Liver transplantation for biliary atresia:A single-center study from mainland China
AIM: To summarize our single-center experience with liver transplantation(LT) for biliary atresia(BA).METHODS: From October 2006 to December 2012, 188 children with BA were analyzed retrospectively. The stage?Ⅰ?group(from October 2006 to December 2010) comprised the first 74 patients, and the stage...
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description | AIM: To summarize our single-center experience with liver transplantation(LT) for biliary atresia(BA).METHODS: From October 2006 to December 2012, 188 children with BA were analyzed retrospectively. The stage?Ⅰ?group(from October 2006 to December 2010) comprised the first 74 patients, and the stage Ⅱ group(from January 2011 to December 2012) comprised the remaining 114 patients. Finally, 123 liver transplants were performed in 122(64.9%) patients, whereas 66 patients did not undergo LT due to denial by their parents or lack of suitable liver grafts. The selection of graft types depended on the patients’ clinical status and whether a suitable living donor was available. The characteristics of patients in stages?Ⅰ?and Ⅱ were described, and the surgical outcomes of LT recipients were compared between the two stages. The KaplanMeier method was used to estimate the cumulative patient and graft survival rates, and the equality of survival distributions was evaluated using the log-rank test.RESULTS: The 188 children consisted of 102 boysand 86 girls. Their ages ranged from 3 to 144 mo with a median of 8 mo. One hundred and fifteen(61.2%) patients were born in rural areas. Comparing stage?Ⅰ?and stage Ⅱ patients, the proportion of patients referred by pediatricians(43.2% vs 71.1%, respectively; P < 0.001) and the proportion of patients who previously received a Kasai procedure(KP)(32.4% vs 44.7%, respectively; P = 0.092) obviously increased, and significantly more parents were willing to treat their children with LT(73% vs 86%, respectively; P = 0.027). Grafts from living donors(102/122, 83.6%) were the most commonly used graft type. Surgical complications(16/25, 64.0%) were the main reason for posttransplant mortality. Among the living donor liver transplantation recipients(n = 102), the incidence of surgical complications was significantly reduced(34.1% vs 15.5%, respectively; P = 0.029) and survival rates of patients and grafts were greatly improved(81.8% vs 89.7%, respectively, at 1 year; 75.0% vs 87.8%, respectively, at 3 years; P = 0.107) from stage?Ⅰ?to stage Ⅱ.CONCLUSION: The status of surgical treatments for BA has been changing in mainland China. Favorable midterm outcomes after LT were achieved as centers gained greater technical experience. |
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fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4548125</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><cqvip_id>90888889504849535150485049</cqvip_id><sourcerecordid>1709393047</sourcerecordid><originalsourceid>FETCH-LOGICAL-c440t-86383181a1902dc96618b7b7a0edd00ab8e13f89228d6d37449dcb3c7b2d7dcd3</originalsourceid><addsrcrecordid>eNpVUU1P4zAUtBCrpcDeOaEcuaQ8fyS2OSChavmQKu1hl7PlxE5rlNjFTov49-uIUoEly0_2zHjeG4QuMMwpZ-L67WU13xE8d5TMZU3FEZoRgmVJBINjNMMAvJSU8BN0mtILAKG0Ij_RCanzJedkhv4u3c7GYozap02v_ahHF3zRhVg0rnc6vhd6jDY5fXNXJOdXvS1b68fMSePWvBddDEMxaOcz2RSLtfP6HP3odJ_sr_15hp7vf_9bPJbLPw9Pi7tl2TIGYymyYYoF1lgCMa2saywa3nAN1hgA3QiLaSckIcLUJvfLpGkb2vKGGG5aQ8_Q7YfuZtsM1ky2ou7VJroh-1ZBO_X9xbu1WoWdYhUTmFRZ4GovEMPr1qZRDS61ts-t2LBNCnOQVFJgPEPhA9rGkFK03eEbDGrKQuUsVM5C5SzUlEWmXH61dyB8Dj8D6F5zHfzqNQ_3gJEgpiUrYILJilZ4qvKW9D-bJJdk</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1709393047</pqid></control><display><type>article</type><title>Liver