Human fitting of pediatric and infant continuous-flow total artificial heart: visual and virtual assessment.

congenital heart disease infant total artificial heart mechanical circulatory support pediatric heart failure pediatric total artificial heart

Journal

Frontiers in cardiovascular medicine
ISSN: 2297-055X
Titre abrégé: Front Cardiovasc Med
Pays: Switzerland
ID NLM: 101653388

Informations de publication

Date de publication:
2023
Historique:
received: 25 03 2023
accepted: 03 07 2023
medline: 2 8 2023
pubmed: 2 8 2023
entrez: 2 8 2023
Statut: epublish

Résumé

This study aimed to determine the fit of two small-sized (pediatric and infant) continuous-flow total artificial heart pumps (CFTAHs) in congenital heart surgery patients. This study was approved by Cleveland Clinic Institutional Review Board. Pediatric cardiac surgery patients ( P-CFTAH pump fit in 21 out of 40 patients (fit group, 52.5%) but did not fit in 19 patients (non-fit group, 47.5%). I-CFTAH pump fit all of the 33 patients evaluated. There were critical differences due to dimensional variation ( This study demonstrated the range of proper fit for the P-CFTAH and I-CFTAH in congenital heart disease patients. These data suggest the feasibility of both devices for fit in the small-patient population.

Sections du résumé

Background UNASSIGNED
This study aimed to determine the fit of two small-sized (pediatric and infant) continuous-flow total artificial heart pumps (CFTAHs) in congenital heart surgery patients.
Methods UNASSIGNED
This study was approved by Cleveland Clinic Institutional Review Board. Pediatric cardiac surgery patients (
Results UNASSIGNED
P-CFTAH pump fit in 21 out of 40 patients (fit group, 52.5%) but did not fit in 19 patients (non-fit group, 47.5%). I-CFTAH pump fit all of the 33 patients evaluated. There were critical differences due to dimensional variation (
Conclusions UNASSIGNED
This study demonstrated the range of proper fit for the P-CFTAH and I-CFTAH in congenital heart disease patients. These data suggest the feasibility of both devices for fit in the small-patient population.

Identifiants

pubmed: 37529709
doi: 10.3389/fcvm.2023.1193800
pmc: PMC10387526
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1193800

Informations de copyright

© 2023 Miyagi, Ahmad, Karimov, Polakowski, Karamlou, Yaman, Fukamachi and Najm.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Chihiro Miyagi (C)

Department of Biomedical Engineering, Cleveland Clinic Lerner Research Institute, Cleveland, OH, United States.

Munir Ahmad (M)

Department of Thoracic and Cardiovascular Surgery, Cleveland Clinic, Cleveland, OH, United States.

Jamshid H Karimov (JH)

Department of Biomedical Engineering, Cleveland Clinic Lerner Research Institute, Cleveland, OH, United States.
Department of Biomedical Engineering, Cleveland Clinic Lerner College of Medicine of Case Western Reserve University, Cleveland, OH, United States.

Anthony R Polakowski (AR)

Department of Biomedical Engineering, Cleveland Clinic Lerner Research Institute, Cleveland, OH, United States.

Tara Karamlou (T)

Department of Thoracic and Cardiovascular Surgery, Cleveland Clinic, Cleveland, OH, United States.

Malek Yaman (M)

Department of Pediatric Cardiology, Cleveland Clinic Children's Hospital, Cleveland, OH, United States.

Kiyotaka Fukamachi (K)

Department of Biomedical Engineering, Cleveland Clinic Lerner Research Institute, Cleveland, OH, United States.
Department of Biomedical Engineering, Cleveland Clinic Lerner College of Medicine of Case Western Reserve University, Cleveland, OH, United States.

Hani K Najm (HK)

Department of Thoracic and Cardiovascular Surgery, Cleveland Clinic, Cleveland, OH, United States.

Classifications MeSH