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MELD-NaAssesses the severity of chronic liver diseaseChild-Pugh ScoreAssesses the prognosis of chronic liver disease, mainly cirrhosisFIB-4 IndexLiver fibrosis scoring indexAPRIAST to platelet ratio — liver fibrosisMaddrey's DFAlcoholic hepatitis severityGlasgow-BlatchfordUpper GI bleed risk stratificationGAHSGlasgow alcoholic hepatitis scoreMontreal IBDIBD classification — CD & UCMayo ScoreUlcerative colitis activityBISAP ScoreBedside index for severity of pancreatitisCLIF-SOFAOrgan failure scoring in cirrhosisAlcohol ContentStandard drinks & alcohol grams calculatorAARC-ACLFAcute-on-chronic liver failure gradePELD / CR ScorePediatric end-stage liver diseaseHarvey-BradshawCrohn's disease activity indexCTSICT severity index — pancreatitisRockall ScoreGI bleed rebleeding & mortality riskCAGEAlcohol use disorder screening (4 questions)MELD 3.0Updated MELD — sex-inclusive formulaAUDIT ScoreAlcohol use disorders identification testVOCAL-Penn ScorePost-operative mortality risk in cirrhosis surgery

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17
ALBI GradeAlbumin-bilirubin liver function grade in HCCUKELD ScoreUK model for end-stage liver diseaseMELD-XIMELD excluding INR — for anticoagulated patientsWest Haven CriteriaHepatic encephalopathy gradingMilan CriteriaLiver transplant eligibility in hepatocellular carcinomaLI-RADS v2018 (CT/MRI)Liver observation category from size, APHE and major featuresBCLC StagingHepatocellular carcinoma stage and treatment allocationSimplified AIH CriteriaSimplified criteria for autoimmune hepatitisRevised Original AIH ScoreIAIHG 1999 comprehensive autoimmune hepatitis scoreSAAGSerum-ascites albumin gradient — cause of ascitesR FactorHepatocellular vs cholestatic pattern in liver injuryCLIF-C ACLFMortality prediction in acute-on-chronic liver failureKing's College CriteriaTransplant criteria in acute liver failureGALAD ScoreHCC detection from gender, age, AFP-L3, AFP and DCPMetroticket 2.0AFP-adjusted up-to-seven for HCC transplant eligibilityRUCAMCausality in drug- and herb-induced liver injuryBaveno VII CriteriacACLD, CSPH and sparing screening endoscopy

Fibrosis & MASLD

8
NAFLD Fibrosis ScoreAdvanced fibrosis probability in MASLD/NAFLDBARD ScoreBMI, AST/ALT ratio, diabetes — MASLD fibrosisFatty Liver IndexPredicts hepatic steatosis from routine labsFibrotic NASH Index (FNI)At-risk NASH probability from AST, HbA1c and HDLNAFLD Activity Score (NAS)Histologic activity grade — steatosis, inflammation, ballooningMEFIB IndexMRE + FIB-4 rule for significant fibrosis (≥F2) in MASLDFAST ScoreFibroScan-AST — at-risk NASH from LSM, CAP and ASTSAFE ScoreSteatosis-Associated Fibrosis Estimator for MASLD in primary care

Pancreas & Biliary

8
Ranson's CriteriaAcute pancreatitis severity at 48 hoursGlasgow-Imrie CriteriaAcute pancreatitis severity — the PANCREAS criteriaHAPSHarmless acute pancreatitis scoreTokyo Guidelines — CholangitisTG18 diagnosis and severity grade for acute cholangitisTokyo Guidelines — CholecystitisTG18 diagnosis and severity grade for acute cholecystitisBiliary Pain (Rome IV)Rome IV — defining biliary-type pain before interventionFunctional Pancreatic SODRome IV — pancreatic sphincter of Oddi disorderRevised Atlanta ClassificationAcute pancreatitis severity — mild, moderately severe, severe

