Intranasal Dexmedetomidine Versus Oral Midazolam Premedication for Postoperative Negative Behavior Changes in Children: A Randomized Controlled Trial
Overview
- Phase
- Phase 4
- Intervention
- Dexmedetomidine Hydrochloride
- Conditions
- Behavior Problem
- Sponsor
- Fujian Provincial Hospital
- Enrollment
- 324
- Locations
- 1
- Primary Endpoint
- Incidence of postoperative negative behavior changes
- Status
- Completed
- Last Updated
- 4 months ago
Overview
Brief Summary
The goal of this clinical trial is to learn the effect of dexmedetomidine premedication in postoperative negative behavior changes in children compared to midazolam premedication. It will also learn about the effect of dexmedetomidine and midazolam in emergence delirium. The main questions are:
- Dose dexmedetomidine lower the incidence of postoperative negative behavior changes compared to midazolam?
- Dose dexmedetomidine lower the incidence of emergence delirium compared to midazolam? Researchers will compare dexmedetomidine to midazolam (a common pediatric premedication) to see if dexmedetomidine works to treat postoperative negative behavior change and emergence delirium.
Participants will:
- Take intranasal dexmedetomidine or oral midazolam or placebo (a look-alike substance that contains no drug) premedication
- Fill in the Post hospitalization behavior questionnaire for ambulatory surgery postoperative 1, 3, 7, and 30
Detailed Description
Due to the fear of being separated from parents, fear of venipuncture, and facing unfamiliar operating room environment, children have different degrees of anxiety before surgery. Preoperative anxiety can lead to strong stress response and increase the incidence of emergence delirium. It can even cause psychological trauma and affect children's physical and mental health growth. The study showed that preoperative anxiety was positively correlated with the incidence of emergence delirium and postoperative negative behavior change, and emergence delirium was a risk factor for postoperative negative behavior in children. Currently, midazolam is the most commonly used sedative drug to relieve preoperative anxiety in children. Midazolam has anterograde amnesia effect, reducing the occurrence of intraoperative awareness, and alleviating psychological trauma and memory of malignant stimulation in children. Dexmedetomidine is a highly selective α2 adrenergic agonist with anxiolytic, sedative, and analgesic properties. Our previous study found that preoperative administration of dexmedetomidine can reduce the incidence of emergence delirium in children compared with midazolam However, no clinical studies have directly compared the effects of dexmedetomidine and midazolam premedication on postoperative negative behavior change in children. This prospective randomized controlled trial was conducted to compare the effects of dexmedetomidine and midazolam premedication on preoperative anxiety, the incidence of postoperative delirium, and postoperative negative behavior changes in children to provide a reference for optimizing clinical anesthesia medication regimens.
Investigators
Yao Yusheng
Clinical Professor
Fujian Provincial Hospital
Eligibility Criteria
Inclusion Criteria
- •ASA physical status I or II;
- •Aged 2-5 years;
- •Scheduled for elective tonsillectomy and (or) adenoidectomy.
Exclusion Criteria
- •Parents refusing to allow their children to participate;
- •Intake of sedative or analgesic medication within 48 hours before surgery;
- •Developmental delay;
- •Body mass index \> 30 kg/m2;
- •Allergy to study drugs;
- •Major life changes 1 month before the operation, such as the divorce of parents, death of parents, moving to a new home, changing to a new kindergarten, etc.;
- •Any other conditions that precluded study inclusion.
Arms & Interventions
Dexmedetomidine group
Participants were premedicated with intranasal dexmedetomidine 2 μg/kg and oral sweet solution 0.25 mL/kg.
Intervention: Dexmedetomidine Hydrochloride
Dexmedetomidine group
Participants were premedicated with intranasal dexmedetomidine 2 μg/kg and oral sweet solution 0.25 mL/kg.
Intervention: Glucose solution
Midazolam group
Participants were premedicated with intranasal 0.9% saline 0.02 mL/kg and oral midazolam 0.5 mg/kg.
Intervention: Midazolam
Midazolam group
Participants were premedicated with intranasal 0.9% saline 0.02 mL/kg and oral midazolam 0.5 mg/kg.
Intervention: normal Saline
Placebo group
Participants were premedicated with intranasal 0.9% saline 0.02 mL/kg and oral sweet solution 0.25 mL/kg.
Intervention: normal Saline
Placebo group
Participants were premedicated with intranasal 0.9% saline 0.02 mL/kg and oral sweet solution 0.25 mL/kg.
Intervention: Glucose solution
Outcomes
Primary Outcomes
Incidence of postoperative negative behavior changes
Time Frame: Day 7 postoperatively
Postoperative negative behavior changes will be assessed using the Post Hospitalization Behavior Questionnaire for Ambulatory Surgery (PHBQ-AS).
Secondary Outcomes
- Incidence of emergence delirium(Within 30 min after extubation)
- Length of postanesthesia care unit stay(Up to 60 minutes postoperatively)
- Emergence time(About up to 30 minutes postoperatively)
- Preoperative anxiety(Before the intervention in holding area)
- Incidence of postoperative negative behavior changes(Day 30 postoperatively)
- Parental satisfaction(Postoperative day 1)
- Incidence of adverse events(Up to 24 hours postoperatively)
- Parental separation anxiety(After intervention 30 minutes)
- Postoperative pain intensity(After extubation 10, 20, 30 min, and postoperative 1 day)