{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,17]],"date-time":"2026-09-17T02:36:38Z","timestamp":1789612598161,"version":"build-2803163510"},"reference-count":96,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"4","content-domain":{"domain":["www.ahajournals.org"],"crossmark-restriction":true},"short-container-title":["Circulation"],"published-print":{"date-parts":[[2026,7,28]]},"abstract":"<jats:sec>\n                    <jats:title\/>\n                    <jats:p>Cardiovascular diseases, particularly stroke, are leading causes of dementia. Several common cardiac interventions such as coronary artery bypass grafting and transcatheter aortic valve implantation are also associated with cognitive decline. However, cognitive outcomes continue to be poorly collected in clinical trials of cardiovascular diseases. In this article, we review the limitations of current approaches to cognitive assessment in cardiovascular disease studies. When assessed, there is wide variation in cognitive tasks used, and tasks have limited population-specific validation, are subject to floor and ceiling effects, and may suffer from sociocultural and linguistic biases. Many tasks are not available in multilingual formats and often rely on face-to-face testing with trained coordinators. All conventional cognitive outcomes in cardiovascular trials are associated with substantial incompletion, especially among older and more impaired individuals, the very people most important to capture. This nonrandom missingness generates survivor and attrition biases, an unacceptable situation for any trial outcome. Last, the meaning of measured cognitive outcomes is often unclear for patients, caregivers, clinicians, and regulators. To help address these limitations, we propose a new framework, major adverse cognitive events (MACE-Cog), to better capture cognitive outcomes in stroke and other cardiovascular populations. As an inclusive construct reflecting the multidimensional nature of cognitive decline, major adverse cognitive events do not rely solely on performance on cognitive testing but also consider inability to complete cognitive testing due to cognitive-behavioral factors, reported symptoms of cognitive decline, impairment in activities of daily living as a result of cognitive impairment, new clinical diagnoses of dementia, and care home admission. We hope that the proposed composite outcome and multiple use cases presented spark progress in cardiovascular research toward more inclusive approaches to the study of cognitive outcomes that move beyond the confines of cognitive tests alone.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1161\/circulationaha.125.077180","type":"journal-article","created":{"date-parts":[[2026,7,27]],"date-time":"2026-07-27T18:00:33Z","timestamp":1785175233000},"page":"378-394","update-policy":"https:\/\/doi.org\/10.1161\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":1,"title":["Major Adverse Cognitive Events (MACE-Cog): A New \u201cMACE\u201d Framework for Cognitive Outcomes in Cardiovascular Diseases and Stroke"],"prefix":"10.1161","volume":"154","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-5520-2070","authenticated-orcid":true,"given":"Aravind","family":"Ganesh","sequence":"first","affiliation":[{"name":"Calgary Stroke Program, Departments of Clinical Neurosciences, Radiology, Medicine, and Community Health Sciences; Hotchkiss Brain Institute, Mathison Centre for Mental Health Research and Education, and O\u2019Brien Institute for Public Health; University of Calgary Cumming School of Medicine, AB, Canada (A.G., M.D.H., B.M., T.S., E.E.S.)"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-3128-3977","authenticated-orcid":true,"given":"Sajeevan","family":"Sujanthan","sequence":"additional","affiliation":[{"name":"Institute of Medical Sciences, ON, Canada (S.S., R.T.M., R.H.S.)"},{"name":"Division of Neurology, Department of Medicine, Sunnybrook Health Sciences Centre (J.S.R., S.S., R.T.M., R.H.S.)"},{"name":"University of Toronto, ON, Canada (S.S., R.T.M., J.S.R., K.N.D., M.D.B., K.L.L., D.S.L., S.F., R.H.S.)."},{"name":"Hurvitz Brain Science Program, Sunnybrook Health Sciences Centre, Toronto, ON, Canada (J.S.R., S.S., R.T.M., R.H.S.)."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ryan T.","family":"Muir","sequence":"additional","affiliation":[{"name":"Institute of Medical Sciences, ON, Canada (S.S., R.T.M., R.H.S.)"},{"name":"Division of Neurology, Department of Medicine, Sunnybrook Health Sciences Centre (J.S.R., S.S., R.T.M., R.H.S.)"},{"name":"University of Toronto, ON, Canada (S.S., R.T.M., J.S.R., K.N.D., M.D.B., K.L.L., D.S.L., S.F., R.H.S.)."},{"name":"Hurvitz Brain Science Program, Sunnybrook Health Sciences Centre, Toronto, ON, Canada (J.S.R., S.S., R.T.M., R.H.S.)."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-9554-0701","authenticated-orcid":true,"given":"Raed A.","family":"Joundi","sequence":"additional","affiliation":[{"name":"Population Health Research Institute, McMaster University and Hamilton Health Sciences, ON, Canada 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