Zusammenfassung
Hintergrund
Eine sog. Nierenersatztherapie kann die physiologischen Funktionen der gesunden Niere nur unvollständig ersetzen. Dabei kann jede Nierenersatztherapie zusätzlich mit einer Reihe von relevanten Nebenwirkungen und Komplikationen verbunden sein, die bei kritisch kranken Patienten den Verlauf und die Prognose erheblich beeinflussen können.
Problemstellung
Neben den hämodynamischen Auswirkungen beinhaltet das sog. Nierenersatztrauma v. a. die Induktion von Entzündung durch den extrakorporalen Kreislauf, die Folgen der Antikoagulation sowie insbesondere den meist unerwünschten und oft unerkannten Verlust einer Vielzahl von Substanzen durch das Blutreinigungsverfahren selbst.
Zielsetzung
Ziel muss es daher sein, die Therapie so zu gestalten, dass systemische aber auch renale Nebenwirkungen möglichst gering bleiben oder ausgeglichen werden. Dazu gehört die richtige Verfahrenswahl für jeden individuellen Patienten in der individuellen klinischen Situation, die Festlegung einer individuellen Therapiedosis und die Substitution von unerwünschten Verlusten. Besonderes bei septischen Patienten sollte auf eine adäquate Dosis von Antiinfektiva geachtet werden. In den ersten 72 h besteht hier sonst die Gefahr einer Unterdosierung dieser Substanzen bei laufendem Nierenersatzverfahren.
Abstract
Background
Renal replacement therapy (RRT) is not able to replace all of the physiologic functions of the kidney. Moreover renal replacement therapy can be associated with a number of serious side effects and complications which can alter the natural course and prognosis of critically ill patients.
Problem
Contributing to this RRT trauma are hemodynamic changes induced by RRT, the induction of inflammation by the extracorporeal circuit itself, side effects of anticoagulation, but especially often unwanted and not recognized losses of multiple substances by the blood purification itself.
Aim
Therefore, the aim should be to adapt therapy in a way that systemic and renal side effects can be minimized or replaced. These include the correct selection of the RRT modality for each patient and each individual clinical situation, in prescribing and monitoring an individual dose of RRT, and the substitution of unwanted losses of different substances. Especially in septic patients, antimicrobials have to be prescribed carefully during the first 72 h, during which underdosing of these substances is a real danger in patients on renal replacement therapy.
Literatur
Uchino S, Kellum JA, Bellomo R et al (2005) Acute renal failure in critically ill patients: a multinational, multicenter study. JAMA 294:813–818
Oppert M, Engel C, Brunkhorst FM et al (2008) Acute renal failure in patients with severe sepsis and septic shock–a significant independent risk factor for mortality: results from the German Prevalence Study. Nephrol Dial Transplant 23:904–909
Joannidis M, Metnitz PG (2005) Epidemiology and natural history of acute renal failure in the ICU. Crit Care Clin 21:239–249
Engel C, Brunkhorst FM, Bone HG et al (2007) Epidemiology of sepsis in Germany: results from a national prospective multicenter study. Intensive Care Med 33:606–618
Elseviers MM, Lins RL, Van der Niepen P et al (2010) Renal replacement therapy is an independent risk factor for mortality in critically ill patients with acute kidney injury. Crit Care 14:R221
Payen D, Mateo J, Cavaillon JM et al (2009) Impact of continuous venovenous hemofiltration on organ failure during the early phase of severe sepsis: a randomized controlled trial. Crit Care Med 37:803–810
Palevsky PM, Zhang JH, O’Connor TZ et al (2008) Intensity of renal support in critically ill patients with acute kidney injury. N Engl J Med 359:7–20
Bellomo R, Cass A, Cole L et al (2009) Intensity of continuous renal replacement therapy in critically ill patients. N Engl J Med 361:1627–1638
Joannes-Boyau O, Honoré PM, Perez P et al (2013) High-volume versus standard-volume haemofiltration for septic shock patients with acute kidney injury (IVOIRE study): a multicentre randomized controlled trial. Intensive Care Med 39:1535–1546
Maynar-Moliner J, Sanchez-Izquierdo JA, Herrera-Gutierrez M (2008) Renal support in critically ill patients with acute kidney injury. N Engl J Med 359:1961–1962
