Summary
The goal of the observational APS phenotyping study is to better understand risk factors, potential biomarkers, length and severity of illness, and recovery for adults with ARDS, pneumonia, and/ or sepsis. This study will also generate a biobank of specimens collected from these patients that will be available to investigators for future studies of ARDS, sepsis, and/or pneumonia.
Official Title
The ARDS, Pneumonia, and Sepsis (APS) Consortium: A Prospective Observational Study to Evaluate Phenotypes
Details
The APS phenotyping study will enroll hospitalized adult patients ≥18 years old who have or are at risk of developing ARDS, sepsis, or pneumonia. Participation in this study will involve collection of clinical data, completing questionnaires, and collection of samples such as blood, urine, and stool. Participants who are mechanically ventilated will also provide samples from their respiratory track. Data and samples will be collected both during and after hospitalization. Analyses to understand the mechanisms underlying ARDS, pneumonia, and sepsis will be conducted, with goals including the classification of patients with ARDS, pneumonia, and sepsis into biologically based phenotype categories and identifying new targets for future therapeutic trials.
Keywords
ARDS, Sepsis, Pneumonia, acute respiratory distress syndrome, phenotype, endotype, critical illness, Respiratory Distress Syndrome, Blood Specimen Collection, Urine Specimen Collection, Surveys and Questionnaires, Hand Strength, Muscle Strength, Blood collection, Urine Collection, Nasal, oral, and rectal swabs, Stool collection, Heat Moisture Exchange Filter collection, Non-bronchoscopic bronchoalveolar lavage (NBBAL), Short physical performance battery, Hand grip strength, CNS Vital Signs, Muscle Ultrasound, Spirometry, Lung Diffusion Testing (DLCO), Chest CT Scan, full study protocol - written informed consent, alteration study protocol - alteration of informed consent