Shock
Conditions
Brief summary
To conduct a multicenter observational cohort study to determine the variability in fluid resuscitation in shock in a broad range of areas in hospitals and treatment areas.
Interventions
OTHERFluids
Fluids Administered in Shock
Sponsors
Montefiore Medical Center
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Age ≥ 18 years admitted to the participating hospital. * Patients in the emergency department, intensive care unit, PACU, or any hospital floor. For patients not in the ICU, there must be plans to transfer to an intensive care unit when an ICU bed is available for patient. * Patients with shock as defined by: * Need for vasopressor (dopamine, norepinephrine, or epinephrine at any dose) to keep MAP \> 65 mmHg Or * Systolic BP \< 90 mmHg
Exclusion criteria
* Patients previously enrolled into this study. * Patients who were in the operating room at time of shock and fluid bolus. * Patients admitted to an ICU after cardiac surgery Patients with primarily cardiogenic shock as etiology for their shock * Patients transferred from another hospital or emergency room to the study hospital.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Method used to guide volume resuscitation | 7 days | Characterize the method used to guide volume resuscitation and vasopressor use in patients with shock |
Countries
United States
Outcome results
None listed