Remote versus In-Office Monitoring for Implantable Cardioverter Defibrillators: Results from a Randomized Pragmatic Controlled Study in Portugal
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10400.17/4382 |
Resumo: | Introduction: Remote monitoring (RM) is a safe and effective alternative to in-office conventional follow-up. Objective: We aimed to evaluate patient satisfaction with RM and its impact on healthcare resources in a population with cardiac implantable electronic devices. Methods: Randomized, pragmatic, open-label controlled trial, with adult wearers of implantable cardioverter-defibrillator (ICD) or cardiac resynchronization therapy with ICD (CRT-D), eligible for the CareLink® system. Patients newly implanted or with previous conventional follow-up were randomized to RM or conventional follow-up (control), and followed for 12 months, according to the centers' practice. The number of in-office visits and adverse events were compared between groups. Patient and healthcare professionals' satisfaction with RM were described. Results: Of the 134 randomized patients (69 RM; 65 control, aged 60±13 years), 80% were male, 23% employed, 72% ICD wearers and 54% newly implanted. Most patients (70%) reported travel costs less than 15€/visit, and 46% daily routine interference with in-office visits. Median physician/technician time with patient was 15 min/15 min, per in-office visit. Excluding baseline and final visits, control patients had more in-office visits in total: median 1 vs. 0, p<0.001. In 81% of the in-office visits, no clinical measures were taken. There were 10 adverse events, with no differences between groups. At the final visit, 95% of RM patients considered RM easy/very easy to use, and would all prefer to maintain RM and recommend it to others. All professionals found the CareLink website easy/very easy to use and were satisfied with transmission data. Conclusions: In a Portuguese population with ICD and CRT-D, RM safely reduced the burden of in-office visits, with high levels of satisfaction among patients and healthcare professionals. |
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Remote versus In-Office Monitoring for Implantable Cardioverter Defibrillators: Results from a Randomized Pragmatic Controlled Study in PortugalMonitoração Remota versus Seguimento Hospitalar Presencial em Portadores de Cardioversor-Desfibrilhador: Resultados dum Estudo Randomizado em PortugalHSM CARAdultFemaleMaleHumansCardiac Resynchronization Therapy*Defibrillators, Implantable* / adverse effectsPortugalIntroduction: Remote monitoring (RM) is a safe and effective alternative to in-office conventional follow-up. Objective: We aimed to evaluate patient satisfaction with RM and its impact on healthcare resources in a population with cardiac implantable electronic devices. Methods: Randomized, pragmatic, open-label controlled trial, with adult wearers of implantable cardioverter-defibrillator (ICD) or cardiac resynchronization therapy with ICD (CRT-D), eligible for the CareLink® system. Patients newly implanted or with previous conventional follow-up were randomized to RM or conventional follow-up (control), and followed for 12 months, according to the centers' practice. The number of in-office visits and adverse events were compared between groups. Patient and healthcare professionals' satisfaction with RM were described. Results: Of the 134 randomized patients (69 RM; 65 control, aged 60±13 years), 80% were male, 23% employed, 72% ICD wearers and 54% newly implanted. Most patients (70%) reported travel costs less than 15€/visit, and 46% daily routine interference with in-office visits. Median physician/technician time with patient was 15 min/15 min, per in-office visit. Excluding baseline and final visits, control patients had more in-office visits in total: median 1 vs. 0, p<0.001. In 81% of the in-office visits, no clinical measures were taken. There were 10 adverse events, with no differences between groups. At the final visit, 95% of RM patients considered RM easy/very easy to use, and would all prefer to maintain RM and recommend it to others. All professionals found the CareLink website easy/very easy to use and were satisfied with transmission data. Conclusions: In a Portuguese population with ICD and CRT-D, RM safely reduced the burden of in-office visits, with high levels of satisfaction among patients and healthcare professionals.Elsevier EspañaRepositório do Centro Hospitalar Universitário de Lisboa Central, EPEMartins Oliveira, MFernandes, MReis, HPrimo, JSanfins, VSilva, VSilva Cunha, PSilva, MNicola, PPORTLink Study Investigators2023-02-01T16:04:59Z2022-122022-12-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.17/4382engRev Port Cardiol. 2022;41(12):987-997.10.1016/j.repc.2021.08.017.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-03-10T09:46:18Zoai:repositorio.chlc.min-saude.pt:10400.17/4382Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T17:21:42.724170Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Remote versus In-Office Monitoring for Implantable Cardioverter Defibrillators: Results from a Randomized Pragmatic Controlled Study in Portugal Monitoração Remota versus Seguimento Hospitalar Presencial em Portadores de Cardioversor-Desfibrilhador: Resultados dum Estudo Randomizado em Portugal |
