Sedative agents are routinely administered to critically ill patients, both
on and off extracorporeal membrane oxygenation (ECMO), to enable patients
to be comfortable and facilitate patient management. It has been observed e
mpirically in our paediatric intensive care unit that doses of sedative dru
gs required to achieve desired levels of sedation in ECMO patients are far
greater than those used in non-ECMO patients. These differences could not s
imply be accounted for by differences in patient types, clinical status or
sedation levels. We therefore undertook an in vitro evaluation of drug bind
ing in ECMO circuits.
This study investigated how the polyvinyl chloride (PVC) and silicone rubbe
r components of neonatal ECMO circuits affect drug delivery in patients thr
ough drug sorption.
Phase 1 investigated drug uptake by the two polymers in static solutions of
known concentrations of four commonly used sedative drugs: lorazepam, mida
zolam, diazepam and propofol. Phase 2 involved the setting up of a complete
neonatal ECMO circuit, injecting the drug solutions pre-reservoir at a flo
w rate of 350 ml/min and collecting samples post-oxygenator for analysis. P
hase 1 results revealed significant uptake of drugs with losses in the rang
e 40-98% and in the order propofol > diazepam > midazolam > lorazepam. Phas
e 2 results were similar and in the first 40 min of running an ECMO circuit
only 10% of propofol passed through the circuit. These results may help to
explain observed clinical phenomena and raise important issues regarding d
rug dosing in ECMO patients.