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RECRUITINGOBSERVATIONAL

Fulminant Severe CAP - an Observational Study

Fulminant Cases Among Severe Community-acquired Pneumonia - an Observational Retrospective Study

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

Severe community-acquired pneumonia (CAP) represents a major cause of hospital mortality. Among severe CAP cases, some exhibit a rapidly progressive evolution, leading to severe ARDS/acute respiratory failure and septic shock within hours to a few days. This type of pneumonia, known as "fulminant pneumonia," is characterized by its rapid onset and deterioration, often necessitating immediate medical intervention. Despite its severity, the true incidence and optimal treatment for fulminant pneumonia are not well understood. This knowledge gap is due to the lack of attention towards pneumonia as a potential time-dependent illness and the separation of overlapping clinical topics: severe pneumonia, ARDS, and sepsis. In clinical practice, pneumonia is the most frequent cause of both ARDS and sepsis. However, these conditions are often considered separately, combining ARDS and sepsis from various extra-pulmonary causes with those originating from pneumonia. The COVID-19 pandemic, with its vast number of severe CAP cases in a short period, has highlighted the existence of fulminant pneumonias, underscoring the need for further investigation. Recent randomized clinical trials (RCTs) and experiences from COVID-19 have suggested that early and prolonged corticosteroid administration can reduce mortality in patients with severe SARS-CoV-2 infection and severe CAP/ARDS of bacterial origin. The aim of this observational study is to analyze the rate of fulminant pneumonia and assess the impact of early corticosteroid treatment in a multicentric population of hospitalized patients with severe pneumonia.

Who May Be Eligible (Plain English)

Who May Qualify: severe community acquired pneumonia according to ATS/IDSA - Who Should NOT Join This Trial: incomplete outcome data \- Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: severe community acquired pneumonia according to ATS/IDSA - Exclusion Criteria: incomplete outcome data \-

Treatments Being Tested

OTHER

no intervention

observational study, the patients received corticosteroids according to the physician on duty

Locations (2)

Marco Confalonieri
Trieste, TS, Italy
SC Pneumologia, Azienda Sanitaria Universitaria Giuliano-Isontina
Trieste, Italy