Kidney injury after cardiopulmonary bypass in infants with congenital heart disease
TI Yun-Xing, PAN Zheng-Xia, WU Chun, WANG Gang, LI Hong-Bo, LI Yong-Gang, AN Yong, DAI Jiang-Tao
Key Laboratory of Developmental Diseases in Childhood (Chongqing Medical University), Ministry of Education, Chongqing 400014,China. Email: Panzhengxia@yahoo.com.cn
Abstract:OBJECTIVE: To study kidney injury in infants with congenital heart disease (CHD) who underwent cardiac surgery with cardiopulmonary bypass (CPB). METHODS: Forty CHD infants undergoing cardiac surgery with CPB from October 2009 to July 2010 were enrolled. The concentrations of serum tumor necrosis factor-alpha (TNF-α), interleukin-6 (IL-6), cystatin C (CysC) and urinary N-acetyl-beta-D-glucosaminidase (NAG) were detected using ELISA before bypass, at the end of surgery, and 2 hrs, 6 hrs and 24 hrs after surgery. Serum concentrations of creatinine (Cr) and urea nitrogen (BUN) were measured with conventional biochemistry technique before and after surgery. RESULTS: The concentrations of serum Cr and BUN were normal before and after surgery. After CPB, the concentrations of serum TNF-α and IL-6 and urinary NAG increased significantly (P<0.05). Serum TNF-α was positively correlated with urinary NAG and serum CysC (r=0.195, 0.190,respectively; both P<0.05). Serum IL-6 was positively correlated with urinary NAG (r=0.278, P<0.01). The positive rate in kidney injury was detected by serum CysC and urinary NAG were significantly higher than by serum Cr or BUN (both P<0.01). CONCLUSIONS: CPB can cause acute kidney injury in infants, which may be correlated with the increase in the concentrations of serum TNF-α and IL-6. Serum CysC and urinary NAG may be used as sensitive markers for reflecting the changes of renal function.
TI Yun-Xing,PAN Zheng-Xia,WU Chun et al. Kidney injury after cardiopulmonary bypass in infants with congenital heart disease[J]. CJCP, 2011, 13(5): 385-387.
[1]Randers E, Krue S, Erlandsen EJ, Danielsen H, Hansen LG. Reference interval for serum cystatin C in children[J].Clin Chem, 1999, 45(10): 1856-1858.
[2]Shin HS, Jung YS, Rim H. Reference values for serum cystatin C by nephelometric immunoassay in healthy young Korean men[J].Korean J Nephrol, 2010, 29:17-22.
[3]Nishida M, Kawakatsu H, Komatsu H, Ishiwari K, Tamai M,Tsunamoto K, et al. Values for urinary beta 2-microglobulin and N-acetyl-beta-D-glucosaminidase in normal healthy infants[J].Acta Paediatr Jpn, 1998, 40(5): 424-426.
[4]Pedersen KR, Povlsen JV, Christensen S, Pedersen J, Hjortholm K, Larsen SH, et al. Risk factors for acute renal failure requiring dialysis after surgery for congenital heart disease in children[J].Acta Anaesthesiol Scand, 2007, 51(10): 1344-1349.
[5]Ricci Z, Stazi GV, Di Chiara L, Morelli S, Vitale V, Giorni C, et al. Fenoldopam in newborn patients undergoing cardiopulmonary bypass: controlled clinical trial[J]. Interact Cardiovasc Thorac Surg, 2008, 7(6): 1049-1053.
[6]Parikh CR, Mishra J, Thiessen-Philbrook H, Dursun B, Ma Q, Kelly C, et al. Urinary IL-18 is an early predictive biomarker of acute kidney injury after cardiac surgery[J].Kidney Int, 2006, 70(1):199-203.
[10]Wan S, LeClerc JL, Vincent JL. Inflammatory response to cardiopulmonary bypass: mechanisms involved and possible therapeutic strategies[J].Chest, 1997, 112(3): 676-692.
[11]Wan S, Yim AP. Multi-organ protection during open heart surgery[J].Chin Med J (Engl), 2001, 114(1):3-8.
[13]Dittrich S, Aktuerk D, Seitz S, Mehwald P, Schulte-M-nting J, Schlensak C, et al. Effects of ultrafiltration and peritoneal dialysis on proinflammatory cytokines during cardiopulmonary bypass surgery in newborns and infants[J].Eur J Cardiothorac Surg, 2004, 25(6): 935-940.