Olanzapine-Induced Diabetic Ketoacidosis and Neuroleptic Malignant Syndrome with Rhabdomyolysis: A Case Report.
- Author:
Young Kyoung SA
1
;
Hyeon YANG
;
Hee Kyoung JUNG
;
Jang Won SON
;
Seong Su LEE
;
Seong Rae KIM
;
Bong Yeon CHA
;
Ho Young SON
;
Chi Un PAE
;
Soon Jib YOO
Author Information
- Publication Type:Case Report
- Keywords: Diabetic ketoacidosis; Neuroleptic malignant syndrome; Olanzapine
- MeSH: Acute Kidney Injury; Antipsychotic Agents; Benzodiazepines; C-Peptide; Diabetic Ketoacidosis; Fluid Therapy; Follow-Up Studies; Glucose; Humans; Incidence; Insulin; Movement Disorders; Neuroleptic Malignant Syndrome; Renal Dialysis; Rhabdomyolysis; Schizophrenia
- From:Endocrinology and Metabolism 2013;28(1):70-75
- CountryRepublic of Korea
- Language:English
- Abstract: Atypical antipsychotics have replaced conventional antipsychotics in the treatment of schizophrenia because they have less of a propensity to cause undesirable neurologic adverse events including extrapyramidal symptoms, tardive dyskinesia, and neuroleptic malignant syndrome (NMS). However, atypical antipsychotics have been known to result in various metabolic complications such as impaired glucose tolerance, diabetes and even diabetic ketoacidosis (DKA). In addition, a number of NMS cases have been reported in patients treated with atypical antipsychotics, although the absolute incidence of neurologic side effects is currently significantly low. Here, we report a patient who simultaneously developed DKA, acute renal failure and NMS with rhabdomyolysis after olanzapine treatment. Olanzapine-induced metabolic complications and NMS were dramatically improved with cessation of the olanzapine treatment and initiation of supportive management including fluid therapy, hemodialysis, and intensive glycemic control using insulin. At short-term follow-up, insulin secretion was markedly recovered as evidenced by a restoration of serum C-peptide level, and the patient no longer required any hypoglycemic medications. Despite the dramatic increase in the use of atypical antipsychotics treatment, individualized treatments along with careful monitoring may be prudent for high risk or vulnerable patients in order to avoid the development of metabolic side effects.
