Acute cholangitis
- Overview
- Theory
- Diagnosis
- Management
- Follow up
- Resources
Treatment algorithm
Please note that formulations/routes and doses may differ between drug names and brands, drug formularies, or locations. Treatment recommendations are specific to patient groups: see disclaimer
Look out for this icon: for treatment options that are affected, or added, as a result of your patient's comorbidities.
acutely ill
1st line – intravenous antibiotics + intensive medical management
intravenous antibiotics + intensive medical management
Start intravenous, broad-spectrum antibiotics for all patients with suspected or confirmed cholangitis, with more specific treatment guided by results of blood and bile cultures.[32]Gomi H, Solomkin JS, Schlossberg D, et al. Tokyo Guidelines 2018: antimicrobial therapy for acute cholangitis and cholecystitis. J Hepatobiliary Pancreat Sci. 2018 Jan;25(1):3-16. https://onlinelibrary.wiley.com/doi/full/10.1002/jhbp.518 http://www.ncbi.nlm.nih.gov/pubmed/29090866?tool=bestpractice.com
Bacteria are usually gram-negative, but gram-positive bacteria and anaerobes are also implicated in cholangitis. Options include piperacillin/tazobactam, and imipenem/cilastatin, cefuroxime plus metronidazole, or metronidazole in combination with ciprofloxacin or levofloxacin or gentamicin are alternative regimens for penicillin-allergic patients.
Fluoroquinolones can cause serious, disabling, and potentially irreversible adverse effects including tendonitis, tendon rupture, arthralgia, neuropathies, and other musculoskeletal or nervous system effects.[44]European Medicines Agency. Quinolone- and fluoroquinolone-containing medicinal products. March 2019 [internet publication]. https://www.ema.europa.eu/en/medicines/human/referrals/quinolone-fluoroquinolone-containing-medicinal-products The US Food and Drug Administration has issued warnings about the increased risk of aortic dissection, significant hypoglycaemia, and mental health adverse effects in patients taking fluoroquinolones.[45]US Food and Drug Administration. FDA warns about increased risk of ruptures or tears in the aorta blood vessel with fluoroquinolone antibiotics in certain patients. FDA Drug Safety Communication. December 2018 [internet publication]. https://www.fda.gov/drugs/drug-safety-and-availability/fda-warns-about-increased-risk-ruptures-or-tears-aorta-blood-vessel-fluoroquinolone-antibiotics [46]US Food and Drug Administration. FDA reinforces safety information about serious low blood sugar levels and mental health side effects with fluoroquinolone antibiotics; requires label changes. FDA Drug Safety Communication. October 2018 [internet publication]. https://www.fda.gov/drugs/drug-safety-and-availability/fda-reinforces-safety-information-about-serious-low-blood-sugar-levels-and-mental-health-side
Once biliary drainage has been achieved and the patient shows clinical improvement, consider switching to oral antibiotics for the remainder of the antibiotic course.
Medical management requires attention to several critical factors and assessment of disease severity.[29]Miura F, Okamoto K, Takada T, et al. Tokyo guidelines 2018: initial management of acute biliary infection and flowchart for acute cholangitis. J Hepatobiliary Pancreat Sci. 2018 Jan;25(1):31-40. https://onlinelibrary.wiley.com/doi/full/10.1002/jhbp.509 http://www.ncbi.nlm.nih.gov/pubmed/28941329?tool=bestpractice.com [42]Mayumi T, Okamoto K, Takada T, et al. Tokyo guidelines 2018: management bundles for acute cholangitis and cholecystitis. J Hepatobiliary Pancreat Sci. 2018 Jan;25(1):96-100. https://onlinelibrary.wiley.com/doi/full/10.1002/jhbp.519 http://www.ncbi.nlm.nih.gov/pubmed/29090868?tool=bestpractice.com For severe acute cholangitis, swift and appropriate respiratory and circulatory management is essential.[29]Miura F, Okamoto K, Takada T, et al. Tokyo guidelines 2018: initial management of acute biliary infection and flowchart for acute cholangitis. J Hepatobiliary Pancreat Sci. 2018 Jan;25(1):31-40. https://onlinelibrary.wiley.com/doi/full/10.1002/jhbp.509 http://www.ncbi.nlm.nih.gov/pubmed/28941329?tool=bestpractice.com
Cholangitis can quickly become an acute, septic, life-threatening infection if not identified and treated promptly. Think 'Could this be sepsis?' based on acute deterioration in an adult patient in whom there is clinical evidence or strong suspicion of infection.[22]Royal College of Physicians. National Early Warning Score (NEWS) 2. Standardising the assessment of acute-illness severity in the NHS. Updated report of a working party. December 2017 [internet publication]. https://www.rcplondon.ac.uk/projects/outputs/national-early-warning-score-news-2 [23]NHS England. Sepsis guidance implementation advice for adults. September 2017 [internet publication]. https://www.england.nhs.uk/publication/sepsis-guidance-implementation-advice-for-adults [24]National Institute for Health and Care Excellence. Sepsis: recognition, diagnosis and early management. September 2017 [internet publication]. https://www.nice.org.uk/Guidance/NG51 See Sepsis in adults.
