Changes of lactate, glucose, ionized calcium and glutamate concentrations in cephalic vein blood during brain hypothermia using extracorporeal membrane oxygenation (ECMO) in a newborn infant with hypoxic-ischemic encephalopathy

Introduction: Sufentanil is a potent analgesic drug used for pain management. A few studies describe the pharmacokinetics of sufentanil in neonates; however, no pharmacokinetic data about sufentanil during extracorporeal membrane oxygenation have been published yet. Case report: A 1-day-old neonate with moderate hypoxic–ischemic encephalopathy received veno-arterial extracorporeal membrane oxygenation support for refractory respiratory and circulatory failure. Sufentanil plasma concentrations were determined during both extracorporeal membrane oxygenation (n = 14) and non–extracorporeal membrane oxygenation (n = 17) period. Based on these measurements, individual sufentanil pharmacokinetic parameters were calculated. Discussion: We observed increased sufentanil volume of distribution (11.6 vs 5.6 L/kg) and decreased sufentanil clearance (0.535 vs 0.746 L/h/kg) in extracorporeal membrane oxygenation period. The increment of volume of distribution was attributed to ECMO influence, while difference in clearance was probably due to drug interaction. Conclusions: This is the first description of sufentanil pharmacokinetics in neonate treated with extracorporeal membrane oxygenation. We observed considerably larger volume of distribution during extracorporeal membrane oxygenation period in comparison with non–extracorporeal membrane oxygenation period.

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The effect of temperature on the QTc interval in the newborn infant receiving extracorporeal membrane oxygenation (ECMO)

Early Human Development ◽

10.1016/j.earlhumdev.2006.05.016 ◽

2007 ◽

Vol 83 (4) ◽

pp. 217-223 ◽

Cited By ~ 11

Author(s):

Marie Horan ◽

A. David Edwards ◽

Richard K. Firmin ◽

Tiena Ablett ◽

Hilary Rawson ◽

...

Keyword(s):

Extracorporeal Membrane Oxygenation ◽

Newborn Infant ◽

Effect Of Temperature ◽

Qtc Interval ◽

Membrane Oxygenation

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Changes in cardiac function during extracorporeal membrane oxygenation for persistent pulmonary hypertension in the newborn infant

The Journal of Pediatrics ◽

10.1016/s0022-3476(05)82163-8 ◽

1991 ◽

Vol 118 (3) ◽

pp. 431-436 ◽

Cited By ~ 38

Author(s):

Thomas R. Kimball ◽

Stephen R. Daniels ◽

Richard G. Weiss ◽

Richard A. Meyer ◽

David W. Hannon ◽

...

Keyword(s):

Pulmonary Hypertension ◽

Extracorporeal Membrane Oxygenation ◽

Cardiac Function ◽

Newborn Infant ◽

Persistent Pulmonary Hypertension ◽

Membrane Oxygenation

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Neurosonographic Findings in Infants Treated by Extracorporeal Membrane Oxygenation (ECMO)

Journal of Child Neurology ◽

10.1177/0883073889004001s09 ◽

1989 ◽

Vol 4 (1_suppl) ◽

pp. S52-S61 ◽

Cited By ~ 17

Author(s):

Aurelio Matamoros ◽

Joseph C. Anderson ◽

James McConnell ◽

David L. Bolam

Keyword(s):

Extracorporeal Membrane Oxygenation ◽

Imaging Modality ◽

Major Complication ◽

Hyaline Membrane Disease ◽

Cardiovascular Complications ◽

Membrane Oxygenation ◽

Cranial Sonography ◽

Baseline Evaluation ◽

Ischemic Encephalopathy

Extracorporeal membrane oxygenation (ECMO) is an approved therapy for some neonates who have respiratory failure that is due to hyaline membrane disease, meconium aspiration, persistent pulmonary hypertension, congenital diaphragmatic hernia, or sepsis. The major complication of this therapy is hemorrhage, with intracranial hemorrhage having the highest morbidity and mortality. Seizures, incisional bleeding and bleeding in the pleural space, hypoxic-ischemic encephalopathy, renal failure, and cardiovascular complications account for most of the other complications. Cranial sonography provides an ideal imaging modality for baseline evaluation and daily follow-up; however, computed tomography and magnetic resonance imaging, because of better sensitivity, are important for assessment after ECMO. The changes in intracranial blood flow related to ECMO can be noninvasively evaluated by Doppler ultrasound modalities. (J Child Neurol 1989;4:S52-S61).

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