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Standard Heparin versus Low-Molecular-Weight Heparin
- Source :
- Nephron; March 2002, Vol. 92 Issue: 3 p589-600, 12p
- Publication Year :
- 2002
-
Abstract
- <abstitle>Abstract</abstitle>Background: To compare standard heparin (SH) and low molecular weight heparin (LMWH) in terms of anticoagulation, platelet activation and lipid metabolism, we selected 54 patients who had been on 4-hour hemodialysis three times weekly for at least 12 months, without bleeding disorders or dyslipidemic diseases. 28 were on hemodialysis with Polysulfone low-flux, 26 were on hemodiafiltration with Polysulfone high-flux. All patients underwent EPO. Methods: During the first 18 months, we administered SH 1,500 IU on starting dialysis and 1,500 ± 500 IU in continuous intradialytic infusion per session. In the following 18 months, we administered LMWH 64.6 IU/kg on starting dialysis in a single arterious bolus. We assessed aPTT, anti-factor Xa activity, TAT and FPA, β-TG and PF4. Blood samples were taken monthly at times 0, 30, 60, 180 and 240 min, as well as 1, 4 and 20 h after dialysis end. Predialysis cholesterol, HDL, LDL, triglycerides and lipoprotein(a) were checked monthly. Results: During both LMWH and SH sessions no clotting or major bleeding complications were observed. APTT with LMWH was lower than that found with SH (p &lt; 0.001); aFXa using LMWH was higher than when using SH (p &lt; 0.001); TAT and FPA were lower in LMWH sessions (p &lt; 0.01) than in SH sessions. We also detected lower β-TG (p &lt; 0.05) and PF4 levels (p &lt; 0.05) using LMWH than using SH. As regards lipids, we only observed a significant decrease in triglycerides after 18 months of LMWH treatment. Conclusions: Routine use of LMWH during hemodialysis affords a safe and effective alternative to SH, and causes reduced platelet activation.Copyright © 2002 S. Karger AG, Basel
Details
- Language :
- English
- ISSN :
- 16608151 and 22353186
- Volume :
- 92
- Issue :
- 3
- Database :
- Supplemental Index
- Journal :
- Nephron
- Publication Type :
- Periodical
- Accession number :
- ejs5736643