The clinical risk factors in specimen collection and procedures designed to minimise those risks for different specimen types.
SIGNET INSTITUTE 5. Outline the clinical risk factors in specimen collection and procedures designed to minimise those risks for different specimen types. 6. For the below factors which may affect the chemical analysis of specimens, discuss the impact they might have on collection: a. Appropriate times to collect b. Timing of last dose c. Required fasting times d. Protecting the integrity of the specimen 7. Identify the features, functions and use of the following specimen collection equipment: a. Sterile jars b. 24hr urine containers with and without additives c. Swabs – viral, bacterial, polymerase chain reaction (PCR), deoxyribonucleic acid (DNA) d. Paediatric urine collection bag e. Breath balloons f. Skin scraping equipment g. Nail clipping and scraping equipment
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