Gupta Kunal, Wang Hongyue, Amin Sanjiv B
Department of Pediatrics, Division of Neonatology.
Biostatistics, Golisano Children's Hospital at Strong, University of Rochester Medical Center, Rochester, New York, USA.
JPEN J Parenter Enteral Nutr. 2016 Mar;40(3):335-41. doi: 10.1177/0148607114555161. Epub 2014 Oct 13.
To evaluate whether intravenous lipid (IL) intake is associated with the development of parenteral nutrition-associated cholestasis (PNAC) in infants younger than 32 weeks gestational age (GA).
A retrospective matched case-control study (1:1) was performed including infants younger than 32 weeks GA admitted to the neonatal intensive care unit within 48 hours after birth. Infants with a chromosomal disorder, TORCH infection (toxoplasmosis, syphilis, rubella, cytomegalovirus, herpes, human immunodeficiency virus, and parvovirus), metabolic disorder, and/or surgical abnormality of the hepatobiliary system were excluded. Infants with PNAC (direct bilirubin 2 mg/dL or higher) comprised the case group, while infants without PNAC comprised the control group. Duration of parenteral nutrition, intravenous fluid intake on the day of development of PNAC, and GA were used as matching criteria.
A total of 46 subjects were studied. Daily average intravenous dextrose (ID) intake was significantly higher in infants with PNAC compared with infants without PNAC (12.72 ± 2.5 g/kg/d and 10.64 ± 2.1 g/kg/d, respectively, P = .004). On comparison of receiver operating characteristic curves, the area under the curve for ID intake (0.74) was significantly higher (P = .01) compared with the area under the curve for IL intake (0.59) and intravenous protein (IP) intake (0.52). On logistic regression, daily ID intake was associated with PNAC (odds ratio 1.7; 95% CI, 1.04-2.9, P = .03) after controlling for daily IP and IL intake.
ID intake may be associated with the development of PNAC in premature infants. Our findings suggest that limiting ID intake may be more useful than limiting IL intake in reducing the incidence of PNAC in premature infants.
评估静脉输注脂质(IL)摄入量与胎龄小于32周的婴儿发生肠外营养相关胆汁淤积(PNAC)之间是否存在关联。
进行一项回顾性配对病例对照研究(1:1),纳入出生后48小时内入住新生儿重症监护病房、胎龄小于32周的婴儿。排除患有染色体疾病、TORCH感染(弓形虫病、梅毒、风疹、巨细胞病毒、疱疹、人类免疫缺陷病毒和细小病毒)、代谢紊乱和/或肝胆系统手术异常的婴儿。患有PNAC(直接胆红素≥2mg/dL)的婴儿组成病例组,未患PNAC的婴儿组成对照组。肠外营养持续时间、发生PNAC当天的静脉液体摄入量和胎龄用作匹配标准。
共研究了46名受试者。与未患PNAC的婴儿相比,患PNAC的婴儿每日平均静脉输注葡萄糖(ID)摄入量显著更高(分别为12.72±2.5g/kg/d和10.64±2.1g/kg/d,P = 0.004)。比较受试者工作特征曲线时,ID摄入量的曲线下面积(0.74)显著高于IL摄入量(0.59)和静脉输注蛋白质(IP)摄入量(0.52)的曲线下面积(P = 0.01)。在逻辑回归分析中,在控制每日IP和IL摄入量后,每日ID摄入量与PNAC相关(比值比1.7;95%CI,1.04 - 2.9,P = 0.03)。
ID摄入量可能与早产儿PNAC的发生有关。我们的研究结果表明,在降低早产儿PNAC发生率方面,限制ID摄入量可能比限制IL摄入量更有效。