Prospective Evaluation of Serial Biomarkers in Patients With Intermediate High Risk Acute Pulmonary Embolism: A Single Center Proof-of-Concept Study

Hilamber Subba, Division of Pulmonary and Critical Care Medicine Maine Medical Center Portland Maine USA.
Ariel McKenna, Department of Internal Medicine Maine Medical Center Portland Maine USA.
John Gilboy, Division of Pulmonary and Critical Care Medicine Maine Medical Center Portland Maine USA.
Jacob Gelman, Division of Pulmonary and Critical Care Medicine Maine Medical Center Portland Maine USA.
Jessica Evans, Division of Pulmonary and Critical Care Medicine Maine Medical Center Portland Maine USA.
Alex Smith, Department of Internal Medicine Maine Medical Center Portland Maine USA.
James Kerney, Department of Internal Medicine Maine Medical Center Portland Maine USA.

Abstract

Patients diagnosed with intermediate high-risk pulmonary embolism (IHRPE) are at significant risk for clinical deterioration during hospitalization; however, clinical tools to identify which patients will worsen are imprecise. We designed a proof-of-concept, single-center prospective study to assess IHRPE patients (using 2019 ESC criteria), measuring blood concentrations of N-terminal pro-B-type natriuretic peptide (NT-proBNP), troponin T (TnT), uric acid, and plasma lactate serially during the first 72 h to better understand their kinetics and associations with in-hospital adverse clinical events. Twenty subjects (mean age 62.0 ± 12.6 years) diagnosed by computed tomography angiogram were enrolled. Central pulmonary embolism was seen in 18/20, and lower extremity deep vein thrombosis in 14/20. On presentation, the mean Bova and PESI scores were 5 ± 0.7 and 105 ± 25.2, respectively. At baseline, TnT was elevated in 20/20, NT-proBNP in 18/20, uric acid in 10/20, and lactate in 8/20 subjects. Clinical outcomes included ICU admission in 7/20, clinical deterioration in 10/20, and death in 2/20. Clinical deterioration was associated with persistent elevations of TnT, NT-proBNP, uric acid and lactate (all p < 0.05). The NT-proBNP time from baseline to peak concentration was highly associated with clinical deterioration (ROC AUC = 0.82 [95% CI: 0.62-0.97, p < 0.01, RR = 2.8 at 24 h). The baseline PESI score ROC AUC for clinical deterioration was 0.75 (95% CI: 0.515-0.952, p = NS). Persistently elevated biomarkers show an association with in-hospital adverse clinical events in IHRPE and warrant further study to assist clinical management.