In Vivo Antibiotics Removal During Hemoadsorption Cartridges and Continuous Renal Replacement Therapy in the Intensive Care Unit (ICARO)

In Vivo Antibiotics Removal During Treatment With Hemoadsorption Cartridges and Continuous Renal Replacement Therapy in the Intensive Care Unit

The purpose of this study is to measure the change in plasma concentrations of antibiotics used during passage through the CRRT filter and hemadsorption cartridge in patients with septic shock and renal failure requiring CRRT.

All patients aged > 18 years, admitted to the ICU, diagnosed with septic shock and renal failure requiring CRRT, receiving antibiotic therapy with at least one of the following drugs: meropenem, linezolid, and daptomycin, who provided informed consent, are included in the study.

Patients not admitted to the ICU, patients with renal failure not requiring CRRT, patients aged < 18 years, or those who did not provide informed consent are excluded. The enrollment period will last 12 months and will run from September 2024 to September 2025. The expected number of patients enrolled is twenty. To proceed with the study, after starting antibiotic therapy, a 4 ml dose of blood will be drawn (Vacuette tube ref. 454092) before the cartridge, immediately after, and after the dialysis filter. This measurement will be repeated after 4, 8, and 12 hours, which represents the maximum usage time of the cartridge.

After 12 hours, the cartridge becomes saturated and loses its adsorption capacity.

The CRRT filter, however, remains in place for at least 72 hours before being replaced. Treatment is maintained until clinically necessary.

For patients in intensive care, several blood samples are required throughout the day, both with a blood sample sent to the biochemistry laboratory every 6-8 hours to check clinical conditions, and with an arterial blood sample (blood gas) to check respiratory and metabolic status in patients on mechanical ventilation. Furthermore, in patients undergoing CRRT, electrolyte balance must be monitored every 4 hours. Therefore, the blood sample for the study inevitably coincides with one of the routine blood samples.

The test tube, labeled with a unique code, will be sent to the central laboratory, which will centrifuge the blood and extract the plasma. This aliquot will then be stored at -80°C in a dedicated space and sent to the designated laboratory upon analysis.

Determination of the plasma dosage of the antibiotic in use is commonly performed on patients admitted to the Intensive Care Unit, where clinically necessary. Participation in the study does not change current clinical practices.

Study Overview

• Status: Recruiting
• Conditions: Septic Shock
• Intervention / Treatment: Diagnostic test: Liquid Chromatography - Tandem Mass Spectrometry

Detailed Description

In ICU setting, most empiric antibiotic treatments include a combination of anti-Gram-positive and -negative bacteria, according to the different clinical scenarios. Thus, there are different possible regimen combinations, including two different drugs. We considered meropenem/linezolid (or daptomycin) as the drugs of choice in septic shock empiric treatment.

The motivation for the use of HA380 was to remove inflammatory cytokines. Only one HA 380 application (=12 hours) will be evaluated in this study.

Hemadsorption will be performed using a BBraun OMNI machine: a Jafron HA380 cartridge is assembled in series with a BBraun OMNI PLUS 'open' filter.

Hemadsorption lasts from 2 to 12 hours maximum, at the end the cartridge can be disassembled and CRRT treatment alone can be carried forward.

CRRT is performed according to the Omni machine BBraun protocol . CVVHD is the technique of choice because the diffusion method guarantees membrane stability.

A predilution Trisodium Citrate 4% infusion is performed, and filter anticoagulation is monitored via post filter blood samples with a target post filter ionized calcium (iCa+) values between 0,2- and 0,4 mmol/L. The citrate plasmatic starting dose is 4 mmol/L: the Omni machine automatically adjusts citrate flow in the predilution pump according to blood flow value, and vice versa. Post filter iCa+ values are checked 5 minutes after treatment institution and 5 minutes after every citrate's dose change; periodic checks are performed every 6 to 8 hours.

Blood flow varies according to patients' weight, dialysate to blood flow (expressed in ml/h) is kept constant in a 1:3 ratio, a table with reference values is provided by the manufacturer. A calcium free dialysate solution with an HCO3 concentration < 25 mmol/l is used.

A Calcium Chloride infusion is performed to restore a normal plasmatic iCa+ concentration. Calcium infusion takes place directly in the Omni circuit's venous line via a dedicated tubing. Starting calcium infusion dose is 1,7 mmol/l, patient's plasmatic iCa+ levels are checked before treatment's start, 30 minutes and 2 hours after treatment's start. Routine monitoring samples are performed every 6 to 8 hours.

When antibiotic treatment includes a loading dose, blood samples will be taken one hour after starting the continuous infusion.

Samples will be taken pre cartridge, post cartridge (pre filter) and after filter at baseline (at least 30 minutes after the beginning of CRRT treatment) and after 4-8 and 12 hours, according to the theoretical cartridge saturation time.

Samples will be processed at the same time, at the end of the recruitment time.

