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Identification of priorities for medication safety in neonatal intensive care
Desireé L Kunac1, David M Reith
1School of Pharmacy, University of Otago, Dunedin, New Zealand. desiree.kunac@stonebow.otago.ac.nz
Insights
Neonatal medication errors are a significant risk. A Failure Mode and Effects Analysis (FMEA) identified lack of training and administration process issues as key vulnerabilities in neonatal intensive care units (NICUs).
Area of Science:
- Pediatric Patient Safety
- Health Systems Engineering
- Neonatal Pharmacology
Background:
- Neonates face higher medication error risks than older children.
- Limited understanding of medication error causes in neonates.
- Failure Mode and Effects Analysis (FMEA) is an industrial safety technique.
Purpose of the Study:
- To identify and prioritize potential failures in the neonatal intensive care unit (NICU) medication use process.
- To apply FMEA to enhance medication safety in neonates.
Main Methods:
- A multidisciplinary panel utilized FMEA and a systems-based approach.
- Developed a flow diagram of the NICU medication use process.
- Brainstormed potential failures, causes, and effects, calculating Risk Priority Scores (RPS).
Main Results:
- Identified 72 failures with 193 causes/effects.
- Vulnerabilities occurred throughout the process, notably in prescribing and preparation.
- Top risks included lack of medication safety training (RPS 273) and administration errors (dose, timing, infusion pumps, route).
- Causes included unsafe preparation/storage systems, variable staff skills, and lack of computerization.
Conclusions:
- Interventions should increase staff awareness of medication safety.
- Focusing on medication administration processes is crucial for reducing adverse events in the NICU.
Background:
Although neonates are reported to be at greater risk of medication error than infants and older children, little is known about the causes and characteristics of error in this patient group. Failure mode and effects analysis (FMEA) is a technique used in industry to evaluate system safety and identify potential hazards in advance. The aim of this study was to identify and prioritize potential failures in the neonatal intensive care unit (NICU) medication use process through application of FMEA.
Methods:
Using the FMEA framework and a systems-based approach, an eight-member multidisciplinary panel worked as a team to create a flow diagram of the neonatal unit medication use process. Then by brainstorming, the panel identified all potential failures, their causes and their effects at each step in the process. Each panel member independently rated failures based on occurrence, severity and likelihood of detection to allow calculation of a risk priority score (RPS).
Results:
The panel identified 72 failures, with 193 associated causes and effects. Vulnerabilities were found to be distributed across the entire process, but multiple failures and associated causes were possible when prescribing the medication and when preparing the drug for administration. The top ranking issue was a perceived lack of awareness of medication safety issues (RPS score 273), due to a lack of medication safety training. The next highest ranking issues were found to occur at the administration stage. Common potential failures related to errors in the dose, timing of administration, infusion pump settings and route of administration. Perceived causes were multiple, but were largely associated with unsafe systems for medication preparation and storage in the unit, variable staff skill level and lack of computerised technology.
Conclusion:
Interventions to decrease medication-related adverse events in the NICU should aim to increase staff awareness of medication safety issues and focus on medication administration processes.
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