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Anaphylaxis Jonathan A. Bernstein, M.D. Anaphylaxis Jonathan A. Bernstein, M.D.

Anaphylaxis Jonathan A. Bernstein, M.D. - PowerPoint Presentation

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Anaphylaxis Jonathan A. Bernstein, M.D. - PPT Presentation

Professor of Medicine Department of Internal Medicine Division of ImmunologyAllergy Section Objectives Definition Epidemiology Pathophysiology Signs Symptoms Management Prevention JTF Guidelines Algorithms ID: 909699

allergy anaphylaxis clinical immunologic anaphylaxis allergy immunologic clinical treatment blood epinephrine management presentation asthma immunol vol reaction skin hypotension

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Slide1

Anaphylaxis

Jonathan A. Bernstein, M.D.

Professor of Medicine

Department of Internal Medicine

Division of Immunology/Allergy Section

Slide2

Objectives

Definition

Epidemiology

Pathophysiology

Signs + Symptoms

Management

Prevention

JTF Guidelines Algorithms

Slide3

Allergy and Clinical Immunology

Asthma/COPD and mimickers

Rhinitis

Recurrent sinusitis

With and without nasal polyps

ImmunodeficiencyUrticaria/angioedemaAtopic dermatitisContact dermatitisPruritusChronic cough

Drug reactions

Food allergy/intolerance

Mast cell disorders

Eosinophilia (PIES, GI disorders, HES…)

Occupational respiratory and skin diseases

Headaches

Insect sting reactions

Slide4

Anaphylaxis: No Consensus Definition

Clinical Criteria

Acute onset with skin or

mucosal signs

AND

- Respiratory compromiseOR- Hypotension(Approximately 80% anaphylaxis)

Slide5

Anaphylaxis: Definition Continued

Clinical Criteria

Two of the following after

exposure to known allergen

- Skin/mucosal

- Respiratory- Hypotension- GastrointestinalHypotension after exposure to known allergen

Need to use epinephrine?

Slide6

Slide7

Epidemiology

Anaphylaxis

Risk of death

~

1%

Mortality ~ 500 – 1000 deaths annuallyFood (125 – 200 fatalities/year)Insect (40 – 50 fatalities/year)

Slide8

Pathophysiology

Hypersensitivity Type I

Prior sensitization

IgE/Mast cell mediated

Slide9

Pathophysiology

Histamine

H

1

Smooth muscle contraction, increased vascular permeability, mucus production, coronary artery spasm,

eosinophil+neutrophil chemotaxisH2Increased cardiac contraction, gastric acid secretion, airway mucus production, vascular permeability

Slide10

Anaphylaxis Classification

Immunologic (i.e., IgE mediated)

Non-immunologic (

anaphylactoid

)

Idiopathic – diagnosis by exclusion

Slide11

Causes: Immunologic

Food

Peanuts + tree nuts

80 – 90 % of food

related

rxn in childrenSeafoodCommon cause in adults

Slide12

Causes: Immunologic

Insect

Hymenoptera

Honeybee

Yellow jacket

WaspHornetFire ant

Slide13

Causes: Immunologic

Antibiotics

Penicillin

Cross reaction

Cephalosporins

AztreonamCarbapenemsSkin testing

Slide14

Causes: Immunologic

Latex – resolved with avoidance measures

Risk factors

Cross reaction

Banana Tomato

Avocado CarrotChestnut CeleryHazel nut PapayaKiwi PotatoMelon

Slide15

Other Less Common Immunologic Causes

Progestin Hypersensitivity

Seminal Plasma Hypersensitivity

Alpha Gal Allergy

Slide16

Causes: Non-Immunologic

NSAIDs/Aspirin

No cross reaction

Unclear mechanism

Slide17

Causes: Non-Immunologic

IV Contrast Media

Risk factors

Asthma

Prior reaction

Premedication(benedryl 50mg po and prednisone 50mg 13, 7 and 1 hour prior to contrast, low osmolality contrast)

