AMT RPT flashcards
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32 cards. Read the term and the definition here. The deck at the top of this page is optional.
- Standard precautions
- Infection control practices applied to all patients regardless of diagnosis: hand hygiene, gloves when contact with blood or body fluids is possible, and additional PPE for splash risk.
- Sharps container fill limit
- Sharps containers are replaced when three-quarters full; overfilling allows needles to protrude and prevents the lid from closing, creating injury and exposure risk.
- Hand hygiene duration
- Soap-and-water handwashing lasts at least 20 seconds, while alcohol-based hand rub requires 20 to 30 seconds of friction until the hands feel dry.
- N95 respirator indications
- An N95 respirator is worn for airborne isolation, including tuberculosis, varicella, and measles, and is fit-checked before room entry and removed after exit.
- Post-exposure needlestick procedure
- Wash the puncture site with soap and water, flush mucous membranes, report the exposure immediately, and complete the facility evaluation, which may include HIV prophylaxis and hepatitis testing.
- Biohazard label meaning
- A biohazard label identifies containers, bags, or equipment holding blood or other potentially infectious material; red bags and red containers are considered labeled.
- Two patient identifiers
- Acceptable identifiers are the full name plus date of birth or medical record number; bed number, room number, and diagnosis are never acceptable identifiers.
- Basal state collection
- Basal specimens are obtained after 8 to 12 hours of fasting and about 30 minutes of rest; prolonged fasting increases hemoconcentration and bilirubin concentration.
- Prolonged tourniquet effects
- Tourniquet application longer than one minute causes hemoconcentration and falsely elevates potassium, lactate, protein, and bilirubin; the tourniquet is released once blood flows.
- Fist pumping during collection
- The patient opens and closes the fist gently; vigorous pumping raises potassium and lactate and increases hemolysis, so it is avoided during venipuncture.
- Syncope-safe positioning
- Seat the patient with the arm supported, or place the patient supine with legs elevated when there is a fainting history; a standing patient is never bled.
- Venipuncture needle angle
- Insert the needle bevel up at 15 to 30 degrees; after blood flows, lower the angle toward parallel and advance slightly to keep the bevel inside the lumen.
- Order of draw rationale
- The CLSI sequence prevents additive carryover between tubes; EDTA is drawn after chemistry tubes so potassium and calcium-chelating additives do not contaminate serum or heparin specimens.
- Butterfly discard tube
- When coagulation tubes are collected with a winged set, a discard tube is drawn first to fill the tubing dead space; otherwise the citrate tube is underfilled and rejected.
- Capillary first drop
- The first drop of a dermal puncture is wiped away because it contains tissue fluid that dilutes the specimen; a fresh freely forming drop is then collected.
- Infant heel stick depth
- Lancet depth for an infant heel stick must not exceed 2 mm because the calcaneus lies close to the skin; deeper puncture can cause bone injury or osteochondritis.
- Heel stick puncture site
- Puncture the lateral or medial plantar surface of the heel; the central heel, toes, and previously punctured areas are avoided because of underlying bone and nerve proximity.
- Bedside labeling requirement
- Tubes are labeled at the patient's side immediately after collection with full name, second identifier, date, time, and collector initials; pre-labeling before collection is prohibited.
- Citrate tube fill ratio
- Sodium citrate tubes require nine parts blood to one part anticoagulant and must be filled to the marked volume; underfilled tubes cause falsely prolonged coagulation results and are rejected.
- Additive tube inversion counts
- Invert EDTA and heparin tubes 8 to 10 times, citrate tubes 3 to 4 times, and serum tubes 5 times; shaking causes hemolysis while inadequate mixing causes microclots.
- Specimens requiring ice
- Ammonia, blood gas, and lactate specimens are transported on ice, whereas cryoglobulins and cold agglutinins are maintained at 37 degrees Celsius during transport.
- Chain of custody seal
- Forensic specimens are sealed with tamper-evident tape, labeled, and documented at every handoff with date, time, and signatures so the chain remains unbroken.
- Scope of practice limit
- A phlebotomy technician may collect, label, handle, process, and transport specimens but may not interpret laboratory results or order tests independently.
- Standard of care definition
- The degree of care and skill a reasonably competent phlebotomist would provide under similar circumstances; falling below that level supports a negligence claim.
- Patient right to refuse
- A competent patient may decline any procedure; the refusal is documented, the ordering provider is notified, and no specimen is collected against the patient's will.
- HIPAA privacy principle
- Protected health information may be disclosed only for treatment, payment, or operations; discussing results in hallways, elevators, or waiting rooms violates patient privacy rules.
- Mandatory abuse reporting
- Suspected child abuse, elder abuse, or neglect must be reported to the designated authority under state law, and patient permission is not required for the report.
- Quality control versus assurance
- Quality control tests the analytic system using control materials, while quality assurance covers the entire process from order entry through result reporting.
- Westgard 1-3s rule
- A single control result that exceeds the mean by three standard deviations rejects the run; patient testing stops until the cause is found and corrective action is documented.
- Blood culture contamination rate
- Contamination should remain at or below 3 percent of collected cultures; higher rates increase unnecessary antibiotics, extended length of stay, and hospital costs.
- Delta check purpose
- A delta check compares a current result with the patient's previous result to flag specimen mix-ups, labeling errors, or a genuine rapid change in analyte concentration.
- Root cause analysis
- A structured review of an error that identifies underlying system causes and designs documented corrective actions intended to prevent the same problem from recurring.