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Please use this identifier to cite or link to this item: http://hdl.handle.net/11375/27213
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dc.contributor.authorHolbrook, Anne-
dc.date.accessioned2021-12-06T22:11:11Z-
dc.date.available2021-12-06T22:11:11Z-
dc.date.issued2021-
dc.identifier.urihttp://hdl.handle.net/11375/27213-
dc.descriptionAdditional files include: Coordination and Continuity of Care Questionnaire, Patient Knowledge of OAC Management Quiz, and the Patient/Caregiver Study Satisfaction Survey.en_US
dc.description.abstractIntroduction: Oral anticoagulants (OACs) are very commonly prescribed, have well documented benefits for important clinical outcomes but have serious harms as well. OAC-related thromboembolic and hemorrhagic event rates are especially high shortly after hospital discharge. Expert OAC management involving virtual care is a research priority given its potential to reach far-flung communities in a more convenient, physically distanced and less costly way than in-person care. Objective: To test whether a focused, expert medication management intervention using a mix of in-person consultation and virtual care follow-up, is feasible and might be effective in preventing anticoagulation-related adverse events, for patients transitioning from hospital to home. Methods and Analysis: A randomized parallel multicentre design enrolling consenting adult patients or the caregivers of cognitively impaired patients about to be discharged from medical wards with a discharge prescription including an oral anticoagulant. The interdisciplinary intervention is led by a clinical pharmacologist and includes a detailed discharge medication reconciliation and management plan focused on oral anticoagulants at hospital discharge; a circle of care handover and coordination with patient, hospital team and community providers; early post-discharge follow-up virtual medication check-up visits at 24 hours, 1 week, and 1 month with triage of any problems. The control group will receive usual care plus encouragement to use Thrombosis Canada website. Co-primary outcomes include a) feasibility such as recruitment rate, participant retention rates, trial resources management, and b) clinical outcomes primarily adverse anticoagulant safety events composite (AASE), coordination and continuity of care, medication-related problems, quality of life and health resource utilization. Follow-up is 3 months.en_US
dc.language.isoenen_US
dc.publisherN/Aen_US
dc.subjectOAC Managementen_US
dc.subjectRandomized control trialen_US
dc.subjectcontinuity of careen_US
dc.titleCOACHeD RCT Additional Files 2021en_US
dc.typeArticleen_US
dc.contributor.departmentMedicineen_US
Appears in Collections:Medicine Publications

Files in This Item:
File Description SizeFormat 
CCCQBaseline.pdf
Open Access
48.79 kBAdobe PDFView/Open
OACKnowledgeTest.pdf
Open Access
46.43 kBAdobe PDFView/Open
PatientCaregiverStudySatisfaction.pdf
Open Access
43.83 kBAdobe PDFView/Open
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