{"id":11579,"date":"2016-08-29T19:28:04","date_gmt":"2016-08-29T19:28:04","guid":{"rendered":"http:\/\/phosdev.com\/todaysveterinarypractice\/?p=11579"},"modified":"2022-02-17T21:48:50","modified_gmt":"2022-02-17T21:48:50","slug":"diagnosis-treatmenta-case-canine-acute-pancreatitis","status":"publish","type":"post","link":"https:\/\/navc.sitepreview.app\/todaysveterinarypractice.com\/gastroenterology\/diagnosis-treatmenta-case-canine-acute-pancreatitis\/","title":{"rendered":"From Diagnosis to Treatment: A Case of Canine Acute Pancreatitis"},"content":{"rendered":"<p>Sidney, a 10-year-old female spayed cocker spaniel, presented with a 2-day history of lethargy, anorexia, and diarrhea.<\/p>\n<h2>History &amp; Physical Examination<\/h2>\n<p>Sidney had a history of chronic keratoconjunctivitis sicca that was treated with topical cyclosporine.<\/p>\n<p>Two days before presentation, Sidney began refusing to eat and became lethargic. At that time, she was taken to her primary care veterinarian; basic blood analysis and urinalysis were performed (specific results not available). The urinalysis results indicated a urinary tract infection, and Sidney received amoxicillin\/clavulanic acid.<\/p>\n<p>However, after initiation of antibiotic therapy, Sidney had loose stools that contained gelatinous red clumps. At this point, her primary care veterinarian referred her for further diagnostics and treatment.<\/p>\n<p>Sidney\u2019s physical examination findings on presentation to the referral facility are listed in <strong>Table 1<\/strong>. Differential diagnoses based on history, clinical signs, and physical examination findings are outlined in <strong>Table 2<\/strong>.<\/p>\n<p><a href=\"https:\/\/todaysveterinarypractice.com\/wp-content\/uploads\/sites\/4\/2016\/08\/T1609F03Table01.jpg\"><img fetchpriority=\"high\" decoding=\"async\" class=\"wp-image-11587 size-full alignnone\" src=\"https:\/\/todaysveterinarypractice.com\/wp-content\/uploads\/sites\/4\/2016\/08\/T1609F03Table01.jpg\" alt=\"T1609F03Table01\" width=\"405\" height=\"535\" srcset=\"https:\/\/navc.sitepreview.app\/todaysveterinarypractice.com\/wp-content\/uploads\/sites\/4\/2016\/08\/T1609F03Table01.jpg 405w, https:\/\/navc.sitepreview.app\/todaysveterinarypractice.com\/wp-content\/uploads\/sites\/4\/2016\/08\/T1609F03Table01-227x300.jpg 227w\" sizes=\"(max-width: 405px) 100vw, 405px\" \/><\/a><\/p>\n<p><a href=\"https:\/\/todaysveterinarypractice.com\/wp-content\/uploads\/sites\/4\/2016\/08\/T1609F03Table02.jpg\"><img decoding=\"async\" class=\"size-full wp-image-11588 alignnone\" src=\"https:\/\/todaysveterinarypractice.com\/wp-content\/uploads\/sites\/4\/2016\/08\/T1609F03Table02.jpg\" alt=\"T1609F03Table02\" width=\"377\" height=\"291\" srcset=\"https:\/\/navc.sitepreview.app\/todaysveterinarypractice.com\/wp-content\/uploads\/sites\/4\/2016\/08\/T1609F03Table02.jpg 377w, https:\/\/navc.sitepreview.app\/todaysveterinarypractice.com\/wp-content\/uploads\/sites\/4\/2016\/08\/T1609F03Table02-300x232.jpg 300w\" sizes=\"(max-width: 377px) 100vw, 377px\" \/><\/a><\/p>\n<p>&nbsp;<\/p>\n<h2><strong>Diagnostic Approach<\/strong><\/h2>\n<div class=\"orange-box\">\n<p>Initial workup included a complete blood count (CBC), serum biochemical profile, urinalysis, urine culture, coagulation panel, and patient-side SNAP cPL test (idexx.com); the results of the CBC, serum biochemical profile, and coagulation panel are shown in <strong>Tables 3 and 4<\/strong>, with abnormal results bolded. Blood and urine samples were collected before treatment was initiated.<\/p>\n<\/div>\n<p>In addition, 3-view abdominal radiographs were taken to rule out a gastrointestinal (GI) foreign body and other obvious abdominal organ-related diseases. On the basis of abdominal radiography results, abdominal ultrasonography with abdominocentesis was performed. The collected abdominal fluid was prepared for analysis and cytology.