Safety and efficiency of a common and simplified protocol for pacemaker and defibrillator surveillance based on remote monitoring only: a long-term randomized trial (RM-ALONE)

Abstract Aims This trial aimed to evaluate the safety and efficiency of a common and simplified protocol for the surveillance of cardiac implantable electronic devices based on remote monitoring (RM) in patients with pacemakers (PMs) and implantable cardiac defibrillators (ICDs) for at least 24 mont...

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Published in:European heart journal Vol. 40; no. 23; pp. 1837 - 1846
Main Authors: García-Fernández, Francisco Javier, Osca Asensi, Joaquín, Romero, Rafael, Fernández Lozano, Ignacio, Larrazabal, José María, Martínez Ferrer, José, Ortiz, Raquel, Pombo, Marta, Tornés, Francisco José, Moradi Kolbolandi, Mehrard
Format: Journal Article
Language:English
Published: England Oxford University Press 14-06-2019
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Abstract Abstract Aims This trial aimed to evaluate the safety and efficiency of a common and simplified protocol for the surveillance of cardiac implantable electronic devices based on remote monitoring (RM) in patients with pacemakers (PMs) and implantable cardiac defibrillators (ICDs) for at least 24 months. Methods and results The RM-ALONE is a multicentre prospective trial that randomly assigned 445 patients in two groups, both followed by RM: the home monitoring-only (HMo) based on RM + remote interrogations (RIs) every 6 months and the HM + IO that adds in-office evaluations every 6 months to RM. Four hundred and forty-five patients were enrolled in the study, 294 PMs and 151 ICDs recipients. In the HMo group, 20% of patients experienced ≥1 major adverse cardiac event (MACE) vs. 19.5% in HM + IO group (P = 0.006 for non-inferiority). The proportion of patients with a PM/ICD who experienced ≥1 MACE was 15.2/29.3% in HMo group and 16.1/26.3% in HM + IO group (hazard ratio 0.95/1.15, 95% confidence interval 0.53–1.70/0.62–2.10). There were 789 in-office evaluations (136 in the HMo and 653 in the HM + IO; P < 0.001). There was a 79.2% reduction of in-office evaluations with no significant differences in unscheduled visits between groups: 122 (54.5%) in HMo and 101 (45.3%) in HM + IO; P = 0.15. The time a physician/nurse spent per patient/follow-up was significantly reduced in the HMo group: 4/5 min (0–30)/(1–30) vs. 10/10 min (0–40)/(1–40) in HM + IO (P < 0.0001). Conclusion The RM-ALONE protocol common for ICD and PM surveillance, consisting of RM + RI every 6 months has proven safe and efficient in reducing hospital visits and staff workload.
AbstractList AIMSThis trial aimed to evaluate the safety and efficiency of a common and simplified protocol for the surveillance of cardiac implantable electronic devices based on remote monitoring (RM) in patients with pacemakers (PMs) and implantable cardiac defibrillators (ICDs) for at least 24 months. METHODS AND RESULTSThe RM-ALONE is a multicentre prospective trial that randomly assigned 445 patients in two groups, both followed by RM: the home monitoring-only (HMo) based on RM + remote interrogations (RIs) every 6 months and the HM + IO that adds in-office evaluations every 6 months to RM. Four hundred and forty-five patients were enrolled in the study, 294 PMs and 151 ICDs recipients. In the HMo group, 20% of patients experienced ≥1 major adverse cardiac event (MACE) vs. 19.5% in HM + IO group (P = 0.006 for non-inferiority). The proportion of patients with a PM/ICD who experienced ≥1 MACE was 15.2/29.3% in HMo group and 16.1/26.3% in HM + IO group (hazard ratio 0.95/1.15, 95% confidence interval 0.53-1.70/0.62-2.10). There were 789 in-office evaluations (136 in the HMo and 653 in the HM + IO; P < 0.001). There was a 79.2% reduction of in-office evaluations with no significant differences in unscheduled visits between groups: 122 (54.5%) in HMo and 101 (45.3%) in HM + IO; P = 0.15. The time a physician/nurse spent per patient/follow-up was significantly reduced in the HMo group: 4/5 min (0-30)/(1-30) vs. 10/10 min (0-40)/(1-40) in HM + IO (P < 0.0001). CONCLUSIONThe RM-ALONE protocol common for ICD and PM surveillance, consisting of RM + RI every 6 months has proven safe and efficient in reducing hospital visits and staff workload.
