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Duration of Antibiotic Therapy in Critically Ill Patients: C-reactive Protein-guided Therapy Versus Best Practice

Primary Purpose

Infection Systemic

Status
Completed
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
C-reactive protein
Sponsored by
Federal University of Minas Gerais
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Infection Systemic focused on measuring Intensive care, Sepsis, Biomarkers, C-reactive Protein, Antimicrobial, Systemic infection

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age ≥ 18 years
  • Signed informed consent
  • Assumed or proven infection
  • Patient admitted to the unit participating in the study

Exclusion Criteria:

  • Patients with severe immunosuppression, such as severe neutropenia (<500 neut/mm3), transplantation of solid organs or cells hematopoietic, HIV infection with CD4+ < 200/mm3
  • Patients with multiple trauma, burns or surgery grid size in the last 5 days (Except surgery for focus control)
  • Use of antibiotics supposedly or proven to be effective against the infectious process in for more than 48 hours.
  • Patients undergoing palliative care.
  • Patients with death expectancy for the next 24 hours.
  • Patients with bacteremia caused by Staphylococcus aureus or Candida spp
  • Patients with infections that are known to require prolonged antibiotic therapy

Sites / Locations

  • Hospital das Clínicas - Universidade Federal de Minas Gerais

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

C-reactive Protein

Best Practice

Arm Description

In this group, the attending physicians will be instructed to follow the decision flowchart based on the CRP values. Antibiotic suspension will be encouraged when levels of this marker are <35mg/L (if peak PCR below 100mg/L); or reduce 50% of the highest value (if PCR peak > 100mg/L), with a limit of seven days, if there is clinical improvement. If a given patient has persistently elevated CRP levels (> 100 mg/l or fall less than 50% relative to the time of inclusion), the investigators will encourage attending physicians to maintain antibiotics and to perform a careful search for persistent infection. In case of doubts, if the patient is well clinically and without signs of active infection, the duration of antibiotic therapy should be the same as suggested for the Best Practice group.

Patients will be initially treated according to the current protocols used in the intensive care units. Decisions about interruption or continuation of treatment will be made according to pre-established time and also according to the clinical evolution of the patients. CRP levels will not be measured and will not be considered in the decision to discontinue antimicrobials. Any decision ultimately rests with the clinical assistants. Suggestions on the suspension of antibiotics will be provided by the researchers as follows: 7 full days for most infections 10 full days for pneumonia caused by Gram negative non-fermenting bacteria or Gram negative bacteria carbapenemase producing. 14 days of treatment for necrotizing pneumonia, confirmed by chest computed tomography.

Outcomes

Primary Outcome Measures

Duration of antibiotic therapy for the first episode of infection
Days of treatment with antibiotics after inclusion
Total antibiotic exposure days per 1,000 days

Secondary Outcome Measures

Costs of hospitalization
Considering Brazilian market prices
Clinical cure rate
Disappearance of clinical signs and symptoms present at inclusion
Therapeutic failure
Persistence or recurrence of the pathogen originally causing the infection.
All cause 28-day mortality
All cause 90-day mortality
Length of ICU stay
Length of hospital stay
Nosocomial infection rate
Isolation of multiresistant bacteria
In-hospital mortality

Full Information

First Posted
December 5, 2016
Last Updated
August 7, 2018
Sponsor
Federal University of Minas Gerais
Collaborators
Fundação de Amparo à Pesquisa do estado de Minas Gerais
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1. Study Identification

Unique Protocol Identification Number
NCT02987790
Brief Title
Duration of Antibiotic Therapy in Critically Ill Patients: C-reactive Protein-guided Therapy Versus Best Practice
Official Title
Duration of Antibiotic Therapy in Critically Ill Patients: C-reactive Protein-guided Therapy Versus Best Practice
Study Type
Interventional

2. Study Status

Record Verification Date
August 2018
Overall Recruitment Status
Completed
Study Start Date
January 2017 (Actual)
Primary Completion Date
August 2018 (Actual)
Study Completion Date
August 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Federal University of Minas Gerais
Collaborators
Fundação de Amparo à Pesquisa do estado de Minas Gerais

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The judicious use of antibiotics is one of the main measures to limit the emergence of multidrug-resistant pathogen related to excessive antimicrobial use. A recent study demonstrated that C-reactive protein (CRP) was as useful as procalcitonin (PCT) in reducing the time of antibiotic therapy in adult septic patients treated in the ICU setting. Therefore, the present study proposes to compare the time of use of antimicrobials, costs of hospitalization and clinical outcomes of interest among a group of antibiotic therapy guided by serum levels of CRP and a group of therapy based on the best practices of antibiotic therapy (Best Practice).
Detailed Description
All adult patients (aged> 17 years), hospitalized at the ICU (total of 50 beds) of the Hospital das Clínicas - UFMG, with an assumed or proven infection, will be considered for inclusion. Patients who meet the inclusion and exclusion criteria will be allocated randomly into one of the following groups: 1) PCR group: antibiotic therapy will be discontinued according to serum CRP levels; 2) "Best Practice" group, length of antibiotic therapy based on the most recent guidelines in the medical literature, according to the focus and / or causative micro-organism. PCR assays shall be performed daily on serum obtained from blood collected for routine intensive care examinations up to 2 days after antibiotic withdrawal. In the PCR group, antibiotic suspension will be encouraged when levels of this marker are <35mg / L (if peak PCR below 100mg / L); or reduce 50% of the highest value (if PCR peak > 100mg / L), with a limit of seven days, if there is clinical improvement. Primary outcomes will be duration of antibiotic therapy and antibiotic-free live days corrected for 1000 days of hospitalization. Secondary outcomes will be costs, clinical cure rate, therapeutic failure, 28-day mortality, 90-day mortality, in-hospital mortality, length of hospital stay, nosocomial infection rate, recurrence of infection, and isolation of multidrug-resistant bacteria

