Jashari Ramadan, Van Hoeck Beatrice, Goffin Yves, Vanderkelen Alain
European Homograft Bank, International Association, c/o Queen Astrid Military Hospital, Rue Bruynstraat, 1, B-1120 Brussels, Belgium.
J Heart Valve Dis. 2009 May;18(3):337-44.
The incidence of bicuspidity and quadricuspidity of arterial valves in donor hearts has been assessed in the European Homograft Bank.
Morphologically unacceptable donor valves for clinical use were assessed for cusp or leaflet malformation, identifying the different valve types. The state of the adjacent valve was also evaluated. Histological evaluations of the corresponding conduits were performed, in order to assess the incidence of media degeneration.
Among 3,861 donor hearts, 39 (1.0%) showed congenital cusp or leaflet malformation of one or both arterial valves, 28 (0.7%) showed bicuspid or bileaflet aortic valves (BCAV), four (0.1%) showed bicuspid or bileaflet pulmonary valves (BCPV), and eight (0.2%) showed quadricuspid or quadrileaflet pulmonary valves (QCPV). Only in one case (0.03%) were both arterial valves bicuspid or bileaflet. Among the bicuspid arterial valves, 27 (84%) were isolated aortic valves, three (9%) were isolated pulmonary valves, and in one case (3%) both the aortic and pulmonary valves were bicuspid or bileaflet.
The most frequently identified congenital malformation of the arterial valves was aortic bicuspidity, followed by pulmonary quadricuspidity and bicuspidity. If asymptomatic, these were detected during routine echocardiography, or at autopsy. These malformations might be genetically determined, as they are detected more often among different members of the same families, and in those persons of the same gender or blood group. These valves have a predisposition to accelerated calcification, stenosis, endocarditis and dissection of the ascending aorta. Neither quadricuspid/quadrileaflet nor unicuspid/monoleaflet aortic valves were detected in this study.
欧洲同种移植心脏库对供体心脏动脉瓣二叶式及四叶式的发生率进行了评估。
对临床上形态学上不可接受的供体瓣膜进行瓣叶畸形评估,确定不同的瓣膜类型。同时也评估相邻瓣膜的状态。对相应管道进行组织学评估,以评估中层退变的发生率。
在3861例供体心脏中,39例(1.0%)显示一个或两个动脉瓣存在先天性瓣叶畸形,28例(0.7%)显示二叶式或双叶式主动脉瓣(BCAV),4例(0.1%)显示二叶式或双叶式肺动脉瓣(BCPV),8例(0.2%)显示四叶式或四叶式肺动脉瓣(QCPV)。仅1例(0.03%)两个动脉瓣均为二叶式或双叶式。在二叶式动脉瓣中,27例(84%)为孤立性主动脉瓣,3例(9%)为孤立性肺动脉瓣,1例(3%)主动脉瓣和肺动脉瓣均为二叶式或双叶式。
最常见的动脉瓣先天性畸形是主动脉瓣二叶式,其次是肺动脉瓣四叶式和二叶式。若无症状,这些畸形在常规超声心动图检查或尸检时被发现。这些畸形可能由基因决定,因为在同一家族的不同成员以及相同性别或血型的人群中更常被检测到。这些瓣膜易发生加速钙化、狭窄、心内膜炎及升主动脉夹层。本研究未检测到四叶式/四叶式或单叶式/单叶式主动脉瓣。