20 results on '"Aam, Stina"'
Search Results
2. Diagnostic accuracy of the Clock Drawing Test in screening for early post-stroke neurocognitive disorder: the Nor-COAST study
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Navickaite, Egle, Saltvedt, Ingvild, Lydersen, Stian, Munthe-Kaas, Ragnhild, Ihle-Hansen, Hege, Grambaite, Ramune, and Aam, Stina
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- 2024
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3. Neopterin, kynurenine metabolites, and indexes related to vitamin B6 are associated with post-stroke cognitive impairment: The Nor-COAST study
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Sandvig, Heidi Vihovde, Aam, Stina, Alme, Katinka N., Lydersen, Stian, Magne Ueland, Per, Ulvik, Arve, Wethal, Torgeir, Saltvedt, Ingvild, and Knapskog, Anne-Brita
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- 2024
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4. A Machine Learning Approach to Predict Post-stroke Fatigue. The Nor-COAST study
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Luzum, Geske, Thrane, Gyrd, Aam, Stina, Eldholm, Rannveig Sakshaug, Grambaite, Ramune, Munthe-Kaas, Ragnhild, Thingstad, Pernille, Saltvedt, Ingvild, and Askim, Torunn
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- 2024
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5. Longitudinal brain age prediction and cognitive function after stroke
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Aamodt, Eva B., Alnæs, Dag, de Lange, Ann-Marie G., Aam, Stina, Schellhorn, Till, Saltvedt, Ingvild, Beyer, Mona K., and Westlye, Lars T.
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- 2023
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6. How do busy hospital circumstances affect mortality and readmission within 60 days: A cohort study of 680 000 acute admissions in Norway
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Nilsen, Sara Marie, Asheim, Andreas, Carlsen, Fredrik, Anthun, Kjartan Sarheim, Vatten, Lars Johan, Aam, Stina, Davies, Neil M, and Bjørngaard, Johan Håkon
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- 2022
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7. Plasma Inflammatory Biomarkers Are Associated With Poststroke Cognitive Impairment: The Nor-COAST Study
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Sandvig, Heidi Vihovde, Aam, Stina, Alme, Katinka Nordheim, Askim, Torunn, Beyer, Mona K., Ellekjær, Hanne, Ihle-Hansen, Hege, Lydersen, Stian, Mollnes, Tom Eirik, Munthe-Kaas, Ragnhild, Næss, Halvor, Saltvedt, Ingvild, Seljeseth, Yngve Müller, Thingstad, Pernille, Wethal, Torgeir, and Knapskog, Anne-Brita
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- 2023
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8. Is Frailty Index a better predictor than pre-stroke modified Rankin Scale for neurocognitive outcomes 3-months post-stroke?
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Munthe-Kaas, Ragnhild, Aam, Stina, Saltvedt, Ingvild, Wyller, Torgeir Bruun, Pendlebury, Sarah T., Lydersen, Stian, Hagberg, Guri, Schellhorn, Till, Rostoft, Siri, and Ihle-Hansen, Hege
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- 2022
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9. Clinically accessible neuroimaging predictors of post-stroke neurocognitive disorder: a prospective observational study
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Schellhorn, Till, Aamodt, Eva Birgitte, Lydersen, Stian, Aam, Stina, Wyller, Torgeir Bruun, Saltvedt, Ingvild, and Beyer, Mona Kristiansen
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- 2021
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10. Test Accuracy of the Montreal Cognitive Assessment in Screening for Early Poststroke Neurocognitive Disorder: The Nor-COAST Study
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Munthe-Kaas, Ragnhild, Aam, Stina, Saltvedt, Ingvild, Wyller, Torgeir Bruun, Pendlebury, Sarah T., Lydersen, Stian, and Ihle-Hansen, Hege
