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Antibiotic Therapy in Viral Airway Infections (ATHENIAN)

Primary Purpose

Infectious Disease, Influenza, Respiratory Syncytial Virus (RSV)

Status
Recruiting
Phase
Phase 4
Locations
Norway
Study Type
Interventional
Intervention
Stop antibiotic therapy
Sponsored by
University Hospital, Akershus
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Infectious Disease focused on measuring pragmatic trial, antibiotic stewardship, viral respiratory tract infection

Eligibility Criteria

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

Inclusion Criteria:

  • Hospitalized
  • Adults 18 year or older
  • Moderately severe disease (CRB65 ≤ 2 at time of inclusion)
  • Nasopharyngeal swab positive for influenza virus, parainfluenza virus, respiratory syncytial virus (RSV) or human metapneumovirus (hMPV)
  • On antibiotic therapy as instituted by the receiving physician from the emergency department
  • Signed informed consent must be obtained and documented according to ICH GCP, and national/local regulations.

Exclusion Criteria:

  • Requiring ICU admission at screening
  • Requiring high-flow oxygen therapy or non-invasive ventilation at screening
  • Signs of severe pneumonia (abscesses, massive pleural effusion, a well-defined lobar infiltrate on chest X-ray strongly suggestive of bacterial etiology)
  • Not immunocompetent (i.e. on active chemotherapy, corticosteroid therapy equaling ≥ 20 mg prednisolone daily for ≥ 4 weeks, chronic immunosuppression due to solid organ transplant)
  • SARS-CoV-2 positive
  • Bacteremia
  • Urine antigen test positive for legionella
  • Any other infection necessitating antibiotic treatment
  • Antibiotic use for assumed airway infection within the last 24 hours before admission to hospital

Sites / Locations

  • Haukeland University Hospital
  • Drammen Hospital, Vestre Viken Hospital Trust
  • Akershus University HospitalRecruiting
  • University Hospital of North Norway
  • St. Olavs hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention

Control

Arm Description

Stop antibiotic therapy as instituted by admitting physician

Continue antibiotic therapy at the discretion of the treating physician (no change in ongoing treatment)

Outcomes

Primary Outcome Measures

Early clinical response
Survival with symptom improvement without receipt of rescue antibacterial therapy

Secondary Outcome Measures

In-hospital mortality
Mortality during hospital admission
30-day mortality
Mortality at 30 days after hospital discharge
Duration of hospital admission
Duration of hospital admission
Antimicrobial days of therapy
Number of days on antibiotic therapy
Rescue antibiotic therapy during hospital admission
Rescue antibiotic therapy given to patients randomized to intervention
New antibiotic therapy for presumed airway infection
New antibiotic therapy instituted after hospital discharge
30-day readmission rate
Hospital readmissions up to 30 days after hospital discharge

Full Information

First Posted
September 7, 2021
Last Updated
August 16, 2023
Sponsor
University Hospital, Akershus
Collaborators
University of Oslo
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1. Study Identification

Unique Protocol Identification Number
NCT05045612
Brief Title
Antibiotic Therapy in Viral Airway Infections
Acronym
ATHENIAN
Official Title
Antibiotic Therapy in Viral Airway Infections: An Open Labeled Randomized Controlled Pragmatic Trial to Evaluate the Efficacy and Safety of Discontinuing Antibiotic Therapy in Adult Patients With Respiratory Viruses
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
January 13, 2022 (Actual)
Primary Completion Date
May 2025 (Anticipated)
Study Completion Date
November 2029 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital, Akershus
Collaborators
University of Oslo

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Antimicrobial resistance is one of the most urgent health threats of our time, and Norwegian hospitals were required to reduce the use of broad-spectrum antibiotics with 30% by the end of 2020. In the current proposal, the investigators aim to assess the efficacy and safety of early discontinuation of antibiotic therapy in adult patients infected with respiratory viruses. A general recommendation to treat all instances of community acquired pneumonia (CAP) patients with antibiotics leads to significant antibiotic overtreatment. In 2008, the US Food and Drug Administration approved the first multiplex polymerase chain reaction assay for the detection of multiple respiratory virus nucleic acids simultaneously. The wide availability of such nucleic acid amplification tests (NAAT) for rapid viral detection together with chest radiographs has the potential to define patients who can be managed without antibiotics. Akershus University Hospital is one of the largest hospitals in Norway, with a catchment area of more than 550,000 people. In 2012 to 2013, the majority of patients admitted to Akershus University Hospital with suspected CAP and a positive viral NAAT were treated with antibiotics, a prescription pattern representing antibiotic overtreatment. The investigators accordingly hypothesize that discontinuation of antibiotic therapy in patients with moderately severe disease and airway sample positive for respiratory viruses is safe and non-inferior to continuation of antibiotic therapy.
Detailed Description
In patients with positive airway sample for respiratory viruses, the investigators hypothesize that discontinuation of antibiotic therapy is safe and non-inferior to continuation of antibiotic therapy. More specifically, the investigators hypothesize that the early clinical response assessed at 120 hours after randomization, defined as survival with symptom improvement without receipt of rescue antibacterial therapy, will be similar between patients who discontinue and continue antibiotic therapy. Furthermore, the investigators hypothesize that discontinuation of antibiotic therapy is associated with similar mortality rates, duration of hospital admission and reduced number of defined daily doses of antibiotics. The primary aim is to assess whether discontinuation of antibiotic therapy in patients with positive airway sample for respiratory viruses is safe and associated with early clinical response assessed at 120 hours after randomization that is comparable to patients who continue antibiotic therapy. The secondary aims are to assess whether discontinuation of antibiotic therapy in patients with positive airway sample for respiratory viruses is associated comparable (1) mortality rates, (2) duration of hospital admission, (3) defined daily doses of antibiotic therapy. Specific objectives In patients with positive airway sample for respiratory viruses, assess the impact of discontinuing antibiotic therapy on early clinical response quantified as survival with symptom improvement without receipt of rescue antibacterial therapy. Early clinical response is defined as improvement of one or more levels relative to baseline in two or more symptoms of the investigator's assessment of symptoms of community-acquired bacterial pneumonia and no worsening of one or more levels in other symptoms.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infectious Disease, Influenza, Respiratory Syncytial Virus (RSV), Respiratory Tract Infections
Keywords
pragmatic trial, antibiotic stewardship, viral respiratory tract infection

