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Publications (3 of 3) Show all publications
Gunnarsson, K., Tofiq, a., Mathew, A., Cao, Y., von Euler, M. & Ström, J. O. (2024). Changes in stroke and TIA admissions during the COVID-19 pandemic: A meta-analysis. European Stroke Journal, 9(1), 78-87
Open this publication in new window or tab >>Changes in stroke and TIA admissions during the COVID-19 pandemic: A meta-analysis
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2024 (English)In: European Stroke Journal, ISSN 2396-9873, E-ISSN 2396-9881, Vol. 9, no 1, p. 78-87Article, review/survey (Refereed) Published
Abstract [en]

PURPOSE: To perform a meta-analysis on how the admissions of stroke and transient ischemic attack (TIA) changed during the Corona Virus infection-19 (COVID-19) pandemic and evaluate if the effect was depending on stroke severity.

METHODS: Observational cohort studies comparing the number of stroke and/or TIA admissions during a period of the pandemic compared to a period before the pandemic were identified in PubMed and Embase. After excluding studies with overlapping populations and studies without satisfactory case ascertainment, data was extracted and meta-analyzed.

FINDINGS: A total of 59 studies were included. During the pandemic, there was a decrease in admissions of ischemic stroke (admission rate ratio (ARR) = 0.77, 95% confidence interval (CI): 0.72, 0.82), intracerebral hemorrhage (ARR = 0.79, 95% CI: 0.70, 0.90) and TIA (ARR = 0.66, 95% CI: 0.58, 0.75). Albeit admission rates of both mild (ARR = 0.61, 95% CI: 0.49, 0.77) and severe (ARR = 0.82, 95% CI = 0.71, 0.95) strokes decreased, milder strokes decreased more (proportion ratio (PR) = 0.76, 95% CI: 0.65, 0.89).

DISCUSSION: Potential causes for the admission reduction could be strict prioritizations within the health care, patients' fear of acquiring COVID-19, or decreased access to health care due to lockdowns.

CONCLUSION: During the COVID-19 pandemic, there was a reduction in admissions of stroke and TIA, possibly caused by reluctance to seek medical care.

Place, publisher, year, edition, pages
Sage Publications, 2024
Keywords
Acute ischemic stroke, Corona virus, NIHSS, SARS-CoV-2, TIA, cerebral infarction, intracerebral hemorrhage
National Category
Public Health, Global Health and Social Medicine Neurology
Identifiers
urn:nbn:se:oru:diva-108656 (URN)10.1177/23969873231204127 (DOI)001073208700001 ()37776062 (PubMedID)2-s2.0-85173493290 (Scopus ID)
Available from: 2023-10-02 Created: 2023-10-02 Last updated: 2025-02-20Bibliographically approved
Tofiq, a., Eriksson Crommert, M., Zakrisson, A.-B., von Euler, M. & Nilsing Strid, E. (2024). Physical functioning post-COVID-19 and the recovery process: a mixed methods study. Disability and Rehabilitation, 46(8), 1570-1579
Open this publication in new window or tab >>Physical functioning post-COVID-19 and the recovery process: a mixed methods study
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2024 (English)In: Disability and Rehabilitation, ISSN 0963-8288, E-ISSN 1464-5165, Vol. 46, no 8, p. 1570-1579Article in journal (Refereed) Published
Abstract [en]

PURPOSE: To describe physical functioning after severe COVID-19-infection.

MATERIALS AND METHOD: An explanatory sequential mixed method design was used. Thirty-nine participants performed tests and answered questionnaires measuring physical functioning six months after hospitalisation due to COVID-19. Thirty of these participants participated in semi-structured interviews with questions regarding how they perceived their physical functioning and recovery from COVID-19 at 12 months post-hospitalisation.

RESULTS: At six months, physical functioning measured via chair stand test and hip-worn accelerometers was lower than normal reference values. There was a reduction in breathing muscle strength. Participants estimated their functional status during different activities as lower compared to those before COVID-19-infection, measured with a patient-specific functional scale. At one year after infection, there were descriptions of a rough recovery process and remaining symptoms.

CONCLUSION: Patients recovering from severe COVID-19 seem to have reduced physical functioning and activity levels, and they perceive their recovery to be slow and difficult. They experienced a lack of clinical support and contradictory advice regarding rehabilitation. Coaching in returning to physical functioning after the infection needs to be better co-ordinated and there is a need for guidelines for health professionals to avoid patients receiving contradictory advice.

