Vascular anastomosis using controlled phase transitions in poloxamer gels
By exploiting the thermoreversible properties of the US Food and Drug Administration–approved poloxamer 407 (triblock polymer) and 2-octylcyanoacrylate bioadhesive, Edward Chang et al . have developed a new method of sutureless vascular anastomosis, even in vessels with a diameter of less than 1.0 m...
Gespeichert in:
Veröffentlicht in: | Nature medicine 2011-09, Vol.17 (9), p.1147-1152 |
---|---|
Hauptverfasser: | , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1152 |
---|---|
container_issue | 9 |
container_start_page | 1147 |
container_title | Nature medicine |
container_volume | 17 |
creator | Chang, Edward I Galvez, Michael G Glotzbach, Jason P Hamou, Cynthia D El-ftesi, Samyra Rappleye, C Travis Sommer, Kristin-Maria Rajadas, Jayakumar Abilez, Oscar J Fuller, Gerald G Longaker, Michael T Gurtner, Geoffrey C |
description | By exploiting the thermoreversible properties of the US Food and Drug Administration–approved poloxamer 407 (triblock polymer) and 2-octylcyanoacrylate bioadhesive, Edward Chang
et al
. have developed a new method of sutureless vascular anastomosis, even in vessels with a diameter of less than 1.0 mm. This nonmechanical, sutureless approach compared favorably to the standard hand-sewn approach in long-term (two-year) rat studies.
Vascular anastomosis is the cornerstone of vascular, cardiovascular and transplant surgery. Most anastomoses are performed with sutures, which are technically challenging and can lead to failure from intimal hyperplasia and foreign body reaction. Numerous alternatives to sutures have been proposed, but none has proven superior, particularly in small or atherosclerotic vessels. We have developed a new method of sutureless and atraumatic vascular anastomosis that uses US Food and Drug Administration (FDA)-approved thermoreversible tri-block polymers to temporarily maintain an open lumen for precise approximation with commercially available glues. We performed end-to-end anastomoses five times more rapidly than we performed hand-sewn controls, and vessels that were too small ( |
doi_str_mv | 10.1038/nm.2424 |
format | Article |
fullrecord | <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_888337459</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A268310476</galeid><sourcerecordid>A268310476</sourcerecordid><originalsourceid>FETCH-LOGICAL-c610t-2c0c8bc073a329f41360aed05e826341d017293d4eea6ac29dbacc5555cacf383</originalsourceid><addsrcrecordid>eNqN0llr3DAQAGBTWpo0Lf0HxbTQ48FbHT7kxxB6LAQCPULfxKw89irI0lZjQ_rvq-1ujw37UOlBQvo0SKPJsqecLTiT6q0fF6IU5b3slFdlXfCGfbuf5qxRhWqr-iR7RHTDGJOsah9mJ4KrRraqPs2W10BmdhBz8EBTGANZymeyfshN8FMMzmGXb9ZAmE8RPNnJBk-59fkmuHALI8Z8QEePswc9OMIn-_Es-_r-3ZeLj8Xl1YflxfllYWrOpkIYZtTKsEaCFG1fclkzwI5VqEQtS94x3ohWdiUi1GBE263AmCo1A6aXSp5lr3ZxNzF8n5EmPVoy6Bx4DDNppZSUTVm1ST6_I2_CHH26nFZter9gFU_oxQ4N4FBb34f0SrMNqc9FrSRnZVMnVRxRA3qM4ILH3qblA7844lPvcLTm6IE3Bwe2ucfbaYCZSC8_f_p_e3V9aF_-Y9cIblpTcPOvTzyE-7SaGIgi9noT7Qjxh-ZMb2tM-1FvayzJZ_u0zqsRuz_ud1El8HoHKG35AePfvN-N9RPEedUL</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>897392051</pqid></control><display><type>article</type><title>Vascular anastomosis using controlled phase transitions in poloxamer gels</title><source>MEDLINE</source><source>Nature</source><source>Alma/SFX Local Collection</source><creator>Chang, Edward I ; Galvez, Michael G ; Glotzbach, Jason P ; Hamou, Cynthia D ; El-ftesi, Samyra ; Rappleye, C Travis ; Sommer, Kristin-Maria ; Rajadas, Jayakumar ; Abilez, Oscar J ; Fuller, Gerald G ; Longaker, Michael T ; Gurtner, Geoffrey C</creator><creatorcontrib>Chang, Edward I ; Galvez, Michael G ; Glotzbach, Jason P ; Hamou, Cynthia D ; El-ftesi, Samyra ; Rappleye, C Travis ; Sommer, Kristin-Maria ; Rajadas, Jayakumar ; Abilez, Oscar J ; Fuller, Gerald G ; Longaker, Michael T ; Gurtner, Geoffrey C</creatorcontrib><description>By exploiting the thermoreversible properties of the US Food and Drug Administration–approved poloxamer 407 (triblock polymer) and 2-octylcyanoacrylate bioadhesive, Edward Chang
et al
. have developed a new method of sutureless vascular anastomosis, even in vessels with a diameter of less than 1.0 mm. This nonmechanical, sutureless approach compared favorably to the standard hand-sewn approach in long-term (two-year) rat studies.
