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AATHR / Thrombophilia Profile, Plasma and Whole Testing begins with: ■ (PT), Plasma ■ Activated Partial Time (APTT), Plasma ■ Dilute Russells Viper Venom Time (DRVVT), Plasma ■ Time (Bovine), Plasma ■ , Clauss, Plasma ■ D-Dimer, Plasma ■ Activity, Plasma ■ Activity, Plasma ■ Antigen, Free, Plasma ■ A Mutation, Blood ■ Activated Protein C Resistance V (APCRV), Plasma ■ Thrombophilia Interpretation

PT: ≥14.0 seconds APT T: >37 seconds DIMER: Fibrinogen: DRV V T: ≥1.20 (Bovine) APCRV: Protein C Protein S Antigen, Free: Antithrombin Activity: >500 ng/mL FEU <150 mg/dL ■ Ratio <2.3 or Activity: ■ Males <65% ■ <80% indeterminate ■ <70% ■ Females ■ No evidence of an AND <50 years: <50% acquired deficiency PT Mix 1:1 APTT Mix 1:1 DRVVT Mix ≥1.20 DRVVT Mix <1.20 ■ PT ≤12.5 ≥50 years: <65% Soluble fibrin PT-Fibrinogen DRVVT Confirm ≥1.20 DRVVT Confirm <1.20 15.8–24.9 seconds >24.9 seconds seconds ≥14.0 seconds <14.0 seconds monomer OR OR DRVVT Mix <1.20* DRVVT Mix ≥1.20 DRVVT Confirm ≥1.20 DRVVT Confirm <1.20 Normal–no evidence Reptilase Time Antithrombin Evidence of Evidence of Evidence of inhibition of or dys/ Leiden Protein C Protein S antigen, total antigen inhibition** factor hypofibrinogenemia (R506Q) mutation antigen deficiency** No evidence of heparin in sample Not diagnostic of 14.0–23.9 seconds >23.9 seconds All initial testing within reference ranges for age and gender: Suggestive of ■ No evidence of thrombotic diathesis neutralization coagulation factor Anticoagulant Possible dys/ ■ No further testing is performed procedure (PNP) deficiency or effect*** hypofibrinogenemia** anticoagulation effect** Does not shorten Shortens by 4–5 seconds

Possible factor inhibitor but does Probable if not exclude lupus anticoagulant** anticoagulation effect can be excluded**

*Weak lupus anticoagulant may not inhibit DRVVT mix **Additional assays may be performed if further clari cation or con rmation is necessary. These may include: • Coagulation Factor Assays • Staclot Lupus Anticoagulant • Protein S Activity *** Unfractionated/low-molecular weight heparin or direct thrombin inhibitor (eg, dabigatran, ) or low concentration of direct anti-Xa inhibitor (eg, rivaroxaban, apixaban, or edoxban)

An interpretive report is provided that includes all pro le tests (always performed) and any re ex tests performed (if appropriate). © Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. 04/2020