Aspirin Desensitization in Patients with Coronary Artery Disease

Aspirin Desensitization in Patients with Coronary Artery DiseaseThere are limited data on aspirin desensitization in patients with coronary artery disease (CAD). The aim of this study was to test the safety and efficacy of a rapid desensitization protocol inpatients with a history of aspirin sensitivity about to receive PCI.

 

This was a prospective multicenter observational study, carried out in seven Italian centers including patients with a history of aspirin hypersensitivity in the context of a coronary angiogram and eventual PCI.

 

The study included an overall of 330 patients in said conditions with a history of CAD, suspected as a stable condition, and also patients undergoing ST elevation acute myocardial infarction.

 

Prior aspirin adverse events included:

  • urticaria (n=177, 53.6%),
  • angioedema (n=69, 20.9%),
  • asthma (n=65, 19.7%),
  • anaphylactic reaction (n=19, 5.8%).

 

Among those presenting urticaria/angioedema, 13 also has a history of chronic idiopathic urticaria.

 

The desensitization procedure was done before catheterization, with the exception of patients undergoing ST elevation AMI (n=78, 23.6%), who underwent the procedure after catheterization. In these last patients, the use of IIb/IIIa glycoprotein inhibitors was left to the operator’s criteria.

aspirine

 

Desensitization involved the oral administration of six sequential doses of aspirin (1, 5, 10, 20, 40 y 100 mg) during 5.5 hours. Aspirin administration was immediately interrupted whenever there were systemic, respiratory or mucocutaneoussigns of hypersensitivity. After desensitization, patients continued to take 100 mg aspirin per day. In all elective cases, the use of corticoids, antihistamine or anti leukotrienes was interrupted seven days after desensitization.

 

Of all patients, 71% (n=235) finally required PCI. The desensitization protocol was successful in 315 patients (95.4%) and all those with a history of anaphylactic reaction.

 

The 15 patients (4.6%) that did not respond to treatment only presented minor adverse reactions that were well managed with corticosteroids and antihistamines.

 

80% continued with aspirin for at least 12 months and those who decided to discontinue treatment did so because of medical decision, not because of adverse events.

 

Conclusion

Rapid desensitization protocol resulted safe and effective in a wide range of patients regardless the type of reaction to aspirin they used to have.

 

Original Title: Aspirin Desensitization in Patients with Coronary Artery Disease. Results of the Multicenter ADAPTED Registry (Aspirin Desensitization in Patients with Coronary Artery Disease).

Reference: Roberta Rossini et al. CircCardiovascInterv. 2017 Feb;10(2).


Subscribe to our weekly newsletter

Get the latest scientific articles on interventional cardiology

We are interested in your opinion. Please, leave your comments, thoughts, questions, etc., below. They will be most welcome.

More articles by this author

AHA 2024 | VANISH2 Trial

Cardiac defibrillator implants (CDIs) have been shown to improve survival in patients with ischemic cardiomyopathy and ventricular tachycardia (VT). However, approximately one third of...

AHA 2024 | SUMMIT

It has been previously shown that the pharmacological treatment of obesity (semaglutide) can reduce cardiovascular events in patients with cardiac failure (CF) and preserved...

STEACS and the Use of Bivalirudin vs. Heparin: In Search of BRIGHT-4 Outcomes

Various studies and registries have previously shown the impact of post-percutaneous coronary intervention (PCI) complications on the survival of patients with ST-segment elevation acute...

TAVR and Atrial Fibrillation: What Anticoagulants Should We Use?

The prevalence of atrial fibrillation (AF) in TAVR patients ranges from 15 to 30%, depending on series. This arrhythmia has been associated to higher...

LEAVE A REPLY

Please enter your comment!
Please enter your name here

Related Articles

SOLACI Sessionsspot_img

Recent Articles

Long Term Results of the International Chimney Registry

The International Chimney Registry was an observational study aimed at assessing the use of chimney stenting during TAVR either to predict or treat coronary...

CANNULATE TAVR extended study: Impact of Commissural and Coronary Alignment in Coronary Cannulation Following TAVR with Evolut Fx

The new valve Evolut FX has shown better commissural alignment vs. its predecessor Evolut Pro+. Prior studies have already shown commissure alignment facilitates post...

TRISCEND II: Transcatheter Replacement vs. Medical Treatment for Tricuspid Regurgitation

The EVOQUE device is designed with an intra-annular sealing system that provides excellent anatomical compatibility and an adaptable shape. It is currently available in...