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Two-arm, open label, pragmatic randomized controlled non-inferiority stop trial
Masking
None (Open Label)
Allocation
Randomized
Enrollment
380 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Experimental
Arm Description
Stop antibiotic therapy as instituted by admitting physician
Arm Title
Control
Arm Type
No Intervention
Arm Description
Continue antibiotic therapy at the discretion of the treating physician (no change in ongoing treatment)
Intervention Type
Other
Intervention Name(s)
Stop antibiotic therapy
Intervention Description
Stop antibiotic therapy instituted by the admitting physician
Primary Outcome Measure Information:
Title
Early clinical response
Description
Survival with symptom improvement without receipt of rescue antibacterial therapy
Time Frame
120 hours after randomization
Secondary Outcome Measure Information:
Title
In-hospital mortality
Description
Mortality during hospital admission
Time Frame
Untill hospital discharge (commonly 3-5 days)
Title
30-day mortality
Description
Mortality at 30 days after hospital discharge
Time Frame
30 days after hospital discharge
Title
Duration of hospital admission
Description
Duration of hospital admission
Time Frame
Untill hospital discharge (commonly 3-5 days)
Title
Antimicrobial days of therapy
Description
Number of days on antibiotic therapy
Time Frame
Untill hospital discharge (commonly 3-5 days)
Title
Rescue antibiotic therapy during hospital admission
Description
Rescue antibiotic therapy given to patients randomized to intervention
Time Frame
Untill hospital discharge (commonly 3-5 days)
Title
New antibiotic therapy for presumed airway infection
Description
New antibiotic therapy instituted after hospital discharge
Time Frame
30 days after hospital discharge
Title
30-day readmission rate
Description
Hospital readmissions up to 30 days after hospital discharge
Time Frame
30 days after hospital discharge

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Hospitalized Adults 18 year or older Moderately severe disease (CRB65 ≤ 2 at time of inclusion) Nasopharyngeal swab positive for influenza virus, parainfluenza virus, respiratory syncytial virus (RSV) or human metapneumovirus (hMPV) On antibiotic therapy as instituted by the receiving physician from the emergency department Signed informed consent must be obtained and documented according to ICH GCP, and national/local regulations. Exclusion Criteria: Requiring ICU admission at screening Requiring high-flow oxygen therapy or non-invasive ventilation at screening Signs of severe pneumonia (abscesses, massive pleural effusion, a well-defined lobar infiltrate on chest X-ray strongly suggestive of bacterial etiology) Not immunocompetent (i.e. on active chemotherapy, corticosteroid therapy equaling ≥ 20 mg prednisolone daily for ≥ 4 weeks, chronic immunosuppression due to solid organ transplant) SARS-CoV-2 positive Bacteremia Urine antigen test positive for legionella Any other infection necessitating antibiotic treatment Antibiotic use for assumed airway infection within the last 24 hours before admission to hospital Time from initiation of antibiotic therapy to screening >48 hours
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Magnus N Lyngbakken, MD PhD
Phone
+4793408837
Email
magnus.lyngbakken@medisin.uio.no
First Name & Middle Initial & Last Name or Official Title & Degree
Olav Dalgard, MD PhD
Phone
+4792616800
Email
olav.dalgard@medisin.uio.no
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Magnus N Lyngbakken, MD PhD
Organizational Affiliation
University Hospital, Akershus
Official's Role
Principal Investigator
Facility Information:
Facility Name
Haukeland University Hospital
City
Bergen
ZIP/Postal Code
5021
Country
Norway
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dagfinn L Markussen, MD
Phone
+4799270071
Email
dagfinn.lunde.markussen@helse-bergen.no
Facility Name
Drammen Hospital, Vestre Viken Hospital Trust
City
Drammen
ZIP/Postal Code
3004
Country
Norway
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Karl Erik Müller, MD PhD
Phone
+4797501475
Email
kamull@vestreviken.no
Facility Name
Akershus University Hospital
City
Lørenskog
ZIP/Postal Code
1478
Country
Norway
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Magnus N Lyngbakken, MD PhD
Phone
+4793408837
Email
magnus.lyngbakken@medisin.uio.no
Facility Name
University Hospital of North Norway
City
Tromsø
ZIP/Postal Code
9038
Country
Norway
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Vegard Skogen, MD PhD
Phone
+4791364541
Email
vegard.skogen@unn.no
Facility Name
St. Olavs hospital
City
Trondheim
ZIP/Postal Code
7006
Country
Norway
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jan Kristian Damås, MD PhD
Phone
+4791112046
Email
jan.k.damas@ntnu.no

12. IPD Sharing Statement

Plan to Share IPD
No

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Antibiotic Therapy in Viral Airway Infections

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