Acute pancreatitis resident survival guide
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Vidit Bhargava, M.B.B.S [2]
Diagnostic Criteria
▸ Diagnosis is established by the presence of two of the three following criteria:[1]
- Abdominal pain consistent with acute pancreatitis (acute onset of a persistent, severe, epigastric pain often radiating to the back).
- Serum lipase or amylase ≥ 3 x ULN.
- Characteristic findings on contrast-enhanced CT, MRI, or transabdominal US.
Types
- Interstitial Edematous Pancreatitis
- ▸ Acute inflammation of the pancreatic parenchyma and peripancreatic tissues, but without recognizable tissue necrosis.
- CECT criteria
- ▸ Pancreatic parenchyma enhancement by intravenous contrast agent.
- ▸ No findings of peripancreatic necrosis.
- Necrotizing Pancreatitis
- ▸ Inflammation associated with pancreatic parenchymal necrosis and/or peripancreatic necrosis.
- CECT criteria
- ▸ Lack of pancreatic parenchymal enhancement by intravenous contrast agent.
- ▸ Presence of findings of peripancreatic necrosis.
- Infected Pancreatic Necrosis:
- ▸ Should be considered in patients with necrotizing pancreatitis who deteriorate or fail to improve after 7–10 days of hospitalization.[1]
- ▸ May be presumed by the presence of extraluminal gas on CECT or when fine-needle aspiration is positive for bacteria and/or fungi on Gram stain and culture.[2]
- ▸ Antibiotics able to penetrate pancreatic necrosis (such as carbapenems, quinolones, and metronidazole) may be useful in delaying or sometimes totally avoiding intervention.[3][4]
Complications
Organ Failure
- Modified Marshall Scoring System
Organ System | 0 | 1 | 2 | 3 | 4 |
Respiratory PaO2/FiO2 |
>400 | 301-400 | 201-300 | 101-200 | ≤101 |
Renal‡ Creatinine (μmol/l) Creatinine (mg/dl) |
≤134 <1.4 |
134-169 1.4-1.8 |
170-310 1.9-3.6 |
311-439 3.6-4.9 |
>439 >4.9 |
Cardiovascular Systolic Blood Pressure (mmHg) |
>90 | <90, fluid responsive | <90, not fluid responsive | <90, pH <7.3 | <90, pH <7.2 |
† A score of 2 or more in any system defines the presence of organ failure.
‡ A score for patients with pre-existing chronic renal failure depends on the extent of further deterioration of baseline renal function. No formal correction exists for a baseline creatinine ≥134 μmol/l or ≥1.4 mg/dl.
▸ For non-ventilated patients, the FiO2 can be estimated from below:
Supplemental oxygen (l/min) | FiO2 (%) |
Room air | 21 |
2 | 25 |
4 | 30 |
6–8 | 40 |
9–10 | 50 |
- Transient organ failure = organ failure resolves within 48 h.
- Persistent organ failure = organ failure persists for >48 h.[5][6][7]
Local Complications
▸ Should be suspected when there is persistence/recurrence of abdominal pain, secondary increases in pancreatic enzyme, increasing organ dysfunction, or the development of signs of sepsis.[1]
- Acute Peripancreatic Fluid Collection (APFC)
- ▸ Peripancreatic fluid associated with interstitial edematous pancreatitis with no associated peripancreatic necrosis. This term applies only to areas of peripancreatic fluid seen within the first 4 weeks after onset of interstitial edematous pancreatitis and without the features of a pseudocyst.
- CECT criteria
- ▸ Occurs in the setting of interstitial edematous pancreatitis.
- ▸ Homogeneous collection with fluid density.
- ▸ Confined by normal peripancreatic fascial planes.
- ▸ No definable wall encapsulating the collection.
- ▸ Adjacent to pancreas (no intrapancreatic extension).
- Pancreatic Pseudocyst
- ▸ An encapsulated collection of fluid with a well defined inflammatory wall usually outside the pancreas with minimal or no necrosis. This entity usually occurs more than 4 weeks after onset of interstitial edematous pancreatitis to mature.
- CECT criteria
- ▸ Well circumscribed, usually round or oval.
- ▸ Homogeneous fluid density.
- ▸ No non-liquid component.
- ▸ Well defined wall; that is, completely encapsulated.
- ▸ Maturation usually requires >4 weeks after onset of acute pancreatitis; occurs after interstitial edematous pancreatitis.
- Acute necrotic collection (ANC)
- ▸ A collection containing variable amounts of both fluid and necrosis associated with necrotizing pancreatitis; the necrosis can involve the pancreatic parenchyma and/or the peripancreatic tissues.
