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Test Code:
090-91-0051

Order Name:
POCT - PT/INR

 
Useful For:
  1. The determination of the prothrombin time in patients with suspected deficiencies of coagulation factors of the extrinsic and common pathway, with the exception of fibrinogen
  2. Monitoring of patients on oral anticoagulant therapy with vitamin K antagonist
 
Methodology:
Electrochemical, Human recombinant tissue factor: Coagu-Chek Pro II devices
 
Test List In Profile:
POCT PT
POCT INR
 
AliasesName:
Coagu-Chek PT
POCT PT
POCT INR
 
 
 
Test Code:
090-91-0051

Order Name:
POCT - PT/INR

 
Collection Specimen Or Container:
Fresh whole blood (Bedside testing)
 
Specimen Testing Type:
Fresh whole blood:
Venous blood, Test volume 8 uL
Arterial blood, Test volume 8 uL
Capillary blood, Test volume 8 uL
 
Rejection Criteria:
  1. Clotted specimen will be reject.
  2. Specimen of patients treated with protamine sulfate can not be tested with this system.
 
Specimen Stabillity:
Test should be done Immediately.
 
 
 
Test Code:
090-91-0051

Order Name:
POCT - PT/INR

 
Method detail:
Electrochemical, Human recombinant tissue factor: Coagu-Chek Pro II devices
 
Schedule:
Test Daily (24 Hours)
 
Turnaround Time:
Collected specimen to report within 1 minute (Bedside testing)
 
Performing Location:
POCT, bedside
 
 
 
Test Code:
090-91-0051

Order Name:
POCT - PT/INR

 
 
Clinical Information:
  1. Anti-phospholipid antibodies (APA) such as Lupus antibodies (LA) may prolong the PT depending on the type and concentration of APAs
  2. Anticoagulants other than vitamin K antagonists (e.g. hirudin, dabigatran and other thrombin inhibitors, direct Factor Xa-inhibitors) may prolong PT
 
Reference Value:
Test Reference Value Unit
General patients POCT PT 10.9 - 13.4 Seconds
POCT INR 0.9 - 1.1 -
Patient with wafarin therapy POCT INR 2.0 - 3.0 -
 
Clinical Reference:
  1. CoaguChek Pro II Operator’s Manual; 2015-11 V2.0, Roche Diagnostics.
  2. CoaguChek PT Test strip package insert; 2016-05 V1.0, Roche Diagnostics.