Effects of cyclic parenteral nutrition on parenteral-associated liver dysfunction parameters

被引:16
作者
Arenas Villafranca, Jose J. [1 ]
Nieto Guindo, Miriam [1 ]
Alvaro Sanz, Elena [1 ,2 ]
Moreno Santamaria, Manuela [1 ]
Garrido Siles, Marga [1 ]
Abiles, Jimena [1 ]
机构
[1] Costa Sol Hosp, Pharm & Nutr Serv, A7,Km 187, Marbella 29603, Malaga, Spain
[2] C Fernando Villalon Edf Lorcrisur,Bloque 8,Bajo A, Marbella 29670, Malaga, Spain
关键词
Liver dysfunction; Parenteral nutrition; Cyclic parenteral nutrition; Liver parameters; COMPLICATIONS; CHOLESTASIS; TAURINE;
D O I
10.1186/s12937-017-0289-7
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 [营养与食品卫生学];
摘要
Introduction: One of the most common complications of parenteral nutrition (PN) is liver dysfunction (LD). Therapeutic approaches for LD include, among others, administering cyclic parenteral nutrition (cPN), allowing some hours for metabolic rest. The purpose of this study was to evaluate the effectiveness of cPN in treating PN-associated LD. Materials and methods: A retrospective observational study was carried out at the Costa del Sol Hospital in Spain between 2013 and 2014. The study involved inpatients >= 18 years old prescribed with cPN due to the development of PN-associated LD. The hepatic biochemical parameters measured at baseline and after completion of cPN included aspartate aminotransferase (AST), alanine aminotransferase (ALT), gamma-glutamyltransferase (GGT), alkaline phosphatase (ALP) and total bilirubin (TB). Quantitative values (age, biochemical parameters) were compared using matched Student's t-test; the mean change in qualitative variables (sex, indication of PN, hepatic comorbidities, presence of insulin in cPN, infection during cPN, management of LD prior to cPN administrarion) was estimated using Mann-Whitney U test, and bivariate correlation between quantitative variables was determined by Spearman's coefficient of correlation. Results: Thirty-seven patients met inclusion criteria. All hepatic function parameters except ALP improved after the administration of cPN, with statistically significant differences (p < 0.05) in AST GGT and TB. Conclusion: cPN improves PN-associated LD by restoring abnormal AST, GGT, and BT levels to normal, and reducing ALT levels close to normal. The results obtained suggest that the administration of cPN is effective in reverting PN-associated LD.
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页数:5
相关论文
共 21 条
[1]
Review article: hepatobiliary complications associated with total parenteral nutrition [J].
Angelico, M ;
Della Guardia, P .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2000, 14 :54-57
[2]
[Anonymous], 2002, Journal of Parenteral and Enteral Nutrition, V26, P1
[3]
THE INFLUENCE OF TAURINE ON THE BILE-ACID MAXIMUM SECRETORY RATE IN THE GUINEA-PIG [J].
BELLI, DC ;
FOURNIER, LA ;
LEPAGE, G ;
YOUSEF, IM ;
ROY, CC .
PEDIATRIC RESEARCH, 1988, 24 (01) :34-37
[4]
ESPEN Guidelines on Parenteral Nutrition: Surgery [J].
Braga, M. ;
Ljungqvist, O. ;
Soeters, P. ;
Fearon, K. ;
Weimann, A. ;
Bozzetti, F. .
CLINICAL NUTRITION, 2009, 28 (04) :378-386
[5]
BRIONES ER, 1995, J AM COLL NUTR, V14, P219
[6]
Caglieris S, 2000, HEPATO-GASTROENTEROL, V47, P1045
[7]
LIVER-FUNCTION TESTS IN PATIENTS RECEIVING PARENTERAL-NUTRITION [J].
CLARKE, PJ ;
BALL, MJ ;
KETTLEWELL, MGW .
JOURNAL OF PARENTERAL AND ENTERAL NUTRITION, 1991, 15 (01) :54-59
[8]
TAURINE PREVENTS CHOLESTASIS INDUCED BY LITHOCHOLIC ACID SULFATE IN GUINEA-PIGS [J].
DORVIL, NP ;
YOUSEF, IM ;
TUCHWEBER, B ;
ROY, CC .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1983, 37 (02) :221-232
[9]
Cholestasis induced by total parenteral nutrition; effects of the addition of Taurine (Tauramin®) on hepatic function parameters; possible synergistic action of structured lipids (SMOFlipid®) [J].
Gonzalez-Contreras, J. ;
Villalobos Gamez, J. L. ;
Gomez-Sanchez, A. I. ;
Garcia-Almeida, J. M. ;
Enguix Armanda, A. ;
Rius Diaz, F. ;
Lucena Gonzalez, M. I. .
NUTRICION HOSPITALARIA, 2012, 27 (06) :1900-1907
[10]
Liver dysfunction associated with artificial nutrition in critically ill patients [J].
Grau, Teodoro ;
Bonet, Alfonso ;
Rubio, Mercedes ;
Mateo, Dolores ;
Farre, Merce ;
Antonio Acosta, Jose ;
Blesa, Antonio ;
Carlos Montejo, Juan ;
Garcia de Lorenzo, Abelardo ;
Mesejo, Alfonso .
CRITICAL CARE, 2007, 11 (01)