Source:http://linkedlifedata.com/resource/pubmed/id/16878609
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2006-8-1
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pubmed:abstractText |
The TandemHeart percutaneous ventricular assist device can be used to support patients in cardiogenic shock (until cardiac recovery occurs or as a bridge to definitive therapy) or as a temporary application during high-risk coronary interventions. The TandemHeart is a left atrial-to-femoral artery bypass system comprising a transseptal cannula, arterial cannulae, and a centrifugal blood pump. The pump can deliver flow rates up to 4.0 L/min at a maximum speed of 7500 rpm. From May 2003 through May 2005, the TandemHeart was used to support 18 patients (11 in cardiogenic shock and 7 undergoing high-risk percutaneous transluminal coronary angioplasty). The patients in cardiogenic shock were supported for a mean of 88.8 +/- 74.3 hours (range, 4-264 hr) at a mean pump flow rate of 2.87 +/- 0.56 L/min (range, 1.8-3.5 L/min). The mean cardiac index improved from 1.57 +/- 0.31 L/min/m2 before support to 2.60 +/- 0.34 L/min/m2 during support. The mean duration of support for the high-risk percutaneous transluminal coronary angioplasty patients was 5.5 +/- 8.3 hours (range, 1-24 hr). The mean flow rate was 2.42 +/- 0.55 L/min (range, 1.5-3.0 L/ min). The overall 30-day survival rate was 61%. In our experience, the TandemHeart device was easy to insert and provided a means either to cardiac recovery or to continued support with an implantable left ventricular assist device.
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/16878609-11110291,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16878609-11794191,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16878609-14530729,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16878609-15061632,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16878609-15063283,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16878609-15734771,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16878609-15945107
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:issn |
0730-2347
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
33
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
111-5
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:16878609-Aged,
pubmed-meshheading:16878609-Aged, 80 and over,
pubmed-meshheading:16878609-Angioplasty, Balloon, Coronary,
pubmed-meshheading:16878609-Equipment Design,
pubmed-meshheading:16878609-Female,
pubmed-meshheading:16878609-Heart-Assist Devices,
pubmed-meshheading:16878609-Humans,
pubmed-meshheading:16878609-Male,
pubmed-meshheading:16878609-Middle Aged,
pubmed-meshheading:16878609-Risk Assessment,
pubmed-meshheading:16878609-Shock, Cardiogenic
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pubmed:year |
2006
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pubmed:articleTitle |
Clinical experience with the TandemHeart percutaneous ventricular assist device.
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pubmed:affiliation |
The Heart Failure and Transplant Program, Texas Heart Institute at St. Luke's Episcopal Hospital, Houston, Texas 77030, USA.
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pubmed:publicationType |
Journal Article
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