Seguimiento en fase aguda de catéteres electrodos de estimulación endocavitaria permanente: Comparación de tres modelos

Background: Electrode lead design and materials influence their performance, stability and manipulation characteristics. In our laboratory, we use straight intracardiac, active fixation, steroid eluting leads. These features are shared by three brands of pacemarker distributors. Aim: To compare the...

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Autores principales: Frangini S,Patricia, Vergara S,Ismael, González A,Rolando, Fajuri N,Alejandro, Baeza L,Mariana
Lenguaje:Spanish / Castilian
Publicado: Sociedad Médica de Santiago 2006
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Acceso en línea:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872006001100010
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spelling oai:scielo:S0034-988720060011000102014-01-24Seguimiento en fase aguda de catéteres electrodos de estimulación endocavitaria permanente: Comparación de tres modelosFrangini S,PatriciaVergara S,IsmaelGonzález A,RolandoFajuri N,AlejandroBaeza L,Mariana Cardiac pacemaker, artificial Defibrillators, implantable Heart block Background: Electrode lead design and materials influence their performance, stability and manipulation characteristics. In our laboratory, we use straight intracardiac, active fixation, steroid eluting leads. These features are shared by three brands of pacemarker distributors. Aim: To compare the short term results of three brands of leads used in our laboratory in patients requiring the implant of a pacemarker of cardioverter. Material and methods: One hundred and four patients (mean age 70 years, 59 males) subjected to a pacemarker or cardioverter implant were studied and followed during the first three months post implant. In these patients, 49 Guidant Flextend® 4087 or 4088, 27 Saint Jude Tendril® 1488T and 10 Medtronic Capsurefix® 5076 leads were implanted in the right atrium and 60 Guidant Flextend® 4087 or 4088, 29 Saint Jude Tendril® 1488T and 19 Medtronic Capsurefix® 5076 leads were implanted in the right ventricle. Results: Implant parameters were adequate for all leads. A sub-acute rise in ventricular stimulation threshold was detected in one Flextrend® lead. Three atrial leads (two Flextend® and one Capsurefix®) and one Capsurefix® ventricular lead experienced an acute displacement. One patient with a Flextend® lead, had a cardiac tamponade caused by an atrial perforation. Conclusions: The three brands of leads tested can be successfully implanted with comparable parameters and without differences in the evolution of patients during the first three monthsinfo:eu-repo/semantics/openAccessSociedad Médica de SantiagoRevista médica de Chile v.134 n.11 20062006-11-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872006001100010es10.4067/S0034-98872006001100010
institution Scielo Chile
collection Scielo Chile
language Spanish / Castilian
topic Cardiac pacemaker, artificial
Defibrillators, implantable
Heart block
spellingShingle Cardiac pacemaker, artificial
Defibrillators, implantable
Heart block
Frangini S,Patricia
Vergara S,Ismael
González A,Rolando
Fajuri N,Alejandro
Baeza L,Mariana
Seguimiento en fase aguda de catéteres electrodos de estimulación endocavitaria permanente: Comparación de tres modelos
description Background: Electrode lead design and materials influence their performance, stability and manipulation characteristics. In our laboratory, we use straight intracardiac, active fixation, steroid eluting leads. These features are shared by three brands of pacemarker distributors. Aim: To compare the short term results of three brands of leads used in our laboratory in patients requiring the implant of a pacemarker of cardioverter. Material and methods: One hundred and four patients (mean age 70 years, 59 males) subjected to a pacemarker or cardioverter implant were studied and followed during the first three months post implant. In these patients, 49 Guidant Flextend® 4087 or 4088, 27 Saint Jude Tendril® 1488T and 10 Medtronic Capsurefix® 5076 leads were implanted in the right atrium and 60 Guidant Flextend® 4087 or 4088, 29 Saint Jude Tendril® 1488T and 19 Medtronic Capsurefix® 5076 leads were implanted in the right ventricle. Results: Implant parameters were adequate for all leads. A sub-acute rise in ventricular stimulation threshold was detected in one Flextrend® lead. Three atrial leads (two Flextend® and one Capsurefix®) and one Capsurefix® ventricular lead experienced an acute displacement. One patient with a Flextend® lead, had a cardiac tamponade caused by an atrial perforation. Conclusions: The three brands of leads tested can be successfully implanted with comparable parameters and without differences in the evolution of patients during the first three months
author Frangini S,Patricia
Vergara S,Ismael
González A,Rolando
Fajuri N,Alejandro
Baeza L,Mariana
author_facet Frangini S,Patricia
Vergara S,Ismael
González A,Rolando
Fajuri N,Alejandro
Baeza L,Mariana
author_sort Frangini S,Patricia
title Seguimiento en fase aguda de catéteres electrodos de estimulación endocavitaria permanente: Comparación de tres modelos
title_short Seguimiento en fase aguda de catéteres electrodos de estimulación endocavitaria permanente: Comparación de tres modelos
title_full Seguimiento en fase aguda de catéteres electrodos de estimulación endocavitaria permanente: Comparación de tres modelos
title_fullStr Seguimiento en fase aguda de catéteres electrodos de estimulación endocavitaria permanente: Comparación de tres modelos
title_full_unstemmed Seguimiento en fase aguda de catéteres electrodos de estimulación endocavitaria permanente: Comparación de tres modelos
title_sort seguimiento en fase aguda de catéteres electrodos de estimulación endocavitaria permanente: comparación de tres modelos
publisher Sociedad Médica de Santiago
publishDate 2006
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872006001100010
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