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This is a PatientPlus article. PatientPlus articles are written for doctors and so the language can be technical. However, some people find that they add depth to the articles found in the other sections of this website which are written for non-medical people.

Cholangitis means inflammation of the bile ducts. Jean Charcot first described the condition in 1877, presenting with the triad of jaundice, fever and right upper quadrant pain.1 In 1959, Reynolds and Dargon added mental confusion and septic shock to the list. This occurred in severe disease and the combination of symptoms was called the Reynolds pentad.2

Bile is normally sterile, but if the common bile duct (CBD) is obstructed the flow of bile is reduced (biliary stasis) and infection can occur. Infection can also flow in a retrograde direction up the CBD as a result of acute cholecystitis or instrumentation such as endoscopic retrograde cholangiopancreatography (ERCP). The commonest organisms in the UK are Klebsiella spp., Escherichia coli, Enterobacter spp., enterococci and streptococci. More than one organism may be involved. Outside the UK, cholangitis can be caused by roundworm and liver fluke.3

N.B. Primary sclerosing cholangitis is an aetiologically unrelated idiopathic condition which is dealt with in a separate article.

Epidemiology3

Cholangitis is relatively uncommon in Europe and the US. 1-3% of patients develop it after ERCP. Its racial distribution pattern follows to some extent the races in which there is a high prevalence of gall stones - i.e. fair-skinned people of Northern European descent, Hispanics, native Americans and Pima Indians. There is also a subset of Asian patients who develop cholangitis, mainly secondary to parasitic infection (recurrent pyogenic cholecystitis).4 The male to female ratio is equal. The median age of presentation is 50-60.

Aetiology3
  • Obstruction of the gall bladder or bile duct due to stones
  • ERCP
  • Tumours - pancreatic cancer,cholangiocarcinoma,ampullary cancer,porta hepatis tumors or metastasis
  • Bile duct stricture or stenosis
  • Choledochocele (cyst or diverticulum of the CBD)
  • AIDS cholangiopathy
  • Parasitic infection - roundworm, liver fluke
Presentation

History3

50-70% of patients present with the classic Charcot triad of jaundice, fever and right upper quadrant (RUQ) pain. In elderly patients, the abdominal pain may be poorly localised. 10-20% of patients also present with the additional features of hypotension due to septic shock and mental confusion - the Reynolds pentad. The patient may also report acholic (putty-coloured) stools and pruritus. A history of gallstones, CBD stones, recent cholecystectomy, ERCP or other invasive procedures, HIV or AIDS may assist the diagnosis. Some patients present with several attacks, usually in association with untreated biliary stones (recurrent pyogenic cholangitis).

Examination

Physical signs may include fever, RUQ tenderness, jaundice, mental status changes, hypotension and tachycardia. Peritonism is an unusual sign and should stimulate the search for an alternative diagnosis.

Differential diagnosis
Investigations

Laboratory tests3

  • The white cell count is raised in the majority of cases.
  • Blood cultures are positive in between 20-30% of cases.
  • Liver function tests are likely to show hyperbilirubinaemia, increased alkaline phosphatase and mildly raised aspartate aminotransferase and alanine aminotransferase levels.
  • One third of patients have a raised amylase. This often indicates involvement of the lower part of the CBD.
  • If bile fluid is available (e.g. biliary drainage through intervention has occurred), send a sample off for culture.

Imaging3

  • Abdominal Plain X-ray is the least invasive method, but is generally unhelpful unless the patient has ileus or has air in the biliary tree, which may be seen after endoscopic manipulation, emphysematous cholecystitis, cholangitis or cholecystic-enteric fistula. A ring of calcium is occasionally seen around gallstones (10-30%).
  • Ultrasound may be useful in identifying gallstones, but is less successful in identifying stones in the CBD. It is however, of value in identifying a dilated duct, signifying obstruction. Ultrasound is readily available and useful in identifying complications such as empyema. It is however highly dependent on operator skill and the cystic duct cannot be imaged. A normal scan does not rule out acute cholangitis.
  • CT scanning may well replace ultrasound as the investigation of choice and produces excellent images of the biliary tree, especially when spiral5 or helical6 methods are used. Other pathologies such as ampullary tumours can be viewed and it is also useful in excluding differential diagnoses such as right-sided diverticulitis and ruptured appendix.
  • ERCP is useful in patients in who need intervention as well as imaging. It has a major complication rate of 5.4% and a mortality rate of 0.49% as should not therefore be used solely for diagnostic purposes.3
  • Magnetic resonance cholangiopancreatography (MRCP) is as sensitive as ERCP and is a noninvasive technique particularly useful if biliary stones are suspected.7,8 Contraindications are as for MRI (e.g. presence of a cardiac pacemaker, cerebral aneurysm clips, ocular or cochlear implants and ocular foreign bodies) and it is, in contrast to ERCP, purely a diagnostic rather than therapeutic tool.
  • Biliary scintigraphy uses a radio-active substance which is excreted through the biliary system and can be used in cases of diagnostic doubt to demonstrate obstruction of the CBD. Positive changes (failure of the substance to enter the intestinal tract) may be detected before duct enlargement can be demonstrated on ultrasound. It is less sensitive in patients with high bilirubin levels.9
Staging10

An international symposium has recommended the following staging for acute cholangitis:

  • Mild (grade I) acute cholangitis may be defined as acute cholangitis that responds to the initial medical treatment (general supportive care and antibiotics).
  • Moderate (grade II) acute cholangitis is defined as acute cholangitis that does not respond to the initial medical treatment and is not associated with organ dysfunction.
  • Severe (grade III) acute cholangitis is diagnosed when there is dysfunction of any one of the following organs/systems:
    • Cardiovascular dysfunction (hypotension requiring treatment with dopamine ≥5μg/kg per min, or any dose of dobutamine)
    • Neurological dysfunction (decreased level of consciousness)
    • Respiratory dysfunction (PaO2/FiO2 (Fraction of inspired oxygen) ratio <300)
    • Renal dysfunction (serum creatinine >177 μmol/L (>2 mg/dl))
    • Hepatic dysfunction (PT-INR > 1.5)
    • Haematological dysfunction (platelet count <100 x 109/L)
Management
  • Resuscitation may be required for patients with septic shock and due attention should be given to oxygenation and correction of fluid and electrolyte imbalance.
  • Vital signs should be monitored.
  • Parenteral antibiotics should be administered once blood cultures have been taken.The drugs selected should be effective against anaerobes and Gram negative organisms. These may include ampicillin, piperacillin and gentamicin.3
  • Patients who fail to respond to 24-48 hours of antibiotics, or those with a rapidly deteriorating clinical picture, will require urgent biliary decompression:
    • Endoscopic decompression with removal of any associated stones is the usual initial procedure. If large stones and/or a considerable degree of sepsis is present, a biliary stent may be employed either as an adjunct to or as a replacement for endoscopic decompression.
    • Transhepatic biliary drainage is reserved for endoscopic failures and surgical biliary decompression via open laparotomy is rarely required.
    • Further surgery may be required electively once the patient stabilises, if the initial cause has not been dealt with at the time of emergency surgery.11
    • Recurrent pyogenic cholangitis may require more radical surgery such as liver resection.12
  • The international symposium on acute cholangitis recommended the following:10
    • Stage I - observation
    • Stage II - early biliary drainage
    • Stage III - urgent biliary drainage

At any stage, the underlying aetiology needs treatment (e.g. endoscopic treatment and surgery).

Complications3

Patients with severe sepsis can develop liver abscesses and liver failure, bacteraemia and Gram-negative sepsis. Acute renal failure can also ensue. Patients treated with percutaneous or endoscopic drainage can develop intra-abdominal or percutaneous bleeding, sepsis, fistulae and bile leakage.

Prognosis3

The current mortality figures are 7-40%. A poor prognosis is associated with:

  • Hypotension
  • Acute renal failure
  • Liver abscess
  • Cirrhosis
  • Inflammatory bowel disease
  • High malignant strictures
  • Radiologic cholangitis (post percutaneous transhepatic cholangiography)
  • Female gender
  • Age older than 50 years
  • Failure to respond to antibiotics and conservative therapy
  • A white cell count on admission of ≥20 x 109/L and total bilirubin of ≥880 μmol/L (10mg/dL)13

Document references
  1. Jean Charcot; whonamedit.com; whonamedit.com
  2. Reynolds BM, Dargan EL; Acute obstructive cholangitis; a distinct clinical syndrome. Ann Surg. 1959 Aug;150(2):299-303.
  3. Rosh A,Manko J; Cholangitis, eMedicine, updated December 2008.
  4. Lim JH, Ko YT, Lee DH, et al; Oriental cholangiohepatitis: sonographic findings in 48 cases. AJR Am J Roentgenol. 1990 Sep;155(3):511-4. [abstract]
  5. Sajjad Z, Oxtoby J, West D, et al; Biliary imaging by spiral CT cholangiography--a retrospective analysis. Br J Radiol. 1999 Feb;72(854):149-52. [abstract]
  6. Hanau LH, Steigbigel NH; Acute (ascending) cholangitis. Infect Dis Clin North Am. 2000 Sep;14(3):521-46. [abstract]
  7. Aube C, Delorme B, Yzet T, et al; MR cholangiopancreatography versus endoscopic sonography in suspected common bile duct lithiasis: a prospective, comparative study. AJR Am J Roentgenol. 2005 Jan;184(1):55-62. [abstract]
  8. Jain M, Agarwal A; MRCP findings in recurrent pyogenic cholangitis. Eur J Radiol. 2008 Apr;66(1):79-83. Epub 2007 Jun 27. [abstract]
  9. Imaging Tests, Merck Manual 2006
  10. Mayumi T, Takada T, Kawarada Y et al; Results of the Tokyo Consensus Meeting Tokyo Guidelines. J Hepatobiliary Pancreat Surg. 2007;14(1):114-21. Epub 2007 Jan 30
  11. Bornman PC, van Beljon JI, Krige JE; Management of cholangitis. J Hepatobiliary Pancreat Surg. 2003;10(6):406-14. [abstract]
  12. Al-Sukhni W, Gallinger S, Pratzer A, et al; Recurrent pyogenic cholangitis with hepatolithiasis--the role of surgical therapy in North America. J Gastrointest Surg. 2008 Mar;12(3):496-503. Epub 2007 Nov 13. [abstract]
  13. Rosing DK, De Virgilio C, Nguyen AT, et al; Cholangitis: analysis of admission prognostic indicators and outcomes. Am Surg. 2007 Oct;73(10):949-54. [abstract]
Acknowledgements EMIS is grateful to Dr Laurence Knott for writing this article. The final copy has passed scrutiny by the independent Mentor GP reviewing team. ©EMIS 2009.
Document ID: 1949
Document Version: 22
Document Reference: bgp1884
Last Updated: 1 Apr 2009
Planned Review: 1 Apr 2011

The authors and editors of this article are employed to create accurate and up to date content reflecting reliable research evidence, guidance and best clinical practice. They are free from any commercial conflicts of interest. Find out more about updating.

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