Impact of concurrent treatment with omeprazole on phenylbutazone‐induced equine gastric ulcer syndrome (EGUS)

Background Phenylbutazone is commonly prescribed for treatment of various painful or inflammatory disorders in horses, but is associated with gastrointestinal (GI) adverse effects. Anecdotally, many practitioners prescribe omeprazole concurrently with phenylbutazone to reduce development of equine g...

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Veröffentlicht in:Equine veterinary journal 2021-03, Vol.53 (2), p.356-363
Hauptverfasser: Ricord, Megan, Andrews, Frank M., Yñiguez, Francisco J. M., Keowen, Michael, Garza, Frank, Paul, Linda, Chapman, Ann, Banse, Heidi E.
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container_end_page 363
container_issue 2
container_start_page 356
container_title Equine veterinary journal
container_volume 53
creator Ricord, Megan
Andrews, Frank M.
Yñiguez, Francisco J. M.
Keowen, Michael
Garza, Frank
Paul, Linda
Chapman, Ann
Banse, Heidi E.
description Background Phenylbutazone is commonly prescribed for treatment of various painful or inflammatory disorders in horses, but is associated with gastrointestinal (GI) adverse effects. Anecdotally, many practitioners prescribe omeprazole concurrently with phenylbutazone to reduce development of equine gastric ulcer syndrome (EGUS), but the efficacy and safety of this practice remains unknown. Objectives To evaluate the effect of omeprazole on phenylbutazone‐induced equine glandular gastric disease (EGGD) and equine squamous gastric disease (ESGD). Study design Randomised block experimental design. Methods Twenty‐two horses with EGGD and ESGD scores ≤2 were included. Horses were assigned to treatment groups: phenylbutazone (4.4 mg/kg PO q 12 h; PBZ), phenylbutazone plus omeprazole (4 mg/kg PO q. 24 h; PBZ/OME) or placebo (CON) in a randomised block design based upon initial EGGD score. Horses were treated for up to 14 days. Gastroscopy was performed weekly; CBC and biochemistry were performed at Day 0 and study end. Horses were monitored for signs of colic and/or diarrhoea. Results EGGD score increased in PBZ (median change 1, inter‐quartile range, [IQR], 0‐2) compared to PBZ/OME (median change 0, IQR −1 to 0; P = .05). PBZ/OME (6/8) had more intestinal complications than CON (0/6; difference between proportions = 75%; 95% CI, 23%‐93%; P = .03). Plasma protein concentrations decreased in PBZ, compared to CON (mean difference between groups, 14 g/L; 95% CI, 1.04‐27; P = .03). Five horses were withdrawn from the study due to intestinal complications (n = 3 PBZ/OME and n = 2 PBZ); one horse (PBZ) was withdrawn due to severe grade 4 EGGD. Main limitations Small sample size and changes in management for the 2‐3 days prior to study initiation; variable treatment duration among groups due to development of complications. Conclusions Administration of omeprazole ameliorated PBZ‐induced EGGD, but was associated with an increase in intestinal complications. Caution should be exercised when co‐prescribing NSAIDs and omeprazole in horses, particularly in association with change in management.
doi_str_mv 10.1111/evj.13323
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M. ; Keowen, Michael ; Garza, Frank ; Paul, Linda ; Chapman, Ann ; Banse, Heidi E.</creator><creatorcontrib>Ricord, Megan ; Andrews, Frank M. ; Yñiguez, Francisco J. M. ; Keowen, Michael ; Garza, Frank ; Paul, Linda ; Chapman, Ann ; Banse, Heidi E.</creatorcontrib><description>Background Phenylbutazone is commonly prescribed for treatment of various painful or inflammatory disorders in horses, but is associated with gastrointestinal (GI) adverse effects. Anecdotally, many practitioners prescribe omeprazole concurrently with phenylbutazone to reduce development of equine gastric ulcer syndrome (EGUS), but the efficacy and safety of this practice remains unknown. Objectives To evaluate the effect of omeprazole on phenylbutazone‐induced equine glandular gastric disease (EGGD) and equine squamous gastric disease (ESGD). Study design Randomised block experimental design. Methods Twenty‐two horses with EGGD and ESGD scores ≤2 were included. Horses were assigned to treatment groups: phenylbutazone (4.4 mg/kg PO q 12 h; PBZ), phenylbutazone plus omeprazole (4 mg/kg PO q. 24 h; PBZ/OME) or placebo (CON) in a randomised block design based upon initial EGGD score. Horses were treated for up to 14 days. Gastroscopy was performed weekly; CBC and biochemistry were performed at Day 0 and study end. Horses were monitored for signs of colic and/or diarrhoea. Results EGGD score increased in PBZ (median change 1, inter‐quartile range, [IQR], 0‐2) compared to PBZ/OME (median change 0, IQR −1 to 0; P = .05). PBZ/OME (6/8) had more intestinal complications than CON (0/6; difference between proportions = 75%; 95% CI, 23%‐93%; P = .03). Plasma protein concentrations decreased in PBZ, compared to CON (mean difference between groups, 14 g/L; 95% CI, 1.04‐27; P = .03). Five horses were withdrawn from the study due to intestinal complications (n = 3 PBZ/OME and n = 2 PBZ); one horse (PBZ) was withdrawn due to severe grade 4 EGGD. Main limitations Small sample size and changes in management for the 2‐3 days prior to study initiation; variable treatment duration among groups due to development of complications. Conclusions Administration of omeprazole ameliorated PBZ‐induced EGGD, but was associated with an increase in intestinal complications. Caution should be exercised when co‐prescribing NSAIDs and omeprazole in horses, particularly in association with change in management.