Management of A Patient With Acute Pancreatitis

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Presentation transcript:

Management of A Patient With Acute Pancreatitis M Khoshbaten, M.D. Professor of Gastroenterology & Hepatology Management of A Patient With Acute Pancreatitis

Initial Management Consists of supportive care with: Fluid resuscitation Pain control Nutritional support

Fluid replacement We provide aggressive hydration at a rate of 5 to 10 mL/kg per hour of isotonic crystalloid solution (eg, normal saline or lactated Ringer's solution) to all patients with acute pancreatitis, unless cardiovascular Renal other related comorbid In patients with severe volume depletion that manifests as hypotension and tachycardia 20 mL/kg of intravenous fluid given over 30 minutes followed by 3 mL/kg/hour for 8 to 12 hours In rare patients with acute pancreatitis due to hypercalcemia, lactated Ringer's is contraindicated because it contains 3 mEq/L calcium

Fluid replacement Fluid requirements should be reassessed at frequent intervals in First six hours of admission For the next 24 to 48 hours The rate of fluid resuscitation should be adjusted based on Clinical assessment Hematocrit Blood urea nitrogen (BUN) values Adequate fluid replacement can be assessed by an improvement in Vital signs (goal heart rate <120 beats/minute, mean arterial pressure between 65 to 85 mmhg) Urine output (>0.5 to 1 cc/kg/hour)  Reduction in hematocrit (goal 35 to 44 percent) and BUN over 24 hours, particularly if they were high at the onset

Fluid replacement Monitoring the BUN may be particularly important As both the BUN at the time of admission and the change in BUN during the first 24 hours of hospitalization predict mortality It is important to note that a low urine output may reflect the development of acute tubular necrosis Rather than persistent volume depletion In this setting, aggressive fluid replacement can lead to peripheral and pulmonary edema Without improving the urine output Increased fluid resuscitation should be considered in patients whose BUN levels stay the same or increase

Fluid replacement In the initial stages (within the first 12 to 24 hours) of acute pancreatitis, fluid replacement has been associated with a reduction in Morbidity and mortality Inadequate hydration can lead to Hypotension Acute tubular necrosis

Fluid replacement Persistent hemoconcentration at 24 hours has been associated with development of Necrotizing pancreatitis  vascular leak syndrome  increased third space fluid losses and worsening of pancreatic hypoperfusion It is important to limit fluid resuscitation mainly to the first 24 to 48 hours after onset of the disease Continued is associated with An increased need for intubation Increased risk of abdominal compartment syndrome

Pain Control Abdominal pain is often the predominant symptom in patients with acute pancreatitis Should be treated with analgesics Uncontrolled pain can contribute to the Hemodynamic instability Attention to adequate fluid resuscitation should be the first priority in addressing abdominal pain As hypovolemia from vascular leak and hemoconcentration can cause ischemic pain and resultant lactic acidosis

Pain Control Opioids are Safe Effective Adequate pain control requires the use of intravenous opiates Usually in the form of a patient-controlled analgesia pump Hydromorphone  or  fentanyl  (intravenous) may be used for pain relief

Pain Control Fentanyl is being increasingly used due to its better safety profile Especially in renal impairment It can be given both as a bolus as well as constant infusion The typical dose for the bolus regimen ranges from 20 to 50 micrograms The typical dose for the bolus regimen ranges from 20 to 50 micrograms with a 10-minute lock-out period (time from the end of one dose infusion to the time the machine starts responding to another demand)

Pain Control Meperidine has been favored over morphine for analgesia Morphine caused an increase in sphincter of oddi pressure There are no clinical studies to suggest that morphine can aggravate or cause pancreatitis or cholecystitis In addition, meperidine has a short half-life and repeated doses can lead to accumulation of the metabolite normeperidine that causes Neuromuscular side effects Rarely, seizures

Monitoring  Patients with acute pancreatitis should be monitored closely in First 24 to 48 hours Patients with organ failure will need ongoing monitoring for other complications

Monitoring Vital signs including oxygen saturation should be monitored Supplemental oxygen administered to maintain arterial oxygen saturation of greater than 95 percent Hypoxia may be due to Atelectasis Pleural effusions Opening of intrapulmonary shunts Acute respiratory distress syndrome (ARDS) Patients with persistent or progressive hypoxia should be transferred to Intensive care unit (ICU) for ventilatory support

