Wireless Assessment of Respiratory and Circulatory Distress in Vascular Surgical Patients - An Observational Study (WARD-VASC)

Eske Kvanner Aasvang

Status: Completed

Conditions: Circulatory; Complications; Complication of Surgical Procedure; Respiratory Complication; Complication of Anesthesia

Study type: Observational

Funder types: Other

Identifiers

NCT04628858

H-19086583

Details and patient eligibility

About

Vascular postsurgical patients have a high risk of morbidity and mortality. On top of that, patients undergoing vascular surgery usually have a high burden of comorbidities.

After a short stay in the post-operative ward, patients are usually transferred to a standard surgical ward.

Monitoring of physiological parameters by intermittent manual recordings 8-12 hours apart, is today's standard of care in hospitals. However, no effect on length of hospital stay, morbidity or mortality has been proven. This may be due to the up to 12 hours of unobserved time that can occur, where physiological deviations can progress resulting in clinical adverse outcomes such as myocardial infarction or stroke.

Vital sign micro events are occurrences when patient physiological parameters deviates significantly from what can be understood as normal physiology. Since adverse outcomes in patients rarely happens without deviating physiological parameters, it is to be investigated if micro events can be used to predict clinical adverse outcomes to patients. We acknowledge that during the observation period, the number of false alarms should be kept to a minimum to avoid the risk of 'alarm fatigue'

Enrollment: 40 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Patients admitted to Copenhagen University Hospital
• Patients with Peripheral Arteriel Disease(PAD)
• Patients undergoing open infraligamentary revascularization
• Emergency or subacute surgery
• Admission the day before surgery, and expected length of stay more than 2 days.

Exclusion criteria

• Patient expected not to cooperate
• Patients with dementia or not able to give informed consent
• Patient allergic to plaster, plastic or silicone
• Patients with pacemaker or implantable cardioverter-defibrillator (ICD) unit
• Patients in isolation
• Active therapy withdrawn
• Patients previously included in the other study branches
• Patients with >20 mmHg in difference in systolic blood pressure between the two arms.
• Expected discharge within less than 24 hours from possible inclusion

Trial design

40 participants in 1 patient group

Primary group