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- 2021
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11. The Impact of Classification Models, Stroke Subtype, and Vascular Risk Factors on Courses of Poststroke Cognitive Impairment
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Aam, Stina, Saltvedt, Ingvild, Hansen, Hege Ihle, and Knapskog, Anne Brita
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Medisinske Fag: 700::Klinisk medisinske fag: 750::Nevrologi: 752 [VDP] - Abstract
Forekomsten av hjerneslag og demens øker eksponentielt med alder. Grunnet økende antall eldre i befolkningen de nærmeste årene vil denne forekomsten øke betydelig. Behandlingen av hjerneslag har bedret seg de senere årene og det er derfor flere som overlever hjerneslag. Det er nå omkring 12 000 hjerneslag pr. år i Norge. På verdensbasis er hjerneslag den nest hyppigste årsaken til død og hjerneslag er også en av de hyppigste årsakene til funksjonsnedsettelse. Kognitiv svikt er en av hovedårsakene til funksjonsnedsettelse etter hjerneslag. Med kognitiv svikt menes problemer med å være orientert for tid og sted, gjenkalle hendelser, lære nye ting, tenke abstrakt, forstå det som blir sagt og uttrykke seg forståelig eller ha problemer med oppmerksomhet, bedømme rom-retning eller å planlegge og utføre praktiske handlinger. Kognitiv svikt spenner fra mild kognitiv svikt hvor dagliglivet i liten grad er påvirket til demens hvor den kognitive svikten påvirker dagliglivet i større grad. Tidligere studier har vist at omkring 50 % av pasienter som har gjennomgått hjerneslag har kognitiv etter hjerneslaget og at omkring 15 % av pasienter med hjerneslag har demens før hjerneslaget. Hovedhensikten med prosjektet var å undersøke betydningen av klassifiseringsmetoder samt type hjerneslag og hjerte-karsykdom for forløpet av kognitiv svikt 3- og 18 måneder etter hjerneslag. Prosjektet er et delprosjekt i studien Norwegian Cognitive Impairment After Stroke (Nor-COAST) som er en prospektiv multisenter kohortstudie som inkluderte 815 deltakere innlagt i sykehus med akutt hjerneslag i perioden mai 2015 til mars 2017. Deltakerne ble inkludert ved slagenhetene ved St. Olavs hospital, Oslo Universitetssykehus Ullevål, Vestre Viken HF Bærum sykehus, Haukeland universitetssjukehus og Ålesund sjukehus. 700 av deltakerne ble undersøkt 3 måneder etter hjerneslaget, 599 av deltakerne ble undersøkt 18 måneder etter hjerneslaget og 483 av deltakerne ble undersøkt 36 måneder etter hjerneslaget. I Nor-COAST ble deltakerne testet med kognitive tester og fysiske tester, og det ble tatt blodprøver samt billedundersøkelser av hjernen i form av MR. Studien viste at andelen som klassifiseres med normal kognisjon, mild kognitiv svikt og demens 3 måneder etter hjerneslaget varierer med ulike klassifiseringsmetoder. Samsvaret mellom ulike klassifiseringsmetoder var dårligere for mild kognitiv svikt enn for demens. Kognitiv svikt etter hjerneslag er vanlig både 3 måneder og 18 måneder etter hjerneslaget for hele slagpopulasjonen, for de ulike typene hjerneslag og uavhengig av hjerte-karsykdom forut for hjerneslaget. Deltakere som hadde hjerneslag forårsaket av sykdom i hjernenes store kar hadde redusert oppmerksomhet sammenliknet med deltakere som hadde hjerneslag forårsaket av sykdom i hjernens små kar. Deltakere som hadde kransåresykdom, atrieflimmer eller tidligere hjerneslag, hadde dårligere kognitiv funksjon enn deltakere uten disse sykdommene. Deltakerne hadde stabil kognitiv funksjon fra 3 måneder til 18 måneder etter hjerneslaget, med unntak av at det tilkom noe bedring i språk, oppmerksomhet samt evnen til å planlegge og utføre handlinger.
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- 2021
12. High ward occupancy, bedspacing, and 60 day mortality for patients with myocardial infarction, stroke, and heart failure.
