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Introduction: Delirium is common among hospitalized elderly. Previous short-term studies reported inconsistent associations between APOEε4 allele, in-hospital delirium, and post-delirium cognitive impairment. We examined the association of APOEε4 allele with in-hospital delirium and long-term cognitive outcomes following delirium.
Methods: The electronic medical records were linked to the Korean National Health Insurance Service database of all citizens from January 2002 to July 2019. The study population consisted of 1057 memory clinic visitors with APOE genotype, longitudinal neuropsychological tests, and hospitalization records. Incident in-hospital delirium was defined as the initiation of antipsychotics during hospitalization after excluding prevalent users. Incidence analysis was conducted using Cox proportional hazards models, while longitudinal outcomes were analyzed using multivariable mixed models with an interrupted time series design.
Results: At baseline, APOEε4 carriers (N = 298, 28.2%) performed poorly on cognitive tests compared to non-carriers (CDR-SB mean±SD: 3.3 ± 3.5 vs 2.8 ± 2.9, P = 0.016; MMSE 22.3 ± 5.8 vs 23.2 ± 5.2, P = 0.029). The carriers developed more in-hospital delirium than noncarriers after covariate adjustments (HR 1.96, 95%CI 1.30-2.96, P = 0.002). The APOEε4 allele also had a more detrimental impact on four out of the five cognitive and functional measurements after the delirium (beta estimates of post-delirium change by APOEε4 for CDR-SB = 3.20, P < 0.001; CDR = 0.60, P < 0.001; KIADL = 0.99, P < 0.001; SIADL = 14.07, P < 0.001). These findings remained robust even after adjusting for covariates.
Conclusions: APOEε4 carriers demonstrated robust associations with in-hospital delirium and exhibited more post-delirium cognitive and functional impairment compared to non-carriers. Individuals with APOEε4 allele may need more attention to prevent in-hospital delirium and post-delirium cognitive and functional deterioration.
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http://dx.doi.org/10.1016/j.archger.2023.105204 | DOI Listing |
JMIR Res Protoc
September 2025
Institute of Higher Education and Research in Healthcare, Faculty of Biology and Medicine, University of Lausanne, Lausanne, Switzerland.
Background: In pediatric intensive care units, pain, sedation, delirium, and iatrogenic withdrawal syndrome (IWS) must be managed as interrelated conditions. Although clinical practice guidelines (CPGs) exist, new evidence needs to be incorporated, gaps in recommendations addressed, and recommendations adapted to the European context.
Objective: This protocol describes the development of the first patient- and family-informed European guideline for managing pain, sedation, delirium, and IWS by the European Society of Paediatric and Neonatal Intensive Care.
Minerva Anestesiol
September 2025
Department of Anesthesiology and Perioperative Medicine, University Hospital of A Coruña, A Coruña, Spain.
Nurs Crit Care
September 2025
Department of Nursing, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan.
Background: Delirium is a prevalent and serious ICU complication, particularly in elderly or ventilated patients. Accurate assessment is crucial but often inconsistent. Intensive care unit (ICU) nurses' use of the Intensive Care Delirium Screening Checklist (ICDSC) may be limited without structured training.
View Article and Find Full Text PDFAustralas J Ageing
September 2025
School of Nursing, Hungkuang University, Taichung, Taiwan.
Objective: Although existing evidence suggests a potential link between dementia and adverse outcomes in patients with COVID-19, a definitive relationship is uncertain. This study aimed to evaluate the impact of dementia on in-hospital outcomes of patients in the presence of COVID-19.
Methods: The US Nationwide Inpatient Sample (NIS) was searched for patients 65 years or older hospitalised for COVID-19 in 2020.
Front Immunol
September 2025
Department of Rheumatology and Immunology, The Affiliated Guangdong Second Provincial General Hospital of Jinan University, Guangzhou, China.
Background: The coexistence of neuropsychiatric systemic lupus erythematosus (NPSLE) and primary diffuse large B-cell lymphoma (DLBCL) of the central nervous system (CNS) (PCNS DLBCL) is extremely rare in clinical practice. This article retrospectively analyzes the clinical manifestations, imaging examinations, pathological diagnosis, and treatment process of a patient with NPSLE, from the appearance of intracranial abnormal signal shadows to the final diagnosis of PCNS DLBCL.
Case Summary: A 32-year-old Chinese female patient had previously visited our hospital due to vomiting and delirium and was diagnosed with NPSLE.