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Microtransesophageal Echocardiographic Guidance during Percutaneous Interatrial Septal Closure without General Anaesthesia.
Snijder, Roel J R; Renes, Laura E; Swaans, Martin J; Suttorp, Maarten Jan; Ten Berg, Jurrien M; Post, Martijn C.
Afiliação
  • Snijder RJR; Department of Cardiology, St. Antonius Hospital, Nieuwegein, Netherlands.
  • Renes LE; Department of Emergency Medicine, St. Antonius Hospital, Nieuwegein, Netherlands.
  • Swaans MJ; Department of Cardiology, St. Antonius Hospital, Nieuwegein, Netherlands.
  • Suttorp MJ; Department of Cardiology, St. Antonius Hospital, Nieuwegein, Netherlands.
  • Ten Berg JM; Department of Cardiology, St. Antonius Hospital, Nieuwegein, Netherlands.
  • Post MC; Department of Cardiology, St. Antonius Hospital, Nieuwegein, Netherlands.
J Interv Cardiol ; 2020: 1462140, 2020.
Article em En | MEDLINE | ID: mdl-32982607
ABSTRACT

OBJECTIVE:

To study the safety and efficacy of microtransesophageal echocardiography (micro-TEE) and TEE during percutaneous atrial septal defect (ASD) and patent foramen ovale (PFO) closure.

BACKGROUND:

TEE has proven to be safe during ASD and PFO closure under general anaesthesia. Micro-TEE makes it possible to perform these procedures under local anaesthesia. We are the first to describe the safety and efficacy of micro-TEE for percutaneous closure.

METHODS:

All consecutive patients who underwent ASD and PFO closure between 2013 and 2018 were included. The periprocedural complications were registered. Residual shunts were diagnosed using transthoracic contrast echocardiography (TTCE). All data were compared between the use of TEE or micro-TEE within the ASD and PFO groups separately.

RESULTS:

In total, 82 patients underwent ASD closure, 46 patients (49.1 ± 15.0 years) with TEE and 36 patients (47.8 ± 12.1 years) using micro-TEE guidance. Median device diameter was, respectively, 26 mm (range 10-40 mm) and 27 mm (range 10-35 mm). PFO closure was performed in 120 patients, 55 patients (48.6 ± 9.2 years, median device diameter 25 mm, range 23-35 mm) with TEE and 65 patients (mean age 51.0 ± 11.8 years, median device diameter 27 mm, range 23-35 mm) using micro-TEE. There were no major periprocedural complications, especially no device embolizations within all groups. Six months after closure, there was no significant difference in left-to-right shunt after ASD closure and no significant difference in right-to-left shunt after PFO closure using TEE or micro-TEE.

CONCLUSION:

Micro-TEE guidance without general anaesthesia during percutaneous ASD and PFO closure is as safe as TEE, without a significant difference in the residual shunt rate after closure.
Assuntos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Cateterismo Cardíaco / Ecocardiografia Transesofagiana / Implantação de Prótese / Cirurgia Assistida por Computador / Dispositivo para Oclusão Septal / Comunicação Interatrial Tipo de estudo: Guideline Limite: Female / Humans / Male / Middle aged Idioma: En Revista: J Interv Cardiol Assunto da revista: CARDIOLOGIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Cateterismo Cardíaco / Ecocardiografia Transesofagiana / Implantação de Prótese / Cirurgia Assistida por Computador / Dispositivo para Oclusão Septal / Comunicação Interatrial Tipo de estudo: Guideline Limite: Female / Humans / Male / Middle aged Idioma: En Revista: J Interv Cardiol Assunto da revista: CARDIOLOGIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Holanda