McIntyre CW (2010) Recurrent circulatory stress: the dark side of dialysis. Semin Dial 23:449–451
John S, Griesbach D, Baumgärtel M et al (2001) Effects of continuous haemofiltration vs intermittent haemodialysis on systemic haemodynamics and splanchnic regional perfusion in septic shock patients: a prospective, randomized clinical trial. Nephrol Dial Transplant 16:320–327
Van der Scheuren G, Diltoer M, Laureys M et al (1996) Intermittent hemodialysis in critically ill patients with multiple organ dysfunction syndrome is associated with intestinal intramucosal acidosis. Intensive Care Med 22:747–751
Schneider AG, Bellomo R, Bagshaw SM et al (2013) Choice of renal replacemt therapy modality and dialysis dependence after acute kidney injury: a systematic review and meta-analysis. Intensive Care Med 39:987–997
Vinsonneau C, Camus C, Combes A et al (2006) Continuous venovenous haemodiafiltration versus intermittent haemodialysis for acute renal failure in patients with multiple-organ dysfunction syndrome: a multicentre randomised trial. Lancet 368:379–385
Joannidis M, Oudemanns-van Straaten HM (2007) Patency of the circuit in continuous renal replacement therapy. Crit Care 11:218
Gritters M et al (2006) Citrate anticoagulation abolishes degranulation of polymorphonuclear cells and platelets and reduces oxidative stress during hemodialysis. Nephrol Dial Transplant 21:153–159
Gritters M, Borgdorff P, Grooteman MP et al (2008) Platelet activation in clinical hemodialysis: LMWH as a major contributor to bio-incompatibility? Nephrol Dial Transplant 23:2911–2917
Böhler J, Schollmeyer P, Dressel B et al (1996) Reduction of granulocyte activation during hemodialysis with regional citrate anticoagulation: dissociation of complement activation and neutropenia from neutrophile degranulation. J Am Soc Nephrol 7:234–241
Bos JC, Grooteman MP, Houte AJ van et al (1997) Low polymorphonuclear cell degranulation during citrate anticoagulation: a comparison between citrate and heparin dialysis. Nephrol Dial Transplant 12:1387–1393
Oudemans-van Straaten HM, Bosman RJ, Koopmans M et al (2009) Citrate anticoagulation for continuous venovenous hemofiltration. Crit Care Med 37:545–552
Hetzel GR, Schmitz M, Wissing H et al (2011) Regional citrate versus systemic heparin for anticoagulation in critically ill patients on continuous venovenoushaemofiltration: a prospective randomized multicentre trial. Nephrol Dial Transplant 26:232–239
Zhang Z et al (2012) Efficacy and safety of regional citrate anticoagulation in critically ill patients undergoing continuous renal replacement therapy. Intensive Care Med 38:20–28
Hoste EA, Blot SI, Lameire NH et al (2004) Effect of nosocomial bloodstream infection on the outcome of critically ill patients with acute renal failure treated with renal replacement therapy. J Am Soc Nephrol 15:454–462
Demirjian S, Teo BW, Guzman JA et al (2011) Hypophosphatemia during continuous hemodialysis is associated with prolonged repiratory failure in patients with acute kidney injury. Nephrol Dial Transplant 26:3508–3514
Brain M, Anderson M, Parkes S et al (2012) Critical Care Resusc 14:274–282
Rogiers P, Sun Q, Dimopoulos G et al (2006) Blood warming during hemofiltration can improve hemodynamics and outcome in ovine septic shock. Anesthesiology 104:1216–1222
Joannes-Boyau O, Honore PM, Perez P et al (2013) High-volume versus standard-volume haemofiltration for septic shock patients with acute kidney injury (IVOIRE study): a multicenter randomized controlled trial. Intensive Care Med 39:1535–1546
Roberts DM, Roberts JA, Roberts MS et al (2012) Variability of antibiotic concentrations in critically ill patients receiving continuous renal replcement therapy: a multicentre pharmacokinetic study. Crit Care Med 40:1523–1528
Kellum JA, Ronco C (2010) Dialysis: results of RENAL – what is the optimal CRRT target dose? Nat Rev Nephrol 6:191–192
Einhaltung ethischer Richtlinien
Interessenkonflikt. S. John gibt an, dass kein Interessenkonflikt besteht.
Dieser Beitrag beinhaltet keine Studien an Menschen oder Tieren.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
John, S. Nierenersatztherapie als mögliches Trauma im akuten Nierenversagen. Med Klin Intensivmed Notfmed 109, 342–347 (2014). https://doi.org/10.1007/s00063-013-0338-8
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00063-013-0338-8