Eosinophilic esophagitis

Although the typical onset of EoE is in childhood, the disease can be found in all age groups and symptoms tend to vary depending on the age of presentation [13]. Clinical manifestations in infants and toddlers generally include vomiting, food refusal, choking with meals and, less commonly, failure to thrive. Predominant symptoms in school-aged children and adolescents include dysphagia (difficulty swallowing), food impactions, and choking/gagging with meals, particularly when comprised of foods with coarse textures. Other symptoms in this patient population include abdominal/chest pain, vomiting, and regurgitation. A careful history in children and adolescents with EoE reveals that they have learned to compensate for these symptoms by eating slowly, chewing excessively or taking small bites, drinking excessively with meals, lubricating meals inordinately with sauces, and avoiding specific food consistencies such as meats (or other foods with coarse textures) [14, 15].

The predominant symptom in adults is dysphagia; however, intractable heartburn and food avoidance may also be present. Due to the long-standing inflammation and possible resultant scarring that has gone unrecognized, adults presenting with EoE tend to have more esophageal food impactions as well as other esophageal abnormalities such as Schatzki ring (a narrow ring of tissue located just above the junction of the esophagus and stomach), esophageal webs (small, thin growths of tissue that partially block the esophagus) and, in some cases, achalasia (an esophageal motility disorder characterized by difficulty swallowing and regurgitation). However, it is important to note that some patients with EoE are asymptomatic and suspicion of the disease is based upon incidental findings at endoscopy that is performed for other indications or upon evidence of food impaction in the absence of other symptoms.

Although many of these symptoms overlap with gastroesophageal reflux, the majority of patients with EoE exhibit a poor response to acid-suppression therapy (e.g., proton pump inhibitors [PPIs]), and up to 75% have a personal or family history of atopic disease (e.g., asthma, eczema, rhinitis) and environmental and/or food allergies [13]. Table 1 provides a brief summary of the clinical manifestations of EoE.

In order to help rule out GERD, an empiric 6- to 8-week trial of high-dose acid-suppression therapy is recommended before performing endoscopy in patients with suspected EoE. A barium swallow should also be considered to rule out severe small-calibre esophagus.

Although the endoscopic examination may be unremarkable, endoscopic features of EoE have been well-characterized and include: linear furrowing (ridges or furrows in the esophageal wall), concentric rings, white speckled exudates (eosinophilic abscesses), Schatzki ring, small-calibre esophagus, and linear superficial mucosal tears that occur after introduction of the endoscope [13]. Table 2 provides a more detailed description of each of these features. Images of exudates, linear furrows and tears are provided in Figure 1.

Although endoscopic findings are helpful in identifying patients with EoE [16], they are not diagnostic of the disease. Additionally, it is important to rule out esophageal candidiasis when white exudates are identified. As such, all patients with suspected EoE must undergo esophageal mucosal biopsies to confirm the diagnosis.

Currently, endoscopic mucosal biopsy remains the most important diagnostic test for EoE. Biopsy specimens should be obtained regardless of the gross appearance of the mucosa, and specimens should be obtained from both the proximal and distal esophagus as well as areas revealing endoscopic abnormalities [2]. At least four biopsies are required to obtain a high sensitivity for the detection of EoE (5-6 biopsies are generally recommended) [13].

As discussed earlier, a definitive diagnosis of EoE is based on the presence of at least 15 eosinophils/HPF in the esophageal biopsies of patients who have normal pH studies or are refractory to acid-suppression therapy (i.e., to rule out GERD). GERD can increase eosinophilic infiltration in the distal esophagus, however, eosinophils associated with GERD generally occur at a lower density (i.e., <10/HPF) [1, 17].

A thorough personal and family history of other atopic conditions is recommended in all patients with EoE. Testing for allergic sensitization may be considered, with skin prick testing or blood testing for allergen-specific IgE, and potentially with atopy patch testing. However, it is important to remember that current approaches may not be able to accurately identify EoE triggers. The role of specific evaluation for allergic triggers in EoE remains in evolution, rendering it difficult to make standard recommendations.

