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Abstract Details

Early-onset delirium after spontaneous intracerebral hemorrhage
Cerebrovascular Disease and Interventional Neurology
P10 - Poster Session 10 (8:00 AM-9:00 AM)
13-011
Delirium is an acute, fluctuating and transient disorder of attention and awareness, usually triggered by acute medical conditions. To date, very few studies specifically focused on delirium after ICH, and neither incidence rates nor related clinical and radiological predictors have been fully investigated yet. Moreover, data on the impact of delirium on long-term outcomes after ICH, including mortality and dementia are lacking.

This study aimed at identifying the incidence, predictors and impact on long-term mortality and dementia of early-onset delirium in a cohort of patients with spontaneous intracerebral hemorrhage (ICH).

We prospectively recruited consecutive patients in the Prognosis of InTra-Cerebral Hemorrhage (PITCH) cohort and analyzed incidence rate of early-onset delirium (i.e. during the first 7-days after ICH onset) with a competing risk model. We used a multivariable Fine-Gray model to identify baseline predictors, a Cox regression model to study its impact on the long-term mortality risk and a Fine-Gray model adjusted for pre-specified confounders to analyze its impact on new-onset dementia.

The study population consisted of 248 patients (mean age 70 years, 54% males). Early-onset delirium incidence rate was 29.8% (95% confidence interval [CI] 24.3-35.6). Multivariate analysis showed that pre-existing dementia (subhazard ratio [SHR] 2.08, 95%CI 1.32–3.32, p=0.002), heavy alcohol intake (SHR 1.79, 95%CI 1.13–2.82, p=0.013) and ICH lobar location (SHR 1.56, CI 1.01–2.42, p=0.049) independently predicted early-onset delirium. Median follow-up was 9.5 years. Early-onset delirium was associated with higher mortality rates during the first 5-years of follow-up (HR 1.52, 95%CI 1.00–2.31, p=0.049), but did not predict new-onset dementia (SHR 1.31, 95%CI 0.60–2.87).

Early-onset delirium is a frequent complication after ICH, it is associated with markers of pre-existing brain vulnerability and with higher mortality risk, but not with higher dementia rates during long-term follow-up.

Authors/Disclosures

PRESENTER
No disclosure on file
No disclosure on file
Marco Pasi No disclosure on file
Mathieu Rutgers No disclosure on file
No disclosure on file
Didier Leys, MD, FAAN The institution of Dr. Leys has received personal compensation in the range of $10,000-$49,999 for serving as an Editor, Associate Editor, or Editorial Advisory Board Member for Wiley. Dr. Leys has received personal compensation in the range of $10,000-$49,999 for serving as an Editor, Associate Editor, or Editorial Advisory Board Member for Wiley.
No disclosure on file
Hilde Henon (Hopital Roger- Salengro) No disclosure on file
No disclosure on file