Comparison of two doses of recombinant human bone morphogenetic protein in absorbable collagen sponges for bone healing in dogs
To determine the effects of 2 doses of recombinant human bone morphogenetic protein-2 in an absorbable collagen sponge (rhBMP-2/ACS) on bone healing in dogs. 27 adult dogs. Dogs underwent a mid-diaphyseal (1-mm) tibial osteotomy (stabilized with external skeletal fixation) and received an ACS contai...
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Veröffentlicht in: | American journal of veterinary research 2007-08, Vol.68 (8), p.834-840 |
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creator | Schmiedt, C.W Lu, Y Heaney, K Muir, P Amodie, D.M Markel, M.D |
description | To determine the effects of 2 doses of recombinant human bone morphogenetic protein-2 in an absorbable collagen sponge (rhBMP-2/ACS) on bone healing in dogs.
27 adult dogs.
Dogs underwent a mid-diaphyseal (1-mm) tibial osteotomy (stabilized with external skeletal fixation) and received an ACS containing 0.28 mg (0.2 mg/mL) or 0.56 mg (0.4 mg/mL) of rhBMP-2 or no treatment (control dogs). All dogs were examined daily; bone healing was assessed via radiography and subjective lameness evaluation every 2 weeks. After euthanasia at 8 weeks, tibiae were evaluated biomechanically and histologically.
Control dogs required antimicrobial treatment for pin-site-related complications more frequently than did rhBMP-2/ACS-treated dogs. At 4 and 6 weeks, weight bearing was greater in dogs treated with rhBMP-2/ACS (0.2 mg/mL) than in control dogs, albeit not significantly. Compared with control treatment, both doses of rhBMP-2/ACS accelerated osteotomy healing at 4, 6, and 8 weeks, and the 0.2 mg/mL dose enhanced healing at 2 weeks; healing at 6 weeks was greater for the lower-dose treatment than for the higher-dose treatment. Histologically, healing at 8 weeks was significantly improved for both rhBMP-2/ACS treatments, compared with control treatment. Among groups, biomechanical variables did not differ, although less osteotomy-site failures occurred in rhBMP-2/ACS-treated groups.
In dogs that underwent tibial osteotomy, rhBMP-2/ACS (0.2 mg/mL) appeared to accelerate bone healing and reduce lameness (compared with control treatment) and apparently augmented bone healing more than rhBMP-2/ACS (0.4 mg/mL). Compared with control dogs, rhBMP-2/ACS-treated dogs required antimicrobial treatments less frequently. |
doi_str_mv | 10.2460/ajvr.68.8.834 |
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27 adult dogs.
Dogs underwent a mid-diaphyseal (1-mm) tibial osteotomy (stabilized with external skeletal fixation) and received an ACS containing 0.28 mg (0.2 mg/mL) or 0.56 mg (0.4 mg/mL) of rhBMP-2 or no treatment (control dogs). All dogs were examined daily; bone healing was assessed via radiography and subjective lameness evaluation every 2 weeks. After euthanasia at 8 weeks, tibiae were evaluated biomechanically and histologically.
Control dogs required antimicrobial treatment for pin-site-related complications more frequently than did rhBMP-2/ACS-treated dogs. At 4 and 6 weeks, weight bearing was greater in dogs treated with rhBMP-2/ACS (0.2 mg/mL) than in control dogs, albeit not significantly. Compared with control treatment, both doses of rhBMP-2/ACS accelerated osteotomy healing at 4, 6, and 8 weeks, and the 0.2 mg/mL dose enhanced healing at 2 weeks; healing at 6 weeks was greater for the lower-dose treatment than for the higher-dose treatment. Histologically, healing at 8 weeks was significantly improved for both rhBMP-2/ACS treatments, compared with control treatment. Among groups, biomechanical variables did not differ, although less osteotomy-site failures occurred in rhBMP-2/ACS-treated groups.
In dogs that underwent tibial osteotomy, rhBMP-2/ACS (0.2 mg/mL) appeared to accelerate bone healing and reduce lameness (compared with control treatment) and apparently augmented bone healing more than rhBMP-2/ACS (0.4 mg/mL). Compared with control dogs, rhBMP-2/ACS-treated dogs required antimicrobial treatments less frequently.</description><identifier>ISSN: 0002-9645</identifier><identifier>EISSN: 1943-5681</identifier><identifier>DOI: 10.2460/ajvr.68.8.834</identifier><identifier>PMID: 17669023</identifier><language>eng</language><publisher>United States</publisher><subject>absorbable collagen sponges ; animal models ; Animals ; bone fractures ; bone morphogenetic proteins ; Bone Morphogenetic Proteins - administration & dosage ; Bone Morphogenetic Proteins - pharmacology ; Bone Morphogenetic Proteins - therapeutic use ; Collagen ; dogs ; dosage ; Dose-Response Relationship, Drug ; drug therapy ; fracture fixation ; Fracture Healing - drug effects ; Fractures, Bone - drug therapy ; growth factors ; histology ; Humans ; lameness ; pets ; radiography ; Recombinant Proteins ; Surgical Sponges ; tibia ; tissue repair</subject><ispartof>American journal of veterinary research, 2007-08, Vol.68 (8), p.834-840</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c385t-792e47aedb95dd382eb51a010b883fe28b14e6018a665adef7bad231e5df546a3</citedby><cites>FETCH-LOGICAL-c385t-792e47aedb95dd382eb51a010b883fe28b14e6018a665adef7bad231e5df546a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17669023$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schmiedt, C.W</creatorcontrib><creatorcontrib>Lu, Y</creatorcontrib><creatorcontrib>Heaney, K</creatorcontrib><creatorcontrib>Muir, P</creatorcontrib><creatorcontrib>Amodie, D.M</creatorcontrib><creatorcontrib>Markel, M.D</creatorcontrib><title>Comparison of two doses of recombinant human bone morphogenetic protein in absorbable collagen sponges for bone healing in dogs</title><title>American journal of veterinary research</title><addtitle>Am J Vet Res</addtitle><description>To determine the effects of 2 doses of recombinant human bone morphogenetic protein-2 in an absorbable collagen sponge (rhBMP-2/ACS) on bone healing in dogs.