Use a systematic approach, alongside your clinical judgement, for assessment; urgently consult a senior clinical decision-maker (e.g., ST4 level doctor in the UK) if you suspect sepsis.[23]NHS England. Sepsis guidance implementation advice for adults. September 2017 [internet publication]. https://www.england.nhs.uk/publication/sepsis-guidance-implementation-advice-for-adults [24]National Institute for Health and Care Excellence. Sepsis: recognition, diagnosis and early management. September 2017 [internet publication]. https://www.nice.org.uk/Guidance/NG51 [26]Nutbeam T, Daniels R; The UK Sepsis Trust. Professional resources: clinical. 2022 [internet publication]. https://sepsistrust.org/professional-resources/clinical [28]Academy of Medical Royal Colleges. Statement on the initial antimicrobial treatment of sepsis. October 2022 [internet publication]. https://www.aomrc.org.uk/reports-guidance/statement-on-the-initial-antimicrobial-treatment-of-sepsis-v2-0
Refer to local guidelines for the recommended approach at your institution for assessment and management of the patient with suspected sepsis.
Patients with severe acute cholangitis often require bolused crystalloid fluid administration followed by maintenance fluids, with monitoring for signs of fluid overload.
Intravenous potassium and/or magnesium may be required as indicated by lab testing results.
Repletion of coagulation factors with fresh frozen plasma and platelets may be required in those with abnormal coagulation parameters (low platelets, raised prothrombin time).
Monitor controlled oxygen therapy. An upper SpO2 limit of 96% is reasonable when administering supplemental oxygen to most patients with acute illness who are not at risk of hypercapnia.
Evidence suggests that liberal use of supplemental oxygen (target SpO2 >96%) in acutely ill adults is associated with higher mortality than more conservative oxygen therapy.[50]Chu DK, Kim LH, Young PJ, et al. Mortality and morbidity in acutely ill adults treated with liberal versus conservative oxygen therapy (IOTA): a systematic review and meta-analysis. Lancet. 2018 Apr 28;391(10131):1693-1705. http://www.ncbi.nlm.nih.gov/pubmed/29726345?tool=bestpractice.com
A lower target SpO2 of 88% to 92% is appropriate if the patient is at risk of hypercapnic respiratory failure.[51]O'Driscoll BR, Howard LS, Earis J, et al. BTS guideline for oxygen use in adults in healthcare and emergency settings. Thorax. 2017 Jun;72(suppl 1):ii1-90. http://www.ncbi.nlm.nih.gov/pubmed/28507176?tool=bestpractice.com
Primary options
piperacillin/tazobactam: 4.5 g intravenously every 8 hours, may increase to 4.5 g every 6 hours in severe infections
More piperacillin/tazobactamDose consists of 4 g of piperacillin plus 0.5 g of tazobactam.
OR
imipenem/cilastatin: 500-1000 mg intravenously every 6 hours; or 1000 mg intravenously every 8 hours
More imipenem/cilastatinDose refers to imipenem component.
OR
cefuroxime: 750 mg intravenously every 6-8 hours, may increase to 1500 mg every 6-8 hours in severe infections
and
metronidazole: 500 mg intravenously every 8 hours
Secondary options
metronidazole: 500 mg intravenously every 8 hours
-- AND --
ciprofloxacin: 400 mg intravenously every 8-12 hours
or
levofloxacin: 500 mg intravenously every 12-24 hours
or
gentamicin: 5-7 mg/kg intravenously every 24 hours
More gentamicinAdjust dose according to serum gentamicin level.
These drug options and doses relate to a patient with no comorbidities.
Primary options
piperacillin/tazobactam: 4.5 g intravenously every 8 hours, may increase to 4.5 g every 6 hours in severe infections
More piperacillin/tazobactamDose consists of 4 g of piperacillin plus 0.5 g of tazobactam.
OR
imipenem/cilastatin: 500-1000 mg intravenously every 6 hours; or 1000 mg intravenously every 8 hours
More imipenem/cilastatinDose refers to imipenem component.
