Acute Kidney Injury in Trauma Patients Admitted to Critical Care: Development and Validation of a Diagnostic Prediction Model

被引:38
作者
Haines, Ryan W. [1 ,2 ]
Lin, Shih-Pin [3 ,4 ,5 ]
Hewson, Russell [1 ,2 ]
Kirwan, Christopher J. [1 ,2 ,7 ]
Torrance, Hew D. [1 ,2 ,6 ]
O'Dwyer, Michael J. [1 ,2 ]
West, Anita [6 ]
Brohi, Karim [6 ]
Pearse, Rupert M. [1 ,2 ]
Zolfaghari, Parjam [1 ,2 ]
Prowle, John R. [1 ,2 ,7 ]
机构
[1] Barts Hlth NHS Trust, Royal London Hosp, Adult Crit Care Unit, Whitechapel Rd, London E1 1BB, England
[2] Queen Mary Univ London, William Harvey Res Inst, London, England
[3] Natl Yang Ming Univ, Dept Anesthesiol, Taipei Vet Gen Hosp, Taipei, Taiwan
[4] Natl Yang Ming Univ, Sch Med, Taipei, Taiwan
[5] Natl Taiwan Univ, Div Biostat, Grad Inst Epidemiol & Prevent Med, Coll Publ Hlth, Taipei, Taiwan
[6] Queen Mary Univ London, Ctr Trauma Sci, Blizard Inst, London, England
[7] Barts Hlth NHS Trust, Royal London Hosp, Dept Renal Med & Transplantat, Whitechapel Rd, London E1 1BB, England
来源
SCIENTIFIC REPORTS | 2018年 / 8卷
关键词
ACUTE-RENAL-FAILURE; ILL PATIENTS; RISK-FACTORS; TRANSFUSION; DISEASE; SCORE;
D O I
10.1038/s41598-018-21929-2
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Acute Kidney Injury (AKI) complicating major trauma is associated with increased mortality and morbidity. Traumatic AKI has specific risk factors and predictable time-course facilitating diagnostic modelling. In a single centre, retrospective observational study we developed risk prediction models for AKI after trauma based on data around intensive care admission. Models predicting AKI were developed using data from 830 patients, using data reduction followed by logistic regression, and were independently validated in a further 564 patients. AKI occurred in 163/830 (19.6%) with 42 (5.1%) receiving renal replacement therapy (RRT). First serum creatinine and phosphate, units of blood transfused in first 24 h, age and Charlson score discriminated need for RRT and AKI early after trauma. For RRT c-statistics were good to excellent: development: 0.92 (0.88-0.96), validation: 0.91 (0.86-0.97). Modelling AKI stage 2-3, c-statistics were also good, development: 0.81 (0.75-0.88) and validation: 0.83 (0.74-0.92). The model predicting AKI stage 1-3 performed moderately, development: c-statistic 0.77 (0.72-0.81), validation: 0.70 (0.64-0.77). Despite good discrimination of need for RRT, positive predictive values (PPV) at the optimal cut-off were only 23.0% (13.7-42.7) in development. However, PPV for the alternative endpoint of RRT and/or death improved to 41.2% (34.8-48.1) highlighting death as a clinically relevant endpoint to RRT.
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页数:9
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