Hamostaseologie 1990; 10(02): 84-91
DOI: 10.1055/s-0038-1655188
Originalarbeiten
Schattauer GmbH

Biokompatibilitätsprobleme bei der Hämodialyse

R. Bambauer
1   Abteilung für Dialyse und Nephrologie, Medizinische Universitäts-Klinik und Poliklinik, Homburg/Saar
,
U. Weber
1   Abteilung für Dialyse und Nephrologie, Medizinische Universitäts-Klinik und Poliklinik, Homburg/Saar
,
J. Lissmann
1   Abteilung für Dialyse und Nephrologie, Medizinische Universitäts-Klinik und Poliklinik, Homburg/Saar
› Author Affiliations
Further Information

Publication History

Publication Date:
25 June 2018 (online)

Zusammenfassung

Seit erstmals Interaktionen von Blut und körperfremden Materialien bei der chronischen Hämodialysebehandlung beobachtet wurden, folgten zahlreiche Untersuchungen, um das Phänomen der Biokompatibilität zu ergründen. Dies hatte zur Folge, daß erhebliche Verbesserungen bei den Membranen, Schlauchsystemen, Geräten und der Behandlung selbst erzielt werden konnten. Im folgenden wird versucht, einen Überblick über die auslösenden Ursachen und die Phänomene, die durch die Interaktion von Blut mit körperfremden Oberflächen verursacht werden, aufzuzeigen.

Die Probleme, die bei der Entwicklung biokompatibler Membranen vorhanden sind, scheinen in naher Zukunft noch nicht alle lösbar zu sein. Unsere ganze Sorgfalt muß daher der Hämodialysebehandlung selbst und der Verringerung ihrer möglichen Nebenwirkungen, die z.B. durch Reste von Sterilisationsmitteln, endotoxinhaltige Dialysierflüssigkeiten hervorgerufen werden können, gelten. Besonders im Hinblick darauf, daß die Zahl der Patienten, die Biomaterialien benötigen, rasch zunimmt und diese Patienten länger leben, wodurch sie den Gefahren durch die Biounverträglichkeit der Materialien länger ausgesetzt werden, sind wir alle aufgefordert, unseren Patienten eine risikoarme Hämodialyse zu ermöglichen served in the treatment of chronic hemodialysis, numerous investigations were performed to definite the phenomena of biocompatibility. As a consequence, considerable improvements in membranes, tube systems, equipments and in the treatment itself have been accomplished. The following is an attempt to demonstrate the initiating causes and the phenomena which results from the interaction of blood with artificial surfaces.

The problems being encountered in the development of biocompatible membranes are not likely to all be solved in the near future. We must, therefore, concentrate all our efforts on the hemodialysis treatment itself and on the reduction of its possible side-effects which can, for example, be caused by the remnants of sterilizing agents, dialysis fluid containing endotoxin, etc. Especially in view of the fact that the number of patients requiring biomaterials is rapidly increasing and that these patients are living longer, whereby they are exposed to the dangers of bioincompatibility of the materials for a longer period of time, we are all called upon to provide low-risk hemodialysis for our patients.

