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肾衰竭中的出血:血管性血友病因子是否与之有关?

Bleeding in renal failure: is von Willebrand factor implicated?

作者信息

Remuzzi G, Livio M, Roncaglioni M C, Mecca G, Donati M B, de Gaetano G

出版信息

Br Med J. 1977 Aug 6;2(6083):359-61. doi: 10.1136/bmj.2.6083.359.

DOI:10.1136/bmj.2.6083.359
PMID:302134
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1631138/
Abstract

Normal or increased concentrations of factor VIII procoagulant activity (VIIIC), factor VIII-related antigen (VIIIRA), and factor VIII-von Willebrand activity (VIIIVWF) were found in the predialysis plasma of 10 out of 11 patients with chronic renal failure (CRF). All patients had a bleeding time longer than 15 minutes and platelet retention to glass beads lower than 40%. The only patient who had reduced concentrations of all three factor VIII complex components was subsequently shown to have von Willebrand's disease. In four patients with CRF, very low platelet retention, and slightly prolonged bleeding time none of the three factor VIII COMPLEX COMPONENTS WERE SELECTIVely modified in predialysis samples. These findings suggest that the bleeding tendency common in CRF is not necessarily linked to defective plasma factor VIII-related activities.

摘要

在11例慢性肾衰竭(CRF)患者中,有10例患者的透析前血浆中发现因子VIII促凝血活性(VIIIC)、因子VIII相关抗原(VIIIRA)和因子VIII-血管性血友病因子活性(VIIIVWF)浓度正常或升高。所有患者的出血时间均超过15分钟,血小板对玻璃珠的黏附率低于40%。唯一一例三种因子VIII复合成分浓度均降低的患者随后被诊断为血管性血友病。在4例CRF患者中,血小板黏附率极低且出血时间稍有延长,其透析前样本中三种因子VIII复合成分均未发生选择性改变。这些发现表明,CRF中常见的出血倾向不一定与血浆中因子VIII相关活性缺陷有关。

相似文献

1
Bleeding in renal failure: is von Willebrand factor implicated?肾衰竭中的出血:血管性血友病因子是否与之有关?
Br Med J. 1977 Aug 6;2(6083):359-61. doi: 10.1136/bmj.2.6083.359.
2
Bleeding in renal failure: a possible cause.肾衰竭中的出血:一个可能的原因。
Br Med J. 1976 Sep 11;2(6036):612-5. doi: 10.1136/bmj.2.6036.612.
3
[Reduction of Willebrand activity in patients with chronic kidney failure].[慢性肾衰竭患者血管性血友病因子活性降低]
C R Acad Hebd Seances Acad Sci D. 1976 Jul 19;283(3):287-9.
4
Increased factor VIII/von Willebrand factor antigen and von Willebrand factor activity in renal failure.肾衰竭时因子VIII/血管性血友病因子抗原及血管性血友病因子活性增加。
Am J Med. 1979 Feb;66(2):226-8. doi: 10.1016/0002-9343(79)90531-x.
5
Factor VIII--related protein on vascular intima of patients with chronic renal failure and prolonged bleeding times.慢性肾功能衰竭及出血时间延长患者血管内膜上的Ⅷ因子相关蛋白
Br Med J. 1978 Jan 14;1(6105):70-2. doi: 10.1136/bmj.1.6105.70.
6
Variant von Willebrand's disease: characterization of two subtypes by analysis of multimeric composition of factor VIII/von Willebrand factor in plasma and platelets.血管性血友病:通过分析血浆和血小板中因子VIII/血管性血友病因子的多聚体组成来鉴定两种亚型
J Clin Invest. 1980 Jun;65(6):1318-25. doi: 10.1172/JCI109795.
7
Von Willebrand Factor (VIIIVWF) in lyophilized Factor VIII concentrates.冻干的凝血因子VIII浓缩物中的血管性血友病因子(VIII/vWF)
Am J Hematol. 1980;9(1):39-42. doi: 10.1002/ajh.2830090105.
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Electrophoretic heterogeneity of normal factor VIII/Von Willebrand protein, and abnormal electrophoretic mobility in patients with Von Willebrand's disease.正常因子VIII/血管性血友病因子蛋白的电泳异质性,以及血管性血友病患者的异常电泳迁移率。
J Lab Clin Med. 1976 Feb;87(2):185-94.
9
Carbohydrate deficiency of the factor VIII/von Willebrand factor Protein in von Willebrand's disease variants.血管性血友病变异型中凝血因子VIII/血管性血友病因子蛋白的碳水化合物缺乏
Science. 1976 Apr 2;192(4234):56-9. doi: 10.1126/science.1083071.
10
Quantitative assay of a plasma factor deficient in von Willebrand's disease that is necessary for platelet aggregation. Relationship to factor VIII procoagulant activity and antigen content.对血管性血友病中缺乏的、血小板聚集所必需的一种血浆因子进行定量测定。与凝血因子VIII促凝活性及抗原含量的关系。
J Clin Invest. 1973 Nov;52(11):2708-16. doi: 10.1172/JCI107465.

