An Interaction Between Levodopa and Enteral Nutrition Resulting in Neuroleptic Malignant-Like Syndrome and Prolonged ICU Stay

Author:

Bonnici André1,Ruiner Carola-Ellen2,St-Laurent Lyne3,Hornstein David4

Affiliation:

1. McGill University Health Centre, Université de Montréal, Montreal, Quebec, Canada

2. Cand. Med., Faculty of Medicine, McGill University and McGill University Health Centre

3. Department of Clinical Nutrition, McGill University Health Centre

4. Department of Medicine, Faculty of Medicine, McGill University; Internal Medicine and Critical Care, SMBD Jewish General Hospital, and McGill University Health Center, Montreal General Hospital

Abstract

Objective: To describe a probable interaction between enteral feeds and levodopa leading to neuroleptic malignant-like syndrome (NMLS) in a polytrauma patient with Parkinson's disease (PD). Case Summary: A 63-year-old morbidly obese male polytrauma patient with PD and type 2 diabetes mellitus was admitted to our intensive care unit postoperatively. Enteral feeds were administered per nasogastric tube and provided 0.88 g/kg/day of protein based on ideal body weight (IBW). His PD medications (pramipexole, entacapone, and immediate-release levodopa/carbidopa 100mg/25mg, 1.5 tablets 4 times daily) were administered via nasogastric tube. To achieve better glycemic control, his enteral feeds were changed to a formula that provided 1.8 g/kg/day of protein based on IBW. In the following 24 hours, the patient's mental status deteriorated and he was reintubated, He developed a high fever (40.5°C), leukocytosis, elevated serum creatine kinase (CK) (480-1801 units/L), and acute renal impairment His enteral nutrition was changed to decrease protein intake to 1.0 g/kg/day based on IBW and he was given bromocriptine 5 mg 3 times daily via nasogastric tube. Within 24 hours, the patient's mental status improved, his temperature and CK decreased, and his renal function began to improve; the values returned to baseline levels on the 18th day of admission. Discussion: Withdrawal or dose reduction of levodopa in patients with PD has been reported to precipitate NMLS, which is potentially fatal. Because dietary protein can decrease the absorption of levodopa, a potential for an interaction between levodopa and enteral feedings exists, although published reports of such an interaction are limited. In this patient, the likelihood that a drug-nutrient interaction occurred between levodopa and enteral feedings is considered to be probable based on the Naranjo probability scale and the Horn Drug Interaction Probability Scale. Conclusions: Health-care professionals should be aware of the interaction between levodopa and protein content of enteral nutrition to avoid the occurrence of NMLS in patients with PD.

Publisher

SAGE Publications

Subject

Pharmacology (medical)

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