Venous Thrombosis Embolism
Conditions
Interventions
Intervention group:The intervention group implemented conventional VTE prevention programs and AI-CDSS auxiliary decision support. The explanation is as follows: For patients in the experimental group
Control group:The control group only implemented routine VTE prevention programs, including uniform VTE prevention knowledge training and a unified version of VTE prevention manual provided by the hos
irregular supervision by the medical department.
Sponsors
Ruijin Hospital Affiliated to Medical College of Shanghai Jiaotong University
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Agree to participate in the trial; 2. Aged >=18 years; 3. Admission departments are high-risk departments.
Exclusion criteria
Exclusion criteria: 1. Patients diagnosed with deep venous thrombosis or pulmonary embolism (ICD10 code) on admission; 2. Subjects who are participating in similar clinical trials; 3. Patients with expected hospitalization time less than 24 hours (patients have 24-hour admission and discharge orders on the day of admission); 4. Patients undergoing full anticoagulation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of new deep venous thrombosis in hospital; | — |
Secondary
| Measure | Time frame |
|---|---|
| Detection rate of imported deep venous thrombosis cases;Incidence of fatal pulmonary thromboembolism in hospital;All-cause mortality;Abandonment rate;Implementation rate of appropriate prevention methods for high-risk patients (24 hours after surgery);Implementation rate of appropriate prevention methods for special high-risk patients (at discharge);Incidence of anticoagulant related bleeding events; | — |
Countries
China
Contacts
Public ContactJieming Qu
Ruijin Hospital Affiliated to Medical College of Shanghai Jiaotong University
Outcome results
None listed