Multiple organ dysfunction
Conditions
Interventions
Trial group:In anticipation of the possibility of multiple organ dysfunction, clinical intervention will be carried out in advance.
Control group:None
Sponsors
Pudong New Area People's Hospital, Shanghai
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Age >= 18 years old, gender not restricted; 2. Admitted to the ICU and undergoing continuous monitoring of vital signs and routine laboratory tests; 3. Expected ICU stay time >= 24 hours, with the conditions to continuously observe the risk of multiple organ dysfunction; 4. At the time of enrollment, did not meet the criteria for multiple organ dysfunction; 5. The quality of vital sign monitoring data meets the standard and can be used for real-time analysis by the AI system; 6. The subject or their legal representative signs the informed consent form.
Exclusion criteria
Exclusion criteria: 1. They already had clear multi-organ dysfunction at the time of enrollment; 2. Their expected ICU stay is less than 24 hours or they are about to be transferred out of the ICU; 3. Patients with end-stage diseases or those who have decided to abandon active treatment; 4. There is severe data missing or the monitoring equipment is unable to reliably obtain key data; 5. They are participating in other interventional clinical trials that may affect the main endpoint of this study; 6. Other situations that the investigator deems unsuitable for inclusion in this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Continuous vital signs monitoring data;Laboratory index;Clinical interventions;Clinical outcome; | — |
Countries
China
Contacts
Public ContactWan Jian
Pudong New Area People's Hospital, Shanghai
Outcome results
None listed