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Drug ODPoisoning Transfusion

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Can be done up to 4 hours after ingestion. Not effective for alcohol ... Endoscopy/surgery may be needed for iron overdose or to remove body packages (eg ... – PowerPoint PPT presentation

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Title: Drug ODPoisoning Transfusion


1
Drug OD/PoisoningTransfusion
2
Management of OD/Poisoning
  • Resuscitation/supportive care
  • Protect the airway/respiratory support
  • Fluid resuscitation
  • Maintain acid-base balance
  • Substance ID
  • What drug was taken, how much, by what route
  • Past history
  • Current circumstances
  • Associated trauma

3
Management of OD/Poisoning
  • Investigations
  • Drug ID by blood, urine, or gastric aspirates
  • Alcohol level
  • CXR (pulm edema with salicylate OD)
  • EKG (ischemia with cocaine)
  • Prevention of absorption
  • Gastric lavage
  • Can be done up to 4 hours after ingestion
  • Not effective for alcohol
  • Harmful after ingestion of caustic products or
    petroleums
  • Patient is in left lateral position
  • Ewald tube is used as it has a larger diameter

4
Management
  • Activated charcoal
  • Absorbs drugs and promotes elimination
  • Given after gastric lavage and at 4 hour
    intervals
  • Wont bind iron, lithium, alcohols, acids,
    alkalis, cyanide, or organophosphates
    (pesticides)
  • Causes constipation

5
Management
  • Addition measures
  • Induced vomiting with ipecac is not often doneit
    risks aspiration
  • Cathartics promote diarrhea and reduce drug
    absorption, but risk fluid/electrolyte loss
  • Skin decontamination is essential for toxins
    absorbed through the skin, like pesticides
  • Endoscopy/surgery may be needed for iron overdose
    or to remove body packages (eg-illicit drugs that
    have been packaged and swallowed)

6
Management
  • Enhanced elimination
  • Gut dialysis
  • Uses repeated doses of activated charcoal to bind
    drugs
  • Forced diuresis
  • Increases urine production with IV fluids
  • Risk of fluid overload
  • Hemodialysis
  • Removes low molecular weight, water soluble
    molecules
  • Hemoperfusion
  • Useful to remove lipid-soluble drugs
  • uses charcoal or resin columns
  • May cause hypocalcemia and coagulopathy

7
Specific Management
  • Paracetamol (Tylenol)
  • Depletes hepatic glutathione stores, causing
    accumulation of a hydroxylamine metabolite that
    causes liver and renal damage
  • Treat with N-acetylcysteine (Mucomyst)it
    increases glutathione levels and reduces toxicity
  • Can also be treated with methionine
  • Tricyclic antidepressants
  • Cause most OD fatalities
  • Toxicity is due to anticholinergic effects
    fixed pupils, dry red skin, hyperthermia,
    tachycardia, urine retention, CNS (psychosis,
    seizures, hallucinations)
  • No specific antidote but gastric lavage and
    activated charcoal can reduce toxicity
  • May cause potentially life-threatening
    arrhythmias and hypotension

8
Blood and Blood Components
  • Whole blood is collected into citrate/phosphate/de
    xtrose/adenine anticoagulantone unit is 430 ml
  • It has a longer shelf life if its divided into
    its constituent parts by centrifuge
  • Red cells are then packaged in saline, adenine,
    glucose and mannitol and have a shelf life of 42
    days
  • Platelets last about 7 days
  • Fresh frozen plasma contains all the clotting
    factors but it takes about 4 units to see
    clinical resultscan store up to a year, though
  • Fresh whole blood has all the clotting factors,
    etc but reactions are common
  • Stored blood is still metabolically active pH,
    2,3 DPG, ATP, platelets, and clotting factors all
    decrease while potassium increases (from cell
    rupture)

9
Coagulation Tests
  • Prothrombin Time (PT)
  • Tests the extrinsic pathway
  • Clot formation should occur within 12-14 sec
  • Increased PT caused by
  • Liver dx
  • DIC
  • Warfarin use
  • Vitamin K deficiency
  • Salicylate poisoning
  • Circulating anticoagulants
  • Excessive heparin
  • Activated Partial Thromboplastin Time (APPT)
  • Tests the intrinsic pathway
  • Coagulation should occur within 40 sec
  • Increased APPT caused by
  • Hemophilia
  • Heparin use
  • Von Willebrands dx
  • Inadequate specimen

10
Coagulation Tests
  • Platelet count
  • Bleeding time
  • Tests platelet function
  • Should stop bleeding within 9 minutes
  • Activated clotting time
  • Factor assays
  • Can test for specific factors, such as fibrinogen
  • Or can test for products of factor degradation
  • Fibrinogen degradation products
  • D-dimers

11
Bleeding Disorders
  • Genetic coagulopathies
  • Hemophilia A factor VIII deficiency
  • Hemophilia B factor IX deficiency
  • Von Willebrands
  • Autosomal dominant trait
  • The most common hereditary coagulation dx
  • Decreases factor VIII activity and reduces
    platelet adherence
  • Liver disease
  • Causes vitamin K dependent coagulation factor
    deficiencies
  • Can also get vit K deficiency with malnutrition

12
Bleeding Disorders
  • Anticoagulants
  • Oral anticoagulants cause vit K dependent
    clotting factor deficiencies
  • Heparin potentiates antithrombin III which blocks
    the action of thrombin preventing clotting
  • Antiplatelet agents (like ASA) inhibit platelet
    function for up to 10 days
  • Circulating anticoagulants increase with some
    drugs (eg-Penicillin) and diseases (AIDS/lupus)

13
Bleeding Disorders
  • Disseminated intravascular coagulation (DIC)
  • Follows widespread clotting
  • Bleeding is the most common symptom
  • Causes
  • Spesis
  • Surgery
  • Liver failure
  • Malignancy
  • Incompatible transfusions
  • Shock
  • Poisoning (snake venom)
  • Autoimmune dx
  • Pregnancy-related (eclampsia, sepsis)
  • Thrombocytopenia
  • Decreased platelets
  • Could be decreased production, increased use, or
    loss of platelets

14
Transfusion
  • A full cross-match takes about 45 minutes
  • Blood type determination takes 10 min
  • O negative blood is given when blood is needed
    immediately, but may cause some
    reactionuniversal donor
  • Type specific blood is preferred if time is
    available
  • After 5 units of blood, clotting disorders and
    other problems may developblood filters
    recommended for large transfusions

15
Transfusion
  • Risks of transfusions
  • Acute hemolytic reactions
  • Incompatible blood group
  • half due to administration error
  • Urticaria, rigors, shock, asthma
  • Non-hemolytic reactions
  • Reaction to donor WBCs
  • Fever, chills, urticaria
  • Acute lung injury
  • Delayed immune reactions
  • Massive transfusions can cause
  • Coagulopathy (eg-DIC)
  • Hypothermia
  • Volume overload
  • ARDS
  • Infection
  • Biochemical abnormalities (increased K, decreased
    Ca)
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