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From the Department of Anesthesiology, Henry Ford Hospital, Detroit, Michigan.
Address correspondence and reprint requests to Henry R. Kroll, MD, Department of Anesthesiology, Henry Ford Hospital, 2799 West Grand Blvd, Detroit, MI 48202-9888. Address e-mail to hkroll1{at}hfhs.org.
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| Introduction |
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| CASE REPORT |
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The patient was taken to the operating room, and the preoperative venous blood glucose of 77 mg/dL was used as our baseline measurement. Our laboratory informed us that the peritoneal dialysate icodextrin used by our patient can falsely increase capillary blood glucose determinations made by the AccuCheck Inform glucometer, and that the only accurate method to ascertain her blood glucose levels would be by central laboratory determination. The surgery proceeded uneventfully under general endotrachael intubation, and the patient remained hemodynamically stable, with no intraoperative complications. No intraoperative insulin was administered. At the end of surgery, the muscle relaxant was reversed with neostigmine and glycopyrrolate, but the patient did not meet extubation criteria and remained on mechanical ventilation, sedated with lorazepam.
On arrival at the postanesthesia care unit (PACU), a blood glucose of 127 mg/dL was measured by the Synchron LX20 Pro Clinical System. The patient received no insulin while in the PACU. At the time of transfer of care to the PACU, the necessity of ascertaining blood glucose levels by central laboratory determination was communicated verbally to the PACU nurse and the surgical resident involved with the patients care, and in writing on the PACU order form.
That night, the intubated and sedated patient was transferred to the 40-bed surgical intensive care unit. Ninety minutes after arrival at the surgical intensive care unit, using the units AccuCheck Inform glucometer, the patients capillary glucose was measured to be 300 mg/dL, and an insulin infusion was initiated in accordance with the units tight glycemic control protocol.
On the first postoperative day, the surgical team noted that, despite overnight weaning from sedation, the patient exhibited symptoms of encephalopathy. A head computed tomography scan revealed no intracranial pathology. The patient remained intubated, on an insulin infusion with tight glycemic controls using the Accucheck Inform glucometer, for 24 h, until the first blood glucose measurement was obtained using the Synchron LX20 Pro Clinical System. It revealed a blood glucose of 7 mg/dL.
The patient was treated for severe hypoglycemia with IV dextrose. Despite treatment, she remained comatose secondary to a severe hypoglycemic encephalopathy. She underwent a percutaneous tracheostomy and percutaneous endoscopic gastrostomy and was discharged to a specialized extended care nursing facility, where she later died.
| DISCUSSION |
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-amylase into the oligosaccharides maltose and maltotriose (3). Maltose, consisting of two glucose molecules, accumulates in the systemic circulation because of the normal deficiency in humans of circulating maltase (3). Many bedside glucometers, including the AccuCheck Inform, use glucose dehydrogenase with coenzyme pyrroloquinolinequinone in their test strips, to catalyze the conversion of glucose to gluconic acid and reduced nicotinamide adenine dinucleotide (NADH) (7). The amount of NADH measured by the glucometer is directly proportional to the blood samples glucose concentration. Glucose dehydrogenase with coenzyme pyrroloquinolinequinone, however, can react with the free reducing group of glucose located at the end of the maltose molecule, a breakdown product of icodextrin, producing additional NADH, and thus yielding an overestimation of blood glucose levels.
This case report highlights an additional, underappreciated, perioperative risk present in the ESRD patient undergoing CAPD. Icodextrin dialysate can lead to falsely elevated glucose measurements with bedside glucometers. Therefore, to prevent similar catastrophic outcomes, only central laboratory determination of blood glucose levels should be obtained for ESRD patients undergoing CAPD.
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