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Acute Angioedema

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Acute Angioedema Gabriele de Vos, M.D., M.Sc. Division of Allergy and Immunology Jacobi Medical Center Albert Einstein College of Medicine The role of C1 inhibitor ... – PowerPoint PPT presentation

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Title: Acute Angioedema


1
Acute Angioedema
  • Gabriele de Vos, M.D., M.Sc.
  • Division of Allergy and Immunology
  • Jacobi Medical Center
  • Albert Einstein College of Medicine

2
(No Transcript)
3
Differential diagnosis of acute angioedema
  • IgE mediated allergic reactions to food, drugs,
    venoms etc.
  • Histamine-releasing drugs (e.g. opioids, RCM),
    pseudoallergens in food
  • Adverse reactions to certain medications NSAIDs,
    ACE-inhibitors
  • Chronic urticaria with angioedema
  • Idiopathic or exercise induced anaphylaxis
  • C1-Esterase Inhibitor deficiency (hereditary or
    acquired)
  • Gleich syndrome recurrent angioedema and high
    eosinophil counts of unknown etiology
  • Angioedema in hypereosinophilic syndrome

4
Differential diagnosis of acute angioedema
  • IgE mediated allergic reactions to food, drugs,
    venoms etc.
  • Histamine-releasing drugs (e.g. opioids, RCM),
    pseudoallergens in food
  • Adverse reactions to certain medications NSAIDs,
    ACE-inhibitors
  • Chronic urticaria with angioedema
  • Idiopathic or exercise induced anaphylaxis
  • C1-Esterase Inhibitor deficiency (hereditary or
    acquired)
  • Gleich syndrome recurrent angioedema and high
    eosinophil counts of unknown etiology
  • Angioedema in hypereosinophilic syndrome

5
Differential diagnosis of acute angioedema
  • IgE mediated allergic reactions to food, drugs,
    venoms etc.
  • Immediate type (histamine)
  • Severe reactions (anaphylaxis) almost always
    occur within 1-30 min
  • Anaphylaxis is accompanied by skin symptoms in
    nearly 100
  • Up to 20 late phase reaction 2-24 hours (peak 8
    hours)

6
How do mast cells release histamine?
7
(No Transcript)
8
Presentation of anaphylaxis
Cutaneous 90-100
Urticaria and angioedema 85-90
Flush 45-55
Pruritus without rash 2-5
Respiratory 50
Dyspnea 50
Throat tightness and wheezing 54
Rhinitis 15-20
Abdominal  
Nausea, vomiting, diarrhea, cramping pain 25-30
Other  
Dizziness, syncope, hypotension 30-35
Headache 7
substernal pain 5
seizure 1
9
Causes of anaphylaxis
Food (e.g. peanuts, tree nuts, shellfish) 35
Drugs (e.g. antibiotics, NSAIDs, radio contrast media, anaesthetics) 15-20
Insect bites and stings 5
Latex rare
Allergen vaccines rare
Exercise induced rare
Idiopathic 30
10
Work-up of IgE mediated allergic reactions
  • Skin-testing
  • Drugs no standardized skin tests, except
    penicillin
  • Food best with fresh food
  • NPV thought to be generally gt95
  • PPV 501 95 (milk, egg, peanut, if wheal
    gt8mm)2
  • Refractory period up to 4 weeks after anaphylaxis
    (data from venom anaphylaxis)

1Kagan et al., Ann Allergy Asthma Immunol. 2003
Jun90(6)640-5 2003 2Sporik R, Hill DJ et al.
Clin Exp Allergy. 2000 Nov30(11)1540-6.
11
Work-up of IgE mediated allergic reactions
  • In vitro sIgE testing
  • RAST (RadioAllergoSorbentTest)-outdated test,
    but term still in use!
  • Newer tests Radioactive signal replaced by
    chemiluminescent reaction (DPC Immulite 2000,
    PharmaciaCap)
  • Limited sensitivity and specificity

