The association of cyclic parenteral nutrition and decreased incidence of cholestatic liver disease in patients with gastroschisis

Journal of Pediatric Surgery

Volumn 44, Issue 1, 2009, Pages 183-189

  Jensen, Aaron R ^a   Goldin, Adam B ^a,b   Koopmeiners, Joseph S ^c   Stevens, Jennifer ^b   Waldhausen, John H T ^a,b   Kim, Stephen S ^a,b  

^a UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

^b SEATTLE CHILDREN S RESEARCH INSTITUTE   (United States)

^c UNIVERSITY OF WASHINGTON   (United States)

Author keywords

Cholestasis; Cycled; Cyclic; Gastroschisis; Hyperalimentation; Hyperbilirubinemia; Neonatal; Nutrition; Parenteral; TPN

Indexed keywords

ARTICLE; CONTROLLED STUDY; GASTROSCHISIS; HOSPITAL MANAGEMENT; HUMAN; HYPERBILIRUBINEMIA; INCIDENCE; INFANT; INTRAHEPATIC CHOLESTASIS; MAJOR CLINICAL STUDY; NEWBORN; PARENTERAL NUTRITION; PRIORITY JOURNAL; RETROSPECTIVE STUDY; RISK FACTOR;

CHOLESTASIS; FEMALE; GASTROSCHISIS; HUMANS; HYPERBILIRUBINEMIA; INCIDENCE; INFANT; INFANT, NEWBORN; MALE; PARENTERAL NUTRITION; PROPORTIONAL HAZARDS MODELS; RETROSPECTIVE STUDIES; RISK FACTORS; TREATMENT OUTCOME;

EID: 58249129141     PISSN: 00223468     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpedsurg.2008.10.033     Document Type: Article

References (37)

