Meta-Analysis of Acetylsalicylic Acid Desensitization in Patients With Acute Coronary Syndrome

被引:14
|
作者
Chopra, Amitabh Madhukumar
Diez-Villanueva, Pablo [1 ]
Gabriel Cordoba-Soriano, Juan [2 ]
Lee, Joe K. T. [3 ]
Al-Ahmad, Mona [4 ]
Ferraris, Victor A. [5 ]
Mehta, Monik [6 ]
Kowalski, Marek L. [7 ]
机构
[1] Univ Hosp La Princesa, Dept Cardiol, Madrid, Spain
[2] Hosp Gen Univ Albacete, Dept Cardiol, Albacete, Spain
[3] Pamela Youde Nethersole Eastern Hosp, Dept Med, Chai Wan, Hong Kong, Peoples R China
[4] Kuwait Univ, Fac Med, Dept Microbiol, Safat, Kuwait
[5] Univ Kentucky, Div Cardiothorac Surg, Dept Surg, Lexington, KY USA
[6] Artemis Hosp, Dept Cardiol, Gurgaon, Haryana, India
[7] Med Univ Lodz, Dept Immunol & Allergy, Lodz, Poland
来源
AMERICAN JOURNAL OF CARDIOLOGY | 2019年 / 124卷 / 01期
关键词
ASPIRIN DESENSITIZATION; RAPID DESENSITIZATION; ARTERY-DISEASE; HYPERSENSITIVITY; CHALLENGE; ALLERGY; HISTORY;
D O I
10.1016/j.amjcard.2019.03.047
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Acetylsalicylic acid (ASA) hypersensitivity represents a clinical challenge in acute coronary syndrome (ACS) patients urgently requiring ASA for antiplatelet therapy. ASA desensitization has been reported with successful outcomes in cardiac patients. The aim of this review is to determine the safety and efficacy of ASA desensitization therapy in ACS patients. A PubMed database search was conducted for articles containing combinations of keywords, "aspirin desensitization" or "aspirin hypersensitivity" and "acute coronary syndrome" between January 1, 1990 and August 1, 2018. The primary end point was desensitization protocol success. Secondary end points included hypersensitivity adverse events and ASA discontinuation due to hypersensitivity adverse events at follow-up. Fifteen reports consisting of 480 ACS patients with previous hypersensitivity to ASA were included. The pooled desensitization success rate was 98.3% (95% confidence interval: 97.2% to 99.5%). There was no statistical difference in outcomes between protocols <= 2 hours and > 2 hours in duration (96.3[92.3 to 100.3]% vs 97.2[94.6 to 99.81%; p = 0.71). Protocols with > 6 dose escalations were associated with higher success rates compared to those with <= 6 doses (99.2[97.9 to 100.4]% vs 95.4[93 to 97.8] %; p = 0.007). At follow-up between 1 and 46 months (mode 12 months), zero hypersensitivity adverse events were reported. Consequently, no ASA discontinuations were related to hypersensitivity adverse events. In conclusion, ASA desensitization therapy is safe and effective in patients with ACS. Protocols with > 6 dose escalations may be optimal for ASA desensitization in ACS patients. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:14 / 19
页数:6
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