Study of Platelet Activation by Severe Aortic Stenosis and Its Correction by Transcatheter Aortic Valve Implantation (TAVI)

Toulouse University Hospital

Status: Completed

Conditions: Aortic Stenosis

Treatments: Other: control group; Other: test

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT02504632

14 7078 03

Details and patient eligibility

About

Study of platelet activation by severe aortic stenosis and its correction by Transcatheter Aortic Valve Implantation (TAVI)

Full description

• Background: TAVI has emerged as an alternative to surgical aortic valve replacement for patients with severe, symptomatic aortic stenosis (AS) and is expanding worldwide with more than 50,000 patients treated to date.

• Purpose Changes in haemostasis, particularly in platelet activation or reactivity before, during and after TAVI have never been studied. Valve replacement is known to alleviate von Willebrand factor abnormalities associated with AS. A potential improvement of platelet function could also occur after TAVI. Indeed, circulating platelets may be desensitized and under-reactive due to multiple passages through the stenotic valve and could recover normal reactivity after TAVI. Besides, TAVI presents a risk of major ischemic complications. The investigators can hypothesize the involvement of high reactive platelets in peri-procedural thrombotic or ischemic events. This study of the platelet activation kinetics will be performed by comparing several specific markers before and at various times after valve implantation.

• Primary outcome To evaluate the kinetics of platelet activation before and at various times after valve implantation, by comparing several specific markers in peripheral venous blood samples before (day 0) and at days 1 and 5±1 after the procedure.

• Study design and number of subjects: This is a prospective, monocentric, study. The test group includes up to 15 patients treated by transfemoral TAVI using a MedTronic CoreValve (MCV) prosthesis. Platelet activation will be studied before and after the procedure and compared to a reference established with an age-matched, aspirin-treated, atherosclerotic population (30 patients in the control group).

• Eligibility criteria:

  • inclusion criteria: test group: patients with severe aortic stenosis and transfemoral TAVI with MCV aspirin treatment . Control group: age-matched patients with stable coronary artery disease treated by aspirin but without aortic stenosis.
  • exclusion criteria: recent (1 month) acute coronary syndrome; treatment by anti platelet agents other than aspirin

• Procedures: Specific platelet activation markers, circulating platelet/monocytes aggregates, platelet reactivity and vWF will be assessed in peripheral venous blood before, 1 and 5 days after TAVI and in ascending aorta during the procedure.

Enrollment: 44 patients

Sex: All

Ages: 50+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Test group

  • Severe symptomatic AS (Aortic valve area < 0,6 cm2/m2 SC), deemed, after multidisciplinary heart team evaluation, contra-indicated or at high risk for surgery and suitable for TF TAVI with a MCV prosthesis.
  • Aspirin treatment (75-160 mg/d for at least one week)

• Control group

  • Stable coronary artery disease, unscathed of AS
  • Aspirin treatment (75-160 mg/d for at least one week)

Exclusion criteria

• Test group:

  • Acute coronary syndrome 1 month before inclusion
  • Any co-morbidity limiting life-expectancy < 1 year
  • Terminal chronic kidney disease requiring hemodialysis thrombocytopenia <100 G/L, anemia (Hb < 10 g/dl)
  • Treatment by another antiplatelet agent within 10 days before the procedure

• Control group:

  • Acute coronary syndrome 1 month before inclusion
  • Any co-morbidity limiting life-expectancy < 1 year
  • Terminal chronic kidney disease requiring hemodialysis
  • Thrombocytopenia <100 G/L
  • Treatment by another antiplatelet agent within 10 days before the procedure

Trial design

Primary purpose: Other

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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44 participants in 2 patient groups

test group

Experimental group

Description:

Patient with severe, symptomatic AS (Aortic valve area \< 0,6 cm2/m2 SC), deemed, after multidisciplinary heart team evaluation, contra-indicated or at high risk for surgery and suitable for TF TAVI with a MCV prosthesis.

Treatment:

Other: test

control group

Other group

Description:

Patient with stable coronary artery disease, unscathed of AS Patient under aspirin treatment (75-160 mg/d for at least one week)

Treatment:

Other: control group