Skip Navigation



NDT Advance Access published online on June 21, 2005

Nephrology Dialysis Transplantation, doi:10.1093/ndt/gfh946
This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow All Versions of this Article:
20/9/1848    most recent
gfh946v1
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 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 arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Selby, N. M.
Right arrow Articles by McIntyre, C. W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Selby, N. M.
Right arrow Articles by McIntyre, C. W.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author [2005]. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For Permissions, please email: journals.permissions@oupjournals.org
Received February 10, 2005
Accepted May 11, 2005


Original Articles

Hypertonic glucose-based peritoneal dialysate is associated with higher blood pressure and adverse haemodynamics as compared with icodextrin

Nicholas M. Selby 1, Sally Fonseca 1, Lisa Hulme 1, Richard J. Fluck 1, Maarten W. Taal 1, and Christopher W. McIntyre 2*

1 Department of Renal Medicine, Derby City Hospital, UK
2 Department of Renal Medicine, Derby City Hospital, UK; Centre for Integrated Systems Biology and Medicine, University of Nottingham, UK

* To whom correspondence should be addressed.
Christopher W. McIntyre, E-mail: Chris.McIntyre{at}derbyhospitals.nhs.uk



  Abstract

Background. Little is known about the haemodynamic effects of continuous ambulatory peritoneal dialysis (CAPD) despite its widespread use in the management of end-stage renal failure. We undertook a study to delineate the haemodynamic effects of CAPD using glucose-containing fluids (1.36 and 3.86% glucose) and icodextrin.

Methods. Eight CAPD patients were recruited for a prospective crossover study. Patients attended for two investigatory days (in random order). CAPD was carried out using 1.36% followed by 3.86% glucose (buffered with lactate/bicarbonate, Physioneal®) on one study day and 1.36% glucose followed by 7.5% icodextrin (Extraneal®) on the other day. Dwell times were 150 min. Blood pressure (BP) and a full range of haemodynamic variables including pulse (HR), stroke volume (SV), cardiac output (CO) and total peripheral resistance (TPR) were measured non-invasively using continuous arterial pulse wave analysis.

Results. BP was significantly higher during 3.86% glucose dwells as compared with 1.36% glucose or icodextrin dwells (P<0.0001). TPR during all three dwells was similar; the higher blood pressure was due to an increased HR, SV and, therefore, CO during 3.86% glucose dwells. The higher blood pressure during the 3.86% glucose dwells was present despite the highest ultrafiltration volume and sodium removal.

Conclusion. This study demonstrates large magnitude haemodynamic changes in response to CAPD. In addition to the well-recognized adverse effects on blood glucose and long-term peritoneal membrane viability, CAPD fluids containing high glucose concentrations may also exert undesirable effects on systemic haemodynamics, with potential long-term consequences for patient outcomes.

Keywords: glucose-based dialysate; haemodynamics; icodextrin; peritoneal dialysis; pulse wave analysis.
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
pdiHome page
R. Paniagua, M.-d.-J. Ventura, M. Avila-Diaz, A. Cisneros, M. Vicente-Martinez, M.-d.-C. Furlong, Z. Garcia-Gonzalez, D. Villanueva, O. Orihuela, M.-d.-C. Prado-Uribe, et al.
ICODEXTRIN IMPROVES METABOLIC AND FLUID MANAGEMENT IN HIGH AND HIGH-AVERAGE TRANSPORT DIABETIC PATIENTS
Perit. Dial. Int., July 1, 2009; 29(4): 422 - 432.
[Abstract] [Full Text] [PDF]


Home page
Nephrol Dial TransplantHome page
A. Pletinck, F. Verbeke, L. Van Bortel, C. Dequidt, D. Vijt, W. Van Biesen, and R. Vanholder
Acute central haemodynamic effects induced by intraperitoneal glucose instillation
Nephrol. Dial. Transplant., December 1, 2008; 23(12): 4029 - 4035.
[Abstract] [Full Text] [PDF]


Home page
NDT PlusHome page
C. W. McIntyre, S. G. John, and H. J. Jefferies
Advances in the cardiovascular assessment of patients with chronic kidney disease
NDT Plus, December 1, 2008; 1(6): 383 - 391.
[Abstract] [Full Text] [PDF]


Home page
NDT PlusHome page
C. J. Holmes and W. Smit
Future technologies and techniques in peritoneal dialysis--opportunities and challenges ahead
NDT Plus, October 1, 2008; 1(suppl_4): iv51 - iv55.
[Abstract] [Full Text] [PDF]


Home page
Nephrol Dial TransplantHome page
P. Ivarsen, J. V. Povlsen, and J. D. Jensen
Increasing fill volume reduces cardiac performance in peritoneal dialysis
Nephrol. Dial. Transplant., October 1, 2007; 22(10): 2999 - 3004.
[Abstract] [Full Text] [PDF]


Home page
Nephrol Dial TransplantHome page
N. M. Selby, J. Fialova, J. O. Burton, and C. W. McIntyre
The haemodynamic and metabolic effects of hypertonic-glucose and amino-acid-based peritoneal dialysis fluids
Nephrol. Dial. Transplant., March 1, 2007; 22(3): 870 - 879.
[Abstract] [Full Text] [PDF]


Home page
Nephrol Dial TransplantHome page
H. F. Woods
Icodextrin and haemodynamics
Nephrol. Dial. Transplant., March 1, 2006; 21(3): 820 - 820.
[Full Text] [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.