• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

1984 - 1997年原发性高草酸尿症(PH1)肝肾联合移植的结果。欧洲PH1移植登记报告。欧洲PH1移植研究组。

The results of combined liver/kidney transplantation for primary hyperoxaluria (PH1) 1984-1997. The European PH1 transplant registry report. European PH1 Transplantation Study Group.

作者信息

Jamieson N V

机构信息

Department of Surgery, Addenbrooke's Hospital, Cambridge, U.K.

出版信息

J Nephrol. 1998 Mar-Apr;11 Suppl 1:36-41.

PMID:9604808
Abstract

Between 1984 and 1987 thirty European Centres reported 87 liver transplants (usually in combination with a renal transplant) in 80 patients with an underlying diagnosis of Primary Hyperoxaluria (PH1). Mean age of onset of first symptoms was 5.4 +/- 7.9 years with a mean delay to diagnosis of 4.2 +/- 6.3 years. The mean age at transplantation was 17.3 +/- 11.7 years with a mean duration of dialysis of 3.1 +/- 3.1 years. There was a family history in 43% of cases. Following transplantation one, two and five year patient survival rates were 88%, 80% and 72% and graft survival rates were 82%, 78% and 62% at the same time intervals. Patients who had been on dialysis for less than two years at the time of transplant were more likely to be assessed as being in good general condition at the time of transplantation and had better survival than those who had been on dialysis for longer time periods and carne to transplantation with evidence of marked systemic oxalosis. Combined liver/kidney transplantation appears to give excellent results in patients with PH1 although the results are poor when transplantation is delayed until advanced systemic oxalosis has developed. The registry will continue to collect and analyse data from patients undergoing liver/kidney grafting for PH1.

摘要

1984年至1987年间,30个欧洲中心报告了80例原发性高草酸尿症(PH1)患者接受的87例肝移植手术(通常与肾移植联合进行)。首次出现症状的平均年龄为5.4±7.9岁,平均诊断延迟时间为4.2±6.3年。移植时的平均年龄为17.3±11.7岁,平均透析时间为3.1±3.1年。43%的病例有家族病史。移植后1年、2年和5年的患者生存率分别为88%、80%和72%,同期移植物生存率分别为8

相似文献

1
The results of combined liver/kidney transplantation for primary hyperoxaluria (PH1) 1984-1997. The European PH1 transplant registry report. European PH1 Transplantation Study Group.1984 - 1997年原发性高草酸尿症(PH1)肝肾联合移植的结果。欧洲PH1移植登记报告。欧洲PH1移植研究组。
J Nephrol. 1998 Mar-Apr;11 Suppl 1:36-41.
2
A 20-year experience of combined liver/kidney transplantation for primary hyperoxaluria (PH1): the European PH1 transplant registry experience 1984-2004.原发性高草酸尿症1型(PH1)肝肾联合移植20年经验:欧洲PH1移植登记处1984 - 2004年经验
Am J Nephrol. 2005 May-Jun;25(3):282-9. doi: 10.1159/000086359. Epub 2005 Jun 15.
3
One hundred percent patient and kidney allograft survival with simultaneous liver and kidney transplantation in infants with primary hyperoxaluria: a single-center experience.原发性高草酸尿症婴儿同期肝肾联合移植的患者和肾移植存活率达100%:单中心经验
Transplantation. 2003 Nov 27;76(10):1458-63. doi: 10.1097/01.TP.0000084203.76110.AC.
4
European PH1 transplant registry report on the results of combined liver/kidney transplantation for primary hyperoxaluria 1984 to 1992. European PHI Transplantation Study Group.
Transplant Proc. 1995 Feb;27(1):1234-6.
5
The European Primary Hyperoxaluria Type 1 Transplant Registry report on the results of combined liver/kidney transplantation for primary hyperoxaluria 1984-1994. European PH1 Transplantation Study Group.
Nephrol Dial Transplant. 1995;10 Suppl 8:33-7. doi: 10.1093/ndt/10.supp8.33.
6
Early renal failure after domino liver transplantation using organs from donors with primary hyperoxaluria type 1.多米诺肝移植术后早期肾衰竭,供体为 1 型原发性高草酸尿症患者。
Transplantation. 2010 Oct 15;90(7):782-5. doi: 10.1097/TP.0b013e3181eefe1f.
7
Recent data on results of isolated kidney or combined kidney/liver transplantation in the U.S.A. for primary hyperoxaluria.
J Nephrol. 1998 Mar-Apr;11 Suppl 1:42-5.
8
Transplantation procedures in children with primary hyperoxaluria type 1: outcome and longitudinal growth.1型原发性高草酸尿症患儿的移植手术:结局与纵向生长情况
Transplantation. 2009 May 15;87(9):1415-21. doi: 10.1097/TP.0b013e3181a27939.
9
Clinical expression and long-term outcomes of primary hyperoxaluria types 1 and 2.1型和2型原发性高草酸尿症的临床表现及长期预后
J Nephrol. 1998 Mar-Apr;11 Suppl 1:56-9.
10
Primary hyperoxaluria type 1 in Japan.日本的1型原发性高草酸尿症
Am J Nephrol. 2005 May-Jun;25(3):297-302. doi: 10.1159/000086361. Epub 2005 Jun 15.

引用本文的文献

1
Development and Validation of a New Gas Chromatography-Tandem Mass Spectrometry Method for the Measurement of Enrichment of Glyoxylate Metabolism Analytes in Hyperoxaluria Patients Using a Stable Isotope Procedure.开发和验证一种新的气相色谱-串联质谱法,用于使用稳定同位素程序测量高草酸尿症患者中乙醛酸代谢分析物的富集。
Anal Chem. 2020 Jan 21;92(2):1826-1832. doi: 10.1021/acs.analchem.9b03670. Epub 2020 Jan 3.
2
Liver transplantation for pediatric inherited metabolic disorders: Considerations for indications, complications, and perioperative management.小儿遗传性代谢疾病的肝移植:适应证、并发症及围手术期管理的考量
Pediatr Transplant. 2016 Sep;20(6):756-69. doi: 10.1111/petr.12741. Epub 2016 Jun 21.
3
Liver-kidney transplantation in primary hyperoxaluria type-1: case report and literature review.
1型原发性高草酸尿症的肝肾联合移植:病例报告及文献综述
Int J Organ Transplant Med. 2011;2(3):126-32.
4
Selected AGXT gene mutations analysis provides a genetic diagnosis in 28% of Tunisian patients with primary hyperoxaluria.28%的原发性高草酸尿症突尼斯患者通过分析选定的 AGXT 基因突变可做出基因诊断。
BMC Nephrol. 2011 May 25;12:25. doi: 10.1186/1471-2369-12-25.
5
The role of preemptive liver transplantation in primary hyperoxaluria type 1.抢先肝移植在1型原发性高草酸尿症中的作用
Urol Res. 2005 Nov;33(5):376-9. doi: 10.1007/s00240-005-0495-1. Epub 2005 Nov 13.
6
Kidney stone disease.肾结石病
J Clin Invest. 2005 Oct;115(10):2598-608. doi: 10.1172/JCI26662.
7
Oxalate crystal deposition disease.草酸盐晶体沉积病
Curr Rheumatol Rep. 2002 Jun;4(3):257-64. doi: 10.1007/s11926-002-0074-1.
8
Current approaches to the management of primary hyperoxaluria.原发性高草酸尿症的当前管理方法。
Arch Dis Child. 2000 Jun;82(6):470-3. doi: 10.1136/adc.82.6.470.