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L Fabris

Publications and source records attributed to L Fabris.

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Primary sclerosing cholangitis: clinical presentation, natural history and prognostic variables: an Italian multicentre study. The Italian PSC Study Group.

OBJECTIVE: Because large-scale reports of PSC in the Mediterranean area we are still lacking, in this study we evaluated by Kaplan-Meyer analysis the natural history of primary sclerosing cholangitis (PSC) in Italy and by means of other statistical methods we identified the variables most useful in predicting survival of such patients. DESIGN: Retrospective multicentre study of unselected patients with PSC. Several variables involving sex, age, associated diseases, clinical features, laboratory, cholangiographic and histological findings at presentation and clinical outcome at data recording were collected by means of a detailed questionnaire. SETTING: 16 Italian university and regional hospitals all over the country, thus giving a geographically representative population. PATIENTS: A total of 117 PSC patients (73 men and 44 women); median age 35 years. METHODS: Survival analysis was performed by the Kaplan-Meyer method; the prognostic influence on survival of collected data was evaluated by univariate chi(2) analysis with Wilcoxon and log-rank tests. The same prognostic variables were also evaluated by multivariate analysis (Cox model), using a stepwise regression procedure. All statistical analyses were performed using the SAS statistical software. RESULTS: At presentation 70% of patients were symptomatic; symptoms did not relate to liver histology. Both intra- and extrahepatic bile duct lesions were detected in 46% of patients at cholangiography. Inflammatory bowel disease was found in 54% of symptomatic patients, ulcerative colitis was 36% of total. Clinical outcome (91/117): 15 underwent liver transplantation or died from liver disease (cholangiocarcinoma). Survival at 10 years was 74%. Features of poor prognosis were cholesterol, aspartate aminotransferase (AST), haemoglobin and albumin. CONCLUSION: PSC in Italy mainly follows a benign course and among clinical features recorded at presentation, serum cholesterol, AST, haemoglobin and albumin may provide some objective criteria to assess disease severity.

Adult

[Methylcellulose].

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Chemistry, Pharmaceutical

Diagnostic approach to primary sclerosing cholangitis: open questions.

Over the last ten years the incidence of primary sclerosing cholangitis (PSC) presented a progressive increase, showing an association with chronic inflammatory bowel disease (IBD) in 50-70% of the cases. Nowadays, however, the prevalence of PSC is still unknown, mainly because of its difficult identification. In contrast to primary biliary cirrhosis (PBC), which is strongly associated with the presence of anti-mitochondrial antibodies (AMA) in serum, a similar reliable diagnostic marker has not yet been demonstrated in PSC. In this review we tried to investigate the controversial diagnostic aspects which may interfere with the initial assessment of PSC syndrome. Alkaline phosphatase (ALP) and endoscopic retrograde cholangiography (ERC) are actually the two cornerstones of the clinical setting, but if alone, they do not seem to provide sufficient accuracy. Furthermore, liver biopsy, perhaps more sensitive but not always specific, is generally performed too late. In our opinion, epidemiologic studies are needed in Italy and elsewhere in order to evaluate PSC prevalence. Moreover, the analysis of these results might lead to an earlier detection of the disease and, perhaps, favourably modify its natural history.

Cholangitis, Sclerosing