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| Section | Objectives |
|---|---|
| Specimen Processing and Handling | - Quality control and rejection criteria - Specimen transport and storage - Labeling and documentation |
| Professional Practice | - Communication and professionalism - Ethics and patient confidentiality (HIPAA) |
| Patient Preparation | - Explaining procedures and obtaining consent - Patient identification and communication - Site selection and preparation |
| Specimen Collection | - Capillary puncture procedures - Order of draw and tube handling - Venipuncture techniques |
| Safety and Compliance | - OSHA standards and safety protocols - Needlestick prevention and biohazard disposal - Infection control and PPE usage |
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NEW QUESTION # 105
A phlebotomist completes a venipuncture procedure and activates the safety mechanism on the winged infusion set up to discard it into the sharps container. Which of the following actions should the phlebotomist take if the sharps container is locked?
Answer: D
Explanation:
If the sharps container is locked and cannot accept the used winged infusion set, the phlebotomist should obtain a new sharps container. A contaminated needle or winged infusion set must be discarded immediately into an approved sharps container that is puncture-resistant, leak-resistant, properly labeled or color-coded, closable, and accessible at the point of use. Unlocking or forcing a container is unsafe and may expose the technician to contaminated sharps. A trash container is never acceptable for needle disposal because it creates risk for housekeeping staff, patients, and other personnel. A biohazard bag is also incorrect because bags are for regulated soft biohazard waste, not sharps; needles can puncture the bag and cause injury. The correct action is to maintain control of the activated device safely and use an appropriate replacement sharps container. This is a direct OSHA and standard-precaution issue. Reference topics: Safety and Compliance; sharps disposal; safety-engineered devices; needlestick prevention; OSHA bloodborne pathogen precautions.
NEW QUESTION # 106
At which of the following angles should a phlebotomist insert an antecubital venipuncture needle?
Answer: C
Explanation:
For antecubital venipuncture, the needle is inserted bevel up at approximately a 15° to 30° angle, with 30° commonly used as the upper accepted standard for routine venous access. From the options provided, 30° is the best answer. A 10° angle is usually too shallow for antecubital venipuncture and may cause the needle to skim the skin surface or fail to enter the vein lumen. A 45° angle is too steep and increases the risk of passing through the vein, causing hematoma, pain, or arterial/nerve injury depending on site depth and anatomy. A 25° angle can be clinically workable in some routine venipunctures, but this item is asking for the standard recognized insertion angle, and 30° is the expected test answer. Proper angle must be combined with vein anchoring, bevel-up orientation, stable equipment control, and avoidance of excessive probing. The NHA CPT outline specifically includes needle insertion, angle of needle insertion and withdrawal, and routine venipuncture technique. Reference topics: Routine Blood Collections; antecubital venipuncture; angle of needle insertion; needle withdrawal and safety.
NEW QUESTION # 107
Which of the following agencies enforces workplace standards related to bloodborne pathogens?
Answer: A
Explanation:
OSHA enforces workplace standards related to bloodborne pathogens. In phlebotomy, OSHA's Bloodborne Pathogens Standard is central because technicians routinely handle blood, sharps, contaminated equipment, and potentially infectious materials. OSHA requirements support exposure-control plans, engineering controls, sharps safety, PPE, hepatitis B vaccination access, training, and post-exposure follow-up. The FDA regulates drugs, biologics, and medical devices, but it does not enforce employer bloodborne pathogen workplace standards in the same way OSHA does. CMS administers Medicare and Medicaid and oversees certain healthcare quality and laboratory-related regulatory structures, but it is not the primary workplace bloodborne pathogen enforcement agency. DEA regulates controlled substances, which is unrelated to routine phlebotomy safety. A phlebotomist does not need to be a legal scholar, but they must know which agencies govern common safety and compliance issues. This knowledge supports correct behavior during needlesticks, sharps disposal, PPE use, exposure reporting, and infection-control practice. Reference topics: Safety and Compliance; OSHA; bloodborne pathogens; exposure-control plan; workplace safety.
NEW QUESTION # 108
Which of the following actions should a phlebotomist take when preparing a specimen for transport?
Answer: D
Explanation:
When preparing a specimen for transport, the phlebotomist should keep the tube with the stopper upright whenever practical. Upright positioning helps reduce leakage risk, prevents specimen contact with the stopper area more than necessary, and supports safe handling during movement to the laboratory or processing area. Refrigerating infectious substances is not a universal transport rule; temperature requirements depend on the ordered test and specimen handling instructions. Agitating a tube vigorously is incorrect because it can cause hemolysis, clot disruption, foaming, or cellular damage. Additive tubes are mixed by gentle inversion according to manufacturer guidance, not shaking. Wrapping multiple tubes together is also poor practice because tubes should be protected from breakage, leakage, and cross-contamination using proper specimen transport bags, absorbent material when required, and separated compartments when applicable. Proper transport preserves analyte stability, patient safety, and biohazard control. NHA CPT processing content includes preparing specimens for testing or transport, maintaining specimen integrity based on temperature, light, or time requirements, and following handling, storage, transportation, and disposal requirements. Reference topics: Processing Specimens; specimen transport; tube handling; specimen integrity.
NEW QUESTION # 109
Which of the following actions is required before using a new lot number of point-of-care testing strips?
Answer: A
Explanation:
Quality control testing should be performed before using a new lot number of point-of-care testing strips. Lot-to-lot variation can affect test performance, and QC confirms that the strips, controls, meter, and operator process are producing acceptable results before patient testing begins. Freezing strips is incorrect unless a manufacturer specifically requires a storage condition, and most reagent strips have controlled storage requirements that must not be improvised. Mixing old and new lots is unsafe because it creates traceability problems and can invalidate quality control. Using strips only for "control patients" is meaningless; patient specimens should not be used to validate unverified supplies. For waived testing and point-of-care testing, the phlebotomist must follow manufacturer instructions, document QC results, check expiration dates, store materials properly, and stop patient testing when controls fail. If QC is outside range, patient results should not be reported until corrective action is completed. Reference topics: Safety and Compliance; Special Collections; point-of-care testing; quality control; reagent lot verification.
NEW QUESTION # 110
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