Predicting Fluid Responsiveness Using Transiently Increased Intrathoracic Pressure in Mechanically Ventilated Patients
| Status: | Recruiting |
|---|---|
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 3/23/2019 |
| Start Date: | December 27, 2017 |
| End Date: | June 30, 2019 |
| Contact: | Pierce Stewart, DO |
| Email: | epstewart@ucdavis.edu |
| Phone: | (916) 734-8230 |
The goal of this study is to identify in patients requiring active fluid resuscitation and
mechanical ventilation for circulatory shock, can a controlled increase in intrathoracic
pressure (either by positive-end expiratory pressure (PEEP) or tidal volume (TV)) predict
responsiveness to additional fluid resuscitation.
We hypothesize that a temporary, physiologically-safe increase in positive-end expiratory
pressure (PEEP) and/or a temporary increase in tidal volume (from 6 cc/kg predicted body
weight (PBW) to 8 cc/kg PBW) in patients requiring invasive mechanical ventilation will
predict fluid responsiveness based upon an assessment of the change in pulse pressure and
stroke volume variation.
mechanical ventilation for circulatory shock, can a controlled increase in intrathoracic
pressure (either by positive-end expiratory pressure (PEEP) or tidal volume (TV)) predict
responsiveness to additional fluid resuscitation.
We hypothesize that a temporary, physiologically-safe increase in positive-end expiratory
pressure (PEEP) and/or a temporary increase in tidal volume (from 6 cc/kg predicted body
weight (PBW) to 8 cc/kg PBW) in patients requiring invasive mechanical ventilation will
predict fluid responsiveness based upon an assessment of the change in pulse pressure and
stroke volume variation.
Once an eligible subject is identified and written or telephone consent is obtained from the
patient or surrogate as appropriate, we will record demographic data and clinical information
including age, sex, height, actual body weight, predicted body weight (PBW), APACHE II on
admission, primary diagnosis, reason for ICU admission, and dose of vasopressors.
Patients will be intubated and on assist-control volume ventilation receiving low tidal
volumes. Sedation will be titrated per current MICU protocol to minimize patient discomfort
and minimizing ventilator dyssynchrony. In keeping with standard practice, the dose of
vasoactive medications will be kept constant during the intervention period. The standard
practice is to titrate vasopressor therapy every five minutes, so keeping vasoactive
medications constant for sixty seconds is in keeping with the standard of care. All subjects
will be in an ICU setting and monitored per standard of care (vital signs, telemetry,
ventilator data) by a respiratory therapist, pulmonary and critical care fellow or faculty
member, and critical care nurse at the bedside throughout the entire intervention.
A point of care (POC) echocardiogram will be performed by the investigator performing the
intervention in order to measure the stroke volume index (surrogate for cardiac output).
Subjects will be randomized to either undergo the PEEP challenge or tidal volume challenge
first. After the initial challenge, subjects will cross over to whichever challenge has not
yet been performed.
The simple changes to the ventilator we are proposing to use as challenges in this study are
done frequently and routinely in the ICU with or without the supervision of a physician, but
we will have a physician present throughout the entire proposed intervention. For the
subjects undergoing PEEP challenge first, we will do the following:
1. POC echocardiogram performed to measure SVI
2. The tidal volume will be set to 6 mL/kg PBW and the patients will be monitored for 5
minutes for any variability in vital parameters. The subject's ventilatory parameters,
vitals, hemodynamics, and oxygenation will be recorded on initial ventilator settings.
3. PEEP challenge - PEEP will be increased by 50% for 60 seconds. The subject's ventilatory
parameters, vitals, hemodynamics, and oxygenation will be recorded after 60 seconds.
4. PEEP returned to initial settings.
5. 2 minute washout period to prepare for tidal volume challenge.
6. Tidal volume challenge - tidal volume raised to 8 cc/kg PBW for 60 seconds. The
subject's ventilatory parameters, vitals, hemodynamics, and oxygenation will be recorded
will be recorded after 60 seconds.
7. Subjects ventilator settings returned to initial settings x 2 minutes.
8. 500 cc crystalloid fluid bolus of the ICU team's choosing is then administered to the
patient. The subject's ventilatory parameters, vitals, hemodynamics, and oxygenation
will be measured.
9. POC echocardiogram performed to measure SVI and determine if the subject is a fluid
responder or non-responder.
The procedure for those randomized into the tidal volume challenge first will be similar, but
the tidal volume challenge (e, above), rather than the PEEP challenge (b, above), will be
performed first.