OR
cefuroxime: 750 mg intravenously every 6-8 hours, may increase to 1500 mg every 6-8 hours in severe infections
and
metronidazole: 500 mg intravenously every 8 hours
Secondary options
metronidazole: 500 mg intravenously every 8 hours
-- AND --
ciprofloxacin: 400 mg intravenously every 8-12 hours
or
levofloxacin: 500 mg intravenously every 12-24 hours
or
gentamicin: 5-7 mg/kg intravenously every 24 hours
More gentamicinAdjust dose according to serum gentamicin level.
Drug choice, dose and interactions may be affected by the patient's comorbidities. Check your local drug formulary.
Show drug information for a patient with no comorbidities
Primary options
piperacillin/tazobactam
OR
imipenem/cilastatin
OR
cefuroxime
and
metronidazole
Secondary options
metronidazole
-- AND --
ciprofloxacin
or
levofloxacin
or
gentamicin
biliary decompression: non-operative
Treatment recommended for ALL patients in selected patient group
Biliary decompression and drainage are necessary to allow for clinical improvement.[29]Miura F, Okamoto K, Takada T, et al. Tokyo guidelines 2018: initial management of acute biliary infection and flowchart for acute cholangitis. J Hepatobiliary Pancreat Sci. 2018 Jan;25(1):31-40. https://onlinelibrary.wiley.com/doi/full/10.1002/jhbp.509 http://www.ncbi.nlm.nih.gov/pubmed/28941329?tool=bestpractice.com [40]Mukai S, Itoi T, Baron TH, et al. Indications and techniques of biliary drainage for acute cholangitis in updated Tokyo Guidelines 2018. J Hepatobiliary Pancreat Sci. 2017 Oct;24(10):537-49. https://onlinelibrary.wiley.com/doi/full/10.1002/jhbp.496 http://www.ncbi.nlm.nih.gov/pubmed/28834389?tool=bestpractice.com
Recommended time frames vary according to severity:
Within 12 hours following admission: for patients with a deteriorating status (with persistent abdominal pain, hypotension despite intravenous fluid administration, fever >39°C [>102°F], worsening confusional state)[29]Miura F, Okamoto K, Takada T, et al. Tokyo guidelines 2018: initial management of acute biliary infection and flowchart for acute cholangitis. J Hepatobiliary Pancreat Sci. 2018 Jan;25(1):31-40. https://onlinelibrary.wiley.com/doi/full/10.1002/jhbp.509 http://www.ncbi.nlm.nih.gov/pubmed/28941329?tool=bestpractice.com [30]Manes G, Paspatis G, Aabakken L, et al. Endoscopic management of common bile duct stones: European Society of Gastrointestinal Endoscopy (ESGE) guideline. Endoscopy. 2019 May;51(5):472-91. https://www.thieme-connect.com/products/ejournals/html/10.1055/a-0862-0346 http://www.ncbi.nlm.nih.gov/pubmed/30943551?tool=bestpractice.com
Within 24 to 72 hours after admission: those for whom antibiotic treatment and medical management provide stability can have the decompression procedure.[29]Miura F, Okamoto K, Takada T, et al. Tokyo guidelines 2018: initial management of acute biliary infection and flowchart for acute cholangitis. J Hepatobiliary Pancreat Sci. 2018 Jan;25(1):31-40. https://onlinelibrary.wiley.com/doi/full/10.1002/jhbp.509 http://www.ncbi.nlm.nih.gov/pubmed/28941329?tool=bestpractice.com [30]Manes G, Paspatis G, Aabakken L, et al. Endoscopic management of common bile duct stones: European Society of Gastrointestinal Endoscopy (ESGE) guideline. Endoscopy. 2019 May;51(5):472-91. https://www.thieme-connect.com/products/ejournals/html/10.1055/a-0862-0346 http://www.ncbi.nlm.nih.gov/pubmed/30943551?tool=bestpractice.com [32]Gomi H, Solomkin JS, Schlossberg D, et al. Tokyo Guidelines 2018: antimicrobial therapy for acute cholangitis and cholecystitis. J Hepatobiliary Pancreat Sci. 2018 Jan;25(1):3-16. https://onlinelibrary.wiley.com/doi/full/10.1002/jhbp.518 http://www.ncbi.nlm.nih.gov/pubmed/29090866?tool=bestpractice.com
