T14 - Trombose Venosa Profunda Flashcards

1
Q

DVT?

A

Deep Venous Thrombosis

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2
Q

Importance of DVT?

A
  • 3rd cause of cardiovascular mortality afrter MI and Stroke
  • Incidence increases two-fold per 20y age increase
  • African Americans have an higher incidence, asians lower
  • recurrence rate 10% at one year
  • post-thrombotic syndrome 20-50%; severe 5-10%
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3
Q

Clinical manifestations of DVT?

A
Asymptomatic
Edema
Pain
Decreased mobililty
Feeling of heaviness
Prominent superficial veins
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4
Q

O que pode ocorrer no edema?

A

Oclusão arterial por compressão do edema, por exemplo em situações em que já existe défice

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5
Q

Location of DVT?

A
  • isolated calf 30%
  • iliofemoral 30-40%
  • iliofemoral DVT is more commonly left-sided
  • recanalization rate: 80% calf, 20% iliac
  • overall incidence of venous VTE around 25% higher with thle addition of pulmonary embolism (PE)
  • upper extremity DVT <5%
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6
Q

How to confirm diagnosis of DVT?

A
    • Clinical assessement and pretest probability score (Wells criteria)
    • D-dimer measurement
    • Duplex ultrasound

– other imaging modalities; MRV, CTV, Venography

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7
Q

Disorders that can mimic DVT?

A
  • lymphoedema
  • superficial vein thrombosis
  • post-thrombotic syndrome
  • cellulitis
  • ruptured Baker’s cist
  • trauma
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8
Q

Acute and chronic complications?

A
  • pulmonary embolism
  • phlegmasia alba dolens
  • phlegmasia cerulea dolens
  • venous grangrena
  • post-thrombotic syndrome
  • chronic thromboembolic pulmonar hypertension
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9
Q

Virchow’s triad?

A
    • increased procoagulant activity in the blood
    • vein wall damage
    • impaired venous flow
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10
Q

Aeteological classification?

A
    • Unprovoked

- - Provoked (transient (major or minor) or presistent)

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11
Q

Risk factors for DVT?

A
Hereditary thrombophilia 
Malignancy
Acquired thrombophilia
Surgery trauma
Estrogens
Compression
Inflammation
Immobility
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12
Q

Idade e DVT?

A

Com idades mais avançadas surgem fatores de risco adquiridos

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13
Q

Acquired thrombophilia?

A
    • Auto-immune diseases (Antiphospholipid syndrome)
    • Malignancy (neoplasia predispõem trombose, umas mais q outras e qualquer clinico que lide com doentes com suspeita de DVT pode estar perante uma primeira manifestação de neoplasia oculta)
    • Inflammatory bowel disease
    • Myeloproliferative disorders
    • Hemolytic anemias
    • Acquired AT deficiency
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14
Q

Clinical criteria for Antiphospholipid syndrome?

A
Vascular thrombosis
- Venous thrombosis 50%
- Arterial thrombosis 
- Embolism 4%
Pregnancy morbidity
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15
Q

Laboratory criteria for Antiphospholipid syndrome?

A

Lupus anticoagulant
Anti-aCL antibodies (cardiolipina)
Anti-B2-GPI antibodies

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16
Q

Inherited thrombophilia?

A
    • VTE (Venous thromboembolism) before 40-50 years of age
    • unprovoked thrombosis at any age
    • recurrent thrombosis at any age
    • thrombosis at unusual or multiple sites
    • strong family history of VTE
17
Q

Etiology of Inherited thrombophilia??

A
    • Venous thromboembolism (DVT, Pulmonary embolism, VT as unusual sites)
    • Purpura fulminans
    • Obstetric problems
    • Arterial thrombosis
18
Q

Marcadores Laboratoriais de Inherited thrombophilia?

A
    • Natural coagulation inhibitors deficiencies
    • Raise of levels / function of clotting factors
    • Impaired fibrinolysis
19
Q

Incidence of recurrent VTE?

A

Unprovoked VTE has a higher predictive value of recurrence than the presence of thrombophilia

20
Q

Who not to test for thrombophilia?

A
    • unselected patients presenting with a first episode of VTE
    • to assess the thrombotic risk in patients admitted to hospital
    • asymptomatic relatives of those with low-risk thrombophilia
    • center venous catheter-related VTE
21
Q

When should not be tested for Thrombophilia?

A
    • do not test for thrombophilia at the time of VTE (treatment not influenced by test results, reduction of natural anticoagulants)
    • do not test under anticoagulation therapy (Heparin, AVKs)
22
Q

VTE treatment objectives?

A
Prevent clot extension, including PE
PREVENT:
- Post-thrombotic syndrome
- Chronic thromboembolic pulmonary hypertension
PREVENTION of recurrence
23
Q

Anticoagulation?

A
Gold standard treatment for VTE
Active Treatment:
- Initial phase 5-7 days
- Long-term phase 3-6 months
Extended Treatment: 3 months to indefinite
  • Warfarin
  • Dabigatran
  • Edoxaban
  • Rivaroxaban
  • Apixaban
24
Q

Duration of therapy?

A

Duration of therapy should be individualized after careful assessment of treatment benefit against risk of bleeding
Shot duration (at least 3 months):
- Proximal DVT associated with risk factors
- Distal DVT
Extended treatment: Unprovoked DVT or DVT associated with permanent risk factors

25
Q

Risk of recurrence?

A
    • Provoking factor for VTE (major reversible risk factor & persistent or progressive risk factor)
    • Unprovoked VTE (several parameters can be evaluated)
    • Previous (a second episode of VTE has a 50% higher risk of recurrence compared with the first one)
26
Q

Risk of recurrence - unprovoked VTE?

A
    • Sex (men)
    • Site of TVE (proximal vs distal)
    • D-dimer (1 month after stopping anticoagulation, when positive)
    • Antiphospholipid syndrome
    • Hereditary thrombophilias
    • Post-Thrombotic syndrome
27
Q

Risk of bleeding?

A

Patient characteristics (>75y, previous bleeding, cancer, hypertension, diabetes, cerebrovascular disease, IR, liver disease)
Antithrombotics
Recent surgery
Frequent falls

28
Q

Anticoagulation + what?

A
    • compression: elastic stockings
    • inferior vena cava filter
    • early thrombus removal
  • surgical thrombectomy
  • catheter-directed thrombolysis
  • pharmacomechanical catheter directed thrombolysis