Shifa A Kalokhe*, Shrutik Devdikar, Lisha Suraj
Department of General Surgery, MGM Medical College, Navi Mumbai, MGM Institute of Health Sciences, India
*Corresponding Author: Shifa A Kalokhe, Department of General Surgery, MGM Medical College, Navi Mumbai, MGM Institute of Health Sciences, India
Received: 19 June 2022; Accepted: 27 June 2022; Published: 13 July 2022
Background
Acute pancreatitis (AP) is a common inflammatory disease of pancreas, mainly characterized by local inflammation of the pancreas due to activation of pancreatic enzymes and increase in serum amylase and lipase levels. As studies suggests 20% of patients with acute pancreatitis develop necrotizing pancreatitis. The aim of our study was to determine whether patients with necrotizing pancreatitis had any significant correlation with Serum Amylase and Lipase Level and if it helps in Early predictability of percentage of Necrosis.
Aim
Methods
To determine correlation between Serum Amylase and Serum Lipase Level with Percentage of necrosis on CECT in patients with Acute Necrotising Pancreatitis. We will be assessing all patients presenting to Institution and diagnosed as a case of Acute Necrotizing Pancreatitis. All Routine Investigation along with Amylase and Lipase done for the Patient, CECT of the Patients were done after 72 hrs of onset of attack. Comparison was done between the relation of Serum Amylase-Lipase level and the percentage of Pancreatic Necrosis mentioned on CECT.
Results
In this retrospective study done from January 2021 to January 2022, 40 cases of Acute Necrotising Pancreatitis were evaluated, it was found that there was no significant correlation between Serum Amylase and Lipase level and the percentage of Necrosis on CECT abdomen.
Conclusion
It was found that level of serum amylase and serum lipase on admission is not a good predictor to assess the percentage of necrosis of pancreas on CECT abdomen. The level of serum amylase and lipas
Serum amylase, Serum lipase, Acute necrotizing pancreatitis, Necrosis percentage
Acute pancreatitis (AP) is a common inflammatory disease of pancreas which can be mild and self-limiting without complications or severe with prolonged hospitalization, high morbidity, and high mortality. Acute pancreatitis (AP), mainly characterized by local inflammation of the pancreas due to activation of pancreatic enzymes, accompanied or not by the involvement of proximal tissues and distal organs [1]. It is a common acute abdomen seen in clinical practice and its incidence is increasing [2,3]. Worldwide, the incidence of acute pancreatitis ranges between 5 and 80 per 100,000 population, with the highest incidence recorded in the United States and Finland. Prevalence rate for Pancreatitis in India is 7.9 per 100,000. Prevalence rate for men and women 8.6 and 8.0 per 100,000 respectively in India. According to the The revised Atlanta classification system, introduced in 2012, the clinical course of acute pancreatitis is subdivided into early (1 week) phases relative to disease onset, and the late phase may persist for weeks to months. AP can be subcategorised into interstitial oedematous pancreatitis (IEP) and Necrotising pancreatitis (NP) which can be classified into three types according to the necrotic area involved: pancreatic parenchymal necrosis with peripancreatic necrosis, pancreatic parenchymal necrosis alone, or peripancreatic necrosis alone. As studies and literature suggests 20% of patients with acute pancreatitis develop necrotizing pancreatitis, with a mortality of 8% to 30%. Activated pancreatic enzymes, microcirculatory impairment, and the release of inflammatory mediators lead to rapid worsening of pancreatic damage and necrosis of the gland causing acute necrotising pancreatitis. Necrotizing pancreatitis has a more severe prognosis and a higher mortality rate than interstitial pancreatitis. CECT is the gold standard of investigation. The aim of our study was to determine whether patients with necrotizing pancreatitis had any significant correlation with serum Amylase and Serum Lipase Level and if Level of Serum Amylase-Lipase level helps in Early predictability of percentage of Necrosis.
To determine correlation between Serum Amylase and Serum Lipase Level with Percentage of necrosis on CECT in patients with Acute Necrotising Pancreatitis.
Inclusion criteria
1.Patients diagnosed as case of Acute Necrotising Pancreatitis.
2.Either Sex - Male, Female.
3.Age - Above 18 years.
Exclusion criteria
1.Patient with interstitial oedematous pancreatitis.
2.Under 18 years of age.
3.All patients above the age of 18 years with severe debilitating diseases.
Acute pancreatitis is a common inflammatory disease of the pancreas with increasing incidence in the western world. It is a complex process in which pancreatic enzyme activation causes local pancreatic damage, resulting in an acute inflammatory response. Acute pancreatitis remains a disease of unpredictable outcome, with a mortality rate of between 10% and 15%. The most common causes of acute pancreatitis are biliary tract stones and alcohol abuse. Other Causes of Pancreatitis include Idiopathic, Iatrogenic, Anatomical obstruction, Drug induced (sulfonamides, metronidazole, erythromycin, tetracyclines, thiazides, furosemide, HMG-CoA reductase inhibitors (statins), azathioprine, 6-mercaptopurine, 5-aminosalicylic acid, sulfasalazine, valproic acid, andacetaminophen), Metabolic (hypertriglyceridemia, hypercalcemia), Miscellaneous (Blunt, penetrating abdominal trauma).

Figure 1: Pathophysiology of Severe Acute Pancreatitis
The cardinal symptom of AP is epigastric or periumbilical pain that radiates to the back. Upto 90% of patients have nausea or vomiting that typically does not relieve the pain. The nature of the pain is constant; therefore, if the pain disappears or decreases, another diagnosis should be considered [6]. Abdomen may be normal or reveal only mild epigastric tenderness. Significant abdominal distention, associated with generalized rebound and abdominal rigidity, is present in severe pancreatitis [6]. According to the The revised Atlanta classification system, introduced in 2012, AP can be subcategorised into interstitial oedematous pancreatitis (IEP) and Necrotising pancreatitis (NP). Pancreatic necrosis is the presence of nonviable pancreatic parenchyma or peripancreatic fat; it can be manifested as a focal area or diffuse involvement of the gland. The acute inflammatory injury that occurs during the first 48 to 72 hours causes mucosal ischemia and reperfusion injury. Both effects favor bacterial overgrowth because they alter local immunity. Mucosal ischemia also produces an increase in the permeability of intestinal cells, which is initiated 72 hours after the acute episode but typically peaks 1 week later. These transient episodes of bacteremia are associated with pancreatic necrosis infection. Less frequently, distant sources of infection, such as pneumonia and vascular or urinary tract infection associated with central lines and catheters, are associated with bacteremia and pancreatic necrosis. Finally, local contamination after surgery or interventional procedures such as ERCP is responsible for necrosis infection. Contrast-enhanced CT is the most reliable technique to diagnose pancreatic necrosis. In acute pancreatitis, serum amylase activity is increased within 2-12 hours of the onset of disease with maximal levels in 12-72 hours which return to normal by the 3rd-4th days [7]. In acute pancreatitis, increased lipase activity in blood is seen after 4-8 h of an attack, peaks at about 24h, and comes back to the normal level by 8-14 days [7]. Serum lipase measurement is a highly specific marker of pancreatic disease than amylase, its activity remains increased for longer than that of serum amylase, and there are no other sources of lipase to reach the blood. Sensitivity for serum amylase is 63.6% and for serum lipase it is 99.5%, whereas specificity for serum amylase 99.4 % and for lipase 99.2% [8].

Figure 2: Pathophysiology of Pancreatic Necrosis Infection
As per the Atlanta classification, Pancreatic necrosis was defined as area of non-enhancement of pancreatic parenchyma after intravenous administration of contrast media. EPN includes peripancreatic and contiguous retro peritoneal fat necrosis; defined by fat infiltration, collection of fluid/solid components and with increased attenuation (more than 20-30 HU) with heterogeneous appearance [4,5]. The study is based on level of Serum Amylase and Serum Lipase in Early predictability of percentage of Necrosis which can guide towards early and aggressive management of the patients to reduce morbidity and mortality.

Figure 3: Correlation between serum Amylase level and Necrosis percentage

Figure 4: Correlation between serum Lipase level and Necrosis percentage