Endoscopic retrograde cholangiopancreatography (ERCP) performed within 48 hours of admission is associated with lower 30-day mortality and shorter hospital stays than ERCP performed after 48 hours.[33]Buxbaum JL, Buitrago C, Lee A, et al. ASGE guideline on the management of cholangitis. Gastrointest Endosc. 2021 Aug;94(2):207-21. http://www.ncbi.nlm.nih.gov/pubmed/34023065?tool=bestpractice.com [38]Du L, Cen M, Zheng X, et al. Timing of performing endoscopic retrograde cholangiopancreatography and inpatient mortality in acute cholangitis: a systematic review and meta-analysis. Clin Transl Gastroenterol. 2020 Mar;11(3):e00158. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7145040 http://www.ncbi.nlm.nih.gov/pubmed/32352721?tool=bestpractice.com [47]Mok SR, Mannino CL, Malin J, et al. Does the urgency of endoscopic retrograde cholangiopancreatography (ercp)/percutaneous biliary drainage (pbd) impact mortality and disease related complications in ascending cholangitis? (deim-i study). J Interv Gastroenterol. 2012 Oct;2(4):161-7. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3655387 http://www.ncbi.nlm.nih.gov/pubmed/23687602?tool=bestpractice.com [39]Iqbal U, Khara HS, Hu Y, et al. Emergent versus urgent ERCP in acute cholangitis: a systematic review and meta-analysis. Gastrointest Endosc. 2020 Apr;91(4):753-60. http://www.ncbi.nlm.nih.gov/pubmed/31628955?tool=bestpractice.com
ERCP with or without sphincterotomy and placement of a drainage stent allows for biliary tree decompression and stone extraction, and is the first-line therapy for acute cholangitis.[30]Manes G, Paspatis G, Aabakken L, et al. Endoscopic management of common bile duct stones: European Society of Gastrointestinal Endoscopy (ESGE) guideline. Endoscopy. 2019 May;51(5):472-91. https://www.thieme-connect.com/products/ejournals/html/10.1055/a-0862-0346 http://www.ncbi.nlm.nih.gov/pubmed/30943551?tool=bestpractice.com [33]Buxbaum JL, Buitrago C, Lee A, et al. ASGE guideline on the management of cholangitis. Gastrointest Endosc. 2021 Aug;94(2):207-21. http://www.ncbi.nlm.nih.gov/pubmed/34023065?tool=bestpractice.com [40]Mukai S, Itoi T, Baron TH, et al. Indications and techniques of biliary drainage for acute cholangitis in updated Tokyo Guidelines 2018. J Hepatobiliary Pancreat Sci. 2017 Oct;24(10):537-49. https://onlinelibrary.wiley.com/doi/full/10.1002/jhbp.496 http://www.ncbi.nlm.nih.gov/pubmed/28834389?tool=bestpractice.com Percutaneous trans-hepatic cholangiography (PTC) can be performed initially for those who are poor ERCP candidates (e.g., status post-Roux-en-Y gastric bypass, presence of oesophageal stricture) or for those who do not obtain relief of bile duct obstruction from ERCP.[33]Buxbaum JL, Buitrago C, Lee A, et al. ASGE guideline on the management of cholangitis. Gastrointest Endosc. 2021 Aug;94(2):207-21. http://www.ncbi.nlm.nih.gov/pubmed/34023065?tool=bestpractice.com [40]Mukai S, Itoi T, Baron TH, et al. Indications and techniques of biliary drainage for acute cholangitis in updated Tokyo Guidelines 2018. J Hepatobiliary Pancreat Sci. 2017 Oct;24(10):537-49. https://onlinelibrary.wiley.com/doi/full/10.1002/jhbp.496 http://www.ncbi.nlm.nih.gov/pubmed/28834389?tool=bestpractice.com
Both ERCP and PTC can be utilised for the purposes of common bile duct stone extraction and stent placement.
Endoscopic stent insertion by ERCP with decompression by aspiration is an option for patients too unwell to undergo either ERCP with sphincterotomy or PTC, or for those who do not obtain adequate drainage subsequent to performance of one or the other of those procedures.
Nasobiliary drains can also be used in this setting, but are difficult to place and often dislodge spontaneously.[40]Mukai S, Itoi T, Baron TH, et al. Indications and techniques of biliary drainage for acute cholangitis in updated Tokyo Guidelines 2018. J Hepatobiliary Pancreat Sci. 2017 Oct;24(10):537-49. https://onlinelibrary.wiley.com/doi/full/10.1002/jhbp.496 http://www.ncbi.nlm.nih.gov/pubmed/28834389?tool=bestpractice.com While effective, nasobiliary drain placement is rarely performed in practice as these patients can usually undergo endoscopic stenting.
