We appreciate the insightful comments by Prof. Honoré and colleagues regarding our target trial emulation on the effect of erythromycin in critically ill patients with sepsis [
1,
2]. Prof. Honoré and colleagues suggest that, in theory, removal of erythromycin from the circulation by renal replacement therapy (RRT) could dilute the potential effect of erythromycin, and that it may therefore be necessary to exclude patients undergoing RRT.
To test their hypothesis, we reanalysed our data after excluding patients that received RRT
within 72 h of ICU admission (the exposure period) and considered RRT initiated > 72 h
after admission as a secondary outcome (these patients were not excluded to avoid immortal time bias and selection bias). After excluding 43/235 (18.3%) erythromycin-treated patients and 75/470 (16.0%) control patients, 192 patients remained in the erythromycin group and 395 patients in the control group (Additional file
1: Table S1). When compared with the original study population [
2], this subpopulation was similar in terms of baseline demographics, comorbidities and chronic medications, but demonstrated lower disease severity (e.g. APACHE-IV score in the original erythromycin group mean [standard deviation] 90.9 [28.5], new erythromycin group 84.8 [24.1]; in the original control group 85.0 [28.4], new control group 81.4 [26.9]). Within this subpopulation, the number of patients receiving RRT > 72 h after admission was low and not different between groups: 13/192 (6.8%) in the erythromycin group and 26/395 (6.6%) in the control group. Propensity score (PS) matching and (inverse probability of treatment) weighting resulted in well-balanced groups. After matching and weighting, we found no differences in mortality rate up to 90 days: matching HR 0.87 (95% confidence interval [CI] 0.59–1.26), weighting HR 0.91 (95% CI 0.60–1.37) nor in secondary clinical outcomes (aside from a slightly longer ICU length of stay in the erythromycin group in the weighted analysis;
P = 0.025).
Thus, in our study, RRT does not appear to impact the effect of erythromycin on 90-day mortality to a clinically relevant degree. We would like to emphasize that the pharmacokinetics of macrolide antibiotics in the critically ill are complex, understudied, and affected by other factors, such as accumulation in white blood cells (which are not removed by RRT) [
3,
4]. We would very much welcome new studies aimed at better characterizing the pharmacokinetics of macrolide antibiotics in critically ill patients, including the possible elimination by RRT—particularly if these studies also attempt to quantify minimum dosages needed to achieve measurable immunomodulatory effects.
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.
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.