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Pediatric allergies: Clinical practice

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Pediatric allergies: Clinical practice

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A 5-year-old boy comes to the emergency department with his mother because of a skin rash on his face that is very itchy for 20 minutes.  His mother says that within minutes of eating peanut butter, he vomited and developed hives on his face. Physical examination shows hives that appear red, raised, and are localized to his face. His medical history is noncontributory and he is up-to-date on his immunizations. His pulse is 90/min, respirations are 22/min, and blood pressure is 120/85 mm Hg. He does not have stridor on auscultation. Which of the following is the most likely explanation for this patient’s physical findings?

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Content Reviewers:

Rishi Desai, MD, MPH

Allergies are an IgE-mediated Type I hypersensitivity reaction against a specific allergen. These include environmental triggers, like viral infections, animal dander, latex, pollen, and insect stings; foods, like nuts, shellfish, and eggs; and medications, like penicillins and sulfonamides. And these usually present first during childhood.

Now, allergic reactions happen in two steps.

Step one - exposure to the allergen causes allergen-specific IgE antibodies to bind to the surface of mast cells and basophils.

Step two - a repeat exposure to the allergen causes those mast cells and basophils to release proinflammatory molecules like histamine.

Generally, there are acute allergic reactions which resolve within 6 weeks, and chronic allergies which persist for more than 6 weeks.

Among the acute allergic reactions, the most common trigger is a viral upper respiratory tract infection.

One outcome is urticaria, also called hives, which are slightly raised, well-defined wheals that are 1 mm to 10 cm in diameter. They’re usually red, blanch with pressure, are extremely itchy, and can pop up anywhere in the body.

The key feature is that these lesions come and go very rapidly - meaning one might appear on the leg as another disappears from the arm. The reaction involves the epidermis and dermis layers of the skin, and the whole thing typically resolves within 24 hours.

Typically no treatment is needed, but if the itching is really bad, topical cooling moisturizers or oral second-generation histamine H1 blockers can be used like loratadine, desloratadine, fexofenadine, cetirizine, or levocetirizine. If these don’t work, immunomodulatory agents, like cyclosporine or methotrexate can also be used.

Now, if there’s recurrent urticaria, it’s good to try to identify a trigger, so that it can be avoided.

One way is with in vivo skin prick tests, which is where small drops of up to 40 allergens, like pollens, fungi, animal dander, house dust mites, and various foods, are pricked into the skin on the forearm or upper back. After that, if there are signs of urticaria within about 20 minutes, that implies that the substance is a trigger. Unfortunately, it’s a bit uncomfortable and requires that the individual doesn’t take any antihistamines and doesn’t have any other skin disease.

Another way is with in vitro blood tests that look for IgE antibodies against specific allergens, such as foods, insect venoms, pollen, mold, latex, or antibiotics. This takes longer, is more expensive, but is more convenient, and isn’t affected by medications or skin diseases.

Unfortunately, both of these tests can have lots of false positives, meaning that the test might suggest a problem allergen, even though a person might really have no symptoms from that allergen, and the tests can have lots of false negatives, meaning that the test might suggest that an allergen causes no reaction, even though a person might really have symptoms from that allergen in their daily life.

Occasionally, in addition to urticaria an individual might also develop angioedema.

Angioedema is often triggered by foods, latex, or insect stings, but it can also be hereditary, which is caused by deficiency of the complement C1 inhibitor or caused by medications, like ACE-inhibitors.

Angioedema can happen almost anywhere on the skin, like in the hands, feet, trunk and urogenital area, but it’s most common, on the face, like around the eyes or nose. It involves even deeper skin layers, like the subdermis and mucosal layers, like the submucosal tissue.

When it involves the skin, angioedema doesn’t cause intense itching, but can cause tenderness and burning.

Angioedema can also happen internally - involving the gastrointestinal mucosa, and causing nausea, vomiting, or diarrhea, or the mucosa of the mouth, lips or tongue, which can progress down to the larynx, closing off the airway.

Now in rare situations, urticaria or angioedema can worsen and cause anaphylaxis.

To diagnose anaphylaxis, at least one of three criteria has to be met.

One criteria is a rapid onset of symptoms that involve skin or mucosa -like urticaria or angioedema, plus at least one other organ system, like the respiratory system, causing dyspnea, the cardiovascular system causing hypotension, or the nervous system, causing syncope.

The second criteria is exposure to a likely allergen, followed by symptoms in any two organ systems.

The third criteria is exposure to a known allergen, for example something that they have been previously tested positive for, followed by hypotension.

Usually anaphylaxis symptoms peak within 30 minutes, and then fade, but sometimes there’s a biphasic reaction, where the symptoms resurge again within a day without reexposure to the allergen.

Other times, there might be a protracted anaphylactic reaction which can last for days.

Both acute angioedema and anaphylaxis are medical emergencies, so they have to be treated right away - that means an intramuscular shot of 1:1000 epinephrine with an EpiPen shot in the thigh. This contains 1 mg/mL of epinephrine and the dose is 0.01 mg/kg with a maximum of 0.5 mg.

Ιf the child has severe trouble breathing or inspiratory stridor, this is followed by immediate airway management, with intubation or cricothyroidotomy, along with supplemental oxygen.

At the same time, in the case of anaphylaxis, if there is hypotension, fluid resuscitation should be started immediately. Specifically, these children are given boluses of normal saline of 20 mL/kg, each over 5 to 10 minutes, which are repeated as needed. In severe cases, though, large volumes of fluid- up to 100 mL/kg may be required to bring the blood pressure back up to normal.

Oral, second- generation antihistamines, such as cetirizine, can also be used to relieve some of the symptoms.

Close monitoring for at least a day after symptoms resolve is important, in case there’s a biphasic reaction and another wave of symptoms.

Before they leave, it’s important that these children should be given epinephrine autoinjectors that they can use right away if there’s a future attack. For children weighing less than 30 kg, an EpiPen Junior Autoinjector is used which delivers 0.15 mg of epinephrine, and for those over 30 kg, an adult EpiPen with 0.3 mg of epinephrine is used.

Now, if symptoms of urticaria or angioedema persist for more than 6 weeks, then it’s considered a chronic allergy. Here, the treatment requires a stepwise approach.

First, a second-generation antihistamine, like 5 mg of levocetirizine or desloratadine, is given on a daily basis. Two weeks later, if symptoms persist, the dose can be increased up to two to four times, so to 10 or 20 mg daily.

Four weeks later, if symptoms persist, then a different second- generation H1 blocker can be given or a first-generation H1 blocker, such as diphenhydramine, chlorpheniramine or hydroxyzine is given. These medications act faster, but they also cross the blood-brain barrier, causing side effects like drowsiness and sedation, as well as antimuscarinic side effects, like dry eyes, dry mouth, urinary retention, and constipation.

In other cases, a histamine H2 blocker, such as cimetidine and ranitidine, may be added. H2 blockers block histamine receptors in the stomach, so they have no direct effect on allergic symptoms. But they also interfere with H1 blocker metabolism by liver enzymes, raising H1 blocker levels in the blood.

Alternatively, other medications can be added, including a leukotriene receptor antagonist, such as zafirlukast and montelukast, or even a three to 10-day burst of oral corticosteroids, such as prednisone or prednisolone.