引用本文的文献

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Hemostatic Abnormalities in Severe Renal Failure: Do They Bark or Bite?严重肾衰竭中的止血异常:它们是虚张声势还是会造成危害?
Indian J Nephrol. 2018 Mar-Apr;28(2):135-142. doi: 10.4103/ijn.IJN_104_17.
2
Coagulation factors as biological risk markers of endothelial dysfunction. Association with the thrombotic episodes of chronic hemodialysis patients.凝血因子作为内皮功能障碍的生物学风险标志物。与慢性血液透析患者血栓形成事件的关联。
Hippokratia. 2009 Oct;13(4):237-41.
3
Factor VIII complex in uraemia and effects of haemodialysis.尿毒症中的凝血因子 VIII 复合物及血液透析的影响
Br Med J (Clin Res Ed). 1981 May 23;282(6277):1653-6. doi: 10.1136/bmj.282.6277.1653.
4
Intermittent heparin treatment does not induce hypercoagulability in haemodialysed patients.间歇性肝素治疗不会在血液透析患者中诱发高凝状态。
J Clin Pathol. 1980 Jul;33(7):631-4. doi: 10.1136/jcp.33.7.631.
5
Platelet function and factor VIII in uremia.尿毒症中的血小板功能与凝血因子VIII
Korean J Intern Med. 1987 Jan;2(1):74-8. doi: 10.3904/kjim.1987.2.1.74.
6
Factor VIII related antigen in the assessment of vasculitis.血管炎评估中的VIII因子相关抗原
Ann Rheum Dis. 1987 Jun;46(6):441-7. doi: 10.1136/ard.46.6.441.
7
Effect of pretreatment with acetylsalicylate on surgical bleeding and peroperative mortality in rats undergoing kidney transplantation.乙酰水杨酸预处理对肾移植大鼠手术出血及围手术期死亡率的影响
Experientia. 1978 May 15;34(5):664-5. doi: 10.1007/BF01937021.

本文引用的文献

1
Platelet function in renal failure.肾衰竭中的血小板功能。
N Engl J Med. 1969 Mar 27;280(13):677-81. doi: 10.1056/NEJM196903272801301.
2
Uremic toxins and platelet function.尿毒症毒素与血小板功能。
Arch Intern Med. 1970 Nov;126(5):823-6.
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Platelet adhesiveness in von Willebrand's disease. A study with a new modification of the glass bead filter method.血管性血友病中的血小板黏附性。一项采用玻璃珠滤器法新改良方法的研究。
Scand J Haematol. 1970;7(5):374-82.
4
AHF related protein in clinical praxis.临床实践中的急性心力衰竭相关蛋白
Scand J Haematol. 1974;12(3):221-31. doi: 10.1111/j.1600-0609.1974.tb00202.x.
5
Bleeding in uremia.尿毒症出血
Med Clin North Am. 1972 Jan;56(1):221-33. doi: 10.1016/s0025-7125(16)32437-3.
6
Letter: Nature of the von Willebrand factor.信件:血管性血友病因子的性质。
N Engl J Med. 1974 Feb 21;290(8):464. doi: 10.1056/NEJM197402212900820.
7
Clues to the pathogenesis of bleeding in von Willebrand's disease.血管性血友病出血发病机制的线索。
N Engl J Med. 1973 Nov 29;289(22):1182-3. doi: 10.1056/NEJM197311292892209.
8
Quantitative assay of a plasma factor deficient in von Willebrand's disease that is necessary for platelet aggregation. Relationship to factor VIII procoagulant activity and antigen content.对血管性血友病中缺乏的、血小板聚集所必需的一种血浆因子进行定量测定。与凝血因子VIII促凝活性及抗原含量的关系。
J Clin Invest. 1973 Nov;52(11):2708-16. doi: 10.1172/JCI107465.
9
The bleeding disorder of uraemia. A qualitative platelet defect.
Lancet. 1966 Jul 9;2(7454):66-9. doi: 10.1016/s0140-6736(66)91802-2.
10
Immunological characterization of purified anti-haemophilic factor A (factor VIII) which corrects abnormal platelet retention in Von Willebrand's disease.可纠正血管性血友病中异常血小板滞留的纯化抗血友病因子A(因子VIII)的免疫学特性
Nat New Biol. 1972 Mar 29;236(65):104-6. doi: 10.1038/newbio236104a0.