 2025

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Introduction

There is limited recent information regarding cytomegalovirus (CMV) infection in people living with HIV (PLHIV) and severe immunosuppression. The objectives of this study were to describe the frequencies of CMV DNAemia and CMV target organ disease (CMV-TOD) in this population, their characteristics, and to assess whether high DNAemia levels and CMV-TOD are associated with in-hospital mortality.

Methods

Observational, retrospective cohort study conducted at a tertiary hospital in São Paulo. All hospitalized PLHIV over a 12-month period who met the following criteria were included: (i) CD4 count ≤ 100 cells/µL, and (ii) CMV plasma viral load measurement at admission, as per institutional routine. Frequencies of DNAemia (presence of CMV DNA in plasma) and confirmed CMV-TOD were calculated. DNAemia ≥ 10,000 IU/mL was considered high. Chi-square or Fisher’s exact tests were used as appropriate. Factors associated with in-hospital mortality were identified through multivariate logistic regression. The study was approved by the Ethics Committee.

Results

During the study period, 830 PLHIV were hospitalized, and 245 (29.5%) met inclusion criteria. Median (IQR) age was 38 (30–46) years, and 183 (74.7%) were male. Median (IQR) CD4 count was 25 (10–53) cells/µL. Median (IQR) hospital stay was 20 (8–37) days, and 57 (23%) patients died. DNAemia was identified in 150 (61.1%) cases, of which 18 (12%) had high DNAemia. Seventeen (6.9%) patients had CMV-TOD: neurological = 6 and non-neurological = 11 (gastrointestinal tract = 10, retinitis = 3, pneumonitis = 2). Forty-seven (19.1%) patients received preemptive anti-CMV antiviral therapy. Neurological CMV-TOD was associated with high DNAemia (P < 0.001, Fisher’s exact test). Confirmed bacterial infection (OR 7.5, 95% CI 3.4–16.7), antiretroviral use prior to admission (OR 3.8, 95% CI 1.8–8.1), and age ≥ 50 years (OR 3.7, 95% CI 1.6–8.4) were associated with in-hospital mortality.

Conclusion

CMV DNAemia was frequent (∼60%), and CMV-TOD was observed in 7% of cases. One in five patients received preemptive anti-CMV therapy. Neurological CMV-TOD was associated with high DNAemia in exploratory analysis. In contrast to high DNAemia and CMV-TOD, confirmed bacterial infection, prior antiretroviral use, and age ≥ 50 years were independently associated with in-hospital mortality.

Keywords:
Cytomegalovirus
Diagnosis
HIV
AIDS
Brazil
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