Abstract
Numerous biomarkers are now available to monitor the resolution of infection and the effectiveness of therapy against infection. Of the more than 180 biomarkers that have been identified, three are used most frequently in clinical practice—C-reactive protein, procalcitonin and N-terminal prohormone of brain natriuretic peptide. Unfortunately, each of these can be eliminated by continuous renal replacement therapy especially when using new adsorptive membranes. In addition to these three biomarkers of infection, we analyze seven other prominent biomarkers that are also unfortunately subject to removal with continuous renal replacement therapy. There is therefore currently no reliable marker of infection during continuous renal replacement therapy. Thus during continuous dialysis in intensive care unit patients, we are unable to know if infection is being treated effectively because we have no reliable biomarkers. We need to rely upon other methods like clinical evaluation, hemodynamic improvement, and organ failure improvement to cite a few. In the meantime, the odyssey for the search of the right biomarker during continuous dialysis continues.
This is a preview of subscription content, log in via an institution.
Buying options
Tax calculation will be finalised at checkout
Purchases are for personal use only
Learn about institutional subscriptionsReferences
Pierrakos C, Vincent JL. Sepsis biomarkers: a review. Crit Care. 2010;14:R15.
Honore PM, Jacobs R, De Waele E, Van Gorp V, Spapen HD. Biomarkers of inflammation during continuous renal replacement therapy: sensors, players, or targets? Blood Purif. 2014;38:102–3.
Tillett WS, Francis T. Serological reactions in pneumonia with a non-protein somatic fraction of pneumococcus. J Exp Med. 1930;52:561–71.
McFadyen JD, Kiefer J, Braig D, et al. Dissociation of C-reactive protein localizes and amplifies inflammation: evidence for a direct biological role of C-reactive protein and its conformational changes. Front Immunol. 2018;9:1351.
Taylor KE, van den Berg CW. Structural and functional comparison of native pentameric, denatured monomeric and biotinylated C-reactive protein. Immunology. 2007;120:404–11.
Dahaba AA, Elawady GA, Rehak PH, List WF. Procalcitonin and proinflammatory cytokine clearance during continuous venovenous haemofiltration in septic patients. Anaesth Intensive Care. 2002;30:269–74.
Matsui T, Nakagawa T, Kikuchi H, Horio H, Hashimura K. The effect of continuous renal replacement therapy with the AN69ST membrane on inflammatory markers and the level of consciousness of hemodialysis patients with stroke: comparison with hemodialysis with low blood flow rate. Pril (Makedon Akad Nauk Umet Odd Med Nauki). 2018;39:29–35.
Taylor R, Jones A, Kelly S, et al. A review of the value of procalcitonin as a marker of infection. Cureus. 2017;9:e1148.
Vijayan AL, Ravindran S, Saikant R, Lakshmi S, Kartik R. Procalcitonin: a promising diagnostic marker for sepsis and antibiotic therapy. J Intensive Care. 2017;5:51.
Level C, Chauveau P, Guisset O, et al. Mass transfer, clearance and plasma concentration of procalcitonin during continuous veno-venous hemofiltration in patients with septic shock and acute oliguric renal failure. Crit Care. 2003;6:R160–6.
Honore PM, Jacobs R, Joannes-Boyau O, et al. Newly designed CRRT membranes for sepsis and SIRS—a pragmatic approach for bedside intensivists summarizing the more recent advances: a systematic structured review. ASAIO J. 2013;59:99–106.
N L, Zhang Y, Fan S, Xing J, Liu H. BNP and NT-proBNP levels in patients with sepsis. Front Biosci (Landmark Ed). 2013;18:1237–43.
Pirracchio R, Salem R, Mebazaa A. Use of B natriuretic peptide in critically ill patients. Biomark Med. 2009;3:541–7.
Wahl HG, Graf S, Renz H, Fassbinder W. Elimination of the cardiac natriuretic peptides B-type natriuretic peptide (BNP) and N-terminal proBNP by hemodialysis. Clin Chem. 2004;50:1071–4.
Yumoto M, Nishida O, Moriyama K, et al. In vitro evaluation of high mobility group box 1 protein removal witvarious membranes for continuous hemofiltration. Ther Apher Dial. 2011;15:385–93.
