Clinically Significant Thromboembolic Disease in Adult Spinal Deformity Surgery: Incidence and Risk Factors in 737 Patients. Academic Article uri icon

Overview

abstract

  • STUDY DESIGN: Retrospective cohort study. OBJECTIVES: Describe the rate and risk factors for venous thromboembolic events (VTEs; defined as deep venous thrombosis [DVT] and/or pulmonary embolism [PE]) in adult spinal deformity (ASD) surgery. METHODS: ASD patients with VTE were identified in a prospective, multicenter database. Complications, revision, and mortality rate were examined. Patient demographics, operative details, and radiographic and clinical outcomes were compared with a non-VTE group. Multivariate binary regression model was used to identify predictors of VTE. RESULTS: A total of 737 patients were identified, 32 (4.3%) had VTE (DVT = 14; PE = 18). At baseline, VTE patients were less likely to be employed in jobs requiring physical labor (59.4% vs 79.7%, P < .01) and more likely to have osteoporosis (29% vs 15.1%, P = .037) and liver disease (6.5% vs 1.4%, P = .027). Patients with VTE had a larger preoperative sagittal vertical axis (SVA; 93 mm vs 55 mm, P < .01) and underwent larger SVA corrections. VTE was associated with a combined anterior/posterior approach (45% vs 25%, P = .028). VTE patients had a longer hospital stay (10 vs 7 days, P < .05) and higher mortality rate (6.3% vs 0.7%, P < .01). Multivariate analysis demonstrated osteoporosis, lack of physical labor, and increased SVA correction were independent predictors of VTE (r2 = .11, area under the curve = 0.74, P < .05). CONCLUSIONS: The incidence of VTE in ASD is 4.3% with a DVT rate of 1.9% and PE rate of 2.4%. Osteoporosis, lack of physical labor, and increased SVA correction were independent predictors of VTE. Patients with VTE had a higher mortality rate compared with non-VTE patients.

authors

  • Kim, Han Jo
  • Iyer, Sravisht
  • Diebo, Basel G
  • Kelly, Michael P
  • Sciubba, Daniel
  • Schwab, Frank
  • Lafage, Virginie
  • Mundis, Gregory M
  • Shaffrey, Christopher I
  • Smith, Justin S
  • Hart, Robert
  • Burton, Douglas
  • Bess, Shay
  • Klineberg, Eric O

publication date

  • September 12, 2017

Identity

PubMed Central ID

  • PMC5958487

Scopus Document Identifier

  • 85046804679

Digital Object Identifier (DOI)

  • 10.1177/2192568217724781

PubMed ID

  • 29796369

Additional Document Info

volume

  • 8

issue

  • 3