The Effects of Vertical Position on Gas Exchange in Patients With Respiratory Failure

Respiratory Failure Clinical Trial

Official title:

The Effects of Vertical Position on Gas Exchange in Patients With Respiratory Failure

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT01705119
• Other study ID #: 12-1773
• Status: Active, not recruiting
• Phase: N/A
• Start date: October 1, 2012
• Est. completion date: December 2024

Study information

• Verified date: May 2023
• Source: University of Chicago
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to investigate how changing from a supine to upright position affects gas exchange for patients with hypoxemic respiratory failure. The research question is: will oxygen saturation and/or partial pressure of oxygen in the blood change when a patient with hypoxemic respiratory failure moves from a supine to upright position?

Description:

Our hypothesis is that blood oxygen tension will not decrease and may even increase when a patient with respiratory failure stands up. Supine positioning often causes partial lung collapse, which results in a decreased amount of lung being available for gas exchange. In patients with Acute Respiratory Distress Syndrome (ARDS), tilting the patient up in bed has been shown to increase oxygen tension and improve lung compliance. Positional changes are sometimes used as a "rescue" intervention in patients with severe hypoxemia from ARDS. The investigators hope to conclude that severe hypoxemia should not be viewed as a contraindication to physical therapy, but rather physical therapy may be a potential intervention for patients with marginal gas exchange. After sedative interruption, physical therapists and nursing staff will assist mechanically ventilated patients in moving to the side of the bed. They will assess the extremity strength using the MRC scale. If lower extremity strength is at least 4/5, the patient will be assisted to assume the upright position. The investigators will monitor the patient continuously and the session will be stopped at any point for A. Mean arterial pressure <65 B. Heart rate <40, >130 beats/min C. Respiratory rate <5, >40 breaths/ min D. Pulse oximetry <88% E. Marked ventilator dyssynchrony F. Patient distress G. New arrhythmia H. Concern for myocardial ischemia I. Concern for airway device integrity J. Endotracheal tube removal At this point, the patient's vital signs, pulse oximetry, and measures of lung compliance will be obtained. If an arterial line is in place and there have been ventilator adjustments since the morning arterial blood gas, the investigators will draw an arterial blood gas. The physical therapists and nursing staff will then help the patient stand up. After one minute, the investigators will record another set of vital signs, pulse oximetry, and measures of lung compliance from the mechanical ventilator. If an arterial line is in place, the investigators will draw another arterial blood gas. The patient will then be assisted back into bed. One hour later, the investigators will record the patient's vital signs, pulse oximetry, and measures of lung compliance from the mechanical ventilator.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 16
• Est. completion date: December 2024
• Est. primary completion date: June 10, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients aged =18 years who are mechanically ventilated
• An oxygen saturation of 88-94% or an arterial line

Exclusion Criteria:

• Mean arterial pressure <65
• Heart rate < 40 or > 130 beats/min
• Respiratory rate < 5 or > 40 breaths/min
• Pulse oximetry < 88%
• Evidence of elevated intracranial pressure
• Active gastrointestinal blood loss
• Active myocardial ischemia
• Pregnancy
• Actively undergoing a procedure
• Patient agitation requiring increased sedative administration in the last 30 mins
• Insecure airway (device)
• The patient was not ambulatory prior to hospitalization
• The patient's body habitus and/or mental status make it unsafe to stand up
• The patient has been placed on strict bed rest by the treating physicians

Related Conditions & MeSH terms

• Respiratory Failure
• Respiratory Insufficiency

Intervention

Other:
• Standing

Locations

Country	Name	City	State
United States	University of Chicago Medical Center	Chicago	Illinois

Sponsors (1)

Lead Sponsor	Collaborator
University of Chicago

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Tidal Volume		change from baseline to 1 hr
Other	Vital Signs		change from baseline to 1hr
Primary	PaO2 to FiO2 ratio		change from baseline to 1 hr
Secondary	Oxygen Saturation		change from baseline to 1 hr
Secondary	change in blood PCO2		change from baseline to 1 hr
Secondary	Change in blood pH		change from baseline to 1hr