Vascular anastomosis is the cornerstone of vascular, cardiovascular and transplant surgery. Most anastomoses are performed with sutures, which are technically challenging and can lead to failure from intimal hyperplasia and foreign body reaction. Numerous alternatives to sutures have been proposed, but none has proven superior, particularly in small or atherosclerotic vessels. We have developed a new method of sutureless and atraumatic vascular anastomosis that uses US Food and Drug Administration (FDA)-approved thermoreversible tri-block polymers to temporarily maintain an open lumen for precise approximation with commercially available glues. We performed end-to-end anastomoses five times more rapidly than we performed hand-sewn controls, and vessels that were too small (<1.0 mm) to sew were successfully reconstructed with this sutureless approach. Imaging of reconstructed rat aorta confirmed equivalent patency, flow and burst strength, and histological analysis demonstrated decreased inflammation and fibrosis at up to 2 years after the procedure. This new technology has potential for improving efficiency and outcomes in the surgical treatment of cardiovascular disease.</description><identifier>ISSN: 1078-8956</identifier><identifier>EISSN: 1546-170X</identifier><identifier>DOI: 10.1038/nm.2424</identifier><identifier>PMID: 21873986</identifier><language>eng</language><publisher>New York: Nature Publishing Group US</publisher><subject>639/301/54/990 ; 692/699/75/593 ; 692/700/565/545/576/402 ; Anastomosis ; Anastomosis, Surgical - methods ; Animals ; Aorta - surgery ; Biomedical and Life Sciences ; Biomedical materials ; Biomedicine ; Blood vessels ; Cancer Research ; Cardiovascular diseases ; Care and treatment ; Diagnosis ; Elastic Modulus ; Immunohistochemistry ; Infectious Diseases ; Male ; Metabolic Diseases ; Methods ; Microscopy, Electron, Scanning ; Microvessels - surgery ; Molecular Medicine ; Neurosciences ; Phase Transition ; Phase transitions ; Poloxamer - therapeutic use ; Polymers ; Rats ; Rheology ; Surgery ; Surgical anastomosis ; Surgical techniques ; technical-report</subject><ispartof>Nature medicine, 2011-09, Vol.17 (9), p.1147-1152</ispartof><rights>Springer Nature America, Inc. 2011</rights><rights>COPYRIGHT 2011 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Sep 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c610t-2c0c8bc073a329f41360aed05e826341d017293d4eea6ac29dbacc5555cacf383</citedby><cites>FETCH-LOGICAL-c610t-2c0c8bc073a329f41360aed05e826341d017293d4eea6ac29dbacc5555cacf383</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21873986$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chang, Edward I</creatorcontrib><creatorcontrib>Galvez, Michael G</creatorcontrib><creatorcontrib>Glotzbach, Jason P</creatorcontrib><creatorcontrib>Hamou, Cynthia D</creatorcontrib><creatorcontrib>El-ftesi, Samyra</creatorcontrib><creatorcontrib>Rappleye, C Travis</creatorcontrib><creatorcontrib>Sommer, Kristin-Maria</creatorcontrib><creatorcontrib>Rajadas, Jayakumar</creatorcontrib><creatorcontrib>Abilez, Oscar J</creatorcontrib><creatorcontrib>Fuller, Gerald G</creatorcontrib><creatorcontrib>Longaker, Michael T</creatorcontrib><creatorcontrib>Gurtner, Geoffrey C</creatorcontrib><title>Vascular anastomosis using controlled phase transitions in poloxamer gels</title><title>Nature medicine</title><addtitle>Nat Med</addtitle><addtitle>Nat Med</addtitle><description>By exploiting the thermoreversible properties of the US Food and Drug Administration–approved poloxamer 407 (triblock polymer) and 2-octylcyanoacrylate bioadhesive, Edward Chang
et al
. have developed a new method of sutureless vascular anastomosis, even in vessels with a diameter of less than 1.0 mm. This nonmechanical, sutureless approach compared favorably to the standard hand-sewn approach in long-term (two-year) rat studies.
