Emergence Delirium Clinical Trial
Official title:
Determining the Incidence of Parasomnias (PS) and Emergence Delirium (ED)in the American Family Children's Hospital Patient Population
Emergence delirium (ED), also called emergence agitation or post-anesthetic excitement, is
defined as a dissociated state of consciousness, occurring on awakening from general
anesthesia, in which children exhibit psychomotor agitation, crying and thrashing and are
not consolable for a period of time, usually 5-15 minutes. Emergence delirium is a common
problem in pre-school children, with estimates of the incidence ranging from 10-70% of
children in this age group. These children are agitated, seemingly unaware of their
surroundings, and typically do not respond to parents or caregivers. They are therefore at
risk for self-inflicted traumatic injury and complications secondary to disruptions of
intravenous lines, surgical incisions, or drains. Children with ED typically require more
resources in the postoperative period than children who do not exhibit ED. Predicting the
likelihood of ED would allow for better allocation of resources in the post-anesthetic care
unit (PACU).
The peak incidence of ED in children occurs in the same age range at which the peak
incidence of parasomnias (PS) occurs. The description of parasomnias is strikingly similar
to the description of ED; the American Academy of Sleep Medicine defines parasomnias as
"undesirable physical events or experiences that occur during entry into sleep, within sleep
or during arousals from sleep." Parasomnias can be diagnosed using a sleep questionnaire.
The purpose of this pilot study is to determine the incidence of ED and PS in our
population, in order to determine the number of patients necessary to enroll in a larger
study to either confirm or reject the hypothesis that ED and PS are correlated.
Status | Completed |
Enrollment | 100 |
Est. completion date | January 2016 |
Est. primary completion date | January 2016 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 1 Year to 6 Years |
Eligibility |
Inclusion Criteria: 1. Pediatric patients age 1-6 (inclusive) scheduled for elective ENT or urologic surgery 2. ASA I or II 3. Presence of a caregiver who is familiar with the child's sleep history Exclusion Criteria: 1. Autism 2. Severe developmental delay 3. Children receiving clonidine 4. Medication for seizures 5. Children who have received ED treatment prior to a diagnosis of ED (clonidine, dexmedetomidine, or propofol) |
Observational Model: Cohort, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
University of Wisconsin, Madison |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Prevalence of parasomnias (PS) and emergence delirium (ED) in children | 6 months | No | |
Secondary | score on Childrens Sleep Habits Questionnaire correlated with ED | 6 months | No |
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