IBD

9
Truelove & Witts CriteriaAcute severe ulcerative colitis — admission decisionUCEISUlcerative colitis endoscopic index of severitySCCAISimple clinical colitis activity index — symptoms onlyCDAICrohn's disease activity index — the trial standardSES-CDEndoscopic severity in Crohn's diseasePUCAIPaediatric ulcerative colitis activity indexTravis (Oxford) CriteriaDay 3 colectomy risk in acute severe ulcerative colitisHo IndexDay 3 steroid failure risk in acute severe ulcerative colitisRutgeerts ScorePostoperative Crohn's recurrence at ileocolonoscopy

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7
EVendo ScorePredicts oesophageal varices needing treatmentForrest ClassificationPeptic ulcer bleeding — rebleeding risk at endoscopyAIMS65 ScoreUpper GI bleed mortality — five bedside criteriaOakland ScoreSafe-discharge risk for acute lower GI bleedingABC ScoreAge, blood tests, comorbidities — GI bleed mortalitySarin ClassificationEndoscopic classification of gastric varicesEGUS (Gastric Ulcer)Malignancy risk in a gastric ulcer, and who needs repeat endoscopy

Alcohol

2
ABIC ScoreAge, bilirubin, INR, creatinine — alcoholic hepatitisLille ModelSteroid response at day 7 in alcoholic hepatitis

Upper GI

4
Chicago Classification v4.0Oesophageal motility pattern from high-resolution manometryLA Classification (Oesophagitis)Los Angeles grade A–D for erosive oesophagitisPrague C & M CriteriaCircumferential and maximal extent of Barrett's oesophagusEREFS (Eosinophilic Oesophagitis)Endoscopic reference score — oedema, rings, exudates, furrows, stricture

Colorectal

3
Boston Bowel Prep ScaleColonoscopy preparation adequacy by segmentStool Osmotic GapOsmotic vs secretory diarrhoea from stool electrolytesATLAS Score (C. difficile)Predicted response to therapy in Clostridioides difficile infection

Functional GI

37
Bristol Stool ScaleStool form types 1–7 and colonic transitRome IV Criteria for IBSIrritable bowel syndrome diagnosis and subtypeFunctional ConstipationRome IV — two of six items, IBS excludedOpioid-Induced ConstipationRome IV — constipation tied to opioid therapyFunctional DiarrhoeaRome IV — loose stools without predominant painFunctional Bloating / DistensionRome IV — bloating without other bowel disorder criteriaUnspecified Functional Bowel DisorderRome IV — bowel symptoms fitting no other categoryCentrally Mediated Abdominal Pain (CAPS)Rome IV — continuous pain unrelated to gut eventsNarcotic Bowel SyndromeRome IV — opioid-induced hyperalgesia of the gutFaecal Incontinence (Rome IV)Rome IV — the criteria, and why nobody is askedFunctional Anorectal PainLevator ani, unspecified pain and proctalgia fugaxFunctional Defecation DisordersRome IV — dyssynergia and inadequate propulsionInfant RegurgitationRome IV — the happy spitter, and the alarm features that rule it outInfant ColicRome IV — recurrent unexplained crying in a well infant under 5 monthsInfant DyscheziaRome IV — straining before a soft stool, and why not to intervenePaediatric Functional ConstipationRome IV — two of six over one month, with overflow soiling as a criterionToddler's DiarrhoeaRome IV functional diarrhoea of childhood — painless, thriving childPaediatric Cyclic Vomiting SyndromeRome IV — both age bands, with different criteria for eachPaediatric Rumination SyndromeRome IV — infant and child/adolescent criteriaFunctional Nausea & Vomiting (Children)Rome IV — two separate disorders that can be met togetherAerophagiaRome IV — distension that increases through the dayPaediatric Functional DyspepsiaRome IV — four times a month, with PDS and EPS subtypingPaediatric Irritable Bowel SyndromeRome IV — plus the constipation clause clinicians missAbdominal MigraineRome IV — stereotypical incapacitating episodes weeks apartFunctional Abdominal Pain — NOSRome IV — the residual category, reached after the other threeNonretentive Faecal IncontinenceRome IV — soiling without retention, where laxatives make it worseFunctional DyspepsiaRome IV — with PDS and EPS subtypingRumination SyndromeRome IV — effortless regurgitation without retchingCyclic Vomiting SyndromeRome IV — stereotypical episodic vomitingCannabinoid HyperemesisRome IV — CVS pattern relieved by cannabis cessationChronic Nausea & VomitingRome IV — chronic nausea and vomiting syndromeBelching DisordersRome IV — supragastric vs gastric belchingFunctional HeartburnRome IV — heartburn with normal acid exposureReflux HypersensitivityRome IV — normal acid exposure, positive symptom associationFunctional Chest PainRome IV — non-cardiac, non-reflux chest painGlobusRome IV — painless lump-in-throat sensationFunctional DysphagiaRome IV — dysphagia with normal endoscopy and manometry
  1. Calculators
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  3. Tokyo Guidelines — Cholangitis
Pancreas & Biliary

Tokyo Guidelines — Cholangitis

TG18 diagnosis and severity grade for acute cholangitis

A — Systemic inflammation

Either item counts.

B — Cholestasis

Either item counts.

C — Imaging

Either item counts.

Organ dysfunction (Grade III)

Any single one of these makes it Grade III (severe), whatever the other findings show. Grade III is assessed first and overrides everything below.

Grade II criteria

Any TWO of these five make it Grade II (moderate), provided no organ dysfunction is present.

A higher bar than the 38 °C used for diagnosis. The two temperatures do different jobs.

Also a higher bar than the 2 mg/dL used for diagnosis.

Two separate questions in one tool: whether this IS acute cholangitis (criteria A, B and C) and, if so, how severe (Grade I–III). The severity grade is what drives timing of biliary drainage, which is the decision that actually changes outcome.

When to use
Use it in any patient with suspected biliary sepsis, both to decide whether this is cholangitis and to grade it — and then again during the admission, because the grade is not fixed at presentation. It replaced Charcot's triad as the diagnostic standard for a specific reason: the triad is highly specific but insensitive, so relying on it means missing patients who need urgent drainage. It applies to acute cholangitis rather than cholecystitis, which has separate criteria despite sharing the Tokyo Guidelines name, and the two are graded by different rules.
Why use it
Because the treatment for cholangitis is drainage, not antibiotics, and the only question that matters is how quickly. Charcot's triad — fever, jaundice and right upper quadrant pain — is present in only a minority of patients with proven cholangitis, so using it as a diagnostic gate delays decompression in exactly the group who cannot afford delay. TG18 splits the problem in two: a sensitive diagnostic framework built from routinely available data, and a severity grade that maps directly onto the urgency of drainage. The grading is also what makes audit and handover meaningful, since 'unwell with cholangitis' means different things to different clinicians while 'Grade II' does not.
Formula, evidence and interpretation

About the Tokyo Guidelines 2018 (TG18) for Acute Cholangitis

Diagnosis first, then grade. A suspected diagnosis needs one item from A (systemic inflammation) plus one from either B (cholestasis) or C (imaging); a definite diagnosis needs one from each of A, B and C. Grading then runs top-down: Grade III (severe) is any single organ dysfunction, Grade II (moderate) is any two of five criteria — abnormal white cell count, fever ≥ 39 °C, age ≥ 75, bilirubin ≥ 5 mg/dL, hypoalbuminaemia — and Grade I is everything else. The grade determines the timing of biliary drainage, which is the decision that changes outcome: urgent at Grade III, early at Grade II, and within 24 hours at Grade I if there is no response to medical treatment.

On this page

  • Formula
  • Interpreting the result
  • Inputs
  • What it returns
  • How it is calculated
  • Facts & figures
  • Evidence
  • How it compares
  • Pearls & pitfalls
  • Critical actions
  • Why it exists
  • About the creator
  • Limitations
  • If you are the patient
  • FAQ
  • Related calculators
  • References

Formula

Diagnosis: suspected = A + (B or C) definite = A + B + C Severity, assessed in this order: Grade III = any ONE organ dysfunction Grade II = any TWO of five criteria (no organ dysfunction) Grade I = neither of the above
A — systemic inflammation
Fever above 38 °C and/or rigors; or WBC below 4 or above 10 ×10⁹/L, or CRP ≥ 1 mg/dL.
B — cholestasis
Total bilirubin ≥ 2 mg/dL; or ALP, γGT, AST or ALT above 1.5 × the upper limit of normal.
C — imaging
Biliary dilatation; or evidence of the aetiology (stricture, stone, stent).
Grade III organ dysfunction
Cardiovascular, neurological, respiratory, renal, hepatic or haematological, at the TG18 thresholds. Any one is sufficient.
Grade II criteria
WBC above 12,000 or below 4,000/mm³; fever ≥ 39 °C; age ≥ 75; bilirubin ≥ 5 mg/dL; albumin below 0.7 × lower limit of normal. Two are required.
  • Severity is assessed top-down. A patient with organ dysfunction is Grade III whether or not any Grade II criteria are met — the counts do not add together.
  • Three thresholds appear twice at different values, and mixing them up is the commonest error: fever is 38 °C for diagnosis but 39 °C for Grade II; bilirubin is 2 mg/dL for diagnosis but 5 mg/dL for Grade II; white cell count is outside 4–10 ×10⁹/L for diagnosis but outside 4,000–12,000/mm³ for Grade II.
  • Grade II requires TWO of its five criteria. Cholecystitis, confusingly, requires only ONE of its four — the two Tokyo scores differ here.
  • The grade is not fixed at presentation. TG18 explicitly expects reassessment, and a Grade I patient who fails to respond within 24 hours is managed as though escalated.
  • TG18 kept the TG13 severity grading for cholangitis unchanged; the 2018 revision altered the diagnostic performance data and management flowchart rather than the grading table.

Interpreting the result

Read the diagnosis and the grade as two separate answers. A suspected diagnosis is not a weaker version of a definite one for treatment purposes: a patient can be Grade III on a suspected diagnosis and needs drainage just as urgently. The grade maps onto timing. Grade III means urgent biliary drainage alongside organ support, and the classic error here is waiting for the patient to stabilise before decompressing — they will not stabilise until the biliary tree is drained, because the sepsis is being driven by an obstructed, infected duct under pressure. Grade II means early drainage rather than a trial of antibiotics. Grade I permits initial medical management, but with an explicit 24-hour review: no response by then is an indication for drainage. Because the grade can change within hours, it should be recalculated rather than carried forward from the admission note.

ScoreBandWhat it meansAction
Grade IMildNo organ dysfunction and fewer than two Grade II criteria. Usually responds to initial medical managementAntimicrobials and observation, with a defined 24-hour review — biliary drainage if there is no response
Grade IIModerateAny two of: abnormal WBC, fever ≥ 39 °C, age ≥ 75, bilirubin ≥ 5 mg/dL, hypoalbuminaemia. Deteriorates if drainage is deferredEarly biliary drainage alongside antimicrobials, not a trial of antibiotics alone
Grade IIISevereDysfunction of any one of six organ systems. The highest-mortality group and the one most sensitive to delayUrgent biliary drainage with organ support in parallel — do not defer drainage for physiological stability
Criteria not metNot diagnosticDoes not exclude cholangitis. TG18 is a diagnostic framework, not a rule-out testContinue investigating if the picture fits; imaging is most often the missing item rather than a genuinely negative one

What the Tokyo Guidelines — Cholangitis needs (8 inputs)

A-1: Fever above 38 °C and/or shaking chills
Note this is a lower threshold than the 39 °C used in the Grade II severity criteria. The two temperatures do different jobs and are frequently conflated.
A-2: Evidence of an inflammatory response
White cell count below 4 or above 10 ×10⁹/L, or CRP of 1 mg/dL or above.
B-1: Jaundice
Total bilirubin of 2 mg/dL or above. Again lower than the 5 mg/dL used for Grade II severity.
B-2: Abnormal liver function tests
ALP, γGT, AST or ALT above 1.5 times the upper limit of normal. Any one of the four counts.
C-1: Biliary dilatation on imaging
Ultrasound, CT, MRCP or EUS all count.
C-2: Evidence of the aetiology on imaging
A stricture, a stone or a stent. Duct dilatation is not required if the cause itself is visible.
Organ dysfunction (six systems)
Cardiovascular (dopamine ≥ 5 µg/kg/min or any noradrenaline), neurological (disturbed consciousness), respiratory (PaO₂/FiO₂ below 300), renal (oliguria or creatinine above 2.0 mg/dL), hepatic (PT-INR above 1.5), haematological (platelets below 100,000/mm³). Any one makes it Grade III.
Grade II criteria (five items)
White cell count above 12,000 or below 4,000/mm³; fever 39 °C or above; age 75 or over; bilirubin 5 mg/dL or above; albumin below 0.7 × the lower limit of normal. Any TWO make it Grade II.

Units. Bilirubin thresholds are given in mg/dL: 2 mg/dL for diagnosis is about 34 µmol/L, and 5 mg/dL for Grade II is about 86 µmol/L — divide µmol/L by 17.1 to convert. Creatinine above 2.0 mg/dL for renal dysfunction is about 177 µmol/L. White cell counts appear in two conventions in the original guideline: ×10⁹/L for the diagnostic criteria and per mm³ for the Grade II criteria, but these are the same units — 10 ×10⁹/L is 10,000/mm³.

What it returns

Diagnostic status
Definite, suspected, or criteria not met. Definite requires an item from all three of A, B and C.
Severity grade
Grade I (mild), II (moderate) or III (severe). Assessed top-down, so organ dysfunction settles it regardless of anything else.
Which organ systems are failing
Listed explicitly, because the grade alone does not tell the receiving team what needs supporting.

How it is calculated

The Tokyo Guidelines were built to solve a diagnostic problem that Charcot's triad had created. The triad is specific enough that its presence more or less confirms cholangitis, but its sensitivity is poor — most patients with proven cholangitis do not have all three findings — so a triad-based approach systematically under-diagnoses the condition in which delay is most costly. The guideline group therefore replaced a single conjunctive rule with a three-category framework built from data available in any emergency department: a marker of systemic inflammation, a marker of cholestasis, and imaging. Requiring one item from each for a definite diagnosis preserves specificity, while allowing A plus either B or C to raise suspicion preserves sensitivity for the patient who needs treating before imaging is complete. Severity grading was constructed separately, around the observation that what distinguishes patients is not how loudly they present but whether organs are failing and how much physiological reserve they have — which is why age and albumin sit alongside white cell count and bilirubin in the Grade II list.

Facts & figures

The diagnostic criteria
CategoryItemsThreshold
A — systemic inflammationA-1 fever and/or rigorsAbove 38 °C
A-2 inflammatory responseWBC below 4 or above 10 ×10⁹/L, or CRP ≥ 1 mg/dL
B — cholestasisB-1 jaundiceTotal bilirubin ≥ 2 mg/dL
B-2 abnormal liver testsALP, γGT, AST or ALT above 1.5 × upper limit of normal
C — imagingC-1 biliary dilatationAny modality
C-2 aetiology visibleStricture, stone or stent

Suspected = one item in A plus one item in B or C. Definite = one item in each of A, B and C.

Thresholds that appear twice at different values
ParameterFor diagnosisFor Grade II severity
FeverAbove 38 °C39 °C or above
Total bilirubin≥ 2 mg/dL≥ 5 mg/dL
White cell countBelow 4 or above 10 ×10⁹/LAbove 12,000 or below 4,000/mm³

This is the single commonest source of error with TG18. The diagnostic thresholds are deliberately lower — they exist to catch the disease — while the severity thresholds are higher because they exist to grade it.

Evidence

TG18 diagnostic criteria and severity grading — Kiriyama et al.

2018

The 2018 revision of the Tokyo Guidelines, developed by an international consensus group and published alongside validation data comparing the criteria against clinical diagnosis and against Charcot's triad. The severity grading was carried forward unchanged from TG13.

The TG criteria substantially outperform Charcot's triad on sensitivity while retaining acceptable specificity — the triad's poor sensitivity being the specific problem the guideline set out to solve.

TG13 — the grading that TG18 retained

2013

The 2013 revision, which introduced the diagnostic criteria and the three-tier severity grading in their current form.

Established the A/B/C diagnostic framework and the Grade I–III severity assessment, both of which TG18 carried forward with the grading table unaltered.

Independent validation against clinician assessment

2022

Comparison of TG18 criteria against assessment by gastroenterology fellows in patients undergoing evaluation for acute cholangitis.

TG18 provided improved specificity and accuracy compared with fellow assessment, supporting its use as a structured framework rather than relying on unaided clinical impression.

How it compares

Tokyo Guidelines — Cholangitis vs Tokyo Guidelines for acute cholecystitis

Different diseases with different criteria that share a name — pick by which organ is infected, not by which tool is to hand.

Cholangitis is infection of an obstructed biliary tree and is treated by draining it; cholecystitis is inflammation of the gallbladder and is treated by removing or draining that. The criteria differ accordingly: cholangitis uses systemic inflammation, cholestasis and imaging with B and C interchangeable for suspicion, while cholecystitis uses local signs, systemic signs and requires imaging for a definite diagnosis. The Grade II rules differ too — two of five here, one of four there. They can coexist, and when they do both need addressing.

Open the Tokyo Guidelines for acute cholecystitis calculator →Yokoe M, Hata J, Takada T, et al. Tokyo Guidelines 2018: diagnostic criteria and severity grading of acute cholecystitis (with videos). J Hepatobiliary Pancreat Sci. 2018;25(1):41-54.

Tokyo Guidelines — Cholangitis vs Charcot's triad and Reynolds' pentad

Superseded for diagnosis. The triad is specific but too insensitive to use as a gate, which is precisely why TG18 exists.

Charcot's triad — fever, jaundice and right upper quadrant pain — confirms cholangitis when complete but is absent in most patients who have it. Reynolds' pentad adds hypotension and altered mental status and describes a patient who is already in septic shock, which in TG18 terms is simply Grade III. Both remain useful shorthand at the bedside; neither should be used to decide whether to investigate for cholangitis.

Tokyo Guidelines — Cholangitis vs Revised Atlanta classification

Complementary — gallstones cause both conditions, and a patient with gallstone pancreatitis and cholangitis needs grading under both systems.

The revised Atlanta classification grades acute pancreatitis by organ failure and its duration; TG18 grades biliary infection. They frequently apply to the same admission, since an impacted ampullary stone can produce both. The distinction matters practically: pancreatitis severity does not indicate urgent ERCP, whereas coexisting cholangitis does.

Open the Revised Atlanta classification calculator →

Pearls & pitfalls

  • Three parameters appear twice at different thresholds. Fever is 38 °C for diagnosis and 39 °C for Grade II; bilirubin is 2 mg/dL then 5 mg/dL; white cell count is outside 4–10 ×10⁹/L then outside 4,000–12,000/mm³. Carrying the diagnostic value into the severity assessment over-grades the patient.
  • Grade II needs TWO criteria for cholangitis but only ONE for cholecystitis. The two Tokyo scores are not symmetrical and this is where they most often get confused.
  • Severity is assessed top-down, not additively. One organ dysfunction is Grade III regardless of how many Grade II criteria are also present.
  • Charcot's triad is not the diagnostic standard and has not been since TG07. It is specific but insensitive, so most patients with cholangitis do not have all three.
  • A suspected diagnosis still needs treating. Grade III on a suspected diagnosis is a drainage emergency; the diagnostic tier is not a measure of urgency.
  • Do not defer drainage to stabilise a Grade III patient. The sepsis is driven by an obstructed infected duct under pressure, and it will not settle until that is decompressed.
  • Recalculate the grade during the admission. It is a snapshot, and a Grade I patient failing to respond by 24 hours is an indication for drainage.
  • Take blood cultures before the first dose of antimicrobials, and send bile for culture at the time of drainage — the yield from bile is high and it frequently changes therapy.

Critical actions

  • Grade III: arrange urgent biliary drainage and provide organ support in parallel, not sequentially.
  • Grade II: arrange early biliary drainage rather than a trial of antibiotics alone.
  • Grade I: start antimicrobials with an explicit 24-hour review point, and drain if there is no response.
  • Take blood cultures before antimicrobials and bile cultures at drainage in every grade.
  • Choose the drainage route by availability and anatomy — ERCP first line, with percutaneous transhepatic or EUS-guided drainage as alternatives.
  • Recalculate the grade at each review rather than carrying the admission grade forward.
  • Plan definitive treatment of the underlying cause, usually cholecystectomy or stone clearance, once the acute episode has settled.

Why this score exists

The guideline's central editorial decision was to stop treating diagnosis as a single conjunctive rule. Charcot's triad had held for over a century precisely because when all three are present the diagnosis is nearly certain — but that is a property of specificity, and using a specific rule as a gate for a disease whose treatment is time-critical means the patients you miss are the ones who most needed finding. Splitting the criteria into three categories and allowing partial combinations to raise suspicion converts the framework from a confirmation test into a triage tool, which is what the clinical problem actually requires. The severity grading reflects a second judgement: that reserve matters as much as the acute insult, which is why age and albumin appear alongside the inflammatory markers.

About the creator

  • Seiki Kiriyama

    First author, TG13 and TG18 cholangitis diagnostic criteria and severity grading

    Led the cholangitis diagnostic criteria and severity grading chapters of both the 2013 and 2018 guidelines.

  • Kazuto Kozaka

    Co-author of the TG18 cholangitis diagnostic criteria and severity grading chapter.

  • Tadahiro Takada

    Chair of the Tokyo Guidelines revision committee

    Led the Tokyo Guidelines programme across the 2007, 2013 and 2018 editions.

Limitations

  • The diagnostic criteria depend on imaging being performed, and category C is often the missing element rather than genuinely absent — which can under-call the diagnosis in a patient who has not yet been scanned.
  • Several items are subjective or laboratory-dependent, and the guideline does not specify which imaging modality or which local reference range should be used.
  • The severity grading is consensus-derived rather than regression-derived, so the Grade II item list and the two-of-five rule are expert judgement rather than a fitted model.
  • The albumin criterion is expressed relative to the local lower limit of normal rather than an absolute value, which introduces between-laboratory variation into the grade.
  • Grading is a snapshot with no built-in mechanism for the trajectory, despite the guideline expecting reassessment — a deteriorating Grade I and a stable Grade I look identical in the output.
  • Validation has largely been retrospective and in populations where ERCP is readily available; performance where drainage is not promptly accessible is less well characterised.
  • It does not identify the cause, choose the drainage route, or indicate antimicrobial selection, all of which need separate decisions.

If you are the patient

Cholangitis is an infection in the bile ducts, the tubes that carry bile from the liver to the gut. It usually happens because something — most often a gallstone — is blocking a duct, so the bile cannot drain and becomes infected. It can make people very unwell quickly. The Tokyo Guidelines are a checklist doctors use to decide two things: first, whether the illness really is cholangitis, using a combination of signs of infection, blood tests showing the bile is not draining, and a scan; and second, how severe it is, graded from I to III. The grade matters because it decides how urgently the blockage needs to be relieved. Antibiotics alone are not enough — the blocked duct has to be drained, usually with a camera test called an ERCP, and the more severe the grade, the sooner that needs to happen. Grade III means it is being done as an emergency alongside intensive care support.

