• Safety & Recalls
  • Regulatory Updates
  • Drug Coverage
  • COPD
  • Cardiovascular
  • Obstetrics-Gynecology & Women's Health
  • Ophthalmology
  • Clinical Pharmacology
  • Pediatrics
  • Urology
  • Pharmacy
  • Idiopathic Pulmonary Fibrosis
  • Diabetes and Endocrinology
  • Allergy, Immunology, and ENT
  • Musculoskeletal/Rheumatology
  • Respiratory
  • Psychiatry and Behavioral Health
  • Dermatology
  • Oncology

Suppressive therapy manages clopidogrel hypersensitivity

Article

Clopidogrel hypersensitivity, which affects 6% of patients, can be successfully treated using short-course corticosteroids and antihistamines without interrupting drug therapy, reported researchers at Jefferson Medical College in Philadelphia.

Clopidogrel hypersensitivity, which affects 6% of patients, can be successfully treated using short-course corticosteroids and antihistamines without interrupting drug therapy, reported researchers at Jefferson Medical College in Philadelphia.

The study population consisted of 25 consecutive patients showing clopidogrel hypersensitivity after percutaneous coronary intervention. They had developed clopidogrel hypersensitivity 6 ± 2 days after drug initiation. The patients were treated with corticosteroids (5 patients), antihistamines (5 patients), or corticosteroids and antihistamines (15 patients). Patients treated with corticosteroids received a tapering course for a mean of 10 ± 8 days.

Suppressive therapy resulted in sustained symptom resolution in 22 of 25 patients (88%). Patients who were successfully desensitized continued clopidogrel therapy for 417 ± 369 days; 16 patients with drug-eluting stents continued for 529 ± 376 days. No deaths, myocardial infarctions, or stent thrombosis occurred during the extended follow-up period.

"Clopidogrel hypersensitivity can be successfully treated using short-course corticosteroids and antihistamines without interrupting therapy," the authors concluded. "This technique enables long-term continuation of clopidogrel and confers a low risk of adverse cardiac events.”

The report was published in the March 15th edition of the American Journal of Cardiology.

Related Content
© 2024 MJH Life Sciences

All rights reserved.