BIOTRONIK, a leading manufacturer of cardiovascular technology, today announced an extension of its ProMRI® technology. BIOTRONIK has combined advanced pacemaker and ICD technology with the option for patients to undergo MR scans. This makes BIOTRONIK the only company worldwide to allow ICD and heart failure patients (CRT-D and CRT-P) to take advantage of potentially life-saving MR scans. The new extension of ProMRI® technology means that even full-body scans are now available for pacemaker patients, placing BIOTRONIK's implants firmly at the forefront of cardiac device innovation.
Thanks to BIOTRONIK's Lumax 7, the Ilesto and Iforia ICDs/CRT-Ds, as well as the Evia HF-T, patients can have more than 88%1 of all required MR scans. Furthermore, patients implanted with the Evia single and dual chamber devices can now undergo 100% of all required scans, including liver and heart scans. BIOTRONIK received CE mark for its full-body scan ProMRI® technology with a backwards compatibility in mid August.
Each of BIOTRONIK's cardiac devices are also equipped with BIOTRONIK's Home Monitoring®, which rapidly detects deterioration in patients' clinical status and automatically transmits data on a daily basis. This enables physicians to adapt patient therapy at a very early stage.
Late-breaking results from the BIOTRONIK IN-TIME Study, which evaluated the influence of implant-based BIOTRONIK Home Monitoring® on the clinical management of heart failure patients, will also be presented at the ESC Congress 2013 by Prof. Gerhard Hindricks, MD, Heart Center, University Leipzig, Germany, and discussed with Prof. Angelo Auricchio, Past President of the European Heart Rhythm Association (EHRA).
"Throughout our 50-year history, our goal has been to grant as many patients as possible access to leading-edge technology, ensuring the best therapies available", explains Christoph Böhmer, President International at BIOTRONIK. "We've kept our promises to patients and physicians since our founding in 1963. Our technologies, like ProMRI® enabling full-body scans and BIOTRONIK Home Monitoring®, have proven our reliability, making a real difference in patients' lives."
Dates and places
- Hot Line Session IN-TIME Study: Sunday, September 1st, 15.30,
Room: Amsterdam - Central-Village
- BIOTRONIK booth: B315
References
1 Barmer Arzt report 2011
Thanks to BIOTRONIK's Lumax 7, the Ilesto and Iforia ICDs/CRT-Ds, as well as the Evia HF-T, patients can have more than 88%1 of all required MR scans. Furthermore, patients implanted with the Evia single and dual chamber devices can now undergo 100% of all required scans, including liver and heart scans. BIOTRONIK received CE mark for its full-body scan ProMRI® technology with a backwards compatibility in mid August.
Each of BIOTRONIK's cardiac devices are also equipped with BIOTRONIK's Home Monitoring®, which rapidly detects deterioration in patients' clinical status and automatically transmits data on a daily basis. This enables physicians to adapt patient therapy at a very early stage.
Late-breaking results from the BIOTRONIK IN-TIME Study, which evaluated the influence of implant-based BIOTRONIK Home Monitoring® on the clinical management of heart failure patients, will also be presented at the ESC Congress 2013 by Prof. Gerhard Hindricks, MD, Heart Center, University Leipzig, Germany, and discussed with Prof. Angelo Auricchio, Past President of the European Heart Rhythm Association (EHRA).
"Throughout our 50-year history, our goal has been to grant as many patients as possible access to leading-edge technology, ensuring the best therapies available", explains Christoph Böhmer, President International at BIOTRONIK. "We've kept our promises to patients and physicians since our founding in 1963. Our technologies, like ProMRI® enabling full-body scans and BIOTRONIK Home Monitoring®, have proven our reliability, making a real difference in patients' lives."
Dates and places
- Hot Line Session IN-TIME Study: Sunday, September 1st, 15.30,
Room: Amsterdam - Central-Village
- BIOTRONIK booth: B315
References
1 Barmer Arzt report 2011