Abstract Aims This trial aimed to evaluate the safety and efficiency of a common and simplified protocol for the surveillance of cardiac implantable electronic devices based on remote monitoring (RM) in patients with pacemakers (PMs) and implantable cardiac defibrillators (ICDs) for at least 24 months. Methods and results The RM-ALONE is a multicentre prospective trial that randomly assigned 445 patients in two groups, both followed by RM: the home monitoring-only (HMo) based on RM + remote interrogations (RIs) every 6 months and the HM + IO that adds in-office evaluations every 6 months to RM. Four hundred and forty-five patients were enrolled in the study, 294 PMs and 151 ICDs recipients. In the HMo group, 20% of patients experienced ≥1 major adverse cardiac event (MACE) vs. 19.5% in HM + IO group (P = 0.006 for non-inferiority). The proportion of patients with a PM/ICD who experienced ≥1 MACE was 15.2/29.3% in HMo group and 16.1/26.3% in HM + IO group (hazard ratio 0.95/1.15, 95% confidence interval 0.53–1.70/0.62–2.10). There were 789 in-office evaluations (136 in the HMo and 653 in the HM + IO; P < 0.001). There was a 79.2% reduction of in-office evaluations with no significant differences in unscheduled visits between groups: 122 (54.5%) in HMo and 101 (45.3%) in HM + IO; P = 0.15. The time a physician/nurse spent per patient/follow-up was significantly reduced in the HMo group: 4/5 min (0–30)/(1–30) vs. 10/10 min (0–40)/(1–40) in HM + IO (P < 0.0001). Conclusion The RM-ALONE protocol common for ICD and PM surveillance, consisting of RM + RI every 6 months has proven safe and efficient in reducing hospital visits and staff workload.
This trial aimed to evaluate the safety and efficiency of a common and simplified protocol for the surveillance of cardiac implantable electronic devices based on remote monitoring (RM) in patients with pacemakers (PMs) and implantable cardiac defibrillators (ICDs) for at least 24 months. The RM-ALONE is a multicentre prospective trial that randomly assigned 445 patients in two groups, both followed by RM: the home monitoring-only (HMo) based on RM + remote interrogations (RIs) every 6 months and the HM + IO that adds in-office evaluations every 6 months to RM. Four hundred and forty-five patients were enrolled in the study, 294 PMs and 151 ICDs recipients. In the HMo group, 20% of patients experienced ≥1 major adverse cardiac event (MACE) vs. 19.5% in HM + IO group (P = 0.006 for non-inferiority). The proportion of patients with a PM/ICD who experienced ≥1 MACE was 15.2/29.3% in HMo group and 16.1/26.3% in HM + IO group (hazard ratio 0.95/1.15, 95% confidence interval 0.53-1.70/0.62-2.10). There were 789 in-office evaluations (136 in the HMo and 653 in the HM + IO; P < 0.001). There was a 79.2% reduction of in-office evaluations with no significant differences in unscheduled visits between groups: 122 (54.5%) in HMo and 101 (45.3%) in HM + IO; P = 0.15. The time a physician/nurse spent per patient/follow-up was significantly reduced in the HMo group: 4/5 min (0-30)/(1-30) vs. 10/10 min (0-40)/(1-40) in HM + IO (P < 0.0001). The RM-ALONE protocol common for ICD and PM surveillance, consisting of RM + RI every 6 months has proven safe and efficient in reducing hospital visits and staff workload.
Author García-Fernández, Francisco Javier
Pombo, Marta
Fernández Lozano, Ignacio
Osca Asensi, Joaquín
Martínez Ferrer, José
Tornés, Francisco José
Moradi Kolbolandi, Mehrard
Ortiz, Raquel
Larrazabal, José María
Romero, Rafael
AuthorAffiliation 3 Hospital Nuestra Señora de la Candelaria, Ctra. Gral. del Rosario 145, Sta. Cruz de Tenerife, Spain
9 Hospital Torrecárdenas, Calle Hermandad de Donantes de Sangre s/n, Almería, Spain
2 Hospital Universitario y Politécnico La Fe, Av de Fernando Abril Martorell 106, Valencia, Spain
6 Hospital Universitario Araba, Jose Atxotegi s/n, Vitoria-Gasteiz, Spain
8 Hospital Costa del Sol, A-7 Km 187, Marbella, Málaga, Spain
7 Hospital General de la Palma, Ctra. de la Cumbre 28, Las Palmas de Gran Canaria, Spain
10 Hospital Vall d`Hebron, Passeig de la Vall d'Hebron 119-129, Barcelona, Spain
4 Hospital U Puerta de Hierro, Manuel de Falla 1, Madrid, Spain
5 Hospital San Pedro de Alcántara, Av Pablo Naranjo s/n, Cáceres, Spain
1 Arrythmia Unit, Cardiology Department, Hospital Universitario de Burgos, Av. Islas Baleares 3, Burgos, Spain
AuthorAffiliation_xml – name: 4 Hospital U Puerta de Hierro, Manuel de Falla 1, Madrid, Spain
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– name: 9 Hospital Torrecárdenas, Calle Hermandad de Donantes de Sangre s/n, Almería, Spain
– name: 5 Hospital San Pedro de Alcántara, Av Pablo Naranjo s/n, Cáceres, Spain
