Nummi Annu, Nieminen Tuomo, Pätilä Tommi, Lampinen Milla, Lehtinen Miia L, Kivistö Sari, Holmström Miia, Wilkman Erika, Teittinen Kari, Laine Mika, Sinisalo Juha, Kupari Markku, Kankuri Esko, Juvonen Tatu, Vento Antti, Suojaranta Raili, Harjula Ari
Heart and Lung Center, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Department of Internal Medicine, South Karelia Central Hospital, Lappeenranta, Finland.
Pilot Feasibility Stud. 2017 Dec 20;3:74. doi: 10.1186/s40814-017-0217-9. eCollection 2017.
The atrial appendages are a tissue reservoir for cardiac stem cells. During on-pump coronary artery bypass graft (CABG) surgery, part of the right atrial appendage can be excised upon insertion of the right atrial cannula of the heart-lung machine. In the operating room, the removed tissue can be easily cut into micrografts for transplantation. This trial aims to assess the safety and feasibility of epicardial transplantation of atrial appendage micrografts in patients undergoing CABG surgery.
METHODS/DESIGN: Autologous cardiac micrografts are made from leftover right atrial appendage during CABG of 6 patients. Atrial appendage is mechanically processed to micrografts consisting of atrial appendage-derived cells (AADCs) and their extracellular matrix (ECM). The micrografts are epicardially transplanted in a fibrin gel and covered with a tissue-engineered ECM sheet. Parameters including echocardiography-reflecting cardiac insufficiency-are studied pre- and post-operatively as well as at 3 and 6 months of the follow-up. Cardiac functional magnetic resonance imaging is performed preoperatively and at 6-month follow-up. The primary outcome measures are patient safety in terms of hemodynamic and cardiac function over time and feasibility of therapy administration in a clinical setting. Secondary outcome measures are left ventricular wall thickness, change in the amount of myocardial scar tissue, changes in left ventricular ejection fraction, plasma concentrations of N-terminal pro-B-type natriuretic peptide (NT-proBNP) levels, New York Heart Association class, days in hospital, and changes in the quality of life. Twenty patients undergoing routine CAGB surgery will be recruited to serve as a control group.
This study aims to address the surgical feasibility and patient safety of epicardially delivered atrial appendage micrografts during CABG surgery. Delivery of autologous micrografts and AADCs has potential applications for cell and cell-based gene therapies.
ClinicalTrials.gov Identifier: NCT02672163. Date of registration: 02.02.2016.
心耳是心脏干细胞的组织储存库。在体外循环冠状动脉旁路移植术(CABG)手术期间,插入心肺机的右心耳插管时可切除部分右心耳。在手术室中,切除的组织可轻松切成微移植物用于移植。本试验旨在评估在接受CABG手术的患者中进行心外膜移植心耳微移植物的安全性和可行性。
方法/设计:自体心脏微移植物由6例患者CABG手术期间剩余的右心耳制成。心耳经机械处理制成由心耳来源细胞(AADCs)及其细胞外基质(ECM)组成的微移植物。微移植物在心外膜处以纤维蛋白凝胶进行移植,并用组织工程ECM片覆盖。术前、术后以及随访3个月和6个月时研究包括反映心功能不全的超声心动图在内的参数。术前和随访6个月时进行心脏功能磁共振成像。主要结局指标是患者随时间推移在血流动力学和心脏功能方面的安全性以及在临床环境中进行治疗给药的可行性。次要结局指标是左心室壁厚度、心肌瘢痕组织量的变化、左心室射血分数的变化、N端前脑钠肽(NT-proBNP)水平的血浆浓度、纽约心脏协会分级、住院天数以及生活质量的变化。将招募20例接受常规CAGB手术的患者作为对照组。
本研究旨在探讨在CABG手术期间心外膜递送心耳微移植物的手术可行性和患者安全性。自体微移植物和AADCs的递送在细胞和基于细胞的基因治疗中具有潜在应用。
ClinicalTrials.gov标识符:NCT02672163。注册日期:2016年2月2日。