2002
DOI: 10.1054/clnu.2002.0554
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Prevalence, outcome and associated factors of deranged liver function tests in patients on home parenteral nutrition

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Cited by 116 publications
(91 citation statements)
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“…17,[82][83][84][85] The incidence of advanced liver disease (fibrosis or cirrhosis) varies between 0% and 50% of patients in retrospective cohorts on long-term PN, with an associated reported mortality rate of up to 22%. 17,[82][83][84][85] This discrepancy in the incidence in severe liver disease between different patient cohorts may reflect an increased use of parenteral lipid predisposing to higher rates of severe liver disease. 17 Patients with ultra-short bowel (<50 cm) are at greatest risk of severe liver disease, which this may, of course, reflect their greater calorie requirement.…”
Section: Liver Diseasementioning
confidence: 99%
“…17,[82][83][84][85] The incidence of advanced liver disease (fibrosis or cirrhosis) varies between 0% and 50% of patients in retrospective cohorts on long-term PN, with an associated reported mortality rate of up to 22%. 17,[82][83][84][85] This discrepancy in the incidence in severe liver disease between different patient cohorts may reflect an increased use of parenteral lipid predisposing to higher rates of severe liver disease. 17 Patients with ultra-short bowel (<50 cm) are at greatest risk of severe liver disease, which this may, of course, reflect their greater calorie requirement.…”
Section: Liver Diseasementioning
confidence: 99%
“…En nuestra serie sólo destacaron alteraciones menores de las enzimas hepáticas, sin hiperbilirrubinemia, como ocurre con frecuencia en los pacientes que utilizan NP [25][26][27] . Creemos que se esto se relaciona al rápido inicio del aporte enteral en nuestros pacientes.…”
Section: Discussionunclassified
“…It has been reported consistently that around 50% of children on PN for 4-12 weeks have cholestasis [2,6,7], but in adults there is a much wider variation in the frequency of IFALD with around 30-50% having a mild disturbance of liver function tests and between 2% [8] and 30% [9] becoming cholestatic after a median of 6 months of PN. These variations in the incidence and subsequent natural history of IFALD reflect differences in case mix, health care systems, and the management of PN solutions, but it is reasonable to assume that one half of children and a third of adults on PN will develop mild liver disease with the potential to progress if not managed actively (see later in this chapter).…”
Section: Incidence and Prevalencementioning
confidence: 99%
“…In contrast to children, the progression of IFALD was slower with a mortality of 22% for the group as a whole, with a 6-year survival of 84% in the patients aged less than 40 years and 53% 6-year survival for older patients. (See also In the United Kingdom, complicated IFALD in adults is uncommon with only around 2% of long-term PN patients becoming frankly jaundiced [8]. The reason for the difference in frequency of jaundice between different units is unclear but may reflect differences in exposure to intravenous lipid and the availability of Nutritional Support Teams.…”
Section: Clinicalmentioning
confidence: 99%