Honore PM, Jacobs R, Hendrickx I, De Waele E, Van Gorp V, Spapen HD. To counteract or to clear high-mobility group box-1 protein in influenza A (H1N1) infection? That may become the question. Crit Care. 2015;19:401.
Honore PM, De Bels D, Attou R, Redant S, Gallerani A, Kashani K. Endocan removal during continuous renal replacement therapy: does it affect the reliability of this biomarker? Crit Care. 2019;23:184.
Hureau M, Gaudet A, De Freitas Caires N, et al. Endocan is a reliable biomarker during continuous renal replacement therapy. Crit Care. 2019;23:296.
De Freitas Caires N, Gaudet A, Portier L, Tsicopoulos A, Mathieu D, Lassalle P. Endocan, sepsis, pneumonia, and acute respiratory distress syndrome. Crit Care. 2018;22:280.
Mueller T, Gegenhuber A, Kronabethleitner G, Leitner I, Haltmayer M, Dieplinger B. Plasma concentrations of novel cardiac biomarkers before and after hemodialysis session. Clin Biochem. 2015;48:1163–6.
Elke G, Bloos F, Wilson DC, et al. The use of mid-regional proadrenomedullin to identify disease severity and treatment response to sepsis—a secondary analysis of a large randomised controlled trial. Crit Care. 2018;22:79.
Honore PM, De Bels D, Attou R, Redant S, Kashani K. The challenge of removal of sepsis markers by continuous hemofiltration. Crit Care. 2019;23:173.
Hansen MB, Rasmussen LS, Garred P, Bidstrup D, Madsen MB, Hyldegaard O. Pentraxin-3 as a marker of disease severity and risk of death in patients with necrotizing soft tissue infections: a nationwide, prospective, observational study. Crit Care. 2016;20:40.
Schilder L, Nurmohamed SA, ter Wee PM, et al. Putative novel mediators of acute kidney injury in critically ill patients: handling by continuous venovenous hemofiltration and effect of anticoagulation modalities. BMC Nephrol. 2015;16:178.
Honore PM, Spapen HD. Pentraxin-3 to better delineate necrotizing soft tissue infection: not really! Crit Care. 2016;20:173.
Zhang X, Liu D, Liu YN, Wang R, Xie LX. The accuracy of presepsin (sCD14-ST) for the diagnosis of sepsis in adults: a meta-analysis. Crit Care. 2015;19:323.
Honore PM, Jacobs R, Hendrickx I, De Waele E, Van Gorp V, Spapen HD. Presepsin and sepsis-induced acute kidney injury treated with continuous renal replacement therapy: will another promising biomarker bite the dust? Crit Care. 2015;19:428.
Honore PM, De Bels D, Barreto Gutierrez L, Redant S, Spapen HD. Heparin-binding protein in sepsis: player! predictor! positioning? Ann Intensive Care. 2019;9:71.
Tverring J, Vaara ST, Fisher J, Poukkanen M, Pettilä V, Linder A, FINNAKI Study Group. Heparin-binding protein (HBP) improves prediction of sepsis-related acute kidney injury. Ann Intensive Care. 2017;7:105.
Honore PM, Jacobs R, Hendrickx I, De Waele E, Van Gorp V, Spapen HD. ‘Biomarking’ infection during continuous renal replacement therapy: still relevant? Crit Care. 2015;19:232.
Schadler D, Pausch C, Heise D, et al. The effect of a novel extracorporeal cytokine hemoadsorption device on IL-6 elimination in septic patients: a randomized controlled trial. PLoS One. 2017;12:e0187015.
Honore PM, Hoste E, Molnár Z, et al. Cytokine removal in human septic shock: where are we and where are we going? Ann Intensive Care. 2019;9:56.
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2020 Springer Nature Switzerland AG
About this chapter
Cite this chapter
Honore, P.M., Redant, S., De Bels, D. (2020). Biomarkers of Sepsis During Continuous Renal Replacement Therapy: Have We Found the Appropriate Biomarker to Use Under This Condition?. In: Vincent, JL. (eds) Annual Update in Intensive Care and Emergency Medicine 2020. Annual Update in Intensive Care and Emergency Medicine. Springer, Cham. https://doi.org/10.1007/978-3-030-37323-8_10
Download citation
DOI: https://doi.org/10.1007/978-3-030-37323-8_10
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-030-37322-1
Online ISBN: 978-3-030-37323-8
eBook Packages: MedicineMedicine (R0)