<\/p>\n<p><a href=\"https:\/\/todaysveterinarypractice.com\/wp-content\/uploads\/sites\/4\/2016\/08\/T1609F03Table03.jpg\"><img decoding=\"async\" class=\"alignnone  wp-image-11589\" src=\"https:\/\/todaysveterinarypractice.com\/wp-content\/uploads\/sites\/4\/2016\/08\/T1609F03Table03.jpg\" alt=\"T1609F03Table03\" width=\"569\" height=\"764\" srcset=\"https:\/\/navc.sitepreview.app\/todaysveterinarypractice.com\/wp-content\/uploads\/sites\/4\/2016\/08\/T1609F03Table03.jpg 716w, https:\/\/navc.sitepreview.app\/todaysveterinarypractice.com\/wp-content\/uploads\/sites\/4\/2016\/08\/T1609F03Table03-224x300.jpg 224w\" sizes=\"(max-width: 569px) 100vw, 569px\" \/><\/a><\/p>\n<p><a href=\"https:\/\/todaysveterinarypractice.com\/wp-content\/uploads\/sites\/4\/2016\/08\/T1609F03Table04.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-11590\" src=\"https:\/\/todaysveterinarypractice.com\/wp-content\/uploads\/sites\/4\/2016\/08\/T1609F03Table04.jpg\" alt=\"T1609F03Table04\" width=\"710\" height=\"246\" srcset=\"https:\/\/navc.sitepreview.app\/todaysveterinarypractice.com\/wp-content\/uploads\/sites\/4\/2016\/08\/T1609F03Table04.jpg 710w, https:\/\/navc.sitepreview.app\/todaysveterinarypractice.com\/wp-content\/uploads\/sites\/4\/2016\/08\/T1609F03Table04-300x104.jpg 300w\" sizes=\"(max-width: 710px) 100vw, 710px\" \/><\/a><\/p>\n<h3><strong>CBC Results<\/strong><\/h3>\n<p>The number of red blood cells (RBCs) was normal at first and mildly decreased later. The normal number of RBCs upon presentation may have been related to the mild dehydration. With aggressive fluid therapy, the patient became mildly anemic due to a dilutional effect on the number of RBCs.<\/p>\n<p>Moderate thrombocytopenia together with the coagulation panel results indicated disseminated intravascular coagulation (DIC). DIC can occur in patients with severe pancreatitis and other serious systemic diseases, such as sepsis due to peritonitis or neoplasia.<\/p>\n<h3><strong>Serum Biochemical Profile Results<\/strong><\/h3>\n<p>Decreases in total protein and albumin are common in dogs with severe acute pancreatitis and other causes of peritonitis due to albumin loss into the peritoneal effusion. However, the pathogenesis may vary and there are many other differential diagnoses for decreased albumin, including:<\/p>\n<ul>\n<li><em>Decreased production<\/em> due to pregnancy, lactation, intestinal malabsorption, malnutrition, cachexia secondary to neoplasia, exocrine pancreatic insufficiency, or chronic liver disease<\/li>\n<li><em>Accelerated loss<\/em> due to protein losing enteropathy or nephropathy, hemorrhage, severe exudative skin disease, burns, intestinal parasitism, or high-protein effusions<\/li>\n<li><em>Acute tissue injury\/inflammation<\/em> as a negative acute phase reactant (eg, pancreatitis, peritonitis).<\/li>\n<\/ul>\n<p>The mildly decreased total calcium was attributed to hypoalbuminemia, while the mildly decreased magnesium may have been caused by decreased GI absorption.<\/p>\n<p>The mild to moderate increase in alkaline phosphatase activity was most likely due to cholestasis secondary to pancreatitis, based on history and other findings. This finding is common in dogs with acute pancreatitis. Elevated alkaline phosphatase activity in adult dogs can also be caused by:<\/p>\n<ul>\n<li>Intrahepatic or extrahepatic cholestasis<\/li>\n<li>Endogenous or exogenous glucocorticoids or other drugs<\/li>\n<li>Bone lesions (lytic or proliferative)<\/li>\n<li>Active bone resorption (primary or secondary hyperparathyroidism).