Duration of Antibiotics for the Treatment of Gram-negative Bacilli Bacteremia

Not Applicable

Completed

• Conditions: Gram Negative Bacteremia
• Interventions: Drug: short-course antibiotic treatment; Drug: accepted prolonged antibiotic treatment

• Registration Number: NCT01737320
• Lead Sponsor: Rabin Medical Center

Brief Summary

The investigators plan an open label randomized controlled trial to compare short-course antibiotic therapy (\<=7 days) versus longer treatment (\>7 days). The investigators will include hospitalized patients with gram-negative bacteremia. The investigators primary objective is to investigate the safety and efficacy of short-course antibiotics.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2012-11-14
• Study First Submitted QC: 2012-11-26
• Study First Posted: 2012-11-29
• Study Start: 2013-01
• Primary Completion: 2018-03
• Study Completion: 2018-03-04
• Status Verified: 2019-04
• Last Update Submitted: 2019-04-06
• Last Update Posted: 2019-04-09

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 604

Inclusion Criteria

• patients with gram-negative aerobic bacilli bacteremia, defined as growth of a single gram-negative microorganism in one or more blood cultures, associated with evidence of infection (hyper- or hypothermia, a localized infection, sepsis or septic shock).
• We will include patients receiving appropriate antibiotic treatment for 7 days and are afebrile / not hypothermic for the last 48 hours. Both community and hospital acquired gram-negative bacteremias will be included, regardless of antibiotic susceptibility patterns. We will allow the inclusion of patients receiving less than 7 days if clinically stable and discharge from hospital is considered. We will then recruit the patient before discharge, if stable at least for 48 hours before randomization.

We will include the following sources of bacteremia:

1. Primary bacteremia / unknown source
2. Urinary tract
3. Abdominal
4. Respiratory tract
5. Central venous catheter(CVC), when the catheter was removed before randomization
6. Skin and soft tissue, including surgical site infection

Exclusion Criteria

1. Gram-negative bacteremia due to specific infections as detailed here:

   1. Endocarditis / endovascular infections
   2. Necrotizing fasciitis
   3. Osteomyelitis
   4. Abdominal abscesses and other unresolved abdominal sources requiring surgical intervention (e.g., cholecystitis)
   5. Central nervous system infections
   6. Empyema
   7. CVC- related or CVC-associated bloodstream infections when the catheter is retained. We will permit the inclusion of patients with retained CVCs in whom the source of the bacteremia is not the CVC.

2. Polymicrobial growth in blood cultures involving gram-positive or anaerobes in addition to gram-negatives (defined as either growth of two or more different species of microorganisms in the same blood culture, or growth of different species in two or more separate blood cultures within the same episode (< 48 h) and with clinical or microbiological evidence of the same source).

3. Specific pathogens including:

   1. Salmonella spp.
   2. Brucella spp.

4. Immunosuppression, including:

   1. HIV infection
   2. Hematopoietic stem-cell transplantation
   3. Neutropenia on day of randomization or in the 48 hours prior to randomization. Patients with neutropenic fever at presentation that are afebrile and non-neutropenic in the 48 hours before randomization will be included.

5. Clinical instability during the 48 hours before randomization, defined as mean blood pressure<60 mmHg despite adequate fluid resuscitation or vasopressors support.

6. Repeated positive blood cultures for the same organism separated by at least 24 hours, regardless of antibiotic treatment. Patients with repeated isolates on the first 24 hours will be included.

7. Uncontrolled focus of infection: e.g. an abscess that was not drained sufficiently; non-drained moderate to severe hydronephrosis in a patient with bacteremia of urinary source; deep seated intra-abdominal infections that were not drained properly.

8. Fever > 38.0C measured at least twice in the 48 h prior to recruitment; or > 38.5C once during the 48 h; or hypothermia <35.5C measured once during the 48 h.

