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December 2019 A Peer-Reviewed Journal | cliniciansbrief.com CASE: EYE COLOR CHANGE IN THIS ISSUE IN A DOG Socialization for Puppies & Kittens Top 5 Canine Biliary Diseases Overview of Mast Cell Tumors Step-by-Step Urinary Catheter Placement in Dogs Differential Diagnosis List: Hyperphosphatemia Volume 17 Number 12 THE OFFICIAL CLINICAL PRACTICE JOURNAL OF THE WSAVA
HELP KEEP YOUR PATIENTS STRONG Hill’s Prescription Diet k/d1 is clinically shown in a recent GREAT TASTING study2 to outperform Royal Canin3 at managing CKD. SIX-MONTH CLINICAL RESULTS Compared to Royal Canin Veterinary Diet Renal Support A Feline,3 cats with chronic kidney disease (CKD) fed Prescription Diet k/d Feline1 with E.A.T (Enhanced Appetite Trigger) Technology: 1 Voluntarily consumed 23% more calories2 2 Increased their body weight by 5.8% while Royal Canin3 cats lost 13%2 3 Maintained their muscle mass while Royal Canin3 cats lost over 11%2 TAKE CONTROL TODAY — recommend the clinical strength of Prescription Diet k/d.1 1 Hill’s® Prescription Diet® k/d® Feline with chicken dry food. 2Data on file. Hill’s Pet Nutrition, Inc. 2018. Results are average values with statistical significance (p value less than or equal to 0.05). 3Royal Canin Veterinary Diet Renal Support A Feline, dry food sold in the US market. ©2019 Hill’s Pet Nutrition, Inc. ®/™ Hill’s, Prescription Diet, k/d and E.A.T. Technology are trademarks owned by Hill’s Pet Nutrition, Inc. Royal Canin is a registered trademark owned by ROYAL CANIN SAS.
PUBLISHER OF CLINICIAN’S BRIEF TEAM EDITOR IN CHIEF CHIEF VETERINARY DIRECTOR OF MANAGING EDITOR J. SCOTT WEESE OFFICER & EDITOR INTEGRATIVE CONTENT SAMANTHA FARLEY DVM, DVSc, DACVIM INDU MANI JENNIFER L. SCHORI MPS dr.weese@briefmedia.com DVM, ScD VMD, MS sam@briefmedia.com Professor dr.indu@briefmedia.com dr.jen@briefmedia.com Ontario Veterinary College Ontario, Canada CEO/FOUNDER CHIEF OF CONTENT STRATEGY EDITORIAL ASSISTANT DESIGN & PRODUCTION AMY MOHL CAROL WATKINS JEANNE MISTRETTA ELIZABETH GREEN DVM carol@briefmedia.com Mistretta Design Group, LLC elizabeth@briefmedia.com dr.amy@briefmedia.com jeanne@mistrettadesigngroup.com EDITOR AT LARGE SENIOR DIRECTOR OF CONTENT ANTOINETTE PASSARETTI SENIOR GRAPHIC DESIGNER ADVERTISING AMANDA BILBERY MICHELLE N. MUNKRES toni@briefmedia.com JOHN O’BRIEN MA amanda@briefmedia.com john@briefmedia.com michelle@briefmedia.com MANAGER, DIGITAL CONTENT EMILY FAISON MEDICAL EDITORS BRIDGETT GREEN ASSOCIATE EDITORS MA PEGGY BURRIS bridgett@briefmedia.com DRUE A. GINDLER emily@briefmedia.com DVM drue@briefmedia.com dr.peggy@briefmedia.com JOANNA LUNDBERG DIGITAL CONTENT COORDINATOR joanna@briefmedia.com ALEXIS USSERY JANE GARDINER SARAH TYLER alexis@briefmedia.com DVM sarah@briefmedia.com NAOMI MURRAY, DVM dr.jane@briefmedia.com dr.naomi@briefmedia.com PROJECTS EDITOR CREATIVE DIRECTOR ALYSSA WATSON LINDSAY ROBERTS AARON MAYS SHELLEY HURLEY DVM lindsay@briefmedia.com aaron@briefmedia.com shelley@briefmedia.com dr.alyssa@briefmedia.com MELISSA ROBERTS melissa@briefmedia.com TO SUBSCRIBE OR FOR SUBSCRIPTION INQUIRIES: CLINICIANSBRIEF.COM/SUBSCRIBE OR 1-847-763-4909 MEGAN WHITWORTH Providing Domestic subscription rate: $65.00 per year. Single copy: $8.00. Payments by check megan@briefmedia.com small animal must be in US funds on a US branch of a US bank only; credit cards also accepted. Copyright © 2019 Brief Media, an Educational Concepts company. All rights reserved. DRAKE BOONE drake@briefmedia.com practitioners and Reproduction in whole or in part without expressed written permission is prohibited. POSTMASTER: Send address changes to Brief Media, PO Box 1084, Skokie, IL 1084 their teams with 60076-9969. Canada Post publications mail agreement #40932038: Return unde- liverable Canadian mailings to Circulation Dept; 7496 Bath Rd, Unit #2; Mississauga, practical, relevant ON L4T 1L2. Periodicals postage paid at Tulsa, OK, and at additional mailing offices BRIEF MEDIA: 2021 S Lewis Avenue #760, Tulsa, OK 74104 information on T 918-749-0118 | F 918-749-1987 | briefmedia.com | info@briefmedia.com Clinician’s Brief (ISSN 1542-4014) is published monthly by Brief Media, an Educational the latest topics Concepts company, 2021 S Lewis Avenue, #760, Tulsa, OK 74104. in veterinary medicine December 2019 cliniciansbrief.com 1
From Clinician’s Brief on Social Media WE ASKED … What is the strangest thing a Do you prefer an open or closed technique patient has regurgitated prior for routine canine neutering? to surgery? “A quarter and a penny. We took it off the owner’s bill.”—Missie B “A very fresh mouse. A cat was being kept overnight and was being fasted before surgery the next morning. Apparently, the mouse had gotten into the 43 kennel and the cat killed and ate it for breakfast.” —Darlene J % “A doll head.”—Erin S Open 57 “A whole hummingbird—not chewed. We could still see the beak.”—Lilia W % “The patient’s own tail.”—Michael K Closed “The item we were planning to surgically remove.” —Jennifer M What is your favorite team-building exercise? “Ice cream Fridays.”—Lindsey A “We went curling. It was actually a lot of fun!” Do you use corticosteroid-containing —Ciara R sprays on hot spots? “Pizza in the breakroom.”—Jenn P 55% Yes “Escape room.”—Judy S 45% No “Pug nail trims!”—Andrea B FOLLOW US facebook.com/cliniciansbrief @CliniciansBrief clinicians.brief 2 cliniciansbrief.com December 2019
