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年轻受者中主动脉瓣同种异体移植物的退变

Degeneration of aortic valve allografts in young recipients.

作者信息

Clarke D R, Campbell D N, Hayward A R, Bishop D A

机构信息

Childrens Hospital, Denver, Colo. 80218.

出版信息

J Thorac Cardiovasc Surg. 1993 May;105(5):934-41; discussion 941-2.

PMID:8487572
Abstract

Aortic allograft fibrocalcification and valvular insufficiency have been observed in patients less than 3 years of age at initial replacement of the left ventricular outflow tract. From June 1985 through May 1992, 47 children have undergone aortic root replacement with cryopreserved aortic valve allografts. Thirty-three children were 3 years of age or older and 14 were less than 3 years of age at operation. In the older patient group, there were three (9%) hospital deaths and one child underwent cardiac transplantation 30 hours after aortic root replacement because of left ventricular failure. Clinical follow-up of the 29 surviving older children is from 4 months to 6.6 years (mean 3.0 years). One patient was lost to follow-up. Two children (7%) have required reoperation, but primary allograft degeneration was not observed. In the younger patient group, there were three (21%) hospital deaths. Follow-up ranged from 2.5 months to 4.7 years (mean 2.3 years). Among 11 operative survivors, one late death resulted from a pulmonary embolus. Seven of 10 (70%) remaining allograft recipients had progressive allograft calcification or insufficiency. Six of them have required reoperation to explant the allograft, and one child is currently receiving cyclosporine therapy with the original valve allograft. The cause of allograft failure is possibly immunologic. The prevalence of early aortic valve allograft degeneration has prompted the consideration of nonviable allografts or xenografts, pulmonary autografts, or minimal immunosuppression as alternatives when left ventricular outflow tract reconstruction is necessary in children less than 3 years of age.

摘要

在左心室流出道初次置换时,已在3岁以下的患者中观察到主动脉同种异体移植物纤维钙化和瓣膜功能不全。从1985年6月至1992年5月,47名儿童接受了带冷冻保存主动脉瓣同种异体移植物的主动脉根部置换术。33名儿童手术时年龄为3岁或以上,14名儿童手术时年龄小于3岁。在年龄较大的患者组中,有3例(9%)住院死亡,1名儿童在主动脉根部置换术后30小时因左心室衰竭接受了心脏移植。29名存活的年龄较大儿童的临床随访时间为4个月至6.6年(平均3.0年)。1例患者失访。2名儿童(7%)需要再次手术,但未观察到原发性同种异体移植物退变。在年龄较小的患者组中,有3例(21%)住院死亡。随访时间为2.5个月至4.7年(平均2.3年)。在11名手术存活者中,1例晚期死亡是由肺栓塞导致的。10名剩余同种异体移植物接受者中有7名(70%)出现了同种异体移植物进行性钙化或功能不全。其中6名已需要再次手术取出同种异体移植物,1名儿童目前正在接受环孢素治疗,仍保留原瓣膜同种异体移植物。同种异体移植物失败的原因可能是免疫性的。早期主动脉瓣同种异体移植物退变的发生率促使人们在3岁以下儿童需要进行左心室流出道重建时,考虑使用无活性同种异体移植物或异种移植物、肺动脉自体移植物或最小化免疫抑制作为替代方案。

相似文献

1
Degeneration of aortic valve allografts in young recipients.年轻受者中主动脉瓣同种异体移植物的退变
J Thorac Cardiovasc Surg. 1993 May;105(5):934-41; discussion 941-2.
2
Ten year experience with pulmonary allografts in children.儿童肺移植十年经验
J Heart Valve Dis. 1995 Jul;4(4):384-91.
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The Ross procedure in children and young adults with congenital aortic valve disease.儿童和年轻成人先天性主动脉瓣疾病的罗斯手术
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Midterm results of Ross aortic valve replacement: a single-institution experience.罗斯主动脉瓣置换术的中期结果:单机构经验
Ann Thorac Surg. 2009 Aug;88(2):601-7; discussion 607-8. doi: 10.1016/j.athoracsur.2009.05.014.
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Pediatric autograft aortic root replacement: a prospective follow-up study.小儿自体主动脉根部置换术:一项前瞻性随访研究。
Ann Thorac Surg. 2005 Nov;80(5):1628-33. doi: 10.1016/j.athoracsur.2005.04.057.
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Aortic valve replacement with pulmonary or aortic allografts.
Circulation. 1991 Nov;84(5 Suppl):III89-93.
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Allografts for aortic valve or root replacement: insights from an 18-year single-center prospective follow-up study.用于主动脉瓣或根部置换的同种异体移植物:一项18年单中心前瞻性随访研究的见解
Eur J Cardiothorac Surg. 2007 May;31(5):851-9. doi: 10.1016/j.ejcts.2007.02.009. Epub 2007 Mar 12.
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The Ross-Konno procedure in children: outcomes, autograft and allograft function, and reoperations.儿童Ross-Konno手术:手术结果、自体移植物和同种异体移植物功能以及再次手术情况
Ann Thorac Surg. 2006 Oct;82(4):1301-6. doi: 10.1016/j.athoracsur.2006.05.001.
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The Ross operation in children: effects of aortic annuloplasty.儿童Ross手术:主动脉瓣环成形术的效果
Ann Thorac Surg. 2007 Oct;84(4):1326-30. doi: 10.1016/j.athoracsur.2007.03.097.
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Comparison of the aortic homograft and the pulmonary autograft for aortic valve or root replacement in children.
J Thorac Cardiovasc Surg. 1991 Jul;102(1):51-60; discussion 60-1.

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