Qureshi Muhammad Y, Cabalka Allison K, Khan Shakila P, Hagler Donald J, Haile Dawit T, Cannon Bryan C, Olson Timothy M, Cantero-Peral Susana, Dietz Allan B, Radel Darcie J, Taggart Nathan W, Kelle Angela M, Rodriguez Vilmarie, Dearani Joseph A, O'Leary Patrick W
Division of Pediatric Cardiology, Mayo Clinic, Rochester, MN.
Division of Pediatric Hematology and Oncology, Mayo Clinic, Rochester, MN.
Mayo Clin Proc Innov Qual Outcomes. 2017 Aug 2;1(2):185-191. doi: 10.1016/j.mayocpiqo.2017.07.002. eCollection 2017 Sep.
Myocardial dysfunction after Fontan palliation for univentricular congenital heart disease is a challenging clinical problem. The medical treatment has a limited impact, with cardiac transplant being the ultimate management step. Cell-based therapies are evolving as a new treatment for heart failure. Phase 1 clinical trials using regenerative therapeutic strategies in congenital heart disease are ongoing. We report the first case of autologous bone marrow-derived mononuclear cell administration for ventricular dysfunction, 23 years after Fontan operation in a patient with hypoplastic left heart syndrome. The cells were delivered into the coronary circulation by cardiac catheterization. Ventricular size decreased and several parameters reflecting ventricular function improved, with maximum change noted 3 months after cell delivery. Such regenerative therapeutic options may help in delaying and preventing cardiac transplant.
单心室先天性心脏病进行Fontan姑息治疗后出现的心肌功能障碍是一个具有挑战性的临床问题。药物治疗效果有限,心脏移植是最终的治疗手段。基于细胞的疗法正在成为治疗心力衰竭的一种新方法。目前正在进行针对先天性心脏病采用再生治疗策略的1期临床试验。我们报告了第一例在左心发育不全综合征患者接受Fontan手术后23年,因心室功能障碍给予自体骨髓来源的单个核细胞治疗的病例。通过心导管术将细胞注入冠状动脉循环。心室大小减小,反映心室功能的几个参数得到改善,在细胞注入后3个月变化最大。这种再生治疗选择可能有助于延迟和预防心脏移植。