The joint effects of inflammation and renal function status on in-hospital outcomes in patients with acute ischemic stroke treated with intravenous thrombolysis

BMC Neurol. 2024 Dec 31;24(1):493. doi: 10.1186/s12883-024-04002-6.

Abstract

Objective: We aimed to determine the predictive value of renal function status [estimating glomerular filtration rate (eGFR)] in conjunction with inflammatory biomarkers [white blood cell(WBC) and C-reactive protein (CRP)] for in-hospital outcomes in acute ischemic stroke (AIS) patients treated with intravenous thrombolysis (IVT).

Methods: We retrospectively screened a total of 409 AIS patients treated with IVT. The study participants were classified into two groups according to post-stroke pneumonia or functional outcome. They were divided into four groups according to the cut-offs of inflammatory biomarkers and eGFR by receiver operating characteristics(ROC) curves for two outcomes of post-stroke pneumonia and functional status: WBC↓/eGFR↑, WBC↓/eGFR↓, WBC↑/eGFR↑, and WBC↑/eGFR↓for post-stroke pneumonia; and CRP↓/eGFR↑, CRP↓/eGFR↓, CRP↑/eGFR↑, and CRP↑/eGFR↓for functional outcome. Logistic regression models were used to calculate the odds ratios (ORs) and 95% confidence intervals (CIs) of post-stroke pneumonia or at-discharge functional outcome, using the WBC↓/eGFR↑group or CRP↓/eGFR↑group as the reference. The Net Reclassification Index (NRI) and the Integrated Discrimination Improvement (IDI) were calculated to analyze the combined predictive value.

Results: Compared with patients in WBC↓/eGFR↑group, those in WBC↑/eGFR↑group had increased risk of post-stroke pneumonia (OR 5.15, 95% CI 1.67-15.87) and poor functional outcome (OR 5.95, 95% CI 2.25-15.74). Furthermore, patients in WBC↑/ eGFR↓group had the highest risk of clinical outcomes (all P value for trend < 0.001), the multivariable-adjusted ORs (95% CIs) were 7.04 (2.42-20.46) for post-stroke pneumonia and 8.64 (3.30-22.65) for poor functional outcome. The addition of WBC and eGFR to the basic model significantly improved risk prediction for post-stroke pneumonia (category-free NRI 69.0%, 95% CI 47.3%-90.7%; IDI 5.4%, 95% CI 2.6%-8.3%) and functional outcome (category-free NRI 59.4%, 95% CI 39.2%-79.9%; IDI 5.3%, 95% CI 2.9%-7.8%). Similarly, when we added CRP and eGFR to the basic model with conventional risk factors, the risk discrimination and prediction for post-stroke pneumonia and functional outcome was also significantly improved.

Conclusion: Combining renal function status and inflammatory biomarkers within 4.5 h after onset could better predict in-hospital outcomes of AIS patients with IVT.

Keywords: Acute ischemic stroke; C-reactive protein; Estimating glomerular filtration rate; Intravenous thrombolysis; Joint prediction; Prognosis; White blood cell.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Biomarkers / blood
  • C-Reactive Protein* / analysis
  • C-Reactive Protein* / metabolism
  • Female
  • Fibrinolytic Agents / administration & dosage
  • Fibrinolytic Agents / therapeutic use
  • Glomerular Filtration Rate* / physiology
  • Humans
  • Inflammation* / blood
  • Inflammation* / drug therapy
  • Ischemic Stroke* / blood
  • Ischemic Stroke* / complications
  • Ischemic Stroke* / drug therapy
  • Male
  • Middle Aged
  • Pneumonia / blood
  • Pneumonia / diagnosis
  • Pneumonia / drug therapy
  • Retrospective Studies
  • Thrombolytic Therapy* / methods
  • Treatment Outcome

Substances

  • C-Reactive Protein
  • Biomarkers
  • Fibrinolytic Agents