Retrospective two-cohort study to determine the effect of chronic antihypertensive therapy on new onset atrial fibrillation and clinical outcomes in septic shock.
This will be a retrospective two-cohort study to determine the effect of chronic antihypertensive therapy on new onset atrial fibrillation and clinical outcomes in septic shock. The two cohorts will be septic shock patients that were: 1) not on either a chronic β-blocker or angiotensin-converting-enzyme inhibitor (ACE inhibitor) or 2) on a chronic β-blocker, on chronic ACE-Inhibitor, or on both chronic β-blocker and ACE-inhibitor
Study Type
OBSERVATIONAL
Enrollment
133
Rush Univeristy Medical Center
Chicago, Illinois, United States
Cumulative percent (%) of patients with new onset atrial fibrillation at 48 hours
New onset atrial fibrillation defined as atrial fibrillation not present on admission to MICU
Time frame: 48 hours
Heart rate > 100
Total number of times with heart rate greater than 100 in 48 hours.
Time frame: 48 hours
New onset of other arrhythmias
Total onset of other arrhythmias not present on admission. Examples include, ventricular fibrillation, ventricular tachycardia, heart blocks, etc
Time frame: 48 hours
Peak lactate
Peak lactate level during the first 48 hours of admission
Time frame: 48 hours
Duration of mechanical ventilation
Time frame: During admission
In hospital mortality
Time frame: During admission
28 day mortality
Time frame: 28 days after discharge
90 day mortality
Time frame: 90 days after discharge
New onset atrial fibrillation for patients on other antiarrhythmics
Antiarrhythmic agents that are used to suppress abnormal rhythms of the heart (cardiac arrhythmias), such as atrial fibrillation, atrial flutter, ventricular tachycardia, and ventricular fibrillation. Will include any single or combination of class I, II, III, IV antiarrhythmic agents
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Time frame: 24 and 48 hours
Cumulative percent (%) of patients with new onset atrial fibrillation at 24 hours
Time frame: 24 hours