search
Back to results

Optimal Antibiotic Treatment of Moderate to Severe Bacterial Infections (CDSS)

Primary Purpose

Community-associated Infections, Health-care Acquired Infections, Nosocomial Infections

Status
Unknown status
Phase
Phase 3
Locations
Israel
Study Type
Interventional
Intervention
antibiotic treatment of by TREAT/PCR
Sponsored by
Rabin Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Community-associated Infections focused on measuring computerized decision support system, PCR, antibiotic treatment

Eligibility Criteria

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

Inclusion Criteria:

The rationale of the study will be to address patients for whom antibiotic treatment is, or should be, considered. Thus we will include consecutive patients detected in medical departments according to the following criteria:

  1. Patients from whom blood cultures were drawn or
  2. All patients for whom antibiotic treatment (but not prophylaxis or intra-peritoneal, inhalation or local antibiotics therapy ) is started within the last 96 days or
  3. Patients fulfilling the CDC diagnostic criteria for any infection (see appendix C) or
  4. Patients with temperature ≥38.3 measured orally (or 38 axillary or 38.5 rectal) on a single measurement or ≥38 / < 36 on at least 2 consecutive measurements separated at least 1 hr apart and one of the next criteria:

    (a) heart rate >90 beats/minute; (b) respiratory rate >20 breaths/minute or partial pressure of CO2 <32 mm Hg; and (c) white blood cell count >12,000/ L, <4000 L, or >10% immature (band) forms. or

  5. Patients with shock compatible with septic shock. As defined as hypotension (arterial blood pressure <90 mmHg systolic, or 40 mmHg less than patient's normal blood pressure) for at least 1 h despite adequate fluid resuscitation; Or Need for vasopressors to maintain systolic blood pressure >90 mmHg or mean arterial pressure >70 mmHg and a suspected source of infection.

Exclusion Criteria:

  1. HIV positive patients with opportunistic infection (suspected or proven)and / or AIDS defining illness in the last 6 months prior to data collection.
  2. Children<18 years.
  3. Suspected travel infections.
  4. Suspected tuberculosis.
  5. Pregnancy.
  6. We will exclude patients not able to sign informed consent or not having a legal guardian willing to do so.

Sites / Locations

  • Rabin Medical Center, Beilinson HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Management by TREAT/PCR

Usual management

Arm Description

The data available at the time of patient recruitment will be entered into TREAT. TREAT will provide advice for the empirical antibiotic treatment and unless the caring physician can justify a deviation from this recommendation, TREAT's recommendation will be implemented (yes or no antibiotic treatment and type of antibiotic). TREAT will also recommend whether a blood sample for PCR should be obtained. Blood will be collected aseptically and the test will be performed once daily between 1000AM-1700PM (results available daily at 1700 PM). PCR results and a PCR-revised TREAT recommendation will be reported to the patient's physician in charge and treatment will be revised accordingly.

Patients will be managed by physicians as in regular clinical practice.

Outcomes

Primary Outcome Measures

Clinical success defined as 30-day survival and clinical stability on day 4
patient alive at day 30; on day 4: no fever, no intra-tracheal tube, hemodynamic stable, no vasopressor support, empirical treatment appropriate (and thus not changed).

Secondary Outcome Measures

Appropriate empirical antibiotic treatment
Appropriateness of the antibiotic treatment given during the first 48 hours, before identification of the causative pathogen and its antibiotic susceptibilities
Survival
Hospital stay
Length of hospital stay
Antibiotic miuse of broad spectrum antibiotics and total costs of antibiotic treatment Superfluous antibiotic treatment
Use of broad spectrum antibiotics and total costs of antibiotic treatment
Costs
Costs incurred during hospital stay
Adverse events
Allergy, nephrotoxicity, diarrhea, clostridium-difficile associated diarrhea and others

Full Information

First Posted
March 30, 2011
Last Updated
April 6, 2016
Sponsor
Rabin Medical Center
search

1. Study Identification

Unique Protocol Identification Number
NCT01338116
Brief Title
Optimal Antibiotic Treatment of Moderate to Severe Bacterial Infections
Acronym
CDSS
Official Title
Optimal Antibiotic Treatment of Moderate to Severe Bacterial Infections: Integration of PCR Technology and Medical Informatics/Artificial Intelligence
Study Type
Interventional

2. Study Status

Record Verification Date
April 2016
Overall Recruitment Status
Unknown status
Study Start Date
April 2016 (undefined)
Primary Completion Date
January 2018 (Anticipated)
Study Completion Date
January 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rabin Medical Center

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Severe bacterial infections are associated with mortality of about 30%. Patients with moderate to severe bacterial infections given early and appropriate empirical antibiotic treatment are at a lesser risk for a fatal outcome, with odds ratios ranging from 1.6 to 6.9. However only about 2/3 of patients worldwide are given early and appropriate empirical antibiotic treatment. About 40% of patients treated with antibiotics are given superfluous treatment. TREAT is a computerized decision support system for antibiotic treatment in inpatients with common bacterial infections. TREAT is based on a state of the art stochastic model of the domain (a causal probabilistic network) and uses a cost benefit model for antibiotic treatment, including costs assigned to future resistance. It was tested in a randomized controlled trial in 3 countries and shown to improve the percentage of appropriate empirical antibiotic treatment while at the same time reduce hospital stay and the use of broad-spectrum antibiotics. The main limitation of TREAT is inherent in the limited information available within hours of presentation. A second attractive approach to improve antibiotic treatment is to use techniques that do not depend on cultures, and thus shorten the time to identification of the pathogen to a few hours only. The LightCycler® SeptiFast test from Roche performs in vitro nucleic acid amplification test for pathogens causing bloodstream infections. The purpose of the clinical trial is to show that the combined system TREAT/PCR assays will improve the outcome of inpatients with moderate to severe bacterial infections, while at the same time reducing the use of broad-spectrum antibiotics, with no or little additional costs. A secondary objective will be to assess the sensitivity and specificity of whole blood PCR, using TREAT as the reference standard.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Community-associated Infections, Health-care Acquired Infections, Nosocomial Infections
Keywords
computerized decision support system, PCR, antibiotic treatment

