Key result
Intraoperative FiO2 ≥60% linked to ~5-fold higher risk of postoperative interstitial pneumonia exacerbation.
Why the study?
Risk factors for acute exacerbation of interstitial pneumonia (AE-IP) after noncardiac surgery have been studied in small samples, leaving few established factors and unclear postoperative mortality.
Does intraoperative FiO2 ≥ 60% increase the risk of postoperative acute exacerbation of interstitial pneumonia in patients with interstitial pneumonia undergoing noncardiac surgery?
Observational (n=482)
No
Does intraoperative FiO2 ≥ 60% increase the risk of postoperative acute exacerbation of interstitial pneumonia in patients with interstitial pneumonia undergoing noncardiac surgery?
Odds Ratio: 5.22 (95% CI 1.37–22.68)
Absolute Event Rate: 8.16% vs 2.09%
p-value: p=0.018
In patients with interstitial pneumonia undergoing noncardiac surgery, high intraoperative oxygen (FiO2 ≥ 60%) and elevated preoperative CRP are significant risk factors for postoperative acute exacerbation, which carries a high mortality risk.
May warrant cautious oxygen titration in interstitial pneumonia; leaves open whether restriction reduces exacerbations in prospective trials.
BACKGROUND: Acute exacerbation of interstitial pneumonia (AE-IP) is associated with high mortality rates. Although the risk factors for AE-IP have been extensively studied, given the small sample sizes, only a few risk factors have been established. This study aimed to investigate the postoperative mortality and factors associated with AE-IP. METHODS: This retrospective study included 482 patients with a preoperative diagnosis of IP who underwent noncardiac surgery between December 2012 and April 2020. AE-IP was diagnosed by a radiologist using computed tomography when worsening respiratory symptoms were observed within 1 month postoperatively. The Cox proportional hazards model was used to compare mortality rates. Candidate factors associated with AE-IP were identified through logistic regression analysis using the variable selection method, followed by case-control analysis using propensity score matching to determine possible factors associated with AE-IP. RESULTS: The multivariable-adjusted hazard ratios for all-cause and IP-related deaths were significantly higher in patients with AE-IP than in those without AE-IP. Multivariable analysis with variable selection suggested that male sex, higher C-reactive protein (CRP) levels, fraction of inspired oxygen (FiO2) ≥ 60%, and non-lung surgery were candidate factors associated with AE-IP. Case-control analysis using propensity score matching demonstrated that patients with AE-IP had higher CRP levels (P = 0.044) and frequency of FiO2 ≥ 60% (P = 0.035) than those without AE-IP. Furthermore, a positive, nearly linear relationship was observed between FiO2 ≥ 60% duration and AE-IP incidence. CONCLUSIONS: Intraoperative management with FiO2 ≥ 60% and high preoperative CRP levels were significantly associated with postoperative AE-IP.
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Shirozu et al. (2025) conducted an observational in Interstitial pneumonia undergoing noncardiac surgery (n=482). Intraoperative fraction of inspired oxygen (FiO2) ≥ 60% vs. Intraoperative fraction of inspired oxygen (FiO2) < 60% was evaluated on Postoperative acute exacerbation of interstitial pneumonia (AE-IP) within 1 month (OR 5.22, 95% CI 1.37-22.68, p=0.018). Intraoperative administration of a fraction of inspired oxygen (FiO2) ≥ 60% was significantly associated with a 5.22-fold increased odds of postoperative acute exacerbation of interstitial pneumonia.
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