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. 2021 May 1;19:62. doi: 10.1186/s12969-021-00548-8

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© The Author(s) 2021

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.

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Fig. 3 — The association between IFX dose intensity and serum trough concentrations based on diagnosis. Dose intensity was determined as the average weight adjusted dose of IFX (i.e. mg/kg) per day, based on the timing between the last dose of IFX and the time at which the serum trough IFX concentrations were measured. a The association of IFX dose intensity and serum trough concentrations of IFX were evaluated by Spearman’s correlation analysis. The Spearman’s correlation coefficient (ρ) and associated p-value are provided. b Dose intensity stratified based on patient diagnosis is presented as a box and whisker plot and evaluated by unpaired analysis using the Wilcoxon rank-sum test and the resulting p-values are provided