Endoscopy 2008; 40(3): 214-218
DOI: 10.1055/s-2007-967024
Original article

© Georg Thieme Verlag KG Stuttgart · New York

Poor outcome in progressive sclerosing cholangitis after septic shock

H.  Kulaksiz1 , 2 , D.  Heuberger2 , S.  Engler2 , A.  Stiehl2
  • 1Department of Internal Medicine, Division of Gastroenterology, University Hospital Ulm, Germany
  • 2Department of Internal Medicine, Division of Gastroenterology, University Hospital Heidelberg, Germany
Further Information

Publication History

submitted 13 May 2007

accepted after revision 18 September 2007

Publication Date:
11 February 2008 (online)

Background and study aims: Progressive sclerosing cholangitis after septic shock is an increasingly diagnosed disease entity. We evaluated the outcome after long-term follow-up of 29 patients treated in our institution between 1995 and 2007.

Patients and methods: Patients with cholestatic liver disease without evidence of pre-existing hepatobiliary disease and who previously required long-term treatment in an intensive care unit for septic shock due to following reasons were included in the study: severe trauma (n = 10; five with burn injury and five following accident), cardiac operation (n = 9), bacterial infection (n = 5), sigmoidectomy (n = 2), operation of aortic aneurysm (n = 3).

Results: In all patients, endoscopic retrograde cholangiopancreatography showed multiple stenoses, pre-stenotic dilatations, and in part rarefication of intrahepatic small bile ducts. The bile ducts were partially filled by black-pigmented or necrotic material. In 18 of 29 patients, liver biopsies were performed and showed fibrosing cholangitis. The endoscopic therapy comprised removal of occluding material, dilation of stenoses, and intermittent stenting if necessary. All endoscopic procedures were done under antibiotic prophylaxis. During follow-up, 19 of the 29 patients died. Three patients received orthotopic liver transplantation. Four patients have been registered for transplantation, and the remaining three patients show signs of severe cholestasis. The actuarial estimate (Kaplan-Meier) indicated a survival free of liver transplantation of 55 % after 1 year, and only 14 % after 6 years. The median survival was 1.1 years.

Conclusions: Progressive sclerosing cholangitis after septic shock is a recently described disease characterized by extremely short survival free of liver transplantation. This disease should be considered in patients who develop cholestasis following treatment of septic shock in an intensive care unit.

References

  • 1 Engler S, Elsing C, Flechtenmacher C. et al . Progressive sclerosing cholangitis after septic shock: a new variant of vanishing bile duct disorders.  Gut. 2003;  52 688-693
  • 2 Benninger J, Grobholz R, Oeztuerk Y. et al . Sclerosing cholangitis following severe trauma: description of a remarkable disease entity with emphasis on possible pathophysiologic mechanisms.  World J Gastroenterol. 2005;  11 4199-4205
  • 3 Jaeger C, Mayer G, Henrich R. et al . Secondary sclerosing cholangitis after long-term treatment in an intensive care unit: clinical presentation, endoscopic findings, treatment, and follow-up.  Endoscopy. 2006;  38 730-734
  • 4 Gossard A A, Angulo P, Lindor K D. Secondary sclerosing cholangitis: a comparison to primary sclerosing cholangitis.  Am J Gastroenterol. 2005;  100 1330-1333
  • 5 Abdalian R, Heathcote E J. Sclerosing cholangitis: a focus on secondary causes.  Hepatology. 2006;  44 1063-1074
  • 6 de Carpi J M, Tarrado X, Varea V. Sclerosing cholangitis secondary to hepatic artery ligation after abdominal trauma.  Eur J Gastroenterol Hepatol. 2005;  17 987-990
  • 7 Hohn D, Melnick J, Stagg R. et al . Biliary sclerosis in patients receiving hepatic arterial infusions of floxuridine.  J Clin Oncol. 1985;  3 98-102
  • 8 Sebagh M, Farges O, Kalil A. et al . Sclerosing cholangitis following human orthotopic liver transplantation.  Am J Surg Pathol. 1995;  19 81-90
  • 9 Tsimoyiannis E C, Grantzis E, Moutesidou K. et al . Secondary sclerosing cholangitis: after injection of formaldehyde into a hyatid cyst in the liver.  Eur J Surg. 1995;  161 299-300
  • 10 Heneghan M A, Sylvestre P B. Cholestatic diseases of liver transplantation.  Semin Gastrointest Dis. 2001;  12 133-147
  • 11 Chand N, Sanyal A J. Sepsis-induced cholestasis.  Hepatology. 2007;  45 230-241
  • 12 Gelbmann C M, Rümmele P, Wimmer M. et al . Ischemic-like cholangiopathy with secondary sclerosing cholangitis in critically ill patients.  Am J Gastroenterol. 2007;  102 1221-1229
  • 13 Bambha K, Kim W R, Talwalkar J. et al . Incidence, clinical spectrum, and outcomes of primary sclerosing cholangitis in a United States community.  Gastroenterology. 2003;  125 1364-1369
  • 14 Batts K P. Ischemic cholangitis.  Mayo Clin Proc. 1998;  73 380-385
  • 15 Le Thi Huong D, Valla D, Franco D. et al . Cholangitis associated with paroxysmal nocturnal hemoglobinuria: another instance of ischemic cholangiopathy?.  Gastroenterology. 1995;  109 1338-1343
  • 16 O’Mahony C A, Vierling J M. Etiopathogenesis of primary sclerosing cholangitis.  Sem Liv Dis. 2006;  26 3-21

H. Kulaksiz, MD

University Hospital Ulm
Department of Internal Medicine
Division of Gastroenterology

Robert-Koch-Str. 8
D-89081 Ulm
Germany

Fax: +49-731-50044502

Email: hasan.kulaksiz@uniklinik-ulm.de

    >