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Adverse Reactions to Contrast Media

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Title: Adverse Reactions to Contrast Media


1
Adverse Reactions to Contrast Media
  • Ri ???

2
Articles
  • Acute serious and fatal reactions to
    contrast media our current understanding
  • S K Morcos, FRCS, FRCR
  • British Journal of Radiology (2005) 78, 686-693
  • Adverse Reactions to Intravenous Iodinated
    Contrast Media An Update
  • Saravanan Namasivayam MD, DNB, DHA, Mannudeep K.
    Kalra MD, DNB, William E. Torres MD and William
    C. Small MD, PhD
  • Current Problems in Diagnostic Radiology Volume
    35, Issue 4 , July-August 2006, Pages 164-169

3
Introduction
  • unpredictable and not dose related
  • CM particles absorbed into the circulation
  • all the features of anaphylaxis
  • but IgE negative in most cases
  • developed within 530 min after exposure to CM
  • may present as generalized skin reactions, airway
    obstruction, angioedema or cardiovascular
    collapse
  • intermediate risk for anaphylaxis with CM

4
Prevalence of life threatening and fatal
reactions to contrast media
  • severe and very severe reactions (IV push of CM)
  • 0.22 and 0.04 after high-osmolar
    contrast media (HOCM)
  • 0.04 and 0.004 after low-osmolar
    contrast media (LOCM)
  • However ? no difference in fatal reactions
    (1170 000)
  • UK USA(FDA) ? (per million examinations) high
    with low osmolar CM
  • 194 vs 44 for all reactions
  • 37 vs 11 for severe reactions
  • 3.9 vs 2.1 for fatal reactions.
  • high osmolar agents V.S.ioxaglate (a low osmolar
    ionic dimer)
  • total reactions 194 vs 143
  • severe reactions 37 vs 34
  • fatal reactions 3.9 vs 6.4
  • low osmolar non ionic CM is the best, besides no
    definite reduction in fatal reactions,

5
Risk factors
  • 1. A history of previous severe adverse reaction
    to a contrast agent ? 6 (both ionic and non-ionic
    CM)
  • 2. Asthma ?610
  • 3. A strong history of allergic reactions to
    different substances (hay fever.)
  • 4. Treated with ß-adrenergic blockers and
    interleukin-2 (IL-2) ? acute adverse reactions to
    CM. (including the ophthalmic preparations)
  • 5. Iodinated CM ? 3
  • 6. Female lt-gt the fatality rate men with old
    age?!
  • 7. Race
  • 8. Malignant tumours ? an increase in histamine
    release
  • Pre-testing with an intravenous injection of a
    small amount of CM is not useful
  • High awareness !!

6
Table 1. European Society of Urogenital Radiology
(ESUR) guidelines on prevention of generalized
contrast medium reactions in adults
7
Pathophysiology of life threatening/fatal
reactions to contrast media
  • adverse reactions to drugs ? type B reactions,
    not dose dependent and unpredictable
  • Aronson and Ferner a new classification (DoTS)
    based on dose relatedness (Do), timing (T) and
    patient susceptibility (S)
  • drug (pharmacology and the dose dependence of its
    effects)
  • the properties of the reaction (time course of
    its appearance and its severity)
  • properties of the individual (the genetic,
    pathological and other biological differences
    that confer susceptibility)
  • Do-hyper susceptibility T first dose S not
    understood.

8
Pathophysiology
  • Type 1 hypersensitivity reaction (anaphylaxis)
    --- lack of consistency in demonstrating
    antibodies to CM
  • Within minutes
  • Chemotactic, vasoactive and spasmogenic
    compounds. leukotrienes, prostaglandins, enzymes
  • basophils and mast cells ? degranulation ?
    Histamine? primary mediator intense immediate
    manifestations. (be reproduced by histamine
    infusion)
  • ? vasodilatation, increasing vascular
    permeability ? edema
  • ? contraction of smooth muscle cells ?
    bronchospasm increasing mucus secretion of
    airways
  • ? recruit WBC ? additional waves of
    cytokines
  • direct effect of CM particles on these cells
  • non ionic monomers ? low levels of histamine
    release
  • Hyperosmolarity ? yes
  • Increasing the size and complexity of the
    molecule ? enhance the release of histamine