<\/li>\n<\/ul>\n<h3><strong>Urinalysis &amp; Urine Culture Results<\/strong><\/h3>\n<p>Isosthenuria (urine specific gravity, 1.012) with mild proteinuria (sulfosalicylic acid test result, 1+) was present but, otherwise, unremarkable. Isosthenuria may have resulted from IV fluid administration during hospitalization.<\/p>\n<p>The urine culture was negative; this result may have been affected by the antibiotic therapy initiated 2 days prior to presentation. The antibiotic was discontinued during hospitalization because there was no evidence of a urinary tract infection and the diarrhea was considered a potential side effect of antibiotic therapy.<\/p>\n<h3><strong>Coagulation Panel Results<\/strong><\/h3>\n<p>DIC was indicated on the basis of thrombocytopenia, mildly prolonged prothrombin time and partial thromboplastin time, decreased antithrombin III, and increased D-dimers, but there were no clinical signs of thrombosis or bleeding.<\/p>\n<h3>Canine cPL Result<\/h3>\n<ul>\n<li>Abnormal SNAP cPL (<strong>Figure 1<\/strong>) indicated a value in the gray zone (200\u2013400 mcg\/L) or one consistent with pancreatitis (&gt; 400 mcg\/L).<\/li>\n<\/ul>\n<div id=\"attachment_11584\" style=\"width: 297px\" class=\"wp-caption alignnone\"><a href=\"https:\/\/todaysveterinarypractice.com\/wp-content\/uploads\/sites\/4\/2016\/08\/T1609F03Fig01.jpg\"><img loading=\"lazy\" decoding=\"async\" aria-describedby=\"caption-attachment-11584\" class=\"size-medium wp-image-11584\" src=\"https:\/\/todaysveterinarypractice.com\/wp-content\/uploads\/sites\/4\/2016\/08\/T1609F03Fig01-287x300.jpg\" alt=\"FIGURE 1. Positive result on a SNAP cPL test. The spot on the right (patient spot) is darker than the control spot on the left side, indicating a serum cPL concentration either in the gray zone or diagnostic for pancreatitis, and requiring a serum Spec cPL test to differentiate between them.\" width=\"287\" height=\"300\" srcset=\"https:\/\/navc.sitepreview.app\/todaysveterinarypractice.com\/wp-content\/uploads\/sites\/4\/2016\/08\/T1609F03Fig01-287x300.jpg 287w, https:\/\/navc.sitepreview.app\/todaysveterinarypractice.com\/wp-content\/uploads\/sites\/4\/2016\/08\/T1609F03Fig01.jpg 573w\" sizes=\"(max-width: 287px) 100vw, 287px\" \/><\/a><p id=\"caption-attachment-11584\" class=\"wp-caption-text\">FIGURE 1. Positive result on a SNAP cPL test. The spot on the right (patient spot) is darker than the control spot on the left side, indicating a serum cPL concentration either in the gray zone or diagnostic for pancreatitis, and requiring a serum Spec cPL test to differentiate between them.<\/p><\/div>\n<ul>\n<li>Follow-up Spec cPL (idexx.com) was 1678 mcg\/L (reference range, \u2264 200 mcg\/L) and, thus, consistent with pancreatitis.<\/li>\n<\/ul>\n<h3><strong>Abdominal Radiographs<\/strong><\/h3>\n<p>Loss of serosal detail in the right cranial abdomen was consistent with peritoneal effusion, while a mildly enlarged and rounded liver was consistent with hepatic venous congestion, hyperadrenocorticism, diabetes mellitus, neoplasia, or an acute inflammatory hepatopathy.<\/p>\n<p>Considering the patient\u2019s clinical signs and radiographic findings, the top differential diagnosis was pancreatitis with extrahepatic biliary obstruction. However, inflammatory hepatopathy, such as a gallbladder mucocele with possible bile peritonitis or hepatic neoplasia with hemorrhagic or neoplastic effusion, were also considered differential diagnoses.<\/p>\n<h3><strong>Abdominal Ultrasonography<\/strong><\/h3>\n<p>Ultrasonographic findings (<strong>Figure 2<\/strong>) included:<\/p>\n<ul>\n<li>Moderate volume of anechoic free abdominal fluid, with a few echoes throughout, consistent with modified transudate or possibly exudate<\/li>\n<li>Enlarged hypoechoic pancreas<\/li>\n<li>Hyperechoic mesenteric fat, consistent with saponification of fat secondary to inflammation<\/li>\n<li>Enlarged liver with multiple hyperechoic nodules likely suggesting a regenerative process, but neoplasia could not be excluded<\/li>\n<li>Undulating, but not plicated, duodenum<\/li>\n<li>Periportal, pancreatic, and gastric lymph node enlargement.