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| Section | Weight | Objectives |
|---|---|---|
| Special Collections | 12% | - Blood cultures & sterile collection - Glucose tolerance & dynamic tests - Therapeutic drug monitoring - Blood alcohol & legal collections - Pediatric & geriatric collections |
| Routine Blood Collections | 28% | - Venipuncture techniques & equipment - Post-collection care & labeling - Tourniquet use & vein assessment - Capillary puncture procedures - Order of draw & tube selection |
| Patient Preparation | 20% | - Patient positioning & comfort - Patient identification & verification - Site selection & preparation - Informed consent & communication - Requisition review & test verification |
| Specimen Processing & Handling | 14% | - Aliquoting & preservation - Documentation & tracking - Transport & storage requirements - Specimen rejection criteria - Processing & centrifugation |
| Safety and Compliance | 26% | - Quality control & error prevention - HIPAA & patient confidentiality - Bloodborne pathogens & exposure control - Infection control & OSHA standards - PPE & sharps disposal |
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NEW QUESTION # 89
Which of the following actions should the phlebotomist take when labelling inpatient specimens?
Answer: A
Explanation:
For inpatient specimens, the phlebotomist should label the specimen collection container immediately after collection using the patient's wristband information as the identification source. The key control is bedside labeling in the presence of the patient, after positive identification and collection, so the specimen is tied to the correct patient before it leaves the room. Labeling the lid is unsafe because lids can be removed, switched, or separated from the specimen. Having the patient write demographic information is not an acceptable patient-identification process and does not satisfy laboratory labeling requirements. Provider pre-labeling is also unsafe because it creates a risk of wrong-patient collection if the container is later used for another patient or if identification is not verified at collection. Correct labeling usually includes patient name, second identifier, date and time of collection, collector identity, and any facility-required information. The NHA CPT outline specifically includes patient identifiers, labeling procedures and requirements, documentation, and the task of labeling all specimens. Reference topics: Routine Blood Collections; patient identification; specimen labeling; documentation requirements.
NEW QUESTION # 90
Which of the following blood components is primarily responsible for oxygen transport?
Answer: A
Explanation:
Erythrocytes are primarily responsible for oxygen transport. They contain hemoglobin, the iron-containing protein that binds oxygen in the lungs and releases it to tissues. Platelets are involved in hemostasis and clot formation, not oxygen transport. Leukocytes are white blood cells that support immune defense. Plasma proteins perform functions such as maintaining oncotic pressure, transporting substances, and supporting clotting through proteins such as fibrinogen, but they are not the primary oxygen carriers. This foundational knowledge matters because phlebotomy technicians work with specimens used to evaluate red blood cell count, hemoglobin, hematocrit, indices, anemia, blood loss, and hemolysis. If a specimen is hemolyzed, red blood cells rupture and release intracellular contents, which can alter laboratory values. Understanding blood components helps the technician connect collection technique to specimen integrity. For example, rough handling, excessive suction, improper needle size, or vigorous shaking can damage erythrocytes and compromise results. Reference topics: Phlebotomy Fundamentals; blood components; erythrocytes; hemoglobin; CBC testing.
NEW QUESTION # 91
Which of the following agencies is responsible for setting guidelines for bloodborne exposure incidents?
Answer: C
Explanation:
The Occupational Safety and Health Administration is responsible for workplace safety regulation, including requirements related to bloodborne pathogen exposure. In phlebotomy, bloodborne exposure incidents include needlesticks, blood splashes, mucous membrane exposure, and contact with non-intact skin. OSHA's Bloodborne Pathogens Standard requires employers to maintain exposure control plans, provide training, use engineering controls such as safety needles and sharps containers, support appropriate PPE, and establish procedures for exposure reporting and follow-up. CMS is primarily linked to Medicare, Medicaid, and healthcare payment/quality oversight, not direct bloodborne exposure incident standards. The FDA regulates medical devices, drugs, biologics, and related safety approvals. CLIA governs laboratory testing quality standards, not occupational blood exposure response. The option wording on the screen says "Occupational Safety of Health Administration," but the correct agency is OSHA: Occupational Safety and Health Administration. NHA CPT safety content includes OSHA, bloodborne pathogens, sharps disposal, biohazards, exposure control protocols, needlestick reporting, and workplace safety regulations. Reference topics: Safety and Compliance; OSHA; Bloodborne Pathogens Standard; exposure control protocols.
NEW QUESTION # 92
Which of the following can cause a preanalytic error for serum bilirubin?
Answer: D
Explanation:
Light exposure can cause a preanalytic error for serum bilirubin because bilirubin is light-sensitive. If a bilirubin specimen is exposed to light for too long, photodegradation can occur, leading to falsely decreased bilirubin results. This is why bilirubin specimens are commonly protected from light by using an amber container or wrapping the specimen in foil according to facility procedure. "Population" is not a specimen-handling variable that directly causes bilirubin degradation. "Pollutants" is too vague and does not identify the specific preanalytical issue tested here. "Location" may matter for collection site selection in some contexts, but it is not the classic handling error for bilirubin. The phlebotomist must know which specimens require special handling for light, temperature, time, transport, and processing. Failure to protect light-sensitive analytes can compromise specimen integrity before testing even begins, producing inaccurate laboratory results despite correct venipuncture technique. The NHA CPT outline directly includes maintaining specimen integrity based on handling requirements such as temperature, light, and time, as well as recognizing the impact of preanalytical errors on test results. Reference topics: Processing Specimens; bilirubin handling; light protection; preanalytical error.
NEW QUESTION # 93
A patient states they ate breakfast 1 hour before a fasting lipid panel. Which of the following actions should the phlebotomist take?
Answer: C
Explanation:
The phlebotomist should ask the provider or follow facility policy to determine whether the specimen should still be collected. A fasting lipid panel can be affected by recent food intake, especially triglyceride-related measurements and specimen lipemia. The phlebotomist must not falsely mark the specimen as fasting because that creates inaccurate documentation and can mislead clinical interpretation. Telling the patient to drink water and wait 30 minutes does not restore the required fasting state. Changing the order to another test is outside the phlebotomist's scope; only an authorized provider can change laboratory orders. The proper role is to verify patient preparation, document noncompliance if the draw proceeds, and communicate the issue through the appropriate workflow. Patient preparation is a major preanalytical control point. A technically perfect venipuncture can still produce clinically misleading results if fasting, medication timing, posture, or timing requirements are ignored. Reference topics: Patient Preparation; fasting requirements; patient compliance; requisition review; preanalytical variables.
NEW QUESTION # 94
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