Arch Craniofac Surg Search

CLOSE


Arch Craniofac Surg > Volume 22(2); 2021 > Article
Kim, Lee, Yu, Min, Chung, and Kim: Ketamine-induced generalized convulsive seizure during procedural sedation

Abstract

Ketamine is used widely in emergency departments for a variety of purposes, including procedural sedation for facial laceration in pediatric patients. The major benefits are its rapid onset of effects, relatively short half-life, and lack of respiratory depression. The known side effects of ketamine are hallucinations, dizziness, nausea, and vomiting. Seizure is not a known side effect of ketamine in patients without a seizure history. Here, we present the case of a patient in whom ketamine likely induced a generalized tonic-clonic seizure when used as a single agent in procedural sedation for facial laceration repair. The aim of this article is to report a rare and unexpected side effect of ketamine used at the regular dose for procedural sedation. This novel case should be of interest to not only emergency physicians but also plastic surgeons.

INTRODUCTION

Ketamine is an effective and versatile drug used commonly in the emergency department. It has been in clinical use since 1965 as a general anesthetic for humans and has an excellent medical safety profile [1]. Ketamine is desirable as an anesthetic in procedural sedation owing to its rapid onset of effects, relatively short half-life, and lack of respiratory depression. Additionally, it has been used for its antidepressant, analgesia, and anti-inflammatory effects, and in the treatment of schizophrenia. However, the side effects of ketamine include hallucinations, visual disturbances, dizziness, nausea, and vomiting, and it has potential for abuse [2]. Although literature regarding the convulsant potential of ketamine is currently unclear, some authors have mentioned that ketamine demonstrates anticonvulsant and neuroprotective properties and can be used as an effective medication for treating refractory status epilepticus [3]. Despite recent reports on the use of ketamine for the treatment of seizures, we here report a case of a healthy 7-year-old male patient who underwent ketamine procedural sedation and developed a new-onset generalized tonic-clonic seizure.

CASE REPORT

A healthy 7-year-old boy weighing 20 kg presented to the emergency department with a history of complaints of a 1-cm laceration on his nose. He had no past medical history. He was comfortable, and not distressed, and his initial vital signs were normal. Physical examination findings were normal, except for a laceration on his nose. After a discussion with the patient’s parents, a decision was made to perform laceration closure under procedural sedation. Ketamine was chosen as the sedating agent for the procedure at a dose of 80 mg (4 mg/kg), which is in the accepted intramuscular dosage range. Consent for sedation was obtained from the patient’s parents after a full discussion about the risks and benefits of procedural sedation and the known side effects of ketamine. Ketamine was administered as a onetime dose intramuscularly. The patient was on a cardiac monitor with pulse oximetry and end-tidal carbon dioxide monitoring throughout the procedure, and he remained normoxic. About 5 minutes after ketamine injection, the patient suddenly developed twitches and stiffness followed by bilateral symmetrical rhythmic tonic-clonic movements with up-rolling of the eyeballs. The seizure lasted for about 90 seconds before it was terminated with two consecutive injections of lorazepam (1 mg intramuscular and 1 mg intravenous). The patient was admitted to the pediatric department for further observation and evaluation. Additional history taking at that time revealed no risk factors for seizures; normal growth and development; no history of febrile seizures, prior head trauma or other neurological disorders; and no family history of seizures. His vital signs were normal, and neurological examination showed no focal deficits, except a drowsy mental state. A post-ictal blood test revealed changes in the increased levels of lactate (3.5 mmol/L) and decreased levels of pH (7.294) consistent with recent convulsions. Complete blood count, chemical analysis, urinalysis, and chest radiography findings were normal, and he was fully awake for 10 hours after the event. Electroencephalography (EEG) was performed on the day after the event, and the results showed a normal waking record with no focal slowing area, epileptiform discharge, or electrographic seizure. He had no further seizure activity throughout his hospital stay, and he was discharged in a stable condition. Follow-up of the patient up to 1 year revealed no recurrence of seizure.

