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Multicenter phase I/II trial of the safety of allogeneic endothelial cell implants after the creation of arteriovenous access for hemodialysis use: the V-HEALTH study.用于血液透析的动静脉通路建立后同种异体内皮细胞植入安全性的多中心I/II期试验:V-HEALTH研究
J Vasc Surg. 2009 Dec;50(6):1359-68.e1. doi: 10.1016/j.jvs.2009.07.108.
2
Advances and new frontiers in the pathophysiology of venous neointimal hyperplasia and dialysis access stenosis.静脉内膜增生和透析通路狭窄病理生理学的进展与新前沿
Adv Chronic Kidney Dis. 2009 Sep;16(5):329-38. doi: 10.1053/j.ackd.2009.06.009.
3
Effect of dipyridamole plus aspirin on hemodialysis graft patency.双嘧达莫加阿司匹林对血液透析移植物通畅性的影响。
N Engl J Med. 2009 May 21;360(21):2191-201. doi: 10.1056/NEJMoa0805840.
4
CKD accelerates development of neointimal hyperplasia in arteriovenous fistulas.慢性肾脏病会加速动静脉内瘘中新生内膜增生的发展。
J Am Soc Nephrol. 2009 Jun;20(6):1236-45. doi: 10.1681/ASN.2007121312. Epub 2009 May 7.
5
Cellular phenotypes in human stenotic lesions from haemodialysis vascular access.血液透析血管通路中人类狭窄病变的细胞表型
Nephrol Dial Transplant. 2009 Sep;24(9):2786-91. doi: 10.1093/ndt/gfn708. Epub 2009 Apr 17.
6
Longitudinal assessment of hyperplasia using magnetic resonance imaging without contrast in a porcine arteriovenous graft model.在猪动静脉移植模型中使用无对比剂磁共振成像对增生进行纵向评估。
Acad Radiol. 2009 Jan;16(1):96-107. doi: 10.1016/j.acra.2008.05.019.
7
Neointimal hyperplasia associated with synthetic hemodialysis grafts.与合成血液透析移植物相关的新生内膜增生。
Kidney Int. 2008 Nov;74(10):1247-61. doi: 10.1038/ki.2008.318. Epub 2008 Jul 30.
8
Effect of clopidogrel on early failure of arteriovenous fistulas for hemodialysis: a randomized controlled trial.氯吡格雷对血液透析动静脉内瘘早期失功的影响:一项随机对照试验。
JAMA. 2008 May 14;299(18):2164-71. doi: 10.1001/jama.299.18.2164.
9
Genetic deficiency of heme oxygenase-1 impairs functionality and form of an arteriovenous fistula in the mouse.血红素加氧酶-1的基因缺陷会损害小鼠动静脉内瘘的功能和形态。
Kidney Int. 2008 Jul;74(1):47-51. doi: 10.1038/ki.2008.110. Epub 2008 Mar 26.
10
Vascular stenosis: biology and interventions.血管狭窄:生物学与干预措施
Curr Opin Nephrol Hypertens. 2007 Nov;16(6):516-22. doi: 10.1097/MNH.0b013e3282efa57f.

透析通路术前严重静脉内膜增生。

Severe venous neointimal hyperplasia prior to dialysis access surgery.

机构信息

Department of Clinical and Experimental Medicine, Federico II University Medical School, Naples, Italy.

出版信息

Nephrol Dial Transplant. 2011 Jul;26(7):2264-70. doi: 10.1093/ndt/gfq733. Epub 2011 Jan 10.

DOI:10.1093/ndt/gfq733
PMID:21220751
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3145379/
Abstract

BACKGROUND

Venous neointimal hyperplasia is the most common cause of arteriovenous (AV) fistula and graft dysfunction following dialysis access surgery. However, the pathogenetic impact of pre-existing venous neointimal hyperplasia at the time of AV access creation on final clinical success is currently unknown in the setting of advanced chronic kidney disease (CKD) and end-stage renal disease (ESRD) patients. The aim of this study was to perform a detailed histological, morphometric, and immunohistochemical analysis of vein specimens in advanced CKD and ESRD patients collected at the time of new vascular access placement.

METHODS

Vein samples from 12 patients were collected at the time of AV access creation near the site of AV anastomosis. Histological, immunohistochemistry and morphometric studies were performed on these vein samples.

RESULTS

Examination of the tissue specimens obtained at the time of surgery showed neointimal hyperplasia in 10 of 12 specimens, ranging from minimal to very severe. The majority of cells within the neointima were myofibroblasts with a minority of contractile smooth muscle cells present.

CONCLUSION

Our work represents a detailed description of the morphometric and cellular phenotypic lesions present in the veins of CKD and ESRD patients, prior to dialysis access placement. These studies (i) suggest the future possibility of a new predictive marker (pre-existing venous neointimal hyperplasia) for AV dialysis access dysfunction and (ii) open the door for the future development of novel local therapies for optimization of the venous substrate on which the dialysis access is created.

摘要

背景

静脉性内膜增生是透析通路手术后动静脉(AV)瘘和移植物功能障碍的最常见原因。然而,在晚期慢性肾脏病(CKD)和终末期肾病(ESRD)患者中,AV 通路创建时存在的静脉性内膜增生对最终临床成功的发病机制影响目前尚不清楚。本研究旨在对新血管通路放置时收集的晚期 CKD 和 ESRD 患者静脉标本进行详细的组织学、形态计量学和免疫组织化学分析。

方法

在 AV 吻合口附近 AV 通路创建时收集 12 名患者的静脉样本。对这些静脉样本进行组织学、免疫组织化学和形态计量学研究。

结果

手术时获得的组织标本检查显示,12 个标本中有 10 个存在内膜增生,从轻度到重度不等。新生内膜中的大多数细胞是肌成纤维细胞,少数存在收缩性平滑肌细胞。

结论

我们的工作代表了对 CKD 和 ESRD 患者静脉中存在的形态计量学和细胞表型病变的详细描述,这些病变发生在透析通路放置之前。这些研究表明(i)未来可能会出现一种新的预测标志物(预先存在的静脉性内膜增生),用于预测 AV 透析通路功能障碍;(ii)为未来开发优化透析通路所创建的静脉基质的新型局部治疗方法开辟了道路。