Vascular anastomosis is the cornerstone of vascular, cardiovascular and transplant surgery. Most anastomoses are performed with sutures, which are technically challenging and can lead to failure from intimal hyperplasia and foreign body reaction. Numerous alternatives to sutures have been proposed, but none has proven superior, particularly in small or atherosclerotic vessels. We have developed a new method of sutureless and atraumatic vascular anastomosis that uses US Food and Drug Administration (FDA)-approved thermoreversible tri-block polymers to temporarily maintain an open lumen for precise approximation with commercially available glues. We performed end-to-end anastomoses five times more rapidly than we performed hand-sewn controls, and vessels that were too small (<1.0 mm) to sew were successfully reconstructed with this sutureless approach. Imaging of reconstructed rat aorta confirmed equivalent patency, flow and burst strength, and histological analysis demonstrated decreased inflammation and fibrosis at up to 2 years after the procedure. This new technology has potential for improving efficiency and outcomes in the surgical treatment of cardiovascular disease.</description><subject>639/301/54/990</subject><subject>692/699/75/593</subject><subject>692/700/565/545/576/402</subject><subject>Anastomosis</subject><subject>Anastomosis, Surgical - methods</subject><subject>Animals</subject><subject>Aorta - surgery</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedical materials</subject><subject>Biomedicine</subject><subject>Blood vessels</subject><subject>Cancer Research</subject><subject>Cardiovascular diseases</subject><subject>Care and treatment</subject><subject>Diagnosis</subject><subject>Elastic Modulus</subject><subject>Immunohistochemistry</subject><subject>Infectious Diseases</subject><subject>Male</subject><subject>Metabolic Diseases</subject><subject>Methods</subject><subject>Microscopy, Electron, Scanning</subject><subject>Microvessels - surgery</subject><subject>Molecular Medicine</subject><subject>Neurosciences</subject><subject>Phase Transition</subject><subject>Phase transitions</subject><subject>Poloxamer - therapeutic use</subject><subject>Polymers</subject><subject>Rats</subject><subject>Rheology</subject><subject>Surgery</subject><subject>Surgical anastomosis</subject><subject>Surgical techniques</subject><subject>technical-report</subject><issn>1078-8956</issn><issn>1546-170X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqN0llr3DAQAGBTWpo0Lf0HxbTQ48FbHT7kxxB6LAQCPULfxKw89irI0lZjQ_rvq-1ujw37UOlBQvo0SKPJsqecLTiT6q0fF6IU5b3slFdlXfCGfbuf5qxRhWqr-iR7RHTDGJOsah9mJ4KrRraqPs2W10BmdhBz8EBTGANZymeyfshN8FMMzmGXb9ZAmE8RPNnJBk-59fkmuHALI8Z8QEePswc9OMIn-_Es-_r-3ZeLj8Xl1YflxfllYWrOpkIYZtTKsEaCFG1fclkzwI5VqEQtS94x3ohWdiUi1GBE263AmCo1A6aXSp5lr3ZxNzF8n5EmPVoy6Bx4DDNppZSUTVm1ST6_I2_CHH26nFZter9gFU_oxQ4N4FBb34f0SrMNqc9FrSRnZVMnVRxRA3qM4ILH3qblA7844lPvcLTm6IE3Bwe2ucfbaYCZSC8_f_p_e3V9aF_-Y9cIblpTcPOvTzyE-7SaGIgi9noT7Qjxh-ZMb2tM-1FvayzJZ_u0zqsRuz_ud1El8HoHKG35AePfvN-N9RPEedUL</recordid><startdate>20110901</startdate><enddate>20110901</enddate><creator>Chang, Edward I</creator><creator>Galvez, Michael G</creator><creator>Glotzbach, Jason P</creator><creator>Hamou, Cynthia D</creator><creator>El-ftesi, Samyra</creator><creator>Rappleye, C Travis</creator><creator>Sommer, Kristin-Maria</creator><creator>Rajadas, Jayakumar</creator><creator>Abilez, Oscar J</creator><creator>Fuller, Gerald G</creator><creator>Longaker, Michael T</creator><creator>Gurtner, Geoffrey C</creator><general>Nature Publishing Group US</general><general>Nature Publishing Group</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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20110901</creationdate><title>Vascular anastomosis using controlled phase transitions in poloxamer