<\/li>\n<\/ul>\n<div id=\"attachment_11585\" style=\"width: 635px\" class=\"wp-caption alignnone\"><a href=\"https:\/\/todaysveterinarypractice.com\/wp-content\/uploads\/sites\/4\/2016\/08\/T1609F03Fig02.jpg\"><img loading=\"lazy\" decoding=\"async\" aria-describedby=\"caption-attachment-11585\" class=\"wp-image-11585 \" src=\"https:\/\/todaysveterinarypractice.com\/wp-content\/uploads\/sites\/4\/2016\/08\/T1609F03Fig02.jpg\" alt=\"FIGURE 2. Abdominal ultrasonographic image of the pancreas. The pancreas appears hypoechoic (arrows) next to a cross section of duodenum (arrowheads). Note the hyperechoic mesenteric fat surrounding the pancreas and duodenum. These ultrasonographic findings are typical features of acute pancreatitis. Courtesy Dr. Kathy Spaulding, Texas A&amp;M University\" width=\"625\" height=\"472\" srcset=\"https:\/\/navc.sitepreview.app\/todaysveterinarypractice.com\/wp-content\/uploads\/sites\/4\/2016\/08\/T1609F03Fig02.jpg 795w, https:\/\/navc.sitepreview.app\/todaysveterinarypractice.com\/wp-content\/uploads\/sites\/4\/2016\/08\/T1609F03Fig02-300x226.jpg 300w, https:\/\/navc.sitepreview.app\/todaysveterinarypractice.com\/wp-content\/uploads\/sites\/4\/2016\/08\/T1609F03Fig02-768x580.jpg 768w\" sizes=\"(max-width: 625px) 100vw, 625px\" \/><\/a><p id=\"caption-attachment-11585\" class=\"wp-caption-text\">FIGURE 2. Abdominal ultrasonographic image of the pancreas. The pancreas appears hypoechoic (arrows) next to a cross section of duodenum (arrowheads). Note the hyperechoic mesenteric fat surrounding the pancreas and duodenum. These ultrasonographic findings are typical features of acute pancreatitis. <em>Courtesy Dr. Kathy Spaulding, Texas A&amp;M University<\/em><\/p><\/div>\n<p>These findings were most likely suggestive of pancreatitis, with no evidence of gallbladder mucocele or obvious pancreatic neoplasia. However, hepatic neoplasia could not be completely ruled out. Further diagnostic workup for possible neoplasia and other causes of enlargement of several abdominal lymph nodes was refused by the client.<\/p>\n<h3><strong>Analysis &amp; Cytology of Abdominal Fluid<\/strong><\/h3>\n<p>Findings from abdominocentesis indicated a modified transudate (total protein, 2.7 g\/dL; total nucleated cell counts, 10,195\/mcL). Cytology showed marked nondegenerative neutrophilic inflammation and mild histiocytic inflammation.<\/p>\n<h2><strong>Diagnosis<\/strong><\/h2>\n<p>Acute pancreatitis was diagnosed based on history, physical examination findings, nonspecific findings on general blood analysis, abnormal pancreatic lipase immunoreactivity (cPLI) based on abnormal SNAP cPL and\/or increased Spec cPL results, abdominal radiographs, and ultrasonographic findings.<\/p>\n<h2><strong>Therapeutic Approach<\/strong><\/h2>\n<h3><strong>Therapy for Acute Pancreatitis<\/strong><\/h3>\n<ul>\n<li><em>IV fluid therapy: <\/em>Lactated Ringer\u2019s solution was initiated and adjusted on the basis of regular monitoring of hydration status.<\/li>\n<li><em>Analgesia: <\/em>Lidocaine (25 mcg\/kg\/H) was initially given IV as a constant rate infusion (CRI), with buprenorphine added (0.4 mg IV Q 8 H). On day 3 of hospitalization, fentanyl (3 mcg\/kg\/H IV CRI) was started, with lidocaine and buprenorphine discontinued.<\/li>\n<li><em>Nausea control:<\/em> Maropitant was initially administered alone at 10.4 mg SC Q 24 H; ondansetron was added on day 2 at 3.12 mg IV Q 12 H.