<?xml version="1.0" encoding="UTF-8"?>
<?xml-stylesheet href="/rss.css" type="text/css"?>
<rdf:RDF xmlns="http://purl.org/rss/1.0/"
    xmlns:cc="http://web.resource.org/cc/"
    xmlns:dc="http://purl.org/dc/elements/1.1/"
    xmlns:extra="http://www.w3.org/1999/xhtml"
    xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/"
    xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#">
    <channel rdf:about="http://www.aacijournal.com/feeds/mostaccessed/journal?quantity=&amp;format=rss&amp;version=">
        <title>Allergy, Asthma &amp; Clinical Immunology - Most accessed articles</title>
        <link>http://www.aacijournal.com</link>
        <description>The most accessed research articles published by Allergy, Asthma &amp; Clinical Immunology</description>
        <dc:date>2012-04-26T00:00:00Z</dc:date>
        <items>
            <rdf:Seq>
                                <rdf:li rdf:resource="http://www.aacijournal.com/content/8/1/4" />
                                <rdf:li rdf:resource="http://www.aacijournal.com/content/7/1/2" />
                                <rdf:li rdf:resource="http://www.aacijournal.com/content/7/S1/S2" />
                                <rdf:li rdf:resource="http://www.aacijournal.com/content/5/1/5" />
                                <rdf:li rdf:resource="http://www.aacijournal.com/content/5/1/10" />
                                <rdf:li rdf:resource="http://www.aacijournal.com/content/7/S1/S11" />
                                <rdf:li rdf:resource="http://www.aacijournal.com/content/8/1/3" />
                                <rdf:li rdf:resource="http://www.aacijournal.com/content/6/1/14" />
                                <rdf:li rdf:resource="http://www.aacijournal.com/content/7/S1/S3" />
                                <rdf:li rdf:resource="http://www.aacijournal.com/content/7/S1/S10" />
                            </rdf:Seq>
        </items>
                 <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </channel>
        <item rdf:about="http://www.aacijournal.com/content/8/1/4">
        <title>Management of anaphylaxis in schools: Evaluation of an epinephrine auto-injector (EpiPen(R)) use by school personnel and comparison of two approaches of soliciting participation</title>
        <description>Background:
There has been no large study characterizing selection bias in allergy and evaluating school personnel&apos;s ability to use an epinephrine auto-injector (EpiPen(R)). Our objective was to determine if the consent process introduces selection bias by comparing 2 methods of soliciting participation of school personnel in a study evaluating their ability to demonstrate the EpiPen(R).
Methods:
School personnel from randomly selected schools in Quebec were approached using a 1) partial or 2) full disclosure approach and were assessed on their ability to use the EpiPen(R) and identify anaphylaxis.
Results:
343 school personnel participated. In the full disclosure group, the participation rate was lower: 21.9% (95%CI, 19.0%-25.2%) versus 40.7% (95%CI, 36.1%-45.3%), but more participants achieved a perfect score: 26.3% (95%CI, 19.6%-33.9%) versus 15.8% (95%CI, 10.8%-21.8%), and identified 3 signs of anaphylaxis: 71.8% (95%CI, 64.0%-78.7%) versus 55.6% (95%CI, 48.2%-62.9%).
