PMID- 15464325 OWN - NLM STAT- MEDLINE DCOM- 20041027 LR - 20220408 IS - 0735-1097 (Print) IS - 0735-1097 (Linking) VI - 44 IP - 7 DP - 2004 Oct 6 TI - Surgical ventricular restoration in the treatment of congestive heart failure due to post-infarction ventricular dilation. PG - 1439-45 AB - OBJECTIVES: The purpose of this study was to test how surgical ventricular restoration (SVR) affects early and late survival in a registry of 1,198 post-anterior infarction congestive heart failure (CHF) patients treated by the international Reconstructive Endoventricular Surgery returning Torsion Original Radius Elliptical shape to the left ventricle (RESTORE)team. BACKGROUND: Congestive heart failure may be caused by late left ventricular (LV) dilation after anterior infarction. The infarcted segment is often akinetic rather than dyskinetic because early reperfusion prevents transmural necrosis. Previously, only dyskinetic areas were treated by operation. Surgical ventricular restoration reduces LV volume and creates a more elliptical chamber by excluding scar in either akinetic or dyskinetic segments. METHODS: The RESTORE group applied SVR to 1,198 post-infarction patients between 1998 and 2003. Early and late outcomes were examined, and risk factors were identified. RESULTS: Concomitant procedures included coronary artery bypass grafting in 95%, mitral valve repair in 22%, and mitral valve replacement in 1%. Overall 30-day mortality after SVR was 5.3% (8.7% with mitral repair vs. 4.0% without repair; p < 0.001). Perioperative mechanical support was uncommon (<9%). Global systolic function improved postoperatively. Ejection fraction (EF) increased from 29.6 +/- 11.0% preoperatively to 39.5 +/- 12.3% postoperatively (p < 0.001). The left ventricular end-systolic volume index (LVESVI) decreased from 80.4 +/- 51.4 ml/m(2) preoperatively to 56.6 +/- 34.3 ml/m(2) postoperatively (p < 0.001). Overall five-year survival was 68.6 +/- 2.8%. Logistic regression analysis identified EF or=80 ml/m(2), advanced New York Heart Association (NYHA) functional class, and age >or=75 years as risk factors for death. Five-year freedom from hospital readmission for CHF was 78%. Preoperatively, 67% of patients were NYHA functional class III or IV and postoperatively, 85% were class I or II. CONCLUSIONS: Surgical ventricular restoration improves ventricular function and is highly effective therapy in the treatment of ischemic cardiomyopathy with excellent five-year outcome. FAU - Athanasuleas, Constantine L AU - Athanasuleas CL AD - Norwood Clinic and Kemp Carraway Heart Institute, Birmingham, Alabama, USA. FAU - Buckberg, Gerald D AU - Buckberg GD FAU - Stanley, Alfred W H AU - Stanley AW FAU - Siler, William AU - Siler W FAU - Dor, Vincent AU - Dor V FAU - Di Donato, Marisa AU - Di Donato M FAU - Menicanti, Lorenzo AU - Menicanti L FAU - Almeida de Oliveira, Sergio AU - Almeida de Oliveira S FAU - Beyersdorf, Friedhelm AU - Beyersdorf F FAU - Kron, Irving L AU - Kron IL FAU - Suma, Hisayoshi AU - Suma H FAU - Kouchoukos, Nicholas T AU - Kouchoukos NT FAU - Moore, Wistar AU - Moore W FAU - McCarthy, Patrick M AU - McCarthy PM FAU - Oz, Mehmet C AU - Oz MC FAU - Fontan, Francis AU - Fontan F FAU - Scott, Meredith L AU - Scott ML FAU - Accola, Kevin A AU - Accola KA CN - RESTORE group LA - eng PT - Journal Article PL - United States TA - J Am Coll Cardiol JT - Journal of the American College of Cardiology JID - 8301365 SB - IM CIN - J Am Coll Cardiol. 2005 Aug 2;46(3):562; author reply 562-3. PMID: 16053978 MH - Aged MH - Blood Pressure MH - Coronary Artery Bypass MH - Dilatation, Pathologic/complications/etiology/surgery MH - Female MH - Heart Failure/etiology/pathology/*physiopathology/*surgery MH - Heart Valve Prosthesis MH - Heart Ventricles/*pathology/physiopathology/*surgery MH - Humans MH - Male MH - Middle Aged MH - Mitral Valve/surgery MH - Myocardial Infarction/*complications/pathology/physiopathology MH - Severity of Illness Index MH - Stroke Volume MH - Treatment Outcome EDAT- 2004/10/07 09:00 MHDA- 2004/10/28 09:00 CRDT- 2004/10/07 09:00 PHST- 2004/05/12 00:00 [received] PHST- 2004/06/24 00:00 [revised] PHST- 2004/07/06 00:00 [accepted] PHST- 2004/10/07 09:00 [pubmed] PHST- 2004/10/28 09:00 [medline] PHST- 2004/10/07 09:00 [entrez] AID - S0735-1097(04)01443-3 [pii] AID - 10.1016/j.jacc.2004.07.017 [doi] PST - ppublish SO - J Am Coll Cardiol. 2004 Oct 6;44(7):1439-45. doi: 10.1016/j.jacc.2004.07.017.