MI後の僧帽弁修復による有益性はほとんどまたは全くない(Abstract 20772)

Routinely adding mitral valve repair to coronary artery bypass graft surgery for myocardial infarction (MI) patients may not be warranted in patients with moderate mitral valve damage, according to an NIH-funded study. Patients treated with both procedures versus the bypass graft alone showed no differences at one year in recovery from structural damage to the heart's left ventricle, nor in secondary measures such as heart failure, stroke, functional status or quality of life.
The results of the Surgical Interventions for Moderate Ischemic Mitral Regurgitation (IMR) study, supported by NIH's National Heart, Lung, and Blood Institute (NHLBI), were presented at the American Heart Association Scientific Sessions in Chicago and published simultaneously in the New England Journal of Medicine.
Of patient suffering a myocardial infarction, about half are left with functional damage to the mitral valve due to the injury and changes to the heart muscle. This damage can result ischemic mitral regurgitation.
Doctors typically treat MI patients with this condition by performing coronary artery bypass graft surgery, sometimes adding mitral valve repair to fix the leaky mitral valve. The study is the first large-scale randomized clinical trial to assess whether adding the repair procedure leads to a measurable benefit for patients.
The study included 301 patients with moderate IMR who had been treated with one or both surgical procedures. Researchers assessed each patient's condition at six and 12 months by measuring the amount of blood remaining in the left ventricle after a heart contraction. Both patient groups showed similar rates of improvement at the 12-month assessment.
At 1 year, when compared with CABG alone, the addition of mitral valve repair to CABG did not result in a greater degree of left ventricular reverse remodeling or an improvement in mortality, MACE, hospital readmission or quality of life. However the addition of MV repair was associated with more neurologic events, increased cross clamp and cardiopulmonary bypass times, and longer ICU and hospital lengths of stay. Longer-term follow-up is ongoing.
This research was conducted as part of NHLBI's Cardiothoracic Surgical Trials Network and was co-funded by the National Institute for Neurological Diseases and Stroke and the Canadian Institutes for Health Research.