Rationale and study design of the REM-HF study: remote management of heart failure using implanted devices and formalised follow-up procedures

Aims: we wish to assess the clinical and cost-effectiveness of remote monitoring of heart failure patients with cardiac implanted electronic devices. Methods: REM-HF is a multicentre, randomized, non-blinded, parallel trial designed to compare weekly remote monitoring-driven management with usual c...

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Main Authors: Morgan, John M. (Author), Dimitrov, Borislav D (Author), Gill, Jas (Author), Kitt, Sue (Author), Ng, G Andre (Author), McComb, Janet M. (Author), Raftery, James (Author), Roderick, Paul (Author), Seed, Alison (Author), Williams, Simon G. (Author), Witte, Klaus K. (Author), Wright, D. Jay (Author), Yao, Guiqing Lily (Author), Cowie, Martin R. (Author)
Format: Article
Language:English
Published: 2014-09.
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Online Access:Get fulltext
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042 |a dc 
100 1 0 |a Morgan, John M.  |e author 
700 1 0 |a Dimitrov, Borislav D  |e author 
700 1 0 |a Gill, Jas  |e author 
700 1 0 |a Kitt, Sue  |e author 
700 1 0 |a Ng, G Andre  |e author 
700 1 0 |a McComb, Janet M.  |e author 
700 1 0 |a Raftery, James  |e author 
700 1 0 |a Roderick, Paul  |e author 
700 1 0 |a Seed, Alison  |e author 
700 1 0 |a Williams, Simon G.  |e author 
700 1 0 |a Witte, Klaus K.  |e author 
700 1 0 |a Wright, D. Jay  |e author 
700 1 0 |a Yao, Guiqing Lily  |e author 
700 1 0 |a Cowie, Martin R.  |e author 
245 0 0 |a Rationale and study design of the REM-HF study: remote management of heart failure using implanted devices and formalised follow-up procedures 
260 |c 2014-09. 
856 |z Get fulltext  |u https://eprints.soton.ac.uk/367476/1/2014_REM-HF%2520Study%2520Design%2520-%2520published.pdf 
520 |a Aims: we wish to assess the clinical and cost-effectiveness of remote monitoring of heart failure patients with cardiac implanted electronic devices. Methods: REM-HF is a multicentre, randomized, non-blinded, parallel trial designed to compare weekly remote monitoring-driven management with usual care for patients with cardiac implanted electronic devices (ICD, CRT-D, or CRT-P). The trial is event driven, and the final analysis will be performed when 546 events have been observed or the study is terminated at the interim analysis. We have randomized 1650 patients to be followed up for a minimum of 2 years. Patients will remain in the trial up to study termination. The first patient was randomized in September 2011 and the study is expected to complete in early 2016. The primary combined endpoint is time to first event of all-cause death or unplanned hospitalization for cardiovascular reasons. An economic evaluation will be performed, estimating the cost per quality-adjusted lifeyear, with direct costs estimated from the National Health Service perspective and quality of life assessed by the EQ-5D, Short-Form12, and Kansas City Cardiomyopathy Questionnaires. The study design has been informed by a feasibility study. Conclusion: REM-HF is a multicentre randomized study that will provide important data on the effect of remote monitoring-driven management of implanted cardiac devices on morbidity and mortality, as well as the cost-effectiveness of this approach 
655 7 |a Article