MedPath

Pharmacokinetic and pharmacodynamic target attainment of cefuroxime in adult patients on general wards with different degrees of renal function: a prospective observational cohort study

Recruiting
Conditions
Infections
Renal impairment
10004018
10038430
Registration Number
NL-OMON52078
Lead Sponsor
oordwest Ziekenhuisgroep
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
45
Inclusion Criteria

Receiving cefuroxime therapy intravenous (iv) as part of standard care
Age >= 18 years
Admitted to a general ward of Noordwest Ziekenhuisgroep location Alkmaar
Informed consent is obtained

Exclusion Criteria

Mentally incapacitated patients , i.e. a minor or legally incompetent adult
Renal replacement therapy during treatment with cefuroxime
Patients admitted to the intensive care unit (ICU)
Severely burned patients, defined as a burned surface >= 10%
Patients with cystic fibrosis
Informed consent is not obtained

Study & Design

Study Type
Observational invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>Percentage of patients attaining the cefuroxime PK-PD target of 50%T>MIC. This<br /><br>will be investigated for patients with adequate renal function receiving a<br /><br>regular cefuroxime dose and impaired renal function receiving a guideline<br /><br>recommended reduced dose.</p><br>
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath