Prevention of heterotopic ossification: an experimental study using a plasma expander in a murine model
Heterotopic ossification (HO) is a frequent complication following orthopedic and trauma surgery. It often leads to substantial morbidity as many affected patients suffer from pain and joint contractures. Current prophylactic measures include nonsteroidal anti-inflammatory drugs (NSAID) and local ra...
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description | Heterotopic ossification (HO) is a frequent complication following orthopedic and trauma surgery. It often leads to substantial morbidity as many affected patients suffer from pain and joint contractures. Current prophylactic measures include nonsteroidal anti-inflammatory drugs (NSAID) and local radiation. However, several disadvantages such as delayed fracture healing and impaired ossification have been reported. For this reason, a novel approach for prevention of HO was searched for. We hypothesized that systemic administration of hydroxyethyl starch (HES), a substance known to influence microcirculation, would reduce formation of HO in a murine model.
A pre-established murine model was used where HO has been shown to develop following Achilles tendon tenotomy. Twenty CD1 mice were randomly assigned to a control (n = 10) or treatment group (n = 10). The treatment group received two intravenous HES injections perioperatively, while the control group underwent tenotomy only. After ten weeks, the mice were euthanized and micro CT scans of the hind limbs were performed. HO was manually identified and quantitatively assessed. A Wilcoxon rank sum test was used for comparison of both groups.
The mean heterotopic bone volume in the control group was significantly larger compared to the HES group (2.276 mm(3) vs. 0.271 mm(3), p = 0.005). A reduction of mean ectopic bone volume of 88 % was found following administration of HES.
A substantial reduction of HO formation was found following perioperative short-term administration of HES. This work represents a preliminary study, necessitating further studies before drawing ultimate conclusions. However, this simple addition to current prophylactic measures might lead to a more effective prevention of HO in the future. |
doi_str_mv | 10.1186/s12893-016-0144-3 |
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A pre-established murine model was used where HO has been shown to develop following Achilles tendon tenotomy. Twenty CD1 mice were randomly assigned to a control (n = 10) or treatment group (n = 10). The treatment group received two intravenous HES injections perioperatively, while the control group underwent tenotomy only. After ten weeks, the mice were euthanized and micro CT scans of the hind limbs were performed. HO was manually identified and quantitatively assessed. A Wilcoxon rank sum test was used for comparison of both groups.
The mean heterotopic bone volume in the control group was significantly larger compared to the HES group (2.276 mm(3) vs. 0.271 mm(3), p = 0.005). A reduction of mean ectopic bone volume of 88 % was found following administration of HES.
A substantial reduction of HO formation was found following perioperative short-term administration of HES. This work represents a preliminary study, necessitating further studies before drawing ultimate conclusions. However, this simple addition to current prophylactic measures might lead to a more effective prevention of HO in the future.</description><identifier>ISSN: 1471-2482</identifier><identifier>EISSN: 1471-2482</identifier><identifier>DOI: 10.1186/s12893-016-0144-3</identifier><identifier>PMID: 27145776</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Achilles Tendon - surgery ; Animals ; Complications and side effects ; Disease Models, Animal ; Dislocations ; Hydroxyethyl Starch Derivatives - therapeutic use ; Male ; Mice ; Ossification ; Ossification, Heterotopic - etiology ; Ossification, Heterotopic - prevention & control ; Plasma Substitutes - therapeutic use ; Prevention ; Random Allocation ; Risk factors ; Tenotomy - adverse effects ; Tomography, X-Ray Computed</subject><ispartof>BMC surgery, 2016-05, Vol.16 (1), p.29-29, Article 29</ispartof><rights>COPYRIGHT 2016 BioMed Central Ltd.</rights><rights>Copyright BioMed Central 2016</rights><rights>Zimmermann et al. 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c494t-c0a009382adc70ae84092017b722783239b26a0f4fda0e7a092a0fa1295e2bfe3</citedby><cites>FETCH-LOGICAL-c494t-c0a009382adc70ae84092017b722783239b26a0f4fda0e7a092a0fa1295e2bfe3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4857383/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4857383/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27145776$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zimmermann, Stefan M</creatorcontrib><creatorcontrib>Schwitter, Lukas W</creatorcontrib><creatorcontrib>Scheyerer, Max J</creatorcontrib><creatorcontrib>Jentzsch, Thorsten</creatorcontrib><creatorcontrib>Simmen, Hans-Peter</creatorcontrib><creatorcontrib>Werner, Clément M L</creatorcontrib><title>Prevention of heterotopic ossification: an experimental study using a plasma expander in a murine model</title><title>BMC surgery</title><addtitle>BMC Surg</addtitle><description>Heterotopic ossification (HO) is a frequent complication following orthopedic and trauma surgery. It often leads to substantial morbidity as many affected patients suffer from pain and joint contractures. Current prophylactic measures include nonsteroidal anti-inflammatory drugs (NSAID) and local radiation. However, several disadvantages such as delayed fracture healing and impaired ossification have been reported. For this reason, a novel approach for prevention of HO was searched for. We hypothesized that systemic administration of hydroxyethyl starch (HES), a substance known to influence microcirculation, would reduce formation of HO in a murine model.
