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Risk Factors for Early Infection in Pediatric Spinal Deformity Surgery: A Multivariate Analysis
Jerry Y Du1, Connie Poe-Kochert1, George H Thompson1
1Division of Pediatric Orthopaedics, Rainbow Babies & Children's Hospitals/University Hospitals Cleveland Medical Center, Case Western Reserve University, 11100 Euclid Ave., Cleveland, OH 44106, USA.
Insights
Nonidiopathic scoliosis and increased intraoperative crystalloid fluids are key risk factors for early deep surgical site infections (SSIs) after pediatric spinal fusion surgery. Understanding these factors can help reduce infection rates in children undergoing spinal deformity correction.
Area of Science:
- Pediatric Orthopedics
- Surgical Site Infections
- Spinal Surgery
Background:
- Deep surgical site infections (SSIs) are a significant complication following pediatric spinal deformity surgery.
- Early SSIs (within three months) can lead to considerable patient morbidity.
Purpose of the Study:
- To identify independent risk factors for early deep SSIs after primary, single-stage pediatric posterior spinal fusion and instrumentation (PSFI).
Main Methods:
- Retrospective case-control study of 616 patients undergoing PSFI between 2001 and 2016.
- Multivariate analysis of demographics, comorbidities, and perioperative factors to identify independent risk factors for early deep SSI.
Main Results:
- Eleven patients (1.6%) developed early deep SSIs.
- Independent risk factors identified were nonidiopathic scoliosis etiologies (OR: 8.384) and increased intraoperative crystalloid administration (OR: 1.547 per liter).
- Mean crystalloid volume was significantly higher in the SSI group (3.3 L) compared to the noninfected group (2.4 L).
Conclusions:
- Nonidiopathic scoliosis and the amount of intraoperative crystalloids are independently associated with early postoperative SSIs.
- Further research into intraoperative fluid management may reveal modifiable strategies to decrease SSI risk in pediatric spinal fusion patients.
Study Design:
Retrospective case-control study.
Objectives:
To identify risk factors for early deep surgical site infections (SSIs; within three months of index procedure) following pediatric spinal deformity surgery.
Background:
Deep surgical site infections (SSIs) following pediatric spinal deformity surgery are a source of significant morbidity. We sought to identify independent risk factors for early infection following primary, definitive single-stage pediatric posterior spinal fusion and instrumentation (PSFI).
Methods:
A total of 616 consecutive patients (2001-2016) from an institutional prospectively maintained Pediatric Orthopaedic Spine database were identified that met inclusion criteria of definitive single-stage PSFI. Early deep SSI was defined as infection within three months of index procedure requiring surgical intervention. A multivariate analysis of demographics, comorbidities, and perioperative factors was performed and independent risk factors were identified.
Results:
Eleven patients (1.6%) developed an early deep SSI. Independent risk factors for SSI identified were nonidiopathic (neuromuscular, syndromic, and congenital) etiologies of scoliosis (adjusted odds ratio [aOR]: 8.384, 95% confidence interval [CI]: 1.784-39.386, p = .007) and amount of intraoperative crystalloids (aOR: 1.547 per additional liter of fluid, 95% CI: 1.057-2.263, p = .025). Mean crystalloid administered in the SSI group was 3.3 ± 1.2 L versus 2.4 ± 1.0 L in the noninfected group (p = .019). On univariate analysis, there was no significant difference in weight of patients between cohorts (p = .869) or surgery time (p = .089). There was also no significant difference in infection rates from redosing of antibiotics intraoperatively after 3 hours of surgery (p = .231).
Conclusions:
Nonidiopathic scoliosis and amount of intraoperative crystalloids were independently associated with early postoperative SSI. Further investigation into intraoperative fluid management may identify modifiable risk factors for early postoperative SSI in primary pediatric spinal deformity posterior spinal fusion patients.
Level Of Evidence:
Level III, case-control study.
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