osteolysis, aseptic loosening, and periprosthetic fracture or malposition
Conditions
Interventions
experimental group:Patients were transfused autologous blood intraoperatively
control group:Patients were not transfused autologous blood intraoperatively
Sponsors
West China Hospital, Sichuan University
Eligibility
Sex/Gender
All
Age
40 Years to 83 Years
Inclusion criteria
Inclusion criteria: Patients who were scheduled for revision THA for osteolysis, aseptic loosening, and periprosthetic fracture or malposition were considered eligible for inclusion in the trial.
Exclusion criteria
Exclusion criteria: Patients on the presence of current infection and dysfunction of blood coagulation, patients with a history of hemophilia, pulmonary embolism or ischemic heart disease.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Allogenic transfusion units and rate;intraoperative blood loss and postoperative drainage volume. ; | — |
Secondary
| Measure | Time frame |
|---|---|
| HB and HCT drop;postoperative hospital stay; | — |
Countries
China
Contacts
Public ContactFuxing Pei
West China Hospital, Sichuan University
Outcome results
None listed