This is a slide on approach and mangement of cholangitis which is a surgical emergency, this slide is based on the Tokyo guideline - 2018 and has references from sabiston text book of surgery
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Approach and Management of Cholangitis.pptx
1. Approach and management to
cholangitis
Dikshanta Acharya
Department of Surgery
Patan Academy of Health Sciences
2. Introduction
• Occurs when biliary obstruction results in cholestasis and biliary infection
• Benign causes (often bile duct stones) or tumor
• Elevated pressure within the biliary system flushes the microorganisms
or endotoxins from the infected bile into systemic circulation SIRS
• Mortality risk is high if the condition is not treated
• Need to be able to reliably diagnose and assess the severity of cholangitis
3. Main bile duct
6 mm in diameter; 10-12 cm in length
A. Upper- common hepatic duct (CHD)
1. Situated above cystic duct
2. Hepatic artery -> right branch of hepatic artery which crosses posteriorly to CHD (
in 20 % crosses anteriorly)
3. Cystic artery branch of right branch of hepatic artery can cross CHD anteriorly or
posteriorly
B. Lower- common bile duct
• After union of CHD and cystic duct
• 7.5 cm length
• Divided into – hilar, supraduodenal and retropancreatic
4. Blood supply of bile duct
• Right branch of the hepatic artery (a),
• 9 o’clock artery (b),
• retroduodenal artery (c),
• left branch of the hepatic artery (d),
• hepatic artery (e),
• 3 o’clock artery (f),
• common hepatic artery (g),
• gastroduodenal artery (h).
5. Clinical manifestations
• Reynauds' pentad :
• Collection of signs and symptoms consistent with obstructive ascending
cholangitis, a serious infection of the biliary tract.
• Charcot's triad + shock + altered mental status.
• Patients with acute cholangitis can also present with complications from
bacteremia, including hepatic abscess, sepsis, multiple organ system dysfunction,
and shock.
Charcot’s traid
(all 3 occur in <50% cases)
Fever Abdominal
pain
Jaundice
(least common)
6. TG-18 Guidelines : Diagnosis
• A. Systemic Inflammation
• B. Cholestasis
• C. Imaging
7. Systemic Inflammation
• A1 - Fever / or shaking chills
• Defined as body temperature > 38 °C
• A2 - Laboratory Evidence of Inflammatory Response
• WBC count(x1000/ul) <4 or >10
• CRP (mg/dl) ≥1
8. Cholestasis
• B1 – Jaundice
• Total Bilirubin ≥2 (mg/dL)
• B2- Abnormal Liver Function Test
• ALP >1.5 × STD
• AST >1.5 × STD
• ALT >1.5 × STD
• γGT >1.5 × STD
9. Imaging
• C1 – Biliary dilatation
• C2 – Evidence of the etiology on imaging (stricture, stone, stent etc.)
10. Lab investigations
• CBC (elevated TLC with neutrophil predominance),
• LFT (shows cholestatic pattern - ↑ed ALP, GGT and conjugated
bilirubin)
• PT/INR - Derangement
• Electrolytes
• Pregnancy test
• Blood cultures (in all patients )
• Cultures should also be obtained from bile or stents removed at ERCP
11. • Leukocytosis with abnormal liver panel is common.
• 1st screening test USG (shows dilatation of biliary tree/ bile duct stones).
• CT Scan useful to know site of obstruction.
• MRCP - > If USG and CT scan are unclear. It helps in identifying cause of
biliary obstruction.
• Most valuable (diagnostic + therapeutic) Cholangiography through ERCP
or PTCs
• EUS - > occasionally used as a diagnostic tool for evaluating suspected
choledocholithiasis in patients who cannot undergo MRCP and can be
therapeutic.
13. Severe (suppurative) cholangitis
• Onset of dysfunction in at least any one of the following
organs/systems:
• Cardiovascular dysfunction – Hypotension requiring dopamie ≥5
micrograms/kg per min, or any dose of norepinephrine
• Neurological dysfunction – Disturbance of consciousness
• Respiratory dysfunction – PaO2/FiO2 ratio <300
• Renal dysfunction – Oliguria, serum creatinine >2.0 mg/dl
• Hepatic dysfunction – Prothrombin time-international normalized ratio >1.5
• Hematological dysfunction – Platelet count <100,000/mm
14. Moderate acute cholangitis
• associated with any two of the following:
• Abnormal WBC count (>12,000/mm3, <4,000/mm3)
• Fever 39°C (102.2°F)
• Age (≥75 years)
• Hyperbilirubinemia (total bilirubin ≥5 mg/dl)
• Hypoalbuminemia
15. • Mild acute cholangitis — Mild acute cholangitis does not meet the
criteria for moderate or severe cholangitis at initial diagnosis.
16. Management
• General measures:
• Admission in hospital.
• Based on the severity, intravenous hydration and correction of associated
electrolyte disorders
• IV antibiotics
• Analgesics for pain control.
• Close monitoring for organ dysfunction and septic shock.
• Definitive:
• Emergent decompression of the biliary tree (endoscopic/ percutaneous
drainage > surgical intervention).
17. IV antibiotics
• Empiric regimens for intra-abdominal infections include
antimicrobials with activity against enteric streptococci, coliforms,
and anaerobes
• Choice of antibiotics - whether the infection is community-acquired
versus healthcare-associated,
18. A) For patients with community-acquired
acute cholangitis of low to-moderate risk
Single-agent regimen
Piperacillin-tazobactam* 3.375 g IV every 6 hours
Combination regimen with metronidazole*
One of the following:
Cefazolin 1 to 2 g IV every 8 hours
or
Cefuroxime 1.5 g IV every 8 hours
or
Ceftriaxone 2 g IV once daily
or
Cefotaxime 2 g IV every 8 hours
or
Ciprofloxacin
400 mg IV every 12 hours or
500 mg PO every 12 hours
or
Levofloxacin 750 mg IV or PO once daily
Plus:
Metronidazole¶ 500 mg IV or PO every 8 hours
19. B) For patients with community-acquired
acute cholangitis of high risk
Single-agent regimen
Imipenem-cilastatin 500 mg IV every 6 hours
Meropenem 1 g IV every 8 hours
Doripenem 500 mg IV every 8 hours
Piperacillin-tazobactam 4.5 g IV every 6 hours
Combination regimen with metronidazole
ONE of the following:
Cefepime 2 g IV every 8 hours
OR
Ceftazidime 2 g IV every 8 hours
PLUS:
Metronidazole 500 mg IV or orally every 8 hours
20. C) For patients with healthcare-associated
acute cholangitis
Single-agent regimen
Imipenem-cilastatin 500 mg IV every 6 hours
Meropenem 1 g IV every 8 hours
Doripenem 500 mg IV every 8 hours
Piperacillin-tazobactam 4.5 g IV every 6 hours
Combination regimen
ONE of the following:
Cefepime 2 g IV every 8 hours
OR
Ceftazidime 2 g IV every 8 hours
PLUS:
Metronidazole 500 mg IV or orally every 8 hours
PLUS ONE of the following (in some cases*):
Ampicillin 2 g IV every 4 hours
OR
Vancomycin 15 to 20 mg/kg IV every 8 to 12 hours
21. Definitive : Biliary drainage
• 70-80 % of patients respond to initial antibiotic therapy
• Mild to moderate cholangitis, biliary drainage should be performed
within 24 to 48 hours
• Mild to moderate cholangitis that fail to respond to conservative
management for 24 hours, and patients with severe cholangitis
require urgent (within 24 hours) biliary decompression
23. Endoscopic Drainage
• Sphincterotomy with stone extraction and/or stent insertion
• Associated with significantly lower overall rates of mortality and
morbidity compared with surgical decompression (10% vs 50%)
• Large or impacted stones require mechanical lithotripsy or
cholangioscopy with electrohydraulic or laser lithotripsy for
fragmentation prior to removal
24. • Patients with coagulopathy - Placing a stent within the bile duct
without first performing a sphincterotomy
• Placement of a nasobiliary catheter
• EUS-guided cholangiopancreatography with biliary drainage and
stent placement - if ERCP fails or not possible due to obstructing
tumors
25. Percutaneous Drainage
• When endoscopic drainage is unavailable or unsuccessful
• Transhepatic insertion of a needle into a bile duct
• Drainage of infected bile, extraction of biliary tract stones, dilation of
benign biliary strictures, or placement of a stent across a malignant
stricture
26. • Requires a dilated biliary system
• Require International normalized ratio (INR) <1.8 (and ideally <1.5)
and platelet count ≥50,000/microL
• Percutaneous cholecystostomy tube in patients with an intact
gallbladder and non dilated biliary system
27. Surgical Drainage
• Reserved for patients in whom other methods of biliary drainage
cannot be performed or have failed
• Obstructing stone - Accomplished with open or laparoscopic common
bile duct exploration, with choledocholithotomy, with or without
placement of a T tube
• Hemodynamically stable patients can undergo a cholecystectomy at
the same time
28. • Malignant biliary obstruction-
• resection (eg, Whipple or bile duct resection),
• Bypass (eg, hepaticojejunostomy),
• T tube drainage
• Iatrogenic bile duct injury/obstruction - Hepaticojejunostomy
29. Addressing the underlying Cause
• Gallstone disease – elective cholecystectomy after the resolution of
cholangitis
• Benign biliary stricture – Endoscopic or surgical repair
• Malignant stenoses, management -stent placement at the time of
endoscopic biliary drainage
33. Transfer Criteria
• Severe Acute Cholangitis
• Patients who require emergency biliary drainage as well as critical care should
be transferred immediately to where this can be provided
• Moderate Acute Cholangitis
• Patients should be treated in a hospital where biliary drainage can be
performed
• Mild Acute Cholangitis
• If no response to initial treatment (within 24 hours), biliary drainage
34. Management Bundle
• When acute cholangitis is suspected, perform a diagnostic
assessment every 6 to 12 h using TG18 diagnostic criteria until a
diagnosis is reached
• Abdominal Ultrasonography, followed by a CT scan, MRI, MRCP, and
HIDA scan as required
• As soon as a diagnosis has been made, provide initial treatment.
35. • Initial management consists of sufficient fluid replacement,
electrolyte compensation, and intravenous administration of
analgesics and full-dose antimicrobial agents
• In patients with Grade I (mild) disease, if no response to the initial
treatment is observed within 24 h, perform biliary tract drainage
immediately
36. • In Grade II (moderate) disease, perform biliary tract drainage
immediately along with the initial treatment
• If early drainage cannot be performed because of a lack of facilities or skilled
personnel, consider transferring the patient
• In Grade III (severe) disease, perform urgent biliary tract drainage
along with the initial treatment and give general supportive care
• If early drainage cannot be performed because of a lack of facilities or skilled
personnel, consider transferring the patient
37. • In patients with Grade III (severe) disease, supply organ support (e.g.
noninvasive/invasive positive pressure ventilation, use of
vasopressors and antimicrobial agents) immediately.
• Perform blood culture or bile culture, or both, in Grade II (moderate)
and III (severe) patients.
38. • Consider treating the etiology of acute cholangitis with endoscopic,
percutaneous, or operative intervention once the acute illness has resolved
• Cholecystectomy should be performed for cholecystolithiasis after the
acute cholangitis has resolved
• If the hospital is not equipped to perform endoscopic or percutaneous
transhepatic biliary drainage or provide intensive care, transfer patient
with moderate or severe cholangitis to a hospital capable of providing
these treatments.
39. References
• Blumgart’s Surgery of Liver, Biliary Tract and Pancreas – 7th edition
• Tokyo Guidelines 2018: initial management of acute biliary infection
and flowchart for acute cholangitis
• Uptodate
Most common pathogens: Klebsiella, E.coli, Enterobacter, Pseudomonas, Citrobacter spp.
The bile duct blood supply. Note the axial arrangement
of the vasculature of the supraduodenal portion of the main bile duct
and the rich network enclosing the right and left hepatic ducts: right
branch of the hepatic artery (a), 9 o’clock artery (b), retroduodenal artery
(c), left branch of the hepatic artery (d), hepatic artery (e), 3 o’clock artery
(f), common hepatic artery (g), gastroduodenal artery (h).
Charcot's triad shows very high specificity. The presence of Charcot's triad strongly suggests the presence of acute cholangitis. However, due to the low sensitivity, it is not applicable in using as diagnosis criteria for acute cholangitis. (Level D)
Hepatocellular injury from the infection and inflammation elevate serum transaminase and alkaline phosphatase levels.
Surgical intervention includes common duct exploration with placement of T tube.
The chosen antimicrobial agents should subsequently be tailored to culture and susceptibility results when they become available. The duration of antibiotics depends on the adequacy of control of infection and the clinical stability of the patient [7,24]. Once the source of infection is controlled, antimicrobial therapy for patients with acute cholangitis is continued for an additional duration of four to five days.
Low-risk community-acquired intra-abdominal infections are those that are of mild to moderate severity in the absence of risk factors for antibiotic resistance or treatment failure. Such risk factors include recent travel to areas of the world with high rates of antibiotics-resistant organisms, known colonization with such organisms, advanced age, immunocompromising conditions, or other major medical comorbidities
High-risk community-acquired intra-abdominal infections are those that are severe or in patients at high risk for adverse outcomes or antimicrobial resistance. These include patients with recent travel to areas of the world with high rates of antibiotics-resistant organisms, known colonization with such organisms, advanced age, immunocompromising conditions, or other major medical comorbidities. For empiric therapy of high-risk community-acquired intra-abdominal infections, we cover streptococci, Enterobacteriaceae resistant to third-generation cephalosporins, Pseudomonas aeruginosa, and anaerobes.
For empiric therapy of health care-associated intra-abdominal infections, we cover streptococci, enterococci, Enterobacteriaceae that are resistant to third-generation cephalosporins and fluoroquinolones, Pseudomonas aeruginosa, and anaerobes. We include coverage against methicillin-resistant Staphylococcus aureus (MRSA) with vancomycin in those who are known to be colonized, those with prior treatment failure, and those with significant prior antibiotic exposure