Ten Years of Experience with Liver Transplantation for Familial Amyloid Polyneuropathy in Japan: Outcomes of Living Donor Liver Transplantations

Object We summarize 10 years of experience with liver transplantation for FAP patients in Japan and review the current opinions regarding this treatment for FAP. Methods and Patients All basic report data on patients at the time of transplantation were registered with the Japanese Liver Transplantat...

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Veröffentlicht in:Internal Medicine 2005, Vol.44(11), pp.1151-1156
Hauptverfasser: TAKEI, Yo-ichi, IKEDA, Shu-ichi, IKEGAMI, Toshihiko, HASHIKURA, Yasuhiko, MIYAGAWA, Shin-ichi, ANDO, Yukio
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container_end_page 1156
container_issue 11
container_start_page 1151
container_title Internal Medicine
container_volume 44
creator TAKEI, Yo-ichi
IKEDA, Shu-ichi
IKEGAMI, Toshihiko
HASHIKURA, Yasuhiko
MIYAGAWA, Shin-ichi
ANDO, Yukio
description Object We summarize 10 years of experience with liver transplantation for FAP patients in Japan and review the current opinions regarding this treatment for FAP. Methods and Patients All basic report data on patients at the time of transplantation were registered with the Japanese Liver Transplantation Society (JLTS). Based on the JLST report data, more detailed information on FAP patients was requested from each center. Results Living donor liver transplantation (LDLT) for FAP patients was first performed in Japan in 1993. LDLT has since been performed in 41 FAP patients, including nine cases of temporary auxiliary partial orthotopic liver transplantation (APOLT). Orthotopic liver transplantation (OLT) from cadaveric donors for FAP patients began in 1999, but only one FAP patient has subsequently undergone this procedure. Of these total of 43 FAP patients, 36 are currently alive: the one-year survival rate of patients after transplantation was 93%, and the five-year survival rate of these cases was 77%. Preoperative clinical severity and the nutritional status of patients are correlated with their outcome after liver transplantation. Domino (sequential) liver transplantation has been carried out in 20 domino recipients with end-stage liver diseases. Of the 20 domino recipients, 12 are currently alive. Conclusion For FAP patients, these outcomes after the operation were very similar to those of OLT from cadaveric donors reported in other countries. Therefore, we concluded that for the treatment of FAP, LDLT from a living donor is equally effective as OLT from a cadaveric donor.
doi_str_mv 10.2169/internalmedicine.44.1151
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Methods and Patients All basic report data on patients at the time of transplantation were registered with the Japanese Liver Transplantation Society (JLTS). Based on the JLST report data, more detailed information on FAP patients was requested from each center. Results Living donor liver transplantation (LDLT) for FAP patients was first performed in Japan in 1993. LDLT has since been performed in 41 FAP patients, including nine cases of temporary auxiliary partial orthotopic liver transplantation (APOLT). Orthotopic liver transplantation (OLT) from cadaveric donors for FAP patients began in 1999, but only one FAP patient has subsequently undergone this procedure. Of these total of 43 FAP patients, 36 are currently alive: the one-year survival rate of patients after transplantation was 93%, and the five-year survival rate of these cases was 77%. Preoperative clinical severity and the nutritional status of patients are correlated with their outcome after liver transplantation. Domino (sequential) liver transplantation has been carried out in 20 domino recipients with end-stage liver diseases. Of the 20 domino recipients, 12 are currently alive. Conclusion For FAP patients, these outcomes after the operation were very similar to those of OLT from cadaveric donors reported in other countries. Therefore, we concluded that for the treatment of FAP, LDLT from a living donor is equally effective as OLT from a cadaveric donor.