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Asheim, Andreas, Nilsen, Sara Marie, Aam, Stina, Anthun, Kjartan Sarheim, Carlsen, Fredrik, Janszky, Imre, Vatten, Lars Johan, and Bjørngaard, Johan Håkon
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MYOCARDIAL infarction ,HEART failure ,HEART failure patients ,HOSPITAL patients ,ODDS ratio - Abstract
Aims To study the consequences of crowded wards among patients with cardiovascular disease. Methods and results This is a cohort study among 201 801 patients with 258 807 admissions who were acutely admitted for myocardial infarction (N = 107 895), stroke (N = 87 336), or heart failure (N = 63 576) to any Norwegian hospital between 2008 and 2016. The ward admitting most patients with the given clinical condition was considered a patient’s home ward. We compared patients with the same condition admitted when home ward occupancy was different, at the same hospital and during comparable time periods. Occupancy was standardized such that a one-unit difference corresponded to the interquartile range in occupancy in the given month. One interquartile increase in home ward occupancy was associated with 7% higher odds of admission to an alternate ward [odds ratio (OR) 1.07, 95% confidence interval (CI) 1.09 to 1.11], and length of stay was shorter ((0.10 days, 95% CI (0.18 to (0.09). Patients with heart failure had 15% higher odds of admission to alternate wards (OR 1.15, 95% CI 1.08 to 1.23) and increased mortality [hazard ratio (HR) 1.08, 95% CI 1.03 to 1.15]. We found no apparent effect on mortality for patients with myocardial infarction (HR 0.99, 95% CI 0.94 to 1.05) or stroke (HR 1.00, 95% CI 0.96 to 1.05). Conclusions Patients with heart failure had higher risk of admission to alternate wards when home ward occupancy was high. These patients may be negatively affected by full wards. [ABSTRACT FROM AUTHOR]
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- 2022
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13. The Risk of Selection Bias in a Clinical Multi-Center Cohort Study. Results from the Norwegian Cognitive Impairment After Stroke (Nor-COAST) Study
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Kuvås, Karen Rosmo, Saltvedt, Ingvild, Aam, Stina, Thingstad, Pernille, Ellekjær, Hanne, and Askim, Torunn
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stroke registry ,Clinical Epidemiology ,cardiovascular diseases ,neurocognitive disorder ,Original Research ,dementia ,cerebrovascular disease - Abstract
Karen Rosmo Kuvås,1 Ingvild Saltvedt,1,2 Stina Aam,1,2 Pernille Thingstad,1,3 Hanne Ellekjær,1,4 Torunn Askim1,4 1Department of Neuromedicine and Movement Science, Faculty of Medicine and Health Science, NTNU-Norwegian University of Science and Technology, Trondheim, Norway; 2Department of Geriatrics, Clinic of Medicine, St. Olavs Hospital, Trondheim University Hospital, Trondheim, Norway; 3Department of Health and Social Services, City of Trondheim, Trondheim, Norway; 4Department of Stroke, Clinic of Medicine, St Olavs Hospital, Trondheim University Hospital, Trondheim, NorwayCorrespondence: Torunn AskimDepartment of Neuromedicine and Movement Science, Faculty of Medicine and Health Science, NTNU-Norwegian University of Science and Technology, MTFS, Trondheim 7491, NorwayTel +47 99 58 92 35Email Torunn.askim@ntnu.noPurpose: The Norwegian Cognitive Impairment After Stroke (Nor-COAST) study aimed to estimate the prevalence and incidence of neurocognitive disorder in an unselected stroke cohort. The aim of the present study was to investigate whether selection bias occurred by comparing baseline characteristics from participants with non-participants in Nor-COAST.Patients and Methods: Nor-COAST is a prospective cohort multi-center study, recruiting participants from five Norwegian hospitals. Patients with the diagnosis of acute stroke were screened for inclusion. Baseline data from the participants recruited between May 2015 and March 2017 were compared to corresponding data from those not participating in Nor-COAST but registered in the Norwegian Stroke Registry. Regression analysis was used to assess whether age, stroke severity, sex and stroke subtype were independently associated with inclusion in the study.Results: Out of 2505 available patients, 815 (32.5%) were included in Nor-COAST. There were no differences between participants and non-participants with respect to age (mean (SD) age 73.5 (11.7) versus 74.2 (14.5) years) or sex (44.8% versus 46.9% women). A significantly larger proportion of the participants were independent prior to stroke (87% versus 78%), had mild strokes (69% versus 55%) and suffered from cerebral infarction (90% versus 84%). The regression analysis showed decreased odds ratio (OR) of being included for those with higher degree of pre-stroke dependency (OR 0.895, 95% CI 0.825 to 0.971, p=0.007) and a more severe stroke (OR 0.952, 95% CI 0.939 to 0.966, p< 0.001).Conclusion: The participants in Nor-COAST had a better pre-stroke health condition and milder strokes compared to non-participants. However, the participants should be regarded as representative of the majority of the stroke population which suffers from mild strokes. Nevertheless, baseline information for non-participants should be available also in future clinical studies to make it easier to identify which part of the stroke population the results can be generalized to.Keywords: neurocognitive disorder, dementia, cerebrovascular disease, stroke registry
