Nonsevere Hemophilia A Profile

CPT: 80503; 85240(x2); 85730
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Test Includes

aPTT; factor VIII activity; factor VIII chromogenic; pathologist interpretation


Expected Turnaround Time

4 - 7 days


Related Documents


Specimen Requirements


Specimen

Plasma


Volume

4 mL platelet-poor, frozen, citrated plasma divided into two tubes


Minimum Volume

2 mL


Container

Blue-top (sodium citrate) tube


Collection

Plasma must be separated from cells within three hours of venipuncture and plasma centrifuged a second time before being placed in plastic transport tubes. Freeze within four hours and keep frozen until testing is performed.


Storage Instructions

Freeze


Causes for Rejection

Noncitrated plasma; gross hemolysis; fibrin clot in plasma; sample received thawed


Test Details


Use

This profile is appropriate for the evaluation of individuals suspected of or previously identified as having nonsevere (mild or moderate) hemophilia A, in order to determine if there is a twofold discrepancy in the one stage and chromogenic factor VIII activities as has been described in discrepant hemophilia A. Evaluation for nonsevere hemophilia A using a one stage (clot-based) activity assay only may lead to missed diagnosis or misclassification of disease severity.


Methodology

See individual tests.


LOINC® Map

Order Code Order Code Name Order Loinc Result Code Result Code Name UofM Result LOINC
504297 Non-Severe Hemophilia A Prof. 500513 APTT sec 14979-9
504297 Non-Severe Hemophilia A Prof. 500666 Factor VIII Activity % 3209-4
504297 Non-Severe Hemophilia A Prof. 500193 FVIII Chromogenic % 49865-9
504297 Non-Severe Hemophilia A Prof. 500684 Pathologist Interpretation 21026-0

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