Antibiotic Dosing in Geriatric Patients at the Emergency Department

  • STATUS
    Recruiting
  • participants needed
    180
  • sponsor
    University Hospital, Ghent
Updated on 19 February 2024
antibiotics
antibiotic therapy
temocillin
beta-lactam
amoxicillin
lactam antibiotics
lactam
piperacillin-tazobactam
piperacillin
clavulanate
hemoculture
amoxicillin-clavulanate

Summary

In this pilot study, we will investigate whether - with the current dosing regimens, used in the Ghent University Hospital - pharmacodynamic targets regarding beta-lactam antibiotics (more specific Amoxicilline-Clavulanate, Piperacillin-Tazobactam and Temocillin) are attained in frail patients admitted to the geriatric department.

Description

In drug research studies, older people - and especially patients with a geriatric profile or frailty risk - are very frequently excluded. Moreover, drug dosing is often extrapolated from studies in younger adults with failure to consider potential differences in pharmacokinetics (PK) and pharmacodynamics (PD).

Studies on dosing of beta-lactam antibiotics in geriatric or frail patients aged 75 years or older have, to the best of our knowledge, never been performed.

In this pilot study, we will investigate whether - with the current dosing regimens, used in the Ghent University Hospital - pharmacodynamic targets regarding beta-lactam antibiotics (more specific Amoxicilline-Clavulanate, Piperacillin-Tazobactam and Temocillin) are attained in frail patients admitted to the geriatric department.

This monocentric, prospective, observational trial is currently ongoing at the emergency department and geriatric department of the Ghent University Hospital.

Amoxicillin/clavulanic acid 1000/200mg of piperacillin-tazobactam 4000mg or temocillin 2000mg was infused intravenously over 30 minutes using a syringe pump. The standard dosing regimes were used.

An infusion catheter of minimum 18-gauge was placed in the contralateral arm to the arm in which the antibiotic dose was administered. Blood samples were collected from this catheter at first dose and assumed steady state conditions. Steady state was assumed to be reached after minimal 24h (> 4 doses at four - six hourly interval) of therapy. The goal was to obtain 5 first dose and 5 steady dose samples in every patient.

Material for bacteriological analysis, such as blood cultures, urine samples, sputum, were collected in every patient according to standard care. In case of bacterial growth, MIC's were measured on the reported strains when possible.

Amoxicillin, clavulanic acid, piperacillin, tazobactam and temocillin were measured using a validated ultra-performance liquid chromatographic method with tandem mass spectrometric detection.

Serum creatinine, cystatin C, procalcitonin, infection parameters (CRP, WBC count) and albumin were obtained from standard blood samples performed in these patients at day one and also later on during their therapy.

Three frailty score systems (KATZ, Geriatric 8 - G8, Cumulative Illness Rating Scale - CIRS) were calculated.

Details
Condition Bacterial Infection, Frailty, Frail Elderly Syndrome, Elderly Infection
Age 75years - 100years
Treatment blood sampling, Sputum sample, Hemoculture, Urine sample
Clinical Study IdentifierNCT04436991
SponsorUniversity Hospital, Ghent
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

Patients presenting at the emergency department and later on admitted to the geriatric department
Patient age 75 years or older
Patients with geriatric profile according to KATZ scale, G8 screening test or CIRS score
Patient receiving antibiotic treatment (amoxicillin-clavulanate, piperacillin-tazobactam)
Intravenous access available for blood sampling. For measurement of the peak concentration an intravenous access other than the drug infusion line is required

Exclusion Criteria

Admission to other units than the geriatric department incl. the ICU
Absence of informed consent
Known hypersensitivity to beta-lactam antibiotics
Patients who received oral amoxicillin-clavulanate prior to admission will not be included in the iv. amoxicillin-clavulanate group
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