Omeprazole-associated rhabdomyolysis

Proton pump inhibitors (PPIs) are commonly used in ICUs. Here, we report a severe case of rhabdomyolysis associated with omeprazole. A 20-year-old man, who previously had been healthy, visited a hospital with epigastric pain. An upper gastrointestinal endoscopy revealed a duodenal ulcer in an active stage. He was admitted to the hospital and received intravenous omeprazole (20 mg) twice a day. On day 14 of admission, he developed muscular pain, predominantly in the lower extremities, and had elevated serum creatinine phosphokinase (CPK) (28,314 IU/L; normal is less than 25 IU/L) (Figure 1). The patient was transferred to the hospital’s ICU on day 16, since the serum CPK (112,240 IU/L) and myoglobin (25,082 ng/mL; normal is less than 154 ng/mL) levels were extremely high. After potential causes of elevated CPK were considered, omeprazoleassociated rhabdomyolysis seemed the most probable diagnosis. We discontinued intravenous omeprazole administration and started aggressive fluid repletion, continuous renal replacement therapy, and urine alkalization. The CPK and myoglobin levels successively decreased and reached within the normal range on day 31. The patient recovered completely and was discharged on day 38. No allergic symptom was detected in this case. The results of a drug-induced lymphocyte stimulation test for omeprazole were negative. Altered pharmacokinetics of omeprazole has been reported in patients with genetic variations in CYP2C19, which encodes a principal enzyme to metabolize omeprazole [1]; therefore, we performed DNA sequencing of the entire coding regions in CYP2C19. The analysis revealed no serious loss-of-function variations in the gene (intermediate metabolizer genotype) [1]. The plasma omeprazole level on day 15 was within normal range (380 ng/mL; normal is less than 400 ng/mL) [1]. Thus, the metabolism and plasma levels of omeprazole were not likely to be associated with rhabdomyolysis.