transplantation for biliary atresia:A single-center study from mainland China</title><source>Open Access: PubMed Central</source><source>MEDLINE</source><source>Baishideng "World Journal of" online journals</source><source>Alma/SFX Local Collection</source><source>EZB Electronic Journals Library</source><creator>Li, Qi-Gen ; Wan, Ping ; Zhang, Jian-Jun ; Chen, Qi-Min ; Chen, Xiao-Song ; Han, Long-Zhi ; Xia, Qiang</creator><creatorcontrib>Li, Qi-Gen ; Wan, Ping ; Zhang, Jian-Jun ; Chen, Qi-Min ; Chen, Xiao-Song ; Han, Long-Zhi ; Xia, Qiang</creatorcontrib><description>AIM: To summarize our single-center experience with liver transplantation(LT) for biliary atresia(BA).METHODS: From October 2006 to December 2012, 188 children with BA were analyzed retrospectively. The stage?Ⅰ?group(from October 2006 to December 2010) comprised the first 74 patients, and the stage Ⅱ group(from January 2011 to December 2012) comprised the remaining 114 patients. Finally, 123 liver transplants were performed in 122(64.9%) patients, whereas 66 patients did not undergo LT due to denial by their parents or lack of suitable liver grafts. The selection of graft types depended on the patients’ clinical status and whether a suitable living donor was available. The characteristics of patients in stages?Ⅰ?and Ⅱ were described, and the surgical outcomes of LT recipients were compared between the two stages. The KaplanMeier method was used to estimate the cumulative patient and graft survival rates, and the equality of survival distributions was evaluated using the log-rank test.RESULTS: The 188 children consisted of 102 boysand 86 girls. Their ages ranged from 3 to 144 mo with a median of 8 mo. One hundred and fifteen(61.2%) patients were born in rural areas. Comparing stage?Ⅰ?and stage Ⅱ patients, the proportion of patients referred by pediatricians(43.2% vs 71.1%, respectively; P &lt; 0.001) and the proportion of patients who previously received a Kasai procedure(KP)(32.4% vs 44.7%, respectively; P = 0.092) obviously increased, and significantly more parents were willing to treat their children with LT(73% vs 86%, respectively; P = 0.027). Grafts from living donors(102/122, 83.6%) were the most commonly used graft type. Surgical complications(16/25, 64.0%) were the main reason for posttransplant mortality. Among the living donor liver transplantation recipients(n = 102), the incidence of surgical complications was significantly reduced(34.1% vs 15.5%, respectively; P = 0.029) and survival rates of patients and grafts were greatly improved(81.8% vs 89.7%, respectively, at 1 year; 75.0% vs 87.8%, respectively, at 3 years; P = 0.107) from stage?Ⅰ?to stage Ⅱ.CONCLUSION: The status of surgical treatments for BA has been changing in mainland China. Favorable midterm outcomes after LT were achieved as centers gained greater technical experience.</description><identifier>ISSN: 1007-9327</identifier><identifier>EISSN: 2219-2840</identifier><identifier>DOI: 10.3748/wjg.v21.i32.9638</identifier><identifier>PMID: 26327772</identifier><language>eng</language><publisher>United States: Baishideng Publishing Group Inc</publisher><subject>atresia;Liver ; Biliary ; Biliary Atresia - diagnosis ; Biliary Atresia - mortality ; Biliary Atresia - surgery ; Child ; Child, Preschool ; China ; Databases, Factual ; Female ; Graft Survival ; Health Services Accessibility ; Humans ; Infant ; Kaplan-Meier Estimate ; Liver Transplantation - adverse effects ; Liver Transplantation - methods ; Liver Transplantation - mortality ; Living Donors - supply & distribution ; Male ; Observational Study ; Postoperative Complications - etiology ; Retrospective Studies ; Risk Factors ; Time Factors ; transplantation;Kasai;Living ; Treatment Outcome</subject><ispartof>World journal of gastroenterology : WJG, 2015-08, Vol.21 (32), p.9638-9647</ispartof><rights>The Author(s) 2015. Published by Baishideng Publishing Group Inc. All rights reserved. 