Ontology highlight
ABSTRACT: Objectives
To prospectively validate that the inability to decrease procalcitonin levels by more than 80% between baseline and day 4 is associated with increased 28-day all-cause mortality in a large sepsis patient population recruited across the United States.Design
Blinded, prospective multicenter observational clinical trial following an Food and Drug Administration-approved protocol.Setting
Thirteen U.S.-based emergency departments and ICUs.Patients
Consecutive patients meeting criteria for severe sepsis or septic shock who were admitted to the ICU from the emergency department, other wards, or directly from out of hospital were included.Interventions
Procalcitonin was measured daily over the first 5 days.Measurements and main results
The
SUBMITTER: Schuetz P
PROVIDER: S-EPMC5389588 | biostudies-literature | 2017 May
REPOSITORIES: biostudies-literature