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Cell therapy and left ventricular restoration for ischemic cardiomyopathy: long-term results of a perspective, randomized study

医学 射血分数 缺血性心肌病 安慰剂 心脏病学 心肌病 内科学 心力衰竭 人口 干细胞疗法 不利影响 队列 围产期心肌病 外科 移植 病理 替代医学 环境卫生
作者
Guglielmo Stefanelli,Fabrizio Pirro,Alina Olaru,Paolo Giovanardi,Marco Meli,M. Concari,Paolo L Weltert
出处
期刊:Minerva Cardioangiologica [Edizioni Minerva Medica]
卷期号:67 (1) 被引量:4
标识
DOI:10.23736/s0026-4725.18.04800-4
摘要

Aim of this study is to verify the potential advantages and benefits of bone-marrow derived autologous stem cells implantation associated to surgical left ventricular restoration (SVR), to report a new modality of cell delivery to myocardium, and to identify possible side effects of this procedure.Between March 2007 and March 2013, 30 patients affected by ischemic dilative cardiomyopathy who received a SVR operation were enrolled in the study. The population was divided in two groups:16 patients were randomly assigned to receive stem cells therapy in addition to SVR (groupA), 14 patients received a placebo (group B). The two groups were homogeneous in respect of age, gender, preoperative NYHA class, mitral incompetence and left ventricular sizes and volumes. The patients were evaluated by echo and pet-scan before surgery and at 6 months follow-up, and by echo at subsequent follow-up.Overall 30 days-in hospital mortality was 0 for the entire cohort. At last follow-up ejection fraction increased from 25.3% before surgery to 36.3% in group A, and from 31.8% to 45.6% in group B. Reduction of LVEDD was 6% in group A, 9% in group B. ESLVV and EDLVD decreased more significantly in patients receiving stem cells (55% vs. 35%). Late cardiac mortality at 9 years follow-up was similar in the two groups of patients. No early or late adverse reaction nor cases of infections were observed.Patients affected by ischemic cardiomyopathy have a favourable outcome after SVR. A higher reduction of LVEDV and LVESV assessed by CT-Scan evaluation in patients receiving cell therapy, when compared to control group, encourages the evolution and refinement of myocardial regenerative therapy added to SVR.

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