Abnormal bleeds Flashcards

(21 cards)

1
Q

What bleeding is associated with dentistry?

A
  • Tooth extraction
  • Surgery, biopsies and trauma
  • Periodontal therapy (and even probing)
  • Exposure of vital pulp
  • Spontaneous (local and systemic causes)
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2
Q

What are the effects of blood loss?

A
  • Patient distress
  • Blood in the tissues (bruising, infection)
  • Blood in the stomach (vomiting) – irritant in stomach so causes vomiting
  • Blood in airway (obstruction) – quite rare
  • Hypovolaemia (reduced blood volume), shock (rare)
  • Reduced oxygen carrying capacity (decreased Hb)
  • Reduced protein (water holding, clotting) – protein responsible for transporting drugs, calcium balance so problems occur.
  • Reduced platelets (less capacity to arrest haemorrhage).
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3
Q

How can you manage bleeding?

A
  • Be prepared
  • Patient expectations
  • Check bleeding/clotting history
  • Careful surgical technique
  • Local measures:
    o Pressure
    o Suture
    o “Surgicel”
    o Patience
  • Careful post-op and follow up.
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4
Q

What is haemostasis?

A
  • Prevention of blood loss
  • Whenever a vessel is severed or ruptured, haemostaiss is achieved by several different mechanisms
  • Squeezing blood vessel will activate vascular spasm, activating clotting cascade, so can avoid using sutures to fix blood vessel.
  • Vascular spasm
  • Platelet plug
  • Blood coagulation
  • Growth of fibrous tissue in the hole in the vessel permanently
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5
Q

What is vascular spasm?

A
  • Prevents excessive blood loss in the body
  • Smooth muscle in the blood vessel wall contracts and reduces blood loss.
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6
Q

What is the formation of the platelet plug?

A
  • Platelet adhesion – platelets adhere to exposed tissue collagen
  • Platelet release reaction – release of Thromboxane A2 causes increased stickiness
  • Platelet aggregation – effect on nearby platelets causes them to adhere to platelet plug
  • Tissue damage
  • Exposure of subendothelial collagen
  • Platelet activation
  • Enhanced platelet adhesion and aggregation
  • Enhanced activation of factor X and prothrombin
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7
Q

How does aspirin and clopidogrel work?

A
  • Aspirin irreversibly binds to platelets
  • It inactivates platelet COX (cyclooxygenase) required for thromboxane A2 mediated aggregation
  • Clopidogrel binds to the P2Y12 receptor irreversibly and prevents Adenosine Di Phosphate (ADP) mediated aggregation
  • Platelets are renewed over about 10 days
  • Ibuprofen binds to platelets reversibly.
  • Takes a couple weeks for aspiring affect to be reversed as that’s when platelets get renewed.
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8
Q

Which patients are likely to be taking clopidogrel or aspirin?

A
  • Vascular disease
  • Including ischaemic heart disease
  • Or thromboembolic disease
  • Or stroke
  • Or peripheral vascular disease
  • In whom thrombi (platelet aggregations) are likely to form within the vascular system
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9
Q

How do you manage patients on aspirin?

A
  • Do not stop the aspirin
  • Takes weeks for effect to be reversed
  • Risk of stopping is greater than risk of continuing
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10
Q

How does the clotting cascade work?

A
  • Factors activate X to convert to Xa
  • Xa converts prothrombin to thrombin
  • Thrombin converts soluble fibrinogen to insoluble fibrin.
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11
Q

What are the different tests for bleeding function?

A
  • INR (International Normalised Ratio) – Patient’s prothrombin time, used to asses warfarin anticoagulation
  • Platelet count – normal 200-400 * 109/L, bleeding a problem if lower than 100 *109/L
  • APTT (Activated Partial Thromboplastin Time) – used to assess heparin anticoagulation
  • Bleeding time (rarely used – direct cut to forearm)
  • Others may be undertaken if an abnormally found in one of these.
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12
Q

Which patients are likely to be taking warfarin?

A
  • Atrial fibrillation
  • Heart valve abnormalities or replacement
  • Thromboembolic disease – deep venous thrombosis and pulmonary embolus
  • Some other cardiac and vascular abnormalities including some patients with ischaemic (inadequate blood supply) heart disease.
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13
Q

How does warfarin work?

A
  • It prevents the action of vitamin K (produced in the gut by bacteria)
  • Vitamin K is required in the liver to produce of Factors II, VII, IX, and X
  • Warfarin prevents carboxylation of clotting factor precursors
  • Clotting factor half lives vary up to 60h
  • Full impact of drug not seen for about 7 days
  • Similar long delay when stopped
  • Many antibiotics enhance effect of warfarin e.g. metronidazole
  • What clotting factors does warfarin affect:
    o 2, 7, 9, 10 factors, produced in liver, using metabolism of Vitamin K usually.
  • At what INR is it safe to perform a tooth extraction on a patient?
    o <4.0
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14
Q

What should you do as a clinician for patients with abnormal bleeding and are taking warfarin?

A
  • Manage expectations
  • Check INR records
  • If stable, check INR 72hrs before extraction
  • If not check within 24 hours
  • Early in the week
  • Early in the day
  • Careful explanations
  • 2.0-3.0:
    o Consider one side at a time
  • 3.0-4.0
    o Forceps extraction
    o One quadrant at a time
    o Caution with IDB
  • Surgical
  • Suture
  • Check clotting before pt leaves
  • Give contact information
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15
Q

What is wrong with warfarin?

A

o Difficult to get stable anticoagulation

o Multiple interactions
 Drugs
* Metronidazole
* Carbamazepine
* Fluconazole
* Miconazole
* St Johns Wort

 Food:
* Cranberry juice

o Need for monitoring

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16
Q

Who takes the new anticoagulant medications?

A

o AF
o Thromboembolic disease (DVT/PE)
o Heart valve replacements
o CVA

17
Q

What are the advantages of the new anticoagulants?

A

o Single point of action
o Predictable effect
o No need for INR monitoring
o No interaction with food

18
Q

What are the disadvantages of the new anticoagulants?

A

o No antidote
o Half-life up to 17hrs.

19
Q

How do you manage patients on the new anticoagulants?

A
  • Do not stop the medication
  • Manage patients expectations
  • Local measures
  • If taking twice daily may consider missing a single pre-op dose.
20
Q

How do you ask patients if they have coagulopathies?

A
  • “Do you have a coagulopathy?”
  • Do you have any problems with bleeding or bruising
  • Are you taking any medicines to thin the blood
  • Do you have any liver problems
21
Q

How do you manage patients with coagulopathy?

A
  • E.g. clotting factor deficiencies, haemophillia, liver disease.
  • Ask advice of haematologist
  • Check clotting factors/INR/aptt preoperatively
  • Adjust if necessary
  • Manage patient expectations
  • Local measures:
    o Pressure
    o Gauze
    o Suture
    o Oxidised cellulose – Surgical/curacel
    o Tranexamic acid mouthwash