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WMLM1318 - CME/CMLE - LMU 16 (Fundamentals) Operat ...
WMLM1318 - Pre-Reading Assignment
WMLM1318 - Pre-Reading Assignment
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Pdf Summary
The document discusses the importance of quality assurance (QA) in laboratory medicine to enhance patient safety by minimizing errors. It highlights the role of laboratory science in improving patient outcomes by implementing quality-management systems that focus on various phases of the total testing process. The preanalytical phase involves test ordering, specimen collection, transport, and identification, which are prone to errors. The analytical phase includes specimen testing, while the postanalytical phase focuses on result reporting and action-taking. The document emphasizes the need for continuous monitoring, training, and implementing SOPs to reduce errors in each phase.<br /><br />To prevent errors, it is crucial to identify high-risk activities and implement error-detecting systems targeting all testing phases. Measures include appropriate test ordering, patient and specimen identification, specimen handling, maintaining integrity, and automated workstations to reduce human errors. The analytical phase's quality has improved with the introduction of EQAS and internal QC programs. To enhance patient safety, critical values reporting, multidisciplinary team collaboration, and the use of information technology are recommended.<br /><br />Challenges, such as staff shortages and system consolidation, are noted, emphasizing the need for a culture shift, transparency, and interprofessional teamwork to achieve quality improvement. Adoption of patient-centric approaches, national/international accreditation, and technology integration to enhance patient safety are suggested. Continuous education, training, and evaluation of examination procedures are essential for error prevention and quality enhancement in laboratory medicine.
Keywords
Quality assurance
Laboratory medicine
Patient safety
Total testing process
Preanalytical phase
Analytical phase
Postanalytical phase
Error detection systems
EQAS
Internal QC programs
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