Historically, all patients with cholangitis were admitted to hospital following ERCP. However, a significant number of patients may be able to be treated as outpatients after ERCP, once drainage has been achieved and antibiotics started.[48]Parbhu SK, Siddiqui AA, Taylor LJ, et al. Initial report of outpatient management of acute cholangitis via ERCP. Dig Dis Sci. 2017 Jun;62(6):1676-7. http://www.ncbi.nlm.nih.gov/pubmed/28315026?tool=bestpractice.com
lithotripsy
Additional treatment recommended for SOME patients in selected patient group
For bile duct stones that are large or difficult to remove, endoscopic lithotripsy may be performed for stone fragmentation during endoscopy to facilitate endoscopic removal.[30]Manes G, Paspatis G, Aabakken L, et al. Endoscopic management of common bile duct stones: European Society of Gastrointestinal Endoscopy (ESGE) guideline. Endoscopy. 2019 May;51(5):472-91. https://www.thieme-connect.com/products/ejournals/html/10.1055/a-0862-0346 http://www.ncbi.nlm.nih.gov/pubmed/30943551?tool=bestpractice.com [41]Yasuda I, Itoi T. Recent advances in endoscopic management of difficult bile duct stones. Dig Endosc. 2013 Jul;25(4):376-85. http://onlinelibrary.wiley.com/doi/10.1111/den.12118/full http://www.ncbi.nlm.nih.gov/pubmed/23650878?tool=bestpractice.com
opioid analgesic + paracetamol
Additional treatment recommended for SOME patients in selected patient group
Use a strong opioid (e.g., morphine, oxycodone) in combination with paracetamol for pain management.
Primary options
oxycodone: 5 mg orally (immediate-release) every 4-6 hours initially, adjust dose according to response, maximum 400 mg/day; 1-10 mg intravenously every 4 hours when required
or
morphine sulfate: 5-10 mg orally (immediate-release)/subcutaneously/intravenously/intramuscularly every 4 hours initially, adjust dose according to response
-- AND --
paracetamol: oral: 500-1000 mg orally every 4-6 hours when required, maximum 4000 mg/day; intravenous (<51 kg body weight): 15 mg/kg intravenously every 4-6 hours when required, maximum 60 mg/kg/day; intravenous (≥51 kg body weight): 1000 mg intravenously every 4-6 hours when required, maximum 4000 mg/day (3000 mg/day if risk factors for hepatotoxicity)
These drug options and doses relate to a patient with no comorbidities.
Primary options
oxycodone: 5 mg orally (immediate-release) every 4-6 hours initially, adjust dose according to response, maximum 400 mg/day; 1-10 mg intravenously every 4 hours when required
or
morphine sulfate: 5-10 mg orally (immediate-release)/subcutaneously/intravenously/intramuscularly every 4 hours initially, adjust dose according to response
-- AND --
paracetamol: oral: 500-1000 mg orally every 4-6 hours when required, maximum 4000 mg/day; intravenous (<51 kg body weight): 15 mg/kg intravenously every 4-6 hours when required, maximum 60 mg/kg/day; intravenous (≥51 kg body weight): 1000 mg intravenously every 4-6 hours when required, maximum 4000 mg/day (3000 mg/day if risk factors for hepatotoxicity)
Drug choice, dose and interactions may be affected by the patient's comorbidities. Check your local drug formulary.
Show drug information for a patient with no comorbidities
Primary options
oxycodone
or
morphine sulfate
-- AND --
paracetamol
biliary decompression: surgical
Non-operative procedures have largely replaced emergency surgery for accomplishing biliary decompression due to their superior risk-benefit ratio.[40]Mukai S, Itoi T, Baron TH, et al. Indications and techniques of biliary drainage for acute cholangitis in updated Tokyo Guidelines 2018. J Hepatobiliary Pancreat Sci. 2017 Oct;24(10):537-49. https://onlinelibrary.wiley.com/doi/full/10.1002/jhbp.496 http://www.ncbi.nlm.nih.gov/pubmed/28834389?tool=bestpractice.com
If adequate biliary decompression/drainage is not accomplished via non-operative means, laparoscopic choledochotomy with T-tube placement or cholecystectomy with common bile duct exploration may need to be performed.[40]Mukai S, Itoi T, Baron TH, et al. Indications and techniques of biliary drainage for acute cholangitis in updated Tokyo Guidelines 2018. J Hepatobiliary Pancreat Sci. 2017 Oct;24(10):537-49. https://onlinelibrary.wiley.com/doi/full/10.1002/jhbp.496 http://www.ncbi.nlm.nih.gov/pubmed/28834389?tool=bestpractice.com
Patients with a deteriorating course of acute cholangitis are at significant risk of surgical morbidity (bleeding, tissue infection, abscess formation acutely; adhesion formation and small bowel obstruction more remotely) and mortality.
