Intravenous dextrose versus ondansetron for prevention of postoperative vomiting in children: a randomized

Andrea Vasquez-Camargo1, Jonathan Gamble2, Kelly A Fedoruk3

  • 1Department of Academic Family Medicine, University of Saskatchewan, 172-1621 Albert Street, Regina, SK, S4P 2S5, Canada. a.vasquez@usask.ca.

Insights

Intravenous dextrose did not effectively prevent postoperative vomiting (POV) in children undergoing ambulatory surgery, unlike ondansetron. These findings do not support dextrose as a substitute for ondansetron in pediatric dental procedures.

Area of Science:

  • Pediatric Anesthesiology
  • Pharmacology

Background:

  • Postoperative vomiting (POV) is common in children.
  • Dextrose-containing IV fluids show promise for POV reduction in adults.
  • Pediatric studies on dextrose for POV prevention are limited.

Purpose of the Study:

  • To evaluate the efficacy of intraoperative intravenous dextrose for antiemetic prophylaxis in pediatric ambulatory surgery.
  • To determine if dextrose is non-inferior to ondansetron in preventing POV.

Main Methods:

  • A non-inferiority randomized clinical trial involving healthy children (3-9 years) undergoing ambulatory dental surgery.
  • Comparison of dexamethasone + ondansetron versus dexamethasone + intravenous dextrose.
  • Primary outcome: POV in the postanesthetic care unit (PACU) within 2 hours.

Main Results:

  • Vomiting in the PACU occurred in 7.6% of the dextrose group and 3.5% of the ondansetron group.
  • The risk difference was 4.2%, exceeding the non-inferiority margin of 7.5%.
  • Non-inferiority of dextrose compared to ondansetron was not demonstrated.

Conclusions:

  • Intravenous dextrose is not a satisfactory alternative to ondansetron for preventing POV in pediatric ambulatory dental surgery.
  • Further research may be needed to explore alternative antiemetic strategies.
Abstract

Related Concept Videos

Chemotherapy-Induced Nausea and Vomiting: 5-HT3 Receptor Antagonists01:27

Chemotherapy-Induced Nausea and Vomiting: 5-HT3 Receptor Antagonists

5-HT3 receptor antagonists, such as dolasetron, granisetron (Kytril), ondansetron (Zofran), and palonosetron (Axoli), are crucial in managing chemotherapy-induced nausea and vomiting (CINV) and postoperative nausea. These drugs selectively block 5-HT3 receptors in the visceral vagal and spinal afferent nerves, chemoreceptor trigger zone, and the vomiting center. They have a rapid onset of action and can be given as a single dose before chemotherapy. Ondansetron and granisetron, in particular,...
494
Chemotherapy-Induced Nausea and Vomiting: Dopamine Receptor Antagonists01:29

Chemotherapy-Induced Nausea and Vomiting: Dopamine Receptor Antagonists

Dopamine receptor antagonists, also known as antipsychotic agents, are critical in managing chemotherapy-induced vomiting. These antiemetic agents block dopamine receptors in the chemoreceptor trigger zone (CTZ), inhibiting signal transmission to the vomiting center. Antipsychotic agents encompass phenothiazines (PTZ), butyrophenones, benzamides, and thienobenzodiazepines (Zyprexa), which are utilized for their antiemetic and sedative properties.
Phenothiazines, such as prochlorperazine...
699
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...
153
Chemotherapy-Induced Nausea and Vomiting: Neurokinin-1 Receptor Antagonists01:28

Chemotherapy-Induced Nausea and Vomiting: Neurokinin-1 Receptor Antagonists

Neurokinin 1 (NK1) receptors are distributed across the GI tract, vagal afferents, and key CNS regions including the central vomiting center and chemoreceptor trigger zone (CTZ) Chemotherapy agents stimulate enterochromaffin cells in the gastrointestinal (GI) tract to release large amounts of substance P (SP). SP is a neuropeptide released by specific sensory nerves in response to many different stressors, including those in the GI mucosa affected by chemotherapy.  SP binds and activates...
428
Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption01:23

Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption

Understanding the physiological differences in the pediatric population is crucial for effective pharmacotherapy. Neonates, infants, and children exhibit significant variations in gastric pH, gastric emptying time, intestinal transit time, and biliary function. These variations profoundly affect oral drug absorption, necessitating a nuanced approach to pediatric dosing.Neonates present with a unique physiological profile, having a gastric pH greater than 4 and faster and more irregular gastric...
148
Pathophysiology of Vomiting01:22

Pathophysiology of Vomiting

Vomiting is a complex physiological response to expel harmful or irritating substances from the body. It's a defensive mechanism triggered by stimuli like poisons, microbial toxins, cytotoxic drugs, and mechanical abdominal distension. The process is centrally coordinated by the vomiting (or emetic) center located in the medulla of the brainstem. This area, rich in muscarinic M1, histamine H1, neurokinin 1 (NK1), and serotonin 5-HT3 receptors, coordinates the act of vomiting through...
2.3K