AI Article Synopsis

  • A study examined aspirin (ASA) hypersensitivity in a cardiology practice, reviewing medical records of over 11,000 patients from 2012 to 2013.
  • The prevalence of ASA hypersensitivity was found to be 1.88%, with skin reactions being the most common, and many patients misclassified based on symptoms like gastrointestinal issues.
  • The findings indicate a significant lack of proper documentation and management of ASA hypersensitivity, highlighting the need for better referral processes for desensitization and addressing unwarranted avoidance of ASA in affected patients.

Article Abstract

Data are lacking with concern to the prevalence and management of aspirin (ASA) hypersensitivity. To study the prevalence, different types of reactions, and implications for clinical management of ASA hypersensitivity in a cardiology practice. We conducted an electronic medical record review of 11,375 individuals, 5052 (44%) in the ambulatory setting, and 6323 (56%) admitted for percutaneous coronary intervention (PCI), from January 2012 to December 2013. The prevalence of ASA hypersensitivity was 1.88% (n = 214). Skin reactions were the most common (40 [19%]), followed by angioedema (10 [4.6%]), respiratory (9 [4.2%]), and anaphylaxis (6 [2.8%]). No records were found for 74 patients (34.5%), and 69 patients (32.2%) were mistakenly labeled as allergic for having gastrointestinal symptoms. Of the 214 patients who had documented ASA hypersensitivity, 108 individuals (50.46%) had coronary artery disease. The medications at discharge were the following: ASA (30 [14%]), thienopyridine (48 [22%]), a combination of ASA and thienopyridine (13 [6%]), anticoagulation only (26 [12%]), and no antiplatelet (97 [43%]). ASA hypersensitivity is often not documented correctly or is often misdiagnosed or not appropriately managed. There is a need for improved management of ASA hypersensitivity, including appropriate referral for ASA desensitization and combating unnecessary avoidance in patients with intolerance due to adverse effects.

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Source
http://dx.doi.org/10.2500/aap.2020.41.190032DOI Listing

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