- CECT criteria
- ▸ Occurs only in the setting of acute necrotising pancreatitis.
- ▸ Heterogeneous and non-liquid density of varying degrees in different locations (some appear homogeneous early in their course).
- ▸ No definable wall encapsulating the collection.
- ▸ Location—intrapancreatic and/or extrapancreatic.
- Walled-off necrosis (WON)
- ▸ A mature, encapsulated collection of pancreatic and/or peripancreatic necrosis that has developed a well defined inflammatory wall. WON usually occurs >4 weeks after onset of necrotising pancreatitis.
- CECT criteria
- ▸ Heterogeneous with liquid and non-liquid density with varying degrees of loculations (some may appear homogeneous).
- ▸ Well defined wall, that is, completely encapsulated.
- ▸ Location—intrapancreatic and/or extrapancreatic.
- ▸ Maturation usually requires 4 weeks after onset of acute necrotizing pancreatitis
Systemic Complications
▸ Defined as exacerbation of pre-existing co-morbidity, such as coronary artery disease or chronic lung disease, precipitated by the acute pancreatitis.
Grades of Severity
The definitions of severity in acute pancreatitis according to the revised Atlanta classification is as follows.[1]
- Mild acute pancreatitis
- ▸ No organ failure
- ▸ No local or systemic complications
- Moderately severe acute pancreatitis
- ▸ Organ failure that resolves within 48 h (transient organ failure) and/or
- ▸ Local or systemic complications without persistent organ failure
- Severe acute pancreatitis
- ▸ Persistent organ failure (>48 h)
- – Single organ failure
- – Multiple organ failure
Causes
Life Threatening Causes
Life-threatening causes include conditions which may result in death or permanent disability within 24 hours if left untreated.
Acute pancreatitis from any cause may be life-threatening especially if it progresses to necrotizing pancreatitis.
Common Causes
- Gallstones 35-40% [9]
- Hypertriglyceridemia 1-4% cases [10]
- Medication such as 5-mercaptopurine, azathioprine, 5-DDI[11]
- Post - ERCP
Management
Shown below is a diagram depicting the management of acute pancreatitis according to the American College of Gastroenterology (ACG).[13]
Characterize the symptoms: ❑ Severe abdominal pain and/or ❑ Breathing difficulty and/or ❑ Nausea & vomiting and/or ❑ Hiccups sometimes | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Examine the patient: ❑ Fever and/or ❑ Hypotension and/or ❑ Cullen's sign and/or ❑ Grey-Turner's sign and/or ❑ Tachypnea and/or ❑ Abdominal distension and/or tenderness | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Hemodynamic stability? | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Stable | Unstable | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Order Labs: (Urgent) ❑ CBC ❑ Hematocrit ❑ BUN ❑ Creatinine ❑ Amylase ❑ Lipase ❑ Triglyceride ❑ Total bilirubin ❑ Direct bilirubin ❑ Albumin ❑ AST ❑ ALT ❑ Alkaline phosphatase ❑ GGT ❑ Chest X-ray Order imaging studies: (Urgent) Trans abdominal USG (TAUSG) | Stabilize the patient | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Diagnostic criteria: Any 2 out of 3 ❑ Abdominal pain consistent with disease ❑ Serum amylase or lipase values > 3 times normal ❑ Consistent findings from abdominal imaging | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Acute Pancreatitis | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Systemic inflammatory response syndrome? (Urgent) | Yes | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
No | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Risk stratification (Marshall scoring)(Urgent) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Lower risk | Higher risk | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Admit to medical ward | Admit to ICU (Urgent) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Fluids: (Urgent) ❑ Aggressive hydration at 250-500 ml/hr with Ringer's lactate in first 12-24 hrs ❑ Reassess within 6 hrs after admission and for next 24-48 hrs Analgesics: (Urgent) Nutrition: (Urgent) ❑ Immediate oral feeding as soon as pain, vomiting, nausea subside | Fluids: (Urgent) ❑ Initiate with a fluid bolus ❑ Aggressive hydration at 250-500 ml/hr with Ringer's lactate in first 12-24 hrs ❑ Reassess within 6 hrs after admission and for next 24-48 hrs Analgesics: (Urgent) Nutrition: (Urgent) ❑ Nasogastric or nasojejunal feeding may be initiated once pain, vomiting, nausea subside ❑ Consider enteral feeding if above not tolerated | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Cholangitis or biliary obstruction | Yes | ERCP within 24 hrs/Cholecystectomy to prevent recurrence | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
No | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Consider MRCP/EUS | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Clinical improvement within 48-72 hrs | Yes | Assess for ability to maintain oral feeding at the end of 1 week | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
N o | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
CECT/MRI | Recovery | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Pancreatic necrosis | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Failure to improve clinically after 7-10 days of hospitalization | Yes | Supportive treatment | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
No | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Suspect Infected necrosis | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
❑ CT guided FNA ❑ Empiric antibiotics, necrosis penetrating:
| Gram stain & Culture (-) | ❑ Supportive treatment ❑ Consider repeat CT FNA every 7 days if no improvement | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Gram stain & Culture(+) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Infected necrosis | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Clinically stable | Clinically unstable | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
❑ Continue antibiotics & observe ❑ If asymptomatic no debridement, else consider surgical consultation | Prompt surgical consultation (Urgent) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
†ALT: Alanine aminotransferase; AST: Aspartate aminotransferase; BUN: Blood urea nitrogen; CBC: Complete blood count; CECT: Contrast-enhanced computed tomography; CT: Computed tomography; ERCP: Endoscopic retrograde cholangiopancreatography; EU: Endoscopic ultrasound; FNA: Fine-needle aspiration; GGT: Gamma-glutamyl transpeptidase; ICU: Intensive care unit; IV: Intravenous; MRCP: Magnetic resonance cholangiopancreatography; MRI: Magnetic resonance imaging; Q8h: Every 8 hours; Q12h: Every 12 hours
Do's
- Patients who fail to improve clinically (e.g., persistent abdominal pain, fever, nausea, unable to begin oral intake) within the first 48-72 h after admission.
- Patients in whom the diagnosis is unclear.
- Perform abdominal USG in all patients.
- Check serum triglycerides if stones/alcohol not an etiology, consider etiology if serum triglycerides >1000 mg/dl.
- Consider pancreatic tumor if age > 40 years.
- Use Ringer's Lactate(RL) as first choice agent, use normal saline if RL not available.
- Pancreatic duct stents or post-procedure NSAID's are recommended to prevent post-ERCP pancreatitis.
- Perform elective cholecystectomy for gallstones to prevent recurrences.
- Antibiotics are given for extra-pancreatic infections such as cholangitis, catheter-acquired infections, bacteremia, UTI's, pneumonia.
- Use antibiotics for infected necrosis, with high penetrance such as carbapenems, quinolones & metronidazole.
- Presence of asymptomatic pancreatic necrosis or asymptomatic pseudocysts do not warrant intervention, regardless of size, location, extension.
Dont's
- ERCP is not needed in most pts. with gallstone pancreatitis, especially if they lack clinical or laboratory evidence of ongoing biliary obstruction.
- Do not shift patients with sepsis/organ failure to general ward.
- Do not perform emergency surgery, radiologic or endoscopic drainage in stable patients with infected necrosis, wait for 3-4 weeks for the development of a fibrous wall around the necrosis.
- Routine use of antibiotics as prophylaxis is not recommended in acute pancreatitis.
- In patients with sterile necrosis, routine antibiotics are not recommended to prevent development of infected necrosis.
- Anti-fungal agents are not recommended for prophylaxis or therapeutic use along with routine antibiotics.
- In a pt. with necrotizing biliary AP, cholecystectomy should be delayed until active inflammation has subsided to prevent infection.
References
- ↑ 1.0 1.1 1.2 1.3 Banks, PA.; Bollen, TL.; Dervenis, C.; Gooszen, HG.; Johnson, CD.; Sarr, MG.; Tsiotos, GG.; Vege, SS.; Acosta, JM. (2013). "Classification of acute pancreatitis--2012: revision of the Atlanta classification and definitions by international consensus". Gut. 62 (1): 102–11. doi:10.1136/gutjnl-2012-302779. PMID 23100216. Unknown parameter
