Expanded hemodialysis: Is anticoagulation of the dialysis circuit different from online hemodiafiltration and high-flux hemodialysis?


Journal

Therapeutic apheresis and dialysis : official peer-reviewed journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis Therapy
ISSN: 1744-9987
Titre abrégé: Ther Apher Dial
Pays: Australia
ID NLM: 101181252

Informations de publication

Date de publication:
Feb 2022
Historique:
revised: 13 04 2021
received: 30 01 2021
accepted: 17 04 2021
pubmed: 24 4 2021
medline: 11 2 2022
entrez: 23 4 2021
Statut: ppublish

Résumé

Expanded hemodialysis (HDx) has a high capacity for removing medium and medium-large molecules; however, there are no specific recommendations during HDx for anticoagulation of the dialysis circuit. We aimed to evaluate the differences in the efficacy of anticoagulation procedures using the venous port and 40 mg enoxaparin in HDx compared to high-flux hemodialysis (HF-HD) and postdilution online hemodiafiltration (HDF). We compared anticoagulant activity in 11 patients in HDx, HF-HD, and HDF under similar dialysis conditions. In the 33 dialysis sessions, 40 mg enoxaparin was administered through the venous port, and pre- and postdialysis antifactor Xa activity (aXa) and activated partial thromboplastin time (APTT), postdialysis clotting time of the vascular access, visual clotting score of the dialyzer, and any complications with the extracorporeal circuit or bleeding were registered. APTT postdialysis in HDx was not significantly different from that in HF-HD and HDF. Postdialysis aXa in HDx was not significantly different from that in HF-HD and HDF. We found no significant differences in visual clotting score of the dialyzer. Enoxaparin administered through the venous port was sufficient for anticoagulation within the extracorporeal circuit in HDx, HF-HD, and HDF. There were no differences in postdialysis aXa or APTT, most likely because when low molecular-weight heparin is applied through venous port, lesser enoxaparin concentration reaches the dialyzer. Thus, we conclude that the dose of enoxaparin administered through the venous port should not be adjusted according to dialysis technique.

Identifiants

pubmed: 33890717
doi: 10.1111/1744-9987.13652
doi:

Substances chimiques

Anticoagulants 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

147-153

Informations de copyright

© 2021 International Society for Apheresis, Japanese Society for Apheresis, and Japanese Society for Dialysis Therapy.

