Aspirin sensitivity - Implications for patients with coronary artery disease
被引:123
作者:
Gollapudi, RR
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机构:Scripps Clin, Div Allergy Asthma & Immunol, La Jolla, CA 92037 USA
Gollapudi, RR
Teirstein, PS
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h-index: 0
机构:Scripps Clin, Div Allergy Asthma & Immunol, La Jolla, CA 92037 USA
Teirstein, PS
Stevenson, DD
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机构:Scripps Clin, Div Allergy Asthma & Immunol, La Jolla, CA 92037 USA
Stevenson, DD
Simon, RA
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机构:Scripps Clin, Div Allergy Asthma & Immunol, La Jolla, CA 92037 USA
Simon, RA
机构:
[1] Scripps Clin, Div Allergy Asthma & Immunol, La Jolla, CA 92037 USA
[2] Scripps Clin, Div Cardiovasc Dis, La Jolla, CA 92037 USA
[3] Scripps Res Inst, La Jolla, CA 92037 USA
来源:
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
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2004年
/
292卷
/
24期
关键词:
D O I:
10.1001/jama.292.24.3017
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Context Although acetylsalicylic acid (aspirin) is commonly used for patients with chronic cardiovascular disease, a minority of patients have a sensitivity to acetylsalicylic acid and other nonsteroidal anti-inflammatory drugs. Objective To provide a diagnostic strategy for evaluating and treating patients with aspirin sensitivity, with additional consideration for issues specific to patients with coronary artery disease (CAD). Evidence Acquisition Published articles were identified through a search of MEDLINE and the Cochrane databases using the dates 1966 to June 2004 and the search terms aspirin allergy, coronary artery disease, aspirin desensitization, and aspirin sensitivity. References of retrieved articles were also reviewed for pertinent studies. Articles were included in this review if they were controlled studies, published in the English language, and appeared in a peer-reviewed journal. Evidence Synthesis The prevalence of aspirin-exacerbated respiratory tract disease is approximately 10% and for aspirin-induced urticaria the prevalence varies from 0.07% to 0.2% of the general population. Aspirin sensitivity is most often manifested as rhinitis and asthma or urticaria/angioedema induced by cross-reacting nonsteroidal anti-inflammatory drugs that inhibit cyclooxygenase 1. The primary mechanism of sensitivity is less often related to drug-specific IgE antibody production leading to urticaria/angioedema and rarely to anaphylaxis. Most patients with acetylsalicylic acid sensitivity are able to undergo desensitization therapy safely and successfully except in cases of chronic idiopathic urticaria. However, there have not been any randomized trials that specifically focus on the efficacy of aspirin desensitization. Furthermore, experience with acetylsalicylic acid desensitization in patients with CAD is very limited. After successful desensitization, acetylsalicylic acid therapy must be indefinitely continued to prevent resensitization. Conclusions Acetylsalicylic acid sensitivity is common and desensitization can be performed safely in many patients. Large-scale trials are warranted to determine the safety and efficacy of acetylsalicylic acid desensitization therapy in patients with concomitant CAD because data are currently limited to small case series.