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Prophylactic Antibiotics in Comatose Survivors of Out-of-hospital Cardiac Arrest

Prophylactic Versus Clinically-driven Antibiotics in Comatose Survivors of Out-of-hospital Cardiac Arrest

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02899507
Enrollment
60
Registered
2016-09-14
Start date
2013-09-30
Completion date
2015-04-30
Last updated
2016-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Out-of-hospital Cardiac Arrest

Keywords

Out-of-hospital cardiac arrest, Prophylactic antibiotics

Brief summary

The purpose of this study is to determine whether there is potential benefits of prophylactic antibiotic treatment in comatose survivors of out-of-hospital cardiac arrest (OHCA) treated in intensive care unit with therapeutic hypothermia.

Detailed description

Postresuscitation management of comatose survivors of out-of-hospital cardiac arrest (OHCA) significantly improved and bundle of care including therapeutic hypothermia, immediate coronary angiography, percutaneous coronary intervention (PCI) and contemporary intensive care nowadays leads to survival with good neurological recovery. Benefit of prophylactic antibiotics, which may suppress development of postresuscitation infection and especially early onset pneumonia and thereby decrease the severity of postresuscitation systemic inflammatory response, is controversial. Because of these uncertainties, the investigators performed a single-center randomized clinical trial comparing prophylactic versus clinically-driven administration of antibiotics in comatose survivors of OHCA. The investigators hypothesized that prophylactic antibiotics may decrease the severity of postresuscitation systemic inflammatory response by reducing the incidence of postresuscitation infection and especially pneumonia which was further addressed by repeat microbiological sampling.

Interventions

Patients without evidence of tracheobronchial aspiration were randomized to immediate prophylactic Amoxicillin-Clavulanic acid 1,2 gr/8h

Sponsors

University Medical Centre Ljubljana
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Female and male over 18 years old * Comatose survivors of out-of-hospital cardiac arrest treated in intensive care unit with therapeutic hypothermia

Exclusion criteria

* Suspected or confirmed pregnancy * Allergy to amoxicillin-clavulanic acid * Tracheobronchial aspiration * Antibiotic therapy before cardiac arrest * Need of antibiotics due to other causes * Candidates for immediate veno-arterial extracorporeal membrane oxygenation (VA ECMO) * Patients in whom no active treatment was decided on admission

Design outcomes

Primary

MeasureTime frameDescription
Value of C-reactive protein (CRP) at day threeThree days after admission to Intensive care unit (ICU)Expressed in milligram/litre (normal \<5 mg/L)

Secondary

MeasureTime frameDescription
Severity of systemic inflammatory response estimated by peak value of procalcitonin (PCT)First measurement at admission in hospital and afterwards in 24 hours intervals during stay in the intensive care unite (ICU) but not longer then first seven daysExpressed in microgram/litre (normal \<0.5 microgram/L)
Severity of systemic inflammatory response estimated by peak value of neutrophil Cluster of differentiation 64 (CD 64)First measurement at admission in hospital and afterwards in 24 hours intervals in the first three daysNeutrophil CD 64 expression was used as an index of sepsis with \>1.2 indicating greater likelihood of sepsis
Appearance of pneumonia on chest X rayChest X ray was taken on admission and afterwards on daily basis during the stay in the intensive care unite but not longer than first week
Incidence of positive blind mini bronchoalveolar lavage (Mini-BAL) on day 3Mini-BAL was performed on the third day after the sudden cardiac arrest
Severity of systemic inflammatory response estimated by peak white blood cell count (WBC)First measurement at admission in hospital and afterwards in 24 hours intervals during stay in the intensive care unite (ICU) but not longer then first seven daysExpressed in number of white blood cells x 109 per litre (L)
Duration of tracheal intubationFrom the day of admission until the extubation. This was always during the ICU stay- one monthDuration of intubation was expressed as days of intubation started with admission until the extubation. Because this is being done in intensive care unite, the time frame is duration of ICU stay
Duration of mechanical ventilationFrom the admission until spontaneous breathing . This was during ICU stay-one monthDuration of mechanical ventilation was expressed as days the patient needed the mechanical support for breathing regardless of mode of support
ICU stayFrom the admission until the patient was transferred to ward, usually less than one month
Survival with good neurological outcomeUp to six months after the eventGood neurological outcome was characterised using cerebral performance category (CPC) with 1-2 indicating good neurological recovery.
Incidence of positive hemoculturesFrom the admission until the patient was transferred to the ward. This was always during the ICU stay-one month

Countries

Slovenia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 11, 2026