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Use of ultrasound to determine changes in diaphragm mechanics during a spontaneous breathing trial

Use of ultrasound to determine changes in diaphragm mechanics during a spontaneous breathing trial

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12616000596404
Acronym
DUET
Enrollment
18
Registered
2016-05-09
Start date
2016-08-17
Completion date
2018-01-24
Last updated
2020-02-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Weaning from mechanical ventilation is one of the most common activities undertaken in intensive care. Currently, the gold standard for weaning and assessing for extubation is a spontaneous breathing trial (SBT). There is still a proportion of patients (up to 20%) that fail extubation due to recurrent respiratory failure following a successful SBT. Both diaphragmatic ultrasound and electromyography are emerging tools that may have considerable utility in augmenting the decision making process surrounding weaning and extubation. This study will aim to assess diaphragmatic function via ultrasound and electromyographic activity analysis at the start and end of a spontaneous breathing trial. This data should enable the identification of the role of diaphragmatic function in both successful and unsuccessful SBTs. Completing this study will aid in understanding the role of diaphragmatic ultrasound and EMG in ventilator weaning and extubation.

Interventions

Weaning from mechanical ventilation is one of the most common activities undertaken in intensive care. Currently, the gold standard for weaning and assessing for extubation is a spontaneous breathing trial (SBT). Diaphragmatic ultrasound is an emerging tools that may have considerable utility in augmenting the decision making process surrounding weaning and extubation. We aim to assess diaphragmatic function via ultrasound and electromyographic activity analysis at the start and end of a spontan

Weaning from mechanical ventilation is one of the most common activities undertaken in intensive care. Currently, the gold standard for weaning and assessing for extubation is a spontaneous breathing trial (SBT). Diaphragmatic ultrasound is an emerging tools that may have considerable utility in augmenting the decision making process surrounding weaning and extubation. We aim to assess diaphragmatic function via ultrasound and electromyographic activity analysis at the start and end of a spontaneous breathing trial. A spontaneous breathing trial consists of the patient being placed on a T-piece without PEEP and given enough supplemental oxygen to maintain adequate oxygen saturation. For a spontaneous breathing trial to be considered successful, it must last at least 30 minutes. Patients who are planned to undergo a spontaneous breathing trial as part of their usual care will be considered for the trial. Ultrasound assessment of the right hemidiaphragm will be conducted within the first 5 minutes of the SBT and at 30 minutes. This will be conducted by a qualified ultrasonographer with the patient lying at 45 degrees. Measurement of diaphragmatic excursion, speed of diaphragmatic contraction and diaphragmatic thickness (at end-inspiration and end-expiration) will be conducted at both assessments.

Sponsors

Dr Hayden White
Lead SponsorIndividual

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient intubated and mechanically ventilated for at least 24 hours over the age of 18 * Planned to undergo spontaneous breathing trial as per unit protocol

Exclusion criteria

* Neuromuscular disease likely to result in diaphragmatic dysfunction * Inability to visualise diaphragm on ultrasound * Inability to access right chest wall due to dressings or surgical site * Inability to sit at 45 degrees * Diaphragmatic injury as a result of trauma or surgery * Pregnancy * Unilateral diaphragmatic or phrenic nerve pathology * Patients whom life support would be withheld, withdrawn, or who are not expected to survive their ICU admission Specific to Edi patients * Nasogastric catheter placement contra-indicated * Inability to place Edicatheter * Edi capable ventilator not available

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026