Understanding the 30-day mortality burden after revision total hip arthroplasty.

Abstract

Revision total hip arthroplasty (THA) is a challenging procedure that burdens the healthcare system. Despite being associated with worse outcomes relative to its primary counterpart, postoperative mortality after revision THA remains ill-defined. The present study aimed to (1) establish the overall 30-day mortality rate after revision THA and (2) explore the mortality rate stratified by age, comorbidity burden, and aseptic versus septic failure. The American College of Surgeons - National Surgical Quality Improvement Program (ACS-NSQIP) database was retrospectively reviewed for all patients who underwent revision THA from 2011 to 2019. A total of 23,501 patients were identified and grouped into mortality (<i>n</i> <i>=</i> 161) and mortality-free (<i>n</i> <i>=</i> 23,340) cohorts. Patient demographics, comorbidities, and aseptic/septic failure were evaluated. The overall 30-day mortality was 0.69%. The mortality rate by age group (normalised per 1000 patients) was 0 (18-39 years [Y]), 0.67 (40-49 Y), 1.10 (50-59 Y), 2.58 (60-69 Y), 6.15 (70-79 Y) 19.32 (80-89 Y), and 58.22 (90+Y) (<i>p</i> <i><</i> 0.001). The mortality rate by ASA classification (normalised per 1000 patients) was 0 (ASA I), 1.47 (ASA II), 6.94 (ASA III), 45.42 (ASA IV), and 200 (ASA V) (<i>p</i> <i><</i> 0.001). The 30-day mortality rate for the septic and aseptic cohorts was 1.03% and 0.65%, respectively (<i>p</i> <i>=</i> 0.038). CCI scores (<i>p</i> <i><</i> 0.001), diabetes (<i>p</i> <i><</i> 0.001), systematic sepsis (<i>p</i> <i><</i> 0.001), poor functional status (<i>p</i> <i><</i> 0.001), BMI < 24.9 kg/m² (<i>p</i> <i><</i> 0.001), and dirty/infected wounds (<i>p</i> <i><</i> 0.001) were all associated with increased mortality risk. 1 in 145 patients will suffer mortality during the 30 days after revision THA. PJI-related revision THA was associated with 1.5-fold increase in 30-day mortality rate compared to its aseptic counterpart. Certain patient determinants and baseline comorbidities, as measured by ASA and CCI scores, were associated with higher 30-day mortality rates. Therefore, it is imperative to identify such risk factors and implement perioperative patient optimisation pathways to mitigate the risk among vulnerable patients.