gels</title><author>Chang, Edward I ; Galvez, Michael G ; Glotzbach, Jason P ; Hamou, Cynthia D ; El-ftesi, Samyra ; Rappleye, C Travis ; Sommer, Kristin-Maria ; Rajadas, Jayakumar ; Abilez, Oscar J ; Fuller, Gerald G ; Longaker, Michael T ; Gurtner, Geoffrey C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c610t-2c0c8bc073a329f41360aed05e826341d017293d4eea6ac29dbacc5555cacf383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>639/301/54/990</topic><topic>692/699/75/593</topic><topic>692/700/565/545/576/402</topic><topic>Anastomosis</topic><topic>Anastomosis, Surgical - methods</topic><topic>Animals</topic><topic>Aorta - surgery</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedical materials</topic><topic>Biomedicine</topic><topic>Blood vessels</topic><topic>Cancer Research</topic><topic>Cardiovascular diseases</topic><topic>Care and treatment</topic><topic>Diagnosis</topic><topic>Elastic Modulus</topic><topic>Immunohistochemistry</topic><topic>Infectious Diseases</topic><topic>Male</topic><topic>Metabolic Diseases</topic><topic>Methods</topic><topic>Microscopy, Electron, Scanning</topic><topic>Microvessels - surgery</topic><topic>Molecular Medicine</topic><topic>Neurosciences</topic><topic>Phase Transition</topic><topic>Phase transitions</topic><topic>Poloxamer - therapeutic use</topic><topic>Polymers</topic><topic>Rats</topic><topic>Rheology</topic><topic>Surgery</topic><topic>Surgical anastomosis</topic><topic>Surgical techniques</topic><topic>technical-report</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chang, Edward I</creatorcontrib><creatorcontrib>Galvez, Michael G</creatorcontrib><creatorcontrib>Glotzbach, Jason P</creatorcontrib><creatorcontrib>Hamou, Cynthia D</creatorcontrib><creatorcontrib>El-ftesi, Samyra</creatorcontrib><creatorcontrib>Rappleye, C Travis</creatorcontrib><creatorcontrib>Sommer, Kristin-Maria</creatorcontrib><creatorcontrib>Rajadas, Jayakumar</creatorcontrib><creatorcontrib>Abilez, Oscar J</creatorcontrib><creatorcontrib>Fuller, Gerald G</creatorcontrib><creatorcontrib>Longaker, Michael T</creatorcontrib><creatorcontrib>Gurtner, Geoffrey C</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection (ProQuest)</collection><collection>Environmental Sciences and Pollution Management</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 Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Science Database (ProQuest)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Biotechnology and BioEngineering Abstracts</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 Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Nature medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chang, Edward I</au><au>Galvez, Michael G</au><au>Glotzbach, Jason P</au><au>Hamou, Cynthia D</au><au>El-ftesi, Samyra</au><au>Rappleye, C Travis</au><au>Sommer, Kristin-Maria</au><au>Rajadas, Jayakumar</au><au>Abilez, Oscar J</au><au>Fuller, Gerald G</au><au>Longaker, Michael T</au><au>Gurtner, Geoffrey C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Vascular anastomosis using controlled phase transitions in poloxamer gels</atitle><jtitle>Nature medicine</jtitle><stitle>Nat Med</stitle><addtitle>Nat Med</addtitle><date>2011-09-01</date><risdate>2011</risdate><volume>17</volume><issue>9</issue><spage>1147</spage><epage>1152</epage><pages>1147-1152</pages><issn>1078-8956</issn><eissn>1546-170X</eissn><abstract>By exploiting the thermoreversible properties of the US Food and Drug Administration–approved poloxamer 407 (triblock polymer) and 2-octylcyanoacrylate bioadhesive, Edward Chang
et al
. have developed a new method of sutureless vascular anastomosis, even in vessels with a diameter of less than 1.0 mm. This nonmechanical, sutureless approach compared favorably to the standard hand-sewn approach in long-term (two-year) rat studies.
