Which of the following is the minimum required number of unique patient identifiers a phlebotomist should use prior to a blood draw?
One
Two
Three
Four
The Correct Answer is C
Choice A Reason:
Using only one patient identifier is not sufficient to ensure patient safety and accuracy in healthcare settings. It increases the risk of misidentification, which can lead to serious medical errors. Therefore, one identifier is not the standard practice for patient verification before a blood draw.
Choice B Reason:
While two identifiers are commonly used in many healthcare settings as a minimum requirement, they may not always provide enough differentiation, especially in larger facilities where patient names may be similar. Two identifiers are often the minimum standard, but they are not the most comprehensive approach.
Choice C Reason:
Three unique patient identifiers provide a more robust method for verifying a patient's identity, significantly reducing the likelihood of errors. According to the Clinical and Laboratory Standards Institute (CLSI), three identifiers are recommended to ensure the correct patient is being collected. This may include the patient's full name, date of birth, and medical record number or another unique identifier.
Choice D Reason:
While using four unique identifiers could further reduce the risk of patient misidentification, it is not typically required as the standard minimum. Three identifiers are generally considered adequate for most healthcare settings to ensure patient safety and proper identification.
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is A
Explanation
Choice A reason:
The date of specimen collection is crucial for a laboratory report as it provides the context for the test results. It helps in assessing the timeliness and relevance of the results, especially when monitoring conditions that can change rapidly over time.
Choice B reason:
While the phlebotomist's initials may be recorded as part of the internal process for tracking specimen collection, they are not typically included in the patient's laboratory report. The focus of the report is on the patient and the test results, rather than on the personnel who collected the sample.
Choice C reason:
Patient diagnosis is not usually included in a laboratory report because the purpose of the report is to provide test results that may inform a diagnosis. The diagnosis is made by the healthcare provider based on the test results, along with other clinical information.
Choice D reason:
Values of previous tests may be referenced in a patient's medical record but are not a required element on a laboratory report. Each report typically presents the results of the current tests only. Comparisons to previous values, if needed, are made by the healthcare provider.
Correct Answer is A
Explanation
Choice A Reason:
Taking the specimen temperature before 4 minutes is the correct procedure according to the Department of Transportation (DOT) guidelines. The DOT Rule 49 CFR Part 40 Section 40.65 states that the temperature of the specimen must be checked no later than four minutes after the employee has given the specimen. The acceptable temperature range is 32–38 °C/90–100 °F, which helps to verify the validity of the specimen.
Choice B Reason:
Taking the specimen temperature at 5 minutes is not within the DOT guidelines. The temperature must be taken before 4 minutes have passed to ensure the specimen's integrity and to comply with the regulatory requirements.
Choice C Reason:
At 15 minutes, the temperature check would be too late. The DOT guidelines specify that the temperature should be checked no later than four minutes after collection to ensure the specimen has not been tampered with and is within the acceptable temperature range.
Choice D Reason:
After 30 minutes, the temperature of the urine specimen would not reflect the body temperature at the time of collection, which is necessary for the validity of the test. This delay could allow for the temperature to fall outside of the acceptable range, potentially invalidating the specimen.
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