posterior pelvic ring injuries
Conditions
Interventions
Surgical Robot Group:None
freehand group:None
Sponsors
Ningbo no.6 hospital
Eligibility
Sex/Gender
All
Age
20 Years to 60 Years
Inclusion criteria
Inclusion criteria: (1) Patients with a clinical diagnosis of fresh posterior pelvic ring injury who underwent percutaneous sacroiliac screw fixation; (2) Patients who underwent sacroiliac screw fixation alone without concurrent anterior fixation or other surgeries (except for staged external fixator surgery); (3) Fracture AO/OTA classification of 61B, 61C1.2, or 61C1.3 ; (4) Routine blood tests before and after surgery; (5) No history of thrombosis, abnormal coagulation function, or other high-risk bleeding diseases; no history of preoperative blood transfusion or long-term anticoagulant use; (6) The amount of fluid replacement within 24 hours after surgery did not exceed 2000 ml ; (7) Complete clinical data.
Exclusion criteria
Exclusion criteria: (1) Old posterior pelvic ring injury (2) Concomitant surgery with other plate fixation (3) History of bleeding disease (4) Incomplete clinical data
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Hidden blood loss; | — |
Secondary
| Measure | Time frame |
|---|---|
| Total blood loss; | — |
Countries
china
Contacts
Public Contactdingxu
Ningbo no.6 hospital
Outcome results
None listed