Approximately two-thirds of patients with EoE have positive skin tests to at least one food allergen, most commonly dairy, eggs, wheat, soy and peanuts [2]. Unfortunately, the positive and negative predictive values for these tests have not been well established in this condition.

Atopy patch testing is a newer approach being used for the potential identification of non-IgE (cell-mediated) reactions. It is similar to patch testing for contact dermatitis and involves placing a small quantity of an allergen directly on the skin and then examining for a local, delayed reaction after a set time. Although atopy patch testing appears promising for the identification of foods that may elicit non-IgE-mediated reactions, this type of testing has not yet been standardized, and the positive and negative predictive values remain unknown. More studies are needed to assess the reliability and validity of atopy patch testing before it can be recommended for routine use in the diagnosis and monitoring of EoE.

Three dietary approaches for the management of EoE have emerged over the past decade: (1) the elemental diet, (2) empiric dietary restrictions (also referred to as the empiric six-food elimination diet), and (3) targeted dietary restrictions. The elemental diet involves the removal of all sources of potentially allergenic protein from the patient’s diet through the use of an amino acid-based formula for nutritional support. Assuming there is a favorable clinical and histologic response, one new food per week is reintroduced in a sequential fashion, beginning with the least allergenic foods (fruits and vegetables) to the most highly allergenic (e.g., dairy, soy, egg, wheat, and peanuts). A repeat endoscopic assessment is performed after the reintroduction of every 3-5 foods to ensure that the inflammation has not recurred.

Although the elemental diet is associated with high rates of clinical and histologic improvement in both adults and children with EoE (i.e., 90%), symptoms often recur after normalization of the patient’s diet [12, 18]. Furthermore, given the unpalatable taste of the formula, most patients require feeding by nasogastric tube which may lead to adherence issues and impaired quality of life, particularly in adolescents and adults.

Targeted and empiric dietary restrictions are often employed before considering an elemental diet. Targeted dietary restrictions involve the elimination of foods based on the results of skin prick and atopy patch testing. Although response rates noted with this approach are lower than those noted with the elemental diet, targeted dietary restrictions have still been shown to be effective in approximately 70-80% of patients and may result in better patient adherence [12]. However, clinically-irrelevant positive results and false negative results complicate this dietary approach and, therefore, further studies examining both the positive and negative predictive value of targeted dietary restrictions in EoE are necessary.

Rather than basing dietary elimination on skin prick testing and atopy patch testing, empiric dietary restrictions involve the elimination of the six most common allergic foods (regardless of the results of allergy testing): dairy, eggs, wheat, soy, peanuts, and fish/shellfish. Like targeted dietary restrictions, the empiric food elimination diet has been shown to be effective in approximately 75% of patients with EoE, and may also be associated with better patient adherence than the elemental diet [19].

With all dietary approaches, it remains unclear how long specific foods need to be avoided, and whether or not the patient’s diet can be normalized over time. Clearly, more studies on this approach are necessary, including an attempt to evaluate patient quality of life given the extensive dietary restrictions often required, including a great many “staple” foods. Furthermore, if several foods are to be eliminated simultaneously, enlisting the assistance of a dietitian may be beneficial, particularly in the pediatric population. This may help ensure nutritional requirements continue to be met in order to facilitate adequate growth and development.

Medical therapies for EoE include corticosteroids, leukotriene modifiers and biologic agents. Systemic (oral) corticosteroids were one of the first treatment options shown to be effective in patients with EoE. Both clinical and histologic improvement have been noted in approximately 95% of EoE patients using systemic corticosteroids; however, upon discontinuation of therapy, 90% of patients experience a recurrence in symptoms [20]. Furthermore, given that prolonged use of systemic corticosteroids are associated with well-known and potentially serious adverse effects, their long-term use is not recommended. Systemic corticosteroids should be reserved for emergent cases such as patients with dysphagia requiring hospitalization or patients experiencing significant weight loss or dehydration due to swallowing difficulties [2].

