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| Section | Weight | Objectives |
|---|---|---|
| Special Collections | 12% | - Therapeutic drug monitoring - Pediatric & geriatric collections - Blood alcohol & legal collections - Blood cultures & sterile collection - Glucose tolerance & dynamic tests |
| Routine Blood Collections | 28% | - Capillary puncture procedures - Post-collection care & labeling - Tourniquet use & vein assessment - Order of draw & tube selection - Venipuncture techniques & equipment |
| Patient Preparation | 20% | - Patient identification & verification - Site selection & preparation - Patient positioning & comfort - Requisition review & test verification - Informed consent & communication |
| Safety and Compliance | 26% | - Quality control & error prevention - HIPAA & patient confidentiality - Infection control & OSHA standards - PPE & sharps disposal - Bloodborne pathogens & exposure control |
| Specimen Processing & Handling | 14% | - Processing & centrifugation - Transport & storage requirements - Specimen rejection criteria - Aliquoting & preservation - Documentation & tracking |
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NEW QUESTION # 111
Using outdated supplies can result in which of the following?
Answer: D
Explanation:
Using outdated supplies can result in specimen rejection because expired collection materials may fail to preserve the specimen correctly or meet laboratory acceptance criteria. Expired evacuated tubes may have inadequate vacuum, degraded additives, compromised sterility, or incorrect blood-to-additive performance. These problems are preanalytical errors, meaning they occur before testing and can make results unreliable. The laboratory may reject the specimen rather than risk reporting inaccurate data. Stat processing refers to urgent priority handling and is unrelated to supply expiration. Postanalytical error occurs after testing, such as reporting or result-delivery mistakes, not from using expired collection supplies during acquisition. Claim rejection is a billing or insurance issue, not a specimen integrity issue. A competent phlebotomist prevents rejection by checking tube expiration dates, inspecting supplies, confirming required specimen type, filling tubes properly, mixing additives correctly, and following transport requirements. NHA CPT processing and routine collection content covers specimen integrity, preanalytical errors, equipment quality control, expiration checks, and recollection when required. Reference topics: Processing Specimens; preanalytical error; specimen rejection; equipment quality control.
NEW QUESTION # 112
Which of the following agencies is responsible for setting guidelines for bloodborne exposure incidents?
Answer: D
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 # 113
Which of the following actions should a phlebotomist take to identify a patient who was admitted to a facility?
Answer: A
Explanation:
For an admitted patient, the phlebotomist should check the patient's identification band. Inpatient identification depends on matching the patient's wristband to the requisition or collection order using required identifiers, commonly full name and date of birth or medical record number. Stating the patient's name and date of birth for the patient to confirm is weaker because it allows passive agreement and does not require the patient to actively provide identifiers. Using the medical chart alone is not sufficient because charts can be misplaced, opened to the wrong patient, or outdated. Comparing the wristband to bedside equipment is also unsafe because equipment stickers may be incorrect, moved, or not patient-specific enough to serve as the primary identifier. The correct process protects against wrong-patient collection, mislabeling, transfusion risk, diagnostic error, and specimen rejection. Reference topics: Patient Preparation; inpatient identification; wristband verification; two patient identifiers; requisition matching; specimen labeling. NHA places patient identification and preparation procedures under core CPT exam domains.
NEW QUESTION # 114
Which of the following is a possible complication of venipuncture collection for a patient who has been on warfarin therapy?
Answer: A
Explanation:
Prolonged bleeding is the expected complication for a patient on warfarin therapy. Warfarin is an anticoagulant, meaning it interferes with normal clot formation and can increase bleeding time after venipuncture. The phlebotomist should be alert for delayed hemostasis, apply firm pressure after needle removal, avoid having the patient bend the arm sharply, and confirm that bleeding has stopped before applying a bandage and leaving the patient. Blood clotting is the opposite of the expected medication effect. Hemostasis is the normal stopping of bleeding, not a complication. Petechiae can occur from tourniquet pressure, fragile capillaries, or platelet-related issues, but in this question the medication-specific risk is prolonged bleeding. Proper technique reduces complications: release the tourniquet, withdraw the needle smoothly, activate the safety device, apply pressure, and monitor the puncture site. Reference topics: Routine Blood Collections; post-procedure care; anticoagulant therapy; bleeding complications; hemostasis; patient observation. NHA includes routine venipuncture complications and post-collection care within the CPT test plan.
NEW QUESTION # 115
Which of the following actions should a phlebotomist take to prevent reflux during venipuncture?
Answer: C
Explanation:
To prevent reflux, the patient's arm should be kept in a downward position so the collection tube remains below the puncture site. Reflux occurs when blood or tube additive flows backward from the tube into the patient's vein. Keeping the tube below the venipuncture site and allowing tubes to fill properly reduces this risk. Holding the tube above the puncture site increases the chance of backflow. Removing the tube before it fills can create incorrect blood-to-additive ratios and does not prevent reflux. Inserting the needle bevel down is incorrect technique; venipuncture needles are inserted bevel up to enter the vein smoothly and reduce trauma. Reflux prevention also includes using proper tube position, avoiding excessive movement, not pushing tube contents toward the patient, and releasing the tourniquet appropriately. This is especially important with additive tubes because additive contamination of the patient's circulation, while uncommon, is a preventable safety concern. Reference topics: Routine Blood Collections; reflux prevention; evacuated tube technique; arm positioning; tube handling.
NEW QUESTION # 116
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