A pre-established murine model was used where HO has been shown to develop following Achilles tendon tenotomy. Twenty CD1 mice were randomly assigned to a control (n = 10) or treatment group (n = 10). The treatment group received two intravenous HES injections perioperatively, while the control group underwent tenotomy only. After ten weeks, the mice were euthanized and micro CT scans of the hind limbs were performed. HO was manually identified and quantitatively assessed. A Wilcoxon rank sum test was used for comparison of both groups.
The mean heterotopic bone volume in the control group was significantly larger compared to the HES group (2.276 mm(3) vs. 0.271 mm(3), p = 0.005). A reduction of mean ectopic bone volume of 88 % was found following administration of HES.
A substantial reduction of HO formation was found following perioperative short-term administration of HES. This work represents a preliminary study, necessitating further studies before drawing ultimate conclusions. However, this simple addition to current prophylactic measures might lead to a more effective prevention of HO in the future.</description><subject>Achilles Tendon - surgery</subject><subject>Animals</subject><subject>Complications and side effects</subject><subject>Disease Models, Animal</subject><subject>Dislocations</subject><subject>Hydroxyethyl Starch Derivatives - therapeutic use</subject><subject>Male</subject><subject>Mice</subject><subject>Ossification</subject><subject>Ossification, Heterotopic - etiology</subject><subject>Ossification, Heterotopic - prevention & control</subject><subject>Plasma Substitutes - therapeutic use</subject><subject>Prevention</subject><subject>Random Allocation</subject><subject>Risk factors</subject><subject>Tenotomy - adverse effects</subject><subject>Tomography, X-Ray Computed</subject><issn>1471-2482</issn><issn>1471-2482</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNptkstu1TAQhiMEoqXwAGyQJTZsUnxL7LBAqipuUiVYwNqa40xOXSV2sJOKvj0TnVJahCzL9sw34xn7r6qXgp8KYdu3RUjbqZqLlqbWtXpUHQttRC21lY_v7Y-qZ6VccS6MbZqn1ZE0QjfGtMfV_lvGa4xLSJGlgV3igjktaQ6epVLCEDxsvncMIsNfM-YwEQ0jK8va37C1hLhnwOYRygQbAbHHzEIk47TmEJFNqcfxefVkgLHgi9v1pPrx8cP388_1xddPX87PLmqvO73UngPnnbISem84oNW8k1T2zkhprJKq28kW-KCHHjgaIC-dQMiuQbkbUJ1U7w9553U3Ye-p2Ayjm6luyDcuQXAPPTFcun26dto2RllFCd7cJsjp54plcVMoHscRIqa1OHpCo43uuCX09T_oVVpzpPaI6oxWWsrmL7WHEV2IQ6J7_ZbUnelGaMW5bIk6_Q9Fo8cp-BRxCGR_ECAOAT7TR2Uc7noU3G3qcAd1OFKH29Thtt5e3X-cu4g_clC_AYAHtUE</recordid><startdate>20160504</startdate><enddate>20160504</enddate><creator>Zimmermann, Stefan M</creator><creator>Schwitter, Lukas W</creator><creator>Scheyerer, Max J</creator><creator>Jentzsch, Thorsten</creator><creator>Simmen, Hans-Peter</creator><creator>Werner, Clément M L</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><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>3V.</scope><scope>7QO</scope><scope>7QP</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160504</creationdate><title>Prevention of heterotopic ossification: an experimental study using a plasma expander in a murine model</title><author>Zimmermann, Stefan M ; Schwitter, Lukas W ; Scheyerer, Max J ; Jentzsch, Thorsten ; Simmen, Hans-Peter ; Werner, Clément M L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c494t-c0a009382adc70ae84092017b722783239b26a0f4fda0e7a092a0fa1295e2bfe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Achilles Tendon - surgery</topic><topic>Animals</topic><topic>Complications and side effects</topic><topic>Disease Models, Animal</topic><topic>Dislocations</topic><topic>Hydroxyethyl Starch Derivatives - therapeutic use</topic><topic>Male</topic><topic>Mice</topic><topic>Ossification</topic><topic>Ossification, Heterotopic - etiology</topic><topic>Ossification, Heterotopic - prevention & control</topic><topic>Plasma Substitutes - therapeutic use</topic><topic>Prevention</topic><topic>Random Allocation</topic><topic>Risk factors</topic><topic>Tenotomy - adverse effects</topic><topic>Tomography, X-Ray Computed</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zimmermann, Stefan M</creatorcontrib><creatorcontrib>Schwitter, Lukas W</creatorcontrib><creatorcontrib>Scheyerer, Max J</creatorcontrib><creatorcontrib>Jentzsch, Thorsten</creatorcontrib><creatorcontrib>Simmen, Hans-Peter</creatorcontrib><creatorcontrib>Werner, Clément M L</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 Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BMC surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zimmermann, Stefan M</au><au>Schwitter, Lukas W</au><au>Scheyerer, Max J</au><au>Jentzsch, Thorsten</au><au>Simmen, Hans-Peter</au><au>Werner, Clément M L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prevention of heterotopic ossification: an experimental study using a plasma expander in a murine model</atitle><jtitle>BMC surgery</jtitle><addtitle>BMC Surg</addtitle><date>2016-05-04</date><risdate>2016</risdate><volume>16</volume><issue>1</issue><spage>29</spage><epage>29</epage><pages>29-29</pages><artnum>29</artnum><issn>1471-2482</issn><eissn>1471-2482</eissn><abstract>Heterotopic ossification (HO) is a frequent complication following orthopedic and trauma surgery. It often leads to substantial morbidity as many affected patients suffer from pain and joint contractures. Current prophylactic measures include nonsteroidal anti-inflammatory drugs (NSAID) and local radiation. However, several disadvantages such as delayed fracture healing and impaired ossification have been reported. For this reason, a novel approach for prevention of HO was searched for. We hypothesized that systemic administration of hydroxyethyl starch (HES), a substance known to influence microcirculation, would reduce formation of HO in a murine model.
A pre-established murine model was used where HO has been shown to develop following Achilles tendon tenotomy. Twenty CD1 mice were randomly assigned to a control (n = 10) or treatment group (n = 10). The treatment group received two intravenous HES injections perioperatively, while the control group underwent tenotomy only. After ten weeks, the mice were euthanized and micro CT scans of the hind limbs were performed. HO was manually identified and quantitatively assessed. A Wilcoxon rank sum test was used for comparison of both groups.
The mean heterotopic bone volume in the control group was significantly larger compared to the HES group (2.276 mm(3) vs. 0.271 mm(3), p = 0.005). A reduction of mean ectopic bone volume of 88 % was found following administration of HES.
A substantial reduction of HO formation was found following perioperative short-term administration of HES. This work represents a preliminary study, necessitating further studies before drawing ultimate conclusions. However, this simple addition to current prophylactic measures might lead to a more effective prevention of HO in the future.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>27145776</pmid><doi>10.1186/s12893-016-0144-3</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Achilles Tendon - surgery Animals Complications and side effects Disease Models, Animal Dislocations Hydroxyethyl Starch Derivatives - therapeutic use Male Mice Ossification Ossification, Heterotopic - etiology Ossification, Heterotopic - prevention & control Plasma Substitutes - therapeutic use Prevention Random Allocation Risk factors Tenotomy - adverse effects Tomography, X-Ray Computed |
title | Prevention of heterotopic ossification: an experimental study using a plasma expander in a murine model |
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