Please use this identifier to cite or link to this item: https://doi.org/10.1007/s12471-014-0587-z
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dc.titlePatient perspective on remote monitoring of cardiovascular implantable electronic devices: Rationale and design of the REMOTE-CIED study
dc.contributor.authorVersteeg, H
dc.contributor.authorPedersen, S.S
dc.contributor.authorMastenbroek, M.H
dc.contributor.authorRedekop, W.K
dc.contributor.authorSchwab, J.O
dc.contributor.authorMabo, P
dc.contributor.authorMeine, M
dc.date.accessioned2020-10-27T11:12:41Z
dc.date.available2020-10-27T11:12:41Z
dc.date.issued2014
dc.identifier.citationVersteeg, H, Pedersen, S.S, Mastenbroek, M.H, Redekop, W.K, Schwab, J.O, Mabo, P, Meine, M (2014). Patient perspective on remote monitoring of cardiovascular implantable electronic devices: Rationale and design of the REMOTE-CIED study. Netherlands Heart Journal 22 (10) : 423-428. ScholarBank@NUS Repository. https://doi.org/10.1007/s12471-014-0587-z
dc.identifier.issn15685888
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/181528
dc.description.abstractBackground: Remote patientmonitoring is a safe and effective alternative for the in-clinic follow-up of patients with cardiovascular implantable electronic devices (CIEDs). However, evidence on the patient perspective on remote monitoring is scarce and inconsistent.Objectives: The primary objective of the REMOTE-CIED study is to evaluate the influence of remote patient monitoring versus in-clinic follow-up on patient-reported outcomes. Secondary objectives are to: 1) identify subgroups of patients who may not be satisfied with remote monitoring; and 2) investigate the cost-effectiveness of remote monitoring.Methods: The REMOTE-CIED study is an international randomised controlled study that will include 900 consecutive heart failure patients implanted with an implantable cardioverter defibrillator (ICD) compatible with the Boston Scientific LATITUDE® Remote Patient Management system at participating centres in five European countries. Patients will be randomised to remote monitoring or in-clinic followup. The In-Clinic group will visit the outpatient clinic every 3– 6 months, according to standard practice. The Remote Monitoring group only visits the outpatient clinic at 12 and 24 months post-implantation, other check-ups are performed remotely. Patients are asked to complete questionnaires at five time points during the 2-year follow-up.Conclusion: The REMOTE-CIED study will provide insight into the patient perspective on remote monitoring in ICD patients, which could help to support patient-centred care in the future. © The Author(s) 2014.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectadult
dc.subjectaged
dc.subjectanxiety
dc.subjectArticle
dc.subjectcardiovascular monitoring device
dc.subjectcontrolled study
dc.subjectcost effectiveness analysis
dc.subjectdepression
dc.subjectheart arrhythmia
dc.subjectheart failure
dc.subjectheart left ventricle ejection fraction
dc.subjecthuman
dc.subjectimplantable cardioverter defibrillator
dc.subjectmajor clinical study
dc.subjectprospective study
dc.subjectquality adjusted life year
dc.subjectquestionnaire
dc.subjectrandomized controlled trial
dc.subjecttelemonitoring
dc.subjecttype D behavior
dc.subjectweight change
dc.typeArticle
dc.contributor.departmentSAW SWEE HOCK SCHOOL OF PUBLIC HEALTH
dc.description.doi10.1007/s12471-014-0587-z
dc.description.sourcetitleNetherlands Heart Journal
dc.description.volume22
dc.description.issue10
dc.description.page423-428
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