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Is ABO blood type a risk factor for adjacent segment degeneration after lumbar spine fusion? | LitMetric

AI Article Synopsis

  • This study investigated the relationship between ABO blood types and the risk of postoperative adjacent segment degeneration (ASD) after lumbar spine fusion surgery.
  • It included 445 patients with various blood types and assessed factors like spinopelvic alignment, perioperative care, and patient outcomes, finding no significant differences in recovery and complications based on blood type, except for increased epidural hematomas in A+ patients.
  • The research concluded that ABO blood type is a non-modifiable risk factor linked to a higher likelihood of developing ASD, particularly in B+ patients, marking a significant first step in understanding this association.

Article Abstract

Purpose: This study aimed to explore associations between ABO blood type and postoperative adjacent segment degeneration/disease (ASD) following lumbar spine fusion, as well as evaluate differences in spinopelvic alignment, perioperative care, postoperative complications, and patient-reported outcome measures (PROMs).

Methods: An ambispective study was performed. Patients who underwent posterolateral or posterior lumbar interbody fusion were included. Demographic, perioperative and postoperative, clinical, and blood type information was recorded. Pre- and post-operative radiographic imaging was analyzed for alignment parameters and development of ASD.

Results: 445 patients were included, representing O+ (36.0%), O- (5.2%), A+ (36.2%), A- (6.3%), B+ (12.1%), B- (1.6%), and AB+ (2.7%) blood types. Most patients were female (59.1%), and had a mean age of 60.3 years and BMI of 31.1 kg/m. Postoperatively, groups did not differ in duration of the hospital (p = 0.732) or intensive care unit (p = 0.830) stay, discharge disposition (p = 0.504), reoperation rate (p = 0.192), or in-hospital complication rate (p = 0.377). Postoperative epidural hematoma was most common amongst A + patients (p = 0.024). Over a mean of 11.0 months of follow-up, all patients exhibited similar improvement in PROMs, with 132 (29.7%) patients developing radiographic evidence of ASD. B + patients were significantly more likely than A + and O + patients to develop spondylolisthesis and ASD (p < 0.05). No significant differences in sagittal alignment parameters and number of levels of fusion were found (p > 0.05).

Conclusions: This is the first large-scale study to address and demonstrate proof-of-principle that ABO blood type, a non-modifiable risk factor, is associated with ASD following lumbar spine fusion.

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Source
http://dx.doi.org/10.1007/s00586-024-08516-yDOI Listing

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