J Pediatr Intensive Care 2015; 04(03): 162-165
DOI: 10.1055/s-0035-1559822
Case Report
Georg Thieme Verlag KG Stuttgart · New York

Posterior Reversible Encephalopathy Syndrome as a Result of Withdrawal from Prolonged Dexmedetomidine

Autoren

  • Grace Brouillette

    1   Department of Pediatrics, University of Kansas Medical Center, Kansas City, Kansas, United States
  • Shaji Pillai

    1   Department of Pediatrics, University of Kansas Medical Center, Kansas City, Kansas, United States
  • K. Sarah Hoehn

    1   Department of Pediatrics, University of Kansas Medical Center, Kansas City, Kansas, United States
Weitere Informationen

Publikationsverlauf

29. August 2014

20. Oktober 2014

Publikationsdatum:
20. August 2015 (online)

Abstract

Dexmedetomidine is a selective α-adrenergic agonist with high α-2 receptor affinity that is used for sedation, analgesia, and as an anxiolytic. Withdrawal symptoms, although rare, include agitation, irritability, headache, and rebound hypertension, which can occur following abrupt cessation of the medication. Posterior reversible encephalopathy syndrome is a clinical condition presenting secondary to acute hypertension that results in neurologic symptoms including headache, seizures, altered sensorium, and loss of vision. These symptoms are coupled with typically reversible characteristic magnetic resonance imaging changes. We present the first reported case of posterior reversible encephalopathy syndrome after a hypertensive crisis likely precipitated by dexmedetomidine withdrawal.