Community acquired biliary sepsis (ascending cholangitis & calculus cholecystitis) (2024)

by Josh Farkas

Community acquired biliary sepsis (ascending cholangitis & calculus cholecystitis) (1)

CONTENTS

  • Rapid Reference 🚀
  • Introduction
  • Diagnostic tests
    • Labs
    • Ultrasonography
    • CT scan
    • HIDA scan
    • Diagnostic criteria
  • Treatment
    • Antibiotics
    • Interventional tx for ascending cholangitis
    • Interventional tx for cholecystitis
  • Podcast
  • Pitfalls

rapid reference

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community-acquired biliary sepsis checklist ✅

investigations

  • Electrolytes, CBC with differential, coags.
  • Liver function tests (including direct bilirubin), lipase.
  • Blood cultures.
  • Procalcitonin, lactate.
  • Imaging:
    • Right upper-quadrant ultrasonography. (more)
    • CT scan if diagnosis unclear or possible gangrene/perforation. (more)

antibiotics (more)

  • Piperacillin-tazobactam is generally front-line therapy.
  • High-risk for ESBL species: may consider meropenem instead.
  • (⚠️ No need for vancomycin.)

source control

  • Ascending cholangitis: Consult gastroenterology for ERCP. (more)
  • Cholecystitis: If not responding to medical therapy, consider percutaneous drain. (more)

sepsis resuscitation as needed (more)

  • Fluid, vasopressors, inotropes, echocardiography as needed.
  • Consider hydrocortisone 50 mg IV q6hr.

Community acquired biliary sepsis (ascending cholangitis & calculus cholecystitis) (2)

introduction

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This chapter discusses acute calculus cholecystitis and ascending cholangitis together, because they have several similarities:

  • Similar epidemiology and presentation.
  • Same antibiotic therapies.
  • Similar imaging modalities.
  • They can rarely occur together.

That being said, there are obviously important differences between them. As foci of septic shock, they behave in fundamentally different ways:

  • Cholecystitis is usually self-contained.
    • The disease process is usually limited to the gallbladder.
    • Cholecystitis tends to have a more gradual, smoldering disease course (unless it progresses to gangrenous or emphysematous cholecystitis).
    • Patients more often respond to medical management.
  • Ascending cholangitis is never self-contained:
    • Bacteria under pressure spread readily up bile ducts, across hepatic sinusoids, and into the blood. This physiology generates characteristic bacteremia and rigors.
    • Ascending cholangitis has a greater tendency to evolve rapidly into septic shock.
    • Timely source control in ascending cholangitis is more important, as this decompresses the biliary tree and stops the reflux of bacteria into the blood.
    • Ascending cholangitis are less likely to respond to medical management alone (although in many cases the obstructing stone may pass spontaneously).

symptoms

  • Both may cause similar symptoms:
    • Right upper quadrant pain.
    • Nausea/vomiting, anorexia.
    • Fever.
  • Ascending cholangitis
    • Bacteremia is common, often leading to frank rigors. Occasionally, patients may present with sepsis and bacteremia in the absence of any localizing symptoms (typically gram-negative organisms, most often E. coli).
    • Jaundice is more common.

common causes of both

  • Most often due to gallstones.
  • Can be caused by strictures (e.g., primary sclerosing cholangitis) or malignancy (e.g., pancreatic cancer).
    • Among patients with known biliary pathology or recent biliary procedures, there should be a higher index of suspicion for biliary sepsis.

differential diagnosis

  • Combination diagnoses:
    • (a) Simultaneous cholecystitis plus ascending cholangitis.
    • (b) Simultaneous ascending cholangitis plus pancreatitis.
    • (c) Simultaneous ascending cholangitis plus liver abscess.
  • Pancreatitis.
  • Pyelonephritis.
  • Liver abscess(es).
  • Septic portal vein thrombosis (pylephlebitis).
  • Pelvic inflammatory disease (can extend to cause right upper quadrant pain, fever, and pericholecystic fluid).
  • Procedural complication (e.g., bile duct leak due to laparoscopic cholecystectomy).

