D Zhu, S Z Wang, J B Gao, Z L Luo, K Yang, C M Xie, P X Kong, S Y Feng, H Jiang, X B Pan
{"title":"[Animal study results of a novel designed transcatheter mitral valve replacement system].","authors":"D Zhu, S Z Wang, J B Gao, Z L Luo, K Yang, C M Xie, P X Kong, S Y Feng, H Jiang, X B Pan","doi":"10.3760/cma.j.cn112148-20250126-00069","DOIUrl":null,"url":null,"abstract":"<p><p><b>Objective:</b> To preliminarily assess the biocompatibility and durability of the TruDelta<sup>TM</sup> transcatheter mitral valve replacement (TMVR) system. <b>Method:</b> Six adult sheep were divided into 3 groups based on the duration of follow-up: 30 days (<i>n</i>=1), 90 days (<i>n</i>=3) and 180 days (<i>n</i>=2). The TruDelta<sup>TM</sup> TMVR system was implanted through a transapical approach under transesophageal echocardiographic guidance. The operability of the TMVR system was evaluated using an instrument performance evaluation scale (consisting of 39 items), with scores ranging from 1 (worst) to 10 (best) assigned by the operator. Echocardiography was conducted preoperatively, immediately after surgery, and at 30, 90, and 180 days post-implantation. At the last follow-up time point, the intervention mitral valve membrane and major organs were dissected for observation. The artificial valves were taken for hematoxylin eosin (HE) staining and observed under a scanning electron microscope. <b>Result:</b> All six procedures were successfully completed using 29S size TruDelta<sup>TM</sup> TMVR device. At the final follow-up, echocardiogram demonstrated good valve function without obvious paravalvular leakage, with a transvalvular gradient of (7.8±3.2) mmHg (1 mmHg=0.133 kPa) and a mitral valve orifice area of (1.8±0.2) cm<sup>2</sup>. Autopsy findings revealed no structural valve failure and almost complete endothelialization (>75%) with 90 to 180 days. Both HE staining and scanning electron microscopy confirmed optimal endothelialization of the valve stent. <b>Conclusion:</b> The preclinical animal study indicates that the TruDelta<sup>TM</sup> device exhibits favorable biocompatibility and durability.</p>","PeriodicalId":38755,"journal":{"name":"中华心血管病杂志","volume":"53 3","pages":"287-292"},"PeriodicalIF":0.0000,"publicationDate":"2025-03-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"中华心血管病杂志","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3760/cma.j.cn112148-20250126-00069","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
Abstract
Objective: To preliminarily assess the biocompatibility and durability of the TruDeltaTM transcatheter mitral valve replacement (TMVR) system. Method: Six adult sheep were divided into 3 groups based on the duration of follow-up: 30 days (n=1), 90 days (n=3) and 180 days (n=2). The TruDeltaTM TMVR system was implanted through a transapical approach under transesophageal echocardiographic guidance. The operability of the TMVR system was evaluated using an instrument performance evaluation scale (consisting of 39 items), with scores ranging from 1 (worst) to 10 (best) assigned by the operator. Echocardiography was conducted preoperatively, immediately after surgery, and at 30, 90, and 180 days post-implantation. At the last follow-up time point, the intervention mitral valve membrane and major organs were dissected for observation. The artificial valves were taken for hematoxylin eosin (HE) staining and observed under a scanning electron microscope. Result: All six procedures were successfully completed using 29S size TruDeltaTM TMVR device. At the final follow-up, echocardiogram demonstrated good valve function without obvious paravalvular leakage, with a transvalvular gradient of (7.8±3.2) mmHg (1 mmHg=0.133 kPa) and a mitral valve orifice area of (1.8±0.2) cm2. Autopsy findings revealed no structural valve failure and almost complete endothelialization (>75%) with 90 to 180 days. Both HE staining and scanning electron microscopy confirmed optimal endothelialization of the valve stent. Conclusion: The preclinical animal study indicates that the TruDeltaTM device exhibits favorable biocompatibility and durability.
Khalid Ghanim Aljuaid, Mohammad Abdulwahab Albuoderman, Emad Abdullah AlAhmadi, J. Iqbal
来源期刊
中华心血管病杂志Medicine-Cardiology and Cardiovascular Medicine
CiteScore
1.40
自引率
0.00%
发文量
10577
期刊介绍:
The Chinese Journal of Cardiology , established in February 1973, is one of the major academic medical journals sponsored by the Chinese Medical Association and a leading periodical in the field of cardiology in China. It specializes in cardiology and related disciplines with a readership of more than 25 000. The journal publishes editorials and guidelines as well as important original articles on clinical and experimental investigations, reflecting achievements made in China and promoting academic communication between domestic and foreign cardiologists. The journal includes the following columns: Editorials, Strategies, Comments, Clinical Investigations, Experimental Investigations, Epidemiology and Prevention, Lectures, Comprehensive Reviews, Continuing Medical Education, etc.