9
Pathophysiology--2
  • Activation of factor XII (Hageman factor) ? kinin
    system ?production of bradykinin ? induce
    vasodilatation, bronchospasm and increase
    vascular permeability.
  • Bradykinin ? arachidonic acid ? cyclooxygenase
    and lipooxygenase pathways? synthesis of PGs
    LTs
  • Patients who are asthmatic or allergic ?
    increased concentration of factor XII products
  • CM DOESNT act as happens (non-reactive
    chemically)
  • p-I concept ? drugs may directly activate T cells
    via receptors that can interact with the drug. ?
    unlikely ? T cell VS. acute life threatening CM ?
    not clear
  • IgE antibodies?
  • Complement system (C3a, C4a and C5a) ? ? no
    significant difference

10
Diagnosis of serious or fatal reaction to
contrast media
  • Histamine --- basophils and mast cells,
    tryptase---mast cells
  • Tryptase 12 h after the reaction (not greater
    than 6 h)
  • Only very high concentrations of serum tryptase
    should be regarded specific
  • Histamine 10 min to 1 h after the reaction
  • Methylhistamine, the main metabolite of histamine
    ? measured in urine
  • Specific IgE antibodies? reliable drug RAST tests
    are not widely available
  • Positive intradermal tests ? some severe reaction
    to CM
  • it is advisable to measure serum tryptase
    routinely in severe or fatal patients (AMI or
    severe vasovagal attack may develop during
    examinations)
  • Post-mortem findings --- High level of seum
    tryptase, macroscopic findings including
    pulmonary oedema, signs of asthma (mucous
    plugging and/or hyperinflated lungs), petechial
    haemorrhages and pharyngeal/laryngeal oedema

11
Prevention of acute reactions to contrast media
  • Explained to the patient the resuscitation team
  • Non-iodinated CM
  • 1. carbon dioxide (CO2) --- nausea, abdominal and
    leg pain may be observed with its administration
  • 2. gadolinium based CM--- intravascular, no above
    0.3 mmol kg1 body weight ? induce nephrotoxicity
    (not sure)
  • Non-ionic contrast media (sure)
  • The prophylactic use of corticosteroids ---
    mechanism unclear
  • Antihistamines (H1 and H2) and ephedrine --- (not
    sure)
  • Corticosteroids? complex with the cytoplasmic
    receptor?migrate into the cell nucleus ? activate
    DNA dependent RNA synthesis ? accelerated
    formation of specific enzymes inhibitors ? take
    time
  • 1. significant elevation in functional
    C1-esterase inhibitor levels,
  • 12 h after inhibits the activated form of
    factor XII
  • 2. Decreased arachidonic acid from cell membranes
  • ? production of PGs LTs (not sure)

12
Prevention of acute reactions to contrast media-2
  • fatality may still occur in patients who received
    pre-medication and low osmolar CM
  • Prompt recognition and treatment of adverse side
    effects to CM ? invaluable
  • never be left alone for at least 20 min after CM
    injection
  • the venous access
  • Emergency administration of contrast media in
    high-risk patients
  • 1. pre-treatment with hydrocortisone, 200 mg
    intravenously, immediately, and every 4 h until
    the procedure is completed
  • 2. diphenhydramine, 50 mg intravenously before
    the procedure
  • 3. low osmolar non-ionic CM

13
Treatment of acute severe reactions to contrast
media
  • Important first-line management
  • 1. Adequate airway, oxygen supplementation,
    (adrenaline use)
  • 2. IV physiological fluids, measuring BP HR
    (most effective treatment for hypotension)
  • 3. Adrenaline ? effective drug ? increases BP,
    reverses peripheral vasodilatation, decreases
    angioedema and urticaria, reverses
    bronchoconstriction, and produces positive
    inotropic and chronotropic cardiac effects
    (avoided in the pregnant patient)
  • Only one concentration (11000) ? IM of
    0.5 ml of 11000 adrenaline preparation
  • IV IS NOT GOOD? requires careful ECG
    monitoring (arrhythmia)
  • Antihistamine H1 receptor blockers ? reduce
    symptoms from skin reactions ? slow onset of
    action, and they cannot block ALREADY events
  • H2-antagonists ? not essential
  • IV injection of high-dose corticosteroids ? an
    immediate stabilizing effect on the cell membrane
    ? second-line treatment. ? reducing delayed
    recurrent symptoms
  • Inhaled ß-2-adrenergic agonists (albuterol,
    metaproterenol and terbutaline) ? bronchodilating
  • Atropine blocks vagal stimulation of the cardiac
    conduction system.
  • Large doses of aptropine (0.61.0 mg)
    are indicated 

14
Table 2. First-line emergency drugs and
instruments that should be in the room where
contrast medium is injected
15
Table 3. Simple guidelines for first-line
treatment of acute severe reactions to contrast
media
16
Thanks for your attention! ?
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