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ANAESTHESIA AND ANTICOAGULANTS

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Mechanical heart valves. Cardiac arrhythmias. Who are patient at risk for DVT? ... Post prosthetic heart valve replacement. Treatment of DVT or PE. ... – PowerPoint PPT presentation

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Title: ANAESTHESIA AND ANTICOAGULANTS


1
ANAESTHESIA AND ANTICOAGULANTS
  • Done by
  • Dr. Ahmad Alrefaie

2
Hemostasis
  • Prevention of blood loss whenever a vessel is
    severed or ruptured.
  • It is a combination of events that occur due to
    physical and chemical forces.
  • Achieved by several mechanisms
  • Vascular spasm.
  • Formation of platelet plug.
  • Formation of blood clot as a result of
    coagulation.
  • Growth of fibrous tissue.

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  • The ultimate step in clot formation is conversion
    of FIBRINOGEN , a soluble plasma protein into
    FIBRIN , an insoluble thread like molecule.
  • The conversion is catalyzed by the enzyme
    THROMBEN at the site of injury.
  • Thrombin exist in the plasma in the form of an
    inactive precursor called PROTHROMBIN.

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  • Prothrombin converts into thrombin by FACTOR X,
    a plasma clotting factor.
  • Factor X present in the blood in inactive form
    and must be converted into its active form by
    another activated factor, and so on.

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Anticoagulants
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Why we use anticoagulants?
  • Prophylaxis and treatment for deep venous
    thrombosis (DVT) and pulmonary embolism which are
    commonly associated with surgical procedures.
  • Mechanical heart valves.
  • Cardiac arrhythmias.

9
Who are patient at risk for DVT?
  • Major lower limb or pelvic surgery.
  • Trauma patient.
  • Malignancy ( increase the risk 7-fold).
  • Central neuraxial block significantly reduces the
    incidence of DVT after orthopaedic surgery but
    additional prophylaxis is necessary to reduce the
    rate to acceptable levels.

10
Aspirin
  • Also called acytelsalicylic acid.
  • Impair platelet function by inhibiting platelet
    cyclo-oxygenase (COX).
  • Aspirin inhibits COX irreversibly, Therefore the
    antiplatelet effect of aspirin persists until a
    new platelet population is manufactured (at least
    7 days).

11
Indications
  • Local analgesic effect.
  • Antipyretic.
  • Anti-inflammatory.
  • Antiplatelet.

12
COX 1
  • Continuously stimulated by the body.
  • Its concentration in the body remain stable.
  • Creates prostaglandins used for basic house
    keeping throughout body.
  • Prostaglandins stimulate normal body functions
    such as stomach mucous production, regulation of
    gastric acid and kidney water excretion.

13
COX 2
  • Induced ( normally not present in cells).
  • Built only in special cells (A549 lung cells).
  • Used for signaling pain and inflammation.
  • Produces prostaglandins for inflammatory
    response.
  • Stimulated only as part of immune response.

14
  • It is safe to proceed with central and periphral
    nerve block in patients taking Aspirin.

15
NSAIDs
  • Analgesic, antipyretic and, in higher doses,
    anti-inflammatory drugs.
  • Impair platelet function by inhibiting platelet
    cyclo-oxygenase (COX).
  • NSAIDs inhibit COX reversibly.
  • Platelet function returns to normal within 3
    days after stopping NSAIDs.
  • It is safe to proceed with central and periphral
    nerve block in patients taking NSAIDs.

16
COX 2 inhibitors
  • Anti-inflammatory drugs that selectively inhibit
    COX 2.
  • They do not affect platelet function.
  • It is safe to proceed with central and periphral
    nerve block in patients taking COX 2 alone.
  • They can potentiate the effect of warfarin by
    increasing the prothrombin time ( PT ).

17
Clopidogrel
  • A thienopyridine derivative.
  • It is a potent antiplatelet agent.
  • It inhibits ADP-induced platelet aggregation and
    binding between platelets and fibrinogen.
  • The effect is irreversible and platelet function
    does not return to normal until at least 7 days
    after stopping the drug.

18
  • It is used in combination with aspirin in
    patients with acute coronary syndrome.
  • It should be discontinued 7 days before surgery,
    central neuraxial and peripheral block.
  • If an antiplatelet effect must be maintained,
    aspirin can be substituted safely.