labs

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liver function tests

  • Both cholecystitis and ascending cholangitis may cause elevation of bilirubin and transaminases, with greater derangements suggesting ascending cholangitis.
    • Marked elevation of bilirubin (e.g., >4 mg/dL) is more consistent with cholangitis.
    • Severe elevation of transaminases (occasionally >1,000 mg/dL) is occasionally seen in cholangitis due to acute biliary obstruction.
  • Sepsis of any etiology can cause mild cholestasis (“cholestasis of sepsis”) with elevated bilirubin & alkaline phosphatase. Such abnormalities shouldn't be misinterpreted to mean that the biliary system is the source of infection.

bacteremia

  • Blood cultures are frequently positive in ascending cholangitis.
  • When gram-negative bacteremia is found without a known source, always consider pyelonephritis or abdominal sources (especially ascending cholangitis).

neutrophil-to-lymphocyte ratio (NLR)

  • General
    • The neutrophil/lymphocyte ratio may be used as an index of physiologic stress caused by various illnesses (further explanation here).
    • For both cholecystitis and ascending cholangitis, the performance of the NLR is superior to the white blood count and similar to the performance of C-reactive protein.(28032577, 29907228)
    • NLR may be conceptualized as a slightly improved version of the white blood cell count.
  • Cholecystitis
    • NLR >3 predicts cholecystitis (~70% sensitivity, 70% specificity).(28032577, 25428640)
    • NLR >4 suggests more severe cholecystitis (e.g., empyema, gangrene, or perforation).(28032577, 30581347)
    • These cutoff values are lower than cutoff values for acute appendicitis (~5 and ~9), suggesting that cholecystitis usually causes less physiologic stress than appendicitis does.
  • Ascending cholangitis
    • NLR >5.3 predicts cholangitis in one study with 68% sensitivity and 95% specificity. (29907228)
    • This cutoff is higher than the cutoff for cholecystitis (~3), reflecting that ascending cholangitis typically causes greater physiologic stress.

Community acquired biliary sepsis (ascending cholangitis & calculus cholecystitis) (3)

ultrasonography

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acute calculus cholecystitis

  • [1] Stones (~95% sensitivity)
    • Cholecystitis is usually caused by stone impaction in the gallbladder neck or cystic duct.
    • An impacted stone won't move if the patient is repositioned.
  • [2] Sonographic Murphy's sign (~90% sensitivity; may be absent in gangrenous cholecystitis).
    • The most specific sign.
    • Sonographic Murphy's sign should replace the traditional (blind) Murphy's sign.
  • [3] Distended gallbladder should be seen (unless the gallbladder has already perforated).
    • Distention is part of the pathophysiology of cholecystitis.
    • A contracted gallbladder with thick-appearing wall may be a normal finding after eating.
  • [4] Adjunctive signs: Thickened gallbladder wall (50-75% sensitive) and pericholecystic fluid:
    • These are relatively nonspecific.
    • These have a variety of possible causes (e.g. volume overload, ascites, hepatitis).

gangrenous cholecystitis

  • May lack sonographic Murphy's sign (gallbladder is dead and insensate).
  • Irregular gallbladder wall thickening.
  • Intraluminal membranes or perforation may be seen.

emphysematous cholecystitis

  • Gas in gallbladder wall may appear as patchy areas of bright signal casting dirty shadows.
  • Emphysematous cholecystitis may be difficult or impossible to distinguish from:
    • (a) Intraluminal air (pneumobilia).
    • (b) Adjacent loops of bowel.
    • (c) Dense calcified stones within the gallbladder (Wall Echo Sign).
    • (d) Calcification of the entire gallbladder wall (“Porcelain gallbladder”).
  • When in doubt, a CT scan is needed (emphysematous cholecystitis is an indication for surgery).

ascending cholangitis

  • The key finding is dilation of common bile duct. Nobody agrees about the normal size of a common bile duct. >7 mm is probably dilated in most patients.(26468310) Patients who have undergone cholecystectomy may have somewhat larger common bile duct dimensions (e.g., up to 10 mm).(22880184)
  • Sensitivity ranges from 38-91%.(34024448) Sonography may be negative very early in the disease course, before the bile ducts have had time to dilate.

serial ultrasonography

  • An ultrasound exam represents a single snapshot in time. In reality, findings will evolve dynamically.
  • The power of ultrasonography may be amplified substantially by serial exams. This may be a useful approach to patients with ambiguous examination findings.
    • A case series by Bosch et al. describes two cases of cholecystitis which evolved dramatically over hours. (PDF is here).
  • Serial ultrasonography may be especially useful in ascending cholangitis:
    • The common bile duct may initially have a normal diameter (in the hyperacute phase), with progressive dilation over time.
    • Occasionally the stone will pass spontaneously, so the common bile duct size will decrease over time.

