Risk of nonsteroidal anti-inflammatory drug-associated renal dysfunction among neonates diagnosed with patent ductus arteriosus and treated with gentamicin

被引:16
作者
Constance, J. E. [1 ]
Reith, D. [2 ]
Ward, R. M. [1 ]
Balch, A. [1 ]
Stockmann, C. [1 ]
Korgenski, E. K. [1 ,3 ]
Thorell, E. A. [1 ]
Sherwin, C. M. T. [1 ]
机构
[1] Univ Utah, Sch Med, Dept Pediat, Div Clin Pharmacol, 295 Chipeta Way, Salt Lake City, UT 84108 USA
[2] Univ Otago, Dunedin Sch Med, Sect Paediat & Child Hlth, Dunedin, New Zealand
[3] Intermt Healthcare, Pediat Clin Program, Salt Lake City, UT USA
关键词
ACUTE KIDNEY INJURY; BIRTH-WEIGHT; PRETERM INFANTS; INTRAVENTRICULAR HEMORRHAGE; PLASMA CREATININE; INDOMETHACIN; IBUPROFEN; CLOSURE; MATURATION; MANAGEMENT;
D O I
10.1038/jp.2017.80
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
OBJECTIVE: To evaluate the risk of nonsteroidal anti-inflammatory drug (NSAID) therapy-associated acute kidney injury (AKI) among neonates diagnosed with patent ductus arteriosus (PDA) who are treated with gentamicin. STUDY DESIGN: Multicenter retrospective observational study of patients <= 44 postmenstrual weeks of age diagnosed with PDA who received gentamicin during hospitalization between January 2006 and December 2014. Patients with and without NSAID exposure were matched on covariates associated with AKI and NSAID therapy. The primary end point, AKI, was defined according to Kidney Disease Improving Global Outcomes neonatal criteria. RESULTS: The rate of AKI for the entire cohort (n = 594) was 12% (n = 71). Among neonates receiving NSAIDS, 14.8% (n = 44) experienced an AKI as compared to 9.1% (n = 27) for those who were not exposed (relative risk, 1.6; 95% confidence interval, 1.0 to 2.6). Therefore, the attributable risk of NSAID use was 5.7% (95% confidence interval, 0.5 to 11.0). CONCLUSION: Among neonates with PDA and receiving gentamicin, NSAID therapy increases the risk of AKI by about 6%.
引用
收藏
页码:1093 / 1102
页数:10
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