Pelvic Ring Tumor Lesions
Conditions
Brief summary
Evaluate early functional outcomes following percutaneous screw fixation or cementoplasty for pelvic ring tumor lesions.
Interventions
None listed
Sponsors
Centre Hospitalier Universitaire de Nice
Study design
Observational model
COHORT
Time perspective
RETROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
Inclusion : \- Individuals with cancer who underwent percutaneous screw fixation or cementoplasty either for prophylactic consolidation or treatment of pathologic fractures in pelvic ring tumors.
Exclusion criteria
: * minors * incompetent adults * refused to participate in the study * pregnant women
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| postoperative weight-bearing ambulation | During hospitalization, mainly less than 3 days | the ability of the patient to walk and bear weight after the procedure and its associated timeframe. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Adverse event | During hospitalization, and follow-up | adverse event during procedure or hospitalization |
| Duration of hospitalization | Mainly less than 3 days | The duration of hospitalization will be measured between the day and time of arrival at the hospital and the day and time of discharge from the hospital |
| Long-term effectiveness in preventing pathological fractures of the pelvic ring | 3 months after the procedure, and during follow-up, up to 5 years | Absence of pelvic ring fracture during follow-up |
Countries
France
Outcome results
None listed