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General Approach of General Approach of Haemostasis Haemostasis MIXING STUDIES MIXING STUDIES Khoa Xet Nghiem Huyet Hoc

General Approach of Haemostasis General Approach of Haemostasis MIXING STUDIES Khoa Xet Nghiem Huyet Hoc

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Page 1: General Approach of Haemostasis General Approach of Haemostasis MIXING STUDIES Khoa Xet Nghiem Huyet Hoc

General Approach of HaemostasisGeneral Approach of Haemostasis

MIXING STUDIESMIXING STUDIES

Khoa Xet Nghiem Huyet Hoc

Page 2: General Approach of Haemostasis General Approach of Haemostasis MIXING STUDIES Khoa Xet Nghiem Huyet Hoc

Mixing studies:

Mixing studies are tests performed on blood plasma used to distinguish factor deficiencies from factor inhibitors

Ex: lupus anticoagulant, or specific factor inhibitors, such as antibodies directed against factor VIII.

Page 3: General Approach of Haemostasis General Approach of Haemostasis MIXING STUDIES Khoa Xet Nghiem Huyet Hoc

Mixing studies:

Mixing studies take advantage of the fact that factor levels that are 50 percent of normal should give a normal Prothrombin time (PT) or Partial Thromboplastins time

Mixing studies can help determine the appropriate next steps to take to diagnose the cause of an abnormal APTT or PT

Page 4: General Approach of Haemostasis General Approach of Haemostasis MIXING STUDIES Khoa Xet Nghiem Huyet Hoc

Test method

The patient plasma is mixed 1:1 with Normal pooled plasma

That contains 100% of the normal factor level results in a level ≥ 50% in the mixture (say the patient has an activity of 0%; the average of 100% + 0% = 50%).

Therefore, correction with mixing indicates factor deficiency; failure to correct indicates an inhibitor.

Page 5: General Approach of Haemostasis General Approach of Haemostasis MIXING STUDIES Khoa Xet Nghiem Huyet Hoc
Page 6: General Approach of Haemostasis General Approach of Haemostasis MIXING STUDIES Khoa Xet Nghiem Huyet Hoc

Some inhibitors are time dependent. The clotting test performed immediately after

the specimens are mixed may show correction because the antibody has not had time to inactivate the added factor (false positive).

A test performed after the mixture is incubated for 2 hours at 37°C will show prolongation.

Test method

Page 7: General Approach of Haemostasis General Approach of Haemostasis MIXING STUDIES Khoa Xet Nghiem Huyet Hoc

• Many specific factor inhibitors are time dependent, and the inhibitor will not be detected unless the test is repeated after incubation (factor VIII inhibitors are notorious for this).

• Nonspecific inhibitors like the lupus anticoagulant usually are not time dependent; the immediate mixture will show prolongation.

Test method

Page 8: General Approach of Haemostasis General Approach of Haemostasis MIXING STUDIES Khoa Xet Nghiem Huyet Hoc

Reagents and Equipment

Pooled Plasma - platelet-poor plasma from 20 or more healthy, male and female adult donors. o DO NOT use a single-sourced normal

plasma. o Pooled plasma must be used to ensure

approximately 100% of all factors are present.

o Do Not Use Lyophilized Normal Control. Other reagents required to perform the

screen test(s) (i.e., PT or PTT).

Page 9: General Approach of Haemostasis General Approach of Haemostasis MIXING STUDIES Khoa Xet Nghiem Huyet Hoc

Quality ControlThe pooled plasma must be evaluated for the test to be performed and results must fall within the reference range or testing is repeated with a fresh aliquot of the pooled plasma.

Reagents and Equipment

Page 10: General Approach of Haemostasis General Approach of Haemostasis MIXING STUDIES Khoa Xet Nghiem Huyet Hoc
Page 11: General Approach of Haemostasis General Approach of Haemostasis MIXING STUDIES Khoa Xet Nghiem Huyet Hoc

Values Expected

Page 12: General Approach of Haemostasis General Approach of Haemostasis MIXING STUDIES Khoa Xet Nghiem Huyet Hoc
Page 13: General Approach of Haemostasis General Approach of Haemostasis MIXING STUDIES Khoa Xet Nghiem Huyet Hoc

Interpretation

The first step when evaluating unexpected prolonged PT or PTT results is to rule out preanalytical interference, e.g., presence of contaminating heparin.

