No interventions
OtherNo intervention, retrospective observational study
NCT Number: NCT07770334
Procalcitonin is a well-known biomarker used to distinguish between bacterial and viral infections, assess a patient's risk category, and serve as a prognostic indicator. However, existing data are derived primarily from relatively young patients in intensive care units; there is a lack of information regarding the prognostic significance of procalcitonin in older patients hospitalized in internal medicine wards.
Trial opening soon.
Get Notified18 year and older
All sexes
Observational
Procalcitonin is a biomarker used to distinguish between bacterial and viral infections, as well as to determine a patient's risk category and serve as a prognostic indicator. Furthermore, monitoring procalcitonin levels and analysing their kinetics during hospitalization improves the management of patients with sepsis and informs decision-making regarding antibiotic use. A wide range of studies has evaluated the diagnostic yield of procalcitonin in sepsis patients, demonstrating its superiority over CRP. However, the studies examined intensive care patients, trauma patients, surgical patients, or relatively young patients (mean age 69). There is significant heterogeneity among the studies, and they do not reach a definitive conclusion: some show an association between high procalcitonin levels and mortality, while others indicate that procalcitonin lacks independent prognostic value. Consequently, there is a significant gap in existing knowledge regarding the value of procalcitonin in a "real-life" setting-specifically, among elderly patients (over age 70) hospitalized in internal medicine wards. The investigators will identify all patients who underwent procalcitonin testing from 2020 onwards and were hospitalized in internal medicine or geriatric wards. Subsequently, the investigators will review medical records and extract relevant data regarding their disease course and outcomes.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
No intervention, retrospective observational study
Time frame: 30 days
Evaluation of procalcitonin as a prognostic marker in patients hospitalized in the internal medicine and geriatric department by examining mortality during hospitalization, within 7 days and within 30 months.
Time frame: 30 days
Comparison of procalcitonin and CRP as predictors of length of hospital stay
Time frame: 30 days
need for vasopressors or mechanical ventilation, need for intensive care, need for invasive intervention
Contact information is provided by the study sponsor or research team.
Daniel Leshin Carmel Head of Infection Prevention and Control, MD
CONTACT
Pnina Nir
CONTACT
Barzilai Medical Center
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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