Real-World Use of AKI Biomarkers: A Quality Improvement Project Using Urinary Tissue Inhibitor Metalloprotease-2 and Insulin-Like Growth Factor Binding Protein 7 ([TIMP-2]*[IGFBP7]).


Journal

American journal of nephrology
ISSN: 1421-9670
Titre abrégé: Am J Nephrol
Pays: Switzerland
ID NLM: 8109361

Informations de publication

Date de publication:
2023
Historique:
received: 15 04 2023
accepted: 19 06 2023
medline: 3 11 2023
pubmed: 26 6 2023
entrez: 25 6 2023
Statut: ppublish

Résumé

Novel urinary biomarkers, including tissue inhibitor metalloprotease-2 and insulin-like growth factor binding protein 7 ([TIMP-2]*[IGFBP7]), have been developed to identify patients at risk for acute kidney injury (AKI). We investigated the "real-world" clinical utility of [TIMP-2]*[IGFBP7] in preventing AKI. We performed a before and after single-center quality improvement study of intensive care unit (ICU) patients at risk for severe (KDIGO stage 2 or 3) AKI. In the prospective cohort, ICU providers were allowed to order [TIMP-2]*[IGFBP7] for patients at their discretion, then offered AKI practice recommendations based on the results. Outcomes were compared to a historical cohort in which biomarker values were not reported to clinical teams. There was no difference in 7-day progression to severe AKI between the prospective (n = 116) and historical cohorts (n = 63) when [TIMP-2]*[IGFBP7] ≥0.3 (24 [28%] versus 8 [21%], p = 0.38) despite more stage 1 AKI at time of biomarker measurement in the prospective cohort (58 [67%] versus 9 [23%], p < 0.001). In the prospective cohort, patients with higher [TIMP-2]*[IGFBP7] values were more likely to receive a nephrology consult. Early consultation (within 24 h of biomarker measurement, n = 20) had a nonsignificant trend toward net negative volume balance (-1,787 mL [6,716 mL] versus + 4,974 mL [15,540 mL]) and more diuretic use (19 [95%] versus 8 [80%]) and was associated with less severe AKI (9 [45%] versus 10 [100%], p = 0.004) and inpatient dialysis (2 [10%] versus 7 [70%], p = 0.002) compared to delayed consultation (n = 10). Despite the prospective cohort having more preexisting stage 1 AKI, there were equal rates of progression to severe AKI in the prospective and historical cohorts. In the setting of [TIMP-2]*[IGFBP7] reporting, there were more nephrology consults in response to elevated biomarker levels. Early nephrology consultation resulted in improved volume balance and favorable outcomes compared to delayed consultation.

Identifiants

pubmed: 37356428
pii: 000531641
doi: 10.1159/000531641
doi:

Substances chimiques

Tissue Inhibitor of Metalloproteinase-2 127497-59-0
Biomarkers 0
Insulin-Like Growth Factor Binding Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

281-290

Informations de copyright

© 2023 S. Karger AG, Basel.

Auteurs

Ashley M La (AM)

Department of Internal Medicine, University of Chicago, Chicago, Illinois, USA.

Samantha Gunning (S)

Section of Nephrology, Department of Internal Medicine, University of Chicago, Chicago, Illinois, USA.

Sharon A Trevino (SA)

Section of Nephrology, Department of Internal Medicine, University of Chicago, Chicago, Illinois, USA.

Alissa Kunczt (A)

Section of Nephrology, Department of Internal Medicine, University of Chicago, Chicago, Illinois, USA.

Lui G Forni (LG)

Department of Intensive Care Medicine, Royal Surrey Hospital and Faculty of Health Sciences, University of Surrey, Guildford, UK.

Varsha Swamy (V)

Department of Internal Medicine, University of Chicago, Chicago, Illinois, USA.

Alexander Zarbock (A)

Department of Anesthesiology, Intensive Care Medicine and Pain Medicine, University Hospital Munster, Munster, Germany.
Outcomes Research Consortium, Cleveland, Ohio, USA.

Sarah Groboske (S)

Section of Clinical Chemistry, Department of Pathology, University of Chicago, Chicago, Illinois, USA.

Edward K Y Leung (EKY)

Section of Clinical Chemistry, Department of Pathology, University of Chicago, Chicago, Illinois, USA.

Kiang-Teck J Yeo (KJ)

Section of Clinical Chemistry, Department of Pathology, University of Chicago, Chicago, Illinois, USA.

Jay L Koyner (JL)

Section of Nephrology, Department of Internal Medicine, University of Chicago, Chicago, Illinois, USA.

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Classifications MeSH