DISCUSSION

Ketamine was introduced commercially in 1970 with the manufacturer’s description of a “rapidly acting, nonbarbiturate general anesthetic” and with a suggestion that it would be useful for short procedures [3]. For more than 50 years, ketamine has been proven to be a safe anesthetic drug with potent analgesic properties [4]. It is considered relatively safe when used with proper precautions in the emergency department and has been successfully administered to patients for procedures, such as laceration repair. As plastic surgeons, we have become more comfortable with the use of this drug regularly for procedural sedation in pediatric patients because of its rapid onset of effects, relatively short half-life, and lack of respiratory depression [5]. Ketamine has been used for the treatment of delirium, depression, and schizophrenia, and for its analgesia and anti-inflammatory effects [2]. Furthermore, the anticonvulsant effects of ketamine have been demonstrated recently, and new reports showed that ketamine can effectively control refractory status epilepticus [6,7]. However, in our case, ketamine injection resulted in generalized tonic-clonic seizure activity in the absence of any known predisposing factors of convulsion. This unusual case emphasizes the possibility of ketamine-induced seizures.
Various reports describe both the proconvulsant and anticonvulsant effects of ketamine. One potential reason is that ketamine exists as asymmetric molecules called enantiomers. This minor variation in the drug’s structure may influence its affinity for a certain receptor binding site and produce different effects for each enantiomer [8]. For example, the S (+) isomer of ketamine is more potent and suppress epileptic activity in the EEG amplitude and frequency, whereas the R (–) isomer is less potent and unable to suppress the similar degree of EEG amplitude and frequency [9]. However, the exact etiology of the proconvulsant effect of ketamine remains unclear.
To manage the side effects of ketamine, the initial drugs recommended are benzodiazepines which are routinely administered along with ketamine to reduce hallucinations [10]. In our case, two consecutive injections of lorazepam (1 mg intramuscular and 1mg intravenous) were used, and the seizure stopped. Only few reports have mentioned the association between ketamine administration and seizures in healthy individuals. To the best of our knowledge, this is the first case report of ketamine-induced seizure with literature review in Korea, aimed at helping recognize the uncommon side effect of ketamine and treatment option. Given the frequency at which ketamine is administered in the emergency department for facial laceration repair or other routine procedures, not only emergency physicians but also plastic surgeons should be aware that ketamine could potentially induce seizures even in healthy individuals.

Notes

Conflict of interest

No potential conflict of interest relevant to this article was reported.

Ethical approval

The study was approved by the Institutional Review Board of Bundang Jesaeng Hospital (IRB No. 2021-03-005) and performed in accordance with the principles of the Declaration of Helsinki. Written informed consent was obtained.

Author contribution

Conceptualization: JHK, CKL, BDM. Methodology: CEC, DCK. Investigation: JHK. Writing - original draft: JHK. Writing - review & editing: JHK, CKL, SHY, BDM.

REFERENCES

1. Dorandeu F, Dhote F, Barbier L, Baccus B, Testylier G. Treatment of status epilepticus with ketamine, are we there yet? CNS Neurosci Ther 2013;19:411-27.
crossref pmid pmc
2. Zanos P, Moaddel R, Morris PJ, Riggs LM, Highland JN, Georgiou P, et al. Ketamine and ketamine metabolite pharmacology: insights into therapeutic mechanisms. Pharmacol Rev 2018;70:621-60.
crossref pmid pmc
3. Kurdi MS, Theerth KA, Deva RS. Ketamine: current applications in anesthesia, pain, and critical care. Anesth Essays Res 2014;8:283-90.
crossref pmid pmc
4. Mion G, Villevieille T. Ketamine pharmacology: an update (pharmacodynamics and molecular aspects, recent findings). CNS Neurosci Ther 2013;19:370-80.
crossref pmid pmc
5. Meaden CW, Barnes S. Ketamine implicated in new onset seizure. Clin Pract Cases Emerg Med 2019;3:401-4.
crossref pmid pmc
6. Borris DJ, Bertram EH, Kapur J. Ketamine controls prolonged status epilepticus. Epilepsy Res 2000;42:117-22.
crossref pmid pmc
7. Borsato GS, Siegel JL, Rose MQ, Ojard M, Feyissa AM, Quinones-Hinojosa A, et al. Ketamine in seizure management and future pharmacogenomic considerations. Pharmacogenomics J 2020;20:351-4.
crossref pmid
8. Modica PA, Tempelhoff R, White PF. Pro- and anticonvulsant effects of anesthetics (Part II). Anesth Analg 1990;70:433-44.
crossref pmid
9. White PF, Schuttler J, Shafer A, Stanski DR, Horai Y, Trevor AJ. Comparative pharmacology of the ketamine isomers: studies in volunteers. Br J Anaesth 1985;57:197-203.
crossref pmid
10. Toft P, Romer U. Comparison of midazolam and diazepam to supplement total intravenous anaesthesia with ketamine for endoscopy. Can J Anaesth 1987;34:466-9.
crossref pmid
TOOLS
Share :
Facebook Twitter Linked In Google+ Line it
METRICS Graph View
  • 2 Crossref
  •   Scopus
  • 3,794 View
  • 66 Download
Related articles in ACFS


ABOUT
ARTICLE CATEGORY

Browse all articles >

BROWSE ARTICLES
AUTHOR INFORMATION
Editorial Office
Dept. of Plastic and Reconstructive Surgery Chonnam National University Medical School, 42 Jebong-ro, Dong-gu, Gwangju 61469, Korea
Tel: +82-62-220-6354    Fax: +82-62-220-6357    E-mail: office_acfs@kcpca.or.kr                

Copyright © 2024 by Korean Cleft Palate-Craniofacial Association.

Developed in M2PI

Close layer
prev next