19
Unfractionated heparin
  • Indications
  • Thromboprophylaxis.
  • Therapeutic anticoagulation.
  • Subcutaneous thromboprophylactic doses are seldom
    associated with bleeding complications.

20
  • Central and periphral block in thromboprophylaxis
    dose the dose should be stoped 4 hours before or
    more than one hour after the procedures.
  • Catheter should be removed 2-4 hours after the
    last dose.
  • In therapeutic dose activated partial
    thromboplastin time (APTT) should be normal
    before attempting a block or removing a catheter.

21
  • Patients who have been receiving unfractionated
    heparin for more than 4 days should have a
    platelet count, because the incidence of
    heparin-induced thrombocytopenia is about 3.

22
LMWHs
  • Indications
  • Thromboprophylaxis.
  • Therapeutic anticoagulation.
  • Have longer half-lives than unfractionated
    heparin, which allows once daily administration.
  • They have anti-Xa activity.
  • There is no monitoring test for routine use.

23
  • Central and periphral block in thromboprophylaxis
    dose the dose should be stoped 12 hours before
    the block or catheter removal.
  • The first dose is given within 6 hours of surgery
    or 2 hours after the block.
  • In therapeutic dose it takes about 24 hours for
    coagulation to return to normal. Therefore, an
    interval of 24 hours should elapse before
    attempting block.

24
Fondaparinux
  • Indications for thromboprophylaxis.
  • It is a synthetic pentasaccharide, which has
    potent anti-Xa activity.
  • It has a longer elimination half-life than LMWH (
    17 hours in young patients and 21 hours in
    healthy elderly patients ).
  • It is administered 6 hours after surgery.
  • An interval of at least 24 hours should elapse
    before removal of neuraxial or peripheral nerve
    catheters.

25
Warfarin
  • Indications
  • Thromboprophylaxis in AF.
  • Post prosthetic heart valve replacement.
  • Treatment of DVT or PE.
  • Central and periphral block INR 1.5, this
    normally takes about 4 days after stoping
    warfarin.
  • If a LMWH or unfractionated heparin has been
    administered in place of warfarin, the
    recommended intervals discussed above should be
    observed before performing any block.

26
Anticoagulants perioperatively
  • Warfarin should be stopped 2-4 days
    preoperatively, and the PT time monitored daily
    (INR 1.5).
  • If INR prolonged
  • Administer vitamin K.
  • Fresh frozen plasma.
  • It is often appropriate to start an alternative
    anticoagulant, such as LMWH or unfractionated
    heparin, until warfarin is re-established and the
    INR is back in the therapeutic range
    postoperatively.

27
  • After minor surgery warfarin may be restarted on
    the first postoperative day.
  • After major surgery an infusion of
    unfractionated heparin may be used to maintain
    anticoagulation ( with control by APTT ) until
    warfarin therapy is restarted.
  • Unfractionated heparin is reversed rapidly with
    protamine 1 mg for every 100 units of heparin.

28
  • Unfractionated heparin is preferable to LMWH
    because it may be monitored more easily and
    reversal titrated more accurately.

29
Summary
  • Aspirin and NSAIDs No contraindication.
  • Clopidogrel Stop 7 days before surgery, central
    and peripheral block.
  • Warfarin INR 1.5.
    After minor surgery start on the first
    postoperative day.
    After major surgery an infusion of
    unfractionated heparin may be used to maintain
    anticoagulation.

30
  • Unfractionated heparin
  • Thromboprophylaxis dose stop 4 hours before or gt
    than one hour after the procedures.
    Catheter should be removed 2-4
    hours after the last dose.
  • Therapeutic dose (APTT) should be normal before
    attempting a block or removing a catheter.

31
  • LMWH
  • Thromboprophylaxis dose the dose should be
    stoped 12 hours before the block or catheter
    removal.
    The first dose is given within 6 hours of
    surgery or 2 hours after the block.
  • Therapeutic dose the dose should be stoped 24
    hours before the block.

32
  • Fondaparinux
    Start 6 hours after surgery.
    Stop 24 hours before removal of neuraxial or
    peripheral nerve catheters.
  • REFERENCE
  • AnaesthesiaUK
  • Europian Journal of Anaesthesiology2007
  • Medical Physiology, Guyton
  • Fundamentals of Physiology
  • Text book of Anaesthesia, Aitkenhead

33
THANK YOU
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