In the management of a critically ill patient in circulatory shock, physicians encounter the
question of whether to administer fluid to the patient or not several times during the course
of the patient's stay in the ICU. To ensure that our study is generalizable and applicable,
we will perform the above protocol up to three times per subject. This is similar to previous
studies using changes in intrathoracic pressure to predict fluid responsiveness.
Additionally, we will have a larger number of interventions in order to better show a clear
difference statistically.
patient or surrogate as appropriate, we will record demographic data and clinical information
including age, sex, height, actual body weight, predicted body weight (PBW), APACHE II on
admission, primary diagnosis, reason for ICU admission, and dose of vasopressors.
Patients will be intubated and on assist-control volume ventilation receiving low tidal
volumes. Sedation will be titrated per current MICU protocol to minimize patient discomfort
and minimizing ventilator dyssynchrony. In keeping with standard practice, the dose of
vasoactive medications will be kept constant during the intervention period. The standard
practice is to titrate vasopressor therapy every five minutes, so keeping vasoactive
medications constant for sixty seconds is in keeping with the standard of care. All subjects
will be in an ICU setting and monitored per standard of care (vital signs, telemetry,
ventilator data) by a respiratory therapist, pulmonary and critical care fellow or faculty
member, and critical care nurse at the bedside throughout the entire intervention.
A point of care (POC) echocardiogram will be performed by the investigator performing the
intervention in order to measure the stroke volume index (surrogate for cardiac output).
Subjects will be randomized to either undergo the PEEP challenge or tidal volume challenge
first. After the initial challenge, subjects will cross over to whichever challenge has not
yet been performed.
The simple changes to the ventilator we are proposing to use as challenges in this study are
done frequently and routinely in the ICU with or without the supervision of a physician, but
we will have a physician present throughout the entire proposed intervention. For the
subjects undergoing PEEP challenge first, we will do the following:
1. POC echocardiogram performed to measure SVI
2. The tidal volume will be set to 6 mL/kg PBW and the patients will be monitored for 5
minutes for any variability in vital parameters. The subject's ventilatory parameters,
vitals, hemodynamics, and oxygenation will be recorded on initial ventilator settings.
3. PEEP challenge - PEEP will be increased by 50% for 60 seconds. The subject's ventilatory
parameters, vitals, hemodynamics, and oxygenation will be recorded after 60 seconds.
4. PEEP returned to initial settings.
5. 2 minute washout period to prepare for tidal volume challenge.
6. Tidal volume challenge - tidal volume raised to 8 cc/kg PBW for 60 seconds. The
subject's ventilatory parameters, vitals, hemodynamics, and oxygenation will be recorded
will be recorded after 60 seconds.
7. Subjects ventilator settings returned to initial settings x 2 minutes.
8. 500 cc crystalloid fluid bolus of the ICU team's choosing is then administered to the
patient. The subject's ventilatory parameters, vitals, hemodynamics, and oxygenation
will be measured.
9. POC echocardiogram performed to measure SVI and determine if the subject is a fluid
responder or non-responder.
The procedure for those randomized into the tidal volume challenge first will be similar, but
the tidal volume challenge (e, above), rather than the PEEP challenge (b, above), will be
performed first.
In the management of a critically ill patient in circulatory shock, physicians encounter the
question of whether to administer fluid to the patient or not several times during the course
of the patient's stay in the ICU. To ensure that our study is generalizable and applicable,
we will perform the above protocol up to three times per subject. This is similar to previous
studies using changes in intrathoracic pressure to predict fluid responsiveness.
Additionally, we will have a larger number of interventions in order to better show a clear
difference statistically.
Inclusion Criteria:
- Mechanically ventilated
- Identified by treatment team as requiring intravenous fluid bolus
- Acute circulatory failure during admission (systolic blood pressure (SBP) ≤90 mmHg or
mean arterial pressure (MAP) ≤70 mmHg or requiring vasopressors to maintain SBP >90
mmHg or MAP >70 mmHg, along with one or more of the following:
- urinary flow ≤0.5 mL/kg/min for ≥2 hours,
- heart rate ≥100 beats per minute
- presence of skin mottling
- blood lactate concentration ≥4 mmol/L
Exclusion Criteria:
- Contraindication to fluid bolus
- Assynchrony Index > 10%
- Clinically significant cardiac arrhythmia
- Severe valvular heart disease
- Chest tubes with air leak
- Abdominal compartment syndrome
- Pregnancy
- Concurrent nebulized medication or inhaled nitric oxide
- Transthoracic echogenicity unsuitable for measuring velocity-time integral of aortic
blood flow (SVI)
- Prisoner
- Clinical brain death
- PEEP > 15 cmH2O
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