Source:http://linkedlifedata.com/resource/pubmed/id/16551899
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2006-3-22
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pubmed:abstractText |
We performed a blinded, randomized pharmacokinetic study of milrinone in 16 neonates with hypoplastic left heart undergoing stage I reconstruction to determine the impact of cardiopulmonary bypass and modified ultrafiltration on drug disposition and to define the drug exposure during a continuous IV infusion of drug postoperatively. Neonates received an initial dose of either a 100 or 250 microg/kg of milrinone into the cardiopulmonary bypass circuit at the start of rewarming. Postoperatively, milrinone was infused to clinical needs. A mixed-effect modeling approach was used to characterize milrinone pharmacokinetics during cardiopulmonary bypass, modified ultrafiltration, and postoperatively using the NONMEM algorithm. All patients in this study demonstrated a modified ultrafiltration concentrating effect that occurred despite a modified ultrafiltration drug clearance of 3.3 mL x kg(-1) x min(-1). The infants in this study demonstrated an impaired renal clearance during the immediate postoperative period. A constant infusion of 0.5 microg x kg(-1) x min(-1) resulted in drug accumulation during the initial 12 h of drug administration. Postoperatively, milrinone clearance was significantly impaired (0.4 mL x kg(-1) x min(-1)), improved by the 12th postoperative hour, and approached steady-state clearance (2.6 mL x kg(-1) x min(-1)) by postoperative day 4. In the postoperative setting of markedly impaired renal function, an infusion rate of 0.2 microg x kg(-1) x min(-1) should be considered.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1526-7598
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pubmed:author |
pubmed-author:AdamsonPeter CPC,
pubmed-author:BarrettJeffrey SJS,
pubmed-author:BurnhamNancyN,
pubmed-author:DavisLauren ALA,
pubmed-author:GaynorJ WilliamJW,
pubmed-author:GreeleyWilliam JWJ,
pubmed-author:HoffmanTimothy MTM,
pubmed-author:MondickJohn TJT,
pubmed-author:NicolsonSusan CSC,
pubmed-author:SprayThomas LTL,
pubmed-author:WernovskyGilG,
pubmed-author:ZuppaAthena FAF
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pubmed:issnType |
Electronic
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pubmed:volume |
102
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1062-9
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:16551899-Cardiopulmonary Bypass,
pubmed-meshheading:16551899-Humans,
pubmed-meshheading:16551899-Hypoplastic Left Heart Syndrome,
pubmed-meshheading:16551899-Infant,
pubmed-meshheading:16551899-Infant, Newborn,
pubmed-meshheading:16551899-Milrinone,
pubmed-meshheading:16551899-Pilot Projects,
pubmed-meshheading:16551899-Reconstructive Surgical Procedures,
pubmed-meshheading:16551899-Statistics, Nonparametric
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pubmed:year |
2006
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pubmed:articleTitle |
Population pharmacokinetics of milrinone in neonates with hypoplastic left heart syndrome undergoing stage I reconstruction.
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pubmed:affiliation |
Division of Clinical Pharmacology and Therapeutics, Department of Pediatrics, Abramson Research Center, Philadelphia, Pennsylvania 19104-4318, USA. zuppa@email.chop.edu
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pubmed:publicationType |
Journal Article,
Comparative Study,
Randomized Controlled Trial,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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