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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
6
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pubmed:dateCreated |
2008-6-6
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pubmed:abstractText |
The Medtronic Sprint Fidelis implantable cardioverter-defibrillator high-voltage lead is prone to fracture. The October 2007 safety advisory recommended lead impedance monitoring to aid in identifying lead fractures.
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pubmed:commentsCorrections |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1556-3871
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pubmed:author |
|
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pubmed:issnType |
Electronic
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pubmed:volume |
5
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
775-9
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pubmed:dateRevised |
2009-10-27
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pubmed:meshHeading |
pubmed-meshheading:18534361-Cardiography, Impedance,
pubmed-meshheading:18534361-Defibrillators, Implantable,
pubmed-meshheading:18534361-Electrodes, Implanted,
pubmed-meshheading:18534361-Equipment Failure,
pubmed-meshheading:18534361-Equipment Failure Analysis,
pubmed-meshheading:18534361-Equipment Safety,
pubmed-meshheading:18534361-Female,
pubmed-meshheading:18534361-Humans,
pubmed-meshheading:18534361-Male,
pubmed-meshheading:18534361-Retrospective Studies
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pubmed:year |
2008
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|
pubmed:articleTitle |
Failure of impedance monitoring to prevent adverse clinical events caused by fracture of a recalled high-voltage implantable cardioverter-defibrillator lead.
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pubmed:affiliation |
Minneapolis Heart Institute Foundation, Minneapolis, Minnesota, USA.
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pubmed:publicationType |
Journal Article
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