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Tytuł pozycji:

Impaired cognition predicts the risk of hospitalization and death in cirrhosis

Tytuł:
Impaired cognition predicts the risk of hospitalization and death in cirrhosis
Autorzy:
Minjee Kim
Eric M. Liotta
Phyllis C. Zee
Daniel R. Ganger
Daniela P. Ladner
Ameeta Karmarkar
John D. Peipert
Farzaneh A. Sorond
Shyam Prabhakaran
Kathryn J. Reid
Andrew M. Naidech
Matthew B. Maas
Temat:
Neurosciences. Biological psychiatry. Neuropsychiatry
RC321-571
Neurology. Diseases of the nervous system
RC346-429
Źródło:
Annals of Clinical and Translational Neurology, Vol 6, Iss 11, Pp 2282-2290 (2019)
Wydawca:
Wiley, 2019.
Rok publikacji:
2019
Kolekcja:
LCC:Neurosciences. Biological psychiatry. Neuropsychiatry
LCC:Neurology. Diseases of the nervous system
Typ dokumentu:
article
Opis pliku:
electronic resource
Język:
English
ISSN:
2328-9503
Relacje:
https://doaj.org/toc/2328-9503
DOI:
10.1002/acn3.50924
Dostęp URL:
https://doaj.org/article/a0b653f8209345cf87977f8bb423d041  Link otwiera się w nowym oknie
Numer akcesji:
edsdoj.0b653f8209345cf87977f8bb423d041
Czasopismo naukowe
Abstract Objective Cognitive impairment, detected in up to 80% of patients with liver cirrhosis, is associated with negative health outcomes but is underdiagnosed in the clinical setting due to the lack of practical testing method. This single‐center prospective observational study aimed to test the feasibility and prognostic utility of in‐clinic cognitive assessment of patients with liver cirrhosis using the NIH Toolbox cognition battery (NIHTB). Methods Patients recruited from a hepatology/transplant clinic underwent cognitive assessments using West‐Haven Grade (WHG) and NIHTB between November 2016 and August 2018 and were prospectively followed until December 2018. The primary outcome was a composite end point of hospitalization related to overt hepatic encephalopathy (OHE) and all‐cause mortality during follow‐up, evaluated by a Cox proportional hazards regression model that adjusted for a priori covariates (age and MELD‐Na). Results Among 127 patients (median age 60 years, 48 [38%] women) assessed, cognitive performance was significantly impaired in 82 [78%] patients with WHG 0 and 22 [100%] patients with WHG 1 and 2. Over a median of 347 days follow‐up, 18 OHE and 8 deaths were observed. Lower cognitive performance was associated with an increased risk of OHE/death adjusting for age and MELD‐Na. Subclinical cognitive impairment detected by NIH Toolbox in WHG 0 patients was significantly associated with greater mortality. Median time to complete the two prognostically informative NIH Toolbox tests was 9.4 min. Interpretation NIH Toolbox may enable a rapid cognitive screening in the outpatient setting and identify patients at high risk for death and hospitalization for severe encephalopathy.
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