医学
小猎犬
生物相容性
动物模型
生物相容性材料
介入心脏病学
外科
心脏病学
内科学
生物医学工程
冶金
材料科学
作者
Haisong Bu,Yifeng Yang,Shijun Hu,Qin Wu,Xueyang Gong,Tianli Zhao
出处
期刊:Interactive Cardiovascular and Thoracic Surgery
[Oxford University Press]
日期:2019-06-25
卷期号:29 (5): 783-792
被引量:11
摘要
Abstract OBJECTIVES The feasibility of an Amplatzer septal occluder closure of ventricular septal defects (VSDs) under echocardiographic guidance has already been proven. However, the technique is not used routinely owing to high-rate atrioventricular blocks and the non-absorbability of the occluder. Here, we aimed to evaluate the safety, biocompatibility and effectiveness of a new biodegradable occluder. METHODS A total of 18 adult beagle dogs [mean body weight 8.85 kg (range 8.10–10.40 kg)] were enrolled in our study from March 2015 to July 2018. VSD animal models were prepared by thoracic intervention, and the new bioabsorbable occluder was implanted under the guidance of transthoracic echocardiography. Laboratory examinations, transthoracic echocardiography and electrocardiography were performed after surgery, and pathological samples from dogs were obtained after euthanasia and examined in the 1st, 3rd, 6th, 9th, 12th and 24th months to evaluate the safety, biocompatibility and effectiveness of the biodegradable occluder. RESULTS All the dogs received successful implantations of the biodegradable occluder and survived, showing no follow-up-related complications (such as dislocation, arrhythmia and recanalization). Biochemical tests showed no significant abnormalities or differences, except for an increase in white blood cells and C-reactive proteins on the day after the operation. Histopathological examinations revealed that the bioabsorbable occluders were biocompatible, while immunohistochemical evaluations and electron microscopy showed endothelial cells growing on the occluder surface. CONCLUSIONS The effective occlusion of VSD, good biocompatibility, rapid endothelialization and lack of complications shown by the biodegradable occluder in this study suggest that the device meets acceptable clinical safety and has potential application prospects.
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