Conclusions:
Selection bias is suspected as school personnel who were fully informed of the purpose of the assessment were less likely to participate; those who participated among the fully informed were more likely to earn perfect scores and identify anaphylaxis. As the process of consent can influence participation and bias outcomes, researchers and Ethics Boards need to consider conditions under which studies can proceed without full consent. Despite training, school personnel perform poorly when asked to demonstrate the EpiPen(R).</description>
        <link>http://www.aacijournal.com/content/8/1/4</link>
                <dc:creator>Nha Uyen Nguyen Luu</dc:creator>
                <dc:creator>Lisa Cicutto</dc:creator>
                <dc:creator>Lianne Soller</dc:creator>
                <dc:creator>Lawrence Joseph</dc:creator>
                <dc:creator>Susan Waserman</dc:creator>
                <dc:creator>Yvan St-Pierre</dc:creator>
                <dc:creator>Ann Clarke</dc:creator>
                <dc:source>Allergy, Asthma &amp; Clinical Immunology 2012, null:4</dc:source>
        <dc:date>2012-04-26T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1710-1492-8-4</dc:identifier>
                            <dc:title>Prior knowledge skews results</dc:title>
                            <dc:description>Where the purpose of studies into participants&apos; &quot;knowledge&quot; is disclosed prior to enrolment there may be a bias towards participants that are confident on the subject. Future study designs should take this into account.</dc:description>
                <prism:require>/content/figures/1710-1492-8-4-toc.gif</prism:require>
                <prism:publicationName>Allergy, Asthma &amp; Clinical Immunology</prism:publicationName>
        <prism:issn>1710-1492</prism:issn>
        <prism:volume>${item.volume}</prism:volume>
        <prism:startingPage>4</prism:startingPage>
        <prism:publicationDate>2012-04-26T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>PDF</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.aacijournal.com/content/7/1/2">
        <title>Canadian clinical practice guidelines for acute and chronic rhinosinusitis</title>
        <description>This document provides healthcare practitioners with information regarding the management of acute rhinosinusitis (ARS) and chronic rhinosinusitis (CRS) to enable them to better meet the needs of this patient population. These guidelines describe controversies in the management of acute bacterial rhinosinusitis (ABRS) and include recommendations that take into account changes in the bacteriologic landscape. Recent guidelines in ABRS have been released by American and European groups as recently as 2007, but these are either limited in their coverage of the subject of CRS, do not follow an evidence-based strategy, or omit relevant stakeholders in guidelines development, and do not address the particulars of the Canadian healthcare environment.Advances in understanding the pathophysiology of CRS, along with the development of appropriate therapeutic strategies, have improved outcomes for patients with CRS. CRS now affects large numbers of patients globally and primary care practitioners are confronted by this disease on a daily basis. Although initially considered a chronic bacterial infection, CRS is now recognized as having multiple distinct components (eg, infection, inflammation), which have led to changes in therapeutic approaches (eg, increased use of corticosteroids). The role of bacteria in the persistence of chronic infections, and the roles of surgical and medical management are evolving. Although evidence is limited, guidance for managing patients with CRS would help practitioners less experienced in this area offer rational care. It is no longer reasonable to manage CRS as a prolonged version of ARS, but rather, specific therapeutic strategies adapted to pathogenesis must be developed and diffused.Guidelines must take into account all available evidence and incorporate these in an unbiased fashion into management recommendations based on the quality of evidence, therapeutic benefit, and risks incurred. This document is focused on readability rather than completeness, yet covers relevant information, offers summaries of areas where considerable evidence exists, and provides recommendations with an assessment of strength of the evidence base and degree of endorsement by the multidisciplinary expert group preparing the document.These guidelines have been copublished in both Allergy, Asthma &amp; Clinical Immunology and the Journal of Otolaryngology-Head and Neck Surgery.</description>
        <link>http://www.aacijournal.com/content/7/1/2</link>
                <dc:creator>Martin Desrosiers</dc:creator>
                <dc:creator>Gerald Evans</dc:creator>
                <dc:creator>Paul Keith</dc:creator>
                <dc:creator>Erin Wright</dc:creator>
                <dc:creator>Alan Kaplan</dc:creator>
                <dc:creator>Jacques Bouchard</dc:creator>
                <dc:creator>Anthony Ciavarella</dc:creator>
                <dc:creator>Patrick Doyle</dc:creator>
