2006
DOI: 10.1161/circulationaha.105.571422
|View full text |Cite
|
Sign up to set email alerts
|

The National Heart, Lung, and Blood Institute Pediatric Circulatory Support Program

Abstract: Abstract-Options for the circulatory support of pediatric patients under the age of 5 years are currently limited to short-term extracorporeal devices, the use of which is often complicated by infection, bleeding, and thromboembolism. Recognizing this void, the National Heart, Lung, and Blood Institute solicited proposals for the development of novel circulatory support systems for infants and children from 2 to 25 kg with congenital or acquired cardiovascular disease. Five contracts were awarded to develop a … Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
111
0
1

Year Published

2008
2008
2023
2023

Publication Types

Select...
6
3
1

Relationship

0
10

Authors

Journals

citations
Cited by 183 publications
(112 citation statements)
references
References 33 publications
(22 reference statements)
0
111
0
1
Order By: Relevance
“…The relatively rapid adoption of this technology by >45 centers in the United States and Canada in a relatively short time frame likely stems from widespread appreciation of the unacceptably high waiting-list mortality in US infants and children with or without ECMO, 1,31,32 the lack of alternative devices, the favorable German EXCOR experience, 6,25 and a foundational shift in the willingness of US clinicians to use emerging circulatory support technologies that were used variably in Germany as early as the mid1990s. 3,[33][34][35][36][37] This fundamental change in US clinical practice represents a major milestone for the field of pediatric heart failure therapy. With a growing number of novel miniaturized pediatric VADs now on the horizon, [38][39][40] FDA approval of the EXCOR marks the beginning of a new era in pediatric mechanical circulatory support.…”
Section: Downloaded Frommentioning
confidence: 99%
“…The relatively rapid adoption of this technology by >45 centers in the United States and Canada in a relatively short time frame likely stems from widespread appreciation of the unacceptably high waiting-list mortality in US infants and children with or without ECMO, 1,31,32 the lack of alternative devices, the favorable German EXCOR experience, 6,25 and a foundational shift in the willingness of US clinicians to use emerging circulatory support technologies that were used variably in Germany as early as the mid1990s. 3,[33][34][35][36][37] This fundamental change in US clinical practice represents a major milestone for the field of pediatric heart failure therapy. With a growing number of novel miniaturized pediatric VADs now on the horizon, [38][39][40] FDA approval of the EXCOR marks the beginning of a new era in pediatric mechanical circulatory support.…”
Section: Downloaded Frommentioning
confidence: 99%
“…Easily adaptable, the MIP could have a great use as a pediatric pump. 20 It implemented on a graft for children suffering of an underdeveloped heart that have undergone a Fontan procedure. 21,22 The pump can be as simple as a gelatin coated graft enliven by a pincher.…”
Section: -9mentioning
confidence: 99%
“…The presence of robust outcome data is essential for measuring patient outcomes, reviewing the emerging field of pediatric mechanical circulatory support, and evaluating novel pediatricspecific devices. 25 INTERMACS analyses are evaluated in light of single-institution studies and published results of FDA IDE trials, both of which appear before publications from INTERMACS because INTERMACS is limited to data from FDA-approved MCSDs.…”
Section: Intermacs: Accomplishments To Datementioning
confidence: 99%