The samples will be processed by a company with expertise in antibiotic TDM. To ensure the highest standards of accuracy and reliability in our data, blood samples collected during this study will be evaluated using state-of-the-art Liquid Chromatography - Tandem Mass Spectrometry (LC-MS/MS) techniques. This advanced analytical method allows for the precise quantification and identification of biochemical compounds within complex biological matrices, providing unparalleled sensitivity and specificity. Following collection, blood is centrifuged to separate serum or plasma, which is then aliquoted to avoid degradation from freeze-thaw cycles. Aliquots are stored at -80°C to preserve sample integrity until analysis. This meticulous pre-analytical preparation ensures that all samples can be analyzed simultaneously, reducing analytical variability, and maintaining the quality of the samples for LC-MS/MS analysis.

Sample size calculation

To assess the variability in concentration levels in patients undergoing Continuous Renal Replacement Therapy (CRRT), a study will be conducted to compare the concentration levels in the blood before and after passing through the CRRT filter. Given the preliminary nature of this study and logistical limitations, the sample size will be set at 10 patients. This sample size is determined based on the ability to detect a clinically significant difference in concentrations of at least 12.53 units, with an assumed standard deviation of 10 units, while maintaining a significance level (α) of 0.05 and a study power (1-β) of 80%. This configuration ensures that the study has the capacity to identify significant differences of relevant magnitude, despite the relatively small number of participants. The decision to limit the sample size to 10 subjects reflects a balance between operational feasibility and the goal of obtaining valid and informative statistical results.

• Study Type: Observational
• Enrollment (Estimated): 20

Contacts and Locations

• Study Contact: Name: Sara Micol Santambrogio, MD; Phone Number: +390264441; Email: saramicol.santambrogio@ospedaleniguarda.it

Study Locations

• Italy
  • Italia
    • Milan, Italia, Italy, 20162
      • Recruiting
      • Niguarda hospital

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: No

• Sampling Method: Non-Probability Sample

Study Population

ICU patients with a diagnosis of infection/sepsis/septic shock

Description

Inclusion Criteria:

• stage 3 KDIGO consensus criteria, indication to CRRT
• use of at least one of the following antibiotics meropenem, linezolid and daptomycin
• < 18 yo

Exclusion Criteria:

• < 18 yo

Study Plan

How is the study designed?

Number of groups / cohorts

1

Cohorts and Interventions

Group / Cohort

Intervention / Treatment

ICU patients with a diagnosis of infection/sepsis/septic shock; stage 3 KDIGO consensus criteria, indication to CRRT; use of at least one of the following antibiotics meropenem, linezolid and daptomycin

Diagnostic test: Liquid Chromatography - Tandem Mass Spectrometry; The samples will be processed by a company with expertise in antibiotic TDM. To ensure the highest standards of accuracy and reliability in our data, blood samples collected during this study will be evaluated using state-of-the-art Liquid Chromatography - Tandem Mass Spectrometry (LC-MS/MS) techniques. This advanced analytical method allows for the precise quantification and identification of biochemical compounds within complex biological matrices, providing unparalleled sensitivity and specificity. Following collection, blood is centrifuged to separate serum or plasma, which is then aliquoted to avoid degradation from freeze-thaw cycles. Aliquots are stored at -80°C to preserve sample integrity until analysis. This meticulous pre-analytical preparation ensures that all samples can be analyzed simultaneously, reducing analytical variability, and maintaining the quality of the samples for LC-MS/MS analysis

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
drug concentration	assess the percentage of drug concentration variation pre and post HA 380 cartridge	4 hours

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
drug concentration variation	assess the percentage of drug concentration variation pre and post HA 380 cartridge	8 and 12 hours

Collaborators and Investigators

• Sponsor: Niguarda Hospital
• Investigators: Principal Investigator: Sara Micol Santambrogio, MD, Niguarda hospital

Study record dates

Study Major Dates

• Study Start (Actual): January 15, 2025
• Primary Completion (Actual): December 15, 2025
• Study Completion (Estimated): August 15, 2026

Study Registration Dates

• First Submitted: August 23, 2025
• First Submitted That Met QC Criteria: November 14, 2025
• First Posted (Actual): November 17, 2025

Study Record Updates

• Last Update Posted (Actual): April 15, 2026
• Last Update Submitted That Met QC Criteria: April 13, 2026
• Last Verified: April 1, 2026

More Information

Terms related to this study

• Keywords: meropenem; antibiotic; linezolid; in vivo; daptomycin; target drug monitoring
• Additional Relevant MeSH Terms: Pathologic Processes; Infections; Sepsis; Systemic Inflammatory Response Syndrome; Inflammation; Shock; Pathological Conditions, Signs and Symptoms; Shock, Septic
• Other Study ID Numbers: 4747

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: UNDECIDED
• IPD Plan Description: Not yet decided

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No