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

Perioperative Morbidity in Adult Scoliotic Surgery: Analysis of a Series From Brest

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT06815861

Acronym

MOSCA-B

Enrollment

Registered

2025-02-10

Start date

2024-12-01

Completion date

2025-01-31

Last updated

2025-02-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adult Scoliosis, Neurosurgery, Spine Deformity

Keywords

adult scoliosis, spine deformity, neurosurgery, spine surgery

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.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

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

Design outcomes

Primary

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

Secondary

Measure	Time frame	Description
ODI SORE	at the time of inclusion	ODI SCORE after the surgery

Countries

France

Outcome results