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Epidemiology of Post-influenza Bacterial Pneumonia Due to a Panton-Valentine Leukocidin Positive Staphylococcus Aureus

Epidemiology of Post-influenza Bacterial Pneumonia Due to a Panton-Valentine Leukocidin Positive Staphylococcus Aureus

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03367624
Acronym
FLUVALENTINE
Enrollment
35
Registered
2017-12-11
Start date
2017-10-01
Completion date
2018-03-31
Last updated
2017-12-11

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

Conditions

Influenza, PV Leukocidin, Staphylococcus Aureus Pneumonia

Keywords

influenza, Staphylococcus Aureus, Pneumonia, PV leukocidin, ICU

Brief summary

Secondary bacterial influenza pneumonia caused by Panton-Valentine Leukocidin Positive Staphylococcus aureus is a rare complication but with poor prognosis. This pathology seems to affect young patients (20-40 years) without any medical history. Since the influenza pandemic of 2009, this complication is more and more mentioned, sought and diagnosed. However, the literature is poor, consisting of case reports, experimental studies on murine models, and low-power studies. The main objective is to evaluate the mortality in intensive care units of patients post-influenza bacterial pneumonia due to a Panton-Valentine Leukocidin positive Staphylococcus aureus

Interventions

None listed

Sponsors

Central Hospital, Nancy, France
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

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

Inclusion criteria

* Patient treated for post-influenza bacterial pneumonia due to a Panton-Valentine Leukocidin positive Staphylococcus aureus in intensive care unit

Exclusion criteria

* Minor patient * Patient under protective measurement * Absence of bacteriological and / or virological documentation

Design outcomes

Primary

MeasureTime frameDescription
Number of dead patientsDuring Length of stay in intensive care unit (an average of 2 weeks)All cause of mortality

Secondary

MeasureTime frameDescription
Clinical data in the initial phase relating to chillsDuring Length of stay in intensive care unit (an average of 2 weeks)chills
Demographic data relating to ageBaselineage
Demographic data relating to sexBaselinesex
Respiratory failureBaselinePaO2/iFO2 value
Demographic data relating to immunosuppressionBaselineAmount of polynuclear neutrophils (G/L)
risk factors for methicillin-resistant Staphylococcus aureusBaselinehospitalization
Clinical data relating to pre-admission antibioticsBaselinetype of antibiotic prescribed
Clinical data in the initial phase relating to SAPS 2 scoreBaselineSimplified acute Physiology score (SAPS2) score between 0 and 163 and a predicted mortality between 0% and 100%
Clinical data in the initial phase relating to SOFA admissionBaselineSequential Organ Failure Assessment (SOFA)
Clinical data in the initial phase relating to neutropeniaDuring Length of stay in intensive care unit (an average of 2 weeks)neutropenia
Clinical data in the initial phase relating to metabolic acidosisDuring Length of stay in intensive care unit (an average of 2 weeks)metabolic acidosis
Clinical data in the initial phase relating to oxygen dependenceDuring Length of stay in intensive care unit (an average of 2 weeks)oxygen dependence
Clinical data in the initial phase relating to headhacheDuring Length of stay in intensive care unit (an average of 2 weeks)headache
Clinical data in the initial phase relating to productive coughDuring Length of stay in intensive care unit (an average of 2 weeks)productive cough
Clinical data in the initial phase relating to dyspnoeaDuring Length of stay in intensive care unit (an average of 2 weeks)dyspnoea
Clinical data in the initial phase relating to acute respiratory failureDuring Length of stay in intensive care unit (an average of 2 weeks)acute respiratory failure
Clinical data in the initial phase relating to hyperthermiaDuring Length of stay in intensive care unit (an average of 2 weeks)hyperthermia
Clinical data in the initial phase relating to uni - or multi - lobar infiltration on chest X - ray or CT scanDuring Length of stay in intensive care unit (an average of 2 weeks)uni - or multi - lobar infiltration on chest X - ray or CT scan
Clinical data in the initial phase relating to pleural effusionDuring Length of stay in intensive care unit (an average of 2 weeks)pleural effusion
Clinical data in the initial phaseDuring Length of stay in intensive care unit (an average of 2 weeks)necrotizing pneumonitis
Clinical data in the initial phase relating to renal failureDuring Length of stay in intensive care unit (an average of 2 weeks)renal failure according to KDIGO classification
Prognostic factors for this pathologyDuring Length of stay in intensive care unit (an average of 2 weeks)Time to diagnosis of influenza infection and Panton-Valentine Leukocidin Positive Staphylococcus aureus Haemoptysis, leukopenia, thrombocytopenia, acute respiratory distress syndrome (ARDS), PaO2 / Fi02, inotropic support
ComplicationsDuring Length of stay in intensive care unit (an average of 2 weeks)Complications related to Septic shock ARDS: according to Berlin 2009 classification Extra corporeal vein-venous or veino-arterial oxygenation membrane (ECMO VV or ECMO VA) Ischemic limb Pneumothorax Acute renal failure according to Kdigo classification Disseminated intravascular coagulation (DIC) (2) Cardiogenic shock / cardiogenic pulmonary acute edema Multi visceral failure syndrome (3) Use of surgery: abscess drainage, lobectomy, amputation, laparotomy and colonic resection ...
Collection of infectious samplesDuring Length of stay in intensive care unit (an average of 2 weeks)Bacteriological, Parasitological, Virological
Probabilistic antibiotherapyDuring Length of stay in intensive care unit (an average of 2 weeks)Collection of probabilistic antibiotherapy
Prescribed antibiotic therapyDuring Length of stay in intensive care unit (an average of 2 weeks)Collection of Prescribed antibiotic therapy
Collection of the date of introduction of adapted antibiotic therapyDuring Length of stay in intensive care unit (an average of 2 weeks)Collection of the date of introduction of adapted antibiotic therapy
Number of patients with Influenza type ADuring Length of stay in intensive care unit (an average of 2 weeks)Number of patients with Influenza type A
Number of patients with Influenza type BDuring Length of stay in intensive care unit (an average of 2 weeks)Number of patients with Influenza type B
Date of initiation of anti-viral treatment in relation to the onset of symptoms and duration of anti-viral treatmentDuring Length of stay in intensive care unit (an average of 2 weeks)Date of initiation of anti-viral treatment in relation to the onset of symptoms and duration of anti-viral treatment
Dosage of antiviral treatmentDuring Length of stay in intensive care unit (an average of 2 weeks)Dosage of antiviral treatment
Number of serious influenza infections per year and per center with early and late deathsDuring Length of stay in intensive care unit (an average of 2 weeks)Mortality caused by serious inflenza infections
Clinical data in the initial phase relating to hemoptysisDuring Length of stay in intensive care unit (an average of 2 weeks)hemoptysis

Countries

France

Outcome results

None listed

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