Hidden Disease. Visible Answer. As your experts in endocrinology, Dechra Veterinary Products is proud to offer ZYCORTAL® Suspension (desoxycorticosterone pivalate injectable suspension) • Replacement therapy for mineralocorticoid deficiency in dogs with primary hypoadrenocorticism (Addison’s Disease) • FDA approved for subcutaneous use • 4mL vial of 25mg/mL suspension • Available direct from your preferred distributor • Three year shelf life from the date of manufacture FREE CE ON ADDISON’S DISEASE Learn how to diagnose and treat Addison’s Disease from one of the top minds in the field of Veterinary Endocrinology, Dr. Audrey Cook. This course is approved by the AAVSB RACE to offer a total of 2.00 CE Credits for both veterinarians and technicians. Each module earns you 1.00 CE Credit in the Scientific category. This course is free to veterinarians and technicians through Dechra Academy at dechra-us.com/CE. NADA 141-444, Approved by FDA CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian. Dechra is a registered trademark of Dechra Pharmaceuticals PLC. Zycortal is a registered trademark of Dechra Limited. Z Y C O R T A L® CONTRAINDICATIONS: Do not use ZYCORTAL Suspension in dogs that have previously had a hypersensitivity reaction to ADVERSE REACTIONS: The field safety analysis included evaluation of 152 dogs. The most common adverse reactions reported are polyuria, polydipsia, depression/lethargy, inappropriate urination, alopecia, SUSPENSION (desoxycorticosterone desoxycorticosterone pivalate. decreased appetite/anorexia, panting, vomiting, diarrhea, shaking/ pivalate injectable suspension) WARNINGS: Use ZYCORTAL Suspension with caution in dogs with trembling, polyphagia, urinary tract infection, urinary tract incontinence congestive heart disease, edema, severe renal disease or primary hepat- and restlessness. Reports of anaphylaxis and anemia have been Mineralocorticoid for subcutaneous use in dogs only. ic failure. Desoxycorticosterone pivalate may cause polyuria, polydipsia, associated with a different desoxycorticosterone pivalate injectable increased blood volume, edema and cardiac enlargement. Excessive suspension product. Z Y C O R T A L® Brief Summary (For Full Prescribing Information, see package insert) weight gain may indicate fluid retention secondary to sodium retention. Distributed by: CAUTION: Federal (USA) law restricts this drug to use by or on the HUMAN WARNINGS: Not for human use. Keep this and all drugs out Dechra Veterinary Products order of a licensed veterinarian. of the reach of children. Consult a physician in case of accidental human SUSPENSION (desoxycorticosterone exposure. 7015 College Boulevard, Suite 525 Overland Park, KS 66211 pivalateDesoxycorticosterone DESCRIPTION: injectable suspension) pivalate is a mineralocorticoid PRECAUTIONS: Any dog presenting with severe hypovolemia, hormone. Zycortal Suspension contains 25mg/ml of ZYCORTAL is a trademark of desoxycorticosterone pivalate. dehydration, pre-renal azotemia and inadequate tissue perfusion Dechra Ltd © 2015, (“Addisonian crisis”) must be rehydrated with intravenous fluid (saline) All rights reserved INDICATION: For use as replacement therapy for mineralocorticoid Z Y C O R T A L® therapy before starting treatment with ZYCORTAL Suspension. The NADA 141-444, deficiency in dogs with primary hypoadrenocorticism (Addison’s effectiveness of ZYCORTAL Suspension may be reduced if disease). Approved by FD potassium-sparing diuretics, such as spironolactone, are administered SUSPENSION (desoxycorticosterone concurrently. 01AD-ZYC50104-0219 pivalate injectable suspension)
ERASING RABIES ONE VACCINE AT A TIME! Rabies is a deadly disease that can affect domestic animals, wild animals, and humans. An estimated 59,000 people die from rabies each year.1 Children are at greatest risk from rabies, with 40% of rabies deaths occur in children 15 years old or younger.2 Outbreaks can be controlled when more than 70% of an area’s canine population is vaccinated.3 In 2015, the world called for action by setting a goal of zero human dog- mediated rabies deaths by 2030, worldwide.4 Merck Animal Health, the makers of Nobivac® vaccines, is committed to making a difference. Every purchase of Nobivac® vaccines helps contribute to the ability to provide ongoing support and vaccine donations to non-profit organizations such as Rabies Free Africa and Mission Rabies. In honor of World Rabies Day, Gallatin Veterinary Hospital brought awareness to this deadly disease by participating in the Nobivac® Paw Print Campaign. Gallatin Veterinary Hospital is proud to show their commitment to the cause to help Erase Rabies by 2030! References: 1. Hampson K, Coudeville L, Lembo T, et al. Estimating the global burden of endemic canine rabies. PLoS Negl Trop Dis. 2015;9(4):e0003709. 2. Rabies. World Health Organization website. https://www.who.int/news-room/fact-sheets/detail/rabies. Accessed September 13, 2019. 3. Morters MK, McNabb S, Horton DL, et al. Effective vaccination against rabies in puppies in rabies endemic regions. Veterinary Record. 2015;177:150. 4. Global Alliance for Rabies Control. Zero by 30: Our catalytic response. https://rabiesalliance.org/policy/united_against_rabies. Accessed September 13, 2019. © 2019 Intervet Inc., d/b/a Merck Animal Health, a subsidiary of Merck & Co., Inc. All rights reserved. US-NOV-190800191
IN THIS ISSUE ON THE COVER CASE IN POINT Eye Color Change in a Dog Andrew Christopher Lewin, BVM&S, DACVO 59 PG NOTICE OF CORRECTION In the article “Responsible Antimicrobial Stewardship” 11 TOP 5 Top 5 Canine Biliary Diseases Stefanie M. DeMonaco, DVM, MS, 62 PROCEDURES PRO Urinary Catheter Placement in Dogs in the November 2019 issue DACVIM (SAIM) Lisa L. Powell, DVM, DACVECC of Clinician’s Brief, the phrase “and the patient does have signs of antimicrobial resis- tance” should have read “and the patient does not have signs 22 CONSULT THE EXPERT Puppy & Kitten Socialization Leslie Sinn, CPDT-KA, DVM, DACVB of antimicrobial resistance” in the following sentence: “Empiric antimicrobial therapy should only be used to treat other infections when the 31 CONSULT THE EXPERT Mast Cell Tumors Brooke Britton, DVM, DACVIM (Oncology) infection is not life threatening, 57 the patient has not had an infection in the past 3 months, DIFFERENTIAL DIAGNOSIS skin infection is superficial, Hyperphosphatemia the infection has a predictable Julie Allen, BVMS, MS, MRCVS, DACVIM antimicrobial susceptibility, (SAIM), DACVP and the patient does have signs of antimicrobial resis- tance.” Clinician’s Brief regrets the error. December 2019 cliniciansbrief.com 5
