Betalactam Pharmacokinetics in Endocarditis Patients

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUppsala University

About this trial

Infectious endocarditis (IE) is associated with mortality rates of 10-12%. Adequate antibiotic therapy is crucial for survival and is administered in high doses due to the severity of the disease. In most cases, beta-lactam antibiotics (e.g. ampicillin, penicillin G, cefotaxime or cloxacillin) are employed. A number of patient characteristics, such as age, body weight, and renal function) influence the pharmacokinetics of these drugs. Yet, the interindividual variability is poorly understood meaning that a large proportion of patients are at risk of subtherapeutic or excessive drug concentrations that might result in treatment failure or side effects, respectively.

In the present study, data will be collected on antibiotic concentrations in patients treated with beta-lactams for infectious endocarditis as well as patient characteristics and treatment outcomes. A mathematical model will be developed to determine which patient factors determine drug pharmacokinetics. Based on this model, predictions will be made by mathematical simulations on which dosing regimens are optimal for individual patients to ensure therapeutic and non-toxic drug concentrations. In total, 150 patients will be included at four University Hospitals in Sweden; Uppsala University Hospital, Sahlgrenska University Hospital in Gothenburg, Skåne University Hospital in Lund and Karolinska University Hospital in Stockholm. Following informed consent to participate blood samples will be collected at 6 time-points during a dose interval and then at 3 time-points weekly during the full treatment episode (maximum 6 weeks).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Verified or suspected left or right sided endocarditis in native or prosthetic valve

Intravenous antibiotic therapy with either ampicillin, penicillin G, cefotaxime or cloxacillin

Signed informed consent to participate in study

Disqualifiers

<18 years of age

Ongoing dialysis

Trial population

Adult patients in Uppsala University Hospital treated for verified or suspected left or right sided endocarditis in nativ or prosthetic valve with intravenous antibiotic therapy (ampicillin, cefotaxime, cloxacillin or penicillin G).

Trial design

Design model

Case-only

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Determinants of the pharmacokinetic profiles of betalactam antibiotics ampicillin, cefotaxime, cloxacillin and penicillin G

Data on drug concentrations will be analysed using non-linear mixed effect modeling to describe correlations between the observed concentrations and the administered dose, patient characteristics (e.g., age, body weight, gender) or biomarkers (e.g. albumin, creatinine, CRP)

Time frame
6 years
2

Maximum drug concentration (Cmax) of betalactam antibiotics ampicillin, cefotaxime, cloxacillin and penicillin G

Data on drug concentrations will be analysed using non-linear mixed effect modeling to determine Cmax.

Time frame
6 years
3

Volume of distribution (Vd) of betalactam antibiotics ampicillin, cefotaxime, cloxacillin and penicillin G

Data on drug concentrations will be analysed using non-linear mixed effect modeling to determine Vd.

Time frame
6 years
4

Clearance (CL) of betalactam antibiotics ampicillin, cefotaxime, cloxacillin and penicillin G

Data on drug concentrations will be analysed using non-linear mixed effect modeling to determine CL.

Time frame
6 years

Secondary outcomes

1

Mortality

All cause mortality

Time frame
12 months
2

Remission of disease

Relapse in infective endocarditis within 6 months

Time frame
12 months
3

Thromboembolic event

Stroke or embolic event related to endocarditis

Time frame
12 months
4

Resistance development

Resistance development in causing pathogen during treatment assessed with repeated blood culture samples for assessment of bacterial growth and antibiotic susceptibility testing

Time frame
12 months

Other outcomes

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