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The COVID-19 pandemic has led to an increased incidence of ventilator-associated pneumonia (VAP) among critically ill patients. However, in a context of high prevalence of multidrug-resistant organisms (MDROs) there is a lack of direct comparison between the incidence of VAP in COVID-19 and non-COVID-19 cohorts.
The investigators conducted a prospective, single-center cohort study comparing COVID-19 patients admitted to the intensive care unit (ICU) of the Città della Salute e della Scienza University Hospital in Turin, Italy, between March 2020 and December 2021 (COVID-19 group), with a historical cohort of ICU-mixed patients admitted between June 2016 and March 2018 (NON-COVID-19 group).
The study aims to explore the occurrence and characteristics of ventilator-associated pneumonia (VAP) in critically ill patients during two distinct periods: the pre-pandemic era and the COVID-19 pandemic. VAP, a serious complication arising from invasive mechanical ventilation (IMV) lasting at least 48 hours, had a crude incidence of 5% to 40% before the COVID-19 pandemic, whereas COVID-19 patients experienced even higher rates, reaching 48-64%.
The COVID-19 pandemic triggered an unprecedented rise in ICU admissions due to severe acute respiratory syndrome caused by the SARS-CoV-2 virus, leading to a considerable number of patients requiring IMV. Mechanical ventilation is a known risk factor for VAP, and COVID-19 exacerbates this risk due to factors like disease-induced immunoparalysis, prolonged mechanical ventilation and sedation, and more frequent application of prone positioning.
Despite the widespread need for prolonged mechanical ventilation in COVID-19 patients, few studies have compared the impact of VAP between pre-pandemic and COVID-19 populations. Additionally, limited research exists on the risk factors for VAP development in COVID-19 patients and the use of scoring systems like SAPS and SOFA as prognostic factors in this specific context. Although the coVAPid study offered insights into VAP risk factors in COVID-19 patients compared to those with influenza, it inadequately addressed the prevalence of multidrug-resistant organisms (MDROs) in this population, particularly carbapenem-resistant Acinetobacter baumannii (CR-Ab). Hence, this study aims to bridge this knowledge gap by investigating VAP's impact in a setting characterized by a high incidence of multidrug resistance.
To achieve this, the study will take place at the Molinette Hospital of the "Città della Salute e della Scienza" University Hospital in Turin, Italy, over a six-year period, spanning from January 2016 to December 2022. This retrospective, observational, and monocentric study will focus on two distinct cohorts: the pre-pandemic cohort (NON-COVID-19) and the COVID-19 cohort.
Researchers will identify ventilator-associated pneumonia (VAP) episodes based on the current definitions provided by the European Center for Disease Prevention and Control (ECDC). Patients will be monitored until hospital discharge to assess outcomes, including ICU mortality, overall mortality, duration of ICU stay, and duration of hospitalization.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Non-COVID-19 cohort | Patients with Ventilator Acquired Pneumonia without COVID-19. The patients belonging to the NON-COVID cohort were admitted to three intensive care units at Molinette Hospital (Turin, Italy):
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| COVID-19 cohort | Patients with Ventilator Acquired Pneumonia with COVID-19. Confirmation of pneumonia was achieved by using the Reverse Transcriptase-Polymerase Chain Reaction (RT-PCR) technique on a sample collected from the lower respiratory tract. The COVID-19 cohort consists of patients admitted at the "Città della Salute e della Scienza" University Hospital (Turin, Italy) in two intensive care units at Molinette Hospital, dedicated to treating critically ill patients with COVID-19. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| COVID-19 | Other | The investigators stratified our population based on COVID-19 virus positivity to identify any risk factors in this population compared to the NON-COVID-19 population. |
| Measure | Description | Time Frame |
|---|---|---|
| Mortality | Mortality within the first 28 days from ICU admission | 28 days |
| Measure | Description | Time Frame |
|---|---|---|
| ICU mortality | Mortality during intensive care unit stay | From date of enrollment until the date of intensive care unit discharge, assessed up to 6 months |
| Hospital mortality | Mortality during hospital stay |
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Inclusion Criteria:
Exclusion Criteria:
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The study population consists of patients diagnosed with ventilator-acquired pneumonia admitted to the intensive care unit of the primary hospital "Molinette," Città della Salute e della Scienza, Turin, Italy.
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| Name | Affiliation | Role |
|---|---|---|
| Luca Brazzi | University of Torino | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| AOU Città della Salute e della Scienza di Torino | Torino | 10100 | Italy |
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| ID | Term |
|---|---|
| D007239 | Infections |
| D016638 | Critical Illness |
| D015163 | Superinfection |
| D009102 | Multiple Organ Failure |
| D053717 | Pneumonia, Ventilator-Associated |
| D012772 | Shock, Septic |
| ID | Term |
|---|---|
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D009894 | Opportunistic Infections |
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| From date of enrollment until the date of hospital discharge, assessed up to 6 months |
| Mechanical ventilation days | Days of mechanical ventilation length of stay | From date of enrollment until the date of intensive care unit discharge, assessed up to 6 months |
| Ventilator acquired pneumonia incidence | Incidence of ventilator acquired pneumonia | From date of enrollment until the date of intensive care unit discharge, assessed up to 6 months |
| Ventilator acquired pneumonia incidence | Incidence of ventilator acquired pneumonia | 28 days |
| Multidrug-resistant micro-organisms incidence | Incidence of Multidrug-resistant micro-organisms | From date of enrollment until the date of intensive care unit discharge, assessed up to 6 months |
| Difficult to treat pathogens incidence | Incidence of difficult to treat pathogens | From date of enrollment until the date of intensive care unit discharge, assessed up to 6 months |
| Hospital length of stay | Duration of hospital length of stay | From date of enrollment until the date of hospital discharge, assessed up to 6 months |
| Intensive care unit length of stay | Duration of intensive care unit length of stay | From date of enrollment until the date of intensive care unit discharge, assessed up to 6 months |
| D012769 | Shock |
| D000077299 | Healthcare-Associated Pneumonia |
| D003428 | Cross Infection |
| D011014 | Pneumonia |
| D012141 | Respiratory Tract Infections |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
| D007049 | Iatrogenic Disease |
| D018805 | Sepsis |
| D018746 | Systemic Inflammatory Response Syndrome |
| D007249 | Inflammation |