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Published on: January 17, 2011
Plasma fentanyl levels in infants undergoing extracorporeal membrane oxygenation
M P Leuschen1, L D Willett, E B Hoie
1Department of Pediatrics, Creighton University University of Nebraska Medical Center, Omaha.
Insights
Low-dose fentanyl infusions provide adequate analgesia for infants on extracorporeal membrane oxygenation (ECMO). Supplementing with lorazepam may improve outcomes, especially for infants with congenital diaphragmatic hernia.
Area of Science:
- Neonatalogy
- Pharmacology
- Critical Care Medicine
Background:
- Extracorporeal membrane oxygenation (ECMO) requires careful pain management in infants.
- Fentanyl is commonly used for analgesia and sedation during ECMO.
- Understanding fentanyl pharmacokinetics is crucial for optimizing its use in this vulnerable population.
Purpose of the Study:
- To analyze plasma fentanyl levels in infants undergoing ECMO.
- To assess the relationship between fentanyl dosage, patient characteristics, and outcomes.
- To evaluate the impact of lorazepam co-administration on fentanyl requirements and survival.
Main Methods:
- Plasma fentanyl concentrations were measured using radioimmunoassay in 12 infants receiving fentanyl.
- Infants received a fentanyl bolus followed by continuous infusion.
- Data on diagnosis, ECMO duration, co-medications (lorazepam), and survival were collected.
Main Results:
- Plasma fentanyl levels varied, with higher concentrations observed in infants with congenital diaphragmatic hernia (CDH).
- Infants with CDH had longer ECMO courses and poorer survival rates.
- Fentanyl clearance correlated with renal dysfunction; lorazepam co-administration was associated with lower fentanyl doses and better outcomes in some cases.
Conclusions:
- A fentanyl regimen of bolus followed by low-dose infusion (1-5 mcg/kg/hr) is effective for ECMO analgesia.
- Adjunctive lorazepam may be beneficial, particularly for CDH infants, to manage movement and potentially improve outcomes.
- Fentanyl pharmacokinetics in ECMO infants are influenced by diagnosis and renal function, necessitating individualized dosing.
Abstract:
Plasma levels of fentanyl were analyzed in 12 infants undergoing extracorporeal membrane oxygenation who received a fentanyl bolus (5 to 10 micrograms/kg) followed by infusion at 1 to 6.3 micrograms/kg/hr. Fentanyl levels, averaging 11 samples/infant, were measured by radioimmunoassay (mean 19.7 +/- 35.7 ng/ml; n = 140). Eight of the infants, all with a primary diagnosis other than congenital diaphragmatic hernia, survived with relatively short (< 7 days) courses on extracorporeal membrane oxygenation; this group of infants did not develop tolerance to fentanyl and could be maintained on infusion rates of < 5 micrograms/kg/hr throughout. The four infants with congenital diaphragmatic hernia had longer extracorporeal membrane oxygenation runs and three did not survive; their plasma fentanyl levels were consistently higher and while the infusion rates were higher early on extracorporeal membrane oxygenation, they did not exceed 7 micrograms/kg/hr and actually decreased after 5 days on extracorporeal membrane oxygenation. Five infants (42%) received lorazepam in addition to fentanyl for at least one sampling time. The fentanyl infusion dose and plasma level were higher in the congenital diaphragmatic hernia nonsurvivors who did not receive lorazepam (p < 0.001). A decrease in fentanyl clearance correlated with renal dysfunction (p < 0.01). A bolus of fentanyl followed by infusion of relatively low doses (1 to 5 micrograms/kg/hr) provides adequate analgesia for infants on extracorporeal membrane oxygenation, particularly when it is supplemented with intravenous lorazepam whenever needed to control infant movement.
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