1. Peden V.H., Witzleben C.L., and Skelton M.A. Total parenteral nutrition. J Pediatr 78 1 (1971) 180-181
2. Rager R., and Finegold M.J. Cholestasis in immature newborn infants: is parenteral alimentation responsible?. J Pediatr 86 2 (1975) 264-269
3. Kubota A., Yonekura T., Hoki M., et al. Total parenteral nutrition-associated intrahepatic cholestasis in infants: 25 years' experience. J Pediatr Surg 35 7 (2000) 1049-1051
4. Albers M.J., de Gast-Bakker D.A., van Dam N.A., et al. Male sex predisposes the newborn surgical patient to parenteral nutrition-associated cholestasis and to sepsis. Arch Surg 137 7 (2002) 789-793
5. Beath S.V., Davies P., Papadopoulou A., et al. Parenteral nutrition-related cholestasis in postsurgical neonates: multivariate analysis of risk factors. J Pediatr Surg 31 4 (1996) 604-606
6. Sondheimer J.M., Asturias E., and Cadnapaphornchai M. Infection and cholestasis in neonates with intestinal resection and long-term parenteral nutrition. J Pediatr Gastroenterol Nutr 27 2 (1998) 131-137
7. Wright K., Ernst K.D., Gaylord M.S., et al. Increased incidence of parenteral nutrition-associated cholestasis with aminosyn PF compared to trophamine. J Perinatol 23 6 (2003) 444-450
8. Wales P.W., de Silva N., Kim J.H., et al. Neonatal short bowel syndrome: a cohort study. J Pediatr Surg 40 5 (2005) 755-762
9. Suita S., Masumoto K., Yamanouchi T., et al. Complications in neonates with short bowel syndrome and long-term parenteral nutrition. JPEN J Parenter Enteral Nutr 23 5 Suppl (1999) S106-S109
10. Yip Y.Y., Lim A.K., R J., et al. A multivariate analysis of factors predictive of parenteral nutrition-related cholestasis (TPN cholestasis) in VLBW infants. J Singapore Paediatr Soc 32 3-4 (1990) 144-148
11. Meehan J.J., and Georgeson K.E. Prevention of liver failure in parenteral nutrition-dependent children with short bowel syndrome. J Pediatr Surg 32 3 (1997) 473-475
12. San Luis V.A., and Btaiche I.F. Ursodiol in patients with parenteral nutrition-associated cholestasis. Ann Pharmacother 41 11 (2007) 1867-1872
13. Teitelbaum D.H., Tracy Jr. T.F., Aouthmany M.M., et al. Use of cholecystokinin-octapeptide for the prevention of parenteral nutrition-associated cholestasis. Pediatrics 115 5 (2005) 1332-1340
14. Forchielli M.L., Gura K.M., Sandler R., et al. Aminosyn PF or trophamine: which provides more protection from cholestasis associated with total parenteral nutrition?. J Pediatr Gastroenterol Nutr 21 4 (1995) 374-382
15. Gura K.M., Duggan C.P., Collier S.B., et al. Reversal of parenteral nutrition-associated liver disease in two infants with short bowel syndrome using parenteral fish oil: implications for future management. Pediatrics 118 1 (2006) e197-e201
16. Kohl M., Wedel T., Entenmann A., et al. Influence of different intravenous lipid emulsions on hepatobiliary dysfunction in a rabbit model. J Pediatr Gastroenterol Nutr 44 2 (2007) 237-244
17. Shin J.I., Namgung R., Park M.S., et al. Could lipid infusion be a risk for parenteral nutrition-associated cholestasis in low birth weight neonates?. Eur J Pediatr 167 2 (2008) 197-202
18. Spencer A.U., Yu S., Tracy T.F., et al. Parenteral nutrition-associated cholestasis in neonates: multivariate analysis of the potential protective effect of taurine. JPEN J Parenter Enteral Nutr 29 5 (2005) 337-343 [discussion 43-4]
19. Javid P.J., Collier S., Richardson D., et al. The role of enteral nutrition in the reversal of parenteral nutrition-associated liver dysfunction in infants. J Pediatr Surg 40 6 (2005) 1015-1018
20. Scribner B.H., Cole J.J., Christopher T.G., et al. Long-term total parenteral nutrition. The concept of an artificial gut. JAMA 212 3 (1970) 457-463
21. Byrne W.J., Halpin T.C., Asch M.J., et al. Home total parenteral nutrition: an alternative approach to the management of children with severe chronic small bowel disease. J Pediatr Surg 12 3 (1977) 359-366
22. Matuchansky C., Morichau-Beauchant M., Druart F., et al. Cyclic (nocturnal) total parenteral nutrition in hospitalized adult patients with severe digestive diseases. Report of a prospective study. Gastroenterology 81 3 (1981) 433-437
23. Messing B., Beliah M., Girard-Pipau F., et al. Technical hazards of using nutritive mixtures in bags for cyclical intravenous nutrition: comparison with standard intravenous nutrition in 48 gastroenterological patients. Gut 23 4 (1982) 297-303
24. Strobel C.T., Byrne W.J., Fonkalsrud E.W., et al. Home parenteral nutrition: results in 34 pediatric patients. Ann Surg 188 3 (1978) 394-403
25. Hwang T.L., Lue M.C., and Chen L.L. Early use of cyclic TPN prevents further deterioration of liver functions for the TPN patients with impaired liver function. Hepatogastroenterology 47 35 (2000) 1347-1350
26. Maini B., Blackburn G.L., Bistrian B.R., et al. Cyclic hyperalimentation: an optimal technique for preservation of visceral protein. J Surg Res 20 6 (1976) 515-525
27. Ternullo S., and Burckart G. Experience with Cyclic Hyperalimentation in Infants (Abstract). JPEN J Parenter Enteral Nutr 3 (1979) 516
28. Collier S., Crouch J., Hendricks K., et al. Use of cyclic parenteral nutrition in infants less than 6 months of age. Nutr Clin Pract 9 2 (1994) 65-68
29. Takehara H., Hino M., Kameoka K., et al. A new method of total parenteral nutrition for surgical neonates: it is possible that cyclic TPN prevents intrahepatic cholestasis. Tokushima J Exp Med 37 3-4 (1990) 97-102
30. Just B., Messing B., Darmaun D., et al. Comparison of substrate utilization by indirect calorimetry during cyclic and continuous total parenteral nutrition. Am J Clin Nutr 51 1 (1990) 107-111
31. Pullicino E., Goldberg G.R., and Elia M. Energy expenditure and substrate metabolism measured by 24 h whole-body calorimetry in patients receiving cyclic and continuous total parenteral nutrition. Clin Sci (Lond) 80 6 (1991) 571-582
32. Lerebours E., Rimbert A., Hecketsweiler B., et al. Comparison of the effects of continuous and cyclic nocturnal parenteral nutrition on energy expenditure and protein metabolism. JPEN J Parenter Enteral Nutr 12 4 (1988) 360-364
33. Matuchansky C., Fabre J., Guillard O., et al. Effects of cyclic (nocturnal) total parenteral nutrition and continuous enteral nutrition on circadian rhythms of blood lipids, lipoproteins and apolipoproteins in humans. Am J Clin Nutr 41 4 (1985) 727-734
34. Yokoyama S., Hirakawa H., Soeda J., et al. Twenty-four-hour profile of growth hormone in cyclic nocturnal total parenteral nutrition. Pediatrics 100 6 (1997) 973-976
35. Messing B., Pontal P.J., and Bernier J.J. Metabolic study during cyclic total parenteral nutrition in adult patients with and without corticosteroid-induced hypercatabolism: comparison with standard total parenteral nutrition. JPEN J Parenter Enteral Nutr 7 1 (1983) 21-25
36. Forsberg E., Soop M., Lepapea A., et al. Metabolic and thermogenic response to continuous and cyclic total parenteral nutrition in traumatised and infected patients. Clin Nutr 13 5 (1994) 291-301
37. Bendorf K., Friesen C.A., and Roberts C.C. Glucose response to discontinuation of parenteral nutrition in patients less than 3 years of age. JPEN J Parenter Enteral Nutr 20 2 (1996) 120-122