Pancreatitis Risk Stratification Systems
Primary Recommendation
Use the BISAP (Bedside Index for Severity in Acute Pancreatitis) score as your first-line risk stratification tool within 24 hours of admission, with a cutoff of ≥2 indicating severe disease, organ failure risk, and increased mortality. 1, 2
Why BISAP is Preferred
The BISAP score has emerged as the optimal initial assessment tool because it:
Can be calculated immediately at the bedside within the first 24 hours using five simple parameters: Blood urea nitrogen >25 mg/dL (or >8.9 mmol/L), Impaired mental status, Systemic inflammatory response syndrome (SIRS), Age >60 years, and Pleural effusion on radiography 1, 2
Demonstrates accuracy comparable to APACHE-II (AUC 0.80 vs 0.88 for severe pancreatitis) but is far simpler to calculate, making it practical for real-world clinical use 1, 2, 3
Excels at predicting organ failure with an AUC of 0.93-0.95, which is the most critical outcome affecting mortality 2, 3
Identifies high-risk patients before organ failure develops, unlike traditional 48-hour scores that only confirm severity after complications have already occurred 1, 2
Critical Cutoff Values
A BISAP score ≥2 is your action threshold for:
- Severe acute pancreatitis prediction 1, 2, 3
- Organ failure risk (sensitivity 71.4%, specificity 99.1%) 3, 4
- Increased mortality risk 3, 5
A BISAP score ≥3 indicates very high risk requiring intensive monitoring and consideration for ICU-level care 5, 4
Complementary Assessment Tools
APACHE-II Score (Use for Ongoing Monitoring)
Calculate APACHE-II (cutoff ≥8) for patients with predicted severe disease based on BISAP or clinical deterioration 1, 2
APACHE-II is superior for daily reassessment to monitor disease progression or recovery, as it can be recalculated throughout hospitalization 1, 2
Perform contrast-enhanced CT after 72 hours in patients with APACHE-II >8 or evidence of organ failure to assess pancreatic necrosis 1
Traditional 48-Hour Scores (Limited Utility)
The Ranson and Glasgow scores require 48 hours to complete, making them less useful for early risk stratification:
- Ranson score ≥3 has modest accuracy (PPV 28.6-49%, sensitivity 75-87%) 1, 2
- Glasgow score ≥3 performs similarly (PPV 59-66%, sensitivity 61-71%) 1, 2
- These scores cannot guide initial triage decisions and are now largely superseded by BISAP 1, 2
Laboratory Markers
C-reactive protein (CRP) ≥150 mg/L at 48 hours (or >210 mg/L within first 4 days) indicates severe disease with ~80% accuracy and should be used as an adjunct to clinical scoring 1, 2
Procalcitonin shows promise with AUC 0.94 for severity prediction and is particularly useful as a negative predictor of infected necrosis 2, 5
CT Severity Index (CTSI)
Calculate CTSI between days 3-10 in patients with predicted severe disease (BISAP ≥2 or APACHE-II ≥8) 1, 2
CTSI ≥3 indicates severe disease, with scores 7-10 correlating with 92% morbidity and 17% mortality 2
Early CT (<72 hours) underestimates necrosis and should be avoided unless there is diagnostic uncertainty or concern for alternative diagnoses 1
Practical Clinical Algorithm
Within First 24 Hours:
- Calculate BISAP score immediately on all pancreatitis patients 1, 2
- Measure baseline CRP, BUN, hematocrit and assess for SIRS criteria 1, 2
- Monitor continuously for organ failure (pulmonary, circulatory, renal) as this defines severe disease regardless of scoring 1, 2
At 48 Hours:
- Recheck CRP (target threshold ≥150 mg/L) 1, 2
- Calculate APACHE-II if BISAP ≥2 or clinical deterioration occurs 1, 2
Days 3-10:
- Perform contrast-enhanced CT with CTSI calculation in all patients with BISAP ≥2, APACHE-II ≥8, or persistent organ failure 1, 2
Ongoing Management:
- Use APACHE-II for daily monitoring in severe cases to track progression 1, 2
- Consider ICU transfer for BISAP ≥3, persistent organ failure, or APACHE-II ≥8 with comorbidities 1
Special Considerations for Older Adults
Age >60 years is already incorporated into BISAP scoring (1 point), making it inherently adjusted for elderly patients 1, 2
BISAP performs equally well in elderly patients (≥60 years) compared to younger patients for predicting severity, unlike Ranson and APACHE-II which show age-dependent performance differences 6
Elderly patients have significantly higher rates of severe disease and mortality, making early risk stratification with BISAP even more critical in this population 6
Common Pitfalls to Avoid
Do not wait 48 hours for Ranson or Glasgow scores before initiating aggressive management in high-risk patients identified by BISAP 1, 2
Do not perform CT in the first 72 hours unless there is diagnostic uncertainty, as it will underestimate necrosis and may lead to false reassurance 1
Do not rely solely on single laboratory values (amylase, lipase, hematocrit, BMI) for risk stratification, as these have poor predictive accuracy compared to multifactorial scores 3, 5
Do not use CTSI alone for initial risk stratification, as it requires delayed imaging and has lower accuracy than BISAP or APACHE-II for predicting mortality 3, 7, 5