Factors associated with medication administration errors in hospitalized pediatric patients: A scoping review

Claudia Lorena Motta Robayo1, Jonathan Martínez Pinto1, Bryan Tabango Goyes1

  • 1Facultad de Enfermería, Universidad Nacional de Colombia, Bogotá, Colombia.

Insights

Medication errors in hospitalized children are common, often due to incorrect dosing and human factors. Prevention requires integrated strategies like education, technology, and a non-punitive safety culture to protect vulnerable pediatric patients.

Area of Science:

  • Pediatric Patient Safety
  • Medication Administration
  • Healthcare Quality Improvement

Background:

  • Medication errors are a significant cause of preventable harm in hospitalized children.
  • The pediatric population faces unique risks due to dosing variability and developmental factors.

Purpose of the Study:

  • To synthesize evidence on factors contributing to medication administration errors in pediatric inpatients.
  • To identify effective strategies for preventing these errors.

Main Methods:

  • Systematic review of 25 studies (quantitative, qualitative, mixed methods) published in English, Spanish, or Portuguese.
  • Searched nine databases and reference lists; followed Joanna Briggs Institute (JBI) methodology.
  • Employed narrative synthesis with thematic analysis for data interpretation.

Main Results:

  • Incorrect dosing was the most frequent error type (72% of studies).
  • Neonates and infants in PICU/NICU settings were most vulnerable.
  • Human factors, especially knowledge deficits (52% of studies), were key contributors.

Conclusions:

  • Pediatric medication errors result from complex interactions of human, environmental, and medication-related factors.
  • Integrated prevention strategies including education, technology, and a non-punitive safety culture are essential.
Abstract

Related Concept Videos

Pharmaceutical Poisoning: Potential Scenarios01:26

Pharmaceutical Poisoning: Potential Scenarios

Pharmaceutical poisoning can occur through various channels, impacting an estimated 2 million hospitalized patients in the U.S. annually with serious adverse drug responses. These scenarios encompass both therapeutic uses, such as drug toxicity, where even standard dosages can lead to severe central nervous system depression, and non-therapeutic exposures, including accidental ingestion by children, and environmental and occupational exposures.Unintentional poisonings often involve exploratory...
Drug Toxicity: Risk factors01:24

Drug Toxicity: Risk factors

Adverse Drug Reactions (ADRs) are potential complications that arise during pharmacotherapy, influenced by multiple risk factors. Age plays a significant role; both neonates and the elderly are at heightened risk due to their respective immature and diminished metabolic and elimination processes. Gender also impacts ADRs, with females experiencing a 1.5 to 1.7-fold greater risk than males, which may be linked to pharmacokinetic, pharmacodynamic, and hormonal differences. Notably, neonates, the...
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...
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, compared...
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...
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...