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Individual variations in fentanyl pharmacokinetics and pharmacodynamics in preterm infants

Norman, Elisabeth (författare)
Neonatology,Neonatologi,Skåne University Hospital
Kindblom, Jenny M. (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicin,Institute of Medicine,University of Gothenburg
Rane, Anders (författare)
Karolinska University Hospital,Karolinska Institute,Karolinska Institutet
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Berg, Ann Cathrine (författare)
Neonatology,Neonatologi,Skåne University Hospital
Schubert, U (författare)
Karolinska University Hospital,Karolinska Institute,Karolinska Institutet,Department of Clinical Science, Intervention and Technology (CLINTEC),Department of Clinical Science, Intervention and Technology (CLINTEC)
Hallberg, B (författare)
Karolinska University Hospital,Karolinska Institute,Karolinska Institutet,Department of Clinical Science, Intervention and Technology (CLINTEC),Department of Clinical Science, Intervention and Technology (CLINTEC)
Fellman, Vineta (författare)
Paediatrics (Lund),Pediatrik, Lund,University of Helsinki,Skåne University Hospital
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 (creator_code:org_t)
2019-03-19
2019
Engelska.
Ingår i: Acta Paediatrica. - : Wiley. - 0803-5253 .- 1651-2227. ; 108:8, s. 1441-1446
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Aim Fentanyl pharmacokinetics and pharmacodynamics are lacking in preterm infants. Our aim was to study these and their relation with a new formulation of fentanyl 5 mu g/mL for procedural pain. Methods Preterm infants were given 0.5 (n = 20, median gestational age 26.5; range 23.3-34.1 weeks) and 2 mu g/kg (n = 8, 27.4; 25.3-30.7 weeks) fentanyl, respectively, before skin-breaking procedures or tracheal intubation. Blood samples were collected after ten minutes, two, four, eight and 24 hours. Physiologic parameters were monitored and pain scores assessed. Results The median fentanyl concentrations were 0.18, 0.15, 0.15 and 0.57, 0.37, 0.35 ng/mL at 15-31 minutes, two and four hours and the half-lives were 1.6 to 20.5 or 4.1 to 32.6 hours for the low- and high-dose groups, respectively. A significant correlation was seen between weight at study inclusion and half-life (Spearman ' s r = -0.9, p < 0.001), volume of distribution (r = -0.8, p < 0.01) and clearance (r = -0.9, p < 0.01) in the low-dose group (n = 9). Pain assessment results were not correlated to pharmacokinetic variables. Fentanyl was well tolerated. Conclusion The inter-individual variation of fentanyl pharmacokinetics is large in preterm infants, and the dose of 0.5 mu g/kg seems not effective for skin-breaking procedures.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Pediatrik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Pediatrics (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Samhällsfarmaci och klinisk farmaci (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Social and Clinical Pharmacy (hsv//eng)

Nyckelord

Fentanyl
Pain
Pharmacokinetics
Preterm infants
continuous-infusion
initial validation
procedural pain
morphine
analgesia
newborns
intubation
management
outcomes
scale
Pediatrics

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