Lab Guide
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Test ID: Factor XIII
Factor XIII Assay
Useful For

To detect deficiency of Factor XIII. Monitoring of substitution therapy with Factor XIII concentrate

Method name and description

Chromogenic.
Test is performed using Sysmex CS5100 analyzer. FXIII in the sample is converted by the action of thrombin in to FXIIIa. Fibrin formed by thrombin also accelerates this reaction. Fibrin produced by the action of thrombin is prevented from forming clots by an aggregation inhibiting Peptide and held in solution.
FXIIIa cross-links a specific peptide substrate to glycine ethyl ester, thereby releasing ammonia. The ammonia released is then determined in a parallel enzymatic reaction.
The decrease in NADH is measured by monitoring the absorbance at 340 nm.

Reporting name

Factor XIII

Clinical information

Factor XIII is responsible for stabilizing  a fibrin  clot. Factor XIII deficiency is an extremely rare autosomal recessive bleeding disorder. Homozygous individuals (FXIII <1%) experience soft tissue hemorrhage, hemarthrosis, and hematomas. Typically, as delayed bleeding start 24 to 48 hours after the initial hemostatic response to an injury. Heterozygous carriers may be asymptomatic; however, may cause recurrent spontaneous abortions in females.
Acquired factor XIII deficiency is rare, occurs as a result of development of autoantibodies and result in adult-onset bleeding.

Specimen type / Specimen volume / Specimen container

Plasma Na Cit. Platelet-poor plasma.
Specimen Volume:2.7 ml.
Container/Tube: Light-blue top (citrate)

Collection instructions / Special Precautions / Timing of collection
  1. Samples collected in HMC facilities MUST reach the coagulation laboratory within 1 hour of collection.
  2. Samples collected in non-HMC facilities / external clients: MUST reach coagulation laboratory within 1 hour of collection, if not applicable, centrifuge the whole blood and carefully remove the plasma (by pipette not by decanting) and send it in a temperature-controlled environment (18- 25 ºC) within 2 hours of centrifugation. If the transportation of the plasma can’t be within a maximum of 2 hours, prepare platelet-poor plasma as follows:
  • Re-centrifuge the plasma again.
  • Remove the top portion of plasma leaving approximately 250 ul in the bottom to discard.
  • The double-centrifuged plasma should be aliquoted into labeled plastic tubes.
  • Freeze immediately at -20 ºC or below
  • Specimens must arrive frozen.
  1. If patient HCT is >55%, test will not be processed. The ordering Physician will be contacted to reorder the test and call the patient to go to Phlebotomy for recollection. Instruct the patient to inform the phlebotomy   about his high HCT% , the phlebotomy will contact the lab to request a coagulation tube after adjusting amount of anticoagulant.

 

Note:

Collection of blood for coagulation testing through intravenous lines that have been previously flushed with heparin should be avoided, if possible. If the blood must be drawn through an indwelling catheter, possible heparin contamination and specimen dilution must be considered. When obtaining specimens from indwelling lines that may contain heparin, the line should be flushed with 5 mL of saline, and the first 5 mL of blood or 6-times the line volume (dead space volume of the catheter) be drawn off and not used for coagulation testing. For those specimens collected from a normal saline lock (capped off venous port) twice the dead space volume of the catheter and extension set should be discarded.

Relevant clinical information to be provided

Patient/family history of bleeding c disorder.  History of chronic diseases .

Storage and transport instructions

Ambient

Specimen Rejection Criteria

Specimens with no label or missing required identification
Broken, leaking or contaminated specimen
Clotted samples 
Under-filled or overfilled sample tubes.
Wrong sample container sample received
Improper specimen transport temperature (e.g. like specimens which are  needed to be sent on ice)
Old specimen (test-dependent) 
Grossly Hemolyzed sample (test-dependent)                                          

Biological reference intervals and clinical decision values

For age > 18 years:    : 70 – 140 %.

For age ≤18 years:  :

* Reference Interval: Factor levels are expressed as percent of blood plasma concentration. By definition, pooled plasma contains 100 %(1unit/ml) of each factor.

 * The reference range is quoted from literature. The reference range values have not been verified /established by lab.

Minutes-4 Days

4 Days-1 Months

1 Months-6 Months

6 Months-1 Years

1 Years-5 Years

5 Years-10 Years

10 Years-18 Years

27-131

44-144

63-152

42-128

71-139

76-133

64-133

 

Factors affecting test performance and result interpretation

No interference up to:
Triglycerides 149 mg/dL.
Hemoglobin 600 mg/dL 600.
Hemoglobin 600 mg/dL 600.

Turnaround time / Days and times test performed / Specimen retention time

For routine ordered test : 3 working days

For stat ordered test :

  • During the Laboratory working hours from 0700 hours to 1500 hours (Sunday to Thursday): TAT is Within 8hrs.
  • After duty hours, weekends and on holidays: TAT is within  12 hrs. with the following requirements:
  • Laboratory should  be notified by telephone about the sending  of a STAT sample.
  • The sample should  be hand-delivered to the central processing area and requesting  them to deliver it immediately to the hematology coagulation lab.

 Test is done : Daily.

Specimen retention time: NA