Peripheral Vascular Disease Intervention in Patients With End-Stage Renal Disease

2001 ◽  
Vol 94 (10) ◽  
pp. 1002-1005
Author(s):  
KELLY L. McCOY ◽  
DAVID R. GOLDSTEIN ◽  
VIVIAN GAHTAN ◽  
GREGORY MAYRO ◽  
MORRIS D. KERSTEIN
2001 ◽  
Vol 94 (10) ◽  
pp. 1002-1005
Author(s):  
KELLY L. McCOY ◽  
DAVID R. GOLDSTEIN ◽  
VIVIAN GAHTAN ◽  
GREGORY MAYRO ◽  
MORRIS D. KERSTEIN

2001 ◽  
Vol 38 (1) ◽  
pp. 57-63 ◽  
Author(s):  
Donal N. Reddan ◽  
Richard J. Marcus ◽  
William F. Owen ◽  
Lynda A. Szczech ◽  
Douglas M. Landwehr

2007 ◽  
Vol 27 (2_suppl) ◽  
pp. 210-214 ◽  
Author(s):  
Heikki H.T. Saha ◽  
Yrjö K.J. Leskinen ◽  
Juha P. Salenius ◽  
Jorma T. Lahtela

In the present article, we review current knowledge of the epidemiology, diagnosis, and treatment of peripheral vascular disease in patients with end-stage renal disease. The main focus is placed on diabetic patients receiving peritoneal dialysis, but studies on patients receiving hemodialysis are also reviewed, because most reports involve this patient group, and the number of reports on peripheral vascular disease in PD patients alone is limited.


2021 ◽  
Vol 74 (3) ◽  
pp. e170
Author(s):  
Ankoor H. Patel ◽  
Murad Elias ◽  
Priya Goyal ◽  
Christopher M. Hall ◽  
Sateesh Babu ◽  
...  

2014 ◽  
Vol 68 (1) ◽  
pp. 16-20
Author(s):  
Danica Labudovic ◽  
Katerina Tosheska-Trajkovska ◽  
Sonja Alabakovska

Abstract Introduction. End-stage renal disease (ESRD) patients undergoing hemodialysis are at an increased risk of arteriosclerotic vascular disease (ASVD). The increased risk is commonly attributed to the traditional risk factors related to ESRD. However, interest for more recent risk factors for ASVD, such as the level of lipoprotein(a) and its specific apoprotein(a) has been promoted. The aim of this paper is to determine whether apo(a) phenotype is a risk factor for arteriosclerotic vascular disease in ESRD patients who are on hemodialysis. Methods. Apo(a) phenotypisation was performed by using the Western Blot Technique of blood samples from 96 end-stage renal disease patients who were undergoing hemodialysis, and from 100 healthy individuals. Results. Frequency distribution of the basic apo(a) isoforms calculated by means of the χ2-test has shown that there was no significant statistical difference in distribution among patients on hemodialysis, and healthy carriers (χ2-0.36, p<0.548-for carriers of single apo(a) isoforms, (χ2-0.10, p<0.7545-for carriers of double apo(a) isoforms). The calculated relative risks have demonstrated that apo(a) phenotype was not a risk factor for ASVD in HD patients. Conclusion. Based on the results obtained, it can be concluded that the apo(a) phenotype is not a risk factor for arteriosclerotic vascular disease in patients undergoing hemodialysis.


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