Percutaneous mitral valve repair using the MitraClip device showed diametrically opposed results in the MITRA-FR and COAPT trials, likely due to differences in patient populations and trial designs.
Does percutaneous mitral valve repair using the MitraClip device improve outcomes in patients with systolic heart failure and severe secondary mitral regurgitation?
Understanding the methodological and population differences between the MITRA-FR and COAPT trials is essential for guiding the clinical application of MitraClip in secondary mitral regurgitation.
Percutaneous mitral valve repair using the MitraClip device has been proposed to correct secondary mitral regurgitation (MR). Recently, the results of two randomized controlled trials, that is MITRA-FR (Percutaneous Repair with the MitraClip Device for Severe Functional/Secondary Mitral Regurgitation) and COAPT (Cardiovascular Outcomes Assessment of the MitraClip Percutaneous Therapy for Heart Failure Patients with Functional Mitral Regurgitation), assessing the efficacy and safety of MitraClip in patients with systolic heart failure and severe secondary MR were published. A priori, these two trials targeted the same patient populations with the same disease using the same device but the results of these trials were diametrically opposed, MITRA-FR being neutral and COAPT being highly positive with respect to efficacy of the MitraClip procedure. The objectives of this viewpoint are: (i) to highlight not only the similarities but also the differences between MITRA-FR and COAPT, which may explain the strikingly different results and conclusions between these two trials and (ii) to derive from these results, implications with regards to the application of the MitraClip procedure in clinical practice.
Pîbarot et al. (Thu,) conducted a review in systolic heart failure and severe secondary mitral regurgitation. MitraClip was evaluated. Percutaneous mitral valve repair using the MitraClip device showed diametrically opposed results in the MITRA-FR and COAPT trials, likely due to differences in patient populations and trial designs.