No More Double Plating The Plate Large Enough for Giant Breed Dogs The new Arthrex 4.5 mm TPLO locking plate was designed after extensive research and includes several key features that make plate placement easier and more consistent. For dogs with severe stifle instability, surgeons have the option to use a knotless anti-rotational lateral stabilization technique (InternalBrace™ ligament augmentation). ■ High-quality, medical-grade material, quality assurance, and superior craftsmanship ■ Locking screws both proximally and distally ■ Shape, contour, and additional features designed to facilitate optimal plate positioning ■ Proximal screw trajectory to optimize bone purchase safely for TPLO and TPLO with InternalBrace augmentation Cranial View © 2019 Arthrex, Inc. All rights reserved vAD1-000098-en-US_B ArthrexVetSystems.com
ON THE WEB THIS MONTH’S FEATURED CLINICAL CONTENT AVAILABLE ONLY ONLINE QUIZ Understanding GI Testing M. Katherine Tolbert, DVM, PhD, DACVIM (SAIM) brief.vet/GI-testing PODCAST Managing Stress-Related Aggression with Dr. Sung Wailani Sung, DVM, MS, PhD, DACVB, discusses managing fear- related aggression and stress in dogs and cats at the clinic, the physical and mental impact severe stress can have on patients, and how to provide low-stress visits. brief.vet/managing-stress 17 SYMPOSIUM CAPSULES 2019 American Veterinary Medical Association Convention 08 OUR AUTHORS 38 FROM PAGE TO PATIENT Tips and techniques from 70 PRACTICE HOTLINE The latest in products and services the research pages 71 ADVERTISERS INDEX 02 GET SOCIAL Currently on Clinician’s Brief social media 72 QUIZ CORNER Test your knowledge Contact us at editor@cliniciansbrief.com Articles archived at cliniciansbrief.com/journal December 2019 cliniciansbrief.com 7
OUR AUTHORS JULIE ALLEN, BVMS, MS, MRCVS, ANDREW CHRISTOPHER LEWIN, DACVIM (SAIM), DACVP, is a former BVM&S, DACVO, is an assistant clinical assistant professor of clinical professor at Louisiana State Univer- pathology at Cornell University. She sity. He earned his veterinary degree earned her veterinary degree from Uni- from University of Edinburgh before versity of Glasgow and her MS from Iowa completing an internship at a private State University, where she completed a practice in the United Kingdom and rotating internship in small animal medi- an ophthalmology residency at cine and surgery and a residency in small University of Wisconsin–Madison. animal internal medicine. She also com- Dr. Lewin’s research interests include pleted a residency in clinical pathology at ocular infectious disease and clinical North Carolina State University. Dr. Allen veterinary ophthalmology. focuses on cachexia/anorexia, endocri- case in point page 59 nology, and hepatobiliary and pancreatic disease and has committed her career to LISA L. POWELL, DVM, DACVECC, is improving the diagnosis of disease. an associate emergency medicine and differential diagnosis page 57 critical care clinician at BluePearl Veterinary Partners in Eden Prairie, BROOKE BRITTON, DVM, DACVIM Minnesota. Her professional interests (Oncology), is a veterinary medical include respiratory emergencies, oncologist at BluePearl Veterinary mechanical ventilation, sepsis, and Partners in New York City, New York. fluid therapy. She earned her DVM from Cornell procedures pro page 62 University and completed a medical oncology residency at University of LESLIE SINN, CPDT-KA, DVM, DACVB, Pennsylvania. Dr. Britton has lectured maintains Behavior Solutions for Pets widely and is active in oncologic research. in Leesburg, Virginia. She earned her Her interests include hematologic malig- DVM from University of Georgia, nancies, the biology of cancer metastasis, where she also completed an intern- and combination drug therapy for the ship in small animal medicine and treatment of various cancers. surgery. Dr. Sinn is a board-certified consult the expert page 31 veterinary behaviorist and a certified professional dog trainer. She has lec- STEFANIE M. DEMONACO, DVM, MS, tured worldwide and is the author of DACVIM (SAIM), is an assistant profes- numerous articles and book chapters. sor of small animal internal medicine at consult the expert page 22 n Virginia–Maryland College of Veterinary Medicine, where she also earned her MS in biomedical veterinary science and com- pleted a residency. Dr. DeMonaco earned her DVM from Kansas State University. Her research interests include feline medicine and hepatobiliary disease. top 5 page 11 8 cliniciansbrief.com December 2019
AAHA-RECOMMENDED AND FDA-APPROVED PRODATA PROSUPPORT PROZINC Backed by the largest prospective study in diabetic cats to date, PROZINC offers predictable glycemic control and efficacy proven to improve clinical signs associated with diabetes.1-3 Another study shows that remission rates with the use of PROZINC were comparable to glargine. 2 Make PROZINC your first-line treatment for diabetic cats.4–6 For more information, contact your Boehringer Ingelheim representative. Important Safety Information for Cats: For use in cats and dogs only. Animals presenting with severe ketoacidosis, anorexia, lethargy, and/or vomiting should be stabilized with short-acting insulin and appropriate supportive therapy until their condition is stabilized. As with all insulin products, careful patient monitoring for hypoglycemia and hyperglycemia is essential to attain and maintain adequate glycemic control and to prevent associated complications. Overdosage can result in profound hypoglycemia and death. Progestogen and glucocorticoid use should be avoided. PROZINC insulin is contraindicated in cats during episodes of hypoglycemia and in cats sensitive to protamine zinc recombinant human insulin or any other ingredients in the PROZINC product. For more information, please see full prescribing information for cats. References: 1. Data on file. Boehringer Ingelheim Animal Health USA Inc. 2. Gostelow R, Scudder C, Hazuchova K, et al. One-year prospective randomized trial comparing effi cacy of glargine and protamine zinc insulin in diabetic cats. In: Proceedings from the American College of Veterinary Internal Medicine Forum; June 8–10, 2017; National Harbor, MD. Abstract EN10. 3. ProZinc ® (protamine zinc recombinant human insulin) [Freedom of Information Summary]. St. Joseph, MO: Boehringer Ingelheim Vetmedica, Inc.; 2009. 4. Rucinsky R, Cook A, Haley S, et al. AAHA diabetes management guidelines for dogs and cats. J Am Anim Hosp Assoc. 2010;46(3):215–224. 5. American Association of Feline Practitioners. AAFP practice guidelines. https://www.catvets.com/guidelines/practice-guidelines. Accessed September 19, 2018. 6. Sparkes AH, Cannon M, Church D, et al. ISFM consensus guidelines on the practical management of diabetes mellitus in cats. J Feline Med Surg. 2015;17(3):235–250. ProZinc® is a registered trademark of Boehringer Ingelheim Animal Health USA, Inc. © 2019 Boehringer Ingelheim Animal Health USA, Inc., Duluth, GA. All rights reserved. PET-0887-PROZ0119. 18371 See page 10 for product information summary.