Références

Davenport A. What are the anticoagulation options for intermittent hemodialysis? Nat Rev Nephrol. 2011;7:499-508.
Davenport A. Anticoagulation options for intermittent hemodialysis. Minerva Urol Nefrol. 2006;58:171-80.
Davenport A. The rationale for the use of low molecular weight heparin for hemodialysis treatments. Hemodial Int. 2013;17 (Suppl 1):S28-32.
Lim W, Cook DJ, Crowther MA. Safety and efficacy of low molecular weight heparins for hemodialysis in patients with end-stage renal failure: a meta-analysis of randomized trials. J Am Soc Nephrol. 2004;15:3192-206.
Palamaner Subash Shantha G, Kumar AA, Sethi M, Khanna RC, Pancholy SB. Efficacy and safety of low molecular weight heparin compared to unfractionated heparin for chronic outpatient hemodialysis in end stage renal disease: systematic review and meta-analysis. PeerJ. 2015;3:e835.
Bramham K, Varrier M, Asgari E, Makanjuola D. Comparison of tinzaparin and unfractionated heparin as anticoagulation on haemodialysis: equal safety, efficacy and economical parity. Nephron Clin Pract. 2008;110:c107-13.
Herrero-Calvo J, González-Parra E, Pérez-García R, Tornero-Molina F. Grupo de Estudio Español Sobre Anticoagulación en Hemodiálisis. Spanish study of anticoagulation in haemodialysis. Nefrologia. 2012;32:143-52.
Ashby D, Borman N, Burton J, Corbett R, Davenport A, Farrington K, et al. Renal Association Clinical Practice Guideline on Haemodialysis. BMC Nephrol. 2019;20:379.
European Best Practice Guidelines Expert Group on Hemodialysis, European Renal Association. Section V: Chronic intermittent haemodialysis and prevention of clotting in the extracorporal system. Nephrol Dial Transplant. 2002;17 (Suppl 7):63-71.
Kerr P, Perkovic V, Petrie J, Agar J, Disney A, Caring for Australians with Renal Impairment (CARI). The CARI guidelines. Dialyisis adequacy (HD) guidelines. Nephrology (Carlton). 2005;10 (Suppl 4):S61.80.
Davenport A. Review article: low-molecular-weight heparin as an alternative anticoagulant to unfractionated heparin for routine outpatient haemodialysis treatments. Nephrology (Carlton). 2009;14:455-61.
Dhont A, Pauwels R, Devreese K, Eloot S, Glorieux G, Vanholder R. Where and when to inject low molecular weight heparin in hemodiafiltration? A cross over randomised trial. PLoS One. 2015;10:e0128634.
Kurtkoti J, Bose B, Hiremagalur B, Sun J, Cochrane T. Arterial line versus venous line administration of low molecular weight heparin, enoxaparin for prevention of thrombosis in the extracoporeal blood circuit of patients on haemodialysis or haemodiafiltration: a randomized cross-over trial. Nephrology (Carlton). 2016;21:663-8.
Klingel R, Schaefer M, Schwarting A, Himmelsbach F, Altes U, Uhlenbusch-Korwer I, et al. Comparative analysis of procoagulatory activity of haemodialysis, haemofiltration and haemodiafiltration with a polysulfone membrane (APS) and with different modes of enoxaparin anticoagulation. Nephrol Dial Transplant. 2004;19:164-70.
Sagedal S, Hartmann A, Sundstrom K, Bjornsen S, Fauchald P, Brosstad F. A single dose of dalteparin effectively prevents clotting during haemodialysis. Nephrol Dial Transplant. 1999;14:1943-7.
Ouseph R, Ward RA. Anticoagulation for intermittent hemodialysis. Semin Dial. 2000;13:181-7.
Polkinghorne KR, McMahon LP, Becker GJ. Pharmacokinetic studies of dalteparin (Fragmin), enoxaparin (Clexane), and danaparoid sodium (Orgaran) in stable chronic hemodialysis patients. Am J Kidney Dis. 2002;40:990-5.
Sridharan S, Berdeprado J, Sivalingam M, Farrington K. Dalteparin dosing in high-flux haemodialysis and haemodiafiltration. Nephron Clin Pract. 2012;122:53-7.
McMahon LP, Chester K, Walker RG. Effects of different dialysis membranes on serum concentrations of epoetin alfa, darbepoetin alfa, enoxaparin and iron sucrosa during dialysis. Am J Kidney Dis. 2004;44:509-16.
Sombolos KI, Fragia TK, Gionanlis LC, Veneti PE, Bamichas GI, Fragidis SK, et al. The anticoagulant activity of enoxaparin sodium during on-line hemodiafiltration and conventional hemodialysis. Hem Int. 2009;13:43-7.
García-Prieto A, Vega A, Linares T, Abad S, Macías N, Aragoncillo I, et al. Evaluation of the efficacy of a medium cut-off dialyser and comparison with other high-flux dialysers in conventional haemodialysis and online haemodiafiltration. Clin Kidney J. 2018;11:742-6.
Reque J, Pérez Alba A, Panizo N, Sánchez-Canel JJ, Pascual MJ, Pons PR. Is expanded hemodialysis an option to online hemodiafiltration for small and middle sized molecules clearance? Blood Purif. 2019;47:126-31.
Macías N, Vega A, Abad S, Aragoncillo I, García-Prieto AM, Santos A, et al. Middle molecule elimination in expanded haemodialysis: only convective transport? Clin Kidney J. 2018 Dec 15;12:447-5.
Tattersall J, Martin-Malo A, Pedrini L, et al. EBPG guideline on dialysis strategies. Nephrol Dial Transplant. 2007 May;22 (Suppl 2):ii5-21.
Kessler M, Moureau F, Nguyen P. Anticoagulation in chronic hemodialysis: progress toward and optimal approach. Semin Dial. 2015;28:474-89.
Santos A, Macías N, Vega A, Abad S, Linares T, Aragoncillo I, et al. Efficacy of enoxaparin in preventing coagulation during high-flux haemodialysis, expanded haemodialysis and haemodiafiltration. Clin Kidney J. 2020;14(4):1120-1125. https://doi.org/10.1093/ckj/sfaa057.
Saltissi D, Morgan C, Westhuyzen J, Healy H. Comparison of low-molecular- weight heparin (enoxaparin sodium) and standard unfractionated heparin for haemodialysis anticoagulation. Nephrol Dial Transplant. 1999;14:2698-703.
Wong SS, Lau WY, Chan PK, Wan CK, Cheng YL. Correlation between activated partial thromboplastin time and anti-Xa activity in patients who reveived low-molecular weight heparin as anticoagulation for haemodialysis. Nephrology (Carlton). 2017;22:921-4.
Soroka S, Agharazii M, Donnelly S, Roy L, Muirhead N, Cournoyer S, et al. An adjustable dalteparin sodium dose regimen for the prevention of clotting in the extracorporeal circuit in hemodialysis: a clinical trial of safety and efficacy (the PARROT study). Can J Kidney Health Dis. 2018;5:2054358118809104.
Whitman-Purves E, Coons JC, Miller T, DiNella JV, Althouse A, Schimidhofer M, et al. Performance of anti-factor Xa versus activated partial thromboplastin time for heparin monitoring using multiple nomograms. Clin Appl Thromb Hemost. 2018;24:310-6.

Auteurs

Alba Santos (A)

Department of Nephrology, Hospital General Universitario Gregorio Marañón, Madrid, Spain.

Nicolás Macías (N)

Department of Nephrology, Hospital General Universitario Gregorio Marañón, Madrid, Spain.

Almudena Vega (A)

Department of Nephrology, Hospital General Universitario Gregorio Marañón, Madrid, Spain.

Soraya Abad (S)

Department of Nephrology, Hospital General Universitario Gregorio Marañón, Madrid, Spain.

Tania Linares (T)

Department of Nephrology, Hospital General Universitario Gregorio Marañón, Madrid, Spain.

Inés Aragoncillo (I)

Department of Nephrology, Hospital General Universitario Gregorio Marañón, Madrid, Spain.

Leonidas Cruzado (L)

Department of Nephrology, Hospital Universitario de Elche, Elche, Spain.

Cristina Pascual (C)

Department of Hematology, Hospital General Universitario Gregorio Marañón, Madrid, Spain.

Marian Goicoechea (M)

Department of Nephrology, Hospital General Universitario Gregorio Marañón, Madrid, Spain.

Juan Manuel López-Gómez (JM)

Department of Nephrology, Hospital General Universitario Gregorio Marañón, Madrid, Spain.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH