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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.
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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Amoxicillin-clavulanate | Administration of amoxicillin-clavulanate as standard care therapy (4x or 6x 1g/d). Blood sampling in early and steady state dose (up to 5 samplings per dose). Collection of hemocultures, urine samples and sputum samples when possible. |
| |
| Piperacillin-tazobactam | Administration of piperacillin-tazobactam as standard care therapy (4x 4g/d). Blood sampling in early and steady state dose (up to 5 samplings per dose). Collection of hemocultures, urine samples and sputum samples when possible. |
| |
| Temocillin | Administration of temocillin as standard care therapy (2x or 3x 2g/d). Blood sampling in early and steady state dose (up to 5 samplings per dose). Collection of hemocultures, urine samples and sputum samples when possible. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Blood sampling | Diagnostic Test | At predefined time points through a venous catheter already in place. Max. volume to be withdrawn: Maximum 4ml/sample. Maximum 10 samples/patient. A last blood sample will be taken, if necessary, after the end of antibiotic therapy, between day 7 and day 14. Though blood results preferably will be used from available data from tests already done during standard treatment. Samples are collected in lithium-heparin tubes (without gel) and centrifuged immediately (within a maximum of 30 minutes after sampling) at room temperature: 8 minutes at 1885g. Plasma is then collected and divided in two separated labelled Eppendorf tubes 1.5 ml and immediately frozen at - 80 °C. If this is not immediately possible, tubes are frozen at - 20 °C and at regular time points transferred to a freezer at - 80 °C (minimum twice a day). |
| Measure | Description | Time Frame |
|---|---|---|
| Blood concentrations of amoxicillin-clavulanate. | To investigate whether blood concentrations with maximum antimicrobial activity are achieved with current dosing regimens in first-dose or early-dose conditions and in steady-state conditions. | Within the first 12 hours (early dose) of treatment and after 24 - 48 hours of treatment (steady state) |
| Blood concentrations of piperacillin-tazobactam. | To investigate whether blood concentrations with maximum antimicrobial activity are achieved with current dosing regimens in first-dose or early-dose conditions and in steady-state conditions. | Within the first 12 hours (early dose) of treatment and after 24 - 48 hours of treatment (steady state) |
| Blood concentrations of temocillin. | To investigate whether blood concentrations with maximum antimicrobial activity are achieved with current dosing regimens in first-dose or early-dose conditions and in steady-state conditions. | Within the first 12 hours (early dose) of treatment and after 24 - 48 hours of treatment (steady state) |
| Measure | Description | Time Frame |
|---|---|---|
| Measured total and unbound concentrations of beta-lactam antibiotics. | To compare measured total and unbound concentrations of beta-lactam antibiotics with predefined pharmacodynamic targets. | Within the first 12 hours (early dose) of treatment and after 24 - 48 hours of treatment (steady state) |
| Response to antimicrobial therapy. |
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Inclusion Criteria:
Exclusion Criteria:
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Frail elderly patients with a minimum of 75 years old, presenting at the emergency department and in need for hospitalization at the geriatric ward, in which a betalactam antibiotic treatment was started.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Peter De Paepe, Prof. Dr. | Contact | 003293325211 | peter.depaepe@uzgent.be | |
| Tania Desmet, Dr. | Contact | 003293321559 | tania.desmet@uzgent.be |
| Name | Affiliation | Role |
|---|---|---|
| Tania Desmet, Dr. | University Hospital, Ghent | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University Hospital Ghent | Recruiting | Ghent | 9000 | Belgium |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 41692875 | Derived | De Clercq A, Desmet T, Boelens J, Somers A, Stove V, Verougstraete N, Brys A, Petrovic M, De Paepe P, De Cock PA. Risk factors for suboptimal target attainment of commonly used ss-lactam antibiotics in older adults: a prospective cohort study. J Antimicrob Chemother. 2026 Feb 2;81(3):dkag048. doi: 10.1093/jac/dkag048. |
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Students participating at the study (registered ethical committee) can consult individual participant data.
During the whole study course.
To be approved by ethical committee.
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| ID | Term |
|---|---|
| D000073496 | Frailty |
| D001424 | Bacterial Infections |
| ID | Term |
|---|---|
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D001423 | Bacterial Infections and Mycoses |
| D007239 | Infections |
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| ID | Term |
|---|---|
| D001800 | Blood Specimen Collection |
| D000071997 | Blood Culture |
| ID | Term |
|---|---|
| D013048 | Specimen Handling |
| D019411 | Clinical Laboratory Techniques |
| D019937 | Diagnostic Techniques and Procedures |
| D003933 | Diagnosis |
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Whole blood, serum, plasma, blood cultures, urine samples, sputum.
|
| Sputum sample | Diagnostic Test | Bacteriological specimen, such as blood cultures, urine samples, sputum ea., which are usually collected in every patient according to standard care will be retained. If there is bacterial growth, MIC's will be calculated on these strains for study purpose. |
|
| Hemoculture | Diagnostic Test | Bacteriological specimen, such as blood cultures, urine samples, sputum ea., which are usually collected in every patient according to standard care will be retained. If there is bacterial growth, MIC's will be calculated on these strains for study purpose. |
|
| Urine sample | Diagnostic Test | Bacteriological specimen, such as blood cultures, urine samples, sputum ea., which are usually collected in every patient according to standard care will be retained. If there is bacterial growth, MIC's will be calculated on these strains for study purpose. |
|
To describe therapeutic response to antimicrobial therapy using procalcitonin. |
| The end of individual antibiotic therapy with an average of 1 week |
| Achievement of pharmacodynamic targets measured by questionnaire, vital signs, blood results and side effects. | To compare achievement of pharmacodynamic targets in early-dose and steady-state conditions. | The end of individual antibiotic therapy with an average of 1 week |
| Clearance of betalactam antibiotics. | To compare clearance of betalactam antibiotics and correlate with renal function using creatinin clearance en cystatin C. | Within the first 12 hours (early dose) of treatment and after 24 - 48 hours of treatment (steady state) |
| D011677 | Punctures |
| D013514 | Surgical Procedures, Operative |
| D008919 | Investigative Techniques |
| D008828 | Microbiological Techniques |