Clinical Utility of a Biomarker to Detect Contrast-Induced Acute Kidney Injury during Percutaneous Cardiovascular Procedures.

John Peabody, David Paculdo, Czarlota Valdenor, Peter A McCullough, Eisei Noiri, Takeshi Sugaya, Jeffrey R Dahlen

Journal: Cardiorenal medicine 2022;12(1):11-19

PMID: 35034025

Abstract

INTRODUCTION

Contrast-induced acute kidney injury (CI-AKI) is a major clinical complication of percutaneous cardiovascular procedures requiring iodinated contrast. Despite its relative frequency, practicing physicians are unlikely to identify or treat this condition.

METHODS

In a 2-round clinical trial of simulated patients, we examined the clinical utility of a urine-based assay that measures liver-type fatty acid-binding protein (L-FABP), a novel marker of CI-AKI. We sought to determine if interventional cardiologists' ability to diagnose and treat potential CI-AKI improved using the biomarker assay for 3 different patient types: pre-procedure, peri-procedure, and post-procedure patients.

RESULTS

154 participating cardiologists were randomly divided into either control or intervention. At baseline, we found no difference in the demographics or how they identified and treated potential complications of AKI, with both groups providing less than half the necessary care to their patients (46.4% for control vs. 47.6% for intervention, p = 0.250). The introduction of L-FABP into patient care resulted in a statistically significant improvement of 4.6% (p = 0.001). Compared to controls, physicians receiving L-FABP results were 2.9 times more likely to correctly identify their patients' risk for AKI (95% CI 2.1-4.0) and were more than twice as likely to treat for AKI by providing volume expansion and withholding nephrotoxic medications. We found the greatest clinical utility in the pre-procedure and peri-procedure settings but limited value in the post-procedure setting.

CONCLUSION

This study suggests L-FABP as a clinical marker for assessing the risk of potential CI-AKI, has clinical utility, and can lead to more accurate diagnosis and treatment.

© 2022 The Author(s). Published by S. Karger AG, Basel.

Address: QURE Healthcare, San Francisco, California, USA.; University of California, School of Medicine, San Francisco, California, USA.; University of California, Fielding School of Public Health, Los Angeles, California, USA.; Texas Christian University and the University of North Texas Health Sciences Center School of Medicine, Dallas, Texas, USA.; Department of Nephrology and Endocrinology, The University of Tokyo Hospital, Tokyo, Japan.; National Center Biobank Network, National Center for Global Health and Medicine, Tokyo, Japan.; Timewell Medical, Tokyo, Japan.; St. Marianna University School of Medicine, Kawasaki, Japan.; Hikari Dx, Inc., San Diego, California, USA.

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