Guideline for Collecting & Handling Specimen
Proper specimen management is the first step in ensuring test accuracy
At ProCare Medical Laboratory, we are committed to delivering accurate and reliable diagnostic results. Adhering to these guidelines ensures that specimens are collected in a manner that minimizes contamination and degradation. Thus, clinicians can enhance the quality of specimens submitted to our laboratory, ultimately leading to more accurate test results.
General Guidelines
Pre-collection
- Each test may have specific criteria due to biological variability, as different markers respond uniquely to factors like food intake and medications. Additionally, various analytical methods require particular specimen handling to maintain sample integrity.
- To ensure optimal diagnostic accuracy, it is essential to provide patients with clear instructions ahead of time regarding fasting and medication restrictions.
- For detailed requirements, please refer to the guidelines outlined in our price book, as each test may have unique specifications.
Specimen collection
All specimens will be collected as soon as the laboratory is informed. Urgent laboratory tests requested by physicians can be arranged.
Different specimen containers may be required for different tests. Please check the "Specimen Requirement" column or phone us if in doubt.
To ensure result accuracy, specimens will be rejected under the conditions in the "Specimen Rejection Principles".
Storage and transportation
- Collected specimens must be stored at room temperature or according to the conditions specified for each test prior to pickup. Time-sensitive tests will be indicated in the specimen requirement column. It is important to inform the laboratory before specimen collection so that any special pickup arrangements can be made.
- Specimens collected can be sent to our locations either on your own or by calling our courier service for pickup. See details here for sending a specimen.
Recommendations for blood specimen collection by Venipuncture
(CLSI GP41-A6 Guidelines)
- Tourniquet Application: The tourniquet must not be applied for more than one minute prior to accessing the vein to prevent hemoconcentration.
- Syringe Use: Syringes should not be used for trace element collections that include testing for cobalt and chromium, as the plunger tip can contaminate the specimen with these elements.
- Order of Draw: Blood-collection tubes must be filled in a proper order to prevent the carryover of additives from one tube to the next. Such carryover can alter the composition of subsequent tubes, leading to erroneous results and potentially misleading physicians, which may result in critical errors in patient management. Adherence to the Clinical Laboratory Standards Institute (CLSI) guidelines for the order of draw is essential.
Improvacuter tubes are recommended for mixing immediately after collection. Insufficient mixing might result in inaccurate test results and the need to re-draw REF: NCCLS H3-A5 Vo 23. No.32, 8.10.2.
Tube Closure Color | Container | Additive | Testing Disciplines | Number of Inversion |
---|---|---|---|---|
No Additive Tube or Blood Culture Bottle | - | Biochemistry test Immunology test |
0 | |
Sodium Citrate 1:9 | Sodium citrate 0.129mol/L 0.109mol/L |
Coagulation determinations on plasma specimens | 3-5 | |
Sodium Citrate 1:4 | Sodium citrate 0.129mol/L 0.109mol/L |
Erythrocyte Sedimentation Rate (ESR) | 3-5 | |
Pro-coagulation | Clot activator | Serum determinations in clinical chemistry | 3-8 | |
Gel & Clot Activator | Gel & Clot activator | Biochemistry test | 3-8 | |
Heparin | Lithium heparin | Plasma determinations in clinical chemistry and hematology | 3-8 | |
Gel & Heparin | Gel & Lithium heparin Gel & Sodium heparin |
Plasma determinations in clinical chemistry | 3-8 | |
EDTA | EDTA K2 EDTA K3 |
Whole blood hematology determinations | Liquid: 3-5 Spray dried: 5-8 |
|
Glucose | Sodium Fluoride/EDTA Sodium Fluoride/oxalate |
Glucose determinations | 5-8 | |
Gel & EDTA K2 | Gel & EDTA K2 | Plasma preparation for molecular diagnostic and virus load testing | 5-8 |
Abbreviation
Abbreviation for Specimens
Short Form | Stands For |
---|---|
ACD | Whole blood |
CB | Clotted blood (gel) |
CB-Plain | Clotted blood (no gel) |
Cit. B | Citrated blood |
EDTA | EDTA blood |
EDTA-Trace wb | EDTA whole blood for trace elements |
FB | Fluoride blood |
Li-Hep | Lithium Heparin blood |
T183 | EDTA blood - metal-free |
T184 | Clotted blood - metal-free |
MSU | Mid-stream urine |
EMU | Early morning urine |
Abbreviation for Test Categories
Letters | Stands For |
---|---|
R | Routine tests performed daily |
S | Special tests performed every 2-6 days |
T | Send-out test (to local or overseas laboratories) |
Preservatives
24-hour Urine Specimen Preservatives
Test Name | Preservative Requirements |
---|---|
5-HIAA | 25mL of 50 Acetic Acid |
Albumin (microalbumin) | No preservative |
Calcium | Refrigerated with no preservative |
Catecholamine Fractions | 25mL of 50 Acetic Acid |
Citrate | Refrigerated with no preservative |
Copper | 25mL of 50 Acetic Acid |
Cortisol | No preservative |
Cortisol, Free | 10g of Boric Acid |
Creatinine | No preservative |
Creatinine Clearance | No preservative |
Metanephrines, Fractionated | 25mL of 50 Acetic Acid |
Phosphorus | No preservative |
Electrolytes (Na, K, Cl) | No preservative |
Uric Acid | No preservative |
Vaillylmandelic Acid (VMA) | 25mL of 50 Acetic Acid |
Specimen rejection principles
To ensure result accuracy, ProCare Medical Laboratory has established specimen rejection criteria in accordance with ISO 15189 requirements and Good Laboratory Practice (GLP) recommendations.
Specimens will be rejected under the following conditions, except in specific cases where the specimen is rare, involves an invasive procedure, or cannot be easily recollected:
- Unlabeled Specimens
- Incorrectly Labeled Specimens/Request Forms
- Improper Containers: This includes incorrect preservatives, inappropriate anticoagulants, or containers that may be contaminated with interfering chemicals or cleaners.
- Inappropriate Specimen Conditions for Testing:
- Specimen is hemolyzed.
- Specimen is milky due to chylomicrons.
- Specimen has been stored too long before collection and transportation.
- Specimen was collected at the wrong time for a timed test.
- Specimen was collected from a non-fasting patient when fasting is required.
- Specimen was taken from patients using drugs or vitamins that may interfere with test results.
- Specimen was collected or transported in an unsuitable medium.
- Urine and stool specimens lack a recorded collection time.
- Urine or stool specimens for routine, culture, or drug sensitivity tests that are kept at room temperature for more than 8 hours or refrigerated for more than 24 hours.
Material Request
Only for requests from healthcare providers. PDF version of the test request form can be downloaded here.
Disclaimer
The information provided on this page is for general guidance only and may not reflect all details. Specific handling may vary depending on individual circumstances, including the specific test required and other factors.
We encourage you to contact us directly at 3529 1983 to discuss your specific needs.