Idiopathic Anaphylaxis. Paul A. Greenberger, MD, FAAAAI 2/28/2014 Course # 1605

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Transcription:

Idiopathic Anaphylaxis Paul A. Greenberger, MD, FAAAAI 2/28/2014 Course # 1605

Objectives Review definition and classification of idiopathic anaphylaxis Consider the differential diagnosis Critique lab tests/procedures used in the work up of patients with idiopathic anaphylaxis Examine treatment recommendations

Definition of Idiopathic Anaphylaxis is anaphylaxis not explained by a proved or presumptive cause or stimulus. It becomes a diagnosis of exclusion after other causes have been considered, such as foods, medications, exercise, food and exercise, insect stings or bites, mastocytosis, and C1 esterase inhibitor deficiency/dysfunction. Greenberger PA. Idiopathic anaphylaxis in Immunol Allergy Clin NA 2007;27:273-93.

Besides The Careful History, The Work Up May include skin and in vitrotests for serum specific IgE to foods and drugs, serum IgE to galactose-alpha-1,3-galactose (alpha-gal), baseline and acute phase serum tryptase, 24- hour urinary histamine metabolites, urinary prostaglandin D 2, oral challenges, peripheral blood for the mutation of the gene D816V and in some cases, a bone marrow examination.

Idiopathic Anaphylaxis Mast cell activation but a diagnosis of exclusion Tryptase elevated acutely Urine Histamine elevated acutely (even with tongue or uvula enlargement) IA-Angioedema B cell activation CD19+CD23+ Responsiveness to prednisone/h1 antagonists Normal C4 and complements + Prick skin tests to foods non-contributory

Conditions/Initials Indolent Systemic Mastocytosis (ISM) Monoclonal mast cell activation syndrome (MMAS) Mast cell activation syndrome (MCAS) Idiopathic anaphylaxis (IA)

Classification of Idiopathic Anaphylaxis IA-Generalized(urticaria, angioedema, respiratory distress, upper airway angioedema, hypotension, abdominal pain, diarrhea) IA-Angioedema(urticaria, upper airway angioedema-obstructive) IA-Questionable(Urticaria without objective evidence of upper/lower airway obstruction, hypotension when syncopal etc)

Atopy in 48% of 333 IA Patients Ann Allergy Asthma Immunol 1996;77:285-91 Allergic rhinitis alone 19% Asthma alone 13% Allergic rhinitis and asthma 11% Food induced anaphylaxis 5% Atopic dermatitis 1.5% Pre-existing urticaria or angioedema 23%

Is There an Effect of Atopy on Anaphylaxis? Yes No Foods Latex Radiocontrast material Asthma Idiopathic anaphylaxis Exercise induced anaphylaxis Aspirin Exacerbated Respiratory Disease Penicillin Muscle relaxants Hymenoptera stings Insulin

Idiopathic Anaphylaxis Considering and excluding other causes of anaphylaxis Being aware of new observations Knowing the patient and disease

SM MMAS MCAS IA Baseline tryptase >20 Normal or mildly increased Normal or mildly increased Normal c-kit D816V + + Multifocal mast cell aggregates + Aberrant CD25 + + 80% UP +/ Mediator release symptoms + + + + Hypotensive episodes +/ +/ +/ +/ Urine N-MH or PGD 2 Increased at baseline Increased during symptoms Increased during symptoms Increased during symptoms Response to antimediator therapy + + + +/

Mast Cell Activation Syndrome JACI 2010;126;1099-1104 1. Episodic symptoms ( 2) of Skin, GI, Cardiovascular, Wheezing, Naso-ocular 2. Decrease/resolution with anti-mediator therapy (H1, H2, LTRA or biosynthesis inhibitor or oral cromolyn) 3. Evidence of an increase in urinary or serum marker on 2 occasions when symptomatic 4. r/o primary or secondary causes of mast cell activation and idiopathic entities

Mast Cell Activation Syndrome JACI 2010;126;1099-1104 If baseline serum tryptase is 15 ng/ml, require an increase during symptoms above baseline

