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- W2893832110 abstract "The growing number of Cardiac Implantable Electronic Devices (CIEDs) being implanted has necessitated additional in-clinic follow-up. Remote monitoring (RM) is a technology that transmits CIED data directly from patients’ home to clinic through a company specific server. Current evidence suggests that RM is a safe alternative to in-clinic follow-up, and is often recommended as a safety measure for CIEDs with lead and battery advisories. Current standard CIED follow-up includes a 1:1 ratio of in-clinic and RM assessment. Given RM’s proven safety, a paradigm shift to exclusive RM has been suggested where patients access clinic only if they have a CIED or lead concern. To date, there is little evidence regarding the patients’ perspective and experience while on RM. Accreditation Canada mandates that all aspects of health care planning, delivery, and evaluation be centred on the patient and family. No patient satisfaction questionnaires regarding RM have been conducted at our center since implementation in 2012. To acquire knowledge regarding the patient perspective on RM and to better understand their level of confidence and satisfaction with this emerging technology. Pending ethics approval a descriptive telephone questionnaire will be conducted with CIED patients currently on RM. Quantitative and qualitative data will be presented and contrasted with literature findings. Results of the study questionnaire will inform guideline and policy makers to ensure our practices remain patient centered, and meet accreditation standards for exclusive RM." @default.
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- W2893832110 date "2018-10-01" @default.
- W2893832110 modified "2023-09-28" @default.
- W2893832110 title "CARDIAC IMPLANTABLE ELECTRONIC DEVICE REMOTE MONITORING FOLLOW-UP: INFORMING FUTURE GUIDELINES AND POLICY FROM THE PATIENTS’ PERSPECTIVE" @default.
- W2893832110 doi "https://doi.org/10.1016/j.cjca.2018.07.459" @default.
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