Predicting Volume Response Study
Status: | Completed |
---|---|
Conditions: | Hospital |
Therapuetic Areas: | Other |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 4/2/2016 |
Start Date: | August 2011 |
End Date: | December 2013 |
Contact: | John J Gallagher, MSN, RN |
Email: | john.gallagher@uphs.upenn.edu |
Phone: | 215-459-2026 |
Change in Stroke Volume During Passive Leg Raise Predicts Volume Challenge Response as Measured by Arterial Pressure Cardiac Output Monitor.
The purpose of this study is to understand and document measurements in heart stroke volume
(the volume or amount of blood pumped per heart beat) and cardiac output (the volume or
amount of blood pumped by your heart per minute) during a passive leg raise maneuver
(elevation of the legs), and to determine if these measurements can predict changes in the
same as a result of fluid or blood product administration.
(the volume or amount of blood pumped per heart beat) and cardiac output (the volume or
amount of blood pumped by your heart per minute) during a passive leg raise maneuver
(elevation of the legs), and to determine if these measurements can predict changes in the
same as a result of fluid or blood product administration.
The administration of intravenous fluid and blood products for treatment of hypovolemia is
common in the ICU setting. Static resuscitation endpoints such as heart rate, blood
pressure, and CVP are frequently used to guide this therapy, despite compelling evidence
they are unreliable in predicting patient response to therapeutic volume administration or
as an endpoint for ongoing therapy. Dynamic parameters such as continuous stroke volume and
cardiac output (index) monitoring, along with pulse pressure and stroke volume variance
measures are more reliable in predicting and measuring response to fluid challenge and
therapeutic volume administration. The purpose of this study is to observe changes in stroke
volume (SV) and cardiac output (CO) during a passive leg raise maneuver (PLR) as a surrogate
to volume challenge, and to determine if these changes can predict changes in the same
parameters with fluid or blood product administration in surgical patients. The PLR maneuver
involves positioning the patient to the supine position and elevating the legs to 45
degrees. The PLR moves blood from the capacitance vessels of the legs to the heart,
potentially improving stroke volume (SV) and cardiac output (CO), without the administration
of intravenous fluids. PLR may predict whether SV or CO would improve with administration of
fluids, and guide decisions on whether fluid administration would be beneficial. Stroke
volume and cardiac output (index) will be calculated by a commercial pulse power arterial
pressure cardiac output system (LIDCORapid), using the patients' measured heart rate and
blood pressure imported from the bedside monitor. By using the combination of a reversible
volume challenge (PLR) and a minimally invasive monitoring system, it is hoped that a more
reliable method will emerge to both predict a response and guide therapeutic volume
administration, while reducing the risk associated with fluid volume overload.
common in the ICU setting. Static resuscitation endpoints such as heart rate, blood
pressure, and CVP are frequently used to guide this therapy, despite compelling evidence
they are unreliable in predicting patient response to therapeutic volume administration or
as an endpoint for ongoing therapy. Dynamic parameters such as continuous stroke volume and
cardiac output (index) monitoring, along with pulse pressure and stroke volume variance
measures are more reliable in predicting and measuring response to fluid challenge and
therapeutic volume administration. The purpose of this study is to observe changes in stroke
volume (SV) and cardiac output (CO) during a passive leg raise maneuver (PLR) as a surrogate
to volume challenge, and to determine if these changes can predict changes in the same
parameters with fluid or blood product administration in surgical patients. The PLR maneuver
involves positioning the patient to the supine position and elevating the legs to 45
degrees. The PLR moves blood from the capacitance vessels of the legs to the heart,
potentially improving stroke volume (SV) and cardiac output (CO), without the administration
of intravenous fluids. PLR may predict whether SV or CO would improve with administration of
fluids, and guide decisions on whether fluid administration would be beneficial. Stroke
volume and cardiac output (index) will be calculated by a commercial pulse power arterial
pressure cardiac output system (LIDCORapid), using the patients' measured heart rate and
blood pressure imported from the bedside monitor. By using the combination of a reversible
volume challenge (PLR) and a minimally invasive monitoring system, it is hoped that a more
reliable method will emerge to both predict a response and guide therapeutic volume
administration, while reducing the risk associated with fluid volume overload.
Inclusion Criteria:
- Patients 18 years or older admitted to the Surgical Intensive Care Unit, anticipated
to receive IV fluid boluses or blood products, with the presence of an arterial
pressure line.
Exclusion Criteria:
- patients under 18 years of age,
- pregnancy,
- prisoners,
- inability to lay in the supine position,
- conditions of the lower extremities,
- pelvis or spine that preclude elevation of the legs
We found this trial at
1
site
3400 Spruce St
Philadelphia, Pennsylvania 19104
Philadelphia, Pennsylvania 19104
(215) 662-4000
Hospital of the University of Pennsylvania The Hospital of the University of Pennsylvania (HUP) is...
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