2015</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c440t-86383181a1902dc96618b7b7a0edd00ab8e13f89228d6d37449dcb3c7b2d7dcd3</citedby><cites>FETCH-LOGICAL-c440t-86383181a1902dc96618b7b7a0edd00ab8e13f89228d6d37449dcb3c7b2d7dcd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/84123X/84123X.jpg</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4548125/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4548125/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26327772$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Qi-Gen</creatorcontrib><creatorcontrib>Wan, Ping</creatorcontrib><creatorcontrib>Zhang, Jian-Jun</creatorcontrib><creatorcontrib>Chen, Qi-Min</creatorcontrib><creatorcontrib>Chen, Xiao-Song</creatorcontrib><creatorcontrib>Han, Long-Zhi</creatorcontrib><creatorcontrib>Xia, Qiang</creatorcontrib><title>Liver transplantation for biliary atresia:A single-center study from mainland China</title><title>World journal of gastroenterology : WJG</title><addtitle>World Journal of Gastroenterology</addtitle><description>AIM: To summarize our single-center experience with liver transplantation(LT) for biliary atresia(BA).METHODS: From October 2006 to December 2012, 188 children with BA were analyzed retrospectively. The stage?Ⅰ?group(from October 2006 to December 2010) comprised the first 74 patients, and the stage Ⅱ group(from January 2011 to December 2012) comprised the remaining 114 patients. Finally, 123 liver transplants were performed in 122(64.9%) patients, whereas 66 patients did not undergo LT due to denial by their parents or lack of suitable liver grafts. The selection of graft types depended on the patients’ clinical status and whether a suitable living donor was available. The characteristics of patients in stages?Ⅰ?and Ⅱ were described, and the surgical outcomes of LT recipients were compared between the two stages. The KaplanMeier method was used to estimate the cumulative patient and graft survival rates, and the equality of survival distributions was evaluated using the log-rank test.RESULTS: The 188 children consisted of 102 boysand 86 girls. Their ages ranged from 3 to 144 mo with a median of 8 mo. One hundred and fifteen(61.2%) patients were born in rural areas. Comparing stage?Ⅰ?and stage Ⅱ patients, the proportion of patients referred by pediatricians(43.2% vs 71.1%, respectively; P &lt; 0.001) and the proportion of patients who previously received a Kasai procedure(KP)(32.4% vs 44.7%, respectively; P = 0.092) obviously increased, and significantly more parents were willing to treat their children with LT(73% vs 86%, respectively; P = 0.027). Grafts from living donors(102/122, 83.6%) were the most commonly used graft type. Surgical complications(16/25, 64.0%) were the main reason for posttransplant mortality. Among the living donor liver transplantation recipients(n = 102), the incidence of surgical complications was significantly reduced(34.1% vs 15.5%, respectively; P = 0.029) and survival rates of patients and grafts were greatly improved(81.8% vs 89.7%, respectively, at 1 year; 75.0% vs 87.8%, respectively, at 3 years; P = 0.107) from stage?Ⅰ?to stage Ⅱ.CONCLUSION: The status of surgical treatments for BA has been changing in mainland China. Favorable midterm outcomes after LT were achieved as centers gained greater technical experience.