 
  • Literatur

  • 1 Absolom D, Thompson C, Hawthorn L, Zingg W, Neumann A. Kinetics of cell adhesion to polymer surfaces. J Biomed Mat Res 1988; 22: 215-29.
  • 2 Adler AJ, Lundin AP, Friedman EA, Berlyne GM. Effect of haemodialysis on plasma ß-TG levels. Trans Amer Soc Artif Int Org 1979; 25: 347-49.
  • 3 Bambauer R. Therapeutischer Plasmaaustausch und verwandte Plasmaseparationsverfahren. Technische Grundlagen, Pathophysiologie und klinische Ergebnisse. Stuttgart, New York: Schattauer: 1988
  • 4 Bambauer R, Jutzler GA, Walther J, Weber U, Jung H. Sterilfiltration der Dialysierflüssigkeit bei der Hämodialyse. Nierenund Hochdruckkrank 1989; 18: 481-87.
  • 5 Bambauer R, Schmidt R, Weber U, El-Saadi R, Oest A, Jung WK. Ultrafiltration of dialysis fluid for hemodialysis. Trans Am Soc Artif Intern Organs 1989; 35: 516-19.
  • 6 Bingel M, Lonnemann G, Shaldon S, Koch KM, Dinarello CA. Human interleukin-1 production during hemodialysis. Nephron 1986; 43: 161-63.
  • 7 Bingel M, Koch KM, Lonnemann G, Dinarello CA, Shaldon S. Enhancement of in vitro human interleukin-1 production by sodium acetate. Lancet 1987; I: 14-16.
  • 8 Bommer J, Becker KP, Urbaschek R, Ritz E, Urbaschek B. No evidence for endotoxin transfer across high flux polysulfone membranes. Clin Nephrol 1987; 27: 278-82.
  • 9 Bowry SK, Courtney JM, Prentice CRM, Douglas JT. Utilization of the platelet release reaction in the blood compatibility assessment of polymers. Biomaterials 1984; 05: 289-93.
  • 10 Brasch JL, Lyman DJ. Dependence of albumin-fibrinogen simple and competitive adsorption on surface properties of biomaterials. J Polymer Sci 1979; 66: 377-82.
  • 11 Brasch JL. Mechanism of adsorption of proteins to solid surfaces on its relationship to blood compatibility. In: Biocompatible Polymers, Metals and Composites. Szycher M. (Ed). Lancaster: Technomic Publ: 1983: 35-40.
  • 12 Breilatt J, Dorson WJ. Quantification of serum complement activation by polymeric membranes and materials. ASAIO J 1984; 07: 57-63.
  • 13 Bruck SD. Polymeric materials: current status of biocompatibility. Biomat Med Dev Artif Org 1973; 01: 79-85.
  • 14 Bryant RE, Stucliffe MC. A method of quantitation of human leucocyte adhesion to glass. Proceedings. Soc f Exp Bio Med 1971; 141: 196-99.
  • 15 Chang G, Absolom D, Strong A, Stubley G, Zingg W. Physical and hydrodynamic factors effecting erythrocyte adhesion to polymer surfaces. J Biomed Mat Res 1988; 22: 13-29.
  • 16 Chenoweth DE, Cooper SW, Hugh TE, Stewart RW, Blackstone EW, Kirklin JW. Complement activation during cardiopulmonary bypass: evidence for generation of C3a and C5a anaphylatoxins. N Engl J Med 1981; 304: 497-503.
  • 17 Chenoweth DE, Cheung A, Ward DM, Henderson LW. Anaphylatoxin formation during hemodialysis : effects of two different dialyzer membranes. Kidney Int 1983; 24: 764-8.
  • 18 Chenoweth DE. Complement activation during hemodialysis: clinical observations, proposed mechanisms and theoretical implications. Artific Organs 1984; 08: 281-7.
  • 19 Cooper NR. The complement system. In: Fundenberg HW, Sites DP, Caldwell JL, Wells JV. (Eds). Basic and Clinical Immunology. Chapter 6. Los Altos (Ca.): Lange Medical Publ; 1976
  • 20 Craddock R, Fehr J, Brigham KL, Kronenberg RS, Jag HS. Complement and leucocyte-mediated pulmonary dysfunction in hemodialysis. N Engl J Med 1977; 296: 769-74.
  • 21 Chuang HYK, King WF, Mason RG. Interactions of plasma proteins with artificial surfaces proteins adsorption isotherms. J Lab Clin Med 1978; 92: 483-91.
  • 22 Dinarello CA, Bendtzen K, Wolff SM. Studies on the active site of human leucocytic pyrogen. Inflammation 1982; 06: 63-78.
  • 23 Dinarello CA. Interleukin-1. Rev Infect Dis 1984; 06: 51-93.
  • 24 Dinarello CA, Cannon JG, Mier JW, Bernheim HA, Lopreste G, Lynn DL, Love RN, Webb AC, Auron PhE, Reuben RC, Rich A, Wolff SM, Putney SD. Multiple biological activities of human recombinant interleukin-1. J Clin Invest 1986; 07: 1734-39.
