Background: Post-stroke delirium (PSD) is a modifiable predictor for worse outcome in stroke. Knowledge of its risk factors would facilitate clinical management of affected patients, but recently updated national guidelines consider available evidence insufficient.

Aims: The study aimed to establish risk factors for PSD incidence and duration using high-frequency screening.

Methods: We prospectively investigated patients with ischemic stroke admitted within 24 h. Patients were screened twice daily for the presence of PSD throughout the treatment period. Sociodemographic, treatment-related, and neuroimaging characteristics were evaluated as predictors of either PSD incidence (odds ratios (OR)) or duration (PSD days/unit of the predictor, ), using logistic and linear regression models, respectively.

Results: PSD occurred in 55/141 patients (age = 73.8 ± 10.4 years, 61 female, National Institutes of Health Stroke Scale (NIHSS) = 6.4 ± 6.5). Age (odds ratio (OR) = 1.06 (95% confidence interval (CI): 1.02-1.10),  = 0.08 (95% CI = 0.04-0.13)), and male gender ( = 0.99 (95% CI = 0.05-1.93)) were significant non-modifiable risk factors. In a multivariable model adjusted for age and gender, presence of pain (OR < sub >  = 1.75 (95% CI = 1.12-2.74)), urinary catheter (OR < sub >   = 3.16 (95% CI = 1.10-9.14)) and post-stroke infection (PSI; OR < sub >   = 4.43 (95% CI = 1.09-18.01)) were predictors of PSD incidence. PSD duration was impacted by presence of pain ( < sub >  = 0.49 (95% CI = 0.19-0.81)), urinary catheter ( < sub >   = 1.03 (95% CI = 0.01-2.07)), intravenous line ( < sub >  = 0.36 (95% CI = 0.16-0.57)), and PSI ( < sub >  = 1.60 (95% CI = 0.42-2.78)). PSD (OR = 3.53 (95% CI = 1.48-5.57)) and PSI (OR = 5.29 (95% CI = 2.92-7.66)) independently predicted inferior NIHSS at discharge. Insular and basal ganglia lesions increased the PSD risk about four- to eight-fold.

Discussion/conclusion: This study identified modifiable risk factors, the management of which might reduce the negative impact PSD has on outcome.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9940154PMC
http://dx.doi.org/10.1177/17474930221109353DOI Listing

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