                <dc:creator>Amin Javer</dc:creator>
                <dc:creator>Eric Leith</dc:creator>
                <dc:creator>Atreyi Mukherji</dc:creator>
                <dc:creator>R Schellenberg</dc:creator>
                <dc:creator>Peter Small</dc:creator>
                <dc:creator>Ian Witterick</dc:creator>
                <dc:source>Allergy, Asthma &amp; Clinical Immunology 2011, null:2</dc:source>
        <dc:date>2011-02-10T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1710-1492-7-2</dc:identifier>
                                <prism:require>/content/figures/1710-1492-7-2-toc.gif</prism:require>
                <prism:publicationName>Allergy, Asthma &amp; Clinical Immunology</prism:publicationName>
        <prism:issn>1710-1492</prism:issn>
        <prism:volume>${item.volume}</prism:volume>
        <prism:startingPage>2</prism:startingPage>
        <prism:publicationDate>2011-02-10T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.aacijournal.com/content/7/S1/S2">
        <title>Asthma</title>
        <description>Asthma is the most common respiratory disorder in Canada. Despite significant improvement in the diagnosis and management of this disorder, the majority of Canadians with asthma remain poorly controlled. In most patients, however, control can be achieved through the use of avoidance measures and appropriate pharmacological interventions. Inhaled corticosteroids (ICSs) represent the standard of care for the majority of patients. Combination ICS/long-acting beta2-agonists (LABA) inhalers are preferred for most adults who fail to achieve control with ICS therapy. Allergen-specific immunotherapy represents a potentially disease-modifying therapy for many patients with asthma, but should only be prescribed by physicians with appropriate training in allergy. Regular monitoring of asthma control, adherence to therapy and inhaler technique are also essential components of asthma management. This article provides a review of current literature and guidelines for the appropriate diagnosis and management of asthma.</description>
        <link>http://www.aacijournal.com/content/7/S1/S2</link>
                <dc:source>Allergy, Asthma &amp; Clinical Immunology 2011, null:S2</dc:source>
        <dc:date>2011-11-10T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1710-1492-7-S1-S2</dc:identifier>
                                <prism:require>/content/figures/1710-1492-7-S1-S2-toc.gif</prism:require>
                <prism:publicationName>Allergy, Asthma &amp; Clinical Immunology</prism:publicationName>
        <prism:issn>1710-1492</prism:issn>
        <prism:volume>${item.volume}</prism:volume>
        <prism:startingPage>S2</prism:startingPage>
        <prism:publicationDate>2011-11-10T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.aacijournal.com/content/5/1/5">
        <title>The role of Probiotics in allergic diseases</title>
        <description>Allergic disorders are very common in the pediatric age group. While the exact etiology is unclear, evidence is mounting to incriminate environmental factors and an aberrant gut microbiota with a shift of the Th1/Th2 balance towards a Th2 response. Probiotics have been shown to modulate the immune system back to a Th1 response. Several in vitro studies suggest a role for probiotics in treating allergic disorders. Human trials demonstrate a limited benefit for the use of probiotics in atopic dermatitis in a preventive as well as a therapeutic capacity. Data supporting their use in allergic rhinitis are less robust. Currently, there is no role for probiotic therapy in the treatment of bronchial asthma. Future studies will be critical in determining the exact role of probiotics in allergic disorders.</description>
        <link>http://www.aacijournal.com/content/5/1/5</link>
                <dc:creator>Sonia Michail</dc:creator>
                <dc:source>Allergy, Asthma &amp; Clinical Immunology 2009, null:5</dc:source>
        <dc:date>2009-10-22T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1710-1492-5-5</dc:identifier>
                                <prism:require>/content/figures/1710-1492-5-5-toc.gif</prism:require>
                <prism:publicationName>Allergy, Asthma &amp; Clinical Immunology</prism:publicationName>
        <prism:issn>1710-1492</prism:issn>
        <prism:volume>${item.volume}</prism:volume>
        <prism:startingPage>5</prism:startingPage>
        <prism:publicationDate>2009-10-22T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.aacijournal.com/content/5/1/10">
        <title>Urticaria and infections</title>
