Physiopathology of Rapid Aspirin Desensitization
Information source: Assistance Publique - Hôpitaux de Paris
Information obtained from ClinicalTrials.gov on October 04, 2010 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Hypersensitivity to Aspirin; Coronary Artery Disease
Phase: N/A
Status: Recruiting
Sponsored by: Assistance Publique - Hôpitaux de Paris Official(s) and/or principal investigator(s): Gabriel STEG, Pr, Principal Investigator, Affiliation: APHP
Overall contact: steg Gabriel, Pr, Phone: (0)1 40 25 86 68, Ext: +33, Email: gabriel.steg@bch.aphp.fr
Summary
Aspirin is very effective in protecting patients with coronary artery disease against
adverse cardiac events, because it is a potent "antiplatelet agent". Some patients may
develop a history of hypersensitivity to aspirin and treatment cannot usually be resumed in
these patients. We have developed a rapid procedure to induce tolerance in these patients
(SILBERMAN et al, Am J CARDIOL 2005;95: 509-10) and wish to test whether aspirin is as
effective as antiplatelet agent in patients with a history of allergy to aspirin and who
undergo desensitization as it is in patients without history of hypersensitivity
Clinical Details
Official title: Physiopathology of Rapid Aspirin Desensitization in Patients With Coronary Artery Disease and a History of Hypersensitivity to Aspirin or NSAIDs
Study design: Observational Model: Case Control, Time Perspective: Prospective
Primary outcome: Platelet aggregation in response to arachidonic acid Basophil activation tests Platelet aggregation in response to arachidonic acid Basophil activation tests
Detailed description:
Previous studies in allergology have proved the safety of desensitization procedures in
allergic patients with an imperative indication for a medication. This tolerance state is
usually obtained after a cumbersome procedure requiring several hours to days. We have
adapted successfully such a procedure to the patients with acute coronary artery disease
requiring urgent aspirin (excluding the ST elevation myocardial infarction) (SILBERMAN et
al, Am J CARDIOL 2005;95: 509-10).
Patients with a history of Aspirin or NonSteroidal Anti-Inflammatory Drugs hypersensitivity
appear to have alterations of eicosanoid metabolism : these drugs trigger an imbalance
toward the leucotriene pathway. This case-control study aims to
- evaluate after desensitization therapy the anti-aggregant effect of aspirin in these
very particular patients : clinical outcome, PFA test, levels of the urinary metabolite
of thromboxane A2 (11 dehydro thromboxane B2) and also usual aggregation tests.
- assess the in VITRO basophil activation induced by aspirin before and after
desensitization procedure by flow cytometric cellular allergen test using basophils
surface marker and mediators' dosage. Before the challenge procedure these tests aim to
confirm the clinically established diagnosis of hypersensitivity. After
desensitization, these tests intend to better assess the efficiency of the induced
tolerance, to attempt to identify predictors of successful desensitization as well as
identify potential cross reactivity with other NSAIDs..
This procedure is indicated in all patients with aspirin or NSAID intolerance with
imperative cardiological indications for aspirin, such as acute coronary syndrome, or
placement of a stent. The desensitization procedure must be performed in a coronary care
unit; the patients are duly informed about benefits and risks of the challenge and provide
written informed consent. Desensitization consists in rapidly escalating aspirin dose
administration with ad hoc aspirin capsules prepared by the hospital pharmacist. Blood and
urinary samples are obtained during the hospital stay for coronary and desensitization care.
An additional blood and urine sample will be obtained 6 to 8 weeks later during an
outpatient visit in the laboratory. Initial biological data will be compared to those of two
control groups matched for age, gender and type of acute coronary syndrome :
- Controls 1: patients with CAD on aspirin, without history of hypersensitivity
- Controls 2: patients without CAD, not on aspirin and without history of
hypersensitivity.
Eligibility
Minimum age: 18 Years.
Maximum age: N/A.
Gender(s): Both.
Criteria:
INCLUSION CRITERIA:
- Age > 18 years
- Admitted to Hospital BICHAT, in Cardiology
- Patients with aspirin or NSAID intolerance due to hypersensitivity
- Imperative cardiological indications for aspirin, such as acute coronary syndrome,
or placement of a stent
- Written informed consent
- Patient with health insurance coverage
EXCLUSION CRITERIA:
- Ongoing ST elevation acute coronary syndrome
- Ongoing signs or symptoms of hypersensitivity or allergy (asthma, urticaria, Quincke'
edema, or other allergic symptoms)
Locations and Contacts
steg Gabriel, Pr, Phone: (0)1 40 25 86 68, Ext: +33, Email: gabriel.steg@bch.aphp.fr
Centre hospitalier Bichat Claude Bernard, Paris, 75018, France; Recruiting Ph Gabriel STEG, MD, Phone: (0)1 40 25 86 68, Ext: +33, Email: gabriel.steg@bch.aphp.fr Estelle Marcault, Phone: 0)1 40 25 79 36, Ext: +33, Email: estelle.marcault@bch.aphp.fr Philippe Gabriel STEG, MD, Principal Investigator
Additional Information
Starting date: February 2007
Last updated: May 5, 2010
|