• 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

尿毒症性多神经病:血液透析和持续性非卧床腹膜透析的不同影响

Uremic polyneuropathy: different effects of hemodialysis and continuous ambulatory peritoneal dialysis.

作者信息

Tegnér R, Lindholm B

出版信息

Acta Med Scand. 1985;218(4):409-16. doi: 10.1111/j.0954-6820.1985.tb08866.x.

DOI:10.1111/j.0954-6820.1985.tb08866.x
PMID:4083083
Abstract

Registrations of clinical signs of neuropathy, quantified according to a fixed protocol, and determinations of vibratory perception thresholds and nerve conduction velocities (NCV) were performed in 22 patients treated with hemodialysis (HD) and in 21 patients treated with continuous ambulatory peritoneal dialysis (CAPD). Measurements were made at the start of dialysis and during a follow-up period of about 30 months. Motor NCV decreased in both groups; vibratory thresholds increased markedly in the CAPD patients, but not in the HD patients; and the clinical signs worsened in the HD patients, but not in the CAPD patients. The difference in outcome of the clinical signs during HD and CAPD was not of such a magnitude that one of these dialysis forms should be preferred before the other as regards neuropathy. We conclude that peripheral neuropathy may deteriorate during both HD and CAPD, but in significantly different ways, indicating that several pathogenetic mechanisms are probably involved in uremic neuropathy.

摘要

按照固定方案对22例接受血液透析(HD)治疗的患者和21例接受持续性非卧床腹膜透析(CAPD)治疗的患者进行了神经病变临床体征的记录,并测定了振动觉阈值和神经传导速度(NCV)。在透析开始时及约30个月的随访期内进行测量。两组患者的运动神经传导速度均下降;CAPD患者的振动觉阈值显著升高,而HD患者未升高;HD患者的临床体征恶化,而CAPD患者未恶化。HD和CAPD期间临床体征结果的差异并不足以使其中一种透析方式在神经病变方面比另一种更具优势。我们得出结论,HD和CAPD期间周围神经病变均可能恶化,但方式显著不同,这表明尿毒症性神经病变可能涉及多种发病机制。

相似文献

1
Uremic polyneuropathy: different effects of hemodialysis and continuous ambulatory peritoneal dialysis.尿毒症性多神经病:血液透析和持续性非卧床腹膜透析的不同影响
Acta Med Scand. 1985;218(4):409-16. doi: 10.1111/j.0954-6820.1985.tb08866.x.
2
[Evaluation of polyneuropathy severity in chronic renal failure patients on continuous ambulatory peritoneal dialysis or on maintenance hemodialysis].[持续性非卧床腹膜透析或维持性血液透析的慢性肾衰竭患者多发性神经病变严重程度的评估]
Przegl Lek. 2007;64(6):423-30.
3
[Uremic neuropathy and the type of dialysis].
Riv Patol Nerv Ment. 1982 Nov-Dec;103(6):271-6.
4
Vibratory perception threshold compared with nerve conduction velocity in the evaluation of uremic neuropathy.在尿毒症性神经病变评估中振动觉阈值与神经传导速度的比较
Acta Neurol Scand. 1985 Apr;71(4):284-9. doi: 10.1111/j.1600-0404.1985.tb03201.x.
5
Control of uremic neuropathy by equilibrium peritoneal dialysis.通过平衡腹膜透析控制尿毒症神经病变
Int J Artif Organs. 1984 Mar;7(2):97-100.
6
Progress of peripheral uremic neuropathy during continuous ambulatory peritoneal dialysis (CAPD).
Trans Am Soc Artif Intern Organs. 1982;28:263-9.
7
Uremic pruritus in patients on hemodialysis or continuous ambulatory peritoneal dialysis (CAPD). The role of plasma histamine and skin mast cells.接受血液透析或持续性非卧床腹膜透析(CAPD)患者的尿毒症瘙痒。血浆组胺和皮肤肥大细胞的作用。
Clin Nephrol. 1990 Sep;34(3):136-41.
8
Increased plasma lipoprotein(a) in continuous ambulatory peritoneal dialysis is related to peritoneal transport of proteins and glucose.持续非卧床腹膜透析患者血浆脂蛋白(a)升高与蛋白质和葡萄糖的腹膜转运有关。
Nephron. 1996;72(2):135-44. doi: 10.1159/000188831.
9
Pruritus in continuous ambulatory peritoneal dialysis and hemodialysis patients.
Perit Dial Int. 1993;13 Suppl 2:S527-32.
10
[Uremic polyneuropathy: a study of vibratory perception threshold in 19 patients].[尿毒症性多发性神经病:19例患者的振动觉阈值研究]
Arq Neuropsiquiatr. 1984 Sep;42(3):215-20. doi: 10.1590/s0004-282x1984000300004.

引用本文的文献

1
Randomised controlled trial of the impact of haemodiafiltration on uraemic neuropathy: FINESSE study protocol.随机对照试验研究血液透析滤过对尿毒症性神经病的影响:FINESSE 研究方案。
BMJ Open. 2019 Jan 15;9(1):e023736. doi: 10.1136/bmjopen-2018-023736.