  • 25 Dinarello CA. Interleukin-1: amino acid sequences, multiple biological activities and comparison with tumor necrosis factor (cachectin). The Year in Immunology 1986; 02: 68-89.
  • 26 Dinarello CA, Lonnemann G, Maxwell R, Shaldon S. Ultrafiltration to reject human interleukin-l-inducing substances derived from bacterial cultures. J Clin Microbiol 1987; 25: 1233-38.
  • 27 Falkenhagen D, Böttcher M, Ramolov W, Falkenhagen U, Courtney JM, Ryan CJ, Holtz M, Klinkmann H. The investigation of biomaterials by sequential plasma-perfusion. In: Biomaterials in Artificial Organs. Paul JP, Gayler JDS, Courtney JM, Gilchrist T. (Eds). London: McMillan; 1984: 228-32.
  • 28 Falkenhagen D, Brown GS, Boettcher M, Falkenhagen U, Schmidt B, Gurland HJ, Klinkmann H. Permeation of complement factors through high-flux dialyzers and plasma separation membranes. In: Therapeutic Plasma Exchange and Selective Plasma Separation. Bambauer R, Malchesky PS, Falkenhagen D. (Eds). Stuttgart, New York: Schattauer: 1987: 215-22.
  • 29 Falkenhagen D, Bosch T, Brown G, Schmidt B, Holtz M, Bauermeister U, Gurland H, Klinkmann H. A clinical study on different cellulosic dialyzer membranes. Nephrol Dial Transpl 1987; 02: 537-45.
  • 30 Farrell PC. Biocompatibility aspects of extracorporeal circulation. In: Biomaterials in Artificial Organs. Paul JP, Gaylor JDS, Courtney JM, Gilchrist T. (Eds). London: McMillan: 1984: 342-50.
  • 31 Forbes DC. Thrombosis and artificial surfaces. Clin Haematol 1981; 10: 653-60.
  • 32 Goldmann M, Lietar N, Lambert P, Thayse C, Vanker-Weghem J. Complement activation and leukopenia on cellulosic hemodialyzer: influence of the membrane area and role of hydroxyl moieties. Life Support Systems 1987; 05: 317-22.
  • 33 Hakim RM, Fearon DT, Lazarus JM, Perzanowski CS. Biocompatibility of dialysis membranes: effect of chronic complement activation. Kidney Int 1984; 26: 194-200.
  • 34 Hamilton RG, Adkinson NF. Mechanismus of acute allergic reactions. Artif Organs 1984; 08: 311-9.
  • 35 Henderson L, Chenoweth D. Cellulose membranes time for a change?. Contr Nephrol 1985; 44: 112-26.
  • 36 Henne W, Dietrich W, Pelger M, Sengbusch G. Residual ethylene oxide in hollo wfiber dialyzers. Artif Organs 1984; 08: 306-09.
  • 37 Herzlinger GA. Activation of complement by polymers in contact with blood. In: Biocompatible Polymers, Metals, and Composites. Szacher M. (Ed). Lancaster: Technomic Publ: 1983
  • 38 Jamieson GA. Role of glycoproteins in platelet functions, in erythrocytes, thrombocytes, leukocytes. In: Recent Advances in Membrane and Metabolic Research. Gerlach E, Moser K, Deutsch E, Wilmanns W. (Eds). Stuttgart: Thieme: 1973: 53-60.
  • 39 Ivanovich P, Chenoweth DE, Schmidt R, Klinkmann H, Boxer LA, Jacob HS, Hammerschmidt DE. Symptoms and activation of granulocytes and complement with two dialysis membranes. Kidney Int 1983; 24: 758-63.
  • 40 Kaplow LS, Goffinet JA. Profound neutropenia during the early phase of hemodialysis. JAMA 1968; 203: 1135-37.
  • 41 Klinkmann H, Wolf H, Schmitt E. Definition of biocompatibility. Contrib Nephrol 1984; 37: 70-80.
  • 42 Klinkmann H, Ivanovich P. Advantages and disadvantages of current dialysis techniques. In: Nephrology. 1984. New York: Springer: 1984: 1528-36.
  • 43 Klinkmann H. The role of biomaterials in the application of artificial organs. In: Biomaterials in Artificial Organs. Paul JP, Gaylor JDS, Courtney JM, Gilchrist T. (Eds). London: McMillan: 1984. -8.:
  • 44 Klinkmann H. Biocompatibility problems in membrane separation processes. In: Therapeutic Plasma Exchange and Selective Plasma Separation. Bambauer R, Malchesky PS, Falkenhagen D. (eds). Stuttgart, New York: Schattauer: 1987: 17-32.
  • 45 Kolmos HJ. Bacterial contamination of the blood compartment originating from the dialysate in haemodialysers. J Hosp Infect 1984; 05: 70-75.
  • 46 Larsson R, Lindahl M. Platelet adhesion and activation of coagulation on surfaces containing heparin and heparin-like substances. Proceedings 2nd Meeding. Int Soc Artif Organs 1979; 239-43.
  • 47 Lee RG, Kim SW. Adsorbed glycoproteins in platelet adhesion onto polymer surfaces: significances of terminal galactose units. Trans Am Soc Art Int Organs 1979; 25: 124-27.
  • 48 Leonhard EF, van Vooren C, Hauglustaino C, Haunson S. Shear-induced formation of aggregates during hemodialysis. Contr Nephrol 1983; 36: 34-39.
  • 49 Luger A, Kovarik J, Stummvoll H-K, Urbanska A, Luger ThA. Blood-membrane interaction in hemodialysis leads to increased cytokine production. Kidney Int 1987; 32: 84-88.
  • 50 Lysaght M. Hemodialysis membranes in transition. Contr Nephrol 1988; 61: 1-17.
  • 51 McLeod BC, Viernes A, Sanetti RJ. Complement metabolism during membrane plasma separation. Artif Organs 1983; 07: 443-49.
  • 52 Mahiout A, Sanchez J, Hampl H, Kessel M. Anaphylatoxin formation and leukokinetics during hemodialysis: effects of different areas by cellulosic membranes. Kidney Int 1984; 26: 574-79.
  • 53 Nichols AJ, Platts MM. Anaphylactoid reactions during hemodialysis are due to ethylene oxide hypersensitivity. Proc EDTA 1984; 21: 173-78.
  • 54 Olijslager J. Blood compatibility testing of synthetic polymers. In: Biocompatibility and Blood-Membrane Interactions. Van Geelen JA, Van Berio A. (Eds). Proceedings, Amsterdam; 1983: 45-51.
  • 55 Port FK, van de Kerkhove KM, Kunkel StL, Kluger MJ. The role of dialysate in the stimulation of interleukin-1 production during clinical hemodialysis. Am J Kidney Dis 1987; 10: 118-22.
  • 56 Raij J, Shapiro FL, Michael AF. Endotoxaemia in febrile reactions during haemodialysis. Kidney Int 1973; 04: 53-59.
  • 57 Ringoir S, Van Holder R. An introduction to biocompatibility. Artif Organs 1986; 10: 20-26.
  • 58 Shaldon S, Deschodt G, Branger B, Granolleras C, Baldamus CA, Koch KM, Lysaght MJ, Dinarello CA. Haemodialysis hypotension: the interleukin hypothesis restated. Proc EDTA-ERA 1985; 22: 229-43.
  • 59 Shaldon S. The interleukin-1 hypothesis: an update. Blood Purification 1988; 06: 162-63.
  • 60 Shaldon S, Dinarello CA, Koch KM, Lonnemann G, Bingel M, Granolleras C, Deschodt G, Branger B, Ouïes R, Fourcade J. Interleukin-1 and dialysis. Adv Nephrol 1988; 17: 423-32.
  • 61 Schäfer R, Rautenberg W, Neumann S, Heidland A, Hörl W. Improvement of dialyzer compatibility by reduction of membrane surface area. Clin Nephrol 1986; 26: 25-38.
  • 62 Swank RL. Alteration of blood on storage: measurement of adhesiveness of “aging” platelets and leukocytes and their removal by filtration. N Engl J Med 1961; 265: 265-71.
  • 63 Szacher M. Thrombosis, hemostasis, and thrombolysis at prosthetic interfaces. In: Biocompatible Polymers, Metals, and Composites. Szacher M. (ed). Lancaster: Technomic Publ: 1983: 1-33.
  • 64 Thaler E, Schmer G. A simple 2 step isolation procedure for human antithrombin II/III and its biological activity after insolubilization to agarose. Trans Am Soc Artif Int Organs 1974; 20: 516-19.
  • 65 Theisen I. Sensibilisierung durch äthylenoxid-sterilisierte Hämodialysatoren und Schlauchsysteme bei Patienten unter chronischer Hämodialysebehandlung. Dissertation. Med. Fakultät der Universität des Saarlandes, Homburg. 1989
  • 66 Vienken J, Baurmeister U. Improved biocompatibility of dialyzers by reduced membrane surface area. Artif Organs 1987; 11: 272-73.
  • 67 Vienken J, Baurmeister U. Aspekte der Biokompatibilität bei der Membranentwicklung. Dialyse J 1988; 4-12.
  • 68 Wegmüller E, Montandon A, Nydegger U, Descoeudres C. Biocompatibility of different hemodialysis membranes : activation of complement and leukopenia. Int J Artif Organs 1986; 09: 85-93.
  • 69 Wetzels E, Colombi A, Dittrich P, Gurland HJ, Kessel M, Klinkmann H. Hämodialyse, Peritonealdialyse, Membranplasmapherese und verwandte Verfahren. 3. Aufl. Berlin, Heidelberg, New York, Tokyo: Springer: 1986