Cargando…

Risk and fate of residual interatrial shunting after transcatheter closure of patent foramen ovale: a long term follow up study

BACKGROUND: Percutaneous transcatheter closure of patent foramen ovale (PFO) in cryptogenic stroke is an alternative to medical therapy. There is still debate on different outcome for each currently available device. The impact of residual shunting after PFO-clo- sure on recurrent arterial embolism...

Descripción completa

Detalles Bibliográficos
Autores principales: Hammerstingl, C, Bauriedel, G, Stüsser, C, Momcilovic, D, Tuleta, I, Nickenig, G, Skowasch, D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3351944/
https://www.ncbi.nlm.nih.gov/pubmed/21345765
http://dx.doi.org/10.1186/2047-783X-16-1-13
_version_ 1782232814399258624
author Hammerstingl, C
Bauriedel, G
Stüsser, C
Momcilovic, D
Tuleta, I
Nickenig, G
Skowasch, D
author_facet Hammerstingl, C
Bauriedel, G
Stüsser, C
Momcilovic, D
Tuleta, I
Nickenig, G
Skowasch, D
author_sort Hammerstingl, C
collection PubMed
description BACKGROUND: Percutaneous transcatheter closure of patent foramen ovale (PFO) in cryptogenic stroke is an alternative to medical therapy. There is still debate on different outcome for each currently available device. The impact of residual shunting after PFO-clo- sure on recurrent arterial embolism is unknown. AIMS: (i) To evaluate the prevalence of residual interatrial shunting after device- closure of PFO, (ii) to identify risk factors predicting residual interatrial shunting after device implantation, and (iii) to investigate the outcome of patients after PFO-closure during long- term follow- up (FU). METHODS AND RESULTS: Between 2000- 2005 PFO-closure was performed in 124 patients using four different devices: Amplatzer PFO-(n = 52), CardioSeal (n = 33), Helex (n = 23) and Premere (n = 16) occluder. All patients underwent serial contrast-enhanced transesophageal echocardiography (TEE) for 24 months after PFO- closure; clinical FU was at minimum 5 years up to 9.75 years (mean 6.67 ± 1.31 years). Overall-closure rate was 87% at 2 years, device-specific closure time curves differed significantly (p-logrank = 0.003). Independent risk factors for residual-shunting were implantation of a Helex occluder (hazard ratio [HR] 12.6, 95% confidence interval [CI] 2.6- 57.4, p = 0.002), PFO- canal- lengths (HR 1.2, 95%CI 1.1- 1.3, p = 0.004) and extend of atrial-septal-aneurysm (HR 1.1, 95%CI 0.9- 1.3; p = 0.05). 4 (3.2%) arterial embolic events occurred during a FU-period of 817.2 patient-years, actuarial annual thromboembolic-risk was 0.49%. All ischemic events were not related to residual PFO-shunting or device-related thrombus- formation. CONCLUSION: Success rates of PFO- closure are mainly dependent on occluder-type, extend of concomitant atrial-septum-aneurysm and PFO-canal- length. Importantly, residual shunting after PFO-closure was not associated with recurrence of arterial embolism during long-term follow-up.
format Online
Article
Text
id pubmed-3351944
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-33519442012-05-16 Risk and fate of residual interatrial shunting after transcatheter closure of patent foramen ovale: a long term follow up study Hammerstingl, C Bauriedel, G Stüsser, C Momcilovic, D Tuleta, I Nickenig, G Skowasch, D Eur J Med Res Research BACKGROUND: Percutaneous transcatheter closure of patent foramen ovale (PFO) in cryptogenic stroke is an alternative to medical therapy. There is still debate on different outcome for each currently available device. The impact of residual shunting after PFO-clo- sure on recurrent arterial embolism is unknown. AIMS: (i) To evaluate the prevalence of residual interatrial shunting after device- closure of PFO, (ii) to identify risk factors predicting residual interatrial shunting after device implantation, and (iii) to investigate the outcome of patients after PFO-closure during long- term follow- up (FU). METHODS AND RESULTS: Between 2000- 2005 PFO-closure was performed in 124 patients using four different devices: Amplatzer PFO-(n = 52), CardioSeal (n = 33), Helex (n = 23) and Premere (n = 16) occluder. All patients underwent serial contrast-enhanced transesophageal echocardiography (TEE) for 24 months after PFO- closure; clinical FU was at minimum 5 years up to 9.75 years (mean 6.67 ± 1.31 years). Overall-closure rate was 87% at 2 years, device-specific closure time curves differed significantly (p-logrank = 0.003). Independent risk factors for residual-shunting were implantation of a Helex occluder (hazard ratio [HR] 12.6, 95% confidence interval [CI] 2.6- 57.4, p = 0.002), PFO- canal- lengths (HR 1.2, 95%CI 1.1- 1.3, p = 0.004) and extend of atrial-septal-aneurysm (HR 1.1, 95%CI 0.9- 1.3; p = 0.05). 4 (3.2%) arterial embolic events occurred during a FU-period of 817.2 patient-years, actuarial annual thromboembolic-risk was 0.49%. All ischemic events were not related to residual PFO-shunting or device-related thrombus- formation. CONCLUSION: Success rates of PFO- closure are mainly dependent on occluder-type, extend of concomitant atrial-septum-aneurysm and PFO-canal- length. Importantly, residual shunting after PFO-closure was not associated with recurrence of arterial embolism during long-term follow-up. BioMed Central 2011-01-27 /pmc/articles/PMC3351944/ /pubmed/21345765 http://dx.doi.org/10.1186/2047-783X-16-1-13 Text en Copyright ©2011 I. Holzapfel Publishers
spellingShingle Research
Hammerstingl, C
Bauriedel, G
Stüsser, C
Momcilovic, D
Tuleta, I
Nickenig, G
Skowasch, D
Risk and fate of residual interatrial shunting after transcatheter closure of patent foramen ovale: a long term follow up study
title Risk and fate of residual interatrial shunting after transcatheter closure of patent foramen ovale: a long term follow up study
title_full Risk and fate of residual interatrial shunting after transcatheter closure of patent foramen ovale: a long term follow up study
title_fullStr Risk and fate of residual interatrial shunting after transcatheter closure of patent foramen ovale: a long term follow up study
title_full_unstemmed Risk and fate of residual interatrial shunting after transcatheter closure of patent foramen ovale: a long term follow up study
title_short Risk and fate of residual interatrial shunting after transcatheter closure of patent foramen ovale: a long term follow up study
title_sort risk and fate of residual interatrial shunting after transcatheter closure of patent foramen ovale: a long term follow up study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3351944/
https://www.ncbi.nlm.nih.gov/pubmed/21345765
http://dx.doi.org/10.1186/2047-783X-16-1-13
work_keys_str_mv AT hammerstinglc riskandfateofresidualinteratrialshuntingaftertranscatheterclosureofpatentforamenovalealongtermfollowupstudy
AT bauriedelg riskandfateofresidualinteratrialshuntingaftertranscatheterclosureofpatentforamenovalealongtermfollowupstudy
AT stusserc riskandfateofresidualinteratrialshuntingaftertranscatheterclosureofpatentforamenovalealongtermfollowupstudy
AT momcilovicd riskandfateofresidualinteratrialshuntingaftertranscatheterclosureofpatentforamenovalealongtermfollowupstudy
AT tuletai riskandfateofresidualinteratrialshuntingaftertranscatheterclosureofpatentforamenovalealongtermfollowupstudy
AT nickenigg riskandfateofresidualinteratrialshuntingaftertranscatheterclosureofpatentforamenovalealongtermfollowupstudy
AT skowaschd riskandfateofresidualinteratrialshuntingaftertranscatheterclosureofpatentforamenovalealongtermfollowupstudy