Place, publisher, year, edition, pages
Taylor & Francis, 2024
Keywords
COVID-19, SARS-CoV-2, exercise, physical activity, qualitative research, recovery of function, rehabilitation, severe acute respiratory syndrome
National Category
Sport and Fitness Sciences
Identifiers
urn:nbn:se:oru:diva-105614 (URN)10.1080/09638288.2023.2201512 (DOI)000971399700001 ()37078388 (PubMedID)2-s2.0-85153473582 (Scopus ID)
Available from: 2023-04-21 Created: 2023-04-21 Last updated: 2025-02-11Bibliographically approved
Tofiq, a., Zetterberg, H., Blennow, K., Basun, H., Cederholm, T., Eriksdotter, M., . . . Freund-Levi, Y. (2021). Effects of Peroral Omega-3 Fatty Acid Supplementation on Cerebrospinal Fluid Biomarkers in Patients with Alzheimer's Disease: A Randomized Controlled Trial-The OmegAD Study. Journal of Alzheimer's Disease, 83(3), 1291-1301
Open this publication in new window or tab >>Effects of Peroral Omega-3 Fatty Acid Supplementation on Cerebrospinal Fluid Biomarkers in Patients with Alzheimer's Disease: A Randomized Controlled Trial-The OmegAD Study
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2021 (English)In: Journal of Alzheimer's Disease, ISSN 1387-2877, E-ISSN 1875-8908, Vol. 83, no 3, p. 1291-1301Article in journal (Refereed) Published
Abstract [en]

BACKGROUND: Studies have suggested a connection between a decrease in the levels of polyunsaturated fatty acids (PUFAs) and Alzheimer's disease (AD). We aimed to assess the effect of supplementation with omega-3 fatty acids (n-3 FAs) on biomarkers analyzed in the cerebrospinal fluid (CSF) of patients diagnosed with AD.

OBJECTIVE: To investigate the effects of daily supplementation with 2.3 g of PUFAs in AD patients on the biomarkers in CSF described below. We also explored the possible correlation between these biomarkers and the performance in the cognitive test Mini-Mental State Examination (MMSE).

METHODS: Thirty-three patients diagnosed with AD were randomized to either treatment with a daily intake of 2.3 g of n-3 FAs (n  =  18) or placebo (n  =  15). CSF samples were collected at baseline and after six months of treatment, and the following biomarkers were analyzed: Aβ 38, Aβ 40, Aβ 42, t-tau, p-tau, neurofilament light (NfL), chitinase-3-like protein 1 (YKL-40), acetylcholinesterase (AChE), butyrylcholinesterase (BuChE), soluble IL-1 receptor type II (sIL-1RII), and IL-6.

RESULTS: There were no significant differences between the groups concerning the level of the different biomarkers in the CSF at baseline. Within the treatment group, there was a small but significant increase in both YKL-40 (p = 0.04) and NfL (p = 0.03), while the other CSF biomarkers remained stable.

CONCLUSION: Supplementation with n-3 FAs had a statistically significant effect on NfL and YKL-40, resulting in an increase of both biomarkers, indicating a possible increase of inflammatory response and axonal damage. This increase in biomarkers did not correlate with MMSE score.

Place, publisher, year, edition, pages
IOS Press, 2021
Keywords
Dementia, Chitinase-3-like protein 1, YKL-40, inflammation, mini-mental state examination, neurodegeneration, neurofilament light
National Category
Neurosciences
Identifiers
urn:nbn:se:oru:diva-93857 (URN)10.3233/JAD-210007 (DOI)000703410000027 ()34420949 (PubMedID)
Funder
Stiftelsen Gamla TjänarinnorAlzheimerfondenThe Swedish Brain Foundation, FO2017-0243European CommissionSwedish Research Council, 2016-0231 22743 22744 2017-00915 2018-02532Stockholm County Council, 20180425Åke Wiberg Foundation, M16-0251
Note

Funding agencies:

Pronova Biocare A/S

Funds of Capio

Odd Fellow

Swedish Society of Physicians

Lion's Sweden

Stohne's Foundation

Alzheimer Drug Discovery Foundation (ADDF), USA RDAPB-201 809-2016615 

2018092016862

ALF ALFGBG-715986

European Union Joint Program for Neurodegenerative Disorders JPND2019466-236

European Research Council (ERC) 681712  

Swedish State Support for Clinical Research ALFGBG-720931

UK Dementia Research Institute at UCL

Sarfond 31 Forskning Senil demens

Region Auvergne-Rhone-Alpes

Region Bourgogne-Franche-Comte

Region Hauts-de-France

Region Nouvelle-Aquitaine

Available from: 2021-08-24 Created: 2021-08-24 Last updated: 2024-01-15Bibliographically approved
Organisations
Identifiers
ORCID iD: ORCID iD iconorcid.org/0000-0003-1712-7510

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