Vascular anastomosis is the cornerstone of vascular, cardiovascular and transplant surgery. Most anastomoses are performed with sutures, which are technically challenging and can lead to failure from intimal hyperplasia and foreign body reaction. Numerous alternatives to sutures have been proposed, but none has proven superior, particularly in small or atherosclerotic vessels. We have developed a new method of sutureless and atraumatic vascular anastomosis that uses US Food and Drug Administration (FDA)-approved thermoreversible tri-block polymers to temporarily maintain an open lumen for precise approximation with commercially available glues. We performed end-to-end anastomoses five times more rapidly than we performed hand-sewn controls, and vessels that were too small (<1.0 mm) to sew were successfully reconstructed with this sutureless approach. Imaging of reconstructed rat aorta confirmed equivalent patency, flow and burst strength, and histological analysis demonstrated decreased inflammation and fibrosis at up to 2 years after the procedure. This new technology has potential for improving efficiency and outcomes in the surgical treatment of cardiovascular disease.</abstract><cop>New York</cop><pub>Nature Publishing Group US</pub><pmid>21873986</pmid><doi>10.1038/nm.2424</doi><tpages>6</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1078-8956 |
ispartof | Nature medicine, 2011-09, Vol.17 (9), p.1147-1152 |
issn | 1078-8956 1546-170X |
language | eng |
recordid | cdi_proquest_miscellaneous_888337459 |
source | MEDLINE; Nature; Alma/SFX Local Collection |
subjects | 639/301/54/990 692/699/75/593 692/700/565/545/576/402 Anastomosis Anastomosis, Surgical - methods Animals Aorta - surgery Biomedical and Life Sciences Biomedical materials Biomedicine Blood vessels Cancer Research Cardiovascular diseases Care and treatment Diagnosis Elastic Modulus Immunohistochemistry Infectious Diseases Male Metabolic Diseases Methods Microscopy, Electron, Scanning Microvessels - surgery Molecular Medicine Neurosciences Phase Transition Phase transitions Poloxamer - therapeutic use Polymers Rats Rheology Surgery Surgical anastomosis Surgical techniques technical-report |
title | Vascular anastomosis using controlled phase transitions in poloxamer gels |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-11T08%3A45%3A18IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Vascular%20anastomosis%20using%20controlled%20phase%20transitions%20in%20poloxamer%20gels&rft.jtitle=Nature%20medicine&rft.au=Chang,%20Edward%20I&rft.date=2011-09-01&rft.volume=17&rft.issue=9&rft.spage=1147&rft.epage=1152&rft.pages=1147-1152&rft.issn=1078-8956&rft.eissn=1546-170X&rft_id=info:doi/10.1038/nm.2424&rft_dat=%3Cgale_proqu%3EA268310476%3C/gale_proqu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=897392051&rft_id=info:pmid/21873986&rft_galeid=A268310476&rfr_iscdi=true |