NADA 141-297, Approved by FDA All cases of hypoglycemia resolved with appropriate therapy and if needed, a dose reduction. ProZinc® Three cats had injection site reactions which were described as either small, punctate, red lesions; lesions on neck; or palpable subcutaneous thickening. All injection site reactions resolved without cessation of therapy. (protamine zinc recombinant human insulin) Four cats developed diabetic neuropathy during the study as evidenced by plantigrade stance. Three cats entered the study with plantigrade stance, one of which resolved by Caution: Federal law restricts this drug to use by or on the order of a licensed Day 45. Four cats were diagnosed with diabetic ketoacidosis during the study. Two were veterinarian. euthanized due to poor response to treatment. Five other cats were euthanized during Description: ProZinc® insulin is a sterile aqueous protamine zinc suspension of the study, one of which had hypoglycemia. Four cats had received ProZinc insulin for recombinant human insulin. less than a week and were euthanized due to worsening concurrent medical conditions. Each mL contains: The following additional clinical observations or diagnoses were reported in cats during recombinant human insulin 40 International Units (IU) the effectiveness field study: vomiting, lethargy, diarrhea, cystitis/hematuria, upper protamine sulfate 0.466 mg respiratory infection, dry coat, hair loss, ocular discharge, abnormal vocalization, zinc oxide 0.088 mg black stool, and rapid breathing. glycerin 16.00 mg Extended Use Field Study dibasic sodium phosphate, heptahydrate 3.78 mg Cats that completed the effectiveness study were enrolled into an extended use field phenol (added as preservative) 2.50 mg study. In this study, 145 cats received ProZinc insulin for up to an additional 136 days. hydrochloric acid 1.63 mg Adverse reactions were similar to those reported during the 45-day effectiveness study water for injection (maximum) 1005 mg and are listed in order of decreasing frequency: vomiting, hypoglycemia, anorexia/ pH is adjusted with hydrochloric acid and/or sodium hydroxide. poor appetite, diarrhea, lethargy, cystitis/hematuria, and weakness. Twenty cats had Indication: ProZinc (protamine zinc recombinant human insulin) is indicated for the signs consistent with hypoglycemia described as: sluggish, lethargic, unsteady, wobbly, reduction of hyperglycemia and hyperglycemia-associated clinical signs in cats with seizures, trembling, or dazed. Most of these were treated by the owner or veterinarian diabetes mellitus. with oral glucose supplementation or food; others received intravenous glucose. One cat had a serious hypoglycemic event associated with seizures and blindness. Dosage and Administration: USE OF A SYRINGE OTHER THAN A U-40 SYRINGE WILL The cat fully recovered after supportive therapy and finished the study. All cases of RESULT IN INCORRECT DOSING. hypoglycemia resolved with appropriate therapy and if needed, a dose reduction. FOR SUBCUTANEOUS INJECTION IN CATS ONLY. Fourteen cats died or were euthanized during the extended use study. In two cases, DO NOT SHAKE OR AGITATE THE VIAL. continued use of insulin despite anorexia and signs of hypoglycemia contributed to the ProZinc insulin should be mixed by gently rolling the vial prior to withdrawing each deaths. In one case, the owner decided not to continue therapy after a presumed episode dose from the vial. One mixed, ProZinc suspension has a white, cloudy appearance. of hypoglycemia. The rest were due to concurrent medical conditions or worsening of Clumps or visible white particles can form in insulin suspensions: do not use the the diabetes mellitus. product if clumps or visible white particles persist after gently rolling the vial. To report suspected adverse reactions, or to obtain a copy of the Material Safety Data Using a U-40 insulin syringe, the injection should be administered subcutaneously Sheet (MSDS), call 1-866-638-2226. on the back of the neck or on the side of the cat. Information for Cat Owners: Please refer to the Cat Owner Information Sheet for Always provide the Cat Owner Information Sheet with each prescription. more information about ProZinc insulin. ProZinc insulin, like other insulin products, The initial recommended ProZinc dose is 0.1 – 0.3 IU insulin/pound of body weight is not free from adverse reactions. Owners should be advised of the potential for (0.2 – 0.7 IU/kg) every 12 hours. The dose should be given concurrently with or right adverse reactions and be informed of the associated clinical signs. Potential adverse after a meal. The veterinarian should re-evaluate the cat at appropriate intervals reactions include: hypoglycemia, insulin antagonism/resistance, rapid insulin and adjust the dose based on both clinical signs and glucose nadirs until adequate metabolism, insulin-induced hyperglycemia (Somogyi Effect), and local or systemic glycemic control has been attained. In the effectiveness field study, glycemic control reactions. The most common adverse reaction observed is hypoglycemia. Signs may was considered adequate if the glucose nadir from a 9-hour blood glucose curve include: weakness, depression, behavioral changes, muscle twitching, and anxiety. was between 80 and 150 mg/dL and clinical signs of hyperglycemia such as polyuria, In severe cases of hypoglycemia, seizures and coma can occur. Hypoglycemia can polydipsia, and weight loss were improved. be fatal if an affected cat does not receive prompt treatment. Appropriate veterinary monitoring of blood glucose, adjustment of insulin dose and regimen as needed, and Further adjustments in the dosage may be necessary with changes in the cat’s diet, stabilization of diet and activity help minimize the risk of hypoglycemic episodes. body weight, or concomitant medication, or if the cat develops concurrent infection, The attending veterinarian should evaluate other adverse reactions on a case-by-case inflammation, neoplasia, or an additional endocrine or other medical disorder. basis to determine if an adjustment in therapy is appropriate, or if alternative therapy Contraindications: ProZinc insulin is contraindicated in cats sensitive to protamine should be considered. zinc recombinant human insulin or any other ingredients in the ProZinc product. Effectiveness: A total of 187 client-owned cats were enrolled in a 45-day field study, ProZinc insulin is contraindicated during episodes of hypoglycemia. with 176 receiving ProZinc insulin. One hundred and fifty-one cats were included in Warnings: User Safety: For use in cats only. Keep out of the reach of children. Avoid the effectiveness analysis. The patients included various purebred and mixed breed contact with eyes. In case of contact, immediately flush eyes with running water for at cats ranging in age from 3 to 19 years and in weight from 4.6 to 20.8 pounds. Of the least 15 minutes. Accidental injection may cause hypoglycemia. In case of accidental cats included in the effectiveness analysis, 101 were castrated males, 49 were spayed injection, seek medical attention immediately. Exposure to product may induce a local females, and 1 was an intact female. or systemic allergic reaction in sensitized individuals. Cats were started on ProZinc insulin at a dose of 0.1-0.3 IU/lb (0.2-0.7 IU/kg) twice daily. Animal Safety: Owners should be advised to observe for signs of hypoglycemia (see Cats were evaluated at 7, 14, 30, and 45 days after initiation of therapy and the dose Cat Owner Information Sheet). Use of this product, even at established doses, has been was adjusted based on clinical signs and results of 9-hour blood glucose curves associated with hypoglycemia. An animal with signs of hypoglycemia should be treated on Days 7, 14, and 30. immediately. Glucose should be given orally or intravenously as dictated by clinical Effectiveness was based on successful control of diabetes which was defined as signs. Insulin should be temporarily withheld and, if indicated, the dosage adjusted. improvement in at least one blood glucose variable (glucose curve mean, nadir, Any change in insulin should be made cautiously and only under a veterinarian’s or fructosamine) and at least one clinical sign (polyuria, polydipsia, or body weight). supervision. Changes in insulin strength, manufacturer, type, species (human, animal) Based on this definition, 115 of 151 cases (76.2%) were considered successful. or method of manufacture (rDNA versus animal-source insulin) may result in the need Blood glucose curve means decreased from 415.3 mg/dL on Day 0 to 203.2 mg/dL for a change in dosage. by Day 45 and the mean blood glucose nadir decreased from 407.9 mg/dL on Day 0 Appropriate diagnostic tests should be performed to rule out other endocrinopathies to 142.4 mg/dL on Day 45. Mean fructosamine values decreased from 505.9 μmol/L in diabetic cats that are difficult to regulate. on Day 0 to 380.7 μmol/L on Day 45. Precautions: Animals presenting with severe ketoacidosis, anorexia, lethargy, and/or Cats that completed the effectiveness study were enrolled in an extended use field vomiting should be stabilized with short-acting insulin and appropriate supportive study. The mean fructosamine value was 342.0 μmol/L after a total of 181 days therapy until their condition is stabilized. As with all insulin products, careful patient of ProZinc therapy. monitoring for hypoglycemia and hyperglycemia are essential to attain and maintain How Supplied: ProZinc insulin is supplied as a sterile injectable suspension in adequate glycemic control and to prevent associated complications. Overdosage can 10 mL multidose vials. Each mL of ProZinc product contains 40 IU recombinant result in profound hypoglycemia and death. Progestogens, certain endocrinopathies human insulin. and glucocorticoids can have an antagonistic effect on insulin activity. Progestogen Storage Conditions: Store in an upright position under refrigeration at 36-46°F and glucocorticoid use should be avoided. (2-8°C). Do not freeze. Protect from light. Use within 60 days of first puncture. Reproductive Safety: The safety and effectiveness of ProZinc insulin in breeding, Manufactured for: pregnant, and lactating cats has not been evaluated. Boehringer Ingelheim Vetmedica, Inc. Use in Kittens: The safety and effectiveness of ProZinc insulin in kittens has not St. Joseph, MO 64506 U.S.A. been evaluated. ProZinc® is a registered trademark of Boehringer Ingelheim Vetmedica, Inc. Adverse Reactions: Effectiveness Field Study © 2017 Boehringer Ingelheim Vetmedica, Inc. All Rights Reserved. In a 45-day effectiveness field study, 176 cats received ProZinc insulin. Hypoglycemia (defined as a blood glucose value of < 50 mg/dL) occurred in 71 of the cats at 449901-03 various times throughout the study. Clinical signs of hypoglycemia were generally Revised 09/2017 mild in nature (described as lethargic, sluggish, weak, trembling, uncoordinated, groggy, glassy-eyed or dazed). In 17 cases, the veterinarian provided oral glucose supplementation or food as treatment. Most cases were not associated with clinical signs and received no treatment. One cat had a serious hypoglycemic event associated with stupor, lateral recumbency, hypothermia and seizures.
