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Safety and efficacy of leadless pacemaker retrieval.
Li, Jianwen; Hou, Wen-Bo; Cao, Ming-Kun; Zhou, Wen-Xiu; Wang, Yan; Fang, Yi; Zhou, Chao; Yin, Yu-Xia; Toft, Egon S; Zhang, Hai-Jun.
Afiliação
  • Li J; R&D Department, National United Engineering Laboratory for Biomedical Material Modification, Dezhou, China.
  • Hou WB; R&D Department, National United Engineering Laboratory for Biomedical Material Modification, Dezhou, China.
  • Cao MK; R&D Department, National United Engineering Laboratory for Biomedical Material Modification, Dezhou, China.
  • Zhou WX; R&D Department, National United Engineering Laboratory for Biomedical Material Modification, Dezhou, China.
  • Wang Y; R&D Department, National United Engineering Laboratory for Biomedical Material Modification, Dezhou, China.
  • Fang Y; R&D Department, National United Engineering Laboratory for Biomedical Material Modification, Dezhou, China.
  • Zhou C; R&D Department, National United Engineering Laboratory for Biomedical Material Modification, Dezhou, China.
  • Yin YX; R&D Department, National United Engineering Laboratory for Biomedical Material Modification, Dezhou, China.
  • Toft ES; Medical and Health Sciences, Qatar University, Doha, Qatar.
  • Zhang HJ; R&D Department, National United Engineering Laboratory for Biomedical Material Modification, Dezhou, China.
J Cardiovasc Electrophysiol ; 30(9): 1671-1678, 2019 09.
Article em En | MEDLINE | ID: mdl-31310416
BACKGROUND AND OBJECTIVES: The success rate of leadless cardiac pacemaker (LP) retrieval remains a major concern for this disruptive technology. The present paper performed a systematic review of the safety and feasibility of the retrieval of LPs. METHODS: Primary publications that performed LP retrieval were collected and included five animal experiments and two worldwide retrieval experiences in human. The procedural details, such as indication, days post implantation, extraction success rate, and complications, were described. The present paper analyzed factors affecting the retrieval and management of the nonfunctional devices. RESULTS: Retrieval animal models was possible at least up to 2.5 years post implantation, and data from humans suggest that removal of a device that was implanted longer (eg, 4 years and 9 months for Nanostim; 4 years for Micra) could be performed within a reasonable safety profile. The fixed mechanism, implant site, and encapsulation of the LP systems may affect the retrieval process. CONCLUSIONS: A high success rate in the relatively chronic retrieval of LPs was demonstrated, which promotes the extensive use of these devices in the treatment arrhythmia in the future.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Marca-Passo Artificial / Estimulação Cardíaca Artificial / Remoção de Dispositivo Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Aged / Aged80 / Animals / Humans / Middle aged Idioma: En Revista: J Cardiovasc Electrophysiol Assunto da revista: ANGIOLOGIA / CARDIOLOGIA / FISIOLOGIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Marca-Passo Artificial / Estimulação Cardíaca Artificial / Remoção de Dispositivo Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Aged / Aged80 / Animals / Humans / Middle aged Idioma: En Revista: J Cardiovasc Electrophysiol Assunto da revista: ANGIOLOGIA / CARDIOLOGIA / FISIOLOGIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China País de publicação: Estados Unidos