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Coag-Sense PT/INR Test Strip Shipment QC Log Sheet 2016 free printable template

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Coarsens PT/INR Test Strip Shipment QC Log Sheet Frequency of QC Testing Each New Shipment / New Lot # Date ReceivedDate TestedTested BPT Test Strips Lot #Lot #Exp. Danelaw Control Expected Range
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How to fill out Coag-Sense PTINR Test Strip Shipment QC

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How to fill out coag-sense ptinr test strip:

01
Ensure that you have the coag-sense ptinr test strip and your coag-sense ptinr testing device ready.
02
Take a clean, dry finger and prick it using a lancet provided with the test kit.
03
Allow a small drop of blood to form on your finger.
04
Gently touch the tip of the coag-sense ptinr test strip to the blood drop on your finger.
05
Make sure that the blood is absorbed into the test strip.
06
Insert the test strip into the coag-sense ptinr testing device, following the manufacturer's instructions.
07
Wait for the device to display the results, which will indicate your INR (International Normalized Ratio) value.

Who needs coag-sense ptinr test strip?

01
Individuals who are prescribed anticoagulant medication, such as warfarin, may need to regularly monitor their INR values using coag-sense ptinr test strips.
02
Patients with certain medical conditions, such as atrial fibrillation, deep vein thrombosis, or pulmonary embolism, may require regular monitoring of their INR levels.
03
People who have recently undergone certain medical procedures, such as heart valve replacement or thrombolytic therapy, may need to monitor their INR to ensure appropriate blood clotting.
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People Also Ask about

The Coag-Sense system simply lifts the fibrin clot from the reaction well which interrupts a simple light beam. The PT time is the actual time from when the blood sample is applied to when the clot is formed. This produces results similar to the gold standard WHO tilt-tube method.
The CoaguChek XS system is extremely accurate and demonstrates (97%) correlation with traditional laboratory testing methods so that you can confidently replace your lab visits with an INR test from home using the a PT/INR Meter.
Coag-Sense does not allow for the use of smaller gauge/ shallow depth lancets such as a 23g diabetes lancet. A 21g lancet must be used in order to obtain a 10 μl sample from the patient. CoaguChek allows the use of diabetes lancets and require less of a patient sample when conducting a test.
CPT Codes: 85610QW: Prothrombin Time (QW indicates a CLIA waived test)
The Coag-Sense® system is used to test prothrombin time (PT) in patients taking Warfarin for oral anticoagulant therapy. Results are reported as International Normalized Ratio, or INR units, and PT seconds. Because the system directly detects clot formation, it reports true PT-seconds.
The Roche CoaguChek® XS performs quantitative prothrombin time testing for the monitoring of warfarin therapy. The monitor provides results in less than a minute and features built-in quality control to ensure each test is accurate.
What is the CoaguChek? The CoaguChek monitor is a hand-held device that is used to measure the international normalised ratio (INR) in individuals taking warfarin. The INR is a laboratory measurement used to determine the effects of oral anticoagulants (warfarin) on the clotting system.

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Coag-Sense PTINR Test Strip Shipment QC refers to the quality control procedures and documentation required for the shipment of Coag-Sense PTINR Test Strips, which are used to measure prothrombin time and INR levels in patients on anticoagulant therapy.
Manufacturers, distributors, and laboratories involved in the shipping of Coag-Sense PTINR Test Strips are required to file Coag-Sense PTINR Test Strip Shipment QC to ensure compliance with quality standards.
To fill out Coag-Sense PTINR Test Strip Shipment QC, enter the necessary details such as the batch number, expiration date, quantity shipped, and any applicable quality control results. Ensure that all sections are completed accurately and submitted as required.
The purpose of Coag-Sense PTINR Test Strip Shipment QC is to ensure that the test strips shipped meet quality and performance standards, thereby ensuring the reliability of INR measurements for patient care.
Information that must be reported includes the product name, lot number, shipping date, quantity shipped, expiration date, and any relevant quality control test results.
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