12
Probability of reacting to egg
Sicherer et al. 2005
13
Treatment of severe allergic reactions
  • 1. Epinephrine (Adrenaline) 11000 solution
    (1mg/ml)
  • gt12 years and adults 0.3-0.5 mg IM
    anterolateral thigh (IV must dilute 0.1-0.3 mg
    (in 10ml) slowly over 10 minutes)
  • gt6 months and lt12 years 0.01 mg/kg
  • 2. Positioning Keep patient lying flat with legs
    up unless respiratory distress increases
  • 3. Oxygen supplementation and beta-agonist
    inhalation (Albuterol)
  • 4. IV access, intravenous fluids (normal saline)
    if still hypotensive after epinephrine
  • Remember 50 of the intravascular volume can be
    shifted to the extravascular space within the
    first 10 min. of anaphylaxis
  • Normal Saline rapid infusion if
    epinephrine-resistant hypotension
  • 5. If patient is on beta-blocker Glucagon
  • Adult 1-5 mg IV (IM,SC), followed by infusion
    5-15 ug/min
  • 6. Antihistamines
  • Adult H1-antagonist (DiphenhydramineBenadryl
    25-50 mg IV) and H2-antagonist (FamotidinePepcid
    20mg IV)
  • Children (2-12y) H1-antagonist
    (DiphenhydramineBenadryl1-1.25 mg/kg IV q6h)
    and H2-antagonist (FamotidinePepcid 0.25-0.5
    mg/kg IV q12h)
  • 7. Steroids do not help acutely but can prevent
    prolonged anaphylaxis
  • Liebermann et al. The diagnosis and management
    of anaphylaxis. An updated practice parameter,
    JACI 2005 115

14
Differential diagnosis of acute angioedema
  • IgE mediated allergic reactions to food, drugs,
    venoms etc.
  • Histamine-releasing drugs (e.g. opioids, RCM),
    pseudoallergens in food
  • Adverse reactions to certain medications NSAIDs,
    ACE-inhibitors
  • Chronic urticaria with angioedema
  • Idiopathic or exercise induced anaphylaxis
  • C1-Esterase Inhibitor deficiency (hereditary or
    acquired)
  • Gleich syndrome recurrent angioedema and high
    eosinophil counts of unknown etiology
  • Angioedema in hypereosinophilic syndrome

15
Differential diagnosis of acute angioedema
  • Food that can enhance allergic skin reactions
  • Any spices and seasoning such as Sazon, Adobo,
    Vegeta, ginger, garlic, onion or celery powder,
    any MSG containing food (e.g. Chinese food) etc.
  • Premixed dressings for salads such as 1000
    islands, blue cheese, French dressing etc. (Only
    oil and a touch of vinegar or lemon juice should
    be used for salad dressing)
  • Canned tomatoes, tomato sauce or paste, canned
    soups, other canned meals
  • Vinegar and vinegar-containing foods such as
    mayonnaise, ketchup, and mustard, salad
    dressings, chili, shrimp sauce, pickles, pickled
    vegetables, relishes, green olives, and
    sauerkraut.
  • Beer, wine and cider
  • Mushrooms.
  • Soy sauce.
  • Pickled and smoked meats and fish including
    sausages, bacon, ham, hot dogs, corned beef,
    pastrami, and pickled tongue.
  • Lobster and shellfish.
  • Soured breads (e.g. pumpernickel, rye) fresh
    rolls, coffee cakes
  • Certain fruits such as melons, especially
    cantaloupe, mango, all tropical fruit (pineapple,
    papaya etc.), grapes, strawberries
  • All dried and candied fruits including raisins,
    apricots, dates, prunes, and figs.
  • Diet soda, sodas containing artificial coloring
    (in particular orange and grape, mountain dew),
    ginger ale, Snapple, fruit punches of any kind,
    iced tea, any powdered drinks, health food
    preparations, any herbal teas (e.g. ginger or
    lemon or orange spice tea), herbal medicines,
    vitamins or tonics unless prescribed.
  • Chocolate, nuts, peanut products, chewing gum,
    breath mints, candy
  • Milk and milk products Cheeses, in particular
    aged cheeses, in some cases also cottage cheese,
    sour cream, and buttermilk
  • Histamine-releasing drugs (e.g. opioids, RCM),
    pseudoallergens in food.
  • Immediate or delayed onset of symptoms
  • Mechanism not well understood
  • Opiates, radio contrast media and vancomycin are
    typical examples
  • There is increasing data that certain food can
    trigger histamine release in susceptible
    individuals (e.g. chronic urticaria)

