Skip Navigation

This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (9)
Right arrowRequest Permissions
Right arrow Disclaimer
Citing Articles
Right arrowScopus Links
Google Scholar
Right arrow Articles by Kim, S.
Right arrow Articles by Park, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kim, S.
Right arrow Articles by Park, J.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nephrology Dialysis Transplantation, Vol 13, Issue 8 2053-2058, Copyright © 1998 by Oxford University Press


ORIGINAL ARTICLES

Effect of increasing serum albumin on haemostatic factors synthesized in the liver in CAPD patients

S Kim, W Yang, S Lee, H Chi and J Park
Department of Internal Medicine and Clinical Pathology, Asan Medical Center, College of Medicine, University of Ulsan, Seoul, Korea; Correspondence to: SB Kim, Department of Internal Medicine, University of Ulsan, College of Medicine, Song-Pa, PO Box 145, Seoul 138-040, Korea

Background. This study was performed to evaluate the relationship between serum albumin and plasma concentration of haemostatic factors and the effect of raising serum albumin on haemostatic factors synthesized in the liver in CAPD patients. Methods. We measured blood levels of albumin, fibrinogen, factor II, factor VII, protein C, free protein S, plasminogen, &agr;2-antiplasmin and antithrombin III in 103 CAPD patients and 30 normal controls. Twenty-two patients with albumin lt;3.5 g/dl were divided into two groups. In the experimental group (n = 11), haemostatic factors and albumin were measured before, after repeated infusion of 20% albumin 100 ml three times per week for 2 weeks, and 4 weeks after withdrawal of albumin infusion. The same parameters were measured in the control group (n = 11) which did not receive albumin infusion. C-reactive protein and haematocrit were followed in both groups as an indicator of acute phase reactant and an indirect measure of volume status. Results. CAPD patients as a whole had lower albumin and higher fibrinogen and factor VII than normal controls. A significant inverse correlation was present between fibrinogen and albumin (r = -0.27, P <0.01). Albumin in the experimental group increased from 2.7 ± 0.4 to 3.5 ± 0.6 g/l at the end of its repeated infusion and haematocrit decreased from 26.6 ± 4.4 to 24.9 ± 5.2%. Fibrinogen and factor VII decreased significantly, even after correction for haematocrit (624 ± 96 vs 556 ± 91 mg/dl, 160 ± 36 vs 121 ± 44%, P <0.05). Four weeks after withdrawal of albumin infusion, serum albumin decreased to 2.7 ± 0.5 g/dl, whereas fibrinogen and factor VII increased to 619 ± 78 mg/dl and 158 ± 32%, respectively (P &;lt;0.05). Albumin, haematocrit and haemostatic factors in the control group did not change. CRP was stable during the study period in both groups. Conclusion. These findings indicate that hypoalbuminaemia is an important trigger factor in the elevation of fibrinogen, and possibly factor VII, in CAPD patients. Keywords: albumin; CAPD; factor VII; fibrinogen
Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Nephrol Dial TransplantHome page
I. Song, W. Yang, S. Kim, J. Lee, T. Kwon, and J. Park
Association of plasma fibrinogen concentration with vascular access failure in hemodialysis patients
Nephrol. Dial. Transplant., January 1, 1999; 14(1): 137 - 141.
[Abstract] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.