        <description>Urticaria is a group of diseases that share a distinct skin reaction pattern. Triggering of urticaria by infections has been discussed for many years but the exact role and pathogenesis of mast cell activation by infectious processes is unclear. In spontaneous acute urticaria there is no doubt for a causal relationship to infections and all chronic urticaria must have started as acute. Whereas in physical or distinct urticaria subtypes the evidence for infections is sparse, remission of annoying spontaneous chronic urticaria has been reported after successful treatment of persistent infections. Current summarizing available studies that evaluated the course of the chronic urticaria after proven Helicobacter eradication demonstrate a statistically significant benefit compared to untreated patients or Helicobacter-negative controls without urticaria (p &lt; 0.001). Since infections can be easily treated some diagnostic procedures should be included in the routine work-up, especially the search for Helicobacter pylori. This review will update the reader regarding the role of infections in different urticaria subtypes.</description>
        <link>http://www.aacijournal.com/content/5/1/10</link>
                <dc:creator>Bettina Wedi</dc:creator>
                <dc:creator>Ulrike Raap</dc:creator>
                <dc:creator>Dorothea Wieczorek</dc:creator>
                <dc:creator>Alexander Kapp</dc:creator>
                <dc:source>Allergy, Asthma &amp; Clinical Immunology 2009, null:10</dc:source>
        <dc:date>2009-12-01T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1710-1492-5-10</dc:identifier>
                                <prism:require>/content/figures/1710-1492-5-10-toc.gif</prism:require>
                <prism:publicationName>Allergy, Asthma &amp; Clinical Immunology</prism:publicationName>
        <prism:issn>1710-1492</prism:issn>
        <prism:volume>${item.volume}</prism:volume>
        <prism:startingPage>10</prism:startingPage>
        <prism:publicationDate>2009-12-01T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.aacijournal.com/content/7/S1/S11">
        <title>Primary immunodeficiency</title>
        <description>Primary immunodeficiency disorder (PID) refers to a heterogeneous group of over 130 disorders that result from defects in immune system development and/or function. PIDs are broadly classified as disorders of adaptive immunity (i.e., T-cell, B-cell or combined immunodeficiencies) or of innate immunity (e.g., phagocyte and complement disorders). Although the clinical manifestations of PIDs are highly variable, most disorders involve at least an increased susceptibility to infection. Early diagnosis and treatment are imperative for preventing significant disease-associated morbidity and, therefore, consultation with a clinical immunologist is essential. PIDs should be suspected in patients with: recurrent sinus or ear infections or pneumonias within a 1 year period; failure to thrive; poor response to prolonged use of antibiotics; persistent thrush or skin abscesses; or a family history of PID. Patients with multiple autoimmune diseases should also be evaluated. Diagnostic testing often involves lymphocyte proliferation assays, flow cytometry, measurement of serum immunoglobulin (Ig) levels, assessment of serum specific antibody titers in response to vaccine antigens, neutrophil function assays, stimulation assays for cytokine responses, and complement studies. The treatment of PIDs is complex and generally requires both supportive and definitive strategies. Ig replacement therapy is the mainstay of therapy for B-cell disorders, and is also an important supportive treatment for many patients with combined immunodeficiency disorders. The heterogeneous group of disorders involving the T-cell arm of the adaptive system, such as severe combined immunodeficiency (SCID), require immune reconstitution as soon as possible. The treatment of innate immunodeficiency disorders varies depending on the type of defect, but may involve antifungal and antibiotic prophylaxis, cytokine replacement, vaccinations and bone marrow transplantation. This article provides a detailed overview of the major categories of PIDs and strategies for the appropriate diagnosis and management of these rare disorders.</description>
        <link>http://www.aacijournal.com/content/7/S1/S11</link>
                <dc:source>Allergy, Asthma &amp; Clinical Immunology 2011, null:S11</dc:source>
        <dc:date>2011-11-10T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1710-1492-7-S1-S11</dc:identifier>
                                <prism:require>/content/figures/1710-1492-7-S1-S11-toc.gif</prism:require>
                <prism:publicationName>Allergy, Asthma &amp; Clinical Immunology</prism:publicationName>
        <prism:issn>1710-1492</prism:issn>
        <prism:volume>${item.volume}</prism:volume>
        <prism:startingPage>S11</prism:startingPage>
        <prism:publicationDate>2011-11-10T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.aacijournal.com/content/8/1/3">
        <title>What are the beliefs of pediatricians and dietitians regarding complementary food introduction to prevent allergy?</title>
        <description>Background:
The timing of complementary food introduction is controversial. Providing information on the timing of dietary introduction is crucial to the primary prevention of food allergy. The American Academy of Pediatrics offers dietary recommendations that were updated in 2008.ObjectiveIdentify the recommendations that general pediatricians and registered dietitians provide to parents and delineate any differences in counselling.
