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Where and When To Inject Low Molecular Weight Heparin in Hemodiafiltration? A Cross Over Randomised Trial

BACKGROUND AND OBJECTIVE: Low molecular weight heparins (LMWHs) are small enough to pass large pore dialysis membranes. Removal of LMWH if injected before the start of the session is possible during high-flux dialysis and hemodiafiltration. The aim of this study was to determine the optimal mode (pl...

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Detalles Bibliográficos
Autores principales: Dhondt, Annemieke, Pauwels, Ruben, Devreese, Katrien, Eloot, Sunny, Glorieux, Griet, Vanholder, Raymond
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4468116/
https://www.ncbi.nlm.nih.gov/pubmed/26076014
http://dx.doi.org/10.1371/journal.pone.0128634
Descripción
Sumario:BACKGROUND AND OBJECTIVE: Low molecular weight heparins (LMWHs) are small enough to pass large pore dialysis membranes. Removal of LMWH if injected before the start of the session is possible during high-flux dialysis and hemodiafiltration. The aim of this study was to determine the optimal mode (place and time) of tinzaparin administration during postdilution hemodiafiltration. STUDY DESIGN, SETTING, PATIENTS: In 13 chronic hemodiafiltration patients, 3 approaches of injection were compared in a randomised cross over trial: i) before the start of the session at the inlet blood line filled with rinsing solution (IN(0)), ii) 5 min after the start at the inlet line filled with blood (IN(5)) and iii) before the start of the session at the outlet blood line (OUT(0)). Anti-Xa activity, thrombin generation, visual clotting score and reduction ratios of urea and beta2microglobulin were measured. RESULTS: Anti-Xa activity was lower with IN(0) compared with IN5 and OUT(0), and also more thrombin generation was observed with IN(0). No differences were observed in visual clotting scores and no clinically relevant differences were observed in solute reduction ratio. An anti-Xa of 0.3 IU/mL was discriminative for thrombin generation. Anti-Xa levels below 0.3 IU/mL at the end of the session were associated with worse clotting scores and lower reduction ratio of urea and beta2microglobulin. CONCLUSIONS: Injection of tinzaparin at the inlet line before the start of postdilution hemodiafiltration is associated with loss of anticoagulant activity and can therefore not be recommended. Additionally, we found that an anti-Xa above 0.3 IU/mL at the end of the session is associated with less clotting and higher dialysis adequacy. TRIAL REGISTRATION: Clinicaltrials.gov NCT00756145