Haematology (clotting) Flashcards

1
Q

What steps should you take to prevent venous thromboembolism?

A
  1. Early ambulation- get them walking
  2. Stockings
  3. Low dose low molecular weigh heparin

Or: low dose Unfractionated heparin/DOAC

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2
Q

What is the acute treatment pathway for haemophilia A?

A

Effectively we replace the factors and make better use of any clots that do form.

  1. Factor 8 concentrate (octocog) 1-3 times per day- replace missing factors
  2. Desmopressin SC,IV or Intranasal- only useful for mild/moderate haemophilia - releases factor 8 stores
  3. Tranexamic acid PO- Antifibrinolytic: inhibits plasminogen, prolonging clots
  4. Orthopaedic evaluation: joint bleeds
  5. Rest, ice, compression and elevation: any joint bleeds
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3
Q

What is the acute treatment pathway for haemophilia B?

A

Effectively we replace the factors and make better use of any clots that do form.

  1. Factor 9 concentrate (nonocog) 1-3 times per day- replace missing factors
  2. Tranexamic acid PO- Antifibrinolytic: inhibits plasminogen, prolonging clots
  3. Orthopaedic evaluation: joint bleeds
  4. Rest, ice, compression and elevation: any joint bleeds
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4
Q

What is the long term treatment for haemophilia? (Same for A and B)

A

Prophylactic factor concentrate (octocog/nonocog) given every week.

  • very expensive
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5
Q

What is the treatment pathway for pulmonary embolism?

Depends on haemodynamic status of the patient

A

If haemodynamically stable:

  1. Fondaparinux or LMWH or Unfractionated heparin (egfr<30)- for five days (Parenteral anticoagulation)
  2. Warfarin or rivaroxaban - after the anticoagulation,for three months

If pharmacological anticoagulation isn’t possible:

  • Inferior vena cava filter

If haemodynamically unstable:

Thrombolytic therapy (reteplase,streptokinase)

Or Embolectomy

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6
Q

What is the treatment pathway for deep vein thrombosis?

A

If haemodynamically stable:

  1. Fondaparinux or LMWH or Unfractionated heparin (egfr<30)- for five days (Parenteral anticoagulation)
  2. Warfarin or rivaroxaban (maintenance treatment after acute treatment) - for 3+ months

If pharmacological anticoagulation isn’t possible:

  • Inferior vena cava filter

If haemodynamically unstable:

Thrombectomy

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7
Q

What is the treatment pathway for von willebrands disease type 1?

A
  1. Desmopressin - causes release of factor 8 AND Von willebrand factor
  2. Tranexamic acid
  3. Possible VW factor concentrate infusion - since type 1 is only a quantitative, not qualitative deficiency, there may be enough

(Same as haemophilia A)

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8
Q

What is the treatment pathway for Von willebrand disease type 2A and 2B?

How do they differ?

A
  1. Von willebrand factor concentrate infusion
  2. For type 2A give desmopressin

Do not give desmopressin for type 2B, can cause severe thrombocytopenia.

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9
Q

What is the treatment pathway for type 3 Von willebrands disease?

A

Von willebrands factor concentrate.

And prophylactic VW factor concentrate.

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10
Q

What is the process for initiating the major haemorrhage pathway?

A
  1. Recognise blood loss
  2. Resuscitate and call for help (4444)- DRS ABCDE
  3. Stop the bleeding - Tranexamic acid (prevents plasminogen activation) and prothrombin complex concentrate
  4. Gather team with emergency runner
  5. Communicate situation to the lab
  6. Locate the emergency 2 units O negative blood (ED resus, theatres, obs and gynae)
  7. Order massive haemorrhage pack 1 or 2
  8. Monitor coagulation tests
  9. Warm the blood: if patient gets hypothermic clotting factors don’t work
  10. Summon anaesthetist and vascular surgeon
  11. Let lab know when they are stable
  12. Send them to ICU: may need organ support (TALI - lungs, kidneys)
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11
Q

How is the haemorrhage controlled?

A

Local measures - pressure and tourniquets

Early intervention - damage limitation

Reverse any anticoagulants - prothrombin complex concentrate for warfarin

Tranexamic acid - only used if within first hour

Blood samples - FBC, UE, LFT, calcium, PT, APTT, fibrinogen and cross match

Request the blood products needed - red cells, FFP or platelets

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12
Q

When is group O RhD negative blood used for transfusion?

A

In an extreme emergency situation when you can’t wait 15 minutes (time it takes to type ABO and RhD)

It is a precious commodity

It takes 15 minutes to find ABO and RhD types

It takes 45-60 minutes to fully screen for all antibodies: this gives you the safest product choice

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13
Q

Why are there major haemorrhage pack 1 AND pack 2?

A

Pack 1 is for initial treatment of major haemorrhage (4 units red cells and 4 units FFP)

Pack 2 is for if the major haemorrhage continues, so pack 2 is only given once pack 1 has been given (4 units red cells, 4 units FFP, 1 dose platelets, 2 packs cryoprecipitate)

The packs provide the coagulation factors and platelets necessary that red cells alone don’t provide.

Targets:

  • we aim for PT and an APTT of <1.5
  • we aim for 80-100 Hb
  • platelets >75
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