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A New Criterion for Pediatric AKI Based on the Reference Change Value of Serum Creatinine
Journal of the American Society of Nephrology ( IF 10.3 ) Pub Date : 2018-09-01 , DOI: 10.1681/asn.2018010090
Xin Xu 1 , Sheng Nie 1 , Aihua Zhang 2 , Mao Jianhua 3 , Hai-Peng Liu 4 , Huimin Xia 5 , Hong Xu 6 , Zhangsuo Liu 7 , Shipin Feng 8 , Wei Zhou 9 , Xuemei Liu 10 , Yonghong Yang 11 , Yuhong Tao 12 , Yunlin Feng 13 , Chunbo Chen 14 , Mo Wang 15 , Yan Zha 16 , Jian-Hua Feng 17 , Qingchu Li 18 , Shuwang Ge 19 , Jianghua Chen 20 , Yongcheng He 21 , Siyuan Teng 22 , Chuanming Hao 23 , Bi-Cheng Liu 24 , Ying Tang 25 , Li-Jun Wang 26 , Jin-Lei Qi 26 , Wenjuan He 1 , Pinghong He 1 , Youhua Liu 1 , Fan Fan Hou 1
Affiliation  

Background Current definitions of AKI do not take into account serum creatinine’s high variability in children.

Methods We analyzed data from 156,075 hospitalized children with at least two creatinine tests within 30 days. We estimated reference change value (RCV) of creatinine on the basis of age and initial creatinine level in children without kidney disease or known AKI risk, and we used these data to develop a model for detecting pediatric AKI on the basis of RCV of creatinine. We defined pediatric AKI according to pediatric reference change value optimized for AKI in children (pROCK) as creatinine increase beyond RCV of creatinine, which was estimated as the greater of 20 μmol/L or 30% of the initial creatinine level.

Results Of 102,817 children with at least two serum creatinine tests within 7 days, 5432 (5.3%) had AKI as defined by pROCK compared with 15,647 (15.2%) and 10,446 (10.2%) as defined by pediatric RIFLE (pRIFLE) and Kidney Disease Improving Global Outcomes (KDIGO), respectively. Children with pROCK-defined AKI had significantly increased risk of death (hazard ratio, 3.56; 95% confidence interval, 3.15 to 4.04) compared with those without AKI. About 66% of patients with pRIFLE-defined AKI and 51% of patients with KDIGO-defined AKI, mostly children with initial creatinine level of <30 μmol/L, were reclassified as non-AKI by pROCK, and mortality risk in these children was comparable with risk in those without AKI by all definitions.

Conclusions pROCK criterion improves detection of “true” AKI in children compared with earlier definitions that may lead to pediatric AKI overdiagnosis.



中文翻译:

基于血清肌酐参考变化值的小儿AKI新判据

背景技术当前对AKI的定义并未考虑儿童血清肌酐的高变异性。

方法我们在30天内对至少156,075名住院儿童进行了至少两次肌酐检测的数据进行了分析。我们根据年龄和未患有肾脏疾病或已知AKI风险的儿童的肌酐初始水平估算了肌酐的参考变化值(RCV),并使用这些数据建立了基于肌酐RCV的儿科AKI检测模型。我们根据儿童(pROCK)为超出肌酸酐RCV肌酐升高,这是估计为20更大的用于AKI优化儿科基准值变化量定义的儿科AKI μ摩尔/ L的初始肌酸酐水平的30%。

结果102 817名儿童在7天内进行了至少两次血清肌酐检测,其中pROCK定义的AKI为5432(5.3%),而儿科RIFLE(pRIFLE)和肾脏疾病为15647(15.2%)和10446(10.2%)分别改善全球成果(KDIGO)。与没有AKI的儿童相比,患有pROCK定义的AKI的儿童的死亡风险显着增加(危险比,3.56; 95%的置信区间,3.15至4.04)。约66%的患者用pRIFLE定义的AKI和患者KDIGO定义的AKI 51%,主要是与<30的初始肌酸酐水平的儿童μ摩尔/ L,被重新分类为非AKI通过pROCK,并且在这些儿童的死亡风险在所有定义中,在没有AKI的患者中,风险具有可比性。

结论与早期定义相比,pROCK标准可改善儿童“真实” AKI的检测,这可能导致儿科AKI过度诊断。

更新日期:2018-09-01
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