CT scan

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acute cholecystitis

  • As with ultrasonography, sensitivity is often greater than specificity. For example, thickening of the gallbladder wall is nonspecific and must be interpreted within clinical context.
  • Strengths of CT scanning include the following:
  • (1) Provides more global imaging of the abdomen, allowing exclusion of more entities (e.g., pancreatitis).
  • (2) Superior to ultrasonography for detection of complicated cholecystitis:
    • (a) Gangrenous cholecystitis (lack of enhancement of the gallbladder wall following IV contrast indicates gangrenous tissue).
    • (b) Emphysematous cholecystitis: CT is excellent at determining the precise location of gas and differentiating this from porcelain gallbladder.
    • (c) Perforated gallbladder.
    • (d) Abscess adjacent to gallbladder, liver abscess.

ascending cholangitis

  • The primary value of CT scanning is in providing a survey of the entire abdomen and excluding other possible foci of sepsis.
  • CT may be less sensitive than ultrasound for detection of stones in the common bile duct (depending on body habitus and sonographic windows).
  • CT scan is superior to ultrasound for determination of some causes of biliary stenosis (e.g., pancreatic cancer).

HIDA scan

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Community acquired biliary sepsis (ascending cholangitis & calculus cholecystitis) (4)

HIDA scan to evaluate for acute calculus cholecystitis

  • Some findings of cholecystitis on ultrasound are nonspecific (e.g., wall thickening and pericholecystic fluid).
  • If ultrasonography is equivocal, HIDA scan can be performed. This is a nuclear medicine test which evaluates the ability of the gallbladder to be filled by bile (reflecting patency of the cystic duct).
    • If the gallbladder fails to fill with radiolabeled bile, this supports the diagnosis of cholecystitis.
    • If the gallbladder fills normally with radiolabeled bile, this largely excludes the possibility of cholecystitis.
  • HIDA scan is ~97% sensitive and ~90% specific for acute calculus cholecystitis.
  • Causes of false-positives (failure of the gallbladder to fill with radiolabeled dye, in the absence of cholecystitis):
    • Severe liver disease with inability to secrete radiolabeled tracer into bile.
    • Prolonged fasting, with distention of the gallbladder.
    • Prior biliary sphincterotomy, which promotes drainage of bile directly into intestine.
    • Cystic duct obstruction without superimposed acute cholecystitis.

diagnostic criteria

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Formal diagnostic criteria aren't perfect for every patient (e.g., a patient with severely altered mentation may lack localizing signs). However, these criteria may provide an organized structure for thinking about these diagnoses.

diagnostic criteria for ascending cholangitis

  • Definite diagnosis requires at least one item in each of three categories (based on Tokyo Guidelines 2018 ):(29090866)
  • (1) Evidence of systemic inflammation (any of the following)
    • Fever or rigors
    • WBC outside the range of 4,000-10,000 /uL
    • Elevated C-reactive protein >10 mg/L (neutrophil/lymphocyte ratio may be considered as an alternative)
  • (2) Laboratory evidence of cholestasis (any of the following)
    • Bilirubin >2 mg/dL (>34 uM).
    • Elevated alkaline phosphatase, AST, or ALT (above 1.5 times the upper range of normal).
  • (3) Imaging evidence of dilation of the common bile duct
    • Bolstered by finding a cause of obstruction (e.g. stone or stricture)

diagnostic criteria for acute cholecystitis

  • Definite diagnosis requires at least one item in each of three categories (based on Tokyo Guidelines 2018 ):(29090866)
  • (1) Systemic signs of inflammation
    • Fever
    • Rigors
    • WBC outside the range of 4,000-10,000 /uL
    • Elevated C-reactive protein > 10 mg/L (neutrophil/lymphocyte ratio may be considered as alternative)
  • (2) Local signs of inflammation
    • Murphy's sign
    • Right upper quadrant pain, mass, or tenderness
  • (3) Imaging findings characteristic of acute cholecystitis

antibiotics

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organisms isolated from bile of patients with acute biliary infection (29090866, 34024448)

