Peanut Allergy

Earn CME/CE in your profession:


Continuing Education Activity

Most primary care clinicians will encounter patients with a food allergy. Food items that account for 90% of hypersensitivity reactions include cow's milk, egg, soy, wheat, peanuts, tree nuts, fish, and shellfish. Peanuts are one of the most frequent food allergens and can cause fatal reactions when ingested. A reaction to peanuts will typically occur in the first few years of life. Peanut allergy is usually lifelong and potentially fatal. This activity addresses the evaluation and management of peanut allergies and highlights the role of the interprofessional team in the care of patients with this condition.

Objectives:

  • Describe the epidemiology of peanut allergies.
  • Summarize the evaluation of a patient with a peanut allergy.
  • Review the treatment and management options for a patient with a peanut allergy.
  • Identify some interprofessional team strategies for improving care for patients with a peanut allergy.

Introduction

Most primary care clinicians will encounter patients with a food allergy. Food items that account for 90% of hypersensitivity reactions include cow’s milk, egg, soy, wheat, peanuts, tree nuts, fish, and shellfish. Peanut is one of the most frequent food allergens and can cause fatal reactions when ingested.[1][2] A reaction to peanuts will typically occur in the first few years of life. Peanut allergy is usually lifelong and potentially fatal. 

While avoidance of peanuts can solve the problem, the ubiquitous presence of trace amounts of peanuts in food can make complete avoidance impossible, especially in children. This activity provides data on vaccination and adaptive immune-based interventions to prevent peanut allergies.

Etiology

Several studies have tested age-related peanut exposure in the development of peanut allergy. One study evaluated the prevalence of peanut allergy in Israeli Jewish children compared to Jewish children living in the United Kingdom (UK). Peanut introduction differs in these two populations whereby peanut-containing food is not restricted in Israel while it is typically delayed until the age of 2 in the UK. The results showed that Israeli children have a decreased frequency of developing a peanut allergy compared to the UK group, suggesting that the early introduction of peanuts may offer protection from developing a peanut allergy.[3] Another important study, the Learning Early About Peanut Allergy (LEAP) study, was a prospective randomized trial with one group avoiding peanuts until age 5 while the other group had repeated exposure to peanuts from 4 to 6 months until age 5. The purpose of the study was to compare the incidence of peanut allergy between the two groups after 5 years. The children in this study were at high risk of developing a peanut allergy. They defined high risk as either having severe eczema or egg allergy. The results of the LEAP study showed that early introduction of peanuts to high-risk infants early could prevent the development of a peanut allergy.[4][5] Current guidelines recommend peanut introduction as early as 4 to 6 months of age in high-risk infants.

Risk factors include:

  • History of atopy
  • Family history of peanut allergy
  • Maternal consumption of peanuts during pregnancy
  • Use of certain oils to fry/roast peanuts

Epidemiology

Food allergies affect approximately 4% to 8% of children and 1% to 2% of adults.[1] Peanut allergy typically manifests initially during childhood with symptom occurrence as early as 4 months of age and usually within the first 2 years of life. Approximately 20% of children will naturally outgrow their peanut allergy and tolerate them without events later on in life.  

In general, there appears to have been an increase in peanut allergy over the past 2 decades. The first evidence of peanut allergy may come to light between ages 12-24 months and unlike egg or milk allergies, peanut allergy does not always decrease with time. Some studies indicate that the severity of reactions to peanuts also increases with age.

Pathophysiology

Food allergy classifies as a type I IgE mediated hypersensitivity reaction. Initial sensitization to peanuts stimulates the production of peanut-specific IgE antibodies. The major peanut antigens identified by the specific antibodies response include AraH1, H2, H3. In a sensitized individual, peanut ingestion can trigger specific IgE antibody cross-linking to IgE receptors on effector cells such as basophils and mast cells, which triggers mediator release such as histamine and a variety of cytokines and chemokines. Inflammatory cell recruitment ensues to propagate the allergic response.[1]

The allergy to peanuts is due to low molecular weight proteins that are resistant to heat, proteases, and denaturants. Eleven peanut allergens have been described (Ara h 1-11).

History and Physical

Diagnosis of a peanut allergy relies on patient history and physical exam. The type/amount of food ingested, onset/duration of symptoms, and relieving factors are key in making an accurate diagnosis. A history of eczema is important as it is a significant risk factor for peanut sensitization. Common symptoms of peanut allergy include skin reactions, such as urticaria, erythema, or edema. More severe symptoms include tingling of the mouth and throat, edema of the lips, and dyspnea. These symptoms will often frequently progress to anaphylaxis.

