PICS: Subtitle Cardiac Dysfunction in Older Sepsis Survivors
common.study.values.description
“PICS: Subtitle Cardiac Dysfunction in Older Sepsis Survivors”
The purpose of this study is to define the natural history and causes of chronic critical illness (CCI) in surgical intensive care patients who have had sepsis. The investigator also wants to define the long-term physical and cognitive outcomes of this disease. The investigator will be looking at many clinical variables to try to define CCI.
common.study.values.location
participant.ui.study.affiliations-map.online-study.header-virtual
participant.ui.study.affiliations-map.online-study.text
common.study.values.methods
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Blood collection
Blood will be collected from patient at baseline, day 1, day 4, day 7 and weekly until week 6 as long as the patient is still hospitalized. Blood will also be collected at the one year appointment.
Urine collection
Urine will be collected from patient at baseline, day 1, day 4, day 7 and weekly until week 6 as long as the patient is still hospitalized. Urine will also be collected at the one year appointment.
Bioimpedance Analysis
The bioimpedance analysis will be performed at baseline, day 14 or discharge from hospitalization, month 3, month 6, and month 12.
Cognitive Function Tests
Cognitive function tests will be administered at 3, 6 and 12 months.
Quality-of-life Questionnaires
Quality-of-life questionnaires will be administered at baseline, 3, 6 and 12 months.
Physical Function Tests
Physical function tests will be administered at baseline, day 14 or discharge from hospital 3, 6 and 12 months.
Blood Collection
The healthy volunteer participants will donate a blood sample. These controls will allow the investigators to determine if the values obtained are accurate, reliable, and repeatable.
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participant.views.study.view.scientific-title
Persistent Inflammation, Immunosuppression and Catabolism Syndrome (PICS): A New Horizon for Surgical Critical Care Subtitle: Cardiac Dysfunction in Older Sepsis Survivors
common.study.values.clinical-trial-id
NCT02276417
participant.views.study.view.id
vbmEAb
