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.title | Patient perspective on remote monitoring of cardiovascular implantable electronic devices: Rationale and design of the REMOTE-CIED study | |
dc.contributor.author | Versteeg, H | |
dc.contributor.author | Pedersen, S.S | |
dc.contributor.author | Mastenbroek, M.H | |
dc.contributor.author | Redekop, W.K | |
dc.contributor.author | Schwab, J.O | |
dc.contributor.author | Mabo, P | |
dc.contributor.author | Meine, M | |
dc.date.accessioned | 2020-10-27T11:12:41Z | |
dc.date.available | 2020-10-27T11:12:41Z | |
dc.date.issued | 2014 | |
dc.identifier.citation | Versteeg, 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.issn | 15685888 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/181528 | |
dc.description.abstract | Background: 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.rights | Attribution 4.0 International | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.source | Unpaywall 20201031 | |
dc.subject | adult | |
dc.subject | aged | |
dc.subject | anxiety | |
dc.subject | Article | |
dc.subject | cardiovascular monitoring device | |
dc.subject | controlled study | |
dc.subject | cost effectiveness analysis | |
dc.subject | depression | |
dc.subject | heart arrhythmia | |
dc.subject | heart failure | |
dc.subject | heart left ventricle ejection fraction | |
dc.subject | human | |
dc.subject | implantable cardioverter defibrillator | |
dc.subject | major clinical study | |
dc.subject | prospective study | |
dc.subject | quality adjusted life year | |
dc.subject | questionnaire | |
dc.subject | randomized controlled trial | |
dc.subject | telemonitoring | |
dc.subject | type D behavior | |
dc.subject | weight change | |
dc.type | Article | |
dc.contributor.department | SAW SWEE HOCK SCHOOL OF PUBLIC HEALTH | |
dc.description.doi | 10.1007/s12471-014-0587-z | |
dc.description.sourcetitle | Netherlands Heart Journal | |
dc.description.volume | 22 | |
dc.description.issue | 10 | |
dc.description.page | 423-428 | |
Appears in Collections: | Elements Staff Publications |
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