</description><subject>atresia;Liver</subject><subject>Biliary</subject><subject>Biliary Atresia - diagnosis</subject><subject>Biliary Atresia - mortality</subject><subject>Biliary Atresia - surgery</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>China</subject><subject>Databases, Factual</subject><subject>Female</subject><subject>Graft Survival</subject><subject>Health Services Accessibility</subject><subject>Humans</subject><subject>Infant</subject><subject>Kaplan-Meier Estimate</subject><subject>Liver Transplantation - adverse effects</subject><subject>Liver Transplantation - methods</subject><subject>Liver Transplantation - mortality</subject><subject>Living Donors - supply & distribution</subject><subject>Male</subject><subject>Observational Study</subject><subject>Postoperative Complications - etiology</subject><subject>Retrospective Studies</subject><subject>Risk Factors</subject><subject>Time Factors</subject><subject>transplantation;Kasai;Living</subject><subject>Treatment Outcome</subject><issn>1007-9327</issn><issn>2219-2840</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUU1P4zAUtBCrpcDeOaEcuaQ8fyS2OSChavmQKu1hl7PlxE5rlNjFTov49-uIUoEly0_2zHjeG4QuMMwpZ-L67WU13xE8d5TMZU3FEZoRgmVJBINjNMMAvJSU8BN0mtILAKG0Ij_RCanzJedkhv4u3c7GYozap02v_ahHF3zRhVg0rnc6vhd6jDY5fXNXJOdXvS1b68fMSePWvBddDEMxaOcz2RSLtfP6HP3odJ_sr_15hp7vf_9bPJbLPw9Pi7tl2TIGYymyYYoF1lgCMa2saywa3nAN1hgA3QiLaSckIcLUJvfLpGkb2vKGGG5aQ8_Q7YfuZtsM1ky2ou7VJroh-1ZBO_X9xbu1WoWdYhUTmFRZ4GovEMPr1qZRDS61ts-t2LBNCnOQVFJgPEPhA9rGkFK03eEbDGrKQuUsVM5C5SzUlEWmXH61dyB8Dj8D6F5zHfzqNQ_3gJEgpiUrYILJilZ4qvKW9D-bJJdk</recordid><startdate>20150828</startdate><enddate>20150828</enddate><creator>Li, Qi-Gen</creator><creator>Wan, Ping</creator><creator>Zhang, Jian-Jun</creator><creator>Chen, Qi-Min</creator><creator>Chen, Xiao-Song</creator><creator>Han, Long-Zhi</creator><creator>Xia, Qiang</creator><general>Baishideng Publishing Group Inc</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20150828</creationdate><title>Liver transplantation for biliary atresia:A single-center study from mainland China</title><author>Li, Qi-Gen ; Wan, Ping ; Zhang, Jian-Jun ; Chen, Qi-Min ; Chen, Xiao-Song ; Han, Long-Zhi ; Xia, Qiang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c440t-86383181a1902dc96618b7b7a0edd00ab8e13f89228d6d37449dcb3c7b2d7dcd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>atresia;Liver</topic><topic>Biliary</topic><topic>Biliary Atresia - diagnosis</topic><topic>Biliary Atresia - mortality</topic><topic>Biliary Atresia - surgery</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>China</topic><topic>Databases, Factual</topic><topic>Female</topic><topic>Graft Survival</topic><topic>Health Services Accessibility</topic><topic>Humans</topic><topic>Infant</topic><topic>Kaplan-Meier Estimate</topic><topic>Liver Transplantation - adverse effects</topic><topic>Liver Transplantation - methods</topic><topic>Liver Transplantation - mortality</topic><topic>Living Donors - supply & distribution</topic><topic>Male</topic><topic>Observational Study</topic><topic>Postoperative Complications - etiology</topic><topic>Retrospective Studies</topic><topic>Risk Factors</topic><topic>Time Factors</topic><topic>transplantation;Kasai;Living</topic><topic>Treatment Outcome</topic><toplevel>online_resources</toplevel><creatorcontrib>Li, Qi-Gen</creatorcontrib><creatorcontrib>Wan, Ping</creatorcontrib><creatorcontrib>Zhang, Jian-Jun</creatorcontrib><creatorcontrib>Chen, Qi-Min</creatorcontrib><creatorcontrib>Chen, Xiao-Song</creatorcontrib><creatorcontrib>Han, Long-Zhi</creatorcontrib><creatorcontrib>Xia, Qiang</creatorcontrib><collection>维普_期刊</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-医药卫生</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>World journal of gastroenterology : WJG</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Qi-Gen</au><au>Wan, Ping</au><au>Zhang, Jian-Jun</au><au>Chen, Qi-Min</au><au>Chen, Xiao-Song</au><au>Han, Long-Zhi</au><au>Xia, Qiang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Liver transplantation for biliary atresia:A single-center study from mainland China</atitle><jtitle>World journal of gastroenterology : WJG</jtitle><addtitle>World Journal of Gastroenterology</addtitle><date>2015-08-28</date><risdate>2015</risdate><volume>21</volume><issue>32</issue><spage>9638</spage><epage>9647</epage><pages>9638-9647</pages><issn>1007-9327</issn><eissn>2219-2840</eissn><abstract>AIM: To summarize our single-center experience with liver transplantation(LT) for biliary atresia(BA).METHODS: From October 2006 to December 2012, 188 children with BA were analyzed retrospectively. The stage?Ⅰ?group(from October 2006 to December 2010) comprised the first 74 patients, and the stage Ⅱ group(from January 2011 to December 2012) comprised the remaining 114 patients. Finally, 123 liver transplants were performed in 122(64.9%) patients, whereas 66 patients did not undergo LT due to denial by their parents or lack of suitable liver grafts. The selection of graft types depended on the patients’ clinical status and whether a suitable living donor was available. The characteristics of patients in stages?Ⅰ?and Ⅱ were described, and the surgical outcomes of LT recipients were compared between the two stages. The KaplanMeier method was used to estimate the cumulative patient and graft survival rates, and the equality of survival distributions was evaluated using the log-rank test.RESULTS: The 188 children consisted of 102 boysand 86 girls. Their ages ranged from 3 to 144 mo with a median of 8 mo. One hundred and fifteen(61.2%) patients were born in rural areas. Comparing stage?Ⅰ?and stage Ⅱ patients, the proportion of patients referred by pediatricians(43.2% vs 71.1%, respectively; P &lt; 0.001) and the proportion of patients who previously received a Kasai procedure(KP)(32.4% vs 44.7%, respectively; P = 0.092) obviously increased, and significantly more parents were willing to treat their children with LT(73% vs 86%, respectively; P = 0.027). Grafts from living donors(102/122, 83.6%) were the most commonly used graft type. Surgical complications(16/25, 64.0%) were the main reason for posttransplant mortality. Among the living donor liver transplantation recipients(n = 102), the incidence of surgical complications was significantly reduced(34.1% vs 15.5%, respectively; P = 0.029) and survival rates of patients and grafts were greatly improved(81.8% vs 89.7%, respectively, at 1 year; 75.0% vs 87.8%, respectively, at 3 years; P = 0.107) from stage?Ⅰ?to stage Ⅱ.CONCLUSION: The status of surgical treatments for BA has been changing in mainland China. Favorable midterm outcomes after LT were achieved as centers gained greater technical experience.</abstract><cop>United States</cop><pub>Baishideng Publishing Group Inc</pub><pmid>26327772</pmid><doi>10.3748/wjg.v21.i32.9638</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | atresia Liver Biliary Biliary Atresia - diagnosis Biliary Atresia - mortality Biliary Atresia - surgery Child Child, Preschool China Databases, Factual Female Graft Survival Health Services Accessibility Humans Infant Kaplan-Meier Estimate Liver Transplantation - adverse effects Liver Transplantation - methods Liver Transplantation - mortality Living Donors - supply & distribution Male Observational Study Postoperative Complications - etiology Retrospective Studies Risk Factors Time Factors transplantation Kasai Living Treatment Outcome |
title | Liver transplantation for biliary atresia:A single-center study from mainland China |
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