Skip to content

Early Discontinuation of Antibiotic Therapy in Elderly Patients Hospitalized for a Viral Infection

Early Discontinuation of Antibiotic Therapy in Elderly Patients Hospitalized for a Viral Infection

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07030673
Acronym
ABUSIV
Enrollment
256
Registered
2025-06-22
Start date
2025-02-14
Completion date
2027-06-01
Last updated
2026-01-16

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

Conditions

Antibiotics Overuse, Elderly, PCR Multiplex, Viral Infections

Keywords

viral infections, elderly, antibiotics overuse, PCR multiplex

Brief summary

Among winter respiratory viruses, influenza is the most common and therefore responsible for the highest mortality, but parainfluenza and RSV viruses have an even higher risk of mortality (1.6 to 1.9 times), this toll being paid mainly by the elderly and co-morbid population. Futhermore, SARS-Cov2 will probably become endemic and/or epidemic with the same targets of fragile patients. These viral infections are serious, however a bacterial co-infection worsens the prognosis even more: excess risk of mortality = 2.6, 95% CI \[1.9-3.7\]. Although rare, these co-infections are the subject of a prescription of antibiotics in more than 50% of influenza infections or other serious viral infections. Mainly due to this excess risk of mortality associated with the difficulty of diagnosing these co-infections. Proper antibiotic use requires preventing this misuse and its harmful consequences in the short and long term at all costs. It is therefore imperative to have solid (grade A) evidence showing that antibiotic therapy in viral infections is not only futile but also potentially harmful.

Interventions

DRUGantibiotic withdrawal

stop antibiotics on viral or negative results

DRUGAntibiotics

standard of care Antibiotics are : Amoxicilline-acide clavulanique : 1g x3/j, 7j or Ceftriaxone : 1g/j, 7j or Pipéracilline-Tazobactam : 4g x3/j, 7j or Pristinamycine : 1g x 3/j, 7j

Sponsors

Centre Hospitalier Universitaire, Amiens
Lead SponsorOTHER
University Hospital, Rouen
CollaboratorOTHER
Centre Hospitalier de Beauvais
CollaboratorOTHER
University Hospital, Caen
CollaboratorOTHER
Hôpital Les Bateliers, CHU de Lille
CollaboratorUNKNOWN
Centre Hospitalier Roubaix
CollaboratorUNKNOWN
CH SOISSONS
CollaboratorUNKNOWN
Tourcoing Hospital
CollaboratorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

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

Inclusion criteria

* Patients ≥ 65 years affiliated to a social security scheme * Hospitalized for a lower respiratory infection defined as: * the presence of 2 of the following 4 signs: * hyperthermia \>38°C, * hyperleukocytosis ≥12000 or ≤4000, * purulent aspirations/sputum, * rales on pulmonary auscultation indicating parenchymal damage * associated with a pulmonary image (standard X-ray, CT scan or ultrasound) * Microbiological diagnostic sample taken within 48 hours * Informed consent of the patient or their representative

Exclusion criteria

* Hospitalization planned for \< 48 hours or transfer planned to another center within 7 days * Patient in septic shock, * Febrile aplasia * Absence of diagnostic microbiological sampling (\> 48 hours after admission) * Moribund patient, * Death expected within the week * Inhalation proven by endoscopy or eyewitness * Purulent pleurisy, lung abscess, or other concomitant bacterial infection requiring antibiotic therapy.

Design outcomes

Primary

MeasureTime frame
Number of days without antibioticsday 30

Secondary

MeasureTime frameDescription
number of side effects of antibioticsday 30
Mortality at M1day 30
martality at day 180day 180
Length of hospitalization in acute careday 30Length of hospitalization in acute care (days)

Countries

France

Contacts

CONTACTJean-Philippe LANOIX, Pr
lanoix.jean-philippe@chu-amiens.fr33+32668813

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026