Optimal timing for the administration of intranasal dexmedetomidine for premedication in children

V M Yuen1, Theresa W Hui, M G Irwin

  • 1Department of Anaesthesiology, Queen Mary Hospital, Hong Kong, China. vtang131@hku.hk

Anaesthesia
|July 22, 2010
PubMed

Insights

Intranasal dexmedetomidine at 1 μg.kg(-1) effectively sedated pediatric patients for procedures. The onset of sedation occurred at a median of 25 minutes, aiding in intravenous cannulation.

Area of Science:

  • Pediatric Anesthesiology
  • Pharmacology
  • Sedation Techniques

Background:

  • Intranasal dexmedetomidine is used for pediatric sedation.
  • Previous studies indicate efficacy in children aged 2-12 years.
  • The precise onset time requires further investigation.

Purpose of the Study:

  • To evaluate the onset time of intranasal dexmedetomidine for pediatric sedation.
  • To determine the effectiveness of intranasal dexmedetomidine in achieving satisfactory sedation for intravenous cannulation.
  • To assess the duration of sedation induced by intranasal dexmedetomidine.

Main Methods:

  • A randomized controlled trial involving 100 children (aged 1-12 years) undergoing elective surgery.
  • Five groups were established: four received intranasal dexmedetomidine (1 μg.kg(-1)) at different pre-cannulation timings (30, 45, 60, 75 min), and one received placebo.
  • Sedation status, behavior, and vital signs were monitored until anesthesia induction.

Main Results:

  • A significantly higher proportion of children receiving intranasal dexmedetomidine achieved satisfactory sedation compared to placebo (p < 0.001).
  • No significant difference in satisfactory sedation rates was observed among the dexmedetomidine groups.
  • Overall, 62% of children receiving intranasal dexmedetomidine had satisfactory sedation at cannulation.
  • The median onset time for sedation was 25 minutes (95% CI: 25-30 min).
  • The median duration of sedation was 85 minutes (95% CI: 55-100 min).

Conclusions:

  • Intranasal dexmedetomidine at 1 μg.kg(-1) provides effective sedation for pediatric patients.
  • The optimal timing for intranasal dexmedetomidine administration to achieve sedation for intravenous cannulation appears to be around 30-75 minutes prior.
  • The drug demonstrates a rapid onset and a clinically relevant duration of action for procedural sedation in children.

Related Concept Videos

Parenteral Anesthetics: Overview01:24

Parenteral Anesthetics: Overview

Intravenous anesthetics are drugs administered parenterally to induce anesthesia or sedation. Propofol is a widely used agent formulated as a 1% emulsion in soybean oil, glycerol, and egg phosphatide. It induces rapid anesthesia primarily due to its rapid distribution from the bloodstream to target tissues and is metabolized in the liver. However, it can cause significant pain on injection and hypertriglyceridemia. Fospropofol, a water-based prodrug of propofol, lacks these adverse effects.
Drug Dosing: Infants and Children01:29

Drug Dosing: Infants and Children

Pediatric patient dosages diverge from adults due to disparities in body surface area, total body water, and extracellular fluid per kilogram of body weight. The dosing regimen considers the variations in pharmacokinetics and pharmacology across distinct age groups, encompassing preterm newborns, infants, young children, older children, and adolescents. Calculation of pediatric patient doses is predicated on determining body surface area, which exhibits a superior correlation with the child's...
Pharmacokinetics in Pediatric Patients: Drug Excretion01:26

Pharmacokinetics in Pediatric Patients: Drug Excretion

In pediatric medicine, understanding the renal function and drug elimination nuances is crucial for administering safe and effective treatments. Newborns, in particular, display markedly slower renal functions than adults, profoundly affecting how drugs are cleared from their bodies. This slower drug clearance requires clinicians to extend the dosing intervals for many medications to prevent drug accumulation and toxicity while ensuring therapeutic efficacy.One key area where these adjustments...
Drug Delivery: Enteral Route01:18

Drug Delivery: Enteral Route

The enteral drug administration involves three primary routes: oral, sublingual, and buccal. Oral ingestion is the most prevalent, safe, economical, and convenient method for drug administration. However, it has certain drawbacks, including limited absorption due to the drug's low water solubility or poor membrane permeability, possible emesis from GI mucosa irritation, destruction of drugs by digestive enzymes or low gastric pH, and irregular absorption along with food or other drugs.
Drugs in...
Depolarizing Blockers: Pharmocokinetics01:19

Depolarizing Blockers: Pharmocokinetics

Depolarizing blockers are administered through intravenous injection. Succinylcholine is the most common choice of depolarizing blockers in emergency clinical practices. Although they have a rapid onset, they readily diffuse away from the motor end plate into the extracellular fluid. They are metabolized by enzymes such as liver butyrylcholinesterase and plasma pseudocholinesterases. This produces a short duration of action, typically 5-10 minutes long, unlike nondepolarizing blockers, which...
Factors Affecting Drug Response: Overview01:21

Factors Affecting Drug Response: Overview

When it comes to infants and young children, they are typically administered smaller doses of medication in comparison to adults. This is primarily because their organ functions still need to fully develop, meaning their bodies are not as efficient at metabolizing or eliminating drugs. Additionally, their blood-brain barrier is more permeable than in adults. As a result, high concentrations of drugs can easily penetrate the central nervous system (CNS), potentially leading to neurological...