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infection Systemic
Keywords
Intensive care, Sepsis, Biomarkers, C-reactive Protein, Antimicrobial, Systemic infection

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
135 (Actual)

8. Arms, Groups, and Interventions

Arm Title
C-reactive Protein
Arm Type
Experimental
Arm Description
In this group, the attending physicians will be instructed to follow the decision flowchart based on the CRP values. Antibiotic suspension will be encouraged when levels of this marker are <35mg/L (if peak PCR below 100mg/L); or reduce 50% of the highest value (if PCR peak > 100mg/L), with a limit of seven days, if there is clinical improvement. If a given patient has persistently elevated CRP levels (> 100 mg/l or fall less than 50% relative to the time of inclusion), the investigators will encourage attending physicians to maintain antibiotics and to perform a careful search for persistent infection. In case of doubts, if the patient is well clinically and without signs of active infection, the duration of antibiotic therapy should be the same as suggested for the Best Practice group.
Arm Title
Best Practice
Arm Type
No Intervention
Arm Description
Patients will be initially treated according to the current protocols used in the intensive care units. Decisions about interruption or continuation of treatment will be made according to pre-established time and also according to the clinical evolution of the patients. CRP levels will not be measured and will not be considered in the decision to discontinue antimicrobials. Any decision ultimately rests with the clinical assistants. Suggestions on the suspension of antibiotics will be provided by the researchers as follows: 7 full days for most infections 10 full days for pneumonia caused by Gram negative non-fermenting bacteria or Gram negative bacteria carbapenemase producing. 14 days of treatment for necrotizing pneumonia, confirmed by chest computed tomography.
Intervention Type
Other
Intervention Name(s)
C-reactive protein
Intervention Description
PCR assays shall be performed daily on serum obtained from blood collected for routine intensive care examinations up to 2 days after antibiotic withdrawal. In the PCR group, antibiotic suspension will be encouraged when levels of this marker are <35mg / L (if peak PCR below 100mg / L); or reduce 50% of the highest value (if PCR peak> 100mg / L), with a limit of seven days, if there is clinical improvement.
Primary Outcome Measure Information:
Title
Duration of antibiotic therapy for the first episode of infection
Description
Days of treatment with antibiotics after inclusion
Time Frame
1 year
Title
Total antibiotic exposure days per 1,000 days
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Costs of hospitalization
Description
Considering Brazilian market prices
Time Frame
Through study completion, an average of 1 year
Title
Clinical cure rate
Description
Disappearance of clinical signs and symptoms present at inclusion
Time Frame
28 days
Title
Therapeutic failure
Description
Persistence or recurrence of the pathogen originally causing the infection.
Time Frame
28 days
Title
All cause 28-day mortality
Time Frame
28 days
Title
All cause 90-day mortality
Time Frame
90 days
Title
Length of ICU stay
Time Frame
28 days
Title
Length of hospital stay
Time Frame
28 days
Title
Nosocomial infection rate
Time Frame
28 days
Title
Isolation of multiresistant bacteria
Time Frame
28 days
Title
In-hospital mortality
Time Frame
An average of 28 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 18 years Signed informed consent Assumed or proven infection Patient admitted to the unit participating in the study Exclusion Criteria: Patients with severe immunosuppression, such as severe neutropenia (<500 neut/mm3), transplantation of solid organs or cells hematopoietic, HIV infection with CD4+ < 200/mm3 Patients with multiple trauma, burns or surgery grid size in the last 5 days (Except surgery for focus control) Use of antibiotics supposedly or proven to be effective against the infectious process in for more than 48 hours. Patients undergoing palliative care. Patients with death expectancy for the next 24 hours. Patients with bacteremia caused by Staphylococcus aureus or Candida spp Patients with infections that are known to require prolonged antibiotic therapy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vandack Nobre, PhD
Organizational Affiliation
Medical School of the Federal University of Minas Gerais
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Isabela Borges, MSc
Organizational Affiliation
Medical School of the Federal University of Minas Gerais
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital das Clínicas - Universidade Federal de Minas Gerais
City
Belo Horizonte
State/Province
Minas Gerais
Country
Brazil

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
32487263
Citation
Borges I, Carneiro R, Bergo R, Martins L, Colosimo E, Oliveira C, Saturnino S, Andrade MV, Ravetti C, Nobre V; NIIMI - Nucleo Interdisciplinar de Investigacao em Medicina Intensiva. Duration of antibiotic therapy in critically ill patients: a randomized controlled trial of a clinical and C-reactive protein-based protocol versus an evidence-based best practice strategy without biomarkers. Crit Care. 2020 Jun 1;24(1):281. doi: 10.1186/s13054-020-02946-y.
Results Reference
derived

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Duration of Antibiotic Therapy in Critically Ill Patients: C-reactive Protein-guided Therapy Versus Best Practice

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