Hemodynamic Response During Goal Directed Fluid Therapy in the OR

Medtronic - MITG18 enrolled

Overview

The purpose of this study is to retrospectively evaluate the hemodynamic response to goal directed fluid therapy fluid during open abdominal surgery where goal directed fluid therapy is a standard of care after establishing a pre-incision baseline response to fluids.

Electronic and annotated observation data to support an algorithm library

Study Type

INTERVENTIONAL

Allocation

Purpose

OTHER

Masking

NONE

Enrollment

Conditions

Hemodynamic Instability

Interventions

Initial bolus pre-incisionPROCEDURE

Measured hemodynamic response to pre-incision bolus

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. Adults ≥18 years booked for an open abdominal procedure 2. American Society of Anaesthesiologists (ASA) Physical Status 1 - 3 3. Expected duration of surgical procedure to be ≥ 2 hours 4. Standard of care monitoring to include cardiac output Exclusion Criteria: 1. Open chest surgical procedure expected 2. Cardiac arrhythmia such as atrial fibrillation. 3. Right Ventricular Failure 4. Aortic regurgitation

Locations (1)

Duke University Medical Center

Durham, North Carolina, United States

Outcomes

Primary Outcomes

Dynamic Hemodynamic Response to Fluid Resuscitation

Physiological parameters compared before and after fluid bolus for fluid resuscitation.

Time frame: Up to 6 hours but not to exceed duration of surgical procedure

Data from ClinicalTrials.gov

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