<\/li>\n<li><em>Nutritional support:<\/em> Attempts were made to feed several types of commercially available low fat diets for the first 2 days of hospitalization, but Sidney was not interested in eating and seemed to be nauseated despite anti-emetic treatment. On day 3 of hospitalization, a nasoesophageal tube was placed, but the patient pulled it out. On day 4, syringe feeding with canine CliniCare (abbott.com) was tolerated. On day 5, the patient began to eat boiled chicken; CliniCare was adjunctively administered to meet daily energy requirements.<\/li>\n<\/ul>\n<h3><strong>Therapy for Early Stage DIC<\/strong><\/h3>\n<p>Fresh frozen plasma (20 mL\/kg IV) was administered over 4 hours to supplement coagulation factors on days 1, 5, and 6. Clopidogrel (18.75 mg PO Q 24 H) was administered to inhibit platelet activity.<\/p>\n<h3><strong>Additional Supportive Care<\/strong><\/h3>\n<p>On day 7 of hospitalization, all IV fluids and medications were discontinued and Sidney was discharged on oral medications, including tramadol (25 mg PO Q 8 H), clopidogrel (18.75 mg PO Q 48 H), and maropitant (24 mg PO Q 24 H). In an attempt to prevent a recurrent episode of acute pancreatitis, an ultra low fat diet was recommended and any treats with high fat content were discouraged.<\/p>\n<h2><strong>Follow-Up<\/strong><\/h2>\n<p>Sidney was discharged after 7 days of hospitalization and was presented for a recheck 3 days after discharge. Sidney\u2019s owners reported that she had a good appetite, and there were no signs of abdominal pain. No vomiting or diarrhea was identified.<\/p>\n<h2><strong>Prognosis<\/strong><\/h2>\n<p>The prognosis for dogs with acute pancreatitis varies and largely depends on disease severity. There is no universally accepted severity score for pancreatitis that allows prediction of prognosis available in veterinary medicine. In general, systemic complications can indicate severe pancreatitis and a poor prognosis.<sup>1<\/sup><\/p>\n<p>A recent study<sup>2<\/sup> suggested that serum paraoxonase 1 activity, combined with triglyceride and C-reactive protein concentrations, can help evaluate disease severity, but further studies are warranted. In Sidney\u2019s case, prognosis was poor to guarded when she was hospitalized, but upgraded to fair to good upon discharge. However, long-term follow-up was not achieved.<\/p>\n<div class=\"orange-box\">\n<h2><strong>Update on Pathophysiology of Pancreatitis<\/strong><\/h2>\n<p>The exact mechanism of development of naturally occurring acute pancreatitis in dogs is still poorly understood.<\/p>\n<p>It has been postulated that pancreatitis develops as a result of autodigestion and severe inflammation caused by inappropriate premature activation and secretion of proteases (especially trypsinogen to trypsin) within pancreatic acinar cells. Pancreatitis and subsequent peripancreatic fat necrosis can cause focal or generalized peritonitis, and most pancreatitis cases in dogs are sterile.<\/p>\n<p>Several protective mechanisms exist to prevent pancreatic autodigestion, including:<\/p>\n<ul>\n<li>Concurrent secretion of pancreatic secretory trypsin inhibitor (PSTI, also known as SPINK 1) with trypsinogen secretion<\/li>\n<li>Unidirectional flow of pancreatic juice in the pancreatic duct<\/li>\n<li>Plasma protease inhibitors (alpha1-proteinase inhibitor and alpha2-macroglobulin).<\/li>\n<\/ul>\n<p>Studies in human medicine<sup>3,4<\/sup> suggest that a compensatory anti-inflammatory response plays an important role in limiting progression of inflammation locally by upregulating anti-inflammatory cytokines, such as IL-10 or IL-11, but no study has been performed to confirm this in dogs.<\/p>\n<p>When these protective mechanisms fail to prevent damage to pancreatic acinar cells, severe inflammation is caused by secreted proinflammatory cytokines from neutrophils and macrophages. A sterile inflammatory peritoneal effusion can occur due to localized peritonitis and the coagulation cascade can be activated, resulting in DIC.