Predicting acute kidney injury using urinary liver-type fatty-acid binding protein and serum N-terminal pro-B-type natriuretic peptide levels in patients treated at medical cardiac intensive care units

The early prediction of acute kidney injury (AKI) can facilitate timely intervention and prevent complications. We aimed to understand the predictive value of urinary liver-type fatty-acid binding protein (L-FABP) levels on admission to medical (non-surgical) cardiac intensive care units (CICUs) for...

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Veröffentlicht in:Critical care (London, England) England), 2018-08, Vol.22 (1), p.197-197, Article 197
Hauptverfasser: Naruse, Hiroyuki, Ishii, Junnichi, Takahashi, Hiroshi, Kitagawa, Fumihiko, Nishimura, Hideto, Kawai, Hideki, Muramatsu, Takashi, Harada, Masahide, Yamada, Akira, Motoyama, Sadako, Matsui, Shigeru, Hayashi, Mutsuharu, Sarai, Masayoshi, Watanabe, Eiichi, Izawa, Hideo, Ozaki, Yukio
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Sprache:eng
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Zusammenfassung:The early prediction of acute kidney injury (AKI) can facilitate timely intervention and prevent complications. We aimed to understand the predictive value of urinary liver-type fatty-acid binding protein (L-FABP) levels on admission to medical (non-surgical) cardiac intensive care units (CICUs) for AKI, both independently and in combination with serum N-terminal pro-B-type natriuretic peptide (NT-proBNP) levels. We prospectively investigated the predictive value of L-FABP and NT-proBNP for AKI in a large, heterogeneous cohort of patients treated in medical CICUs. Baseline urinary L-FABP and serum NT-proBNP were measured on admission. AKI was diagnosed according to the Kidney Disease: Improving Global Outcomes criteria. We studied 1273 patients (mean age, 68 years), among whom 46% had acute coronary syndromes, 38% had acute decompensated heart failure, 5% had arrhythmia, 3% had pulmonary hypertension, 2% had acute aortic syndrome, 2% had infective endocarditis, and 1% had Takotsubo cardiomyopathy. Urinary L-FABP levels correlated with serum NT-proBNP levels (r = 0.17, p 
ISSN:1364-8535
1466-609X
1364-8535
1366-609X
DOI:10.1186/s13054-018-2120-z