Classification of Idiopathic Anaphylaxis.. Terminology Objective Evidence for Anaphylaxis? Idiopathic Anaphylaxis Generalized Idiopathic Anaphylaxis Angioedema Corticosteroid Dependent Idiopathic Anaphylaxis Malignant Idiopathic Anaphylaxis Undifferentiated Somatoform Idiopathic Anaphylaxis yes yes yes yes no

Idiopathic Anaphylaxis-Tips Atopy often present May co-exist with Exercise Induced Anaphylaxis, chronic idiopathic urticaria and/or food allergy (anaphylaxis) May be followed by PANIC ATTACKS not additional episodes of anaphylaxis Rarely proved to be Indolent Systemic Mastocytosis, Mast Cell Activation Syndrome, Urticaria Pigmentosa.

Anaphylaxis Implies a Risk of Death.. Self injectable epinephrine (verify presence and use of demo) H1 receptor antagonist Oral albuterol (if tolerated) Prednisone for initial therapy

Pharmacologic Approaches to Idiopathic Anaphylaxis Initial Therapy Epinephrine auto-injector Cetirizine (or H1 receptor antagonist) Albuterol orally (if tolerated) Prednisone if severe or frequent If not controlled, not more than cases described LTRA Oral cromolyn Oral ketotifen Azathioprine or tacrolimus (oral) Omalizumab (in literature)

Initial Treatment with Prednisone, H1 antagonist, Epi available Prednisone 60mg o Prednisone alternate mornings Prednisone daily Months

Control of Episodes; Gradual tapering of Prednisone

Practice Parameters on Anaphylaxis JACI 2010;126:477-80 Empiric use of oral steroids/h1 blockers has been demonstrated to reduce the frequency/severity of episodes (C)

Frequency of Idiopathic Anaphylaxis Frequent: 2 attacks in 2 months or 6 in 1 year Infrequent: < 6 attacks in 1 year

Ineffectiveness of Prednisone: Episodes Continue in First Month Consider Undifferentiated Somatoform IA

Undifferentiated Somatoform- Idiopathic Anaphylaxis US-IA..JACI 1995;96:893-900 When prednisone increases attacks When objective evidence cannot be confirmed When there is no response to therapy When the pt meets criteria for a somatoform disorder Manage with non-steroid therapy Pt typically won t obtain psychiatry consultation

Somatoform Condition One or more physical complaints Symptoms/signs lasting 6 months and 1 or 2 1.Exam doesn t confirm objective evidence 2.Symptoms, impairment or physical problems are grossly out of proportion to physical exam findings Urticaria (limited) + passing out (NL BP, pulse)

Idiopathic Anaphylaxis Considering and excluding other causes of anaphylaxis Being aware of new observations Knowing the patient and disease

Considering and ExcludingOther Causes of Anaphylaxis..Northwestern Experience Hidden Foods..is allergic reaction > 3 hrs from onset.or is it from beef, pork or lamb? Non-reported medication Bee pollen (pollens + molds) consumed K 2 S 2 O 5 (1mg, placebo, 5, 10, 25, 50, 100, 200= 391mg or 4x a heavily sulfited restaurant meal) MSG (81mg total challenge) Aspartame Papain (consumed)

Anaphylaxis Questions/Considerations re the oligosaccharide galactose-α-1,3-galactose? Questions: Has glycosylation of the Fab or Fc fragment made an immunoglobulin (cetuximab) immunogenic or did a tick bite sensitize the patient to a SUGAR that caused anaphylaxis? Does the patient report delayed (3-6 hours) onset urticaria (anaphylaxis) after BEEF, PORK or LAMB? Can the patient tolerate chicken, turkey and fish? Have there been tick bites?

Skin Tests to Foods prick, ID in Patients + for anti-alpha Gal IgE JACI 2009;123:426-433 Time to Onset of Anaphylaxis in 10 patients: 1-2 to 6 hours Intradermal Food Tests

The % of Anti-Alpha Gal IgE in the U. VA. Allergy- Immunology Pediatric Service 24% of 142 children/adolescents ages 4-18 seen for wheezing Pediatrics 2013;131:e1345-e1552 Presumably sensitized by tick bites

How Would You Describe the Urticarial Lesions that Accompany Carcinoid Syndrome Pheocromocytoma Scromboid poisoning Non-Scromboid poisoning