<\/p>\n<p>Lungs, kidneys, and livers are especially vulnerable to damage, causing multiple organ failure due to extensive distribution of capillary vessels. In human medicine, multi-organ failure is recognized as having more important relation to mortality in acute pancreatitis than severity of the disease itself<sup>3,5<\/sup> even though no data is available for dogs.<\/p>\n<\/div>\n<h2>Acute Pancreatitis: Diagnostics<\/h2>\n<p>Even with the advanced diagnostic modalities currently available, accurate diagnosis of acute pancreatitis is still challenging. Practically, acute pancreatitis in dogs is usually diagnosed with a combination of history, clinical signs, abnormally high serum cPLI concentration (as measured by Spec cPL), and abdominal ultrasonographic images consistent with pancreatitis. Concurrently, other intra-abdominal diseases that could cause similar clinical signs are excluded by assessment of laboratory test results, survey abdominal radiographs, and abdominal ultrasonography.<\/p>\n<h3><strong>Pancreatic Lipase Immunoreactivity<\/strong><\/h3>\n<p>Measurement of serum cPLI concentration is considered highly sensitive and specific for pancreatitis. The SNAP test provides semiquantitative estimation of cPLI concentration. A negative result rules out pancreatitis with high likelihood, whereas a positive result is consistent with pancreatitis and may require follow-up with the Spec cPL test.<sup>6,7<\/sup><\/p>\n<p>Serum lipase activity has traditionally been used to estimate pancreatic lipase in serum. None of the substrates available (including newer substrates, such as triolein or DGGR [1,2-o-dilauryl-rac-glycero3-glutaric acid 6-methyl resorufin ester]), however, are specific for the measurement of pancreatic lipase, and results of clinical studies using these assays are inconsistent.<sup>6,8<\/sup><\/p>\n<h3><strong>Cytology &amp; Histopathology<\/strong><\/h3>\n<p>Pancreatitis can be confirmed by cytologic evaluation of a fine-needle aspirate of the pancreas.<sup>7<\/sup> Histopathology of the pancreas has traditionally been considered the gold standard for diagnosis and classification of pancreatitis. However, a recent study<sup>9<\/sup> suggests that a negative finding (ie, no inflammatory lesions in the biopsy) does not rule out pancreatitis because pancreatic inflammation can be highly localized.<\/p>\n<h3><strong>Advanced Imaging<\/strong><\/h3>\n<p>Advanced imaging modalities, including contrast-enhanced computed tomography (CECT) and contrast-enhanced multidetector helical computed tomography (CE-MDCT), have been evaluated and shown different utility for diagnosing pancreatitis in dogs. A study using CE-MDCT<sup>10<\/sup> showed low sensitivity for diagnosing pancreatitis in dogs presented with acute abdominal signs even though CE-MDCT was suggested as a good screening test to differentiate between surgical and nonsurgical conditions. A more recent study<sup>11<\/sup> using CECT concluded that CECT under sedation can confirm a clinical suspicion of pancreatitis. However, these modalities have limited availability for general use.<\/p>\n<h2>Acute Pancreatitis: Treatment<\/h2>\n<p>Because most cases of acute pancreatitis in dogs are idiopathic, the mainstay of treatment is supportive care that includes risk factor control, fluid therapy, nutritional support, and pain control.<\/p>\n<h3><strong>Fluid Therapy<\/strong><\/h3>\n<p>Fluids are important to correct hypovolemia, dehydration, and electrolyte and acid\u2013base imbalances as early as possible to prevent any systemic complications, which can be associated with a negative outcome. A study in human medicine<sup>12<\/sup> suggested a possible benefit of using lactated Ringer\u2019s solution because the alkalinizing property of that solution prevented further trypsin activation within the acinar cells, but no data are available for dogs.