Slide18

Causes: Non-Immunologic

Exercise

Urticaria/angioedema

Associated factors

Eating before exercise

Specific foods? Celery? atopyProphylaxis not always effectiveCarry Epi and buddy-up

Slide19

Causes: Immunologic or Non-Immunologic

Anesthesia

Muscle Relaxants

Induction agents

Opioids

Local anestheticsOther IV agentsColloidsBlood productsProtamine

Slide20

Anesthetic Agents Associated With Anaphylaxis

And Proposed Mechanisms

Slide21

Skin Testing To Anesthetic Agents

Slide22

Clinical Presentation

Slide23

Signs and Symptoms of Anaphylaxis

Lieberman P, Nicklas R, Oppenheimer

J, et al. The diagnosis and management of anaphylaxis practice parameter:

2010 update. J Allergy Clin

Immunol

. 2010;126:477e480;

Wood R, Camargo CA, Lieberman P, et al. Anaphylaxis in America: results from a national physician survey.

Ann Allergy Asthma

Immunol

. 2012;109 (

suppl

):A20;

Boyle J, Camargo CA, Lieberman P, et al. Anaphylaxis in America: results from a national telephone survey. J

Allergy Clin

Immunol

. 2012;129 (

suppl

):AB132.

Slide24

Essential Features of History in Evaluation of a

Patient Who Experienced Anaphylaxis

Slide25

Clinical Presentation

Urticaria

Slide26

Clinical Presentation

Angioedema

Slide27

Clinical Presentation

GI

Nausea/vomiting

Abdominal pain

CV

Tachycardia – except Bezold-Jarisch reflexHypotensionDysrhythmias

Slide28

Clinical Presentation

Respiratory

Rhinitis

Bronchospasm

Laryngeal edema

Slide29

Differential Diagnosis of Anaphylaxis

Slide30

Diagnostic Tests For Establishing

Anaphylaxis As A Cause

Slide31

Diagnostic Testing

Serum

tryptase

level

Peak at 1 – 1 ½ hours,

nl in 6 hoursSerum histamine – not recommended

Elevated at five minutes,

nl

in 30 – 60 minutes

Urinary methylhistamine – 24 hour collection more appropriate for systemic

mastocytosis

Slide32

World Health Organization Criteria

For Systemic

Mastocytosis

Slide33

Anaphylaxis

Treatment

ABCs

Epinephrine

0.5 mg

IM/SC every 5 minPediatric (0.01 mg/kg, max 0.3 mg)Hypotension 0.01 mg IVCardiovascular collapse 0.1 to 0.5 mg IVInfusion

Slide34

Anaphylaxis

Treatment

β

agonists/Oxygen

Corticosteroids – biphasic prophylaxis

1 – 2 mg/kg methylprednisolone IVVolumePositioningAntihistamines H1 – DiphenhydramineH2 – Ranitidine

Slide35

Anaphylaxis

Treatment

Dopamine

400 mg in 500 cc D5 at 2-20

ug

/kg/minVasopressinGlucagon1 – 5 mg IV plus infusion 5-15 ug/min

Slide36

Anaphylaxis

Disposition

Observation 4 – 6 hours

Risk of Biphasic reaction 4 – 20%

Hospital Admission

Severe or refractory reactionReactive airway diseaseβ blocker

Slide37

Anaphylaxis

Treatment on Disposition

Corticosteroids

H

1

BlockerConsider 2nd generation

Slide38

Anaphylaxis

Follow-up

Epi-pen

Avoid precipitating allergen

Allergist/PCP

Slide39

Slide40

Slide41

JTF Guideline:

Algorithm For Initial Evaluation of Anaphylaxis

Slide42

Management Of Anaphylaxis In The Outpatient Setting

Slide43

References

Sampson HA. Second Symposium on the Definition and Management of Anaphylaxis: Summary Report – Second National Institute of Allergy and Infectious Disease/Food Allergy and Anaphylaxis Network Symposium.

