Related Experiment Videos
Medication Safety Self-assessment in Hospital Wards Within A Regional Health Services System: A Descriptive Follow-up
Kaisa Mäkinen1,2, Tiina Kortteisto3, Marja Airaksinen4
1Hospital Pharmacy, Tampere University Hospital, Wellbeing Services County of Pirkanmaa, Finland.
Journal of Patient Safety
|June 19, 2026
Summary
Hospital wards improved medication safety practices over one year. A self-assessment procedure identified key areas for development, enhancing patient safety and quality improvement initiatives.
Area of Science:
- Healthcare Management
- Patient Safety
- Quality Improvement
Background:
- Medication safety is a critical component of hospital care.
- Assessing and improving medication practices are essential for patient outcomes.
- A structured self-assessment can identify areas for enhancement in healthcare settings.
Purpose of the Study:
- To evaluate safe medication practices in hospital wards.
- To assess changes in medication safety over a one-year period.
- To utilize a structured self-assessment procedure for quality improvement.
Main Methods:
- A medication safety self-assessment procedure was developed and implemented.
- The assessment involved interprofessional teams in hospital wards.
- Data were collected via an electronic survey and analyzed using descriptive statistics over two years.
Main Results:
- Participation increased from 60 wards in 2022 to 76 in 2023.
- Top practices included supervisor commitment and valid nursing licenses.
- Areas for development included staff onboarding and medication list maintenance.
- Overall implementation of practices increased from 23% to 33%.
Conclusions:
- The self-assessment effectively identified strengths and weaknesses in medication safety management.
- Significant improvements in medication safety were observed within one year.
- The procedure serves as a practical tool for continuous quality improvement in healthcare systems.
Related Concept Videos
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...
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 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 Dosing: Geriatric Patients
Elderly individuals encompass a diverse population with varying degrees of age-related physiological changes. Defining the elderly presents challenges, as the geriatric population is often arbitrarily categorized as individuals older than 65. However, many individuals in this group lead active and healthy lives, with an increasing number surpassing 85 years and falling into the older elderly category. Physiological changes associated with aging impact performance capacity and homeostatic...
Dosage Regimens: Partial Pharmacokinetic Parameters
It is not uncommon for complete drug pharmacokinetic profiles to remain elusive in pharmacokinetics. This necessitates certain educated assumptions by pharmacokineticists to determine appropriate dosage regimens without comprehensive pharmacokinetic data from animal or human studies. One prevalent assumption is setting the bioavailability factor, denoted as F, to 1 or 100%. This assumption caters to the scenario where a drug doesn't achieve full systemic absorption, resulting in the patient...
Healthcare Associated Infections II: Preventive Measures
Essential infection prevention measures are based on the knowledge of the infection chain, the modes of transmission in healthcare settings, and the use of the best practices in all healthcare settings. Compulsory public reporting of healthcare-associated infection rates is needed to allow individuals and the community to make informed choices regarding selecting a healthcare facility.
The best practices for preventing healthcare-associated infections include hand hygiene, patient risk...
The best practices for preventing healthcare-associated infections include hand hygiene, patient risk...
Dosage Regimens: Designs and Approaches
Designing a dosage regimen, which refers to the manner of drug administration, is a complex process involving the selection of drug dose, route, and frequency. This process is underpinned by pharmacokinetic parameters derived from tests and population averages. These parameters are then tailored to patient-specific variables such as diagnosis, demographics, and allergy status. Once therapy commences, therapeutic response monitoring is critical and achieved through clinical and physical...