Frequently asked questions

What are the Tokyo Guidelines for acute cholangitis?#

A two-part framework: diagnostic criteria in three categories (A systemic inflammation, B cholestasis, C imaging) and a three-tier severity grading. A suspected diagnosis needs A plus B or C; a definite diagnosis needs one item from each category.

What is the difference between suspected and definite cholangitis under TG18?#

Suspected means one item from category A plus one item from either B or C. Definite means one item from each of A, B and C. The distinction is diagnostic confidence, not urgency — a suspected diagnosis can still be Grade III and require emergency drainage.

What defines Grade III acute cholangitis?#

Dysfunction of any one of six organ systems: cardiovascular (dopamine ≥ 5 µg/kg/min or any noradrenaline), neurological (disturbed consciousness), respiratory (PaO₂/FiO₂ below 300), renal (oliguria or creatinine above 2.0 mg/dL), hepatic (PT-INR above 1.5), or haematological (platelets below 100,000/mm³).

What are the Grade II criteria for cholangitis?#

Any two of five: abnormal white cell count (above 12,000 or below 4,000/mm³), fever of 39 °C or above, age 75 or over, total bilirubin of 5 mg/dL or above, and hypoalbuminaemia below 0.7 times the lower limit of normal. Two are required — one is not enough.

Why do fever and bilirubin appear twice with different numbers?#

Because the diagnostic thresholds and the severity thresholds do different jobs. Diagnosis uses fever above 38 °C and bilirubin ≥ 2 mg/dL to catch the disease; Grade II severity uses 39 °C and 5 mg/dL to grade it. Carrying the diagnostic value into the severity assessment is the commonest error with TG18.

Is Charcot's triad still used to diagnose cholangitis?#

Not as the diagnostic standard. The triad is highly specific but insensitive — most patients with proven cholangitis do not have all three of fever, jaundice and right upper quadrant pain — so using it as a gate delays treatment in the patients who most need it. That insensitivity is why the Tokyo Guidelines were developed.

How quickly does biliary drainage need to happen?#

It depends on the grade. Grade III needs urgent drainage alongside organ support. Grade II needs early drainage rather than a trial of antibiotics. Grade I can start with medical management, but if there is no response within 24 hours, drainage should follow.

Should a Grade III patient be stabilised before drainage?#

No, and this is the classic error. The septic physiology is being driven by an obstructed, infected duct under pressure, and it will not improve until that duct is decompressed. Organ support and drainage proceed in parallel, not in sequence.

Related calculators

  • Tokyo Guidelines — Cholecystitis — TG18 diagnosis and severity grade for acute cholecystitis
  • Biliary Pain (Rome IV) — Rome IV — defining biliary-type pain before intervention
  • Revised Atlanta Classification — Acute pancreatitis severity — mild, moderately severe, severe
  • BISAP Score — Bedside index for severity of pancreatitis
  • Glasgow-Imrie Criteria — Acute pancreatitis severity — the PANCREAS criteria
  • Functional Pancreatic SOD — Rome IV — pancreatic sphincter of Oddi disorder

References

Original / primary reference

  1. 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;25(1):17-30.
  2. Kiriyama S, Takada T, Strasberg SM, et al. TG13 guidelines for diagnosis and severity grading of acute cholangitis (with videos). J Hepatobiliary Pancreat Sci. 2013;20(1):24-34.

Management

  1. 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;25(1):31-40.
  2. Gomi H, Solomkin JS, Schlossberg D, et al. Tokyo Guidelines 2018: antimicrobial therapy for acute cholangitis and cholecystitis. J Hepatobiliary Pancreat Sci. 2018;25(1):3-16.

Last updated August 1, 2026. Clinical knowledge base written and curated by GastroAGI Team from primary medical literature.

Written from primary literature and not yet independently clinically reviewed.

For use by qualified healthcare professionals. This calculator supports clinical judgement and does not replace it.