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- 2020
14. Test Accuracy of the Montreal Cognitive Assessment in Screening for Early Poststroke Neurocognitive Disorder
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Munthe-Kaas, Ragnhild, Aam, Stina, Saltvedt, Ingvild, Wyller, Torgeir Bruun, Pendlebury, Sarah T., Lydersen, Stian, and Ihle-Hansen, Hege
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Background. Human immunodeficiency virus (HIV)–infected immunological nonresponders (INRs) fail to reconstitute their CD4+ T-cell pool after initiation of antiretroviral therapy, and their prognosis is inferior to that of immunological responders (IRs). A prevailing hypothesis is that the INR phenotype is caused by a persistently disrupted mucosal barrier, but assessments of gut mucosal immunology in different anatomical compartments are scarce. Methods. We investigated circulating markers of mucosal dysfunction, immune activation, mucosal Th17 and Th22 cells, and mucosa-adherent microbiota signatures in gut mucosal specimens from sigmoid colon and terminal ileum of 19 INRs and 20 IRs in addition to 20 HIV-negative individuals. Results. INRs had higher blood levels of the enterocyte damage marker intestinal fatty acid–binding protein than IRs. In gut mucosal biopsies, INRs had lower fractions of CD4+ T cells, higher fractions of interleukin 22, and a tendency to higher fractions of interleukin 17–producing CD4+ T cells. These findings were all restricted to the colon and correlated to circulating markers of enterocyte damage. There were no observed differences in gut microbial composition between INRs and IRs. Conclusions. Restricted to the colon, enterocyte damage and mucosal immune dysfunction play a role for insufficient immune reconstitution in HIV infection independent of the gut microbiota. © The Author(s) 2020. Published by Oxford University Press for the Infectious Diseases Society of America. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/ by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com DOI: 10.1093/infdis/jiaa714
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- 2020
15. The Impact of Vascular Risk Factors on Post-stroke Cognitive Impairment: The Nor-COAST Study.
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Aam, Stina, Gynnild, Mari Nordbø, Munthe-Kaas, Ragnhild, Saltvedt, Ingvild, Lydersen, Stian, Knapskog, Anne-Brita, Ihle-Hansen, Hege, Ellekjær, Hanne, Eldholm, Rannveig Sakshaug, and Fure, Brynjar
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STROKE ,COGNITION disorders ,COGNITION ,EXECUTIVE function ,CORONARY disease ,MONTREAL Cognitive Assessment - Abstract
Introduction: Post-stroke cognitive impairment (PSCI) is common, but evidence on the impact of vascular risk factors is lacking. We explored the association between pre-stroke vascular risk factors and PSCI and studied the course of PSCI. Materials and Methods: Vascular risk factors were collected at baseline in stroke survivors (n = 635). Cognitive assessments of attention, executive function, memory, language, and the Montreal Cognitive Assessment (MoCA) were performed at 3 and/or 18 months post-stroke. Stroke severity was assessed with the National Institutes of Health Stroke Scale (NIHSS). PSCI was measured with global z; MoCA z-score; and z-score of the four assessed cognitive domains. Mixed-effect linear regression was applied with global z, MoCA z-score, and z-scores of the cognitive domains as dependent variables. Independent variables were the vascular risk factors (hypertension, hypercholesterolemia, smoking, diabetes mellitus, atrial fibrillation, coronary heart disease, previous stroke), time, and the interaction between these. The analyses were adjusted for age, education, and sex. There were between 5 and 25% missing data for the variables for PSCI. Results: Mean age was 71.6 years (SD 11.7); 42% were females; and the mean NIHSS score at admittance was 3.8 (SD 4.8). Regardless of vascular risk factors, global z, MoCA, and all the assessed cognitive domains were impaired at 3 and 18 months, with MoCA being the most severely impaired. Atrial fibrillation (AF) was associated with poorer language at 18 months and coronary heart disease (CHD) with poorer MoCA at 18 months (LR = 12.80, p = 0.002, and LR = 8.32, p = 0.004, respectively). Previous stroke was associated with poorer global z and attention at 3 and 18 months (LR = 15.46, p < 0.001, and LR = 16.20, p < 0.001). In patients without AF, attention improved from 3 to 18 months, and in patients without CHD, executive function improved from 3 to 18 months (LR = 10.42, p < 0.001, and LR = 9.33, p = 0.009, respectively). Discussion: Our findings indicate that a focal stroke lesion might be related to pathophysiological processes leading to global cognitive impairment. The poorer prognosis of PSCI in patients with vascular risk factors emphasizes the need for further research on complex vascular risk factor interventions to prevent PSCI. [ABSTRACT FROM AUTHOR]
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- 2021
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16. Current and Future Prevalence Estimates of Mild Cognitive Impairment, Dementia, and Its Subtypes in a Population-Based Sample of People 70 Years and Older in Norway: The HUNT Study.