</description><identifier>ISSN: 0425-1644</identifier><identifier>EISSN: 2042-3306</identifier><identifier>DOI: 10.1111/evj.13323</identifier><identifier>PMID: 32697849</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Animals ; Anti-Inflammatory Agents, Non-Steroidal - adverse effects ; dysbiosis ; equine glandular gastric disease (EGGD) ; horse ; Horse Diseases - chemically induced ; Horse Diseases - drug therapy ; Horses ; non‐steroidal anti‐inflammatory drug (NSAID) ; Omeprazole - adverse effects ; Phenylbutazone - adverse effects ; proton pump inhibitor (PPI) ; Stomach Ulcer - chemically induced ; Stomach Ulcer - drug therapy ; Stomach Ulcer - veterinary ; Ulcers</subject><ispartof>Equine veterinary journal, 2021-03, Vol.53 (2), p.356-363</ispartof><rights>2020 EVJ Ltd</rights><rights>2020 EVJ Ltd.</rights><rights>Copyright © 2021 EVJ Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3883-c2c21c16cb875f2798173a5255ab49123a5fb50529554505e34bd9e0248426153</citedby><cites>FETCH-LOGICAL-c3883-c2c21c16cb875f2798173a5255ab49123a5fb50529554505e34bd9e0248426153</cites><orcidid>0000-0001-7930-6237 ; 0000-0002-0120-0376</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fevj.13323$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fevj.13323$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27926,27927,45576,45577</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32697849$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ricord, Megan</creatorcontrib><creatorcontrib>Andrews, Frank M.</creatorcontrib><creatorcontrib>Yñiguez, Francisco J. M.</creatorcontrib><creatorcontrib>Keowen, Michael</creatorcontrib><creatorcontrib>Garza, Frank</creatorcontrib><creatorcontrib>Paul, Linda</creatorcontrib><creatorcontrib>Chapman, Ann</creatorcontrib><creatorcontrib>Banse, Heidi E.</creatorcontrib><title>Impact of concurrent treatment with omeprazole on phenylbutazone‐induced equine gastric ulcer syndrome (EGUS)</title><title>Equine veterinary journal</title><addtitle>Equine Vet J</addtitle><description>Background Phenylbutazone is commonly prescribed for treatment of various painful or inflammatory disorders in horses, but is associated with gastrointestinal (GI) adverse effects. Anecdotally, many practitioners prescribe omeprazole concurrently with phenylbutazone to reduce development of equine gastric ulcer syndrome (EGUS), but the efficacy and safety of this practice remains unknown. Objectives To evaluate the effect of omeprazole on phenylbutazone‐induced equine glandular gastric disease (EGGD) and equine squamous gastric disease (ESGD). Study design Randomised block experimental design. Methods Twenty‐two horses with EGGD and ESGD scores ≤2 were included. Horses were assigned to treatment groups: phenylbutazone (4.4 mg/kg PO q 12 h; PBZ), phenylbutazone plus omeprazole (4 mg/kg PO q. 24 h; PBZ/OME) or placebo (CON) in a randomised block design based upon initial EGGD score. Horses were treated for up to 14 days. Gastroscopy was performed weekly; CBC and biochemistry were performed at Day 0 and study end. Horses were monitored for signs of colic and/or diarrhoea. Results EGGD score increased in PBZ (median change 1, inter‐quartile range, [IQR], 0‐2) compared to PBZ/OME (median change 0, IQR −1 to 0; P = .05). PBZ/OME (6/8) had more intestinal complications than CON (0/6; difference between proportions = 75%; 95% CI, 23%‐93%; P = .03). Plasma protein concentrations decreased in PBZ, compared to CON (mean difference between groups, 14 g/L; 95% CI, 1.04‐27; P = .03). Five horses were withdrawn from the study due to intestinal complications (n = 3 PBZ/OME and n = 2 PBZ); one horse (PBZ) was withdrawn due to severe grade 4 EGGD. Main limitations Small sample size and changes in management for the 2‐3 days prior to study initiation; variable treatment duration among groups due to development of complications. Conclusions Administration of omeprazole ameliorated PBZ‐induced EGGD, but was associated with an increase in intestinal complications. 