Journal of Orthopaedics and Traumatology (Jun 2024)

Radiographic evaluation of robot-assisted versus manual total hip arthroplasty: a multicenter randomized controlled trial

  • Xianzuo Zhang,
  • Xianyue Shen,
  • Rongwei Zhang,
  • Mo Chen,
  • Ruixiang Ma,
  • Zian Zhang,
  • Haining Zhang,
  • Bo Yang,
  • Chen Zhu

DOI
https://doi.org/10.1186/s10195-024-00773-3
Journal volume & issue
Vol. 25, no. 1
pp. 1 – 8

Abstract

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Abstract Background The effectiveness of robot-assisted surgery remains contentious due to the lack of high-quality randomized controlled trials (RCTs) to elevate the level of evidence. We aimed to evaluate the postoperative radiographic outcomes of robot-assisted (RAS-THA) versus manual (M-THA) total hip arthroplasty. Methods This multicenter RCT was performed from March 1, 2021 to December 1, 2021. Patients were randomly assigned to routine M-THA or to RAS-THA that used the TRex-RS orthopedic joint surgical navigation system. The primary outcome was to compare the acetabular component orientation, femoral stem alignment, femoral canal fill ratio, and leg length discrepancy between RAS-THA and M-THA using postoperative radiography. Subgroup analyses of the two groups stratified by surgical approach, gender, and BMI were also conducted. Results Seventy-three participants were randomly allocated to the RAS-THA group, while seventy-two participants were assigned to the M-THA group. Compared to the M-THA group, the RAS-THA group exhibited less variability in the preoperative planning of the vertical center of rotation (VCOR; P 0.05) between the two groups. Further subgroup analysis also showed that the RAS-THA group had fewer horizontal center of rotation (HCOR) and leg length differences when stratified by surgical approach, gender, and overweight status. Conclusion This RCT found that, regardless of the surgical approach, gender, or body mass index, RAS-THA can effectively improve the postoperative VCOR and significantly reduce the variability of leg length difference. RAS-THA should be considered an effective method to enhance surgical precision by achieving less variability in challenging patients with leg length discrepancies. Trial registration: ChiCTR2100044124.

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