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Gjøra, Linda, Strand, Bjørn Heine, Bergh, Sverre, Borza, Tom, Brækhus, Anne, Engedal, Knut, Johannessen, Aud, Kvello-Alme, Marte, Krokstad, Steinar, Livingston, Gill, Matthews, Fiona E., Myrstad, Christian, Skjellegrind, Håvard, Thingstad, Pernille, Aakhus, Eivind, Aam, Stina, Selbæk, Geir, GjØra, Linda, and Strand, BjØrn Heine
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MILD cognitive impairment ,MEDICAL personnel ,ALZHEIMER'S disease ,DEMENTIA ,COGNITIVE testing ,APOLIPOPROTEIN E4 ,DIAGNOSIS of dementia ,ALZHEIMER'S disease diagnosis ,RESEARCH ,RESEARCH methodology ,MEDICAL cooperation ,EVALUATION research ,SEX distribution ,NEUROPSYCHOLOGICAL tests ,COMPARATIVE studies ,DISEASE prevalence ,FORECASTING - Abstract
Background: Having accurate, up-to-date information on the epidemiology of mild cognitive impairment (MCI) and dementia is imperative.Objective: To determine the prevalence of MCI and dementia in Norway using data from a large population-based study.Methods: All people 70 + years of age, n = 19,403, in the fourth wave of the Trøndelag Health Study (HUNT4) were invited to participate in the study HUNT4 70 + . Trained health personnel assessed participants using cognitive tests at a field station, at homes, or at their nursing home. Interviewers also completed a structured carer questionnaire in regard to participants suspected of having dementia. Clinical experts made diagnoses according to DSM-5 criteria. We calculated prevalence weighing the data to ensure population representativeness.Results: A total of 9,930 (51.2%) of the possible 19,403 people participated, and 9,663 of these had sufficient information for analysis. Standardized prevalence of dementia and MCI was 14.6% (95% confidence interval (CI) 13.9-15.4) and 35.3% (95% CI 34.3-36.4), respectively. Dementia was more prevalent in women and MCI more prevalent in men. The most prevalent dementia subtype was Alzheimer's disease (57%). By adding data collected from a study of persons < 70 years in the same region, we estimate that there are 101,118 persons with dementia in Norway in 2020, and this is projected to increase to 236,789 and 380,134 in 2050 and 2100, respectively.Conclusion: We found a higher prevalence of dementia and MCI than most previous studies. The present prevalence and future projections are vital for preparing for future challenges to the healthcare system and the entire society. [ABSTRACT FROM AUTHOR]- Published
- 2021
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17. Post-stroke Cognitive Impairment—Impact of Follow-Up Time and Stroke Subtype on Severity and Cognitive Profile: The Nor-COAST Study.
