VTE Flashcards

1
Q

What is the difference between DVT and PE

A

DVT -Blood clot in a deep vein

P.E- detachment of blood clot that travels to the lungs and blocks pulmonary artery.

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2
Q

Which patients are at risk of VTE

A

Immobile
Obese
Malignant disease
History of VTE
Over 60
HRT/contraceptive
varicose veins with phlebitis
Pregnancy
Critical care
significant co-morbidities
relative with VTE

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3
Q

Who are at risk of bleeding?

A

Patients on anticoagulants
Systolic hypertension
Thrombocytopenia (low platelet)
Acute stroke
Bleeding disorders
Acquired: liver disease
Inherited:haemophillia

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4
Q

What are different forms of prophylaxis against blot clots?

A

Mechanical prophylaxis:
compression stockings
Pharmacological VTE prophylaxis:
Parenteral anticoagulants and DOACs

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5
Q

What are examples of parenteral anticoagulants?

A

-LMWH
-Unfractionated Heparin in renal failure
-Fondaparinux

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6
Q

When are DOACs used for VTE prophylaxis?

A

Prophylaxis after knee/hip replacement surgery

Edoxaban: treatment and prevention recurrent VTE.

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7
Q

How long would you give VTE prophylaxis for following surgery?

A

General-5-7 days
Major cancer surgery in abdomen or pelvis- 28 days
Knee/hip surgery: extended duration

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8
Q

What is TREATMENT of VTE?and what is length of treatment?

A

LMWH or unfractionated heparin in renal failure

For at least 5 days and until INR at 2 or more for at least 24 hours

Monitor APTTif unfractionated Heparin given

Start oral anticoagulant at the same time(usually warfarin)

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9
Q

What VTE is used in pregnancy and why?

A

LMWH
Lower risk of osteoporosis and heparin induced thrombocytopenia (HIT)

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10
Q

HEPARIN:

Heparin and Fondaparinux (parenteral)
What are common indications?

A

Can be given in ACS to reduce clot progression

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11
Q

HEPARIN:

What is the mechanism of action?

A

It activates antithrombin which inactivates clotting factors (II and Xa) providing a natural break to the clotting process.

Heparin and fondaparinux enhance the anticoagulant effect of antithrombin

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12
Q

What is fondaparinux?

A

A synthetic pentasaccharide that mimics the sequence of the binding site of heparin to antithrombin and is very specific for factor Xa

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13
Q

Heparin and Fondaparinux:

What are common adverse effects and why?

A

Haemorrhage ( lower risk may be with Fonda than with LMWH)

Bruising

Hyperkalaemia- effect on adrenal aldosterone secretion

Rarely: Immune reaction characterised by (HIT Heparin-induced thrombocytopenia)
less likely with LMWH than UFH and far less than with fondaparinux.

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14
Q

What are common interactions with heparin and fondaparinux?

A

Antithrombotic drugs and heparins has an additive effect sometimes desirable such as in treating ACS . Also associated with increased risk bleeding.

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15
Q

Who should be used prescribed with caution?

A

Risk of bleeding:
-clotting disorders
-severe uncontrolled hypertension

Withheld before invasive procedures(especially lumbar puncture and spinal anaesthesia)

Renal impairment-
LMWH and fonda
accumulate so lower dose or UFH should be used instead.

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16
Q

What is the treatment reverse heparin effects?

A

Major bleeding; protamine
Effective for UFH but less for LMWH and ineffective against fondaparinux.

17
Q

What is treatment to reverse fondaparinux?

A

Andexanet Alpha but is unlicensed

18
Q

What are dosages

A

-Dalteparin 5000 SC daily for VTE prophylaxis
- UFH preferred in renal impairment or when rapid onset and offset anticoagulation is required.

( heparin 5000 units SC 12 hourly for VTE prophylaxis)

19
Q

What are monitoring requirements before and after starting?

A

FBC
clotting
renal profiles

In prolonged therapy (>4 days):

platelet count and serum potassium concentration should be monitored because the risk of HYPERKALAEMIA and THROMBOCYTOPOENIA increases with duration of therapy.

20
Q

What is a sign of HIT? and should be done if suspected?

A

Significant decline in platelets

Seek specialist advice, stop heparin

21
Q

What should be prescribed along side warfarin indicated for VTE?

A

LMWH because there is a delay in the onset of the anticoagulant effect while existing clotting factors are cleared.