Assessing medication safety culture in Norwegian pediatric wards: a first nationwide survey

Lavin Kadir1, M Einen2,3, J C Bergman2,3

  • 1Department of Pharmacy, University of Oslo, Oslo, Norway. lavinar@uio.no.

BMC Pediatrics
|July 20, 2026
PubMed

Insights

Pediatric patient safety awareness is positive, but health information technology use in medication management varies. Improving technology and addressing reporting barriers are key for learning and enhancing safety culture in pediatric wards.

Area of Science:

  • Pediatric healthcare
  • Patient safety
  • Health information technology

Background:

  • Limited evidence exists on health information technologies' impact on pediatric medication management and patient safety.
  • Hospitals widely use health information technologies to reduce medication errors, but pediatric-specific data is scarce.

Purpose of the Study:

  • To assess safety culture in pediatric medication management.
  • To evaluate medication error reporting in pediatric wards.
  • To identify areas for improvement in pediatric patient safety.

Main Methods:

  • A survey was developed and distributed to pediatric wards in Norway.
  • The survey targeted physicians, pharmacists, and nurses.
  • The Systems Engineering Initiative for Patient Safety (SEIPS) model guided the analysis.

Main Results:

  • 102 nurses, 24 physicians, and 7 pharmacists responded, representing 86% of pediatric wards.
  • Access to pediatric-adapted health information technology varied across hospitals and medication management stages.
  • Staff desired more involvement in error review and training on patient safety and reporting.

Conclusions:

  • Hospital staff show positive awareness of pediatric patient safety.
  • Health information technology implementation impacts medication management, highlighting needs for pediatric-specific solutions.
  • Barriers in medication error reporting hinder learning and improvement opportunities.
Abstract

Related Concept Videos

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...
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...
Obedience01:08

Obedience

According to obedience research, we may harm others under the forceful pressures of an authority figure (Milgram, 1974). How about if the inappropriate orders were delivered with less force? The increasing interdependence between nurses and physicians compelled Hofling and his colleagues to explore nurses’ reactions to a potentially harmful medical request made by the perceived authority figure, the doctor (Hofling, Brotzman, Dalrymple, Graves, & Pierce, 1966). In this situation, obedience...
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...
Guidelines and Strategies for Safe Computer Charting01:18

Guidelines and Strategies for Safe Computer Charting

The guidelines and strategies provided by the American Nurses Association (ANA) and the Canadian Nurses Association (CNA) offer essential principles for ensuring safe and secure computer charting systems in healthcare settings. Let's break down each recommendation:
Maintain Confidentiality and Security:
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...