Evaluation

Skin testing is the preferred testing method in those patients with a history compatible with food allergies. A skin-prick test is performed by applying a drop of a peanut extract to the skin, commonly on the arm or back. A wheal/flare response is measured approximately 20 minutes after pricking the skin where the drop of peanut extract was placed. Positive testing indicates sensitization to peanuts and can predict the probability of a future reaction. Measurement of peanut-specific IgE antibodies in serum is another useful method to estimate sensitization and the probability of future reaction. It is important to note that this type of testing does not predict the severity of the reaction and is limited by poor sensitivity; results are reassuring when negative. Ultimately a clinician-supervised oral food challenge is the best and most reliable method for diagnosing peanut allergy. Serum-specific IgE and skin-prick testing can aid in determining which patients should have an oral food challenge.[6][7] An oral food challenge can also assist in confirming reactivity in those patients without a clear history or never having ingested peanuts despite sensitization.

Treatment / Management

To date, the recommended management of peanut allergy relies on avoidance of peanut ingestion. Unfortunately, severe reactions such as anaphylaxis may occur despite best efforts in avoidance. Epinephrine is the first-line medication for the treatment of anaphylaxis. Intramuscular (IM) or intravenous (IV) epinephrine should be administered, although the IM route is preferred, with injection placement in the lateral thigh. IV administration ideally should be done in the inpatient setting with appropriate monitoring.[8] Antihistamines, corticosteroids, and bronchodilators, may also be used, but it is essential to realize these medications do not treat anaphylaxis, rather they are adjunctive therapies for anaphylaxis management. IV fluids should be provided to prevent and treat tissue hypoperfusion. In rare cases, the patient may require intubation for airway protection. Severe cases of anaphylaxis should be admitted and monitored at least overnight until stable. Biphasic anaphylaxis may occur in some cases where symptoms recur up to 8 hours after the initial reaction. The treating clinician should take this into account before discharge.[9] In less severe presentations the patient can be observed in the emergency department after standard treatment, and with sufficient improvement safely discharged home. 

Although avoidance is the mainstay of treatment, new strategies are being tested to prevent food allergies. Peanut immunotherapy clinical trials have been promising to date using incremental ingestion of small amounts of peanut over time with oral immunotherapy (OIT). The goal of OIT may be either to prevent a reaction if accidental peanut ingestion occurs or to induce tolerance where the patient can regularly ingest peanuts safely.[1][10] Epicutaneous immunotherapy is another desensitization method tested where peanut is transdermally introduced over time to build up a tolerance.  

Immunization with plasmid DNA encoding food allergens is a novel method to treat peanut allergy. However, this approach requires a large amount of plasmid DNA required for vaccination.

Mutated peanut protein substitutes are another way to manage peanut allergies.

Finally, sublingual immunotherapy involves placing emulsified purified peanut protein under the tongue for 120 seconds and then swallowing. Data show that this can help prevent peanut allergic reactions with time.

Differential Diagnosis

  • Acute urticaria
  • Food intolerance (e.g., lactose intolerance)
  • Toxic reaction (e.g., scombroid poisoning)
  • Oral allergy syndrome
  • Eosinophilic esophagitis

Prognosis

Approximately 20% of patients with a peanut allergy will naturally acquire tolerance to peanuts over time. Unfortunately, peanut allergy is usually lifelong and remains potentially fatal.

Complications

Symptoms can occur within seconds of ingestion, with peak occurrence by 30 minutes but can delay up to 2 hours. Major target organs of an allergic reaction include the skin, gastrointestinal (GI), and respiratory tracts. Skin-related symptoms include urticaria, angioedema, and occasional worsening of existing eczema. GI symptoms include abdominal pain, vomiting, and/or diarrhea. Respiratory symptoms can manifest as repetitive coughing, stridor, and wheezing. Also, it can affect the cardiac and the central nervous systems in the setting of anaphylactic shock whereby diminished tissue perfusion leads to cardiac arrest and syncope.[10] Symptom presentation must be interpreted in the context of the patient's history, i.e., symptoms are relevant to a food allergy when ingestion occurs in the appropriate time frame expected for food-induced allergic reactions.

Deterrence and Patient Education

Patients and parents should be educated on the importance of avoiding peanuts and all peanut-containing products. All caregivers and teachers should be made aware of the allergy as well. It is vital that these patients carry injectable epinephrine with them everywhere they go.

Enhancing Healthcare Team Outcomes

Managing a peanut allergy usually involves an interprofessional team. The majority of patients are first seen by the primary care clinician. While avoidance is the primary means of preventing a food allergy reaction, strict avoidance can place a significant burden on patient quality of life and provoke anxiety in patients and family members.[11][12] Besides avoiding peanuts, nurses should educate patients to be careful not to consume cross-contaminated foods how to interpret food labels to identify sources of food allergens. A self-injectable epinephrine prescription is necessary for patients with peanut allergies. They should receive education on how to recognize the signs and symptoms of food hypersensitivity and how to administer epinephrine. Today there are novel ways to decrease peanut allergy with various types of immunotherapeutic methods. The oral immunotherapy technique has been shown to have the most promise. However, until a definitive method of preventing peanut allergy is available, the key is for all clinicians to encourage allergic patients to carry injectable epinephrine and avoid peanuts.


