An Evaluation of Risperidone Dosing for Pediatric Delirium in Children Less Than or Equal to 2 Years of Age

Christopher T Campbell1,2, Erin Grey1, Jennifer Munoz-Pareja3

  • 1University of Florida College of Pharmacy, Gainesville, FL, USA.

Insights

This study found risperidone to be safe and well-tolerated for treating ICU delirium in infants under two years old. Doses between 0.1-0.25 mg daily, given once or twice, effectively reduced other sedative medications.

Area of Science:

  • Pediatric Intensive Care
  • Pharmacology
  • Critical Care Medicine

Background:

  • Limited data exists on risperidone dosing and safety in pediatric patients under two years old.
  • Antipsychotic use in critically ill infants requires careful consideration of efficacy and safety profiles.

Purpose of the Study:

  • To characterize risperidone dosing strategies, safety, and tolerability in infants aged two years and younger.
  • To provide evidence-based recommendations for risperidone use in a vulnerable pediatric population.

Main Methods:

  • Retrospective study of 17 patients aged ≤2 years receiving risperidone for ICU delirium.
  • Analysis of initial and mean daily doses, dosing frequency, treatment duration, and adverse events.
  • Comparison of concomitant sedative and analgesic medication use before and after risperidone initiation.

Main Results:

  • Initial daily risperidone doses ranged from 0.1 to 0.25 mg (0.01-0.04 mg/kg), with most patients receiving once-daily dosing.
  • Over 80% of patients required a dose increase; however, no adverse events led to discontinuation.
  • Initiation of risperidone was associated with decreased median doses of fentanyl, morphine, ketamine, and midazolam.

Conclusions:

  • Risperidone is safe and well-tolerated at 0.1-0.25 mg/day in patients ≤2 years old for managing ICU delirium.
  • This study offers the largest cohort to date with specific risperidone dosing recommendations for this age group.
  • Further research is needed to explore the impact of antipsychotics on other sedation and analgesic regimens in pediatric ICU patients.

Related Concept Videos

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...
215
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...
177
Drug Dosing: Geriatric Patients01:15

Drug Dosing: Geriatric Patients

Elderly individuals encompass a diverse population with varying degrees of age-related physiological changes. Defining the elderly presents challenges, as the geriatric population is often arbitrarily categorized as individuals older than 65. However, many individuals in this group lead active and healthy lives, with an increasing number surpassing 85 years and falling into the older elderly category. Physiological changes associated with aging impact performance capacity and homeostatic...
189
Pharmacokinetics in Pediatric Patients: Drug Distribution01:17

Pharmacokinetics in Pediatric Patients: Drug Distribution

Drug distribution in the pediatric population exhibits unique challenges and considerations due to the physiological differences between children, particularly neonates and infants, and adults. A crucial aspect of pediatric pharmacology is understanding how these differences impact the pharmacokinetics of various drugs, necessitating age-specific dosing strategies to ensure efficacy and safety.Neonates and infants have a higher total body water content, ~75%–90% of their body weight,...
214
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...
200
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...
2.8K