Effectiveness of granisetron in controlling pediatric gastroenteritis-related vomiting after discharge from the ED

Khajista Qazi1, Hashim M BinSalleeh2, Ubaid H Shah3

  • 1King Fahd Medical City, Emergency Medicine, Riyadh, Riyadh 11525, Saudi Arabia.

Insights

Oral granisetron did not effectively stop vomiting in children with gastroenteritis after emergency department discharge. The study found no significant difference in vomiting rates between granisetron and placebo groups.

Area of Science:

  • Pediatric Emergency Medicine
  • Gastroenterology
  • Pharmacology

Background:

  • Gastroenteritis-related vomiting and dehydration are common in children presenting to emergency departments.
  • Oral rehydration therapy (ORT) is the standard initial treatment, but some patients fail to tolerate it.
  • Controlling vomiting after discharge is crucial for successful rehydration and preventing return visits.

Purpose of the Study:

  • To evaluate the efficacy of oral granisetron, a 5-HT3 receptor antagonist, in managing vomiting in pediatric patients with gastroenteritis.
  • To determine if granisetron reduces vomiting in children who failed initial oral rehydration therapy (ORT) and were discharged from the emergency department (ED).

Main Methods:

  • A randomized, placebo-controlled trial was conducted involving children aged 6 months to 8 years with gastroenteritis-related vomiting and dehydration.
  • Patients who failed initial ORT received either oral granisetron (40 μg/kg) or placebo, with ORT resumed.
  • The primary outcome was the proportion of patients experiencing vomiting at 24 hours post-discharge, with follow-up via telephone.

Main Results:

  • Out of 900 eligible patients, 165 who vomited during initial ORT were randomized.
  • No statistically significant difference in vomiting at 24 hours was observed between the granisetron group (38/83) and the placebo group (45/82) (P = .16).
  • Vomiting trends throughout the follow-up period also showed no significant difference between the groups.

Conclusions:

  • Oral granisetron is not effective in controlling gastroenteritis-related vomiting in pediatric patients discharged from the ED.
  • Granisetron did not alter the natural course of illness for vomiting in this patient population.
  • Further research may be needed to explore alternative antiemetic strategies for refractory vomiting in pediatric gastroenteritis.
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,...
919
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...
816
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...
1.1K
Drugs Affecting GI Tract Motility: Dopamine Receptor Antagonists01:28

Drugs Affecting GI Tract Motility: Dopamine Receptor Antagonists

Prokinetic agents are specialized medications that stimulate gastrointestinal (GI) motility, promoting food movement through the GI tract. Dopamine, an inhibitory neurotransmitter, plays a significant role in this process, reducing GI motility and indirectly controlling the speed of digestion. Dopamine receptor antagonists, such as metoclopramide and domperidone, offer a unique advantage as prokinetic agents. By blocking the dopamine receptors, these drugs increase GI motility, improving food...
1.9K
Prevention of Further Absorption of Poison01:14

Prevention of Further Absorption of Poison

In cases of acute poisoning, the primary objective is to prevent further absorption of the toxic substance into the body. Immediate interventions using various decontamination techniques targeting the gastrointestinal (GI) tract can achieve this. Decontamination is crucial to prevent poison from entering the systemic circulation, which involves washing affected areas with water and mild soap and removing contaminated clothing. Once external decontamination is done, attention must be turned to...
1.4K
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...
4.5K