Elective surgery in stabilised patients carries a much lower risk of morbidity and mortality compared with emergency surgery.
intravenous antibiotics
Treatment recommended for ALL patients in selected patient group
Start iIntravenous, broad-spectrum antibiotics for all patients with suspected or confirmed cholangitis, with more specific treatment guided by results of blood and bile cultures.[32]Gomi H, Solomkin JS, Schlossberg D, et al. Tokyo Guidelines 2018: antimicrobial therapy for acute cholangitis and cholecystitis. J Hepatobiliary Pancreat Sci. 2018 Jan;25(1):3-16. https://onlinelibrary.wiley.com/doi/full/10.1002/jhbp.518 http://www.ncbi.nlm.nih.gov/pubmed/29090866?tool=bestpractice.com
Bacteria are usually gram-negative, but gram-positive bacteria and anaerobes are also implicated in cholangitis. Options include piperacillin/tazobactam, and imipenem/cilastatin, cefuroxime plus metronidazole, or metronidazole in combination with ciprofloxacin or levofloxacin or gentamicin are alternative regimens for penicillin-allergic patients.
Fluoroquinolones can cause serious, disabling, and potentially irreversible adverse effects including tendonitis, tendon rupture, arthralgia, neuropathies, and other musculoskeletal or nervous system effects.[44]European Medicines Agency. Quinolone- and fluoroquinolone-containing medicinal products. March 2019 [internet publication]. https://www.ema.europa.eu/en/medicines/human/referrals/quinolone-fluoroquinolone-containing-medicinal-products The US Food and Drug Administration has issued warnings about the increased risk of aortic dissection, significant hypoglycaemia, and mental health adverse effects in patients taking fluoroquinolones.[45]US Food and Drug Administration. FDA warns about increased risk of ruptures or tears in the aorta blood vessel with fluoroquinolone antibiotics in certain patients. FDA Drug Safety Communication. December 2018 [internet publication]. https://www.fda.gov/drugs/drug-safety-and-availability/fda-warns-about-increased-risk-ruptures-or-tears-aorta-blood-vessel-fluoroquinolone-antibiotics [46]US Food and Drug Administration. FDA reinforces safety information about serious low blood sugar levels and mental health side effects with fluoroquinolone antibiotics; requires label changes. FDA Drug Safety Communication. October 2018 [internet publication]. https://www.fda.gov/drugs/drug-safety-and-availability/fda-reinforces-safety-information-about-serious-low-blood-sugar-levels-and-mental-health-side
Once biliary drainage has been achieved and the patient shows clinical improvement, consider switching to oral antibiotics for the remainder of the antibiotic course.
Primary options
piperacillin/tazobactam: 4.5 g intravenously every 8 hours, may increase to 4.5 g every 6 hours in severe infections
More piperacillin/tazobactamDose consists of 4 g of piperacillin plus 0.5 g of tazobactam.
OR
imipenem/cilastatin: 500-1000 mg intravenously every 6 hours; or 1000 mg intravenously every 8 hours
More imipenem/cilastatinDose refers to imipenem component.
OR
cefuroxime: 750 mg intravenously every 6-8 hours, may increase to 1500 mg every 6-8 hours in severe infections
and
metronidazole: 500 mg intravenously every 8 hours
Secondary options
metronidazole: 500 mg intravenously every 8 hours
-- AND --
ciprofloxacin: 400 mg intravenously every 8-12 hours
or
levofloxacin: 500 mg intravenously every 12-24 hours
or
gentamicin: 5-7 mg/kg intravenously every 24 hours
More gentamicinAdjust dose according to serum gentamicin level.
These drug options and doses relate to a patient with no comorbidities.
Primary options
piperacillin/tazobactam: 4.5 g intravenously every 8 hours, may increase to 4.5 g every 6 hours in severe infections
More piperacillin/tazobactamDose consists of 4 g of piperacillin plus 0.5 g of tazobactam.
OR
imipenem/cilastatin: 500-1000 mg intravenously every 6 hours; or 1000 mg intravenously every 8 hours
More imipenem/cilastatinDose refers to imipenem component.
OR
cefuroxime: 750 mg intravenously every 6-8 hours, may increase to 1500 mg every 6-8 hours in severe infections
and
metronidazole: 500 mg intravenously every 8 hours
Secondary options
metronidazole: 500 mg intravenously every 8 hours
-- AND --
ciprofloxacin: 400 mg intravenously every 8-12 hours
or
levofloxacin: 500 mg intravenously every 12-24 hours
or
gentamicin: 5-7 mg/kg intravenously every 24 hours
More gentamicinAdjust dose according to serum gentamicin level.