TOP 5 h INTERNAL MEDICINE h PEER REVIEWED Top 5 Canine Biliary Diseases Stefanie M. DeMonaco, DVM, MS, DACVIM (SAIM) Virginia–Maryland College of Veterinary Medicine d FIGURE 1 Ultrasonographic image of a GBM showing the classic kiwi-like appearance The number of dogs diagnosed with biliary Following are 5 of the most common canine biliary diseases according to the author. disease is increasing.1-5 Clinical signs and physical 1 examination findings in dogs with biliary disease Gallbladder Mucoceles tend to be nonspecific and overlap with clinical Gallbladder mucoceles (GBMs) result from an accumulation of semisolid mucus signs of GI and systemic diseases; these can include masses and inspissated bile in the gallblad- anorexia, vomiting, abdominal pain, jaundice, and der and are associated with high morbidity and fever. Clinicopathologic abnormalities are similarly mortality.3,6-11 Affected dogs are typically older nonspecific and can include cholestatic to mixed liver enzyme elevations, hyperbilirubinemia, TOP 5 CANINE BILIARY DISEASES hypercholesterolemia, and neutrophilic 1. Gallbladder Mucoceles leukocytosis.1,2,6-8 Diagnosis of biliary disease 2. Extrahepatic Biliary Obstruction usually involves ultrasonography with or without 3. Cholecystitis collection of liver and bile samples. Treatment with 4. Cholelithiasis urgent surgical care versus conservative medical 5. Biliary Neoplasia management should be determined based on the cause and severity of disease. GBM = gallbladder mucocele December 2019 cliniciansbrief.com 11
TOP 5 h INTERNAL MEDICINE h PEER REVIEWED (median age, 10 years) and of a predisposed breed appearances of GBMs include echogenic immobile (ie, cocker spaniel, Shetland sheepdog, miniature biliary sludge filling the gallbladder or a stellate schnauzer, border terrier, Pomeranian).2,3,6-16 pattern (Figure 2).6,10,11 These different GBM Additional risk factors for GBMs include gallbladder appearances on ultrasonographic images likely dysmotility, dyslipidemias, and endocrinopathies represent a continuum of early to mature mucoce- (eg, hyperadrenocorticism, hypothyroidism).14,17,18 les.6 Ultrasonography cannot be used alone to determine the clinical significance of GBMs or Abdominal ultrasonography is key to diagnosis of guide treatment decisions unless there is clear GBMs. The classic description of GBMs is a kiwi- evidence of biliary rupture or obstruction that like appearance of intraluminal gallbladder warrants urgent surgical intervention (see contents with hyperechoic immobile striations Gallbladder Rupture).1,3,10 of inspissated bile in hypoechoic mucus structures (Figure 1, previous page). Other ultrasonographic Preoperative biliary rupture and bile peritonitis can increase the risk for death, but some studies have shown that long-term survival (ie, 2-5 years) is possible in patients that survive the peri- operative period.3,7,8,19,20 Common postoperative complications include pancreatitis and bile peritonitis.2,7,19 Patients with biliary infection at the time of rupture tend to have a higher mortality rate. The best approach to treating GBMs (medical vs surgical) in dogs is controversial. When clinical signs and serum chemistry abnormalities (eg, increased ALP, γ-glutamyl transferase, ALT, and total bilirubin) are supportive of GBMs, cholecys- tectomy is generally recommended over medical management.1,6,10,21,22 A retrospective study found a longer survival time in dogs that underwent sur- d FIGURE 2 Ultrasonographic image of a GBM displaying a gery as compared with those that received medical stellate pattern management.20 Medical therapy is best reserved for clinically inapparent cases of GBMs and when surgery is not an option. Medical therapy includes ursodiol, a low-fat diet, antibiotics, and treatment GALLBLADDER RUPTURE of concurrent diseases associated with GBMs (eg, hyperadrenocorticism, hypothyroidism, dyslipid- Ultrasonography can help determine the presence of emias) and, in most cases, is unlikely to resolve concurrent gallbladder rupture and/or extrahepatic GBMs. A few cases of resolution or improvement biliary obstruction. Pericholecystic hyperechoic fat, with medical management have been reported, pericholecystic fluid, a discontinuous gallbladder wall, with other cases having static disease.2,10,23 Follow- and an unidentifiable discrete gallbladder with free- floating mucoceles in the peritoneum are supportive of up ultrasonography and serum chemistry profile gallbladder rupture.1,6,7 The specificity and sensitivity of performed within 2 to 3 months of diagnosis to ultrasonography in determining gallbladder rupture in assess response to treatment and identify complica- dogs with GBMs varies from 91.7% to 100% and 56.1% to tions are recommended, regardless of whether the 85%, respectively.3,10 patient is treated medically or surgically. 12 cliniciansbrief.com December 2019
2 Extrahepatic Biliary Obstruction The most common cause of extrahepatic biliary obstruction (EHBO) in dogs is pancreatitis. In acute pancreatitis patients, atitis, which is typically characterized by chronic neutrophilic inflammation.4,5 Abdominal radiogra- phy can aid in the diagnosis of cholecystitis, partic- ularly if emphysematous cholecystitis is present pancreatic edema and/or inflammation affecting with a gas-filled gallbladder or gas opacities in the the bile duct results in obstruction, whereas in pericholecystic region. Nonspecific radiographic chronic pancreatitis patients, fibrosis results in duct findings may reveal a right quadrant abdominal obstruction. Other causes can include GBMs, chol- mass effect, poor serosal detail, and/or angiohepatitis, neoplasia, and cholelithiasis.4,13,24 choleliths.9,27 The following abdominal ultrasono- graphic findings can be suggestive of cholecystitis Diagnosis of EHBO is usually made via ultra- and/or cholangiohepatitis: thickened, hyperechoic, sonography and/or exploratory laparotomy. irregular and/or laminar gallbladder wall; echo- Ultrasonographic characteristics of EHBO include genic intraluminal contents; pericholecystic fluid gallbladder enlargement, dilation of the cystic or echogenic abdominal effusion; distended bile and/or bile ducts, and, in cases of obstruction last- duct; and/or heterogeneous or hyperechoic hepatic ing >5 days, intrahepatic duct dilation.9 Because parenchyma.4,9 Bile samples can be obtained with ultrasonography may not always discern the cause percutaneous ultrasound-guided cholecystocente- of obstruction, surgery may