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Therapeutic Monitoring of Antibiotics in Intensive Care Patients: a Cohort Study PopTDM-ICU

P

Poitiers University Hospital

Status

Not yet enrolling

Conditions

Pharmacokinetic
Antibiotic Therapy
Intensive Care Unit

Study type

Observational

Funder types

Other

Identifiers

NCT05367011
PopTDM-ICU

Details and patient eligibility

About

Intensive care patients are exposed to serious infections. Mortality linked to these infections remains high and antibiotic therapy treatment optimization is one of the key points of therapeutic success . Pharmacokinetic therapeutic monitoring and dosage adjustments are recommended for large families of antibiotics such as glycopeptides and aminoglycosides for a long time, but to this day still insufficiently practiced. Concerning Beta-Lactamines this practice is recommended by french society of pharmacology and therapeutic (SFPT) and french society of anesthesiology and intensive care (SFAR) since 2018.

The main goal of the POP-TDM-ICU study is to find the predictive factors of clinical therapeutic efficacy of antibiotic therapy in sepsis or septic shock in intensive care, among which the use of the dosage pharmacokinetics of antibiotic therapy (TDM = Therapeutic Drug Monitoring).

This study is a non-interventional study. Patients bacterial samples already collected in standard care and additional plasma samples will be collected as part of a biological collection with the consent of the patient or family member.

Enrollment

2,500 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient ≥ 18 year-old.
  • Patient hospitalized in intensive care,
  • Patient receiving an antibiotic for sepsis or septic shock
  • Patient or family member who does not object to participating in the study

Exclusion criteria

Patient at risk of death, for a cause other than infectious, within 48 hours following the introduction of antibiotic therapy.

  • Patient receiving antibiotic treatment for antibiotic prophylaxis.
  • Patients benefiting from enhanced protection, namely: minors, persons deprived of their liberty by a judicial or administrative decision, persons staying in a health or social establishment, adults under legal protection.
  • Pregnant and / or lactating women.

Trial contacts and locations

0

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Central trial contact

Karine ESTEVE-GARNIER; Claire DAHYOT-FIZELIER, Pr

Data sourced from clinicaltrials.gov

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