9. Previous enrollment in this trial

10. Concurrent participation in another clinical trial

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
short-course	short-course antibiotic treatment	antibiotic treatment stopped on day 7 if the patient has been afebrile for 48 hours and clinically stable. Continued hospitalization will be left to the discretion of the treating physician. Antibiotics will be restarted if fever recurs in at least 2 consecutive measurements above 38 or in cases of clinically or microbiologically documented infections.
accepted prolonged antibiotic treatment	accepted prolonged antibiotic treatment	antibiotic treatment continued for 14 days according to accepted hospital local guidelines. Duration of hospital stay will also be left to the discretion of the treating physician. Type of empiric antibiotic treatment and later, specific antibiotic treatment, will be chosen by the treating physicians in consultation with the infectious diseases unit. The decision on timing of switch to oral antibiotic therapy will also be left to the discretion of the treating physician.

Primary Outcome Measures

Name	Time	Method
All -cause mortality	Until day 90 after randomization	All- cause mortality
composite of the following	Until day 90 after randomization	The primary outcome is a composite of the following outcome measures
Treatment Failure	Until day 90 after randomization	Failure including any of the following: 1. Relapse: a recurrent bacteraemia due to the same microorganism occurring from day of randomization and until day 9013; 2. Local suppurative complication that was not present at infection onset (e.g. renal abscess in pyelonephritis, empyema in pneumonia); 3. Distant complications of initial infection, defined by growth of the same bacteria as in the initial bacteremia
Hospital re-admissions or extended hospitalization	Until day 90 after randomization	We will define re-admission as a new hospitalization for any cause occurring more than14 days from start of appropriate antibiotic treatment. Patients hospitalized after day 14 (were never discharged or 7-day regimen who were readmitted between days 7-14) will be counted as failures for this outcome.; We will define re-admission as a new hospitalization for any cause occurring more than14 days from start of appropriate antibiotic treatment. Patients hospitalized after day 14 (were never discharged or 7-day regimen who were readmitted between days 7-14) will be counted as failures for this outcome.

Secondary Outcome Measures

Name	Time	Method
Adverse events	Until day 30 after randomization	* Any diarrhea; * Liver function test abnormalities, defined as elevated bilirubin x 1.5 of upper limit of normal or transaminases x 2.5 of upper limit of normal; * Antibiotic rash; * Acute kidney injury - defined according to RIFLE criteria as increased creatinine level x 1.5 from baseline or glomerular filtration rate (GFR) decrease \>25% or urine output of \<0.5 ml/kg/h for 6 hours22
Infection caused by other than gram-negative bacteremia	Until day 90 after randomization	Development of either clinically or microbiologically documented infection other than gram-negative bacteremia. We will use the 2008 CDC/NHSN surveillance definitions of health-care associated infections for bacterial infections
Number of hospital re-admissions	Until day 90 after randomization	Number of hospital re-admissions until day 90
Development of Antibiotic resistance	Until day 30 after randomization	Development of resistance, defined as clinical isolates resistant to antibiotics previously used in the bacteremia episode. Surveillance sampling will not be conducted.
Clostridium difficile associated diarrhea	Until day 30 after randomization	Clostridium difficile associated diarrhea
Carriage of carbapenem resistant Klebsiella pneumonia.	Until day 30 after randomization	Carriage of carbapenem resistant Klebsiella pneumonia (screened routinely)
Total in hospital days	Until day 90 after randomization.	Total in hospital days within 30 and 90 days
Total antibiotic days	Until day 30 after randomization	Total antibiotic days
Functional capacity and time to return to baseline activity	Until day 30 after randomization	Functional capacity and time to return to baseline activity

Trial Locations

Locations (3)

Rambam Health Care Center; 🇮🇱 Haifa, Israel

Rabin medical center, Beilinson Hospital; 🇮🇱 Petah Tikvah, Israel

Policlinico di Modena, Italy; 🇮🇹 Modena, Emilia Romagna, Italy