  • Gram negatives
    • E. coli (~35%)
    • Klebsiella spp. (~15%)
    • Enterobacter spp. (7%)
    • Pseudomonas spp. (0.5-19%)
  • Gram positives
    • Enterococcus spp. (~15%)
    • Streptococcus spp. (2-10%)
  • Anaerobes, including Bacteroides fragilis (4-20%)

comments on the microbes involved:

  • (1) Gram-negatives are most important, especially E. coli, Klebsiella, and Enterobacter.
  • (2) Enterococci are commonly found in the gallbladder, but enterococcus isn't a particularly virulent pathogen. It's debatable whether empiric enterococcal coverage is needed, with some guidelines stating that this is not routinely required.(33153472) If blood cultures are positive for enterococcus, this requires treatment.
  • (3) The pathogenic role of anaerobes is unclear. Anaerobes should be covered in patients with a biliary-enteric anastomosis or gangrenous/emphysematous cholecystitis.(29090866)
  • (4) MRSA is not a community-acquired biliary pathogen!
    • Thus, there is no role for vancomycin.
    • If the blood cultures reveal gram positives and there is concern about the possibility of drug-resistant gram positives, then the addition of linezolid or daptomycin may be considered pending speciation & sensitization (to cover for vancomycin-resistant enterococci).

penetration of various antibiotics into biliary secretions

Community acquired biliary sepsis (ascending cholangitis & calculus cholecystitis) (5)

  • There is no solid evidence to support the use of antibiotics with higher biliary penetration. However, it may be reasonable to give this some consideration.
  • Biliary penetration is probably most relevent for ascending cholangitis. (In cholecystitis, bile doesn't come in contact with the focus of infection within the gallbladder, so biliary penetration is probably unimportant.)

empiric therapy

  • Piperacillin-tazobactam is generally the front-line therapy for empiric treatment of biliary sepsis:
    • Adequate coverage of gram-negatives, enterococci, and anaerobes.
    • Good biliary penetration.
    • Low risk of C. difficile.
  • Meropenem: In locales with a high incidence of extended-spectrum beta-lactamase resistant (ESBL) E. coli, meropenem could be considered as empiric therapy. This should be based upon the frequency of ESBL (+) E. coli in a local antibiogram, possibly using a cutoff of >10-20%.(29090866)
  • For patients with penicillin allergy: Piperacillin-tazobactam or meropenem are generally still fine. (more on this here)

de-escalation

  • These infections are often polymicrobial, so narrowing antibiotics based on a single organism isolated from the blood should be done with caution.

duration of therapy

  • Generally, once source control has been achieved, antimicrobial therapy is recommended for 4-7 days.(29090866)
  • If gram-positive bacteremia is detected (e.g., Enterococcus) then therapy should be extended to 14 days (since these bacteria have a tendency to stick to valves).
  • If the source has been surgically removed (cholecystectomy), then shorter courses of antibiotics may be adequate.

interventional therapy for ascending cholangitis

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importance of drainage

  • Relief of the biliary obstruction is a critical intervention for ascending cholangitis, as this allows pus to drain out of the biliary tree (rather than backing up into the liver and causing bacteremia). This may be required for source control in order to control septic shock.
  • Patients who respond well to antibiotics and fluid resuscitation may not require urgent decompression. However, patients who are more severely ill or who fail to respond to medical management do require expedited drainage.
  • Gastroenterology should be consulted early.

ERCP

  • ERCP is the front-line approach to drainage, with high success rates (>90%).(26961212)
  • ERCP allows for stone removal as well as procedures to keep the bile ducts open (sphincterotomy and/or stent placement).
  • Performing ERCP on a septic patient will often require intubation (because this procedure must be performed in the prone procedure with little ability to monitor the patient's ventilation).
    • ERCP shouldn't be delayed substantially because the patient is “too sick” to tolerate the procedure. On the contrary, severe illness is an indication for ERCP. Profoundly ill patients should ideally be promptly resuscitated and intubated, stabilized on the ventilator, and then taken expeditiously for ERCP.

percutaneous transhepatic cholangiography (PTC)

  • Basics of the procedure:
    • The biliary tree is accessed percutaneously via interventional radiology guidance.
    • The biliary tree may be swept clean of stones.
    • Internal stents may be placed to facilitate drainage. An external drain will often also be inserted.
  • Percutaneous transhepatic cholangiography is generally considered a second-line drainage procedure. It may be required among patients in whom ERCP is technically impossible (e.g., patients who are status post gastric bypass).

