Papers

International journal
Jul 13, 2018

Marked attenuation of the amplitude of transcranial motor-evoked potentials after intravenous bolus administration of ketamine: a case report.

Journal of medical case reports
  • Kenta Furutani
  • ,
  • Mari Matsuhashi
  • ,
  • Hiroyuki Deguchi
  • ,
  • Yusuke Mitsuma
  • ,
  • Nobuko Ohashi
  • ,
  • Hiroshi Baba

Volume
12
Number
1
First page
204
Last page
204
Language
English
Publishing type
Research paper (scientific journal)
DOI
10.1186/s13256-018-1741-9

BACKGROUND: It is believed that ketamine does not affect motor-evoked potential amplitude, whereas various anesthetic drugs attenuate the amplitude of transcranial motor-evoked potential. However, we encountered a patient with marked attenuation of motor-evoked potential amplitude after intravenous bolus administration of ketamine. CASE PRESENTATION: A 15-year-old Japanese girl with a diagnosis of adolescent idiopathic scoliosis was admitted to our hospital to undergo posterior spinal fusion at T4-L3. After induction of general anesthesia using a continuous infusion of propofol and remifentanil, we confirmed that transcranial electrical motor-evoked potentials were being recorded correctly. Ketamine 1.25 mg/kg was administered intravenously for intraoperative and postoperative analgesia. About 3 minutes later, the motor-evoked potential amplitude was markedly attenuated. No other drugs were administered except for ketamine. The patient's vital signs were stable, and the surgery had not yet started. The motor-evoked potential amplitude was recovered at about 6 minutes after administration of ketamine. The surgery was performed uneventfully, and the patient had no neurologic deficit when she emerged from general anesthesia. CONCLUSIONS: Although there is a widely held belief in the field of anesthesiology that ketamine does not affect motor-evoked potential amplitude, it has been suggested that ketamine could affect its monitoring.

Link information
DOI
https://doi.org/10.1186/s13256-018-1741-9
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/30001750
PubMed Central
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6043957
ID information
  • DOI : 10.1186/s13256-018-1741-9
  • Pubmed ID : 30001750
  • Pubmed Central ID : PMC6043957

Export
BibTeX RIS