2018
DOI: 10.1016/j.healun.2017.03.005
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Outcomes following implantation of mechanical circulatory support in adults with congenital heart disease: An analysis of the Interagency Registry for Mechanically Assisted Circulatory Support (INTERMACS)

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Cited by 110 publications
(110 citation statements)
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“…Vanderpluym and colleagues used the INTERMACS registry to evaluate outcomes of circulatory support device use in patients ACHD patients. Over 10 years, there were 126 ACHD patients who received mechanical circulatory support out of 16,182 patients (43). Forty-five of the 126 patients had a systemic morphologic right ventricle.…”
Section: Waiting List and Mechanical Circulatory Support As A Bridgementioning
confidence: 99%
“…Vanderpluym and colleagues used the INTERMACS registry to evaluate outcomes of circulatory support device use in patients ACHD patients. Over 10 years, there were 126 ACHD patients who received mechanical circulatory support out of 16,182 patients (43). Forty-five of the 126 patients had a systemic morphologic right ventricle.…”
Section: Waiting List and Mechanical Circulatory Support As A Bridgementioning
confidence: 99%
“…Currently, VAD use remains limited in ACHD patients, despite favorable outcomes in a recent INTERMACS analysis . In this study, while survival was similar between ACHD and non‐ACHD patients, ACHD patients were three times more likely to undergo a biventricular assist device or total artificial heart.…”
Section: Commentmentioning
confidence: 72%
“…Recent data from the Interagency Registry for Mechanically Assisted Circulatory Support registry have shown similar outcomes between non-CHD patients and patients with CHD with a biventricular circulation requiring LVAD, independent of systemic ventricular morphology. Options for patients with biventricular failure are limited 23. The only Food and Drug Administration-approved total artificial heart is a pneumatically driven device for temporary use (bridge to transplant) based on technology that is more than three decades old.…”
Section: Discussionmentioning
confidence: 99%
“…The only Food and Drug Administration-approved total artificial heart is a pneumatically driven device for temporary use (bridge to transplant) based on technology that is more than three decades old. Additionally, the mortality is higher in patients with CHD requiring biventricular assist devices 23. Finally, novel forms of mechanical support need to be developed for patients with univentricular circulations.…”
Section: Discussionmentioning
confidence: 99%