Implementation of a risk-stratified opioid weaning protocol in a pediatric intensive care unit

L Nelson Sanchez-Pinto1, Lara P Nelson2, Phuong Lieu3

  • 1Division of Critical Care Medicine, Ann & Robert H. Lurie Children's Hospital of Chicago, 225 E. Chicago Ave, Box 73, Chicago, IL 60611-2605, USA.

Journal of Critical Care
|September 18, 2017
PubMed

Insights

A new risk-stratified opioid weaning protocol for critically ill children reduced opioid exposure duration without increasing withdrawal. This approach safely shortens opioid use in pediatric intensive care units.

Area of Science:

  • Pediatric Critical Care Medicine
  • Pharmacology
  • Clinical Protocol Implementation

Background:

  • Opioid use is essential for critically ill children but linked to adverse effects like delirium and dependence.
  • Effective strategies are needed to minimize opioid-related complications in pediatric intensive care units (PICUs).

Purpose of the Study:

  • To implement and evaluate a risk-stratified opioid weaning protocol in a pediatric ICU.
  • To reduce the duration of opioid administration in critically ill children.
  • To assess the protocol's impact on opioid withdrawal incidence.

Main Methods:

  • A prospective, pre- and post-intervention study design was employed in a large children's hospital PICU.
  • The study included 107 critically ill children receiving scheduled opioids for ≥7 days.
  • Key outcomes measured were the duration of opioid use and hospital length of stay (LOS).

Main Results:

  • The post-intervention group showed a significantly shorter duration of opioid exposure (17 vs. 22.5 days, p=0.01) and opioid wean (12 vs. 18 days, p=0.01).
  • No significant increase in opioid withdrawal incidence was observed despite reduced opioid duration.
  • Hospital length of stay did not differ significantly between the pre- and post-intervention groups (29 vs. 33 days, p=0.06).

Conclusions:

  • Implementation of a risk-stratified opioid weaning protocol effectively reduced opioid exposure in critically ill children.
  • The protocol achieved its goal of shortening opioid duration without increasing withdrawal complications.
  • The protocol did not impact overall hospital length of stay.
Abstract

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...
371
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...
302
Drug Dosing: Obese Patients01:21

Drug Dosing: Obese Patients

In the United States, obesity is a prominent concern. It is linked to heightened mortality rates due to increased occurrences of conditions such as hypertension, atherosclerosis, coronary artery disease, and diabetes compared to nonobese individuals. A patient is classified as obese if their actual body weight surpasses the ideal or desirable body weight by 20%, based on Metropolitan Life Insurance Company data. Ideal body weights consider average weights and heights for males and females...
303
IV Infusion to Oral Dosing: Conversion Methods01:28

IV Infusion to Oral Dosing: Conversion Methods

The development of extended-release formulations has facilitated the transition from intravenous to oral medication, offering a more convenient and patient-friendly approach to drug administration. This transition, however, requires careful management to ensure that therapeutic drug levels are maintained, preserving efficacy and avoiding adverse effects. Understanding pharmacokinetic principles and dosage calculations is critical during this process.Pharmacokinetics of the...
47
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,...
356
Pharmacokinetics in Pediatric Patients: Drug Metabolism01:24

Pharmacokinetics in Pediatric Patients: Drug Metabolism

In pediatric care, understanding the nuances of hepatic drug metabolism is crucial, as it significantly differs from that of adults. This divergence is primarily due to the developmental stage of drug-metabolizing enzymes, which affects how medications are processed in the body. In neonates, for instance, the activity of Phase I enzymes—critical for the initial breakdown of drugs—is markedly reduced, functioning at just 20–40% of the levels seen in adults. This reduction poses...
276