Viewing Study NCT03974568



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Last Modification Date: 2024-10-26 @ 1:11 PM
Study NCT ID: NCT03974568
Status: COMPLETED
Last Update Posted: 2020-01-28
First Post: 2019-05-31

Brief Title: Peripheral Perfusion Index in Weaning From Mechanical Ventilation
Sponsor: Cairo University
Organization: Cairo University

Study Overview

Official Title: Evaluation of Peripheral Perfusion Index as a Predictor of Failure of Weaning From Mechanical Ventilation
Status: COMPLETED
Status Verified Date: 2020-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Peripheral perfusion index PPI is variable measured by Radical-7 Masimo device and reflects the ratio between pulsatile and non-pulsatile portions of peripheral circulation PPI is characterized by being non-invasive real time and simple variable Impairment of various perfusion indices such as central venous oxygen saturation and serum lactate during spontaneous breathing trial SBT were previously reported however these indices are characterized by being relatively invasive We hypothesized that impairment of PPI during SBT might be predictive of weaning failure The aim of this work was to evaluate the possible association between PPI and success of SBT
Detailed Description: This prospective observational study will be carried out in surgical intensive care unit SICU unit of trauma and emergency hospital at Cairo University teaching hospital Informed consent will be obtained from patients next-of-kin prior to the enrolment in the study All mechanically ventilated patients for more than 48 hours presented will be consecutively included

The excluded patients are patients 18 years patients with peripheral vascular disease patients on vasopressors and those with hand injuries hindering which would preclude the application of the device probe will be excluded

Assessment of readiness to wean from mechanical ventilation will be done by ICU physician according to the ICU protocol Spontaneous breathing trial SBT will be applied through pressure support PS mode with PS 5 cmH2O and positive end expiratory pressure PEEP 5 cmH2O for 30 minutes then weaning parameters will be assessed again The decision of extubation will be taken by the intensivist in charge who is blinded to peripheral perfusion index PPI measurements Weaning failure will be defined according to the guidelines of international conference on weaning from mechanical ventilation PPI will be continuously monitored using Radical-7 device pulse co-oximeter Masimo corporation Irvine CA via a pulse oximeter probe applied to the third or fourth digit of left hand The probe will be covered with an opaque shield to avoid any error by external light sources A baseline reading for PPI will be obtained followed by a reading each 5 minutes till the end of the SBT We calculated a PPI ratio to evaluate the change in PPI during SBT PPI ratio is defined as PPI by the end of SBT baseline PPI

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None