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Treatment of severe acute pancreatitis and its complications.pptx
1. MANAGEMENT OF SEVERE ACUTE
PANCREATITIS AND ITS COMPLICATIONS
Maj. Hasnain Afzal
Resident General Surgery
2. DEFINITION
Acute Pancreatitis
An acute condition presenting with abdominal pain-
usually associated with raised blood pancreatic
enzymes as a result of pancreatic inflammation
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3. DIAGNOSTIC CRITERIA
Characteristic Abdominal Pain
Elevated Serum Amylase/Lipase >3 Times
Radiological Findings
(2 out of 3 criteria Required For Diagnosis)
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7. SEVERITY CLASSIFICATION
Revised Atlanta Classification
Mild Acute Pancreatitis
no organ failure; no local or systemic complications
Moderately Severe Acute Pancreatitis
organ failure that resolves within 48 hours (transient organ failure);
and/or local or systemic complications without persistent organ
failure
Severe Acute Pancreatitis
persistent organ failure (>48 hours)
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8. EARLY MANAGEMENT OF SEVERE ACUTE
PANCREATITIS
Admission to HDU/ICU
Analgesia
Aggressive fluid rehydration
Supplemental oxygen
Invasive monitoring
Nasogastric drainage (only initially)
Antibiotics if cholangitis suspected
CT scan
ERCP within 72 hours for severe gallstone pancreatitis or signs of cholangitis
Supportive therapy for organ failure
If nutritional support is required, consider enteral (nasogastric) feeding 8
10. A. Acute peripancreatic fluid collection
B. Pancreatic Pseudocyst D. Walled-Off Necrosis
C. Acute Necrotic collection
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11. INDICATIONS FOR PERCUTANEOUS /
ENDOSCOPIC DRAINAGE OF PANCREATIC
COLLECTIONS
Clinical deterioration with signs or strong suspicion of
infected necrotizing pancreatitis is an indication to
perform intervention (percutaneous/endoscopic drainage)
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12. INDICATIONS FOR SURGICAL
INTERVENTION
The following are indications for surgical intervention:
Step-up approach
Abdominal compartment syndrome
Acute on-going bleeding
Bowel ischaemia or acute necrotizing cholecystitis
Bowel fistula
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13. TIMING OF SURGERY
Postponing surgical interventions for more than 4 weeks
after the onset of the disease results in less mortality
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14. SURGICAL APPROACH TO NECROTIZING
PANCREATITIS
OPEN NECROSECTOMY WITH OPEN
PACKING
OPEN NECROSECTOMY WITH CLOSED
PACKING
OPEN NECROSECTOMY WITH
CONTINOUS POSTOPERATIVE LAVAGE
PROGRAMMED OPEN NECROSECTOMY 14
15. CONCLUSION
Classification of complications according to revised Atlanta
Classification system
The step-up Approach
Close monitoring,
Percutaneous or endoscopic drainage,
Minimally invasive Retroperitoneal debridement
Open Necrosectomy
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16. REFERENCES
Leppäniemi et al. World Journal of Emergency Surgery (2019) 14:27
https://doi.org/10.1186/s13017-019-0247-0
Zerem E. Treatment of severe acute pancreatitis and its complications. World
J Gastroenterol 2014; 20(38): 13879-13892
Bailey & Love’s short practice of surgery 27th Edition
Fischer’s Mastery of surgery 7th edition
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Bismillah Arehman Arraheem. Worthy DG surgery Respected seniors and my dear colleagues Assalam o alaikum I am maj. Hasnain resident in gen surgery I will be presenting management of SAP and its complications
It is
According to the revised Atlanta classification, the diagnosis of AP can be made when two of three criteria are met: (1)
characteristic abdominal pain; (2) serum amylase or lipase levels
greater than three times the upper limit of normal; and (3) characteristic
findings on cross-sectional imaging.
Acute pancreatitis has an early phase that usually lasts a week. It is characterised by a systemic inflammatory response syndrome (SIRS) which – if severe – can lead to transient or persistent organ failure (deemed persistent if it lasts for over 48 hours).
The late phase is seen typically in those who suffer a severe attack, and can run from weeks to months. It is characterised by persistent systemic signs of inflammation, and/or local complications, particularly fluid collections and peripancreatic sepsis
The two major causes of acute pancreatitis are Gallstones, which occur in 50–70% of patients, and alcohol abuse, which accounts for 25% of cases.
Rest of the etiologic factors are as flashed
In clinical presentation Pain is the cardinal symptom. Pain is usually experienced first in the epigastrium but may be localised to either upper quadrant or
felt diffusely throughout the abdomen radiating to back in 50% of patients.
Nausea vomiting and abdominal distension are other common presenting symptoms
A Revised Atlanta classification of acute pancreatitis recommends that patients with acute pancreatitis be stratified into 3 groups:
●● Mild acute pancreatitis: in which there is no organ failure; ●● no local or systemic complications.
●● Moderately severe acute pancreatitis: in which organ failure that resolves within 48 hours (transient
organ failure); and/or ●● local or systemic complications without persistent organ failure.
Severe acute pancreatitis: in which persistent organ failure (>48 hours); ●● single organ failure; ●● multiple organ failure.
Early management of SAP includes Continuous vital signs monitoring in high dependency unit if organ dysfunction occurs. Persistent organ dysfunction or organ failure occurrence despite adequate fluid resuscitation is an indication for ICU admission
Analgesia No evidence or recommendation about any restriction in pain medication is available. Nonsteroidal anti-inflammatory drugs (NSAID) should be avoided in acute kidney injury (AKI)
Aggressive fluid rehydration to optimize tissue perfusion targets, without waiting for hemodynamic worsening
Supplemental oxygen
Frequent monitoring of haematological and biochemical parameters
Nasogastric drainage (only initially)
There are no data to support a practice of ‘resting’ the pancreas and feeding only by the parenteral or nasojejunal routes. If nutritional support is felt to be necessary, enteral nutrition (e.g. feeding via a nasogastric tube) should be used.
Antibiotics if cholangitis suspected; prophylactic antibiotics can be considered
CT scan is essential if organ failure, clinical deterioration or signs of sepsis develop
ERCP within 72 hours for severe gallstone pancreatitis or signs of cholangitis
Supportive therapy for organ failure if it develops (inotropes, ventilatory support, haemofiltration, etc.)
The revised Atlanta classification has characterized these fluid collections according to timing (> or <4 weeks) and the presence or
absence of pancreatic necrosis
Peripanreatic fluid collection without necrosis before 4 weeks is termed as Acute peripancreatic fluid collection. Whereas after 4 weeks it is termed as pancreatic pseudocyst
Peripancreatic fluid collection with necrosis before 4 weeks is termed as Acute nectrotic collection and after 4 weeks is called walled-off necrosis
shows an ill-defined peripancreatic collection and stranding around the body and tail of the pancreas (arrows) with mild heterogeneity of the pancreatic tail (*)
acute necrotizing pancreatitis shows ill-defined hypoattenuating areas in the head and body of the pancreas (*) and an ill-defined, heterogeneous peripancreatic collection (white arrows) with interspersed fat (black arrow) and stranding around the head, body, and tail.
well-defined, homogeneous peripancreatic collection around the tail of the pancreas (arrows), a finding that is compatible with a pseudocyst
relatively well-defined, walled-off combined necrosis in the region of the head and body of the pancreas (white arrows), with peripancreatic necrosis seen around the tail (black arrow)
Clinical deterioration with signs or strong suspicion of infected necrotizing pancreatitis is an indication to perform percutaneous/endoscopic Drainage.
After 4 weeks after the onset of the disease:
– On-going organ failure without sign of infected necrosis. On-going gastric outlet, biliary, or intestinal obstruction due to a large walled off necrotic collection
– Disconnected duct syndrome
– Symptomatic or growing pseudocyst
After 8 weeks after the onset of the disease:
– On-going pain and/or discomfort
As a continuum in a step-up approach after percutaneous/ endoscopic procedure with the same indications
Abdominal compartment syndrome
Acute on-going bleeding when endovascular approach is unsuccessful
Bowel ischaemia or acute necrotizing cholecystitis during acute pancreatitis
Bowel fistula extending into a peripancreatic collection
IAH: A sustained or repeated pathological elevation in IAP more than or equal to 12 mmhg
ACS: A sustained IAP . 20 mmHg that is associated with new organ dysfunction/failure.
Surgical approaches include:
OPEN NECROSECTOMY WITH OPEN PACKING
after necrosectomy, the abdomen maybe left open and repeatedly debrided until there is no residual necrosis, and is allowed to close by secondary intention
OPEN NECROSECTOMY WITH CLOSED PACKING
after the removal of necrotic tissue, the abdomen is closed, packing with external drains left in place.
The drains are removed singly every other day, starting 5-7 d postoperatively
OPEN NECROSECTOMY WITH CONTINOUS POSTOPERATIVE LAVAGE
the procedure is based on the insertion of 2 or more double lumen catheters. Repeated open necrosectomy is performed and the packing is removed when there is no residual necrosis. The smaller lumen of the drains is used for the inflow of the lavage, and the larger lumen is used for the outflow. The drains can be removed after 2-3 wk
PROGRAMMED OPEN NECROSECTOMY
necrosectomy of necrotic tissue is performed using multiple procedures. After necrosectomy, the pancreatic bed is packed with sponges and soft drains are placed on the top of the packs. The abdomen is closed using a zipper
In the end I would like to conclude by saying that Classifying the complications of SAP according to the revised Atlanta classification system is important before deciding the appropriate treatment strategy because different complications of SAP are treated in different ways, either conservatively by interventional imaging techniques or by surgery. Although no universally accepted treatment algorithm exists, the step-up approach using close monitoring, percutaneous or endoscopic drainage, followed by minimally invasive video-assisted retroperitoneal debridement has been shown to produce superior outcomes to traditional open necrosectomy and may be considered as the reference standard intervention for this disorder.