16
Differential diagnosis of acute angioedema
  • IgE mediated allergic reactions to food, drugs,
    venoms etc.
  • Histamine-releasing drugs (e.g. opioids, RCM),
    pseudoallergens in food
  • Adverse reactions to certain medications NSAIDs,
    ACE-inhibitors
  • Chronic urticaria with angioedema
  • Idiopathic or exercise induced anaphylaxis
  • C1-Esterase Inhibitor deficiency (hereditary or
    acquired)
  • Gleich syndrome recurrent angioedema and high
    eosinophil counts of unknown etiology
  • Angioedema in hypereosinophilic syndrome

17
Mechanism of action of NSAIDs (non selective
Cox-inhibitors)
Angioedema
18
Mechanism of action of ACE inhibitor
ACE-inhibitor
Angioedema
NOS?NO
19
Differential diagnosis of acute angioedema
  • IgE mediated allergic reactions to food, drugs,
    venoms etc.
  • Histamine-releasing drugs (e.g. opioids, RCM),
    pseudoallergens in food
  • Adverse reactions to certain medications NSAIDs,
    ACE-inhibitors
  • Chronic urticaria with angioedema
  • Idiopathic or exercise induced anaphylaxis
  • C1-Esterase Inhibitor deficiency (hereditary or
    acquired)
  • Gleich syndrome recurrent angioedema and high
    eosinophil counts of unknown etiology
  • Angioedema in hypereosinophilic syndrome

20
Differential diagnosis of acute angioedema
  • IgE mediated allergic reactions to food, drugs,
    venoms etc.
  • Histamine-releasing drugs (e.g. opioids, RCM),
    pseudoallergens in food
  • Adverse reactions to certain medications NSAIDs,
    ACE-inhibitors
  • Chronic urticaria with angioedema
  • Idiopathic or exercise induced anaphylaxis
  • C1-Esterase Inhibitor deficiency (hereditary or
    acquired)
  • Gleich syndrome recurrent angioedema and high
    eosinophil counts of unknown etiology
  • Angioedema in hypereosinophilic syndrome

21
  • C1 inhibitor deficiency (hereditary or acquired)
  • Hereditary
  • au.-dom.,can begin in childhood, 130.000
  • 30 new mutations
  • Depending on gene defect either type I (deficient
    quantitative production) or type II (deficient
    qualitative production) type III with nl C1 inh
    recently described in women, still poorly
    understood
  • Acquired
  • over utilization of the normal C1 inhibitor by
    high levels of antigen-antibody complexes
  • factors formed by lymphoid tumors that destroy
    C1-INH activity
  • autoantibody to the C1-INH that prevents its
    function
  • Attacks are typically triggered by trauma (e.g.
    dental surgery), infection, stress, ACE
    inhibitors, etc.

22
The role of C1 inhibitor and available treatments
Morgan, NEJM 2010
23
The role of C1 inhibitor and available treatments
  • C1 inhibitor concentrates Cinryze (pateurized,
    nanofiltered C1 inh concentrate approved for
    prophylaxis of attacks studies showed 50
    reduction in severity and frequency of attackes
    (50) if infused twice weekly
  • Attenuated Androgens (danazol, stanazol)
    increase C1 inh production in liver
  • Antifibrinolytic agents (tranexamic acid,
    epsilon-aminocaproic acid) inhibit plasminogen
    activation with consequent sparing of C1 inh
    usage

24
Complement levels in C1 inhibitor deficiency
Angioedema syndrome Complement component levels Complement component levels Complement component levels Complement component levels
Angioedema syndrome C1q C4 C2 C1-inhibitor functional/antigenic
HAE type 1 normal low low low/low
HAE type 2 normal low low low/normal
Aquired low low low low/variable
during attack
25
  • Questions ?

26
In vitro sIgE-testing
Allergen Decision point (spec. IgE kU/l) PPV
Egg 7 98
Egg infant lt 2y 2 95
Milk 15 95
Milk infant lt 2y 5  
Peanut 14 100
Fish 20 100
Soybean 30 73
Wheat 26 74
tree nuts 15 95
Sampson et al. JACI 2003.111S542
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