Postoperative care Surgery
Conditions
Interventions
Patients are asked to wear the remote monitoring device for clinical evaluation for the first 3 days after the operation. During the pilot, no alarms will be set on the device. Treatment and monitorin
Sponsors
Vrije Universiteit Amsterdam (VUmc)
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Adult patients who underwent major abdominal surgery with an increased preoperative risk for postoperative pulmonary complications
Exclusion criteria
Exclusion criteria: 1. Withdrawal of informed consent 2. Cancelled surgery 3. Total monitoring time < 8 hours
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Critical early warning scores measured by continuous remote monitoring of the respiratory rate, SpO2 and pulse rate in four postoperative days. | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative pulmonary complications retrospectively scored using patient records. | — |
Countries
Netherlands
Contacts
Public ContactHugo Touw
Outcome results
None listed