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Meta-Analysis of Acetylsalicylic Acid Desensitization in Patients With Acute Coronary Syndrome.
Chopra, Amitabh Madhukumar; Díez-Villanueva, Pablo; Córdoba-Soriano, Juan Gabriel; Lee, Joe K T; Al-Ahmad, Mona; Ferraris, Victor A; Mehta, Monik; Kowalski, Marek L.
Afiliación
  • Chopra AM; Self Employed, Chemical Engineer/Medical Researcher, Mumbai, Maharashtra, India. Electronic address: Amitabh.m.chopra@gmail.com.
  • Díez-Villanueva P; Department of Cardiology, University Hospital La Princesa, Madrid, Spain.
  • Córdoba-Soriano JG; Department of Cardiology, Hospital General Universitario de Albacete, Albacete, Spain.
  • Lee JKT; Department of Medicine, Pamela Youde Nethersole Eastern Hospital, Chai Wan, Hong Kong.
  • Al-Ahmad M; Department of Microbiology, Faculty of Medicine, Kuwait University, Safat, Kuwait.
  • Ferraris VA; Division of Cardiothoracic Surgery, Department of Surgery, University of Kentucky, Lexington, Kentucky.
  • Mehta M; Department of Cardiology, Artemis Hospital, Gurgaon, Haryana, India.
  • Kowalski ML; Department of Immunology and Allergy, Medical University of Lódz, Lódz, Poland.
Am J Cardiol ; 124(1): 14-19, 2019 07 01.
Article en En | MEDLINE | ID: mdl-31027657
ABSTRACT
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 99.8]%; 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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Inhibidores de Agregación Plaquetaria / Aspirina / Desensibilización Inmunológica / Hipersensibilidad a las Drogas / Síndrome Coronario Agudo Tipo de estudio: Guideline / Systematic_reviews Límite: Humans Idioma: En Revista: Am J Cardiol Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Inhibidores de Agregación Plaquetaria / Aspirina / Desensibilización Inmunológica / Hipersensibilidad a las Drogas / Síndrome Coronario Agudo Tipo de estudio: Guideline / Systematic_reviews Límite: Humans Idioma: En Revista: Am J Cardiol Año: 2019 Tipo del documento: Article
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