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Novel Low-Voltage MultiPulse Therapy to Terminate Atrial Fibrillation
FS. Ng, O. Toman, J. Petru, P. Peichl, RA. Winkle, VY. Reddy, P. Neuzil, RH. Mead, NA. Qureshi, ZI. Whinnett, DW. Bourn, MB. Shelton, J. Kautzner, AD. Sharma, M. Hocini, M. Haïssaguerre, NS. Peters, IR. Efimov
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem
Grantová podpora
R43 HL107055
NHLBI NIH HHS - United States
R01 HL115415
NHLBI NIH HHS - United States
R01 HL141470
NHLBI NIH HHS - United States
RG/16/3/32175
British Heart Foundation - United Kingdom
R41 HL114329
NHLBI NIH HHS - United States
Department of Health - United Kingdom
R44 HL107055
NHLBI NIH HHS - United States
- MeSH
- elektrická defibrilace MeSH
- elektrody MeSH
- fibrilace síní * chirurgie MeSH
- lidé MeSH
- srdeční síně MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
- Geografické názvy
- Minnesota MeSH
OBJECTIVES: This first-in-human feasibility study was undertaken to translate the novel low-voltage MultiPulse Therapy (MPT) (Cardialen, Inc., Minneapolis, Minnesota), which was previously been shown to be effective in preclinical studies in terminating atrial fibrillation (AF), into clinical use. BACKGROUND: Current treatment options for AF, the most common arrhythmia in clinical practice, have limited success. Previous attempts at treating AF by using implantable devices have been limited by the painful nature of high-voltage shocks. METHODS: Forty-two patients undergoing AF ablation were recruited at 6 investigational centers worldwide. Before ablation, electrode catheters were placed in the coronary sinus, right and/or left atrium, for recording and stimulation. After the induction of AF, MPT, which consists of up to a 3-stage sequence of far- and near-field stimulation pulses of varied amplitude, duration, and interpulse timing, was delivered via temporary intracardiac leads. MPT parameters and delivery methods were iteratively optimized. RESULTS: In the 14 patients from the efficacy phase, MPT terminated 37 of 52 (71%) of AF episodes, with the lowest median energy of 0.36 J (interquartile range [IQR]: 0.14 to 1.21 J) and voltage of 42.5 V (IQR: 25 to 75 V). Overall, 38% of AF terminations occurred within 2 seconds of MPT delivery (p < 0.0001). Shorter time between AF induction and MPT predicted success of MPT in terminating AF (p < 0.001). CONCLUSIONS: MPT effectively terminated AF at voltages and energies known to be well tolerated or painless in some patients. Our results support further studies of the concept of implanted devices for early AF conversion to reduce AF burden, symptoms, and progression.
Cardialen Inc Minneapolis Minnesota USA
Chelsea and Westminster Hospital NHS Foundation Trust London United Kingdom
George Washington University Washington DC USA
Hôpital Cardiologique du Haut Lévêque Bordeaux Pessac Bordeaux France
Imperial College Healthcare NHS Trust London United Kingdom
Institut Klinické a Experimentální Medicíny Prague Czech Republic
Mount Sinai School of Medicine New York New York USA
Na Homolce Prague Czech Republic
National Heart and Lung Institute Imperial College London London United Kingdom
Citace poskytuje Crossref.org
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