4.6 Article

The Diagnostic Role of Uric Acid to Creatinine Ratio for the Identification of Patients with Adverse Pulmonary Embolism Outcomes

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DIAGNOSTICS
卷 12, 期 1, 页码 -

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MDPI
DOI: 10.3390/diagnostics12010193

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uric acid to creatinine ratio; pulmonary embolism; diagnosis; hospitalization; mortality; prognosis

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This study investigated the potential value of the UA/Cr ratio as a diagnostic tool for the prognosis of patients with acute pulmonary embolism (PE) and its correlation with other parameters. The results showed that UA/Cr levels are associated with disease severity and risk stratification, and may serve as a useful biomarker for identifying patients at risk of adverse outcomes.
Background: Uric acid (UA) is the final product of purine metabolism and a marker of oxidative stress that may be involved in the pathophysiology of cardiovascular and thromboembolic disease. The aim of the current study is to investigate the potential value of UA to creatinine ratio (UA/Cr) as a diagnostic tool for the outcome of patients admitted with acute pulmonary embolism (PE) and the correlations with other parameters. Methods: We evaluated 116 patients who were admitted for PE in a respiratory medicine department. PE was confirmed with computed tomography pulmonary angiography. Outcomes evaluated were hospitalization duration, mortality or thrombolysis and a composite endpoint (defined as mortality or thrombolysis). Patients were assessed for PE severity with the PE Severity Index (PESI) and the European Society of Cardiology (ESC) 2019 risk stratification. Results: The median (interquartile range) UA/Cr level was 7.59 (6.3-9.3). UA/Cr was significantly associated with PESI (p < 0.001), simplified PESI (p = 0.019), and ESC 2019 risk stratification (p < 0.001). The area under the curve (AUC) for prediction of 30-day mortality by UA/Cr was 0.793 (95% CI: 0.667-0.918). UA/Cr levels >= 7.64 showed 87% specificity and 94% negative predictive value for mortality. In multivariable analysis UA/Cr was an independent predictor of mortality (HR (95% CI): 1.620 (1.245-2.108), p < 0.001) and composite outcome (HR (95% CI): 1.521 (1.211-1.908), p < 0.001). Patients with elevated UA/Cr levels (>= 7.64) had longer hospitalization (median (IQR) 7 (5-11) vs. 6 (5-8) days, p = 0.006)), higher mortality (27.3% vs. 3.2%, p = 0.001) and worse composite endpoint (32.7% vs. 3.4%, p < 0.001). Conclusion: Serum UA/Cr ratio levels at the time of PE diagnosis are associated with disease severity and risk stratification, and may be a useful biomarker for the identification of patients at risk of adverse outcomes.

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