Perioperative Morbidity in Adult Scoliotic Surgery: Analysis of a Series From Brest (MOSCA-B)

Active, not recruiting

• Conditions: Neurosurgery; Spine Deformity; Adult Scoliosis

• Registration Number: NCT06815861
• Lead Sponsor: University Hospital, Brest

Brief Summary

Scoliosis surgery is an invasive procedure essential for alleviating significant pain and improving the physical, psychological, aesthetic, professional, and social well-being of patients. However, it carries a considerable risk of perioperative complications. This retrospective study, conducted at Brest University Hospital since 2017, aims to analyze these complications to provide a detailed assessment, particularly since the introduction of the OARM (intraoperative CT navigation), with the goal of optimizing the safety and effectiveness of surgical interventions. The complications studied include neurological, infectious, mechanical, and cardiopulmonary complications, along with an additional "other" category for rare complications. The period analyzed extends from the immediate postoperative phase to the most recent follow-up consultation with the referring surgeon, which varies depending on the duration of follow-up for each patient.

Detailed Description

Not available

Study Timeline

• Status Verified: 2024-10
• Study Start: 2024-12-01
• Primary Completion: 2025-01-31
• Study Completion: 2025-01-31
• Study First Submitted: 2025-02-04
• Study First Submitted QC: 2025-02-06
• Last Update Submitted: 2025-02-06
• Study First Posted: 2025-02-10
• Last Update Posted: 2025-02-10

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 48

Inclusion Criteria

• Adult patient
• Patient affiliated with a social security system
• Who underwent scoliosis surgery between 2017 and 2024 at the Brest University Hospital

Exclusion Criteria

Patients under legal protection (guardianship, curatorship, etc.) Refusal to participate (expressed opposition) History of scoliosis surgery performed by another surgeon, regardless of the center or year

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Number of postoperative complications	at the time of inclusion	Number of complications (raw description), followed by univariate analysis to exclude confounding factors

Secondary Outcome Measures

Name	Time	Method
ODI SORE	at the time of inclusion	ODI SCORE after the surgery

Trial Locations

Locations (1)

Chu Brest; 🇫🇷 Brest, France