Related Experiment Videos

Characteristics of pediatric chemotherapy medication errors in a national error reporting database

Michael L Rinke1, Andrew D Shore, Laura Morlock

  • 1Department of Pediatrics, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.

Cancer
|May 29, 2007
PubMed

Insights

Pediatric chemotherapy errors frequently reached patients, with administration and dispensing errors being most common. Methotrexate and cytarabine were frequently involved, highlighting the need for targeted safeguards in pediatric cancer care.

Area of Science:

  • Pediatric Oncology
  • Medication Safety
  • Pharmacovigilance

Background:

  • Limited data exists on chemotherapy medication errors in pediatric patients.
  • Pediatric medication errors are reported at high rates overall.
  • This study investigates patterns in pediatric chemotherapy errors.

Purpose of the Study:

  • To examine patterns in pediatric chemotherapy medication errors.
  • To identify common error types, causes, and involved agents.
  • To inform the development of targeted medication administration safeguards.

Main Methods:

  • Utilized the United States Pharmacopeia MEDMARX database.
  • Analyzed error reports from 1999-2004 for patients under 18.
  • Focused on reports involving chemotherapy medications.

Main Results:

  • 310 pediatric chemotherapy error reports were analyzed; 85% reached the patient.
  • Administration (48%) and dispensing (30%) phases were primary error origins.
  • Antimetabolites were most frequent (39.5%), with methotrexate and cytarabine commonly involved.
  • Improper dose/quantity (22.9%) and wrong time (22.6%) were leading error types.
  • Performance deficit (41.3%) was the most cited cause of errors.

Conclusions:

  • Pediatric chemotherapy errors are common, often reach patients, and can cause harm.
  • Errors differ between outpatient and inpatient settings.
  • Administration errors and specific agents like methotrexate require focused safety interventions.
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...
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...
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...
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...
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 a challenge in...
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...