ICU sedation, delirium & recovery

Outcomes in critically Ill HIV-infected patients between 1997 and 2020: analysis of the OUTCOMEREA multicenter cohort

Crit CarePublished Retrospective cohort study

Authors' conclusion

Whereas the profile of ICU-admitted HIV patients has evolved over time (HIV better controlled but more associated comorbidities), mortality risk factors remain stable, including AIDS status.

Study context

Population
Adult HIV patients hospitalized in intensive care unit (ICU), French university and non-university hospitals participating in the OutcomeRea database, over 24 yearsfirst ICU stays of 24,298
Participants
630 patients
Exposure
Trends over a 24-year period among ICU-admitted HIV patients
Outcome
Patient profile over time
Methodological detailsmulticentre, prospective database (OutcomeRea)
  • Multicentre
  • Prospective database (OutcomeRea)

Main finding

As reported in the abstract

  • Mean age and number of comorbidities (diabetes, renal and respiratory history, solid neoplasia) increased over time
  • Proportion of HIV diagnosed on ICU admission decreased significantly; median HIV disease duration and % antiviral therapy (ART)-treated increased
  • Main reasons for admission stable over time (acute respiratory distress > shock > coma)
  • Significant drop in active opportunistic infection on admission; active hemopathy qualifying for AIDS increased nonsignificantly, with significant increase in anticancer chemotherapy in ICU
  • Admissions for HIV-associated-non-AIDS (HANA) or non-HIV reasons stable over time

Observational data: associations, not effects.

Further findings

Predictors of 60-day mortality (multivariate analysis)

Advanced age, chronic liver disease, past chemotherapy, SOFA > 4 at admission, hospitalization > 24 h before ICU admission, AIDS status; not period of admission

Original publication

Outcomes in critically Ill HIV-infected patients between 1997 and 2020: analysis of the OUTCOMEREA multicenter cohort. Crit Care. Published 13 March 2023. doi:10.1186/s13054-023-04325-9

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