Phlebotomy · Processing · 6 min read
Specimen Quality, Rejection and Recollection
- Distinguish between the three phases of laboratory testing and identify preanalytical variables controlled by the phlebotomist.
- Recognize visual and physical indicators of compromised specimens, including hemolysis, lipemia, icterus, clots, and improper volume.
- Execute correct protocols for specimen labeling, documenting rejections, notifying healthcare personnel, and handling recollected samples.
The Phases of Testing and Preanalytical Control
Laboratory testing follows a continuous path that is divided into three distinct phases: preanalytical, analytical, and postanalytical. The preanalytical phase begins the moment a healthcare provider orders a test and ends when the actual sample testing begins. The analytical phase consists of performing laboratory tests, whether by instrument or manual method. Finally, the postanalytical phase involves the verification, reporting, and archiving of laboratory test results. The phlebotomist plays a foundational role in this cycle because the majority of all laboratory testing errors occur during the preanalytical phase.
Phlebotomists directly control preanalytical variables within their scope of duties. These essential responsibilities include patient identification, specimen collection, labeling, handling, and transport. Everyday technical choices make a substantial difference in test outcomes. For example, common preanalytical errors include patient misidentification, incorrect tube selection, and improper specimen mixing. Using an incorrect order of draw can cause additive carryover between tubes and compromise subsequent test results.
A specimen's journey after it leaves the patient's arm is just as critical as the collection itself. Delayed specimen transport and improper storage temperatures are preanalytical errors that compromise specimen integrity. Technical errors during venipuncture also alter sample composition before the needle is even withdrawn. For instance, prolonged tourniquet application exceeding one minute causes hemoconcentration, which is an entirely avoidable preanalytical error that distorts blood components. Maintaining strict adherence to standard collection and handling steps preserves sample quality from order entry to processing.
Common mistakes
- Pre-labeling collection tubes before drawing blood, which creates a serious risk of patient misidentification and specimen rejection.
- Attempting to correct a mislabeled tube by crossing out or writing over the existing text instead of rejecting the tube.
- Vigorously shaking an anticoagulated tube rather than using gentle inversion, leading to mechanical hemolysis.
- Accepting a light blue sodium citrate tube that is filled to less than ninety percent of the required indicator line.
Key points
- Laboratory testing is divided into preanalytical, analytical, and postanalytical phases, with the majority of testing errors occurring in the preanalytical phase.
- Hemolyzed specimens appear pink to dark red and falsely elevate potassium, lactate dehydrogenase, and aspartate aminotransferase.
- Lipemic specimens appear milky or turbid due to fats, which cause optical interference with laboratory instruments.
- Anticoagulated tubes with detectable clots must be rejected, and light blue tubes filled to less than ninety percent volume must be rejected due to altered additive ratios.
- Tubes must be labeled immediately after collection in the patient's presence with all required identifiers, and mismatched or unlabeled routine tubes must be rejected without altering the label.
- When a specimen is rejected, the phlebotomist reports the required patient identifiers, any assigned accession number, the rejection reason, and the need for recollection to the nurse or supervisor, and documents the report according to facility policy.
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Sample lesson: Serum, Plasma and Clotting Before Centrifugation25 practice questions on this exam
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