Wireless Assessment of Respiratory and Circulatory Distress in Chronic Obstructive Pulmonary Disease - an Observational Study (WARD-COPD)

University Hospital Bispebjerg and Frederiksberg

Status: Completed

Conditions: Chronic Obstructive Pulmonary Disease

Treatments: Device: Continuous monitoring system

Study type: Observational

Funder types: Other

Identifiers

NCT03660501

WARD-COPD_v1.1

Details and patient eligibility

About

For patients admitted to the medical ward, it is often difficult to predict if their clinical condition will deteriorate, however subtle changes in vital signs are usually present 8 to 24 hours before a life-threatening event such as respiratory failure leading to ICU admission, or unanticipated cardiac arrest. Such adverse trends in clinical observations can be missed, misinterpreted or not appreciated as urgent. New continuous and wearable 24/7 clinical vital parameter monitoring systems offer a unique possibility to identify clinical deterioration before patients condition progress beyond the point-of-no-return, where adverse events are inevitable. The WARD-COPD project aims to determine the correlation between cardiopulmonary micro events and clinical adverse events during the first four days after hospital admission with acute exacerbation of Chronic Obstructive Pulmonary Disease (AECOPD).

Enrollment: 200 patients

Sex: All

Ages: 18 to 100 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Adult patients admitted with AECOPD
• Recruitment and monitoring start is possible within 24 hours after admission

Exclusion criteria

• Patient expected not to cooperate
• Patient allergic to plaster, plastic or silicone
• Active therapy withdrawn
• Patients with dementia or not able to give informed consent
• Patients with pacemaker or implantable cardioverter-defibrillator (ICD) unit
• Expected discharge within less than 24 hours from possible inclusion