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M. ; Keowen, Michael ; Garza, Frank ; Paul, Linda ; Chapman, Ann ; Banse, Heidi E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3883-c2c21c16cb875f2798173a5255ab49123a5fb50529554505e34bd9e0248426153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animals</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - adverse effects</topic><topic>dysbiosis</topic><topic>equine glandular gastric disease (EGGD)</topic><topic>horse</topic><topic>Horse Diseases - chemically induced</topic><topic>Horse Diseases - drug therapy</topic><topic>Horses</topic><topic>non‐steroidal anti‐inflammatory drug (NSAID)</topic><topic>Omeprazole - adverse effects</topic><topic>Phenylbutazone - adverse effects</topic><topic>proton pump inhibitor (PPI)</topic><topic>Stomach Ulcer - chemically induced</topic><topic>Stomach Ulcer - drug therapy</topic><topic>Stomach Ulcer - veterinary</topic><topic>Ulcers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ricord, Megan</creatorcontrib><creatorcontrib>Andrews, Frank M.</creatorcontrib><creatorcontrib>Yñiguez, Francisco J. M.</creatorcontrib><creatorcontrib>Keowen, Michael</creatorcontrib><creatorcontrib>Garza, Frank</creatorcontrib><creatorcontrib>Paul, Linda</creatorcontrib><creatorcontrib>Chapman, Ann</creatorcontrib><creatorcontrib>Banse, Heidi E.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><jtitle>Equine veterinary journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ricord, Megan</au><au>Andrews, Frank M.</au><au>Yñiguez, Francisco J. M.</au><au>Keowen, Michael</au><au>Garza, Frank</au><au>Paul, Linda</au><au>Chapman, Ann</au><au>Banse, Heidi E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of concurrent treatment with omeprazole on phenylbutazone‐induced equine gastric ulcer syndrome (EGUS)</atitle><jtitle>Equine veterinary journal</jtitle><addtitle>Equine Vet J</addtitle><date>2021-03</date><risdate>2021</risdate><volume>53</volume><issue>2</issue><spage>356</spage><epage>363</epage><pages>356-363</pages><issn>0425-1644</issn><eissn>2042-3306</eissn><abstract>Background Phenylbutazone is commonly prescribed for treatment of various painful or inflammatory disorders in horses, but is associated with gastrointestinal (GI) adverse effects. Anecdotally, many practitioners prescribe omeprazole concurrently with phenylbutazone to reduce development of equine gastric ulcer syndrome (EGUS), but the efficacy and safety of this practice remains unknown. Objectives To evaluate the effect of omeprazole on phenylbutazone‐induced equine glandular gastric disease (EGGD) and equine squamous gastric disease (ESGD). Study design Randomised block experimental design. Methods Twenty‐two horses with EGGD and ESGD scores ≤2 were included. Horses were assigned to treatment groups: phenylbutazone (4.4 mg/kg PO q 12 h; PBZ), phenylbutazone plus omeprazole (4 mg/kg PO q. 24 h; PBZ/OME) or placebo (CON) in a randomised block design based upon initial EGGD score. Horses were treated for up to 14 days. Gastroscopy was performed weekly; CBC and biochemistry were performed at Day 0 and study end. Horses were monitored for signs of colic and/or diarrhoea. Results EGGD score increased in PBZ (median change 1, inter‐quartile range, [IQR], 0‐2) compared to PBZ/OME (median change 0, IQR −1 to 0; P = .05). PBZ/OME (6/8) had more intestinal complications than CON (0/6; difference between proportions = 75%; 95% CI, 23%‐93%; P = .03). Plasma protein concentrations decreased in PBZ, compared to CON (mean difference between groups, 14 g/L; 95% CI, 1.04‐27; P = .03). Five horses were withdrawn from the study due to intestinal complications (n = 3 PBZ/OME and n = 2 PBZ); one horse (PBZ) was withdrawn due to severe grade 4 EGGD. Main limitations Small sample size and changes in management for the 2‐3 days prior to study initiation; variable treatment duration among groups due to development of complications. Conclusions Administration of omeprazole ameliorated PBZ‐induced EGGD, but was associated with an increase in intestinal complications. Caution should be exercised when co‐prescribing NSAIDs and omeprazole in horses, particularly in association with change in management.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>32697849</pmid><doi>10.1111/evj.13323</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-7930-6237</orcidid><orcidid>https://orcid.org/0000-0002-0120-0376</orcidid><oa>free_for_read</oa></addata></record>
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source Wiley-Blackwell Journals; MEDLINE
subjects Animals
Anti-Inflammatory Agents, Non-Steroidal - adverse effects
dysbiosis
equine glandular gastric disease (EGGD)
horse
Horse Diseases - chemically induced
Horse Diseases - drug therapy
Horses
non‐steroidal anti‐inflammatory drug (NSAID)
Omeprazole - adverse effects
Phenylbutazone - adverse effects
proton pump inhibitor (PPI)
Stomach Ulcer - chemically induced
Stomach Ulcer - drug therapy
Stomach Ulcer - veterinary
Ulcers
title Impact of concurrent treatment with omeprazole on phenylbutazone‐induced equine gastric ulcer syndrome (EGUS)
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