be necessary to con- sis to assess for inflammation, infectious agents, firm biliary obstruction and further characterize and culture and susceptibility. Culture and suscep- and address the cause.9 tibility testing is particularly important, as resis- tance can occur with empiric broad-spectrum Treatment of EHBO should be aimed toward antimicrobials.5 Common bacterial isolates include addressing the underlying cause of obstruction Escherichia coli, Enterococcus spp, Klebsiella spp, and, if necessary, include biliary decompression. Clostridium spp, and Bacteroides spp.4,5,25,28 Whether surgical or ultrasound-guided percutane- ous biliary decompression is necessary in patients Treatment of cholecystitis includes medical manage- with EHBO secondary to pancreatitis is controver- ment, but surgical intervention may be necessary sial. Most dogs with EHBO secondary to pancreati- depending on the severity of signs and gallbladder tis improve with medical management as acute rupture. Cholecystectomy can reduce morbidity and pancreatitis resolves. Serum chemistry abnormali- mortality in dogs with cholangiohepatitis and/or ties (eg, liver enzymes, bilirubin) can worsen cholecystitis.4 Medical therapy includes antimicro- despite improvement in clinical signs and should bial administration guided by either culture and not be confused with worsening of the patient’s con- dition. Unpublished data suggest that bilirubin lev- els peak in dogs with pancreatitis-associated EHBO when clinical signs of pancreatitis are improving. Cholecystectomy can reduce 3 Cholecystitis Cholecystitis can have acute or chronic pre- sentations. Anorexia, vomiting, abdominal pain, and fever are typical signs of acute morbidity and mortality in dogs with cholangiohepatitis and/or cholecystitis.4 cholecystitis.25,26 Patients with chronic cholecysti- tis may have milder signs of chronic intermittent vomiting, anorexia, weight loss, and/or abdominal EHBO = extrahepatic biliary obstruction pain or no clinical signs at all. Cholecystitis may be GBM = gallbladder mucocele present alone or in combination with cholangiohep- December 2019 cliniciansbrief.com 13
TOP 5 h INTERNAL MEDICINE h PEER REVIEWED susceptibility results or, when culture and suscepti- Ultrasonographic findings are nonspecific but bility results are unavailable, empiric treatment can include a solitary mass or diffuse nodules against common isolates (eg, amoxicillin/clavulanic with or without target lesions.38 Histopathology acid and enrofloxacin). Additional treatment with or without immunohistochemical markers options include ursodiol and supportive care.9,25 is necessary to confirm diagnosis. Cholecystectomy is typically the surgical treatment of choice when surgery is required and in cases in The treatment of choice for biliary carcinomas is which only the gallbladder is affected.9,29 surgical resection unless the disease is diffuse or 4 multifocal in nature. Overall survival is generally Cholelithiasis poor, with survival times typically being ≤6 Choleliths are stones in the biliary system months.34,39 Metastasis to regional lymph nodes and can have varying presentations (ie, and lungs occurs in ≤88% of dogs.35,36 Cholecysto- mixed stones, pigment stones, cholesterol duodenostomy can be performed in patients with stones). In dogs with mixed stones, pigment stones secondary EHBO as a palliative option. n are most commonly seen, with cholesterol stones being less frequent.9,30,31 Middle-aged to older, female, small-breed dogs are predisposed to choleliths, and an increased incidence of cholelithi- asis has been observed in miniature poodles and miniature schnauzers.9,26,29,30,32,33 Choleliths are POLL usually found incidentally on abdominal ultrasono- graphic images or necropsy and can lead to EHBO Have you ever suspected or diagnosed any or cholecystitis. of the following biliary diseases via ultra- sonography? Check all that apply. Diagnosis is made via ultrasonography, which can A. Gallbladder mucocele detect stones >2 mm in size.9,26,27 Medical dissolu- B. Extrahepatic biliary obstruction tion of choleliths is usually unsuccessful. Medical C. Cholecystitis therapy includes ursodiol, S-adenosylmethionine, D. Cholelithiasis antimicrobials, vitamin E, and anti-inflammatory E. Biliary neoplasia medications based on liver histopathology results F. I have never suspected/diagnosed any (eg, chronic nonsuppurative hepatitis). Surgery is of these via ultrasonography. the treatment of choice in patients with concur- rent cholecystitis and/or bile duct obstruction. Scan the QR code to submit your answer and see the 5 other responses! The poll is located at the bottom of Biliary Neoplasia the article. Hepatobiliary neoplasia accounts for 0.6% Using QR codes from your mobile to 1.3% of all canine neoplasms.34 Hepato- device is easy and quick! cellular carcinoma is the most common form of hepatobiliary neoplasia, followed by bili- Simply focus your phone’s camera on ary carcinoma. Labrador retrievers and female the QR code as if taking a picture (but don’t click!). A notification banner will pop up at the dogs are predisposed to biliary carcinomas.34-37 top of your screen; tap the banner to view the linked EHBO = extrahepatic biliary obstruction content. 14 cliniciansbrief.com December 2019
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SYMPOSIUM CAPSULES SYMPOSIUM CAPSULES What Breeds Are makeup. Other coat traits (eg, furnishings, hair length, curl) also involve multiple genes. The 2019 American in My Mixed-Breed list of polygenic traits is long, and environmen- tal factors can impact some polygenic traits; Veterinary Medical Association Convention Dog? therefore, these traits should not be used to make breeding choices. Although crossbreed dogs may theoretically benefit from a lesser concentration of disease-causing recessive August 2-6, 2019 Visual identification of the breed makeup of genes, it is important to consider diseases Washington, DC crossbreed dogs is imprecise. There is often of genetic origin when creating a differential little agreement regarding breed-makeup diagnosis list for patients. When a genetic assumptions among professionals in dog- disease database is being used, however, the related professions, and DNA identification, search should be based on clinical signs rather which is based on gene identification and than breed. comparison, often does not match these assumptions. Implications of misidentification Because visual breed identification is so exist from both legal (eg, breed-related legisla- unreliable, it is recommended that non- tion) and medical standpoints (eg, testing for breed–based terminology be used when genetic disease). describing a dog. Use of generic terms (eg, crossbreed), along with a description of the Breed-related traits that can be visually iden- dog’s characteristics (eg, brindle, short- tified include chondrodysplasia, hair ridge, haired, neutered male dog with upright ears), and hairlessness. Coat colors are determined is preferable to breed-based identification by many different possible gene combinations (eg, pit bull cross).