|month=
ignored (help) - ↑ Banks, PA.; Gerzof, SG.; Langevin, RE.; Silverman, SG.; Sica, GT.; Hughes, MD. (1995). "CT-guided aspiration of suspected pancreatic infection: bacteriology and clinical outcome". Int J Pancreatol. 18 (3): 265–70. doi:10.1007/BF02784951. PMID 8708399. Unknown parameter
|month=
ignored (help) - ↑ Petrov, MS.; Shanbhag, S.; Chakraborty, M.; Phillips, AR.; Windsor, JA. (2010). "Organ failure and infection of pancreatic necrosis as determinants of mortality in patients with acute pancreatitis". Gastroenterology. 139 (3): 813–20. doi:10.1053/j.gastro.2010.06.010. PMID 20540942. Unknown parameter
|month=
ignored (help) - ↑ van Santvoort, HC.; Bakker, OJ.; Bollen, TL.; Besselink, MG.; Ahmed Ali, U.; Schrijver, AM.; Boermeester, MA.; van Goor, H.; Dejong, CH. (2011). "A conservative and minimally invasive approach to necrotizing pancreatitis improves outcome". Gastroenterology. 141 (4): 1254–63. doi:10.1053/j.gastro.2011.06.073. PMID 21741922. Unknown parameter
|month=
ignored (help) - ↑ Johnson, CD.; Abu-Hilal, M. (2004). "Persistent organ failure during the first week as a marker of fatal outcome in acute pancreatitis". Gut. 53 (9): 1340–4. doi:10.1136/gut.2004.039883. PMID 15306596. Unknown parameter
|month=
ignored (help) - ↑ Mofidi, R.; Duff, MD.; Wigmore, SJ.; Madhavan, KK.; Garden, OJ.; Parks, RW. (2006). "Association between early systemic inflammatory response, severity of multiorgan dysfunction and death in acute pancreatitis". Br J Surg. 93 (6): 738–44. doi:10.1002/bjs.5290. PMID 16671062. Unknown parameter
|month=
ignored (help) - ↑ Lytras, D.; Manes, K.; Triantopoulou, C.; Paraskeva, C.; Delis, S.; Avgerinos, C.; Dervenis, C. (2008). "Persistent early organ failure: defining the high-risk group of patients with severe acute pancreatitis?". Pancreas. 36 (3): 249–54. doi:10.1097/MPA.0b013e31815acb2c. PMID 18362837. Unknown parameter
|month=
ignored (help) - ↑ Yang, AL.; Vadhavkar, S.; Singh, G.; Omary, MB. (2008). "Epidemiology of alcohol-related liver and pancreatic disease in the United States". Arch Intern Med. 168 (6): 649–56. doi:10.1001/archinte.168.6.649. PMID 18362258. Unknown parameter
|month=
ignored (help) - ↑ Forsmark, CE.; Baillie, J. (2007). "AGA Institute technical review on acute pancreatitis". Gastroenterology. 132 (5): 2022–44. doi:10.1053/j.gastro.2007.03.065. PMID 17484894. Unknown parameter
|month=
ignored (help) - ↑ Fortson, MR.; Freedman, SN.; Webster, PD. (1995). "Clinical assessment of hyperlipidemic pancreatitis". Am J Gastroenterol. 90 (12): 2134–9. PMID 8540502. Unknown parameter
|month=
ignored (help) - ↑ Yi, GC.; Yoon, KH.; Hwang, JB. (2012). "Acute Pancreatitis Induced by Azathioprine and 6-mercaptopurine Proven by Single and Low Dose Challenge Testing in a Child with Crohn Disease". Pediatr Gastroenterol Hepatol Nutr. 15 (4): 272–5. doi:10.5223/pghn.2012.15.4.272. PMID 24010098. Unknown parameter
|month=
ignored (help) - ↑ Köhler, H.; Lankisch, PG. (1987). "Acute pancreatitis and hyperamylasaemia in pancreatic carcinoma". Pancreas. 2 (1): 117–9. PMID 2437571.
- ↑ Tenner, S.; Baillie, J.; DeWitt, J.; Vege, SS. (2013). "American College of Gastroenterology guideline: management of acute pancreatitis". Am J Gastroenterol. 108 (9): 1400–15, 1416. doi:10.1038/ajg.2013.218. PMID 23896955. Unknown parameter
|month=
ignored (help) - ↑ Arvanitakis, M.; Delhaye, M.; De Maertelaere, V.; Bali, M.; Winant, C.; Coppens, E.; Jeanmart, J.; Zalcman, M.; Van Gansbeke, D. (2004). "Computed tomography and magnetic resonance imaging in the assessment of acute pancreatitis". Gastroenterology. 126 (3): 715–23. PMID 14988825. Unknown parameter
|month=
ignored (help) - ↑ Zaheer, A.; Singh, VK.; Qureshi, RO.; Fishman, EK. (2013). "The revised Atlanta classification for acute pancreatitis: updates in imaging terminology and guidelines". Abdom Imaging. 38 (1): 125–36. doi:10.1007/s00261-012-9908-0. PMID 22584543. Unknown parameter
|month=
ignored (help) - ↑ Bollen, TL.; Singh, VK.; Maurer, R.; Repas, K.; van Es, HW.; Banks, PA.; Mortele, KJ. (2011). "Comparative evaluation of the modified CT severity index and CT severity index in assessing severity of acute pancreatitis". AJR Am J Roentgenol. 197 (2): 386–92. doi:10.2214/AJR.09.4025. PMID 21785084. Unknown parameter
|month=
ignored (help)