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
600 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Management by TREAT/PCR
Arm Type
Experimental
Arm Description
The data available at the time of patient recruitment will be entered into TREAT. TREAT will provide advice for the empirical antibiotic treatment and unless the caring physician can justify a deviation from this recommendation, TREAT's recommendation will be implemented (yes or no antibiotic treatment and type of antibiotic). TREAT will also recommend whether a blood sample for PCR should be obtained. Blood will be collected aseptically and the test will be performed once daily between 1000AM-1700PM (results available daily at 1700 PM). PCR results and a PCR-revised TREAT recommendation will be reported to the patient's physician in charge and treatment will be revised accordingly.
Arm Title
Usual management
Arm Type
No Intervention
Arm Description
Patients will be managed by physicians as in regular clinical practice.
Intervention Type
Other
Intervention Name(s)
antibiotic treatment of by TREAT/PCR
Intervention Description
Management by TREAT/PCR. The data available at the time of patient recruitment will be entered into TREAT. TREAT will provide advice for the empirical antibiotic treatment and unless the caring physician can justify a deviation from this recommendation, TREAT's recommendation will be implemented (yes or no antibiotic treatment and type of antibiotic). TREAT will also recommend whether a blood sample for PCR should be obtained. Blood will be collected aseptically and the test will be performed once daily between 1000AM-1700PM (results available daily at 1700 PM). PCR results and a PCR-revised TREAT recommendation will be reported to the patient's physician in charge and treatment will be revised accordingly. On day 2, when results of blood cultures and other cultures become available TREAT will be re-consulted and will issue a new recommendation based on the full microbiological investigation (negative and positive results).
Primary Outcome Measure Information:
Title
Clinical success defined as 30-day survival and clinical stability on day 4
Description
patient alive at day 30; on day 4: no fever, no intra-tracheal tube, hemodynamic stable, no vasopressor support, empirical treatment appropriate (and thus not changed).
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Appropriate empirical antibiotic treatment
Description
Appropriateness of the antibiotic treatment given during the first 48 hours, before identification of the causative pathogen and its antibiotic susceptibilities
Time Frame
48 hours
Title
Survival
Time Frame
30 days
Title
Hospital stay
Description
Length of hospital stay
Time Frame
30 days
Title
Antibiotic miuse of broad spectrum antibiotics and total costs of antibiotic treatment Superfluous antibiotic treatment
Description
Use of broad spectrum antibiotics and total costs of antibiotic treatment
Time Frame
30 days
Title
Costs
Description
Costs incurred during hospital stay
Time Frame
30 days
Title
Adverse events
Description
Allergy, nephrotoxicity, diarrhea, clostridium-difficile associated diarrhea and others
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: The rationale of the study will be to address patients for whom antibiotic treatment is, or should be, considered. Thus we will include consecutive patients detected in medical departments according to the following criteria: Patients from whom blood cultures were drawn or All patients for whom antibiotic treatment (but not prophylaxis or intra-peritoneal, inhalation or local antibiotics therapy ) is started within the last 96 days or Patients fulfilling the CDC diagnostic criteria for any infection (see appendix C) or Patients with temperature ≥38.3 measured orally (or 38 axillary or 38.5 rectal) on a single measurement or ≥38 / < 36 on at least 2 consecutive measurements separated at least 1 hr apart and one of the next criteria: (a) heart rate >90 beats/minute; (b) respiratory rate >20 breaths/minute or partial pressure of CO2 <32 mm Hg; and (c) white blood cell count >12,000/ L, <4000 L, or >10% immature (band) forms. or Patients with shock compatible with septic shock. As defined as hypotension (arterial blood pressure <90 mmHg systolic, or 40 mmHg less than patient's normal blood pressure) for at least 1 h despite adequate fluid resuscitation; Or Need for vasopressors to maintain systolic blood pressure >90 mmHg or mean arterial pressure >70 mmHg and a suspected source of infection. Exclusion Criteria: HIV positive patients with opportunistic infection (suspected or proven)and / or AIDS defining illness in the last 6 months prior to data collection. Children<18 years. Suspected travel infections. Suspected tuberculosis. Pregnancy. We will exclude patients not able to sign informed consent or not having a legal guardian willing to do so.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mical Paul, MD
Organizational Affiliation
Rabin Medical Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Leonard Leibovici, Prof
Organizational Affiliation
Rabin Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rabin Medical Center, Beilinson Hospital
City
Petah Tikvah
ZIP/Postal Code
49100
Country
Israel
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Laura Farbman
Phone
972-3-9377380
Email
laurafa@clalit.org.il
First Name & Middle Initial & Last Name & Degree
Mical Paul, Md
Phone
972-3-9377380
Email
michalp2@clalit.org.il
First Name & Middle Initial & Last Name & Degree
Mical Paul, MD
First Name & Middle Initial & Last Name & Degree
Leonard Leibovici, MD

12. IPD Sharing Statement

Learn more about this trial

Optimal Antibiotic Treatment of Moderate to Severe Bacterial Infections

We'll reach out to this number within 24 hrs