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Optimization of PK/PD Target Attainment for Meropenem in Critically Ill Patients With Sepsis

U

Universitaire Ziekenhuizen KU Leuven

Status

Completed

Conditions

Critical Illness
Pharmacokinetics

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

WP1.1. PK/PD target attainment: Plasma exposure, Excretion via urine & ELF exposure; WP1.2. Predictive dosing algorithm; WP1.3. ECMO subset

Full description

First, the investigators will document exposure to meropenem in plasma and epithelial lining fluid. Moreover excretion in urine will be documented.

Second, the investigators will try to identify risk factors for not attaining PK/PD target. Based on significant predictors for target non attainment a predictive dosing algorithm will be constructed.

Finally in a small subset of ECMO patients PK exposure will be explored.

Enrollment

116 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Severe sepsis or septic shock
  • Admitted to an ICU ward
  • Treated with meropenem

Exclusion criteria

  • eGFR(CKD-EPI) < 70ml/min/1.73m²
  • Renal replacement therapy
  • Pregnancy
  • DNR code 1-3

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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