<\/p>\n<h3><strong>Nutritional Support<\/strong><\/h3>\n<p>Several studies in both humans and dogs suggest that early enteral nutritional support is superior to parenteral feeding in patients with acute pancreatitis as long as it is tolerated.<sup>13-16<\/sup><\/p>\n<ul>\n<li>Enteral feeding can be achieved by voluntary intake in mild cases or by using different types of feeding tubes (nasoesophageal, nasogastric, esophagostomy, gastrostomy, or jejunostomy tubes) in more severe cases.<sup>17<\/sup><\/li>\n<li>Gradually increasing the volume fed until the full energy requirement is reached is recommended regardless of the method of enteral alimentation.<\/li>\n<li>Generally, an easily digestible food is recommended. The benefit of using a low fat diet is anecdotal, but we feel strongly that an ultra low fat diet should be chosen for feeding. These diets should be fed both during hospitalization and also after discharge.<\/li>\n<li>If patients demonstrate severe nausea, vomiting, or abdominal pain before, during, or after feeding, enteral feeding should be discontinued and attempted later when these signs have been successfully controlled.<\/li>\n<\/ul>\n<h3><strong>Pain Management<\/strong><\/h3>\n<p>Every dog with acute pancreatitis should be considered as having abdominal pain even if it is not clinically apparent. A multimodal approach for pain management is advised for better pain control, lower dosages, and fewer adverse effects.<\/p>\n<ul>\n<li>Most commonly used analgesics include opioids, ketamine, or lidocaine for hospitalized patients.<\/li>\n<li>The use of a CRI of ketamine (5\u201320 mcg\/kg\/min) or lidocaine (25\u201350 mcg\/kg\/min) can decrease the amount of opioids required. Lidocaine may have some anti-inflammatory properties, based on evidence in human medicine.<sup>18<\/sup><\/li>\n<li>Outpatients can receive tramadol (5 mg\/kg PO Q 6\u20138 H), an opioid, gabapentin (5\u201315 mg\/kg PO Q 12 H), <em>and\/or<\/em> a fentanyl patch.<\/li>\n<\/ul>\n<h3><strong>Antiemetic Agents<\/strong><\/h3>\n<p>Antiemetic treatment should be started as early as possible even in dogs without overt nausea or vomiting to encourage patients to eat voluntarily.<\/p>\n<ul>\n<li>Maropitant (1 mg\/kg SC Q 24 H for a maximum 5 days), a neurokinin1 receptor inhibitor, is recommended as a first choice antiemetic due to its high efficacy and visceral analgesic properties.<\/li>\n<li>Dolasetron (0.6 mg\/kg IV or SC Q 12\u201324 H) or ondansetron (0.1\u20130.2 mg\/kg slow IV Q 6\u201312 H), both 5-HT<sub>3<\/sub> antagonists, can also be used.<\/li>\n<li>Because maropitant and the 5-HT<sub>3<\/sub> antagonists act on different receptors, we commonly use both types of drugs concurrently in patients with severe pancreatitis.<\/li>\n<li>Metoclopramide (a dopamine inhibitor), which has been traditionally used, is not currently recommended due to its low efficacy as an antiemetic and its effect on splanchnic perfusion.<sup>19<\/sup><\/li>\n<\/ul>\n<h3><strong>Plasma Transfusion<\/strong><\/h3>\n<p>The proposed advantage of using plasma in dogs with acute pancreatitis includes supplementation of alpha-2-macroglobulin (scavenger proteins for activated proteases in serum), coagulation factors, and anti-inflammatory factors.<sup>20<\/sup> Due to the high cost and lack of confirmed benefits in dogs, however, plasma transfusion is generally reserved for dogs suspected to have DIC.