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Evaluation of clinically available renal biomarkers in critically ill adults: A prospective multicenter observational study

Critical Care, ISSN: 1466-609X, Vol: 21, Issue: 1, Page: 46
2017
  • 41
    Citations
  • 0
    Usage
  • 73
    Captures
  • 1
    Mentions
  • 37
    Social Media
Metric Options:   Counts1 Year3 Year

Metrics Details

  • Citations
    41
  • Captures
    73
  • Mentions
    1
    • News Mentions
      1
      • 1
  • Social Media
    37
    • Shares, Likes & Comments
      37
      • Facebook
        37

Most Recent News

Combining Serum Cystatin C and Urinary N-Acetyl-Beta-D-Glucosaminidase Improves the Precision for Acute Kidney Injury Diagnosis after Resection of Intracranial Space-Occupying Lesions

ABSTRACT Background: Postoperative acute kidney injury (AKI) is frequent and associated with adverse outcomes. Unfortunately, the early diagnosis of AKI remains a challenge. Combining functional

Article Description

Background: Although serum cystatin C (sCysC), urinary N-acetyl-β-d-glucosaminidase (uNAG), and urinary albumin/creatinine ratio (uACR) are clinically available, their optimal combination for acute kidney injury (AKI) detection and prognosis prediction remains unclear. We aimed to assess the discriminative abilities of these biomarkers and their possible combinations for AKI detection and intensive care unit (ICU) mortality prediction in critically ill adults. Methods: A multicenter, prospective observational study was conducted in mixed medical-surgical ICUs at three tertiary care hospitals. One thousand eighty-four adult critically ill patients admitted to the ICUs were studied. We assessed the use of individual biomarkers (sCysC, uNAG, and uACR) measured at ICU admission and their combinations with regard to AKI detection and prognosis prediction. Results: AUC-ROCs for sCysC, uNAG, and uACR were calculated for total AKI (0.738, 0.650, and 0.683, respectively), severe AKI (0.839, 0.706, and 0.771, respectively), and ICU mortality (0.727, 0.793, and 0.777, respectively). The panel of sCysC plus uNAG detected total and severe AKI with significantly higher accuracy than either individual biomarkers or the other two panels (uNAG plus uACR or sCysC plus uACR). For detecting total AKI, severe AKI, and ICU mortality at ICU admission, this panel yielded AUC-ROCs of 0.756, 0.863, and 0.811, respectively; positive predictive values of 0.71, 0.31, and 0.17, respectively; and negative predictive values of 0.81, 0.97, and 0.98, respectively. Moreover, this panel significantly contributed to the accuracy of the clinical models for AKI detection and ICU mortality prediction, as measured by the AUC-ROC, continuous net reclassification index, and incremental discrimination improvement index. The comparable performance of this panel was further confirmed with bootstrap internal validation. Conclusions: The combination of a functional marker (sCysC) and a tubular damage marker (uNAG) revealed significantly superior discriminative performance for AKI detection and yielded additional prognostic information on ICU mortality.

Bibliographic Details

Deng, Yujun; Chi, Ruibin; Chen, Shenglong; Ye, Heng; Yuan, Jie; Wang, Lin; Zhai, Yiling; Gao, Lu; Zhang, Danqing; Hu, Linhui; Lv, Bo; Long, Yi; Sun, Cheng; Yang, Xiaobing; Zou, Xia; Chen, Chunbo

Springer Science and Business Media LLC

Medicine

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