Effect of therapeutic plasma exchange on antimicrobials in critically ill patients

Abstract

Dear Editor,

Therapeutic plasma exchange (TPE) is a procedure in which plasma is separated from the cellular components of whole blood by various methods. The removed plasma is replaced with albumin or fresh frozen plasma (FFP). TPE aims to eliminate disease-related pathogens [1]. Removal of significant amounts of plasma during TPE can alter the pharmacokinetic profiles of antimicrobials, resulting in inadequate therapeutic efficacy. In addition, critically ill patients may have altered pharmacokinetic profiles for many drugs. Data on antimicrobial elimination via TPE in intensive care unit (ICU) patients are scarce. Few studies have examined the effect of TPE on antimicrobials [2].

Several factors may influence antimicrobial elimination during TPE. High plasma protein-binding (> 80%) and low volume of distribution (V_d < 0.2 L/kg) are important pharmacokinetic factors indicating a high rate of removal via TPE [3]. Studies have also shown that allowing an adequate interval for drug distribution significantly decreases drug elimination via TPE [4]. It is important to note that distribution half-life values are not typically available to clinicians through drug monographs. However, because the distribution phase generally has a shorter half-life than the elimination phase, elimination half-life data can be used as a surrogate measure of drug distribution half-life [5].

We report the plasma levels of meropenem, teicoplanin, voriconazole, and amikacin immediately before and after TPE, along with the amounts of antimicrobials in plasmapheresate (removed plasma) from three critically ill ICU patients. All antimicrobials were at steady-state during TPE sessions, with none given immediately before or during TPE. TPE was performed using the Spectra Optia Apheresis System (TERUMOBCT) by continuous-flow-centrifugation. Plasma levels of these drugs are routinely monitored at our hospital using liquid chromatography with tandem mass spectrometry (LC–MS/MS). The amount of drug removed (mg) (Q_TPE) was calculated as follows: drug concentration in plasmapheresate (mg/L) x volume of plasma removed (L). To the best of our knowledge, this study is the first to provide data on the effect of TPE on steady-state plasma levels of meropenem, teicoplanin, and amikacin, as well as the first to report on the effect of TPE on the disposition of amikacin.

A 40-year-old male patient with hemochromatosis, chronic liver disease, type 2 diabetes, and atrial fibrillation was admitted to the medical ICU for neutropenic fever and community-acquired pneumonia (Case 1). He underwent 7 TPE sessions with FFP to treat worsening hyperbilirubinemia associated with hepatic encephalopathy. The patient's antimicrobial therapy included meropenem for neutropenic fever, teicoplanin for gram-positive pathogens due to epididymitis, and voriconazole for Aspergillus fumigatus. Maintenance doses were meropenem 2 g q8h as a prolonged infusion, teicoplanin 12 mg/kg q24h (after a loading dose of 12 mg/kg q12h for 3 doses), and voriconazole 4 mg/kg q12h (after a loading dose of 6 mg/kg q12h). The Q_TPE ranged from 35.64 to 43.22 mg for meropenem, 12.03 mg to 51.86 mg for teicoplanin, and 29.62 mg to 51.68 mg for voriconazole after the 4th, 5th and 6th TPE sessions. Antifungal therapy was changed to liposomal amphotericin B due to supratherapeutic voriconazole levels. The patient's clinical improvement was unaffected by the amount of antimicrobial eliminated, allowing the patient to complete his treatment.

A 76-year-old female patient with myasthenia gravis, metastatic carcinoma, and hypertension was admitted to the medical ICU for a myasthenic crisis (Case 2). She underwent 7 TPE sessions with albumin. The patient was treated with meropenem for hospital-acquired pneumonia caused by extended-spectrum β-lactamase-producing Klebsiella pneumonia. Meropenem was administered at a maintenance dose of 2 g q8h as a prolonged infusion (3-h) after the loading dose. The Q_TPE for meropenem was 27.39 mg after the 6th TPE session. Based on the culture results, antibacterial therapy was escalated to trimethoprim-sulfamethoxazole on day 5 of meropenem treatment.