Methods:
A 9-item survey was distributed to pediatricians and dietitians online and by mail. Information on practitioner type, gender, length of practice and specific recommendations regarding complementary food introduction and exposure was collected.
Results:
181 surveys were returned with a 54% response rate from pediatricians. It was not possible to calculate a meaningful dietitian response rate due to overlapping email databases. 52.5% of all respondents were pediatricians and 45.9% were dietitians. The majority of pediatricians and dietitians advise mothers that peanut abstinence during pregnancy and lactation is unnecessary. Dietitians were more likely to counsel mothers to breastfeed their infants to prevent development of atopic dermatitis than pediatricians. Hydrolyzed formulas for infants at risk of developing allergy were the top choice of formula amongst both practitioners. For food allergy prevention, pediatricians were more likely to recommend delayed introduction of peanut and egg, while most dietitians recommended no delay in allergenic food introduction.
Conclusions:
In the prophylaxis of food allergy, pediatricians are less aware than dietitians of the current recommendation that there is no benefit in delaying allergenic food introduction beyond 4 to 6 months. More dietitians than pediatricians believe that breastfeeding decreases the risk of atopic dermatitis. Practitioners may benefit from increased awareness of current guidelines.</description>
        <link>http://www.aacijournal.com/content/8/1/3</link>
                <dc:creator>Sara Leo</dc:creator>
                <dc:creator>John Dean</dc:creator>
                <dc:creator>Edmond Chan</dc:creator>
                <dc:source>Allergy, Asthma &amp; Clinical Immunology 2012, null:3</dc:source>
        <dc:date>2012-03-21T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1710-1492-8-3</dc:identifier>
                                <prism:require>/content/figures/1710-1492-8-3-toc.gif</prism:require>
                <prism:publicationName>Allergy, Asthma &amp; Clinical Immunology</prism:publicationName>
        <prism:issn>1710-1492</prism:issn>
        <prism:volume>${item.volume}</prism:volume>
        <prism:startingPage>3</prism:startingPage>
        <prism:publicationDate>2012-03-21T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.aacijournal.com/content/6/1/14">
        <title>Acquired angioedema</title>
        <description>Acquired angioedema (AAE) is characterized by acquired deficiency of C1 inhibitor (C1-INH), hyperactivation of the classical pathway of human complement and angioedema symptoms mediated by bradykinin released by inappropriate activation of the contact-kinin system. Angioedema recurs at unpredictable intervals, lasts from two to five days and presents with edema of the skin (face, limbs, genitals), severe abdominal pain with edema of the gastrointestinal mucosa, life-threateing edema of the upper respiratory tract and edema of the oral mucosa and of the tongue. AAE recurs in association with various conditions and particularly with different forms of lymphoproliferative disorders. Neutralizing autoantibodies to C1-INH are present in the majority of patients. The therapeutic approach to a patient with AAE should first be aimed to avoid fatalities due to angioedema and then to avoid the disability caused be angioedema recurrences. Acute attacks can be treated with plasma-derived C1-INH, but some patients become non-responsive and in these patients the kallikrein inhibitor ecallantide and the bradykinin receptor antagonist icatibant can be effective. Angioedema prophylaxis is performed using antifibrinolytic agents and attenuated androgens with antifibrinolytic agents providing somewhat better results. Treatment of the associated disease can resolve AAE in some patients.</description>
        <link>http://www.aacijournal.com/content/6/1/14</link>
                <dc:creator>Marco Cicardi</dc:creator>
                <dc:creator>Andrea Zanichelli</dc:creator>
                <dc:source>Allergy, Asthma &amp; Clinical Immunology 2010, null:14</dc:source>
        <dc:date>2010-07-28T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1710-1492-6-14</dc:identifier>
                                <prism:require>/content/figures/1710-1492-6-14-toc.gif</prism:require>
                <prism:publicationName>Allergy, Asthma &amp; Clinical Immunology</prism:publicationName>
        <prism:issn>1710-1492</prism:issn>
        <prism:volume>${item.volume}</prism:volume>
        <prism:startingPage>14</prism:startingPage>
        <prism:publicationDate>2010-07-28T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.aacijournal.com/content/7/S1/S3">