Drug choice, dose and interactions may be affected by the patient's comorbidities. Check your local drug formulary.
Show drug information for a patient with no comorbidities
Primary options
piperacillin/tazobactam
OR
imipenem/cilastatin
OR
cefuroxime
and
metronidazole
Secondary options
metronidazole
-- AND --
ciprofloxacin
or
levofloxacin
or
gentamicin
intensive medical management
Treatment recommended for ALL patients in selected patient group
Medical management requires attention to several critical factors and assessment of disease severity.[29]Miura F, Okamoto K, Takada T, et al. Tokyo guidelines 2018: initial management of acute biliary infection and flowchart for acute cholangitis. J Hepatobiliary Pancreat Sci. 2018 Jan;25(1):31-40. https://onlinelibrary.wiley.com/doi/full/10.1002/jhbp.509 http://www.ncbi.nlm.nih.gov/pubmed/28941329?tool=bestpractice.com [42]Mayumi T, Okamoto K, Takada T, et al. Tokyo guidelines 2018: management bundles for acute cholangitis and cholecystitis. J Hepatobiliary Pancreat Sci. 2018 Jan;25(1):96-100. https://onlinelibrary.wiley.com/doi/full/10.1002/jhbp.519 http://www.ncbi.nlm.nih.gov/pubmed/29090868?tool=bestpractice.com For severe acute cholangitis, swift and appropriate respiratory and circulatory management is essential.[29]Miura F, Okamoto K, Takada T, et al. Tokyo guidelines 2018: initial management of acute biliary infection and flowchart for acute cholangitis. J Hepatobiliary Pancreat Sci. 2018 Jan;25(1):31-40. https://onlinelibrary.wiley.com/doi/full/10.1002/jhbp.509 http://www.ncbi.nlm.nih.gov/pubmed/28941329?tool=bestpractice.com
Cholangitis can quickly become an acute, septic, life-threatening infection if not identified and treated promptly. Think 'Could this be sepsis?' based on acute deterioration in an adult patient in whom there is clinical evidence or strong suspicion of infection.[22]Royal College of Physicians. National Early Warning Score (NEWS) 2. Standardising the assessment of acute-illness severity in the NHS. Updated report of a working party. December 2017 [internet publication]. https://www.rcplondon.ac.uk/projects/outputs/national-early-warning-score-news-2 [23]NHS England. Sepsis guidance implementation advice for adults. September 2017 [internet publication]. https://www.england.nhs.uk/publication/sepsis-guidance-implementation-advice-for-adults [24]National Institute for Health and Care Excellence. Sepsis: recognition, diagnosis and early management. September 2017 [internet publication]. https://www.nice.org.uk/Guidance/NG51 See Sepsis in adults.
Use a systematic approach, alongside your clinical judgement, for assessment; urgently consult a senior clinical decision-maker (e.g., ST4 level doctor in the UK) if you suspect sepsis.[23]NHS England. Sepsis guidance implementation advice for adults. September 2017 [internet publication]. https://www.england.nhs.uk/publication/sepsis-guidance-implementation-advice-for-adults [24]National Institute for Health and Care Excellence. Sepsis: recognition, diagnosis and early management. September 2017 [internet publication]. https://www.nice.org.uk/Guidance/NG51 [26]Nutbeam T, Daniels R; The UK Sepsis Trust. Professional resources: clinical. 2022 [internet publication]. https://sepsistrust.org/professional-resources/clinical [28]Academy of Medical Royal Colleges. Statement on the initial antimicrobial treatment of sepsis. October 2022 [internet publication]. https://www.aomrc.org.uk/reports-guidance/statement-on-the-initial-antimicrobial-treatment-of-sepsis-v2-0
Refer to local guidelines for the recommended approach at your institution for assessment and management of the patient with suspected sepsis.
Patients with severe acute cholangitis often require bolused crystalloid fluid administration followed by maintenance fluids, with monitoring for signs of fluid overload.
Intravenous potassium and/or magnesium may be required as indicated by lab testing results. Repletion of coagulation factors with fresh frozen plasma and platelets may be required in those with abnormal coagulation parameters (low platelets, raised prothrombin time).
Monitor controlled oxygen therapy. An upper SpO2 limit of 96% is reasonable when administering supplemental oxygen to most patients with acute illness who are not at risk of hypercapnia.
