ACTRN12616001174471
Completed
未知
Efficacy of nasogastric and endotracheal tube securement devices, preventative dressings and topical skin applications for reducing device-related pressure injuries in intensive care patients; a pilot study
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Queensland University of Technology
- Enrollment
- 100
- Status
- Completed
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •All ICU patients \= or \>18 years who have a NGT and/or ETT in situ
- •Patients who are expected to remain in ICU \> 24 hours
- •NGT or ETT inserted a maximum of 12 hours prior to ICU admission
- •Patients readmitted to ICU with no oral or nasal skin injury present
- •NGT arm only \- must have wide bore NGT and an ETT in situ.
Exclusion Criteria
- •Burn patients with an ETT wired in place (ETT arm only)
- •Patients with NGT sutured in place or nasal bridle (NGT arm only)
- •Patients with facial trauma
- •Traumatic brain injured patients requiring intracranial pressure monitoring and/or ventricular drainage of cerebrospinal fluid
- •Cervical spine injured patients who have a hard collar in situ
- •Hirsute patients with beards where patient permission to shave is not possible
- •Patients who are receiving non\-invasive ventilation
- •Patients with a device (NGT or ETT) predicted to be in situ \< 48 hours.
- •Patients with a community or hospital\-acquired NGT or ETT PI diagnosed within 24 hours of admission to the ICU.
- •Patients on whom treatment is withdrawn or who are being palliated.
Outcomes
Primary Outcomes
Not specified
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