title |
Remote versus In-Office Monitoring for Implantable Cardioverter Defibrillators: Results from a Randomized Pragmatic Controlled Study in Portugal |
spellingShingle |
Remote versus In-Office Monitoring for Implantable Cardioverter Defibrillators: Results from a Randomized Pragmatic Controlled Study in Portugal Martins Oliveira, M HSM CAR Adult Female Male Humans Cardiac Resynchronization Therapy* Defibrillators, Implantable* / adverse effects Portugal |
title_short |
Remote versus In-Office Monitoring for Implantable Cardioverter Defibrillators: Results from a Randomized Pragmatic Controlled Study in Portugal |
title_full |
Remote versus In-Office Monitoring for Implantable Cardioverter Defibrillators: Results from a Randomized Pragmatic Controlled Study in Portugal |
title_fullStr |
Remote versus In-Office Monitoring for Implantable Cardioverter Defibrillators: Results from a Randomized Pragmatic Controlled Study in Portugal |
title_full_unstemmed |
Remote versus In-Office Monitoring for Implantable Cardioverter Defibrillators: Results from a Randomized Pragmatic Controlled Study in Portugal |
title_sort |
Remote versus In-Office Monitoring for Implantable Cardioverter Defibrillators: Results from a Randomized Pragmatic Controlled Study in Portugal |
author |
Martins Oliveira, M |
author_facet |
Martins Oliveira, M Fernandes, M Reis, H Primo, J Sanfins, V Silva, V Silva Cunha, P Silva, M Nicola, P PORTLink Study Investigators |
author_role |
author |
author2 |
Fernandes, M Reis, H Primo, J Sanfins, V Silva, V Silva Cunha, P Silva, M Nicola, P PORTLink Study Investigators |
author2_role |
author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Repositório do Centro Hospitalar Universitário de Lisboa Central, EPE |
dc.contributor.author.fl_str_mv |
Martins Oliveira, M Fernandes, M Reis, H Primo, J Sanfins, V Silva, V Silva Cunha, P Silva, M Nicola, P PORTLink Study Investigators |
dc.subject.por.fl_str_mv |
HSM CAR Adult Female Male Humans Cardiac Resynchronization Therapy* Defibrillators, Implantable* / adverse effects Portugal |
topic |
HSM CAR Adult Female Male Humans Cardiac Resynchronization Therapy* Defibrillators, Implantable* / adverse effects Portugal |
description |
Introduction: Remote monitoring (RM) is a safe and effective alternative to in-office conventional follow-up. Objective: We aimed to evaluate patient satisfaction with RM and its impact on healthcare resources in a population with cardiac implantable electronic devices. Methods: Randomized, pragmatic, open-label controlled trial, with adult wearers of implantable cardioverter-defibrillator (ICD) or cardiac resynchronization therapy with ICD (CRT-D), eligible for the CareLink® system. Patients newly implanted or with previous conventional follow-up were randomized to RM or conventional follow-up (control), and followed for 12 months, according to the centers' practice. The number of in-office visits and adverse events were compared between groups. Patient and healthcare professionals' satisfaction with RM were described. Results: Of the 134 randomized patients (69 RM; 65 control, aged 60±13 years), 80% were male, 23% employed, 72% ICD wearers and 54% newly implanted. Most patients (70%) reported travel costs less than 15€/visit, and 46% daily routine interference with in-office visits. Median physician/technician time with patient was 15 min/15 min, per in-office visit. Excluding baseline and final visits, control patients had more in-office visits in total: median 1 vs. 0, p<0.001. In 81% of the in-office visits, no clinical measures were taken. There were 10 adverse events, with no differences between groups. At the final visit, 95% of RM patients considered RM easy/very easy to use, and would all prefer to maintain RM and recommend it to others. All professionals found the CareLink website easy/very easy to use and were satisfied with transmission data. Conclusions: In a Portuguese population with ICD and CRT-D, RM safely reduced the burden of in-office visits, with high levels of satisfaction among patients and healthcare professionals. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-12 2022-12-01T00:00:00Z 2023-02-01T16:04:59Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10400.17/4382 |
url |
http://hdl.handle.net/10400.17/4382 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Rev Port Cardiol. 2022;41(12):987-997. 10.1016/j.repc.2021.08.017. |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier España |
publisher.none.fl_str_mv |
Elsevier España |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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