COLLECTION AND PREPARATION Sample Clauses

COLLECTION AND PREPARATION. The aPTT test cards may be used with citrated whole blood or plasma collected and processed according to the CLSI Guideline: Collection, Transport and Processing of Blood Specimens for Testing Plasma-Based Coagulation Assays and Molecular Hemostasis Assays, H21-A5.3 Add whole blood to 109 mM (3.2%) of the dihydrate form of sodium citrate, in a proportion of nine parts whole blood to one part anticoagulant. Mix the blood by gentle inversion with the anticoagulant immediately on collection. Test whole blood specimens within 30 minutes of collection.10 CAUTION: Clot times may be affected due to improperly filled sodium citrate blood collection tubes. CAUTION: When handling blood specimens, all samples should be treated as biohazards.7-9 Materials provided: The following materials are contained in the Abrazo aPTT Test Kit (Cat. No. 5722).
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COLLECTION AND PREPARATION. Specimen: Plasma obtained from whole blood with 3.8% sodium citrate as an anticoagulant is the specimen of choice. Specimen Collection: Blood may be collected with evacuated test tubes, a 2-syringe technique, or with a butterfly and syringe technique. Accurate coagulation studies depend on the correct whole blood to anticoagulant ratio. For blood specimens with hematocrits (HCT) of 40-50% (normal), 9 parts of freshly collected whole blood should be immediately added to one part anticoagulant. For blood specimens with hematocrits outside the normal range, adjust the amount of whole blood added to the anticoagulant according to the following formula.5 Parts whole blood to 0.6
COLLECTION AND PREPARATION. The c-ACT test cards may be used with noncitrated whole blood collected according to recognized standards for the handling of blood specimens for blood coagulation studies.4 Test noncitrated whole blood specimens immediately after collection. • Cascade POC analyzer • Cascade POC Operator’s Manual • Blood sampling materials such as venipuncture needles, syringes, alcohol swabs, vacuum tubes • Sample transfer devices (pipettes or droppers) capable of delivering approximately 30 to 35 µL • Quality Control material 1. Equilibrate test cards at room temperature (20 to 25°C or 68–77°F) before removing from the foil pouch. CAUTION: The test card must be used within 15 minutes after the pouch is opened. Pouches of cards should not be repeatedly warmed and returned to the refrigerator. 2. Remove the test card from its foil pouch and hold it so that the full test name is right side up and facing you. 3. Pass the test card firmly and steadily through the card reader. The analyzer interprets the encoded information on the test card and displays prompts for each step of the procedure. 4. When prompted, place the test card in the analyzer, and allow to warm.
COLLECTION AND PREPARATION. The aPTT test cards may be used with citrated whole blood or plasma collected and processed according to the CLSI Guidline: Collection, Transport, and Processing of Blood Specimens for Testing Plasma-Based Coagulation Assays and Molecular Hemostasis Assays, H21-A5.3 Add whole blood to 109 mM (3.2%) of the dihydrate form of sodium citrate, in a proportion of nine parts whole blood to one part anticoagulant. Mix the blood by gentle inversion with the anticoagulant immediately after collection. Xxxxxx recommends testing citrated whole blood specimens within 30 minutes of collection. Materials provided: The following materials are contained in the Cascade POC aPTT Test Kit (Cat. No. 5822).
COLLECTION AND PREPARATION. The specimen of choice is citrated whole blood or plasma collected and processed according to the CLSI Guideline: Collection, Transport and Processing of Blood Specimens for Testing and Plasma-Based Coagulation Assays and Molecular Hemostasis Assays, H21-A5.5 Add whole blood to 109 mM (3.2%) of the dihydrate form of sodium citrate, in a proportion of nine parts whole blood to one part anticoagulant. Mix the blood by gentle inversion with the anticoagulant immediately after collection. Xxxxxx recommends testing whole blood specimens within 30 minutes of collection, especially if the patient is being monitored for heparin therapy. Specimen Preparation: Centrifuge the whole blood specimen at 1600-2000 X G for 10 minutes. Immediately separate the plasma from the red blood cells, and place it in a plastic test tube with cap. Storage and Stability: Prior to testing, the plasma should be stored in the capped plastic tubes at 2 to 8°C. If testing is delayed for more than 2 hours, the plasma may be stored at -20°C or colder for up to one month. Thaw quickly at 37°C prior to testing, but do not allow to stand at 37°C for more than 5 minutes. Cat. No. Factor XI Deficient Substrate Plasma 5196 Xxxxxx XXXX-SA Reagent Kits 10 x 10 mL - 500 tests 5389
COLLECTION AND PREPARATION. Specimen: The plasma collected by venipuncture with either 3.2% or 3.8% sodium citrate as an anticoagulant should be used. Centrifuge sample immediately and remove the plasma. Storage and Stability: Store at 2-8°C until testing can be performed. If not tested within 1 hour of collection, the sample must be stored at -70°C and tested within 1 month.
COLLECTION AND PREPARATION. The donor’s identification shall always be verified upon arrival at the collection site. The use of a photo identification card (passport, employee’s license, employee card, etc.) is usually the preferred method of identification, but alternate means, such as the use of an accompanying employee representative is acceptable. Once donor identification has been verified, STEP 1 of the chain of custody requisition should be completed. Contact a company representative for the employee if identification cannot be verified.
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