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De-labeling of Patients With False Diagnosis of Penicillin Allergy

De-labeling of Patients With False Diagnosis of Penicillin Allergy

Recruiting
18-85 years
All
Phase N/A

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Overview

The purpose of this study is to estimate the prevalence of penicillin allergy, evaluate the diagnostic value of the allergologic work-up used in the study, and the health effects of penicillin allergy.

Description

Penicillin allergy is the most common of self-reported drug allergies and un-verified penicillin allergy is a significant and growing public health problem. 10% of all patients report penicillin allergy. However, there is large discrepancy between reported penicillin allergy and true allergy. Despite its high prevalence, greater than 90% of such patients are in fact able to tolerate the medication without allergic reactions.

In this study patients having a penicillin allergy label will be investigated to confirm or to exclude the allergy diagnosis. The diagnostic value of the allergen test panel and the allergologic work-up will be evaluated. Clinical parameters as well as immunological will be assessed.

Eligibility

Inclusion Criteria:

  • Adult patients who are referred to the department of Pulmonary medicine with clinical history suspected of having penicillin allergy.
  • The control group will be healthy adult volunteers with no history of any personal or family history of drug allergy, atopy, inflammatory or autoimmune diseases.

Exclusion Criteria:

  • Systemic reactions such as DRESS, any internal organ involvement
  • Clinical history of Type II-III hypersensitivity reaction
  • Severe Type IV hypersensitivity reaction such as Stevens-Johnson syndrome, toxic epidermal necrolysis, DRESS, vasculitis, acute generalized exanthematous pustulosis
  • Chronic idiopathic urticaria on antihistamine maintenance treatment/anti-IgE treatment
  • Medication which can affect the test outcome
  • Active signs of an underlying disease such as uncontrolled asthma
  • Cardiac disease with increased risk of serious anaphylaxis
  • Pregnancy/Breastfeeding
  • Reaction within the last 4-6 weeks

Study details
    Allergy Drug

NCT03581604

Oslo University Hospital

27 January 2024

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