interventional therapy for cholecystitis

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surgery for the cholecystitis patient with septic shock

  • Surgery is uncommonly performed among septic ICU patients.
    • Tokyo 2018 guidelines suggest that early surgery can be performed in selected septic patients with cholecystitis. However, this should be undertaken only by experienced surgeons at high-volume centers. In practice, this doesn't seem to be pursued often.
  • Indications to consider immediate surgery:
    • (1) Emphysematous cholecystitis.
    • (2) Gangrenous/necrotic cholecystitis.
    • (3) Perforated gallbladder.

percutaneous cholecystostomy drain (via interventional radiology)

  • Benefit: Relief of pressure in gallbladder, drainage of pus.
  • Drawbacks: ? Spillage of bacteria into peritoneum, patients who aren't operative candidates may be stuck with drain.
  • Contraindications: Large-volume ascites, interposed loop of bowel blocking access.
  • This is currently an evidence-free zone:
    • In one RCT of patients with high-risk cholecystitis, there was no benefit to cholecystostomy compared to medical management alone.(12111069)
    • The 2020 World Society of Emergency Surgery recommends that “drainage may be an option in patients who failed conservative management after a variable time of 24-48 hours and who present with strict contraindications to surgery.”(33153472)
  • A reasonable approach might be:
    1. Start with aggressive sepsis resuscitation (antibiotics, vasopressors, fluid, etc.).
    2. If the patient is responding to therapy and clinically improving, continue medical therapy.
    3. If patient is deteriorating or failing therapy (e.g., not improving after ~1-2 days), place a percutaneous drain.

failure of percutaneous cholecystostomy drain

  • Drainage combined with medical therapy should cause clinical improvement within ~1-3 days.
  • Failure to improve may reflect the following:
    • Gangrenous/necrotic or emphysematous cholecystitis.
    • Malpositioned or dysfunctional drain.
    • Liver abscess(es).
    • Septic portal vein thrombosis (pylephlebitis).
    • Superimposed pancreatitis or ascending cholangitis.
  • Evaluation may include liver function tests, ultrasonography, and contrasted CT scan. Depending on the findings, the need for cholecystectomy may need to be reconsidered (e.g., if gangrenous or emphysematous cholecystitis is found).

simultaneous ascending cholangitis and cholecystitis

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simultaneous ascending cholangitis & cholecystitis

  • Rarely, these two diseases may occur together.
  • The pathophysiology may be a proximal stone lodged in the common bile duct, which causes distention of both the gallbladder and the biliary tree.

treatment options may include the following:

  • (1) ERCP may be ideal (to allow for stone removal and stenting of the common bile duct).
  • (2) If the patient is too unstable to tolerate ERCP, then placement of a percutaneous drain in the gallbladder may be adequate to drain both the gallbladder and biliary tree. This has the advantage of being a simple and quick procedure, but it doesn't allow definitive treatment (stone removal).
  • (3) Percutaneous transhepatic cholangiography (PTC) is another percutaneous procedure which may be a bit more involved than a gallbladder drain, but it offers more definitive therapy (stone removal and sweeping of the common bile duct).

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questions & discussion

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Community acquired biliary sepsis (ascending cholangitis & calculus cholecystitis) (7)

  • Under-utilization of repeat right upper-quadrant sonogram in equivocal situations (the exam changes over time!).
  • Failure to consider ascending cholangitis in patients with unexplained gram-negative bacteremia.
  • Vancomycin is over-utilized for community-acquired biliary sepsis.
  • Over-utilization of percutaneous drains for cholecystitis, due to the misconception that if the patient has cholecystitis then they must receive an immediate drain.
  • Underutilization of ERCP for ascending cholangitis, due to the misconception that patient is “too sick” for ERCP.

Guide to emoji hyperlinks Community acquired biliary sepsis (ascending cholangitis & calculus cholecystitis) (8)

  • Community acquired biliary sepsis (ascending cholangitis & calculus cholecystitis) (9) = Link to online calculator.
  • Community acquired biliary sepsis (ascending cholangitis & calculus cholecystitis) (10) = Link to Medscape monograph about a drug.
  • Community acquired biliary sepsis (ascending cholangitis & calculus cholecystitis) (11) = Link to IBCC section about a drug.
  • Community acquired biliary sepsis (ascending cholangitis & calculus cholecystitis) (12) = Link to IBCC section covering that topic.
  • Community acquired biliary sepsis (ascending cholangitis & calculus cholecystitis) (13) = Link to FOAMed site with related information.
  • Community acquired biliary sepsis (ascending cholangitis & calculus cholecystitis) (14) = Link to supplemental media.

