Z Gastroenterol 2025; 63(05): e315-e318
DOI: 10.1055/s-0045-1809195
Abstracts
2. Gastroenterologie

Accounting for comorbidity improves prediction of outcome trajectories in biliary acute pancreatitis

J Prosenz
1   Karl Landsteiner University of Health Sciences, Krems, Austria
2   University Hospital St. Pölten, Department of Internal Medicine 2 Gastroenterology & Hepatology, St. Pölten, Austria
3   Paracelsus Medical University, Medical Science Research Program, Salzburg, Austria
,
M Birkl
1   Karl Landsteiner University of Health Sciences, Krems, Austria
2   University Hospital St. Pölten, Department of Internal Medicine 2 Gastroenterology & Hepatology, St. Pölten, Austria
,
T Hadrigan
1   Karl Landsteiner University of Health Sciences, Krems, Austria
4   University Hospital Tulln, Tulln an der Donau, Austria
,
L Brandl
1   Karl Landsteiner University of Health Sciences, Krems, Austria
,
A Wittmann
1   Karl Landsteiner University of Health Sciences, Krems, Austria
,
F Koutny
1   Karl Landsteiner University of Health Sciences, Krems, Austria
2   University Hospital St. Pölten, Department of Internal Medicine 2 Gastroenterology & Hepatology, St. Pölten, Austria
3   Paracelsus Medical University, Medical Science Research Program, Salzburg, Austria
,
A Maieron
1   Karl Landsteiner University of Health Sciences, Krems, Austria
2   University Hospital St. Pölten, Department of Internal Medicine 2 Gastroenterology & Hepatology, St. Pölten, Austria
3   Paracelsus Medical University, Medical Science Research Program, Salzburg, Austria
› Institutsangaben
 

Introduction Outcome prediction in acute pancreatitis remains difficult. We aimed to identify simple predictors of a clinically significant outcome trajectories in biliary acute pancreatitis.

Material and Methods In this retrospective, multicenter cohort study data from electronic health-records of patients with biliary acute pancreatitis between 2018 and 2021 were extracted. Predictors of outcome were tested using univariable analyses. Outcome categories were defined hierarchically as: (i) death, (ii) severe pancreatitis and/or ICU admission, (iii) early or late interventions (e.g., endoscopic, surgical), (iv) moderately-severe pancreatitis, (v) mild pancreatitis.

Results Of 569 cases of acute pancreatitis, 217 (38.1%) patients with biliary acute pancreatitis, mean age 65.9 years (SD 17.4), median length of stay (LOS) 7 days (IQR 4;11), were included (see [Table 1]). Overall, 62.2% of patients experienced mild, 30.0% moderately severe, and 7.8% severe acute pancreatitis. The all-cause 90-day mortality was 2.3%. Individually, the Bedside Index of Severity in Acute Pancreatitis (BISAP) score and Charlson Comorbidity Index (CCI) classified patients reasonably well, however, large “outcome grey zones” existed (see [Table 2]). When combining BISAP and CCI, 5 distinct risk groups were identified, ranging from low (group 5) to very-high risk (group 1). High health-care resource use and worse outcomes (i-iii) were prevalent in 62.5%, 60%, 27.3%, 9.5%, 2.4% in groups 1-5. Also, LOS was significantly longer in higher risk groups (p<0.001). Importantly, 97.6% of patients in group 5 experienced a mild-to-moderate pancreatitis without ICU admission, persistent organ dysfunction, surgical or endoscopic interventions, and no fatality, and 90.5% in group 4, with groups 4 and 5 comprising approximately 80% of the entire cohort.

Table 1 Baseline characteristics of initial search and biliary acute pancreatitis cohort

Initial search

Acute pancreatitis cases, n

569

Age, mean (SD)

60.3 (17.2)

Sex female, n (%)

251 (44.1%)

LOS, median (IQR)

7 (4;12)

Etiology, n (%)

 Biliary

217 (38.1%)

 Alcohol-related

139 (24.4%)

 Idiopathic

130 (22.8%)

Biliary acute pancreatitis cohort

p-value

Cases, n

217

Age, mean (SD)

65.9 (17.4)

<0.001*

Sex female, n (%)

107 (49.3%)

0.05*

LOS, median (IQR)

7 (4;11)

0.34*

BISAP, median (IQR)

1 (0;2)

CCI, median (IQR)

3 (1;4)

MODS, median (IQR)

0 (0;1)

Suspected/confirmed cholangitis, n (%)

40 (18.4%)

Underwent ERCP, n (%)

148 (68.2%)

Antibiotic treatment, n (%)

133 (61.3%)

Severity of pancreatitis

 mild

135 (62.2%)

 moderately-severe

65 (30.0%)

 severe

17 (7.8%)

Mortality 90 day all-cause, n (%)

5 (2.3%)

Characteristics across severity groups

Mild

Moderately-severe

severe

Age, mean (SD)

64.8 (18.5)

66.2 (15.8)

74.2 (13.2)

0.10

LOS, median (IQR)

6 (3;9)

9 (6;13)

17 (8.5;31.5)

<0.001

BISAP, median (IQR)

1 (0;1)

1 (0;2)

2 (2;3.75)

<0.001

CCI, median (IQR)

3 (1;4)

3 (2;5)

6 (4.5;7)

<0.001

MODS, median (IQR)

*vs. other etiologies/initial search; BISAP=Bedside Index of Severity of Acute Pancreatitis, CCI=Charlson Comorbidity Index, ERCP=Endoscopic retrograde cholangiopancreatography, IQR=interquartile range, LOS=length of stay, MODS=multi-organ dysfunction score (adj. Marshall score), SD=standard deviation

Table 2 Outcome predictors and groups

Outcomes, n (%)

BISAP 0

BISAP 1-2

BISAP 3-5

Mortality 90d all-cause

0 (0.0%)

0 (0.0%)

4 (30.8%)

Severe pancreatitis or ICU admission

2 (3.3%)

12 (9.3%)

3 (23.1%)

Moderately-severe pancreatitis

16 (26.2%)

40 (31.0%)

5 (38.5%)

Mild pancreatitis

44 (72.1%)

81 (62.8%)

1 (7.7%)

CCI 0-2

CCI 3-5

CCI≥6

Mortality 90d all-cause

0 (0.0%)

0 (0.0%)

5 (14.7%)

Severe pancreatitis or ICU admission

2 (2.2%)

9 (9.7%)

6 (17.6%)

Moderately-severe pancreatitis

27 (30.3%)

25 (26.9%)

13 (38.2%)

Mild pancreatitis

62 (69.7%)

61 (65.6%)

11 (32.4%)

Outcome groups*

Group 1

Group 2

Group 3

Group 4

Group 5

Risk

Very-high

High

Mod.-high

Mod.-low

Low

BISAP-class

3-5

0-2

CCI-class

≥6

0-5

≥6

3-5

0-2

Cases, n (%)

8 (4.0%)

5 (2.5%)

22 (10.9%)

84 (41.6%)

83 (41.1%)

LOS, median (IQR)

5 (3;10)

15 (9;106.5)

10 (6;14.25)

7 (4;11)

5 (3;9)

Mortality 90d all-cause

4 (50%)

0 (0%)

0 (0%)

0 (0%)

0 (0%)

Severe pancreatitis or ICU admission

0 (0%)

3 (60%)

6 (27.3%)

6 (7.1%)

2 (2.4%)

Moderately-severe pancreatitis

1 (12.5%)

0 (0%)

0 (0%)

2 (2.4%)

0 (0%)

Mild pancreatitis

2 (25%)

2 (40%)

7 (31.8%)

18 (21.4%)

24 (28.9%)

*Outcome groups 1-5 according to BISAP & CCI-classification: Group 1=BISAP 3-5 & CCI≥6, Group 2=BISAP 3-5 & CCI 0-5, Group 3=BISAP 0-2 & CCI≥6, Group 4=BISAP 0-2 & CCI 3-5, Group 5=BISAP 0-2 & CCI 0-2; BISAP=Bedside Index of Severity of Acute Pancreatitis, CCI=Charlson Comorbidity Index, IQR=interquartile range, LOS=length of stay, MODS=multi-organ dysfunction score, SD=standard deviation

Conclusion Outcome prediction does not necessarily demand complicated or hard to come by parameters. This study supports the combined use of BISAP and CCI, both readily and early-on available scores, in stratifying biliary acute pancreatitis patients.



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Artikel online veröffentlicht:
13. Mai 2025

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