If the APTT or PT is corrected by normal plasma, a factor deficiency is indicated.

If the APTT or PT is not corrected by the addition of nor-mal plasma immediately, a strong inhibitor is indicated.

A weak or time-dependent inhibitor is indicated by a prolonged APTT or PT following incubation at 37°C for 1 to 2 hours ( factor VIII inhibitor).

Page 14: General Approach of Haemostasis General Approach of Haemostasis MIXING STUDIES Khoa Xet Nghiem Huyet Hoc

1:1 Mixing Study Results

Not incubatedIncubated

Factor deficiencyCorrectionCorrection

Immediate acting inhibitorNo correctionNo

correction

Time/temperature dependent inhibitor

Correction (Falsely)

No correction

Table A Differentiation of Factor Deficiency and Inhibitors By Mixing Studies

Table adapted from McKenzie, S.,, Clinical l Laboratory Hematology, 2004, p. 790.

Page 15: General Approach of Haemostasis General Approach of Haemostasis MIXING STUDIES Khoa Xet Nghiem Huyet Hoc

Possible InterpretationsCoagulation Screen Results:PT prolongedPT mixing study results:PT correctsMost likely interpretation:Factor VII deficiencyProbable cause(s):Early response to warfarin, early vitamin K deficiencyRare cause:Congenital factor VII deficit

Coagulation Screen Results:PTT prolongedPTT mixing study results:PTT correctsMost likely interpretation:Factor deficit

Probable cause(s):Factor VIII or IX (male) deficiency, or von Willebrand Disease (female)Possible causeFactor inhibitor

Coagulation Screen Results:PTT markedly prolonged (>200 seconds)PTT mixing study results:PTT correctsMost likely interpretation:Severe Contact Factor deficitProbable cause(s):Factor Prekallikrein, HMWK, XI, or XII

Coagulation Screen Results:PT and PTT prolongedPT & PTT mixing study results:PT and PTT correctMost likely interpretation:Acquired, multiple factor deficiencyProbable cause(s):DIC, Liver Disease, Vitamin K deficiencyPossible cause:Warfarin therapy

Coagulation Screen Results:PTT slightly – moderately prolongedPTT mixing study results:No correctionMost likely interpretation:Immediately reacting antibody inhibitorProbable cause(s):Lupus anticoagulant

Page 16: General Approach of Haemostasis General Approach of Haemostasis MIXING STUDIES Khoa Xet Nghiem Huyet Hoc

Comment The antibody that inhibits factor VIII is most often a

specific IgG antibody (temperature and time dependent) , which will cause only a slightly prolonged APTT on initial testing.

If a factor VIII inhibitor is present, it is important to determine the initial level of factor activity because the development of an inhibitor complicates the management of a patient with hemophilia A when therapy involves AHF* concentrates. These should be monitored periodically.

Repeating the mixing study with 4 parts patient sample and 1 part normal pooled plasma may increase the chance of detecting a weak inhibitor.

Page 17: General Approach of Haemostasis General Approach of Haemostasis MIXING STUDIES Khoa Xet Nghiem Huyet Hoc

NotesNotes::

Be careful when thawing the pooled plasma because prolonged incubation at 37°C will selectively decrease Factor V, prolonging the results and making interpretation of the 1:1 mix test results difficult.

The pooled normal plasma is stable for ~2 hours at room temperature. Initial test results for the pooled normal plasma must be within the reference range or the mix should be repeated with a fresh aliquot of pooled normal plasma.

Page 18: General Approach of Haemostasis General Approach of Haemostasis MIXING STUDIES Khoa Xet Nghiem Huyet Hoc

Next Lecture: Coagulation-instruments

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