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Aam, Stina, Einstad, Marte Stine, Munthe-Kaas, Ragnhild, Lydersen, Stian, Ihle-Hansen, Hege, Knapskog, Anne-Brita, Ellekjær, Hanne, Seljeseth, Yngve, and Saltvedt, Ingvild
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COGNITION disorders ,MONTREAL Cognitive Assessment ,STROKE ,LIKELIHOOD ratio tests ,COGNITION - Abstract
Background: Post-stroke cognitive impairment (PSCI) is common, but evidence of cognitive symptom profiles, course over time, and pathogenesis is scarce. We investigated the significance of time and etiologic stroke subtype for the probability of PSCI, severity, and cognitive profile. Methods: Stroke survivors (n = 617) underwent cognitive assessments of attention, executive function, memory, language, perceptual-motor function, and the Montreal Cognitive Assessment (MoCA) after 3 and/or 18 months. PSCI was classified according to DSM-5 criteria. Stroke severity was assessed with the National Institutes of Health Stroke Scale (NIHSS). Stroke subtype was categorized as intracerebral hemorrhage (ICH), large artery disease (LAD), cardioembolic stroke (CE), small vessel disease (SVD), or un-/other determined strokes (UD). Mixed-effects logistic or linear regression was applied with PSCI, MoCA, and z-scores of the cognitive domains as dependent variables. Independent variables were time as well as stroke subtype, time, and interaction between these. The analyses were adjusted for age, education, and sex. The effects of time and stroke subtype were analyzed by likelihood ratio tests (LR). Results: Mean age was 72 years (SD 12), 42% were females, and mean NIHSS score at admittance was 3.8 (SD 4.8). Probability (95% CI) for PSCI after 3 and 18 months was 0.59 (0.51–0.66) and 0.51 (0.52–0.60), respectively and remained constant over time. Global measures and most cognitive domains were assessed as impaired for the entire stroke population and for most stroke subtypes. Executive function and language improved for the entire stroke population (LR) = 9.05, p = 0.003, and LR = 10.38, p = 0.001, respectively). After dividing the sample according to stroke subtypes, language improved for ICH patients (LR = 18.02, p = 0.003). No significant differences were found in the severity of impairment between stroke subtypes except for attention, which was impaired for LAD and CE in contrast to no impairment for SVD (LR = 56.58, p < 0.001). Conclusions: In this study including mainly minor strokes, PSCI is common for all subtypes, both early and long-term after stroke, while executive function and language improve over time. The findings might contribute to personalizing follow-up and offer new insights into underlying mechanisms. Further research is needed on underlying mechanisms, PSCI prevention and treatment, and relevance for rehabilitation. [ABSTRACT FROM AUTHOR]
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- 2020
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18. Impact of Pre-Stroke Frailty on Outcome Three Years after Acute Stroke: The Nor-COAST Study.
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Munthe-Kaas, Ragnhild, Lydersen, Stian, Quinn, Terry, Aam, Stina, Pendlebury, Sarah T., and Ihle-Hansen, Hege
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STROKE , *LOGISTIC regression analysis , *STROKE patients , *OLDER people , *COGNITION disorders - Abstract
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We aimed to explore the predictive value of pre-stroke frailty index (FI) on functional dependency and mortality 3 years after stroke.Introduction: Based on the Rockwood 36-item FI score, we calculated the pre-stroke FI from medical conditions recorded at baseline in the multicenter prospective Nor-COAST study 2015–2017. Participants with a FI score and a modified Rankin scale (mRS) 0–6 3 years post-stroke were included in this study. We used logistic regression analysis with unfavorable mRS (over 2 vs. 0–2) at 3 years, or dead within 3 years, as dependent variable, and frailty and pre-stroke mRS, one at a time, and simultaneously, as predictors. The analyses were carried out unadjusted and adjusted for the following variables one at a time: Age, sex, years of education, stroke severity at admission, infections treated with antibiotics and stroke progression. We report odds ratio (OR) per 0.10 increase in FI.Methods: At baseline, the 609 included patients had mean age 72.8 (standard deviation [SD] 11.8), 261 (43%) were females, and had a FI mean score of 0.16 (SD 0.12), range 0–0.69. During 3 years, 138 (23%) had died. Both the FI, and pre-stroke mRS, were strong predictors for unfavorable mRS (OR 4.1 and 2.7) and dead within 3 years (OR 2.2 and 1.7). Only adjusting for age affected the result. The OR for pre-stroke mRS decreased relatively more than the OR for FI when entered as predictors simultaneously.Results: FI is a stronger predictor than premorbid mRS for prognostication after stroke. Stroke is a leading cause of dead and disability in the world. It is an acute condition prevalent in older populations. As more older adults surviving previously fatal strokes, the prevalence of stroke survivors with different functional and cognitive impairments increase. There is a great heterogeneity in outcome after stroke, even in milder strokes. We know less of what predict poor outcome. While increasing age in general is associated with poor outcome, at individual plan the relationship with age is more uncertain. Frailty is a concept gaining more attention over the recent years. It is defined as a condition of vulnerability associated with an increased risk of adverse health outcomes such as functional decline and mortality. Frail people have an increased risk of developing disease when something extraordinary occurs. Less is known about the relationship between stroke and frailty. Frailty assessment is not yet part of routine stroke care. In this study, we explored the impact of pre-stroke frailty on functional dependency and mortality 3 years after stroke. We found that the degree of frailty before stroke had a huge impact on functional status and mortality 3 years after stroke, even when we adjusted for important factors, like stroke severity and age. This demonstrates the importance of implementing frailty measures as a routine tool in stroke medicine. It also underline the value of developing preventing mechanisms of frailty in the older population. [ABSTRACT FROM AUTHOR]Conclusions: - Published
- 2024
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19. The Risk of Selection Bias in a Clinical Multi-Center Cohort Study. Results from the Norwegian Cognitive Impairment After Stroke (Nor-COAST) Study.
