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In the general population, increased WBCC and neutrophil count are widely used as markers for infection during inflammatory states 1. However, 32% of geriatric patients with an infection do not develop an increase in WBCC 2. The hypothesis is that with inflammation, geriatric patients have a misadapted response of the immune system (IS) 3.
Our recent retrospective study 4 has shown that total and differential WBCC were not correlated with infection in a geriatric hospitalized population. Therefore, WBCC does not seem to be a reliable marker for infection in geriatric hospitalized patients. The neutrophil/lymphocyte ratio, and CRP, seem to be better markers.
the aim of the study to investigate this hypothesis prospectively and assess the role of aging and chronic diseases (such as cardiovascular diseases (CVD) and risk factors (CVRF) 5, cytomegalovirus (CMV) infection 6, periodontitis 7, onychomycosis 8 ) in this process and assess the role of a geriatric assessment.
To assess the usefulness of WBCC in the diagnosis of infection in geriatric patients and to address the contribution of ongoing chronic co-morbidities and age to WBCC-kinetics during an acute inflammatory syndrome, young and geriatric hospitalized patients with an inflammatory syndrome with and without infection will be compared
Full description
Study design Observational prospective study
The subjects Number of subjects 200 subjects: Average value CRP: group 1: 55; group 2: 84 Average standard deviation: 70.52 Power 80%: 158 deelnemers Power 90%: 202 deelnemers alpha = 0.05 2-sample T-test.
Inclusion criteria
Acute inflammation is defined as a CRP ≥ 10 mg/l. We will include 2 groups of participants:
A) A group with an inflammatory syndrome and infection; infection being defined as:
B) A group with inflammatory syndrome and inflammatory diseases without infection: defined as:
Exclusion criteria Immunosuppressive therapy (NSAIDs, corticosteroids, chemotherapy, immunotherapy), active cancer, antibiotics before admission, hematological diseases
Replacement of subjects None.
Restrictions and prohibitions for the subjects None.
Procedures
A) Questionnaires:
taken at UZ Brussels
D) Follow up of bacterial and viral culture analyses
Observational data from bacterial and viral samples during hospitatalization :
E) Follow up of blood analyses:
Observational data from blood samples during hospitalization:
Flowchart Questionnaires, blood samples: conducted by Hanne Maes. Supervising MD: Dr. Nathalie Compté, UZ Brussels.
Randomisation/blinding Observational study, not applicable.
Prior and concomitant therapy All medication can be continued during this study.
Study analysis Statistical analysis the investigators will perform student t-tests or Mann-Whitney rank sum tests to compare geriatric/young patients with and without infection. To assess the contribution of age, comorbidities and geriatric syndrome in the kinetics of WBCC, the investigators will perform univariate and multivariate analyses.
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Inclusion criteria
Acute inflammation is defined as a CRP ≥ 10 mg/l. We will include 2 groups of participants:
A) A group with an inflammatory syndrome and infection; infection being defined as:
B) A group with inflammatory syndrome and inflammatory diseases without infection: defined as:
Exclusion criteria
Immunosuppressive therapy (NSAIDs, corticosteroids, chemotherapy, immunotherapy), active cancer, antibiotics before admission, hematological diseases
62 participants in 2 patient groups
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Central trial contact
Compté Nathalie, Dr, PhD
Data sourced from clinicaltrials.gov
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