Evidence suggests that liberal use of supplemental oxygen (target SpO2 >96%) in acutely ill adults is associated with higher mortality than more conservative oxygen therapy.[50]Chu DK, Kim LH, Young PJ, et al. Mortality and morbidity in acutely ill adults treated with liberal versus conservative oxygen therapy (IOTA): a systematic review and meta-analysis. Lancet. 2018 Apr 28;391(10131):1693-1705. http://www.ncbi.nlm.nih.gov/pubmed/29726345?tool=bestpractice.com
A lower target SpO2 of 88% to 92% is appropriate if the patient is at risk of hypercapnic respiratory failure.[51]O'Driscoll BR, Howard LS, Earis J, et al. BTS guideline for oxygen use in adults in healthcare and emergency settings. Thorax. 2017 Jun;72(suppl 1):ii1-90. http://www.ncbi.nlm.nih.gov/pubmed/28507176?tool=bestpractice.com
opioid analgesic + paracetamol
Additional treatment recommended for SOME patients in selected patient group
Use a strong opioid (e.g., morphine, oxycodone) in combination with paracetamol for pain management.
Primary options
oxycodone: 5 mg orally (immediate-release) every 4-6 hours initially, adjust dose according to response, maximum 400 mg/day; 1-10 mg intravenously every 4 hours when required
or
morphine sulfate: 5-10 mg orally (immediate-release)/subcutaneously/intravenously/intramuscularly every 4 hours initially, adjust dose according to response
-- AND --
paracetamol: oral: 500-1000 mg orally every 4-6 hours when required, maximum 4000 mg/day; intravenous (<51 kg body weight): 15 mg/kg intravenously every 4-6 hours when required, maximum 60 mg/kg/day; intravenous (≥51 kg body weight): 1000 mg intravenously every 4-6 hours when required, maximum 4000 mg/day (3000 mg/day if risk factors for hepatotoxicity)
These drug options and doses relate to a patient with no comorbidities.
Primary options
oxycodone: 5 mg orally (immediate-release) every 4-6 hours initially, adjust dose according to response, maximum 400 mg/day; 1-10 mg intravenously every 4 hours when required
or
morphine sulfate: 5-10 mg orally (immediate-release)/subcutaneously/intravenously/intramuscularly every 4 hours initially, adjust dose according to response
-- AND --
paracetamol: oral: 500-1000 mg orally every 4-6 hours when required, maximum 4000 mg/day; intravenous (<51 kg body weight): 15 mg/kg intravenously every 4-6 hours when required, maximum 60 mg/kg/day; intravenous (≥51 kg body weight): 1000 mg intravenously every 4-6 hours when required, maximum 4000 mg/day (3000 mg/day if risk factors for hepatotoxicity)
Drug choice, dose and interactions may be affected by the patient's comorbidities. Check your local drug formulary.
Show drug information for a patient with no comorbidities
Primary options
oxycodone
or
morphine sulfate
-- AND --
paracetamol
with choledocholithiasis, PSC, or HIV cholangiopathy
referral for follow-up medical/surgical care
Patients who develop cholangitis due to choledocholithiasis and undergo stone removal from the biliary tree should have subsequent cholecystectomy if cholelithiasis is present.[30]Manes G, Paspatis G, Aabakken L, et al. Endoscopic management of common bile duct stones: European Society of Gastrointestinal Endoscopy (ESGE) guideline. Endoscopy. 2019 May;51(5):472-91. https://www.thieme-connect.com/products/ejournals/html/10.1055/a-0862-0346 http://www.ncbi.nlm.nih.gov/pubmed/30943551?tool=bestpractice.com Patients without cholelithiasis or with prior cholecystectomy who are at low risk of recurrent cholangitis can be followed expectantly. Patients who appear well (i.e., without systemic signs of sepsis) can be treated and managed as outpatients following duct decompression via ERCP.
If primary sclerosing cholangitis (PSC) is present, it will almost always be identified on cholangiogram (obtained via endoscopic retrograde cholangiopancreatography [ERCP] or PTC). Patients with PSC should be referred to a hepatologist for formal evaluation and possible consideration for liver transplantation depending on the severity of disease and model for end-stage liver disease score. The long-term endoscopic management of PSC is complex and individualised, but often includes frequent ERCPs with tissue sampling to rule out cholangiocarcinoma and the use of balloon dilations and stents to manage symptomatic obstructing bile duct strictures.
Patients with HIV cholangiopathy who undergo sphincterotomy should be followed for improvement in liver chemistries and symptoms and should be referred to an HIV specialist for long-term care.
Choose a patient group to see our recommendations
Please note that formulations/routes and doses may differ between drug names and brands, drug formularies, or locations. Treatment recommendations are specific to patient groups. See disclaimer
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