The epidemiology of drug-related hospital admissions in paediatrics - a systematic review

Sonja Eberl1, Pauline Heus2,3, Irmgard Toni4

  • 1Department of Pediatrics and Adolescent Medicine, Faculty of Medicine, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany. sonja.eberl@uk-erlangen.de.

Insights

Medication safety in children is a significant concern, with drug-related hospital admissions occurring frequently. Improving prescribing practices and clinical awareness is crucial for preventing these events.

Area of Science:

  • Pediatric Medicine
  • Pharmacovigilance
  • Public Health

Background:

  • Medication safety in children is a persistent challenge.
  • Drug-related hospital admissions in pediatric populations require further investigation, particularly in outpatient settings.

Purpose of the Study:

  • To systematically review the literature on the frequency and nature of drug-related hospital admissions in children.
  • To identify areas for improvement in pediatric medication safety strategies and guide future research.

Main Methods:

  • Conducted a systematic literature review of studies published between 2000 and 2024.
  • Included 45 studies reporting over 24,000 hospitalizations for adverse drug events (ADEs) or adverse drug reactions (ADRs).
  • Utilized Joanna Briggs Institute recommendations for data extraction and appraisal.

Main Results:

  • Drug-related hospitalizations varied significantly based on monitoring intensity, with intensive ADE monitoring showing higher frequencies.
  • ADR-related hospitalizations ranged from 0.04% to 6.9% depending on monitoring type.
  • Limited data suggested up to one-third of drug-related admissions may be preventable, often due to prescribing issues.

Conclusions:

  • High frequency of drug-related hospitalizations necessitates enhanced pediatric medication safety.
  • Routine identification methods appear unreliable, emphasizing the need for increased clinical awareness.
  • Addressing under-reporting and methodological limitations is vital for future research and improvement strategies.
Abstract

Related Concept Videos

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...
2.0K
Pharmacovigilance01:19

Pharmacovigilance

Post-marketing surveillance is a critical component of pharmaceutical regulation, often uncovering unanticipated adverse drug reactions (ADRs) once a drug is widely used over an extended period.
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
In some cases, there...
825
Prescription, Nonprescription and Orphan Drugs01:02

Prescription, Nonprescription and Orphan Drugs

Prescription drugs require a prescription from a medical practitioner and can only be obtained from a pharmacy. They have many applications, including treating pain, anxiety, and hypertension.
The misuse and addiction to prescription drugs is a growing problem that can affect people of all age groups, specifically teenagers. This can happen when prescription medications are used in ways not intended by the prescriber, such as taking someone else's prescription or using medication for...
720
Drug Regulation01:25

Drug Regulation

Drug regulation encompasses the management of drug usage by evaluating its safety and efficacy through assessments conducted by regulatory authorities. Regrettably, the history of drug regulation is marred by several catastrophic events. One such incident is the Elixir Sulfanilamide tragedy, in which the toxic compound diethyl glycol was included in a sweet-tasting medication, leading to numerous fatalities. This event prompted the enactment of the Food, Drug, and Cosmetic Act in 1938. Under...
1.4K
Drug Abuse and Addiction: Pharmacological Phenomena01:15

Drug Abuse and Addiction: Pharmacological Phenomena

Drug dependence, abuse, and addiction are complex phenomena that can precipitate various abnormal states. Physical dependence refers to a state of pharmacological adaptation to a drug. This adaptation often results in tolerance—a reduced response to the drug after repeated administrations. When the drug use is abruptly stopped, withdrawal symptoms occur due to the body's need to readjust from the pharmacologically induced imbalance. However, tolerance and withdrawal symptoms do not...
465
Drug Dosage Regimen: Overview01:15

Drug Dosage Regimen: Overview

A drug dosage regimen describes the specific instructions and schedule for administering a drug to a patient. It considers factors such as drug dosage, frequency, route of administration, and duration of treatment. Designing an appropriate dosage regimen for a patient aims to achieve a target drug concentration at the site of action.
Typically, the starting dose and dosing interval are guided by the manufacturer's recommendations based on clinical trials conducted during and after drug...
3.5K