8
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      ESO Guideline on covert cerebral small vessel disease

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          ‘Covert’ cerebral small vessel disease (ccSVD) is common on neuroimaging in persons without overt neurological manifestations, and increases the risk of future stroke, cognitive impairment, dependency, and death. These European Stroke Organisation (ESO) guidelines provide evidence-based recommendations to assist with clinical decisions about management of ccSVD, specifically white matter hyperintensities and lacunes, to prevent adverse clinical outcomes. The guidelines were developed according to ESO standard operating procedures and Grading of Recommendations, Assessment, Development, and Evaluation (GRADE) methodology. We prioritised the clinical outcomes of stroke, cognitive decline or dementia, dependency, death, mobility and mood disorders, and interventions of blood pressure lowering, antiplatelet drugs, lipid lowering, lifestyle modifications, glucose lowering and conventional treatments for dementia. We systematically reviewed the literature, assessed the evidence, formulated evidence-based recommendations where feasible, and expert consensus statements. We found little direct evidence, mostly of low quality. We recommend patients with ccSVD and hypertension to have their blood pressure well controlled; lower blood pressure targets may reduce ccSVD progression. We do not recommend antiplatelet drugs such as aspirin in ccSVD. We found little evidence on lipid lowering in ccSVD. Smoking cessation is a health priority. We recommend regular exercise which may benefit cognition, and a healthy diet, good sleep habits, avoiding obesity and stress for general health reasons. In ccSVD, we found no evidence for glucose control in the absence of diabetes or for conventional Alzheimer dementia treatments. Randomised controlled trials with clinical endpoints are a priority for ccSVD.

          Related collections

          Most cited references165

          • Record: found
          • Abstract: found
          • Article: found
          Is Open Access

          The Cochrane Collaboration’s tool for assessing risk of bias in randomised trials

          Flaws in the design, conduct, analysis, and reporting of randomised trials can cause the effect of an intervention to be underestimated or overestimated. The Cochrane Collaboration’s tool for assessing risk of bias aims to make the process clearer and more accurate
            Bookmark
            • Record: found
            • Abstract: found
            • Article: found

            Neuroimaging standards for research into small vessel disease and its contribution to ageing and neurodegeneration

            Summary Cerebral small vessel disease (SVD) is a common accompaniment of ageing. Features seen on neuroimaging include recent small subcortical infarcts, lacunes, white matter hyperintensities, perivascular spaces, microbleeds, and brain atrophy. SVD can present as a stroke or cognitive decline, or can have few or no symptoms. SVD frequently coexists with neurodegenerative disease, and can exacerbate cognitive deficits, physical disabilities, and other symptoms of neurodegeneration. Terminology and definitions for imaging the features of SVD vary widely, which is also true for protocols for image acquisition and image analysis. This lack of consistency hampers progress in identifying the contribution of SVD to the pathophysiology and clinical features of common neurodegenerative diseases. We are an international working group from the Centres of Excellence in Neurodegeneration. We completed a structured process to develop definitions and imaging standards for markers and consequences of SVD. We aimed to achieve the following: first, to provide a common advisory about terms and definitions for features visible on MRI; second, to suggest minimum standards for image acquisition and analysis; third, to agree on standards for scientific reporting of changes related to SVD on neuroimaging; and fourth, to review emerging imaging methods for detection and quantification of preclinical manifestations of SVD. Our findings and recommendations apply to research studies, and can be used in the clinical setting to standardise image interpretation, acquisition, and reporting. This Position Paper summarises the main outcomes of this international effort to provide the STandards for ReportIng Vascular changes on nEuroimaging (STRIVE).
              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              2020 International Society of Hypertension Global Hypertension Practice Guidelines

                Bookmark

                Author and article information

                Journal
                Eur Stroke J
                Eur Stroke J
                ESO
                speso
                European Stroke Journal
                SAGE Publications (Sage UK: London, England )
                2396-9873
                2396-9881
                11 May 2021
                June 2021
                11 May 2021
                : 6
                : 2
                : CXI-CLXII
                Affiliations
                [1 ]Centre for Clinical Brain Sciences, UK Dementia Research Institute, University of Edinburgh, Edinburgh, UK
                [2 ]Bordeaux Population Health Center, University of Bordeaux, INSERM, UM1219, Team VINTAGE
                [3 ]Department of Neurology, Institute for Neurodegenerative Disease, Bordeaux University Hospital, Bordeaux, France
                [4 ]HUS Neurocenter, Division of Neuropsychology, Helsinki University Hospital, University of Helsinki and Department of Psychology and Logopedics, Faculty of Medicine, University of Helsinki, Finland
                [5 ]Radboud University Medical Center, Department of Neurology; Donders Center for Medical Neuroscience, Nijmegen, The Netherlands
                [6 ]Stroke and Dementia Lab, 'Luigi Sacco' Department of Biomedical and Clinical Sciences, University of Milan, Milano, Italy
                [7 ]Department of Neurology, Hopital Lariboisiere, APHP, INSERM U 1161, FHU NeuroVasc, University of Paris, Paris, France
                [8 ]Department of Neurology, School for Cardiovascular Diseases (CARIM), Maastricht UMC+, AZ Maastricht, the Netherlands
                [9 ]Dept of Medicine for the Elderly, University of Edinburgh, Edinburgh, UK
                [10 ]Comprehensive Stroke Center, Department of Neuroscience, Hospital Clínic, Barcelona, Spain
                [11 ]University Clinic of Neurology, Medical University of Graz, Graz, Austria
                [12 ]Department of Applied Clinical Sciences and Biotechnology, University of L’Aquila, L’Aquila, Italy
                [13 ]Univ. Lille, INSERM, CHU Lille, U1172, LilNCog – Lille Neuroscience & Cognition, Lille, France
                [14 ]Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK
                [15 ]Department of Clinical Sciences Lund, Neurology, Lund University; Section of Neurology, Skåne University Hospital, Lund, Sweden
                Author notes
                [*]Joanna M Wardlaw, University of Edinburgh, Edinburgh, UK. Email: Joanna.wardlaw@ 123456ed.ac.uk
                Author information
                https://orcid.org/0000-0002-9812-6642
                https://orcid.org/0000-0001-7357-8530
                https://orcid.org/0000-0002-8775-6884
                Article
                10.1177_23969873211012132
                10.1177/23969873211012132
                8370079
                34414301
                bedf1158-8edb-4606-a0c0-ea28be18f5fe
                © European Stroke Organisation 2021

                This article is distributed under the terms of the Creative Commons Attribution 4.0 License ( https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages ( https://us.sagepub.com/en-us/nam/open-access-at-sage).

                History
                : 18 March 2021
                : 2 April 2021
                Funding
                Funded by: The Stroke Association;
                Funded by: European Stroke Organisation;
                Funded by: Mrs Gladys Row Fogo Charitable Trust, FundRef https://doi.org/10.13039/100012164;
                Funded by: Swedish Research Council;
                Funded by: UK Dementia Research Institute, FundRef https://doi.org/10.13039/501100017510;
                Funded by: Fondation Leducq, FundRef https://doi.org/10.13039/501100001674;
                Categories
                Guidelines
                Custom metadata
                ts2

                white matter hyperintensities,lacunes,cerebral small vessel disease,leukoaraiosis,silent brain infarcts,covert,prevention,stroke,dementia,recommendations,outcome

                Comments

                Comment on this article