Monitoring Urine output should be measured hourly fluids should be titrated to maintain urine output (>0.5 to 1 cc/kg/hour)  Patients in the intensive care unit should be monitored for potential abdominal compartment syndrome With serial measures of urinary bladder pressures

Monitoring Electrolytes should be monitored frequently in the first 48 to 72 hours Especially with aggressive fluid resuscitation Hypocalcemia should be corrected if Ionized calcium is low or There are signs of neuromuscular irritability (chvostek's or trousseau's sign) Low magnesium levels can also cause hypocalcemia Should be corrected

Monitoring Serum glucose levels should be monitored hourly in Patients with severe pancreatitis Hyperglycemia (blood glucose greater than 180 to 200 mg/dl) should be treated as it can Increase the risk of secondary pancreatic infections

Nutrition  Patients with mild pancreatitis can often be managed with intravenous hydration alone allowing patients to resume an oral diet within a week Nutritional support is often required in patients with Moderately severe and severe pancreatitis as they are unlikely to resume oral intake within five to seven days Nasojejunal tube feeding (using an elemental or semi-elemental formula) is preferred to  Total parenteral nutrition (TPN)

Oral In mild pancreatitis, in the absence of ileus, nausea or vomiting, oral feeds can be initiated as soon as Pain is decreasing Inflammatory markers are improving  This usually occurs 24 to 48 hours Start with a low residue, low fat, soft diet

Oral More recent data suggest that early refeeding when patients are subjectively hungry, may be safe Regardless of resolution of Abdominal pain Normalization of pancreatic enzymes

Oral In moderately severe to severe pancreatitis, oral feeding may not be tolerated due to Postprandial pain Nausea or vomiting Related to Gastroduodenal inflammation and/or  Extrinsic compression from fluid collections leading to gastric outlet obstruction When the local complications start improving, oral feeds can be Initiated Advanced as tolerated

Enteral  Enteral feeding rather than parenteral nutrition is recommended in patients with Moderately severe Severe acute pancreatitis Who cannot tolerate oral feeding Initiate enteral feeding when it becomes clear that the patient will not be able to consume nourishment by mouth Transfer to an intensive care unit Development of organ failure Systemic inflammatory response syndrome [SIRS] persisting for 48 hours

Enteral Enteral feeding requires radiologic or endoscopic placement of a jejunal feeding tube Beyond the ligament of treitz If placement of a nasojejunal feeding tube is not possible Nasogastric feeding should be initiated Two controlled trials comparing nasogastric with nasojejunal feedings found no significant differences in Apache II scores CRP levels Pain Analgesic requirements

Enteral Start at 25 cc per hour and advance as tolerated To at least 30 percent of the calculated daily requirement (25 kcal/kg ideal body weight) Even in the presence of ileus The presence of fluid collections or elevated pancreatic enzymes is Not necessarily a contraindication to oral or enteral feeding Signs that the formula is not tolerated include increased abdominal pain, vomiting (with nasogastric feeding), bloating, or diarrhea (>5 watery stools or >500 mL per 24 hours with exclusion of Clostridium difficile toxin and medication-induced diarrhea) that resolves if the feeding is held.

Parenteral Parenteral nutrition should be initiated only in patients who Do not tolerate enteral feeding Enteral nutrition plus either early or late parenteral nutrition was associated with increased mortality as compared with enteral nutrition alone (35 versus 28 percent)

Antibiotics  Up to 20 percent of patients with acute pancreatitis develop an extrapancreatic infection Bloodstream infections Pneumonia Urinary tract infections Extrapancreatic infections are associated with Increase in mortality When an infection is suspected, antibiotics should be started While the source of the infection is being determined If cultures are negative and no source of infection is identified Antibiotics should be discontinued

Antibiotics Prophylactic antibiotics are not recommended Regardless of the type Interstitial or necrotizing Disease severity Mild, moderately severe, or severe

Antifungals Administration of prophylactic antifungal therapy (eg, fluconazole) along with prophylactic or therapeutic antibiotics Is not recommended Fungal infections occur in approximately 9 percent of necrotizing pancreatitis It is not clear if they are associated with higher mortality