Given their substantially better safety profile, topical corticosteroids delivered to the esophagus have become the mainstay of pharmacotherapy for patients with EoE. Both swallowed fluticasone propionate (500-1000 µg/day) and oral viscous (thick) budesonide (500-1000 µg/day) have been shown to be effective in the management of EoE. Fluticasone propionate is delivered via a pressurized metered dose inhaler (pMDI) that is activated into the mouth (without inhaling and without a spacer device) and swallowed. Budesonide is administered orally after the contents of a vial used for nebulization are mixed with an artificial sweetener to increase the viscosity (thickness) of the solution which, theoretically, slows its transit over the esophageal lining [13].

Randomized clinical trials of topical fluticasone propionate therapy have shown both histologic and symptomatic improvements in 50-80% of patients with EoE [21, 22]. The most frequent complications noted with topical fluticasone propionate are superficial oropharyngeal and esophageal candidiasis. Although not as well studied as topical fluticasone propionate, oral viscous budesonide also appears to lead to similar clinical and histologic response rates in pediatric patients with EoE [23, 24]. Oral budesonide has been associated with a lower risk of developing esophageal candidiasis, and given the viscosity of the solution, may provide better delivery to the esophageal surface than swallowed fluticasone. However, budesonide has a slightly higher systemic bioavailability than oral fluticasone propionate and, therefore, may potentially be associated with more systemic effects.

Patients using topical corticosteroids for EoE should be advised not to eat, drink, or rinse their mouth for 20 to 30 minutes after using the medication [13]. After 6-8 weeks of topical therapy, patients should undergo repeat endoscopic assessment to ensure histologic response to therapy. If a therapeutic response is confirmed, treatment should be reduced to the lowest effective dose with appropriate follow up. It is important to note that symptoms and pathological changes often recur after topical corticosteroid therapy is discontinued. Therefore, many patients with EoE will require long-term treatment.

Since inflammatory mediators such as leukotrienes have been theorized to play a role in the esophageal inflammation noted in patients with EoE, leukotriene modifiers may be of value for the management of EoE [2]. A small study of 8 patients with EoE examined the efficacy of the leukotriene receptor antagonist, montelukast, and found a significant improvement in symptoms in the majority of subjects, but no improvement in histology [25]. Given that montelukast is generally well tolerated and potentially useful for the management of other atopic diseases such as asthma, it may be a therapeutic option to consider in patients with EoE and concurrent atopic conditions.

Given that both IL-5 and IgE appear to play a role in the pathogenesis of EoE, humanized monoclonal antibodies against IL-5 (reslizumab, mepolizumab) and IgE (omalizumab) may also be potential therapeutic options for the disease. Results from small case series using anti-IL-5 antibodies in patients with EoE suggest that these biologics are well tolerated and may improve clinical symptoms, histology and quality of life [26]. Two large pediatric trials are currently underway to further examine the efficacy and safety of anti-IL-5 antibodies in the management of EoE.

The anti-IgE antibody omalizumab is used for the management of severe atopic asthma and allergic rhinitis. Since omalizumab has been shown to lower eosinophil counts in the blood and lungs of asthmatic subjects [27], it may be a potential therapeutic approach for EoE. Although no clinical trials of omalizumab in patients with EoE have been conducted, anecdotal reports suggest that this may be a promising treatment option.

Esophageal endoscopic dilatation is a treatment modality most commonly used in adults with established esophageal strictures. Although dilatation is effective for relieving dysphagia, it does not address the underlying inflammation and, therefore, the majority of patients undergoing this procedure develop recurrent symptoms within 3-8 months [4, 28‐30]. Furthermore, in patients with EoE, endoscopic dilatation has been associated with extensive mucosal tearing and perforation. Therefore, dilatation is generally reserved for patients with symptomatic strictures that persist after a trial of pharmacological or dietary therapy [2, 7, 13].

A proposed algorithm for the diagnosis and management of EoE is shown in Figure 2.