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| Name | Class |
|---|---|
| Ullevaal University Hospital | OTHER |
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Norwegian guidelines for empirical antibiotic therapy in suspected community acquired sepsis recommend the combination of narrow spectrum betalactam and aminoglycoside as the first choice, but broad spectrum betalactams are considered equally appropriate, effective, and safe. However, fear of renal complications due to gentamicin and concern for lacking evidence for efficiency commonly leads to the use of broad spectrum betalactam therapy, a larger driver of antibiotic resistance.
In patients with suspected community acquired sepsis, the investigators hypothesize that empirical combination therapy with narrow spectrum betalactams and aminoglycosides is safe and non-inferior to empirical therapy with broad spectrum betalactams. More specifically, the investigators hypothesize that the proportion of patients with acute kidney injury or death will be similar between these two treatment groups. Furthermore, the investigators hypothesize that the aminoglycoside-based regimen has lesser impact on the gut microbiome. Antimicrobial resistance is one of the most urgent health threats of our time, and Norwegian hospitals were required but failed to reduce the use of broad-spectrum antibiotics with 30% by the end of 2020. In this context, novel initiatives aiming at reducing use of antibiotics are direly needed.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Gentamicin + narrow spectrum betalactam | Active Comparator | Empirical therapy for suspected community-acquired sepsis with gentamicin + narrow spectrum betalactam (either one of penicillin, ampicillin, or cloxacillin) |
|
| Cefotaxime or piperacillin-tazobactam | Active Comparator | Empirical therapy for suspected community-acquired sepsis with broad spectrum betalactam (either one of cefotaxime or piperacillin-tazobactam) |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Gentamicin + narrow spectrum betalactam | Drug | Empirical therapy for suspected community-acquired sepsis with gentamicin + narrow spectrum betalactam (either one of penicillin, ampicillin, or cloxacillin) |
| Measure | Description | Time Frame |
|---|---|---|
| 30-day mortality | All-cause mortality up to 30 days after randomization | Up to 30 days after randomization |
| 30-day acute kidney injury | Any acute kidney injury up to 30 days after randomization | Up to 30 days after randomization |
| Measure | Description | Time Frame |
|---|---|---|
| In-hospital mortality | All-cause mortality during index hospitalization | During index hospitalization (commonly up to 30 days) |
| Duration of hospital stay | Duration of index hospitalization (days) |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Magnus N Lyngbakken, MD PhD | Contact | +4793408837 | magnus.lyngbakken@medisin.uio.no | |
| Kristian Tonby, MD PhD | Contact | +4741550565 | kristian.tonby@medisin.uio.no |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Haukeland University Hospital | Not yet recruiting | Bergen | Bergen | Norway |
The dataset used in this study is not publicly available, as the Data Protection Authority approval and patient consent do not allow for such publication. The study group welcomes initiatives for cooperation and data access may be granted upon application.
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| ID | Term |
|---|---|
| D018805 | Sepsis |
| ID | Term |
|---|---|
| D007239 | Infections |
| D018746 | Systemic Inflammatory Response Syndrome |
| D007249 | Inflammation |
| D010335 | Pathologic Processes |
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| ID | Term |
|---|---|
| D005839 | Gentamicins |
| D002439 | Cefotaxime |
| D000077725 | Piperacillin, Tazobactam Drug Combination |
| ID | Term |
|---|---|
| D000617 | Aminoglycosides |
| D006027 | Glycosides |
| D002241 | Carbohydrates |
| D002505 | Cephacetrile |
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| Cefotaxime | Drug | Empirical therapy for suspected community-acquired sepsis with cefotaxime |
|
| Piperacillin-tazobactam | Drug | Empirical therapy for suspected community-acquired sepsis with piperacillin-tazobactam |
|
| During index hospitalization (commonly up to 30 days) |
| Duration of intensive care stay | Duration of stay in intensive care unit (days) | During index hospitalization (commonly up to 30 days) |
| Duration of ventilator therapy | Duration of therapy with invasive mechanical ventilation (days) | During index hospitalization (commonly up to 30 days) |
| Duration of vasopressor therapy | Duration of therapy with vasoactive (vasopressor) (days) | During index hospitalization (commonly up to 30 days) |
| Hospital readmissions | Readmission after discharge from index hospitalization | Up to 30 days after discharge from index hospitalization |
| Post-discharge mortality | All-cause mortality after discharge from index hospitalization | Up to 30 days after discharge from index hospitalization |
| Duration of antibiotic treatment | Duration of antibiotic therapy during index hospitalization (days of therapy, DOT) | During index hospitalization (commonly up to 30 days) |
| Lovisenberg Diakonal Hospital | Not yet recruiting | Oslo | Oslo | Norway |
|
| St. Olav's Hospital | Not yet recruiting | Trondheim | Trondheim | Norway |
|
| Akershus University Hospital | Recruiting | Lørenskog | 1478 | Norway |
|
| Oslo University Hospital Ullevål | Recruiting | Oslo | 0450 | Norway |
|
| D013568 |
| Pathological Conditions, Signs and Symptoms |
| D002511 |
| Cephalosporins |
| D047090 | beta-Lactams |
| D007769 | Lactams |
| D000577 | Amides |
| D009930 | Organic Chemicals |
| D013843 | Thiazines |
| D013457 | Sulfur Compounds |
| D006574 | Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |
| D006571 | Heterocyclic Compounds |
| D000078142 | Tazobactam |
| D010397 | Penicillanic Acid |
| D010406 | Penicillins |
| D010878 | Piperacillin |
| D000667 | Ampicillin |
| D010400 | Penicillin G |
| D013450 | Sulfones |
| D004338 | Drug Combinations |
| D004364 | Pharmaceutical Preparations |