Risk Factor Analysis for Proximal Junctional Kyphosis After Adult Spinal Deformity Surgery: A New Simple Scoring System to Identify High-Risk Patients.

Published

Journal Article

STUDY DESIGN:Retrospective cohort study. OBJECTIVE:Develop a simple scoring system to estimate proximal junctional kyphosis (PJK) risk. METHODS:A total of 417 adult spinal deformity (ASD) patients (80% females, 57.8 years) with 2-year follow-up were included. PJK was defined as a >10° kyphotic angle between the upper-most instrumented vertebra (UIV) and the vertebrae 2 levels above the UIV (UIV+2). Based on a previous literature review, the following point score was attributed to parameters likely to impact PJK development: age >55 years (1 point), fusion to S1/ilium (1 point), UIV in the upper thoracic spine (UIV-UT: 1 point), UIV in the lower thoracic region (UIV-LT: 2 points), flattening of the thoracic kyphosis (TK) relative to the lumbar lordosis (LL; ie, ▵LL - ▵TK) greater than 10° (1 point). RESULTS:At 2 years, the overall PJK rate was 43%. The odds ratios for each risk factor were the following: age >55 years (2.52), fusion to S1/ilium (5.17), UIV-UT (6.63), UIV-LT (8.24), and ▵LL - ▵TK >10° (1.59). Analysis by risk factor revealed a significant impact on PJK (no PJK vs PJK): age >55 years (28% vs 51%, P < .001), LIV S1/ilium (16.3% vs 51.4%, P < .001), UIV in lower thoracic spine (12.0% vs 38.7% vs 52.9%, P < .001), and a >10° surgical reduction in TK relative to LL increase (40.0% vs 51.5%, P < .001). The PJK rate by point score was as follows: 1 = 17%, 2 = 29%, 3 = 40%, 4 = 53%, and 5 = 69%. CONCLUSION:A pragmatic scoring system was developed that is tied to the increasing risk of PJK. These findings are helpful for surgical planning and preoperative counseling.

Full Text

Duke Authors

Cited Authors

  • Lafage, R; Beyer, G; Schwab, F; Klineberg, E; Burton, D; Bess, S; Kim, HJ; Smith, J; Ames, C; Hostin, R; Khalife, M; Shaffrey, C; Mundis, G; Lafage, V

Published Date

  • October 2020

Published In

Volume / Issue

  • 10 / 7

Start / End Page

  • 863 - 870

PubMed ID

  • 32905727

Pubmed Central ID

  • 32905727

Electronic International Standard Serial Number (EISSN)

  • 2192-5690

International Standard Serial Number (ISSN)

  • 2192-5682

Digital Object Identifier (DOI)

  • 10.1177/2192568219882350

Language

  • eng