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Assessment of the return of pulsatile flow by carotid artery ultrasound using cardiac bypass patients as a model of the return of spontaneous circulation

Assessment of the return of pulsatile flow by carotid artery two-dimension or colourDoppler ultrasound using cardiac bypass patients as a model for the return of spontaneous circulation: A Pilot study

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12616001591448
Enrollment
20
Registered
2016-11-17
Start date
2016-08-01
Completion date
2017-01-23
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

Current cardiac arrest algorithms require assessment of the return of spontaneous circulation (ROSC) following rhythm checks. Current recommendations for assessment of ROSC include observation for patient movement or spontaneous respiration, both of which may be absent in sedated and paralysed patients. Healthcare professionals are advised to check the pulse in the presence of an organized rhythm, however previous studies have shown poor ability to correctly detect the presence or absence of a pulse in a simulated pulseless electrical activity (PEA) arrest. In one study, 45% of participants incorrectly diagnosed pulselessness in cardiac surgery patients no longer on bypass, despite systolic pressures greater than 80mmHg. In coronary artery bypass graft (CABG) surgery, when coming off bypass, blood flow changes from continuous to pulsatile. This may offer a model by which to simulate the return of pulsatile flow, and allow a comparison of radial arterial pressures when pulsatile flow becomes first apparent on 2D US and colour flow Doppler US of the carotid artery. This pilot study proposes to investigate whether pulsatile flow can be reliably assessed by the use of carotid artery ultrasound, and whether CABG patients can be used as a model to evaluate this.

Interventions

This is an interventional trial with two arms. The trial will evaluate the use of US to detect pulsatile flow compared to the blood pressure as measured on the radial arterial line. The participants will be randomised to 2D US or colour-Doppler. One of the investigators will ultrasound the carotid artery of patients as they come off bypass and a video of the image recorded. At the same time a video will be recorded of the anaesthetic monintor. Three Independent investigators will assess the ultr

This is an interventional trial with two arms. The trial will evaluate the use of US to detect pulsatile flow compared to the blood pressure as measured on the radial arterial line. The participants will be randomised to 2D US or colour-Doppler. One of the investigators will ultrasound the carotid artery of patients as they come off bypass and a video of the image recorded. At the same time a video will be recorded of the anaesthetic monintor. Three Independent investigators will assess the ultrasound images and will record the time at which they think sustained pulsatile flow occurs, This will then be correlated to the blood presssure of the participants. Those assessing the ultrasound images will not have access to the monitor videos. The assessors will be three anaesthetists (two cardiac and one general anaesthetist). Videos will be recorded as rewarming of the heart begins and continue for approximately 5 minutes after the return of spontaneous circulation

Sponsors

St George Hospital
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Diagnosis
Masking
Open (masking not used)

Eligibility

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

Inclusion criteria

Age > 18. Ability to offer informed consent. Undergoing cardiac surgery requiring cardiac bypass from the perfusion machine.

Exclusion criteria

Previous surgery involving the great blood vessels including aorta or carotid arteries. Patients in whom the cardiac surgeon considers enrolment will be inappropriate due to high surgical risk, patients with intraaortic balloon pump, known peripheral vascular disease.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026