Chronic biochemical cholestasis in patients receiving home parenteral nutrition: prevalence and predisposing factors

Summary Background  Chronic biochemical cholestasis has been shown to be associated with a fivefold increase in histologically advanced liver disease in patients receiving home parenteral nutrition. Aims  To investigate prevalence of chronic biochemical cholestasis in home parenteral nutrition patie...

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Veröffentlicht in:Alimentary pharmacology & therapeutics 2008-04, Vol.27 (7), p.552-560
Hauptverfasser: LLOYD, D. A. J., ZABRON, A. A., GABE, S. M.
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Sprache:eng
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Zusammenfassung:Summary Background  Chronic biochemical cholestasis has been shown to be associated with a fivefold increase in histologically advanced liver disease in patients receiving home parenteral nutrition. Aims  To investigate prevalence of chronic biochemical cholestasis in home parenteral nutrition patients and examine factors influencing its occurrence. Methods  Records of all patients receiving home parenteral nutrition for >6 months treated at a single centre were reviewed and plasma biochemistry recorded. Logistic regression analysis was employed to identify factors associated with prevalence of chronic biochemical cholestasis. Results  Records of 113 patients were reviewed. The point prevalence of chronic biochemical cholestasis was 24%, increasing to 28% if patients receiving parenteral fluid and electrolytes only were excluded. In multivariate analysis, presence of colon in continuity was associated with a significantly lower prevalence of chronic biochemical cholestasis, while total parenteral calorie intake was associated with a higher prevalence of chronic biochemical cholestasis. No association was seen between small intestinal lengths or between parenteral lipid intake and chronic biochemical cholestasis in multivariate analysis. Conclusions  Chronic biochemical cholestasis is common in patients receiving home parenteral nutrition. High parenteral calorie intake and lack of a colon in continuity with small intestine are independently associated with an increased risk of chronic biochemical cholestasis.
ISSN:0269-2813
1365-2036
DOI:10.1111/j.1365-2036.2008.03615.x