Clinical use of percutaneous mechanical circulatory assistance in a patient with end-stage right-sided heart failure and massive tricuspid insufficiency due to congenital heart disease: first-in-the-world case report.

Case report Congenital heart disease Ebstein's anomaly Impella RP Percutaneous mechanical circulatory support Percutaneous right ventricular assist device Right ventricular failure

Journal

European heart journal. Case reports
ISSN: 2514-2119
Titre abrégé: Eur Heart J Case Rep
Pays: England
ID NLM: 101730741

Informations de publication

Date de publication:
Aug 2021
Historique:
received: 13 01 2021
revised: 12 02 2021
accepted: 22 06 2021
entrez: 19 8 2021
pubmed: 20 8 2021
medline: 20 8 2021
Statut: epublish

Résumé

Due to improvement in the management of patients with congenital heart disease (CHD), the likelihood of their survival to adulthood is increasing. A relevant population suffers end-stage right ventricular failure (RVF) in their 3rd-4th decade of life. Hence, heart transplantation is still gold standard of treatment of end-stage heart failure, mechanical circulatory assistance has become a valuable tool in the bridging to heart transplant or definitive therapy. Use of implantable short-term or long-term devices is reported by others. However, within this clinical context, presence of significant tricuspid regurgitation (TR) or CHD is used as exclusion criteria for insertion of a percutaneous right ventricular circulatory support. We described a 36-year-old patient diagnosed with Ebstein's anomaly and severe TR who is admitted to hospital due to RVF refractory to standard medical treatment. After case presentation to the heart team, an Impella RP device insertion was scheduled, in spite of the presence of TR or CHD after evaluation of pulmonary valve competency and 3D reconstruction with virtual device implantation. During support, the patient improved clinically and haemodynamically. Due to device displacement to the right ventricle, it was bedside explanted after 30 days of support. After mechanical unloading during 30 days patients' right ventricle recovered partially, permitting patient to improve his functional class. Although TR and CHD are exclusion criteria for the implantation of the Impella RP device, we report clinical experience in patient with Ebstein's anomaly and severe TR supported with percutaneous device as bridge to heart transplantation during 30 days.

Sections du résumé

BACKGROUND BACKGROUND
Due to improvement in the management of patients with congenital heart disease (CHD), the likelihood of their survival to adulthood is increasing. A relevant population suffers end-stage right ventricular failure (RVF) in their 3rd-4th decade of life. Hence, heart transplantation is still gold standard of treatment of end-stage heart failure, mechanical circulatory assistance has become a valuable tool in the bridging to heart transplant or definitive therapy. Use of implantable short-term or long-term devices is reported by others. However, within this clinical context, presence of significant tricuspid regurgitation (TR) or CHD is used as exclusion criteria for insertion of a percutaneous right ventricular circulatory support.
CASE SUMMARY METHODS
We described a 36-year-old patient diagnosed with Ebstein's anomaly and severe TR who is admitted to hospital due to RVF refractory to standard medical treatment. After case presentation to the heart team, an Impella RP device insertion was scheduled, in spite of the presence of TR or CHD after evaluation of pulmonary valve competency and 3D reconstruction with virtual device implantation. During support, the patient improved clinically and haemodynamically. Due to device displacement to the right ventricle, it was bedside explanted after 30 days of support. After mechanical unloading during 30 days patients' right ventricle recovered partially, permitting patient to improve his functional class.
DISCUSSION CONCLUSIONS
Although TR and CHD are exclusion criteria for the implantation of the Impella RP device, we report clinical experience in patient with Ebstein's anomaly and severe TR supported with percutaneous device as bridge to heart transplantation during 30 days.

Identifiants

pubmed: 34409247
doi: 10.1093/ehjcr/ytab269
pii: ytab269
pmc: PMC8364766
doi:

Types de publication

Case Reports

Langues

eng

Pagination

ytab269

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press on behalf of the European Society of Cardiology.

Références

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pubmed: 22548820
Eur J Heart Fail. 2016 Mar;18(3):226-41
pubmed: 26995592
Circulation. 2018 May 15;137(20):e578-e622
pubmed: 29650544

Auteurs

Mario García Gómez (M)

Department of Cardiology, Hospital Clinico Universitario, Valladolid, Spain.

Aitor Uribarri (A)

Department of Cardiology, Hospital Clinico Universitario, Valladolid, Spain.
Centro de Investigación Biomédica en Red de Enfermedades Cardiovasculares (CIBERVC), Spain.

José Alberto San Román Calvar (JA)

Department of Cardiology, Hospital Clinico Universitario, Valladolid, Spain.
Centro de Investigación Biomédica en Red de Enfermedades Cardiovasculares (CIBERVC), Spain.

Alexander Stepanenko (A)

Department of Cardiology, Hospital Clinico Universitario, Valladolid, Spain.
Centro de Investigación Biomédica en Red de Enfermedades Cardiovasculares (CIBERVC), Spain.

Classifications MeSH