—Ekenstedt KJ and thus cannot be used to ascertain breed Hypertonic Saline vagally mediated hypotension and brady- cardia; electrolytes should be monitored. In cases of shock, HTSs can interrupt the cycle Hypertonic saline solutions (HTSs) are crystal- of reduced perfusion, ischemia, vasocon- loid solutions with NaCl concentrations ranging striction, and endothelial swelling. Cerebral from 3% to 23.4%. Administration of HTSs can blood flow may also be enhanced by the abil- cause water to immediately shift from the inter- ity of HTSs to decrease endothelial swelling. stitial space to the intravascular space due to Administration of HTSs can lower intracranial SAVE THE DATE increased osmolarity, expanding the intravas- hypertension and is generally preferred over cular volume by 2 to 3 times the volume admin- mannitol. HTSs have shown some promise 2020 American istered. Although this effect may only last 1 to in nebulization for patients with respiratory Veterinary Medical 3 hours, it is a desirable effect in patients with disease. Although seemingly counterintui- Association Convention hemorrhagic and/or traumatic shock, in which tive, administration of HTSs with high-dose excessive fluid resuscitation can exacerbate furosemide to patients that have congestive hypothermia, acidosis, and coagulopathy. heart failure has also proven beneficial. HTSs Small volumes of HTSs can improve preload, are inexpensive and easy to administer, and July 31-August 4, 2020 cardiac output, and mean arterial pressure although more clinical studies are needed to San Diego, California and decrease peripheral vascular resistance. investigate their potential role in veterinary Dehydration is not a contraindication of HTS medicine, there are numerous documented administration. A rate of
SYMPOSIUM CAPSULES Tips & Advanced the process, as owners will often take their emotional cues from the staff. double the dose can also be squirted into the mouth. Techniques for Sedatives, often at high doses, can Smaller patients, obese cats, and Challenging help ensure a smooth, less stressful patients with poor venous access may Euthanasias procedure. Overdosing is not a concern, although the possibility of death via require alternative euthanasia routes following sedation; these can include sedative should be communicated. intrahepatic, intrarenal, or intraperito- Sedation prior to IV catheter placement neal injections, although these routes is ideal; vitamin B12 in the sedative generally require larger volumes of Although some euthanasias can present syringe can help reduce stinging on the euthanasia agent and usually take unique challenges, veterinary staff can injection. longer to achieve full effect. Alterna- provide a smooth experience through tive veins (eg, dorsal pedal, sublingual, good planning and communication. Oral premedication at home with ear) can also be considered. Clinicians gabapentin, acepromazine, or should gain experience with alternative Euthanasia appointments should trazodone can be helpful for reactive euthanasia routes to be prepared for be scheduled with plenty of time patients; gabapentin (30 mg/kg) with when a secondary plan is needed; alter- allowed to ensure that all questions crushed acepromazine (10 mg/kg PO) native routes can first be attempted in and concerns are fully addressed. administered in treats on presentation fully sedated patients of owners who Staff members should be calm and will often be effective within 10 to 15 choose nonwitness euthanasias. reassuring to pet owners throughout minutes. Injectable premedication at —Naun C Anesthesia compressed gas, although some use both. The drive mechanism is usually cavity, and/or patients with increased intracranial pressure that also require Ventilators: compressed gas, and most ventilators are dual circuit. With dual-circuit venti- strict regulation of end tidal CO2. Obese patients or those with intra-abdominal How They Work lators, a driving gas provides the pneu- masses may also benefit from ventila- & When to Use matic force that compresses the bellows, which then releases its contents (ie, tion. Debilitated patients may not be good candidates for ventilation due to Them the breathing gas) that are delivered to the patient. The major control variable decreased preload, which may affect cardiac output, and increased thoracic delivers the breath and can be volume positive pressure. or pressure controlled; most are volume Anesthesia ventilators are simpler in controlled and have an alarm and/or Delivery of tidal volume that is greater function than intensive care ventilators pressure relief valve. The cyclic mech- than what is recommended may cause and are intended to provide support to anism generally uses an electric timing barotrauma and lead to interstitial healthy patients. Because veterinary mechanism to cycle from the inspira- emphysema and pneuomothorax; maxi- models are not regulated like human tory to expiratory phase. Most modern mum values for peak inspiratory pressure models are, clinicians are responsible ventilators have ascending or standing should not be exceeded. Minute volume for understanding how to use them. bellows (vs hanging bellows) based on (ie, tidal volume multiplied by respiratory Ventilators are typically classified based the direction of the bellows during expi- rate), positive end expiratory pressure, on power source, drive mechanism, ration. Smaller patients require smaller and peak inspiratory pressure values major control variable, cyclic mecha- bellows. should all be monitored and maintained nism, and bellows. in the appropriate range.—Barletta M Indications for mechanical ventilation The power source in most ventila- include use of neuromuscular blocking tors is electricity or, less commonly, agents, patients with an open thoracic 18 cliniciansbrief.com December 2019
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