27 adult dogs.
Dogs underwent a mid-diaphyseal (1-mm) tibial osteotomy (stabilized with external skeletal fixation) and received an ACS containing 0.28 mg (0.2 mg/mL) or 0.56 mg (0.4 mg/mL) of rhBMP-2 or no treatment (control dogs). All dogs were examined daily; bone healing was assessed via radiography and subjective lameness evaluation every 2 weeks. After euthanasia at 8 weeks, tibiae were evaluated biomechanically and histologically.
Control dogs required antimicrobial treatment for pin-site-related complications more frequently than did rhBMP-2/ACS-treated dogs. At 4 and 6 weeks, weight bearing was greater in dogs treated with rhBMP-2/ACS (0.2 mg/mL) than in control dogs, albeit not significantly. Compared with control treatment, both doses of rhBMP-2/ACS accelerated osteotomy healing at 4, 6, and 8 weeks, and the 0.2 mg/mL dose enhanced healing at 2 weeks; healing at 6 weeks was greater for the lower-dose treatment than for the higher-dose treatment. Histologically, healing at 8 weeks was significantly improved for both rhBMP-2/ACS treatments, compared with control treatment. Among groups, biomechanical variables did not differ, although less osteotomy-site failures occurred in rhBMP-2/ACS-treated groups.
In dogs that underwent tibial osteotomy, rhBMP-2/ACS (0.2 mg/mL) appeared to accelerate bone healing and reduce lameness (compared with control treatment) and apparently augmented bone healing more than rhBMP-2/ACS (0.4 mg/mL). Compared with control dogs, rhBMP-2/ACS-treated dogs required antimicrobial treatments less frequently.</description><subject>absorbable collagen sponges</subject><subject>animal models</subject><subject>Animals</subject><subject>bone fractures</subject><subject>bone morphogenetic proteins</subject><subject>Bone Morphogenetic Proteins - administration & dosage</subject><subject>Bone Morphogenetic Proteins - pharmacology</subject><subject>Bone Morphogenetic Proteins - therapeutic use</subject><subject>Collagen</subject><subject>dogs</subject><subject>dosage</subject><subject>Dose-Response Relationship, Drug</subject><subject>drug therapy</subject><subject>fracture fixation</subject><subject>Fracture Healing - drug effects</subject><subject>Fractures, Bone - drug therapy</subject><subject>growth factors</subject><subject>histology</subject><subject>Humans</subject><subject>lameness</subject><subject>pets</subject><subject>radiography</subject><subject>Recombinant Proteins</subject><subject>Surgical Sponges</subject><subject>tibia</subject><subject>tissue repair</subject><issn>0002-9645</issn><issn>1943-5681</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1r3DAQhkVpabZJjr22OvXmjT4sWT6WJf2AQA9tzmJkjb0OtuRK3pac-tcrsws9lhkYBp55Z5iXkLec7UWt2R08_Up7bfYlZP2C7Hhby0ppw1-SHWNMVK2u1RV5k_MTY1wYrl6TK95o3TIhd-TPIc4LpDHHQGNP19-R-pgxb03CLs5uDBBWejzNEKiLAekc03KMAwZcx44uKa44BloSXI7JgZuQdnGaoCA0LzEMRa6P6Tx9RJjGMGy8j0O-Ia96mDLeXuo1efx0_-PwpXr49vnr4eND1Umj1qppBdYNoHet8l4agU5xYJw5Y2SPwjheo2bcgNYKPPaNAy8kR-V7VWuQ1-TDWbfc-_OEebXzmDssVwaMp2zLw3jLmPovKLjc_igKWJ3BLsWcE_Z2SeMM6dlyZjdr7GZNEbYlZF34dxfhk5vR_6MvXhTg_RnoIVoYiif28btg276mbZWW8i_Tq5ZY</recordid><startdate>20070801</startdate><enddate>20070801</enddate><creator>Schmiedt, C.W</creator><creator>Lu, Y</creator><creator>Heaney, K</creator><creator>Muir, P</creator><creator>Amodie, D.M</creator><creator>Markel, M.D</creator><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>20070801</creationdate><title>Comparison of two doses of recombinant human bone morphogenetic protein in absorbable collagen sponges for bone healing in dogs</title><author>Schmiedt, C.W ; Lu, Y ; Heaney, K ; Muir, P ; Amodie, D.M ; Markel, M.D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c385t-792e47aedb95dd382eb51a010b883fe28b14e6018a665adef7bad231e5df546a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>absorbable collagen sponges</topic><topic>animal models</topic><topic>Animals</topic><topic>bone fractures</topic><topic>bone morphogenetic proteins</topic><topic>Bone Morphogenetic Proteins - administration & dosage</topic><topic>Bone Morphogenetic Proteins - pharmacology</topic><topic>Bone