Emergence delirium
Anesthetic relevance
Anesthetic management

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Emergence delirium or post-anesthetic delirium is a transient state of agitation, confusion/disorientation, and irritability that occurs after the withdrawal of anesthesia.[1] It is associated with prolonged post-op recovery time and increases the risk for other perioperative complications.

This article will discuss risk factors and management considerations. The topic of delayed emergence is a related but separate discussion.

Anesthetic implications

Emergence delirium is a well known phenomenon in pediatric anesthesia. Pediatric anesthesia providers are particularly wary due to concern for laryngospasm. Regardless of age, emergence delirium can carry with it a higher risk of post-op pulmonary and surgical complications in patients with additional comorbidities (low FRC due to morbid obesity, chronic hypoxemia due to COPD or interstitial lung disease, risk of aspiration, delicate surgical sites particularly at the head/neck).

Preoperative optimization

Intraoperative management

A 2022 metanalysis of pediatric cases using sevofluorane as maintenance showed a significant reduction in emergence delirium with the use of Precedex (Dexmedetomidine), Ketamine, and Fentanyl.

Precedex

Precedex is a selective alpha-2 agonist which acts on the central nervous system to treat pain, provide sedation/anxiolysis, and decrease sympathetic tone. It can be bolused in small increments (4 mcg/dose) or run as a low-dose infusion intraoperatively and is commonly used in pediatrics for the prevention of emergence delirium and has been shown to significantly reduce agitation, cough, pain, post-op nausea/vomiting (PONV), and shivering in the PACU.[2] Its use may be limited by hemodynamic effects (bradycardia, hypotension).

Ketamine and Fentanyl

Ketamine is an NMDA receptor antagonist which also has sedative and analgesic effects. In the above study, it had almost equal efficacy in treating emergence delirium when compared to Precedex.[2] Similar to Precedex, it can be given in small boluses (10 mg/dose) or run as a low-dose infusion intraoperatively. Its use may be limited by concern for its dissociative effects. These are usually decreased with perioperative administration of benzodiazepine (i.e. Versed) but can also be prevented with concurrent use of Precedex. In a corresponding manner, ketamine provides hemodynamic stability which may balance/prevent the bradycardia and hypotension observed with Precedex.

Fentanyl is a mu-opioid receptor agonist which may nonspecifically reduce emergence delirium by treating perioperative pain. It may be limited by an increased risk of PONV.

Postoperative management

Related surgical procedures

Pathophysiology

Inhalational agents (Sevofluorane)

Inhalational agents, notable sevofluorane, have been shown to increase the incidence of emergence delirium. In a 2007 study of 189 preschool and school-age children receiving either propofol or sevofluorane as their primary anesthetic, the incidence of emergence delirium was found to be significantly higher in both sevofluorane groups (as high as 42% in the preschool sevofluorane group 5 minutes after extubation

Other risk factors

  • Pediatric patients between the ages of 2 and 5
  • Rapid awakening
  • Preoperative anxiety
  • Preoperative medications (benzodiazepines, opioids, scopolamine)
  • Perioperative pain

Signs and symptoms

Emergence delirium may manifest as:

  • Increased agitation/Hyperexcitability
  • Disinhibition
  • Confusion

Diagnosis

Treatment

Reorientation

Treat acute pain

Consider other sources of discomfort (full bladder, hypothermia)

Medication

Surgery

Prognosis

Epidemiology

References

  1. Barreto, Ana Carolina Tavares Paes; Paschoal, Ana Carolina Rangel da Rocha; Farias, Carolina Barbosa; Borges, Paulo Sérgio Gomes Nogueira; Andrade, Rebeca Gonelli Albanez da Cunha; de Orange, Flávia Augusta (2018-03-01). "Risk factors associated with anesthesia emergence delirium in children undergoing outpatient surgery". Brazilian Journal of Anesthesiology (English Edition). 68 (2): 162–167. doi:10.1016/j.bjane.2017.11.002. ISSN 0104-0014.
  2. 2.0 2.1 login.proxy1.library.jhu.edu https://login.proxy1.library.jhu.edu/login?qurl=https://pubmed.ncbi.nlm.nih.gov%2f35085107%2f. Retrieved 2022-08-30. Missing or empty |title= (help)