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Kuvås KR, Saltvedt I, Aam S, Thingstad P, Ellekjær H, and Askim T
- Abstract
Purpose: The Norwegian Cognitive Impairment After Stroke (Nor-COAST) study aimed to estimate the prevalence and incidence of neurocognitive disorder in an unselected stroke cohort. The aim of the present study was to investigate whether selection bias occurred by comparing baseline characteristics from participants with non-participants in Nor-COAST., Patients and Methods: Nor-COAST is a prospective cohort multi-center study, recruiting participants from five Norwegian hospitals. Patients with the diagnosis of acute stroke were screened for inclusion. Baseline data from the participants recruited between May 2015 and March 2017 were compared to corresponding data from those not participating in Nor-COAST but registered in the Norwegian Stroke Registry. Regression analysis was used to assess whether age, stroke severity, sex and stroke subtype were independently associated with inclusion in the study., Results: Out of 2505 available patients, 815 (32.5%) were included in Nor-COAST. There were no differences between participants and non-participants with respect to age (mean (SD) age 73.5 (11.7) versus 74.2 (14.5) years) or sex (44.8% versus 46.9% women). A significantly larger proportion of the participants were independent prior to stroke (87% versus 78%), had mild strokes (69% versus 55%) and suffered from cerebral infarction (90% versus 84%). The regression analysis showed decreased odds ratio (OR) of being included for those with higher degree of pre-stroke dependency (OR 0.895, 95% CI 0.825 to 0.971, p=0.007) and a more severe stroke (OR 0.952, 95% CI 0.939 to 0.966, p<0.001)., Conclusion: The participants in Nor-COAST had a better pre-stroke health condition and milder strokes compared to non-participants. However, the participants should be regarded as representative of the majority of the stroke population which suffers from mild strokes. Nevertheless, baseline information for non-participants should be available also in future clinical studies to make it easier to identify which part of the stroke population the results can be generalized to., Competing Interests: Nor-COAST was funded by the Norwegian Health Association. The funder had no role in designing the study and has not taken part in the data collection, analysis or interpretation of the results. No authors report competing interests related to this work. However, Dr. Saltvedt reports being an investigator in the Boehringer-Ingelheim drug trial, 1346.0023,) outside the submitted work., (© 2020 Kuvås et al.)
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- 2020
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20. Impact of different methods defining post-stroke neurocognitive disorder: The Nor-COAST study.
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Munthe-Kaas R, Aam S, Ihle-Hansen H, Lydersen S, Knapskog AB, Wyller TB, Fure B, Thingstad P, Askim T, Beyer MK, Næss H, Seljeseth YM, Ellekjær H, Pendlebury ST, and Saltvedt I
- Abstract
Introduction: Post-stroke neurocognitive disorder (NCD) is common; prevalence varies between studies, partially related to lack of consensus on how to identify cases. The aim was to compare the prevalence of post-stroke NCD using only cognitive assessment (model A), DSM-5 criteria (model B), and the Global Deterioration Scale (model C) and to determine agreement among the three models., Methods: In the Norwegian Cognitive Impairment After Stroke study, 599 patients were assessed 3 months after suffering a stroke., Results: The prevalence of mild NCD varied from 174 (29%) in model B to 83 (14%) in model C; prevalence of major NCD varied from 249 (42%) in model A to 68 (11%) in model C. Cohen's kappa and Cohen's quadratic weighted kappa showed fair to very good agreement among models; the poorest agreement was found for identification of mild NCD., Discussion: The findings indicate a need for international harmonization to classify post-stroke NCD., Competing Interests: The authors declare they have no competing interests. ABK and IS have been investigators in the drug trial Boehringer‐Ingelheim 1346.0023, and ABK has also been an investigator for Roche BN29553., (© 2020 The Authors. Alzheimer's & Dementia: Translational Research & Clinical Interventions published by Wiley Periodicals, Inc. on behalf of Alzheimer's Association.)
- Published
- 2020
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