References

  • 12111069 Hatzidakis AA, Prassopoulos P, Petinarakis I, Sanidas E, Chrysos E, Chalkiadakis G, Tsiftsis D, Gourtsoyiannis NC. Acute cholecystitis in high-risk patients: percutaneous cholecystostomy vs conservative treatment. Eur Radiol. 2002 Jul;12(7):1778-84. doi: 10.1007/s00330-001-1247-4 [PubMed]
  • 22880184 Park SM, Kim WS, Bae IH, Kim JH, Ryu DH, Jang LC, Choi JW. Common bile duct dilatation after cholecystectomy: a one-year prospective study. J Korean Surg Soc. 2012 Aug;83(2):97-101. doi: 10.4174/jkss.2012.83.2.97 [PubMed]
  • 25428640 Lee SK, Lee SC, Park JW, Kim SJ. The utility of the preoperative neutrophil-to-lymphocyte ratio in predicting severe cholecystitis: a retrospective cohort study. BMC Surg. 2014 Nov 27;14:100. doi: 10.1186/1471-2482-14-100 [PubMed]
  • 26468310 Zimmer V, Lammert F. Acute Bacterial Cholangitis. Viszeralmedizin. 2015 Jun;31(3):166-72. doi: 10.1159/000430965 [PubMed]
  • 26961212 Sun Z, Zhu Y, Zhu B, Xu G, Zhang N. Controversy and progress for treatment of acute cholangitis after Tokyo Guidelines (TG13). Biosci Trends. 2016 Feb;10(1):22-6. doi: 10.5582/bst.2016.01033 [PubMed]
  • 27307785 Ansaloni L, Pisano M, Coccolini F, et al. 2016 WSES guidelines on acute calculous cholecystitis. World J Emerg Surg. 2016 Jun 14;11:25. doi: 10.1186/s13017-016-0082-5 [PubMed]
  • 28032577 Beliaev AM, Angelo N, Booth M, Bergin C. Evaluation of neutrophil-to-lymphocyte ratio as a potential biomarker for acute cholecystitis. J Surg Res. 2017 Mar;209:93-101. doi: 10.1016/j.jss.2016.09.034 [PubMed]
  • 29032610 Kiriyama S, Kozaka K, Takada T, et al. Tokyo Guidelines 2018: diagnostic criteria and severity grading of acute cholangitis (with videos). J Hepatobiliary Pancreat Sci. 2018 Jan;25(1):17-30. doi: 10.1002/jhbp.512 [PubMed]
  • 29090866 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. doi: 10.1002/jhbp.518 [PubMed]
  • 29907228 Beliaev AM, Booth M, Rowbotham D, Bergin C. Diagnostic inflammatory markers in acute cholangitis. J Surg Res. 2018 Aug;228:35-41. doi: 10.1016/j.jss.2018.02.048 [PubMed]
  • 30581347 Micić D, Stanković S, Lalić N, Đukić V, Polovina S. Prognostic Value of Preoperative Neutrophil-to-lymphocyte Ratio for Prediction of Severe Cholecystitis. J Med Biochem. 2018 Apr 1;37(2):121-127. doi: 10.1515/jomb-2017-0063 [PubMed]
  • 31131353 Mou D, Tesfasilassie T, Hirji S, Ashley SW. Advances in the management of acute cholecystitis. Ann Gastroenterol Surg. 2019 Feb 19;3(3):247-253. doi: 10.1002/ags3.12240 [PubMed]
  • 33153472 Pisano M, Allievi N, Gurusamy K, et al. 2020 World Society of Emergency Surgery updated guidelines for the diagnosis and treatment of acute calculus cholecystitis. World J Emerg Surg. 2020 Nov 5;15(1):61. doi: 10.1186/s13017-020-00336-x [PubMed]
  • 34024448 An Z, Braseth AL, Sahar N. Acute Cholangitis: Causes, Diagnosis, and Management. Gastroenterol Clin North Am. 2021 Jun;50(2):403-414. doi: 10.1016/j.gtc.2021.02.005 [PubMed]
Community acquired biliary sepsis (ascending cholangitis & calculus cholecystitis) (2024)
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