Details

Author

Reena Patel

Editor:

Alan P. Koterba

Updated:

7/4/2023 12:29:12 AM

References


[1]

Al-Muhsen S, Clarke AE, Kagan RS. Peanut allergy: an overview. CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne. 2003 May 13:168(10):1279-85     [PubMed PMID: 12743075]

Level 3 (low-level) evidence

[2]

Sicherer SH, Sampson HA. Peanut and tree nut allergy. Current opinion in pediatrics. 2000 Dec:12(6):567-73     [PubMed PMID: 11106277]

Level 3 (low-level) evidence

[3]

Finkelman FD. Peanut allergy and anaphylaxis. Current opinion in immunology. 2010 Dec:22(6):783-8. doi: 10.1016/j.coi.2010.10.005. Epub 2010 Nov 2     [PubMed PMID: 21051210]

Level 3 (low-level) evidence

[4]

Stiefel G, Anagnostou K, Boyle RJ, Brathwaite N, Ewan P, Fox AT, Huber P, Luyt D, Till SJ, Venter C, Clark AT. BSACI guideline for the diagnosis and management of peanut and tree nut allergy. Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology. 2017 Jun:47(6):719-739. doi: 10.1111/cea.12957. Epub     [PubMed PMID: 28836701]


[5]

Du Toit G, Roberts G, Sayre PH, Bahnson HT, Radulovic S, Santos AF, Brough HA, Phippard D, Basting M, Feeney M, Turcanu V, Sever ML, Gomez Lorenzo M, Plaut M, Lack G, LEAP Study Team. Randomized trial of peanut consumption in infants at risk for peanut allergy. The New England journal of medicine. 2015 Feb 26:372(9):803-13. doi: 10.1056/NEJMoa1414850. Epub 2015 Feb 23     [PubMed PMID: 25705822]

Level 1 (high-level) evidence

[6]

Rabjohn P, Helm EM, Stanley JS, West CM, Sampson HA, Burks AW, Bannon GA. Molecular cloning and epitope analysis of the peanut allergen Ara h 3. The Journal of clinical investigation. 1999 Feb:103(4):535-42     [PubMed PMID: 10021462]


[7]

Stanley JS, King N, Burks AW, Huang SK, Sampson H, Cockrell G, Helm RM, West CM, Bannon GA. Identification and mutational analysis of the immunodominant IgE binding epitopes of the major peanut allergen Ara h 2. Archives of biochemistry and biophysics. 1997 Jun 15:342(2):244-53     [PubMed PMID: 9186485]


[8]

Sicherer SH, Forman JA, Noone SA. Use assessment of self-administered epinephrine among food-allergic children and pediatricians. Pediatrics. 2000 Feb:105(2):359-62     [PubMed PMID: 10654956]


[9]

Boyce JA, Assa'ad A, Burks AW, Jones SM, Sampson HA, Wood RA, Plaut M, Cooper SF, Fenton MJ, Arshad SH, Bahna SL, Beck LA, Byrd-Bredbenner C, Camargo CA Jr, Eichenfield L, Furuta GT, Hanifin JM, Jones C, Kraft M, Levy BD, Lieberman P, Luccioli S, McCall KM, Schneider LC, Simon RA, Simons FE, Teach SJ, Yawn BP, Schwaninger JM, NIAID-Sponsored Expert Panel. Guidelines for the Diagnosis and Management of Food Allergy in the United States: Summary of the NIAID-Sponsored Expert Panel Report. The Journal of allergy and clinical immunology. 2010 Dec:126(6):1105-18. doi: 10.1016/j.jaci.2010.10.008. Epub     [PubMed PMID: 21134568]


[10]

Bublin M, Breiteneder H. Developing therapies for peanut allergy. International archives of allergy and immunology. 2014:165(3):179-94. doi: 10.1159/000369340. Epub 2014 Dec 20     [PubMed PMID: 25531161]


[11]

Sicherer SH, Noone SA, Muñoz-Furlong A. The impact of childhood food allergy on quality of life. Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology. 2001 Dec:87(6):461-4     [PubMed PMID: 11770692]

Level 2 (mid-level) evidence

[12]

Primeau MN, Kagan R, Joseph L, Lim H, Dufresne C, Duffy C, Prhcal D, Clarke A. The psychological burden of peanut allergy as perceived by adults with peanut allergy and the parents of peanut-allergic children. Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology. 2000 Aug:30(8):1135-43     [PubMed PMID: 10931121]