Accuracy of continuous non-invasive blood pressure monitoring Volume clamp method Sepsis Septic shock Hypotension ICU Sepsis Septic Shock Hypotension Blood Pressure Monitoring Arterial Line Catheterization Volume Clamp Method Non-Invasive Hemodynamic Monitoring Critical Care Medicine ICU Monitoring
Conditions
Interventions
Sponsors
No sponsor (Self funding)
Eligibility
Sex/Gender
All
Age
20 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Adult patients (more than or equal 20 years) 2. Diagnosed with sepsis or septic shock based on the Sepsis3 criteria within 24 hours of diagnosis 3. Requiring continuous blood pressure monitoring via an arterial line catheter.
Exclusion criteria
Exclusion criteria: 1. Body mass index (BMI) >= 40 kg/m2 or inability to fit the finger cuff 2. Significant motion artifacts due to conditions such as delirium or Parkinson's disease 3. Peripheral arterial occlusive disease, Raynaud phenomenon 4. severe peripheral edema (grade 3 or above) 5. Pregnancy 6. Inability to maintain non-invasive monitoring due to ongoing treatment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Mean Difference in Blood Pressure (MAP) Between VCM and ALC, Accuracy of Volume Clamp Method in BP Monitoring Baseline, 15 min, 30 min, 60 min, 120 min Systolic, Diastolic, and Mean Arterial Pressure recorded using Acumen IQ Finger Cuff and FloTrac Sensor,Accuracy of Volume Clamp Method in BP Monitoring Baseline, 15 min, 30 min, 60 min, 120 min Systolic, Diastolic, and Mean Arterial Pressure recorded using Acumen IQ Finger Cuff and FloTrac Sensor | — |
Secondary
| Measure | Time frame |
|---|---|
| BP Variability in Response to Fluid Bolus Before and after fluid bolus administration Systolic, Diastolic, and Mean Arterial Pressure recorded using Acumen IQ Finger Cuff and FloTrac Sensor | — |
Countries
Thailand
Contacts
Public ContactWeerapol Borhirunrat
Phramongklutklao hospital
Outcome results
None listed