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. 2016 Jan 4;20:2. doi: 10.1186/s13054-015-1159-3

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© Sponholz et al. 2016

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 2 — Changes in laboratory parameters representing the primary and secondary study endpoints. Total bilirubin levels, albumin-binding capacity (ABiC), total bile acid concentrations and creatinine levels during albumin dialysis, separated by the applied extracorporeal albumin dialysis (ECAD) systems Molecular Adsorbents Recirculating System (MARS) or single-pass albumin dialysis (SPAD). Box plots represent overall values including all 69 performed ECAD cycles, while bounded dots mark changes of each individual ECAD application. *p < 0.05 significant changes within ECAD; ^# p < 0.05 significant differences between both devices. n.s. non-significant difference