A 67-year-old male patient with non-Hodgkin's lymphoma, pancreatic adenocarcinoma, and type 2 diabetes was admitted to the surgical ICU for neurological deterioration (Case 3). He underwent 15 TPE sessions with FFP to treat hyperbilirubinemia associated with hepatic encephalopathy. Amikacin was prescribed at a dose of 15 mg/kg q24h for the treatment of å sepsis associated with intra-abdominal infection. The Q_TPE for amikacin was 23.53 mg after the 14th TPE session. The patient passed away due to cardiac arrest while on amikacin therapy.

Detailed clinical data and TPE parameters for the three patients are presented in Tables 1 and 2.

Table 1 Clinical data and pre-TPE laboratory values of the patients undergoing TPE sessions

Full size table

Table 2 Plasma exchange parameters and drug concentration measurements in patients with TPE

Full size table

In the present study, we assumed adequate time for tissue distribution of meropenem, teicoplanin and amikacin based on their elimination half-lives. For meropenem, this resulted in a Q_TPE range of 27.39 mg to 43.22 mg, with 1.37% to 2.16% after a single administered dose. The Q_TPE for meropenem in our study is lower than that reported in a previous study of patients receiving a 1 g dose of meropenem by 1-h infusion concurrent with TPE, resulting in a mean Q_TPE of 142.23 ± 110.31 mg [6]. These differences may be explained by differing intervals for drug distribution. Similarly, the Q_TPE of teicoplanin in the first patient ranged from 12.03 to 51.86 mg, with 1.25% to 5.4% of the single administered dose removed. Again, this is substantially lower compared to a previous study 12 patients who received intravenous teicoplanin at a dose of 6 mg/kg immediately prior to TPE, resulting in a mean Q_TPE of 74.6 ± 34.6 mg [7].

The amount of voriconazole removed in the plasmapheresate ranged from 29.62 to 51.68 mg, with 9.26% to 16.15% of the single administered dose removed. In a case study where TPE was initiated following a 1-h voriconazole infusion, the calculated Q_TPE was approximately 10.1 mg [8]. The voriconazole plasma level in our first patient was 18.1 mg/L on the non-TPE day between the 4th and 5th TPE sessions. There were no drug interactions with voriconazole. Plasma voriconazole levels were unexpectedly high for unknown reasons. These high levels may have affected our measurements.

The current report is also the first to report on the effect of TPE on amikacin, showing a Q_TPE of 23.53 mg, with 2.09% of the single administered dose removed. Low protein-binding affinity and a 21.6-h interval from the end of infusion to TPE may be related to measurements.

Ibrahim et al. [3] propose that the most reliable method to assess the effect of TPE on drug disposition is to measure the amount of drug removed in the plasmapheresate. In the presented cases, the amount of drug removed via TPE was not significant in comparison to the administered single dose, as shown in Table 2. Therefore, it can be stated that all antimicrobials in our study were minimally affected via TPE.

In conclusion, the results of this real-world study emphasize that attention should be paid to the timing of drug distribution, allowing sufficient time between drug administration and TPE to minimize antimicrobial elimination. In addition, therapeutic drug monitoring may help to improve antimicrobial management during TPE in critically ill patients.

No datasets were generated or analysed during the current study.

1. Connelly-Smith L, Alquist CR, Aqui NA, et al. Guidelines on the use of therapeutic apheresis in clinical practice - evidence-based approach from the writing committee of the American society for apheresis: the ninth special issue. J Clin Apher. 2023;38(2):77–278.

   Article PubMed Google Scholar

2. Krzych LJ, Czok M, Putowski Z. Is antimicrobial treatment effective during therapeutic plasma exchange? Investigating the role of possible interactions. Pharmaceutics. 2020. https://doi.org/10.3390/pharmaceutics12050395.

   Article PubMed PubMed Central Google Scholar

3. Ibrahim RB, Liu C, Cronin SM, et al. Drug removal by plasmapheresis: an evidence-based review. Pharmacotherapy. 2007;27(11):1529–49. https://doi.org/10.1592/phco.27.11.1529.

   Article CAS PubMed Google Scholar

4. Ibrahim RB, Balogun RA. Medications in patients treated with therapeutic plasma exchange: prescription dosage, timing, and drug overdose. Semin Dial. 2012;25(2):176–89. https://doi.org/10.1111/j.1525-139X.2011.01030.x.

