Management of haemorrhage in OS Flashcards

1
Q

What is primary haemorrhage?

A

Bleeding at the time of surgery - blood stained saliva 12-24 hours post surgery

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2
Q

What is reactionary haemorrhage?

A

Bleeding usually occurs 2-3 hours post XLA as the LA vasoconstrictor wears off - call 111

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3
Q

What is secondary haemorrhage?

A

Up to 14 days after the surgery - most likely cause of this is infection

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4
Q

What are the stages of blood clotting?

A

Vasoconstriction - vascular spasm in smooth muscle in the walls of blood vessels

Platelet plug formation - adhesion, interaction and aggregations of platelets

Coagulation cascade - clotting factors in the extrinsic, intrinsic and common pathways leading to the formation of fibrin

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5
Q

What is fibrinolysis?

A

Occurs when plasma enzyme plasminogen activates plasmin which digests the fibrin threads in the clot

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6
Q

Where are the majority of clotting factors produced?

A

Liver

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7
Q

Where are the platelets produced?

A

Red bone marrow

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8
Q

Where do the intrinsic and extrinsic clotting factor pathways converge?

A

Clotting factor X

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9
Q

What happens after the clotting pathways converge?

A

Factor V plus Ca convert prothrombin to thrombin which intern, converts fibrinogen to fibrin (network which stabilises a clot alongside platelets in a plug)

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10
Q

What clotting factor deficiencies can cause post operative bleeds?

A

Haemophilia A - factor 8
Haemophilia B - Factor 9
vWF disease - affects platelet adhesion and causes factor 8 deficiencies
Vit K deficiencies - factor 2, 7, 9 and 10

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11
Q

What acquired liver diseases can cause clotting issues?

A

Hepatitis/cirrhosis
History of alcohol XS

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12
Q

Which thrombocytopenic diseases cause clotting issues?

A

Immune idiopathic thrombocytopenia ITP
Secondary disease - to leukaemia
Drug induced antiplatelet therapy

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13
Q

Which vascular anomolies can cause post op bleeds?

A

Arterio-venous malformations
Hereditary haemorrhagic telangiectasia
Collagen disorders

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14
Q

How to treat pts with haemophilia?

A

X linked disorder
Factor replacement
Fresh frozen plasma
Replacement factors and proteins

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15
Q

How to treat vWF sufferers?

A

vWF - protein required for platelet aggregation
Protects factor 8 from rapid breakdown
Factor 8 deficiencies requiring replacement

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16
Q

Which complications arise from having cirrhosis and hepatitis?

A

Varices which can lead to bleeds and anaemia

17
Q

What are the causes of thrombocytopenia?

A

150-400 x 10^9/L
Drug induced, e.g. NSAIDs/ alcohol, heparin
Aplastic anaemia
Immune driven (idiopathic)
EBV/HIV

18
Q

How to manage patients on vit K antagonists

A

Warfarin, acencoumarol, phenindione

Check INR no more than 24 hours before procedure (up to 72hrs if patient is stably coagulated)

If INR is below 4 - treat without interruption of meds
Stage Tx
Consider suture and packing

If above 4 - delay tx and refer

19
Q

How does warfarin work?

A

Inhibits vit k dependant synthesis of biologically active forms of the clotting factors 1,8,9 and 10 as well as the regulatory factor proteins

Blocking enzyme called vit k epoxide reductase

20
Q

How does aspirin work? (acetylsalicylic acid)

A

NSAID which suppresses platelet fn by blocking formation of thromboxane A2 in platelets producing an inhibitory affect on platelet aggregation during the 8-9 day lifespan of platelet.

Also inhibitors COX 1 and COX 2 which reduce the production of proinflammatory prostaglandins

21
Q

What local measure should be taken in aspirin alone users?

A

Pack and suture
Stage tx
Extensive or complex procedures

22
Q

How does clopidogrel work?

A

antiplatelet meds that reduce risk of MI and stroke
Can be prescribed with aspirin - dual antiplatelet therapy following coronary stent placement
Irreversibly inhibits adenosine diphosphate (ADP) receptor which is important for platelet activation and cross linking of fibrin

23
Q

Which other medications work similarly to clopidogrel?

A

Ticagrelor and prasugrel

24
Q

How do DOACs work?

A

Dabigatrin

Reversibly bind to active site on thrombin preventing thrombin mediated activation of coagulation factors and may enhance fibrinolysis

25
Q

How do apixaban and rivaroxaban work?

A

Direct inhibitors of factors Xa
Do not require INR monitoring

26
Q

What measures are taken for a low bleeding risk?

A

Treat without interruption to medss

27
Q

What steps are taken for higher bleeding risk patients?

A

Advise patients to delay/miss morning dose

28
Q

Which meds are taken 2x/day?

A

Apixaban and dabigatrin

29
Q

How long after XLA can rivaroxaban be taken?

A

4hrs post haemostats

30
Q

What are the subtle signs of leukaemia

A

Purpura of the palate
Bleeding gingival margins

31
Q

How to manage post op bleeds

A

Good light and assistance
Irrigation of socket with 0.9% saline
Suction and remove liver clot to visualise bleed

Apply pressure with damp gauze
Administer LA with adrenaline
Pack with surgicel/fibrin blocks
Silver nitrate/diathermy to bleeding points
Bone wax - possible foreign body reaction
Suture well - horizontal mattress suture/ X stitch
5% tranexamic acid soaked gauze - 1g IV

Discuss with haem/cardiology
Systemic signs and fluid resuscitation

32
Q

When would silver nitrate be used?

A

Difficult to apply finger pressure or suture

e.g. mucosal biopsy hard palate or retromolar pad

After a few mins, agent should be deactivated by swabbing area with saline to avoid damage to surrounding structures

33
Q

What are the alternatives to surgicel?

A

Haemocollagen, gelfoam, kaltostat

34
Q

How does tranexamic acid work?

A

5% mouthwash can be used in planned cases e.g. haemophilia or in cases with persistent bleeding.

Antifibrinolytic - binds to plasminogen and therefore reduces clot breakdown

Given orally pre/post op or IV