Ann

Emer

Med

. Vol 47:4 2006Lieberman P. The diagnosis and management of anaphylaxis: An updated practice parameter. J Allergy Clin Immunol. Vol 115:3 2006; Lieberman P et.al. Anaphylaxis--a practice parameter update 2015. Ann Allergy Asthma Immunol. 2015 Nov;115(5):341-84Gruchalla RS,

Pirmohamed

M. Antibiotic allergy.

NEJM

. Vol 354:6 2006

Freeman TM. Hypersensitivity to Hymenoptera Stings.

NEJM

. Vol 351:9 2004

Simons FE. Advances in H1 antihistamines.

NEJM

. Vol 351:21 2004

Simons FE et.al. World Allergy Organization anaphylaxis guidelines: summary. J Allergy Clin

Immunol

 2011 Mar;127(3):587-93.

Zibners

L,

Laddis

D,

Sadow

KB. Pediatric anaphylaxis: critical aspects of ED management.

Ped

Emer

Med Reports

. 2006

Mackay IR, Rosen FS. Allergy and allergic disease.

NEJM

. Vol 344:2 2001

Hussain AM Vasopressin for the management of catecholamine-resistant anaphylactic shock.

Singapore Med J

49(9) 2008

Jones DH. Time-dependent inhibition of histamine-induced

cutneous

response by oral and intramuscular diphenhydramine and oral fexofenadine.

Ann Allergy Asthma

Immonol

100(5) 2008

Sheikh A H1-antihistamines for the treatment of anaphylaxis with and without shock.

Cochrane Collaboration

2008

Sheikh A Epinephrine for the treatment of anaphylaxis with and without shock.

Cochrane Collaboration

2008

Slide44

Question 1

A 21 year male presents to the ED to with symptoms of diffuse

urticaria

, facial swelling and throat swelling sensation. He relates the symptoms to beginning within 15 minutes after eating at a Chinese restaurant. He has a history of mild allergies and asthma as a child but is otherwise healthy. His vital signs show a blood pressure of 100/60 and a pulse of 95. Physical exam reveals diffuse hives over 85% of his body and upper lip edema. There is no evidence of stridor or posterior pharyngeal swelling on exam

.

Based on this presentation the most appropriate next step is to:

Treat with diphenhydramine 50mg IVP

Treat with

solumedrol

60mg IVP

Treat with epinephrine .05cc 1:1000 IM

Monitor for improvement

Intravenous fluids

Slide45

Discussion

Answer – c

Patients presenting to the ED with hives with or without angioedema are often difficult to differentiate from anaphylaxis. Given the acute onset and no prior history in conjunction with the episode occurring in close proximity to eating, it is important to first consider anaphylaxis in this setting. His slightly low blood pressure and elevated pulse could be subtle clues to the occurrence of anaphylaxis. While all of the other answers are appropriately adjunctively, the treatment of choice for this patient should be with epinephrine.

Slide46

Question 2

A 54 year old obese male was undergoing radical nephrectomy surgery for renal cell carcinoma. Immediately after induction of anesthesia his blood pressure was noted to decrease to 70/P. There was no evidence of hives or angioedema. He had received cefazolin, lidocaine,

rocuronium

, ketamine, fentanyl and midazolam. He was immediately administered epinephrine and IV fluids. His blood pressure stabilized and the surgery was aborted

.

The most appropriate next step would be:

Administration of diphenhydramine 50mg IV

Obtain blood for a

tryptase

level

Administration of

solucortef

120mg IVP

Skin testing to the anesthetic agents

Refer to a cardiologist for cardiovascular work up

Slide47

Discussion

Answer b

This case represents

peri

-operative anaphylaxis which can manifest solely has hypotension without other clinical manifestations. The appropriate treatment was epinephrine and IVFs. While all of the other choices are reasonable to pursue during the hospitalization or as an outpatient, obtaining blood for a

tryptase level would be the best option for determining if the event was indeed anaphylaxis. The earlier blood is drawn after a suspected anaphylaxis event the better chance to observe a positive test as tryptase levels peak within 1-1.5 hours and normalize by 6 hours.