   Article PubMed Google Scholar

5. Mahmoud SH, Buhler J, Chu E, Chen SA, Human T. Drug dosing in patients undergoing therapeutic plasma exchange. Neurocrit Care. 2021;34(1):301–11. https://doi.org/10.1007/s12028-020-00989-1.

   Article CAS PubMed Google Scholar

6. Jaruratanasirikul S, Neamrat P, Jullangkoon M, Samaeng M. Impact of therapeutic plasma exchange on meropenem pharmacokinetics. Pharmacotherapy. 2022;42(8):659–66. https://doi.org/10.1002/phar.2717.

   Article CAS PubMed Google Scholar

7. Alet P, Lortholary O, Fauvelle F, et al. Pharmacokinetics of teicoplanin during plasma exchange. Clin Microbiol Infect. 1999;5(4):213–8. https://doi.org/10.1111/j.1469-0691.1999.tb00126.x.

   Article CAS PubMed Google Scholar

8. Vay M, Foerster KI, Mahmoudi M, Seessle J, Mikus G. No alteration of voriconazole concentration by plasmapheresis in a critically ill patient. Eur J Clin Pharmacol. 2019;75(2):287–8. https://doi.org/10.1007/s00228-018-2582-6.

   Article PubMed Google Scholar

9. Pistolesi V, Morabito S, Di Mario F, Regolisti G, Cantarelli C, Fiaccadori E. A guide to understanding antimicrobial drug dosing in critically ill patients on renal replacement therapy. Antimicrob Agents Chemother. 2019. https://doi.org/10.1128/AAC.00583-19.

   Article PubMed PubMed Central Google Scholar

Download references

Not applicable.

None.

Authors and Affiliations

1. Department of Clinical Pharmacy, Faculty of Pharmacy, Hacettepe University, Ankara, Turkey

   Ugur Balaban, Emre Kara & Kutay Demirkan

2. Division of Intensive Care Medicine, Department of Internal Medicine, Faculty of Medicine, Hacettepe University, Ankara, Turkey

   Esat Kivanc Kaya & Arzu Topeli

3. Division of Hematology, Department of Internal Medicine, Faculty of Medicine, Hacettepe University, Ankara, Turkey

   Osman Ilhami Ozcebe

4. Department of Infectious Diseases and Clinical Microbiology, Faculty of Medicine, Hacettepe University, Ankara, Turkey

   Murat Akova

5. Department of General Surgery, Faculty of Medicine, Hacettepe University, Ankara, Turkey

   Kaya Yorganci

Authors

1. Ugur BalabanView author publications

   You can also search for this author in PubMed Google Scholar

2. Emre KaraView author publications

   You can also search for this author in PubMed Google Scholar

3. Esat Kivanc KayaView author publications

   You can also search for this author in PubMed Google Scholar

4. Osman Ilhami OzcebeView author publications

   You can also search for this author in PubMed Google Scholar

5. Murat AkovaView author publications

   You can also search for this author in PubMed Google Scholar

6. Arzu TopeliView author publications

   You can also search for this author in PubMed Google Scholar

7. Kaya YorganciView author publications

   You can also search for this author in PubMed Google Scholar

8. Kutay DemirkanView author publications

   You can also search for this author in PubMed Google Scholar

Contributions

U.B. was a major contributor in conceptualization, methodology, data analysis, and writing-original draft. E.K. contributed to conceptualization, methodology, and writing-review&editing. E.K.K., O.I.O., M.A., A.T., K.Y., and K.D. contributed to resources and writing-review&editing. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Ugur Balaban.

Ethics approval and consent to participate

Ethical approval was not required. Informed consent was obtained from the patients.

Competing interests

The authors declare no competing interests.

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, 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 you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. 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-nc-nd/4.0/.

Reprints and permissions

Cite this article

Balaban, U., Kara, E., Kaya, E.K. et al. Effect of therapeutic plasma exchange on antimicrobials in critically ill patients. Crit Care 28, 280 (2024). https://doi.org/10.1186/s13054-024-05077-w

Download citation

• Received: 05 July 2024

• Accepted: 21 August 2024

• Published: 28 August 2024

• DOI: https://doi.org/10.1186/s13054-024-05077-w

Share this article

Anyone you share the following link with will be able to read this content:

Get shareable link

Sorry, a shareable link is not currently available for this article.

Copy to clipboard

Provided by the Springer Nature SharedIt content-sharing initiative