        <title>Allergic rhinitis</title>
        <description>Allergic rhinitis is a common disorder that is strongly linked to asthma and conjunctivitis. It is usually a long-standing condition that often goes undetected in the primary-care setting. The classic symptoms of the disorder are nasal congestion, nasal itch, rhinorrhea and sneezing. A thorough history, physical examination and allergen skin testing are important for establishing the diagnosis of allergic rhinitis. Second-generation oral antihistamines and intranasal corticosteroids are the mainstay of treatment. Allergen immunotherapy is an effective immune-modulating treatment that should be recommended if pharmacologic therapy for allergic rhinitis is not effective or is not tolerated. This article provides an overview of the pathophysiology, diagnosis, and appropriate management of this disorder.</description>
        <link>http://www.aacijournal.com/content/7/S1/S3</link>
                <dc:source>Allergy, Asthma &amp; Clinical Immunology 2011, null:S3</dc:source>
        <dc:date>2011-11-10T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1710-1492-7-S1-S3</dc:identifier>
                                <prism:require>/content/figures/1710-1492-7-S1-S3-toc.gif</prism:require>
                <prism:publicationName>Allergy, Asthma &amp; Clinical Immunology</prism:publicationName>
        <prism:issn>1710-1492</prism:issn>
        <prism:volume>${item.volume}</prism:volume>
        <prism:startingPage>S3</prism:startingPage>
        <prism:publicationDate>2011-11-10T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.aacijournal.com/content/7/S1/S10">
        <title>Drug allergy</title>
        <description>Drug allergy encompasses a spectrum of immunologically-mediated hypersensitivity reactions with varying mechanisms and clinical presentations. This type of adverse drug reaction (ADR) not only affects patient quality of life, but may also lead to delayed treatment, unnecessary investigations, and even mortality. Given the myriad of symptoms associated with the condition, diagnosis is often challenging. Therefore, referral to an allergist experienced in the identification, diagnosis and management of drug allergy is recommended if a drug-induced allergic reaction is suspected. Diagnosis relies on a careful history and physical examination. In some instances, skin testing, graded challenges and induction of drug tolerance procedures may be required.The most effective strategy for the management of drug allergy is avoidance or discontinuation of the offending drug. When available, alternative medications with unrelated chemical structures should be substituted. Cross-reactivity among drugs should be taken into consideration when choosing alternative agents. Additional therapy for drug hypersensitivity reactions is largely supportive and may include topical corticosteroids, oral antihistamines and, in severe cases, systemic corticosteroids. In the event of anaphylaxis, the treatment of choice is injectable epinephrine. If a particular drug to which the patient is allergic is indicated and there is no suitable alternative, induction of drug tolerance procedures may be considered to induce temporary tolerance to the drug.This article provides a backgrounder on drug allergy and strategies for the diagnosis and management of some of the most common drug-induced allergic reactions, such allergies to penicillin, sulfonamides, cephalosporins, radiocontrast media, local anesthetics, general anesthetics, acetylsalicylic acid (ASA) and non-steroidal anti-inflammatory drugs.</description>
        <link>http://www.aacijournal.com/content/7/S1/S10</link>
                <dc:source>Allergy, Asthma &amp; Clinical Immunology 2011, null:S10</dc:source>
        <dc:date>2011-11-10T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1710-1492-7-S1-S10</dc:identifier>
                                <prism:require>/content/figures/1710-1492-7-S1-S10-toc.gif</prism:require>
                <prism:publicationName>Allergy, Asthma &amp; Clinical Immunology</prism:publicationName>
        <prism:issn>1710-1492</prism:issn>
        <prism:volume>${item.volume}</prism:volume>
        <prism:startingPage>S10</prism:startingPage>
        <prism:publicationDate>2011-11-10T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <cc:License rdf:about="http://creativecommons.org/licenses/by/2.0/">
        <cc:permits rdf:resource="http://creativecommons.org/ns#Reproduction" />
        <cc:permits rdf:resource="http://creativecommons.org/ns#Distribution" />
        <cc:permits rdf:resource="http://creativecommons.org/ns#DerivativeWorks" />
    </cc:License>
</rdf:RDF>

