Monitoring of Immunity Markers in Intensive Care Patients and Link with Recurrence and Relapse of Ventilator-associated Pneumonia
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Pneumonia, Ventilator-Associated
- Sponsor
- Centre Hospitalier Intercommunal Aix-Pertuis
- Enrollment
- 40
- Locations
- 1
- Primary Endpoint
- Occurrence of a VAP recurrence/relapse
- Status
- Recruiting
- Last Updated
- last year
Overview
Brief Summary
The goal of this observational study is to show the direct correlation between the occurrence of recurrence of VAP and postagressive immunoparalysis, monitored by HLA-DR rate below litterature-acknowledged threshold, in a well conducted antibiotherapy context, in patient admitted in the Intensive Care Unit.
The main questions it aims to answer are:
- evaluation of the association between death and persistence of immunoplegia using HLA-DR monitoring
- search an association between immunoplegia depth and severity of the initial state of shock
- search an association between immunoplegia depth and viral reactivation
- compare association of immunoplegia duration and HLA-DR nadir and VAP occurrence Blood samples will be taken from participants to HLA-DR dosage, at the time of inclusion and once a week then.
Detailed Description
The occurrence of ICU-acquired infections in patients admitted to the intensive care unit (ICU) results in increased morbidity and mortality, increased length of stay in the ICU, and also clearly increased healthcare costs. The incidence of these infections fluctuates between 15% and 40%, depending on the study. A major problem in the ICU is the recurrence and relapse of ventilator-associated pneumonia (VAP), with increased exposure to antibiotics and a probable increase in average length of stay. One of the possible hypothesis that could explain relapses/recurrences of VAP is incorrect conducted antibiotherapy. To prevent this, in the unit, we currently perform antibiotics pharmacological assays and adapt them to the antibiogram. Another possible explanation to treatment failure could be patients' postagressive immunoparalysis. It has clearly been demonstrated that postagressive immunoparalysis is a predisposing state to healthcare related infections. Some markers can be used to monitor this immunoplegia state. Several studies have shown that low HLA-DR expression and reduced CD16 expression (polymorphonuclear neutrophils percentage) is associated with increased susceptibility to develop infections in the ICU. Immunity monitoring could be an interesting tool to identify populations most at risk of developing healthcare-associated infections after a state of shock, and could become an interesting line of thinking for the use of immunomodulatory therapies. To best evaluate these therapies and find a place for them in the current arsenal, it is essential to integrate them into daily practice by linking them to a significant clinical event, such as recurrent healthcare-associated infections, despite properly conducted antibiotic treatment.
Investigators
Laurent LEFEBVRE
Principal investigator
Centre Hospitalier Intercommunal Aix-Pertuis
Eligibility Criteria
Inclusion Criteria
- •Patient over 18 years old
- •Patient admitted in the Intensive Care Unit of the CHIAP
- •Patient under mechanical ventilation
- •Patient with infectious pneumonia
- •Informed Consent Form (ICF) obtained from the patient or emergency ICF obtained from close relatives
- •Patient beneficiary of French social security, whatever the regime
Exclusion Criteria
- •Patient under 18 years old
- •Patient with severe neutropenia (neutrophils \< 0.5 G/L)
- •Patient under immunosuppressive treatment
- •Use of corticosteroids (intravenous or oral) prior to ICU admission
- •Use of therapeutic antibodies
- •Onco-hematological disease (e.g. lymphoma, leukemia...) under treatment or treated in the 5 years prior to inclusion
- •End of chemotherapy 6 months prior to inclusion
- •Patients with innate or acquired immune deficiency (e.g., severe combined immunodeficiency, HIV or AIDS, at any stage)
- •Patients with a decision to limit or discontinue active therapies, at the time of inclusion
- •Patients with an estimated ICU stay of less than 48 hours
Outcomes
Primary Outcomes
Occurrence of a VAP recurrence/relapse
Time Frame: From date of hospital admission until the date of the end of hospitalization or date of death from any cause, whichever came first, assessed up to 100 months
Number of occurrence of a VAP recurrence/relapse
Secondary Outcomes
- Viral reactivation(From date of hospital admission until the date of the end of hospitalization or date of death from any cause, whichever came first, assessed up to 100 months)
- Association between immunoparalysis depth and state of shock severity within the first 24 hours(First 24 hours)
- Persistence of immunoparalysis during hospitalization and care-related infections(From date of hospital admission until the date of the end of hospitalization or date of death from any cause, whichever came first, assessed up to 100 months)
- HLA-DR nadir and link with care-related infections(From date of hospital admission until the date of the end of hospitalization or date of death from any cause, whichever came first, assessed up to 100 months)