– name: 6 Hospital Universitario Araba, Jose Atxotegi s/n, Vitoria-Gasteiz, Spain
– name: 7 Hospital General de la Palma, Ctra. de la Cumbre 28, Las Palmas de Gran Canaria, Spain
– name: 3 Hospital Nuestra Señora de la Candelaria, Ctra. Gral. del Rosario 145, Sta. Cruz de Tenerife, Spain
– name: 1 Arrythmia Unit, Cardiology Department, Hospital Universitario de Burgos, Av. Islas Baleares 3, Burgos, Spain
– name: 10 Hospital Vall d`Hebron, Passeig de la Vall d'Hebron 119-129, Barcelona, Spain
Author_xml – sequence: 1
  givenname: Francisco Javier
  surname: García-Fernández
  fullname: García-Fernández, Francisco Javier
  email: javyergf@secardiologia.es
  organization: Arrythmia Unit, Cardiology Department, Hospital Universitario de Burgos, Av. Islas Baleares 3, Burgos, Spain
– sequence: 2
  givenname: Joaquín
  surname: Osca Asensi
  fullname: Osca Asensi, Joaquín
  organization: Hospital Universitario y Politécnico La Fe, Av de Fernando Abril Martorell 106, Valencia, Spain
– sequence: 3
  givenname: Rafael
  surname: Romero
  fullname: Romero, Rafael
  organization: Hospital Nuestra Señora de la Candelaria, Ctra. Gral. del Rosario 145, Sta. Cruz de Tenerife, Spain
– sequence: 4
  givenname: Ignacio
  surname: Fernández Lozano
  fullname: Fernández Lozano, Ignacio
  organization: Hospital U Puerta de Hierro, Manuel de Falla 1, Madrid, Spain
– sequence: 5
  givenname: José María
  surname: Larrazabal
  fullname: Larrazabal, José María
  organization: Hospital San Pedro de Alcántara, Av Pablo Naranjo s/n, Cáceres, Spain
– sequence: 6
  givenname: José
  surname: Martínez Ferrer
  fullname: Martínez Ferrer, José
  organization: Hospital Universitario Araba, Jose Atxotegi s/n, Vitoria-Gasteiz, Spain
– sequence: 7
  givenname: Raquel
  surname: Ortiz
  fullname: Ortiz, Raquel
  organization: Hospital General de la Palma, Ctra. de la Cumbre 28, Las Palmas de Gran Canaria, Spain
– sequence: 8
  givenname: Marta
  surname: Pombo
  fullname: Pombo, Marta
  organization: Hospital Costa del Sol, A-7 Km 187, Marbella, Málaga, Spain
– sequence: 9
  givenname: Francisco José
  surname: Tornés
  fullname: Tornés, Francisco José
  organization: Hospital Torrecárdenas, Calle Hermandad de Donantes de Sangre s/n, Almería, Spain
– sequence: 10
  givenname: Mehrard
  surname: Moradi Kolbolandi
  fullname: Moradi Kolbolandi, Mehrard
  organization: Hospital Vall d`Hebron, Passeig de la Vall d'Hebron 119-129, Barcelona, Spain
BackLink https://www.ncbi.nlm.nih.gov/pubmed/30793735$$D View this record in MEDLINE/PubMed
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Issue 23
Keywords Implantable cardiac defibrillator
Remote interrogation
Telemedicine
Pacemaker
Remote monitoring
Language English
License This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
The Author(s) 2019. Published by Oxford University Press on behalf of the European Society of Cardiology.
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Varma (2022102607534542600_ehz067-B8) 2014; 35
Varma (2022102607534542600_ehz067-B11) 2015; 65
Varma (2022102607534542600_ehz067-B4) 2010; 122
Saxon (2022102607534542600_ehz067-B13) 2010; 122
Slotwiner (2022102607534542600_ehz067-B17) 2015; 12
Crossley (2022102607534542600_ehz067-B9) 2009; 54
Hindricks (2022102607534542600_ehz067-B10) 2017; 38
Guedon-Moreau (2022102607534542600_ehz067-B5) 2013; 34
Varma (2022102607534542600_ehz067-B21) 2013; 34
Ricci (2022102607534542600_ehz067-B2) 2008; 10
Vogtmann (2022102607534542600_ehz067-B3) 2013; 15
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Guedon-Moreau (2022102607534542600_ehz067-B16) 2014; 16
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Snippet Abstract Aims This trial aimed to evaluate the safety and efficiency of a common and simplified protocol for the surveillance of cardiac implantable electronic...
This trial aimed to evaluate the safety and efficiency of a common and simplified protocol for the surveillance of cardiac implantable electronic devices based...
AIMSThis trial aimed to evaluate the safety and efficiency of a common and simplified protocol for the surveillance of cardiac implantable electronic devices...
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SubjectTerms Fast Track Clinical Research
Title Safety and efficiency of a common and simplified protocol for pacemaker and defibrillator surveillance based on remote monitoring only: a long-term randomized trial (RM-ALONE)
URI https://www.ncbi.nlm.nih.gov/pubmed/30793735
https://search.proquest.com/docview/2185551788
https://pubmed.ncbi.nlm.nih.gov/PMC6568206
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