CRP Versus PCT as Bio-markers for Sepsis and in Guiding Antibiotics in Critically Ill Patients
NCT ID: NCT04049565
Last Updated: 2020-02-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
60 participants
OBSERVATIONAL
2018-10-01
2019-03-15
Brief Summary
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Detailed Description
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Use of appropriate antibiotics in the intensive care unit (ICU) is a major challenge. Studies have shown that up to 50% of antibiotics prescribed in hospital settings are either unnecessary or inappropriate, contributing to increasing rates of resistant organisms, increases in adverse drug reactions, overall length of stay (LOS) and mortality. In addition, in critically ill patients, a long duration of treatment with antibiotics is associated with the development of antimicrobial resistance. Moreover, Sepsis and Systemic Inflammatory Response Syndrome (SIRS) SIRS can closely mimic one another and present a diagnostic challenge. So, determination of the presence or absence of bacterial infection is important to guide appropriate therapy and reduce antibiotic exposure. For microorganism detection, culture sensitivity is used though it has some drawbacks as time consuming, sometimes misleading with negative or positive reports and also they don't give information about the onset of organ dysfunction. Accordingly, it is important to differentiate culture negative sepsis patients from those with noninfectious SIRS, as these disease conditions require different therapeutic regimens. Due to these drawbacks of culture, researchers tried to depend on other more specific blood markers.
Biomarkers of infection, namely C-reactive protein and procalcitonin (PCT) have been shown to be useful in the diagnosis of infection as well as in the assessment of its response to antibiotic therapy. C-reactive protein variations overtime appears to have a good performance for the diagnosis of infection. Procalcitonin shows a better correlation with clinical severity.
Despite being used routinely in several intensive care services as an auxiliary criterion for decisions regarding antibiotic therapy, no C- reactive protein based protocol has been tested in clinical trials to guide the reduction of antibiotic use in patients with sepsis until 2012. In 2013 Oliveira et al. compared a protocol based on serum PCT levels versus a protocol based on serum C-reactive protein levels for reducing the duration of antibiotic treatment in critically ill patients presenting with severe sepsis or septic shock. The latter study showed that C-reactive protein was as useful as procalcitonin in reducing antibiotic use in a predominantly medical population of septic patients, causing no apparent harm.
Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Procalcitonin
septic patients who will receive Procalcitonin
Procalcitonin biomarker and CRP biomarker
collecting blood samples to measure serum CRP and Procalcitonin
C-Reactive Protein
septic patients who will receive C-Reactive ptotein
Procalcitonin biomarker and CRP biomarker
collecting blood samples to measure serum CRP and Procalcitonin
Interventions
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Procalcitonin biomarker and CRP biomarker
collecting blood samples to measure serum CRP and Procalcitonin
Eligibility Criteria
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Inclusion Criteria
* Patients with sepsis or septic shock who received their first doses of antibiotics no longer than 24 h before inclusion into the study
Exclusion Criteria
* Pregnancy and lactation
* Immunocompromised patients or who had high doses of corticosteroids
* Patients with chronic organ failure
* Infections that required long-term treatment, regardless of the etiologic agent (e.g., bacterial endocarditis).
18 Years
69 Years
ALL
No
Sponsors
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Beni-Suef University
OTHER
Responsible Party
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Walid Ahmed Ali
Clinical Pharmacist / Walid Ahmed Ali Abdeltawab
Principal Investigators
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Abdelrahman Dr ElNaggar, Prof
Role: PRINCIPAL_INVESTIGATOR
study official is dead
Locations
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Cairo University Hospital
Cairo, , Egypt
Countries
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Other Identifiers
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PCTCRP
Identifier Type: -
Identifier Source: org_study_id
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