<\/p>\n<h3><strong>Antibiotics<\/strong><\/h3>\n<p>Bacterial complications are extremely rare in dogs with naturally occurring acute pancreatitis. Only dogs with overt bacterial infections or a strong suspicion for such an infection should be given broad spectrum antibiotics.<\/p>\n<p>Amoxicillin\/clavulanate acid (12.5\u201325 mg\/kg PO Q 12 H) or ticarcillin (33\u201350 mg\/kg IV or IM Q 4\u20136 H) has been recommended as first choice antibiotics, if needed, but this recommendation is based on expert opinion rather than critical research.<sup>21<\/sup><\/p>\n<h3>Corticosteroid Therapy<\/h3>\n<p>No prospective studies demonstrate beneficial effects of corticosteroid therapy in dogs with acute pancreatitis. Reserve corticosteroids for patients who have critical illness-related corticosteroid insufficiency causing refractory hypotension, even with aggressive fluid therapy.<\/p>\n<div class=\"orange-box\">\n<h2><strong>Avoiding Risk Factors<\/strong><\/h2>\n<p>If identifiable, any risk factors should be discontinued or avoided when a patient has been diagnosed with pancreatitis (<strong>Table 5<\/strong>). Specifically, medications that have been shown to cause pancreatitis should be considered for discontinuation or replacement with another medication.<\/p>\n<p><a href=\"https:\/\/todaysveterinarypractice.com\/wp-content\/uploads\/sites\/4\/2016\/08\/T1609F03Table05.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-11591\" src=\"https:\/\/todaysveterinarypractice.com\/wp-content\/uploads\/sites\/4\/2016\/08\/T1609F03Table05.jpg\" alt=\"T1609F03Table05\" width=\"674\" height=\"296\" srcset=\"https:\/\/navc.sitepreview.app\/todaysveterinarypractice.com\/wp-content\/uploads\/sites\/4\/2016\/08\/T1609F03Table05.jpg 674w, https:\/\/navc.sitepreview.app\/todaysveterinarypractice.com\/wp-content\/uploads\/sites\/4\/2016\/08\/T1609F03Table05-300x132.jpg 300w\" sizes=\"(max-width: 674px) 100vw, 674px\" \/><\/a><\/p>\n<\/div>\n<h2><strong>In Summary<\/strong><\/h2>\n<p>Canine acute pancreatitis is a reversible disease when diagnosed promptly and managed appropriately. Avoiding known risk factors and careful monitoring after the first episode are important in prevention of progression to chronic pancreatitis or recurrent acute pancreatitis.<\/p>\n<div class=\"orange-box\">\n<h3><strong>Disclosure Statement<\/strong><\/h3>\n<p>Dr. Steiner is a paid consultant for Idexx Laboratories. Both the Gastrointestinal Laboratory at Texas A&amp;M University and Idexx Laboratories offer Spec cPL testing on a fee-for-service basis.<\/p>\n<\/div>\n<p>CBC = complete blood count; CECT = contrast-enhanced computed tomography; CE-MDCT = contrast-enhanced multidetector helical computed tomography; cPLI = pancreatic lipase immunoreactivity; CRI = constant rate infusion; DIC = disseminated intravascular coagulation; GI = gastrointestinal; RBC = red blood cell<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Canine acute pancreatitis is a reversible disease when diagnosed promptly and managed appropriately.<\/p>\n","protected":false},"author":15,"featured_media":11586,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"iawp_total_views":6489,"footnotes":""},"categories":[363],"tags":[13],"class_list":["post-11579","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-september-october-2016","tag-peer-reviewed","column-features","clinical_topics-gastroenterology","clinical_topics-hepatology"],"acf":{"hide_sidebar":false,"hide_sidebar_ad":false,"hide_all_ads":false},"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v24.7 (Yoast SEO v27.3) - https:\/\/yoast.com\/product\/yoast-seo-premium-wordpress\/ -->\n<title>From Diagnosis to Treatment: A Case of Canine Acute Pancreatitis | Today&#039;s Veterinary Practice<\/title>\n<meta name=\"robots\" content=\"noindex, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<meta 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