Morphogenetic Proteins - therapeutic use</topic><topic>Collagen</topic><topic>dogs</topic><topic>dosage</topic><topic>Dose-Response Relationship, Drug</topic><topic>drug therapy</topic><topic>fracture fixation</topic><topic>Fracture Healing - drug effects</topic><topic>Fractures, Bone - drug therapy</topic><topic>growth factors</topic><topic>histology</topic><topic>Humans</topic><topic>lameness</topic><topic>pets</topic><topic>radiography</topic><topic>Recombinant Proteins</topic><topic>Surgical Sponges</topic><topic>tibia</topic><topic>tissue repair</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schmiedt, C.W</creatorcontrib><creatorcontrib>Lu, Y</creatorcontrib><creatorcontrib>Heaney, K</creatorcontrib><creatorcontrib>Muir, P</creatorcontrib><creatorcontrib>Amodie, D.M</creatorcontrib><creatorcontrib>Markel, M.D</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of veterinary research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schmiedt, C.W</au><au>Lu, Y</au><au>Heaney, K</au><au>Muir, P</au><au>Amodie, D.M</au><au>Markel, M.D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison of two doses of recombinant human bone morphogenetic protein in absorbable collagen sponges for bone healing in dogs</atitle><jtitle>American journal of veterinary research</jtitle><addtitle>Am J Vet Res</addtitle><date>2007-08-01</date><risdate>2007</risdate><volume>68</volume><issue>8</issue><spage>834</spage><epage>840</epage><pages>834-840</pages><issn>0002-9645</issn><eissn>1943-5681</eissn><abstract>To determine the effects of 2 doses of recombinant human bone morphogenetic protein-2 in an absorbable collagen sponge (rhBMP-2/ACS) on bone healing in dogs.
27 adult dogs.
Dogs underwent a mid-diaphyseal (1-mm) tibial osteotomy (stabilized with external skeletal fixation) and received an ACS containing 0.28 mg (0.2 mg/mL) or 0.56 mg (0.4 mg/mL) of rhBMP-2 or no treatment (control dogs). All dogs were examined daily; bone healing was assessed via radiography and subjective lameness evaluation every 2 weeks. After euthanasia at 8 weeks, tibiae were evaluated biomechanically and histologically.
Control dogs required antimicrobial treatment for pin-site-related complications more frequently than did rhBMP-2/ACS-treated dogs. At 4 and 6 weeks, weight bearing was greater in dogs treated with rhBMP-2/ACS (0.2 mg/mL) than in control dogs, albeit not significantly. Compared with control treatment, both doses of rhBMP-2/ACS accelerated osteotomy healing at 4, 6, and 8 weeks, and the 0.2 mg/mL dose enhanced healing at 2 weeks; healing at 6 weeks was greater for the lower-dose treatment than for the higher-dose treatment. Histologically, healing at 8 weeks was significantly improved for both rhBMP-2/ACS treatments, compared with control treatment. Among groups, biomechanical variables did not differ, although less osteotomy-site failures occurred in rhBMP-2/ACS-treated groups.
In dogs that underwent tibial osteotomy, rhBMP-2/ACS (0.2 mg/mL) appeared to accelerate bone healing and reduce lameness (compared with control treatment) and apparently augmented bone healing more than rhBMP-2/ACS (0.4 mg/mL). Compared with control dogs, rhBMP-2/ACS-treated dogs required antimicrobial treatments less frequently.</abstract><cop>United States</cop><pmid>17669023</pmid><doi>10.2460/ajvr.68.8.834</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | absorbable collagen sponges animal models Animals bone fractures bone morphogenetic proteins Bone Morphogenetic Proteins - administration & dosage Bone Morphogenetic Proteins - pharmacology Bone Morphogenetic Proteins - therapeutic use Collagen dogs dosage Dose-Response Relationship, Drug drug therapy fracture fixation Fracture Healing - drug effects Fractures, Bone - drug therapy growth factors histology Humans lameness pets radiography Recombinant Proteins Surgical Sponges tibia tissue repair |
title | Comparison of two doses of recombinant human bone morphogenetic protein in absorbable collagen sponges for bone healing in dogs |
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