Antimicrobial Pharmacokinetics in Critically Ill Adults During Sustained Low Efficiency Dialysis (SLED)

Sponsor
Ottawa Hospital Research Institute (Other)
Overall Status
Completed
CT.gov ID
NCT02242006
Collaborator
(none)
90
1
17
5.3

Study Details

Study Description

Brief Summary

Severe acute kidney injury (AKI) is a common complication of critical illness affecting almost half of all patients with septic shock. Extracorporeal renal replacement therapy is a cornerstone in the management of AKI in these patients. Options for renal replacement therapy include continuous renal replacement (CRRT) therapy, intermittent dialysis (IHD) or a hybrid form of the two called sustained low efficiency dialysis (SLED). Globally there is a push to switch from traditional CRRT to SLED. Although there are resource and financial comparative benefits to SLED there is almost no literature describing how to dose antimicrobials (or other drugs for that matter). It appears that drug clearance on SLED may be more efficient than CRRT but not as efficient as IHD making extrapolation from these bodies of literature inappropriate for SLED. The investigators are proposing to conduct the population pharmacokinetic studies for the three most commonly used antimicrobials in critically ill patients receiving SLED therapy (piperacillin-tazobactam, meropenem and vancomycin). Population pharmacokinetic modeling of these drugs will provide estimates and sources of variability around pharmacokinetic parameters that will subsequently be used for Monte Carlo simulation to determine the most appropriate dosing regimens to achieve therapeutic targets while minimizing the risk of toxicity.

Condition or Disease Intervention/Treatment Phase
  • Other: serial serum sampling for quantification of drug concentration

Study Design

Study Type:
Observational
Actual Enrollment :
90 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Antimicrobial Pharmacokinetics in Critically Ill Adults During Sustained Low Efficiency Dialysis (SLED)
Study Start Date :
Oct 1, 2014
Actual Primary Completion Date :
Mar 1, 2016
Actual Study Completion Date :
Mar 1, 2016

Arms and Interventions

Arm Intervention/Treatment
piperacillin/tazobactam

Serial serum sampling of patients receiving piperacillin/tazobactam and SLED simultaneously

Other: serial serum sampling for quantification of drug concentration

meropenem

Serial serum sampling of patients receiving meropenem and SLED simultaneously

Other: serial serum sampling for quantification of drug concentration

vancomycin

Serial serum sampling of patients receiving vancomycin and SLED simultaneously

Other: serial serum sampling for quantification of drug concentration

Outcome Measures

Primary Outcome Measures

  1. drug clearance [During the first run of SLED after study inclusion]

    Serial serum samples will be obtained after drug administration and during SLED to determine drug clearance during SLED.

  2. volume of distribution [During the first run of SLED after study inclusion]

    Serial serum samples will be obtained after drug administration and during SLED to determine drug volume of distribition during SLED.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Critically ill adults [age ≥ 18] admitted to one of two of the medical/surgical intensive care units (ICUs) of The Ottawa Hospital, who require SLED and are or will receive meropenem, piperacillin-tazobactam or vancomycin therapy at any dose.
Exclusion Criteria:
  • Patients for whom participation via the informed consent process is denied.

  • Critically ill patients with a hypermetabolic state due to >25% coverage of body surface area burn, cystic fibrosis, spinal cord injury, bariatric patients (defined as

150kg total body weight)

  • Patient is pregnant as per a positive serum or urine βHCG qualitative assay

  • Patient does not have a closed-system arterial or central venous catheter (to minimize blood wastage)

  • Patients receiving concomitant drugs known to interact with the metabolism or clearance of the antimicrobial of interest according to Micromedex 2.0 (Truven Health Analytics Inc 2013)

Contacts and Locations

Locations

Site City State Country Postal Code
1 The Ottawa Hospital Ottawa Ontario Canada K1H 8L6

Sponsors and Collaborators

  • Ottawa Hospital Research Institute

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ottawa Hospital Research Institute
ClinicalTrials.gov Identifier:
NCT02242006
Other Study ID Numbers:
  • 20140429
First Posted:
Sep 16, 2014
Last Update Posted:
Apr 29, 2021
Last Verified:
Sep 1, 2014
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 29, 2021