Page 1420 - Small Animal Internal Medicine, 6th Edition
P. 1420

1392   PART XIII   Hematology



                   TABLE 87.2
  VetBooks.ir  Interpretation of Hemostasis Screens ACT  OSPT*  aPTT    PLATELETS    FIBRINOGEN      FDP/D-DIMER

                                 BT
             DISORDER
             Thrombocytopenia    ↑        N         N         N         ↓            N               N
             Thrombocytopathia   ↑        N         N         N         N            N               N
             vWD                 ↑        N/↑?      N         N/↑?      N            N               N
             Hemophilias         N        ↑         N         ↑         N            N               N
             Rodenticide toxicity  N/↑    ↑         ↑↑        ↑         N/↓          N/↓             N/↑
             DIC                 ↑        ↑         ↑         ↑         ↓            N/↓             ↑
             Liver disease       N/↑      ↑         N/↑       ↑         N/↓          N/↓             N

            ACT, Activated coagulation test; aPTT, activated partial thromboplastin time; BT, bleeding time; DIC, disseminated intravascular coagulation;
            FDP, fibrin degradation product; N, normal or negative; OSPT, one-stage prothrombin time; vWD, von Willebrand disease; ↑, high or
            prolonged; ↓, decreased or shortened; ?, questionable.
            *OSPT and aPTT are considered prolonged if they are 25% or more than the concurrent controls.


            Unfortunately, the BMBT has high interoperator and intra-   TABLE 87.3
            operator variability (as high as 80%), and the results are not
            reproducible, even by the same operator. The PFA-100 (see   Specimens Required for Laboratory Evaluation
            later) has largely replaced the BMBT in most veterinary   of Hemostasis
            teaching hospitals.
              By performing these simple tests after evaluating the clin-   TUBE TOP
            ical features of the bleeding disorder, the clinician should be   SAMPLE  COLOR  TEST(S)
            able to narrow down the number of differential diagnoses.   EDTA   Purple   Platelet count
            For example, the blood smear evaluation reveals whether   blood
            the patient is thrombocytopenic or not. If the patient is   Citrated   Blue  OSPT, aPTT, fibrinogen, AT,
            not thrombocytopenic but petechiae and ecchymoses are   blood                 vWF, clotting factor assays,
            present, a prolonged bleeding time or PFA-100 closure time                    D-dimer, TEG, PFA-100
            support the existence of a platelet function defect (although   Thrombin  Blue  FDP
            this situation is uncommon). A prolonged ACT or aPTT
            indicates an abnormality in the intrinsic or common path-  aPTT, Activated partial thromboplastin time; AT, antithrombin;
            ways, a prolonged OSPT documents a defect in the extrin-  EDTA, ethylenediamine tetraacetic acid; FDP, fibrin degradation
            sic pathway (i.e., factor VII), and a positive test result for   product; OSPT, one-stage prothrombin time; PFA-100, platelet
            FDPs or  D-dimer supports the presence of primary or     function analyzer; TEG, thromboelastograph; vWF, von Willebrand
            secondary fibrinolysis.                              factor assay.
              If further confirmation of a presumptive diagnosis is
            required, plasma can be submitted to a referral laboratory or   A routine coagulation screen (or hemostatic profile)
            a specialized coagulation laboratory (see  p. 1393). Most   usually contains the OSPT, aPTT, platelet count, fibrino-
            commercial veterinary diagnostic laboratories routinely   gen concentration, and FDP and D-dimer concentration. In
            evaluate hemostatic profiles. Samples should be submitted in   some laboratories, AT activity may also be included. The
            a purple-topped tube (sodium EDTA) for platelet count, a   OSPT primarily evaluates the extrinsic pathway, whereas
            blue-topped tube (sodium citrate) for coagulation studies   the aPTT primarily evaluates the intrinsic pathway. Because
            (OSPT,  aPTT,  fibrinogen  concentration,  D-dimer),  and  a   the end product in these assays is always fibrin formation,
            special blue-topped tube (Thrombo-Wellcotest, Thermo   both tests also evaluate the common pathway (see Fig. 87.2).
            Fisher  Scientific,  Lenexa,  KS)  for  FDP  determination  (the   The D-dimer assay evaluates for systemic fibrinolysis, as does
            last tube is usually supplied by the diagnostic laboratory).   the FDP test; however, as noted, the D-dimer is formed after
            The blue-topped tubes are now primarily available in 3.2%   fibrin has been stabilized by factor XIII. Thus it is more
            sodium citrate concentrations. The results of routine hemo-  indicative of intravascular thrombus formation. The inter-
            stasis assays are not affected by the concentration of citrate   pretation  of  routine  hemostasis  profiles  is  summarized  in
            used (Morales et al., 2007). It is important to submit the right   Table 87.2.
            samples in the appropriate anticoagulant. The guidelines for   New instruments now allow evaluation of other aspects
            sample submission to commercial laboratories are summa-  of hemostasis. For example, the platelet function analyzer
            rized in Table 87.3.                                 PFA-100 (Siemens Healthcare Diagnostics, Deerfield, IL) is
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