Literature DB >> 22568414

Aetio-pathogenesis and the management of spontaneous liver bleeding in the West: a 16-year single-centre experience.

Narendra Battula1, Dimitrios Tsapralis, Arjun Takhar, Chris Coldham, David Mayer, John Isaac, Paolo Muiesan, Robert P Sutcliffe, Ravi Marudanayagam, Darius F Mirza, Simon R Bramhall.   

Abstract

BACKGROUND: Spontaneous liver bleeding (SLB) is a rare but potentially fatal complication. In contrast to the East, various benign pathologies are the source of SLB in the West. An accurate diagnosis and a timely implementation of appropriate treatment are crucial in the management of these patients. The present study presents a large Western experience of SLB from a specialist liver centre.
METHODS: A retrospective analysis of patients presented with SLB between January 1995 and January 2011.
RESULTS: Sixty-seven patients had SLB, 44 (66%) were female and the median age at presentation was 47 years. Abrupt onset upper abdominal pain was the presenting symptom in 65 (97%) patients. The aetiology for SLB was hepatic adenoma in 27 (40%), hepatocellular carcinoma (HCC) in 17 (25%) and various other liver pathologies in the rest. Emergency treatment included a conservative approach in 42 (64%), DSA and embolization in 6 (9%), a laparotomy and packing in 6 (9%) and a liver resection in 11 (16%) patients. Eleven (16%) patients had further planned treatments. Seven (10%) died during the same admission but the mortality was highest in patients with HELLP syndrome. At a median follow-up of 54 months all patients with benign disease are alive. The 1-, 3- and 5-year survival of patients with HCC was 59%, 35% and 17%, respectively.
CONCLUSION: SLB is a life-threatening complication of various underlying conditions and may represent their first manifestation. The management should include initial haemostasis followed by appropriate staging investigations to provide a definitive treatment for each individual patient.
© 2012 International Hepato-Pancreato-Biliary Association.

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Year:  2012        PMID: 22568414      PMCID: PMC3384862          DOI: 10.1111/j.1477-2574.2012.00460.x

Source DB:  PubMed          Journal:  HPB (Oxford)        ISSN: 1365-182X            Impact factor:   3.647


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