Bunton R W, Xabregas A A, Miller A P
Department of Cardiothoracic Surgery, University of Otago, Dunedin, New Zealand.
J Thorac Cardiovasc Surg. 1990 Jul;100(1):99-107.
An experimental study to assess the performance of currently available pericardial substitutes is described with particular reference to their use after coronary artery bypass grafting. Seventy-two ewes, (six groups of 12 animals) had a 7 x 5 cm portion of the pericardium excised. Each group had either the defect left open, primarily resutured, replaced with coarse Dexon No. 2 mesh (American Cyanamid Co., Danbury, Conn.), replaced with fine Dexon No. 8 mesh, replaced with glutaraldehyde-preserved bovine pericardium, or replaced with polytetrafluoroethylene 0.1 mm surgical membrane. Six animals from each group were assessed at 3 months and the remaining six animals were assessed at 6 months. The open-defect and resutured groups served as control animals. None of the substitutes proved superior to the open-defect group in the prevention of chest wall/lung-to-pericardium adhesions at either 3 or 6 months. The limitations of the animal model in assessing this aspect of substitute performance are discussed. Whereas the bovine pericardium, polytetrafluorethylene, and Dexon No. 8 mesh groups were superior to the resutured group in the prevention of pericardium-to-epithelium adhesions in the area of the patch, this advantage was lost at 6 months when resuturing proved as effective as polytetrafluoroethylene and bovine pericardium. In all groups there was little tendency to produce generalized pericardial adhesions. At 3 months Dexon No. 8 mesh and bovine pericardium produced the least amount of significant epicardial reaction. In two animals in the 3-month polytetrafluoroethylene group and in one animal in the 6-month polytetrafluoroethylene group, a "fibrous peel" was encountered on the inner surface of the patch, which had also become adherent to the epicardium and had obscured the underlying anatomy. At 6 months the open-defect, resutured, and bovine pericardium groups had produced no significant epicardial reaction. In one animal at 6 months the bovine pericardium had become markedly thickened and degenerative. We do not recommend routine closure of the pericardium after coronary artery operations with any of the substitutes investigated in our study.
本文描述了一项实验研究,旨在评估当前可用的心包替代物的性能,特别提及了它们在冠状动脉旁路移植术后的使用情况。72只母羊(分为6组,每组12只动物)切除了7×5厘米的心包部分。每组的缺损要么敞开不处理,要么进行一期缝合,要么用2号粗德克松网片(美国氰胺公司,康涅狄格州丹伯里)替代,要么用8号细德克松网片替代,要么用戊二醛保存的牛心包替代,要么用0.1毫米的聚四氟乙烯手术膜替代。每组6只动物在3个月时进行评估,其余6只动物在6个月时进行评估。敞开缺损组和一期缝合组作为对照动物。在3个月或6个月时,没有一种替代物在预防胸壁/肺与心包粘连方面优于敞开缺损组。讨论了动物模型在评估替代物性能这一方面的局限性。虽然牛心包、聚四氟乙烯和8号德克松网片组在预防补片区域的心包与上皮粘连方面优于一期缝合组,但在6个月时,当一期缝合证明与聚四氟乙烯和牛心包一样有效时,这一优势就消失了。在所有组中,产生广泛性心包粘连的倾向很小。在3个月时,8号德克松网片和牛心包产生的显著心外膜反应最少。在3个月的聚四氟乙烯组的两只动物和6个月的聚四氟乙烯组的一只动物中,在补片的内表面遇到了一层“纤维性包膜”,它也与心外膜粘连并掩盖了下面的解剖结构。在6个月时,敞开缺损组、一期缝合组和牛心包组没有产生显著的心外膜反应。在6个月时,有一只动物的牛心包明显增厚并发生退变。我们不建议在冠状动脉手术后常规使用我们研究中所调查的任何替代物来关闭心包。