This document contains summaries of multiple research articles and guidelines related to liver, pancreas, and biliary tract problems. One study found that 46% of chronic pancreatitis patients showed signs of acute inflammation based on cytology samples, and 60% showed signs of acute inflammation based on cytology or biopsy samples. Guidelines for managing severe acute pancreatitis recommend diagnosing and predicting severity early, identifying infection risk, and using evidence-based treatment approaches. Another discussion reviews approaches to diagnosing acute pancreatitis, identifying etiology, providing supportive ICU care, and managing gallstone-induced acute pancreatitis.
This document contains summaries of multiple research articles and guidelines related to liver, pancreas, and biliary tract problems. One study found that 46% of chronic pancreatitis patients showed signs of acute inflammation based on cytology samples, and 60% showed signs of acute inflammation based on cytology or biopsy samples. Guidelines for managing severe acute pancreatitis recommend diagnosing and predicting severity early, identifying infection risk, and using evidence-based treatment approaches. Another discussion reviews approaches to diagnosing acute pancreatitis, identifying etiology, providing supportive ICU care, and managing gallstone-induced acute pancreatitis.
This document contains summaries of multiple research articles and guidelines related to liver, pancreas, and biliary tract problems. One study found that 46% of chronic pancreatitis patients showed signs of acute inflammation based on cytology samples, and 60% showed signs of acute inflammation based on cytology or biopsy samples. Guidelines for managing severe acute pancreatitis recommend diagnosing and predicting severity early, identifying infection risk, and using evidence-based treatment approaches. Another discussion reviews approaches to diagnosing acute pancreatitis, identifying etiology, providing supportive ICU care, and managing gallstone-induced acute pancreatitis.
RESEARCH JOURNAL Republic of the Philippines CAMARINES SUR POLYTECHNIC COLLEGES Nabua, Camarines Sur By: ELAINE FRANCES M. ILLO, RM, GRADUATE SCHOOL RN PATHOLOGICAL ACUTE INFLAMMATION IN CHRONIC PANCREATITIS by: Pavankumar Vijayaraj1, Biju Pottakkat1, Raja Kalayarasan1, Sandip Chandrasekar1, Surinder Kumar Verma2 Published: July 04, 2019 https://pancreas.imedpub.com/pathological-acute-inflammation-in- chronic-pancreatitis.php?aid=25079 ABSTRACT Mechanism of pain in Chronic Pancreatitis is not fully understood. Recurrent acute inflammation is one of the proposed hypotheses for pain in chronic pancreatitis. The actual incidence and prevalence of ongoing acute inflammation in chronic pancreatitis have been under-noticed in literature. This study aims to examine the prevalence of acute pancreatic inflammation in chronic pancreatitis patients. Methods: Fifty patients who underwent surgery for chronic pancreatitis were analyzed. Those with clinical, biochemical or radiological features of acute on chronic pancreatitis were excluded. Intra operative fine needle aspiration cytology was taken from the head and body of pancreas. Pancreatic tissue was sent for histopathological examination in all patients. Results: Intraoperative fine needle aspiration cytology from pancreas showed features of acute inflammation in twenty 23 (46%) cases. Biopsy from pancreas showed features of acute inflammation in 12 patients (24%). 30/50 (60%) patients had some features of acute inflammation in either fine needle aspiration cytology or biopsy. CONCLUSION Significant proportion of patients with chronic pancreatitis has pathological features of acute inflammation in pancreas despite clinical, biochemical and radiological features showing no evidence of acute pancreatitis. Ongoing pathological acute inflammatory process in the pancreas might be a major cause for initiation and progression of chronic fibrosis in chronic pancreatitis. 2019 WSES GUIDELINES FOR THE MANAGEMENT OF SEVERE ACUTE PANCREATITIS by: Ari Leppäniemi, et. al. Published: 13 June 2019 https://wjes.biomedcentral.com/articles/10.1186/s13017- 019-0247-0 ABSTRACT Although most patients with acute pancreatitis have the mild form of the disease, about 20–30% develops a severe form, often associated with single or multiple organ dysfunction requiring intensive care. Identifying the severe form early is one of the major challenges in managing severe acute pancreatitis. Infection of the pancreatic and peripancreatic necrosis occurs in about 20–40% of patients with severe acute pancreatitis, and is associated with worsening organ dysfunctions. While most patients with sterile necrosis can be managed nonoperatively, patients with infected necrosis usually require an intervention that can be percutaneous, endoscopic, or open surgical. These guidelines present evidence-based international consensus statements on the management of severe acute pancreatitis from collaboration of a panel of experts meeting during the World Congress of Emergency Surgery in June 27–30, 2018 in Bertinoro, Italy. The main topics of these guidelines fall under the following topics: Diagnosis, Antibiotic treatment, Management in the Intensive Care Unit, Surgical and operative management, and Open abdomen. DISCUSSION Acute pancreatitis (AP) represents a disease characterized by acute inflammation of the pancreas and histologically acinar cell destruction. The diagnosis of AP requires at least the presence of two of the three following criteria: (i) abdominal pain consistent with the disease, (ii) biochemical evidence of pancreatitis (serum amylase and/or lipase greater than three times the upper limit of normal), and (iii) characteristic findings from abdominal imaging. Most patients (80–85%) will develop a mild disease course (self-limited, mortality < 1–3%), but around 20% will have a moderate or severe episode of AP, with a mortality rate from 13 to 35%. Thus, it is important to diagnose (or better predict) an episode of severe acute pancreatitis (SAP), and to identify the patients with high risk of developing complications. DISCUSSION On admission, the etiology of AP should be determined, to project the need of definitive treatment (e.g., gallstone disease) and to avoid recurrence (e.g., alcohol intake, hypertriglyceridemia). The treatment and follow-up depend on the etiology of the AP. A transabdominal US should be performed on admission (to perform cholecystectomy for biliary pancreatitis when appropriate). Almost all the AP guidelines worldwide (based on revisions and meta-analyses) recommend performing US on admission or in the first 48 h. Serum pancreatic enzyme measurement is the “gold standard” for the diagnosis of AP. In an episode of AP, amylase, lipase, elastase, and trypsin are released into the bloodstream at the same time but the clearance varies depending on the timing of blood sampling. Amylase is an enzyme secreted by the pancreas, and also salivary glands, small intestine, ovaries, adipose tissue, and skeletal muscles. There are two major isoforms of amylase: pancreatic and salivary, and the leading function is digestion of starch, glycogen, and related poly- and oligosaccharides, by hydrolysis. In AP, serum amylase levels usually rise within 6 to 24 h, peak at 48 h, and decrease to normal or near normal levels over the next 3 to 7 days. DISCUSSION Lipase is another enzyme secreted by the pancreas. AP is the main reason for an increase in lipase, and many investigators emphasize that lipase is more specific, but can be found elevated also in non-pancreatic diseases such as renal disease, appendicitis, acute cholecystitis, chronic pancreatitis, bowel obstruction, etc. In AP, serum lipase remains elevated for a longer period than serum amylase. It rises within 4 to 8 h, peaks at 24 h, and decreases to normal or near normal levels over the next 8 to 14 days. Trypsinogen is the zymogen of the pancreatic enzyme trypsin. In AP, the serum and urinary concentrations of trypsinogen usually rise to high levels within a few hours and decrease in 3 days. CONCLUSIONS These guidelines present evidence-based international consensus statements on the management of severe acute pancreatitis from collaboration of a panel of experts. It contains 55 statements on diagnosis, management in the ICU, surgical and operative management, open abdomen, and antibiotic treatment. For some of the statements such as severity grading, imaging, use of prophylactic antibiotics and most aspect of the management in the ICU, the evidence is strong. For others, such as laboratory diagnostics and surgical strategies, for example, the evidence is quite weak requiring further studies. With accumulating knowledge, the statements need to be regularly updated. ACUTE PANCREATITIS: CURRENT PERSPECTIVES ON DIAGNOSIS AND MANAGEMENT By: Adarsh P Shah, Moustafa M Mourad, And Simon R Bramhall Published: March 9. 2018 10.2147/Jir.S135751 ABSTRACT The last two decades have seen the emergence of significant evidence that has altered certain aspects of the management of acute pancreatitis. While most cases of acute pancreatitis are mild, the challenge remains in managing the severe cases and the complications associated with acute pancreatitis. Gallstones are still the most common cause with epidemiological trends indicating a rising incidence. The surgical management of acute gallstone pancreatitis has evolved. In this article, we revisit and review the methods in diagnosing acute pancreatitis. We present the evidence for the supportive management of the condition, and then discuss the management of acute gallstone pancreatitis. Based on the evidence, our local institutional pathways, and clinical experience, we have produced an outline to guide clinicians in the management of acute gallstone pancreatitis. CONCLUSION Acute pancreatitis is frequently encountered on the emergency surgical take. Once the diagnosis is made, clinical efforts should simultaneously concentrate on investigating for the underlying etiology and managing the condition by anticipating its complications, which can be aided by using any of the severity scoring systems described. Management of acute pancreatitis is largely supportive. There is still no consensus on the ideal type and regimen of fluid for resuscitation, but goal-directed fluid therapy is associated with better outcomes. Early enteral nutrition modulates the inflammatory response and improves outcomes by decreasing infective complications of acute pancreatitis. Antibiotics should be used judiciously as prophylactic antibiotics have not shown any benefit in preventing infective complications of acute pancreatitis. Patients with mild acute gallstone pancreatitis should be recommended to undergo a laparoscopic cholecystectomy at the index admission, while those with severe gallstone pancreatitis and evidence of cholangitis and/or choledocholithiasis benefit from early ERCP. Patients with mild acute gallstone pancreatitis and concurrent choledocholithiasis benefit from single-stage laparoscopic cholecystectomy and bile duct exploration, subject to available local expertise. There is no difference in mortality and morbidity between the single-stage and double-stage management of choledocholithiasis. However, the single-stage approach reduces the length of hospital stay and