Platelet disorders Flashcards

1
Q

What are the clinical signs of Thrombocytopenia?

A
  • Petechiae and ecchymoses common
  • Hematomas are rare
  • Bleeding often involves mucus membranes
  • Bleeding usually at multiple sites
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2
Q

Why would patients have petechiae (bleeding)?

A
  • Defect in vessels
  • Defect in primary hemostasis
  • Defect in secondary hemostasis
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3
Q

How are Primary and secondary hemostatic disorders differentiated?

A
  • Primary:
    • Most common: Petechiae, ecchymoses
    • Also: Epistaxis, hematuria, GI hemorrhage, prolonged wound bleeding
  • Secondary:
    • Most common: Hematoma, hemarthrosis, hemoptysis
    • Also: Epistaxis, melena, hematochezia, hematemesis, prolonged hemorrhage
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4
Q

How is Primary Hemostasis tested for?

A
  • Buccal Mucosal Bleeding time
    • not a reliable indicator of vascular integrity
    • Prolonged with vWd and thrombopathy
  • Von Willebrand’s factor Antigen assay
    • Important for certain reeds
  • Platelet count
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5
Q

How is Secondary Hemostasis tested for?

A
  • Partial thromboplastin Time (PTT)
  • Prothrombin time (PT)
  • Proteins induced by vitamin K antagonists (PIVKA)
  • Specific Clotting factor assays
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6
Q

What are the general rules for thrombocytopenia?

A
  • Platelet count <50,000 for bleeding
    • Often <30,000 in dogs
    • <10,000 in cats
  • Severity helps predict disease
  • presence of other diseases ⇢ DIC
  • Bone marrow evaluation not helpful
  • Primary autoimmune disease of cats is rare
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7
Q

What causes thrombocytopenia?

A
  • Decreased production (Bone Marrow disorder)
    • Drug-induced (Cytotoxic drugs, TMS, estrogen)
    • Myelofibrosis (Idiopathic, immune mediated)
    • Neoplasia (-phthisis, -dysplasia, -proliferative disease)
    • Infection (FeLV, FIV, Chronic ehrilichiosis)
  • Increased Consumption
    • Immune-mediated thrombocytopenia (1o, 2o)
  • Increased utilization
    • Disseminated Intravascular Coagulation
    • Hemorrhage
    • Vasculitis (acute, ehrlichiosis, immune, RMSF)
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8
Q

What diagnostic tests are considered when diagnosing thrombocytopenia?

A
  • Platelet indices (MPV): no support in aiding a diagnosis
  • Coagulation panel, d-dimers: rule out DIC
  • Tick-borne disease screening (4DX, serology, PCR)
  • Radiographs, ultrasonography
  • Immunological tests: PSA-Ig, ANA
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9
Q

How is Immune-mediated Thrombocytopenia (ITP) diagnosed?

A
  • Anti-platelet antibody testing
    • Flow cytometry
  • Diagnosis of Exclusion
  • Predicted by platelet count
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10
Q

What is the presentation of Immune-mediated Thrombocytopenia?

A
  • Bleeding (75%)
  • Splenomegaly (60%)
  • Platelet count <30,000 (80%), <8000 (50%)
  • Anemia (40%) from blood loss
  • 90% survival rate
  • 25% recurrence rate
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11
Q

What are the possible outcomes of Immune-mediated Thrombocytopenia?

A
  • Recovery after a single event
  • Recurrent
  • Chronic ITP
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12
Q

What are the treatment options for Immune-mediated thrombocytopenia?

A
  • Blood product options:
    • Fresh Whole Blood/PRBC: used to correct anemia
    • Platelet-rich plasma: misnomer
  • Immunosuppressive Therapy
    • Rapid Acting drugs
      • Prednisone: 2-4 mg/kg/day, inhibits uptake platelets
      • Vincristine: Paralyze RES or Forced maturation
      • Intravenous gamma globulin: Flood RES; anti-idiotypic Abs
    • Moderate acting: cyclosporine, leflunomide
    • Slow acting: Azathioprine, Mycophenolate
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13
Q

What are causes of thrombocytopenia in cats?

A
  • FeLV, FIV
  • FIP
  • Lymphoma/Leukemia
  • Immune-mediated
  • Histoplasmosis
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14
Q

What is Disseminated Intravascular Coagulation (DIC)?

A
  • Consequence/complication of other disease
  • Paradox of thrombosis and hemorrhage
  • Diagnosis:
    • Markedly increased D-dimer and FDPs
    • Prolonged APTT/PT
    • Thrombocytopenia
    • Schistocytes, reduced (fibrinogen)
  • Treat underlying cause, FFP, heparin
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15
Q

What is Systemic Lupus Erythematosus?

A
  • Multi-organ autoimmune disease
  • Variable symptoms/presentations
  • Classic descriptions:
    • Major/Minor signs
    • ANA/LE prep
  • Less rigid/stringent definitions
  • Not all are positive on Anit-Nuclear Antibody (ANA)
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16
Q

What are the signs of SLE?

A
  • Fever: constant or cyclic
  • Polyarthritis (nonerosive)
  • Glomerulopathy
  • Dermatologic lesions
  • IMHA, ITP, Leukopenia
  • Polymyositis, dermatomyositis, pleuritis/pericarditis, polyneuritis/CNS, hepatic disease, rhinitis, pneumonitis
17
Q

What laboratory Diagnostics are used for SLE?

A
  • Anti-Nuclear Antibody
    • Positive in 97-100% of dogs
    • False positive occur
  • Other tests not used in dogs:
    • LE prep test
    • ANti-histone antibodies
    • Anti-extractable nuclear antigen antibodies
    • Anti-SR protein antibodies
18
Q

What is the treatment for SLE?

A

Similar to IMHA or ITP

19
Q

What are Thrombotic Disorders?

A
  • Occurs when conditions promote blood stasis, vascular injury and hypercoagulability
  • Clinical manifestations
    • Acute paralysis
    • Dyspnea
    • Abdominal Pain
  • Diagnostic tests
    • Determined by underlying condition
    • D-dimer, antithrombin, TEG
20
Q

What are the etiologies of Thromboembolic Disease

A
  • Cardiac disease - HCM, DCM, CHF
  • Corticosteroid therapy
  • DIC
  • Endocrine disease - Cushing’s, Hypothyroidism
  • Heartworm disease
  • Immunological disease - IMHA, SLE
  • Neoplasia
  • Acute Pancreatitis
  • Protein-losing nephropathy
  • Protein-losing enteropathy
  • Trauma
21
Q

How is Thromboembolic Disease treated?

A
  • Treat underlying disorder
  • Clopidogrel