</description><identifier>ISSN: 0918-2918</identifier><identifier>EISSN: 1349-7235</identifier><identifier>DOI: 10.2169/internalmedicine.44.1151</identifier><identifier>PMID: 16357452</identifier><language>eng</language><publisher>Tokyo: The Japanese Society of Internal Medicine</publisher><subject>Adult ; Amyloid Neuropathies, Familial - mortality ; Amyloid Neuropathies, Familial - surgery ; Biological and medical sciences ; Cranial nerves. Spinal roots. Peripheral nerves. Autonomic nervous system. Gustation. Olfaction ; familial amyloid polyneuropathy ; Female ; Follow-Up Studies ; General aspects ; Humans ; Japan ; Japan - epidemiology ; Liver Transplantation - methods ; Liver Transplantation - mortality ; living donor liver transplantation ; Living Donors ; Male ; Medical sciences ; Middle Aged ; Nervous system (semeiology, syndromes) ; Neurology ; Retrospective Studies ; Survival Rate - trends ; Time Factors ; Treatment Outcome</subject><ispartof>Internal Medicine, 2005, Vol.44(11), pp.1151-1156</ispartof><rights>2005 by The Japanese Society of Internal Medicine</rights><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c555t-e70354b073e70b9f6210520aacecfc8d42f62febd4e4aab08a0481ddb9c22ec43</citedby><cites>FETCH-LOGICAL-c555t-e70354b073e70b9f6210520aacecfc8d42f62febd4e4aab08a0481ddb9c22ec43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,1883,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=17446168$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16357452$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>TAKEI, Yo-ichi</creatorcontrib><creatorcontrib>IKEDA, Shu-ichi</creatorcontrib><creatorcontrib>IKEGAMI, Toshihiko</creatorcontrib><creatorcontrib>HASHIKURA, Yasuhiko</creatorcontrib><creatorcontrib>MIYAGAWA, Shin-ichi</creatorcontrib><creatorcontrib>ANDO, Yukio</creatorcontrib><creatorcontrib>Japanese Liver Transplantation Society</creatorcontrib><title>Ten Years of Experience with Liver Transplantation for Familial Amyloid Polyneuropathy in Japan: Outcomes of Living Donor Liver Transplantations</title><title>Internal Medicine</title><addtitle>Intern. Med.</addtitle><description>Object We summarize 10 years of experience with liver transplantation for FAP patients in Japan and review the current opinions regarding this treatment for FAP. Methods and Patients All basic report data on patients at the time of transplantation were registered with the Japanese Liver Transplantation Society (JLTS). Based on the JLST report data, more detailed information on FAP patients was requested from each center. Results Living donor liver transplantation (LDLT) for FAP patients was first performed in Japan in 1993. LDLT has since been performed in 41 FAP patients, including nine cases of temporary auxiliary partial orthotopic liver transplantation (APOLT). Orthotopic liver transplantation (OLT) from cadaveric donors for FAP patients began in 1999, but only one FAP patient has subsequently undergone this procedure. Of these total of 43 FAP patients, 36 are currently alive: the one-year survival rate of patients after transplantation was 93%, and the five-year survival rate of these cases was 77%. Preoperative clinical severity and the nutritional status of patients are correlated with their outcome after liver transplantation. Domino (sequential) liver transplantation has been carried out in 20 domino recipients with end-stage liver diseases. Of the 20 domino recipients, 12 are currently alive. Conclusion For FAP patients, these outcomes after the operation were very similar to those of OLT from cadaveric donors reported in other countries. Therefore, we concluded that for the treatment of FAP, LDLT from a living donor is equally effective as OLT from a cadaveric donor.</description><subject>Adult</subject><subject>Amyloid Neuropathies, Familial - mortality</subject><subject>Amyloid Neuropathies, Familial - surgery</subject><subject>Biological and medical sciences</subject><subject>Cranial nerves. Spinal roots. Peripheral nerves. Autonomic nervous system. Gustation. Olfaction</subject><subject>familial amyloid polyneuropathy</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>General aspects</subject><subject>Humans</subject><subject>Japan</subject><subject>Japan - epidemiology</subject><subject>Liver Transplantation - methods</subject><subject>Liver Transplantation - mortality</subject><subject>living donor liver transplantation</subject><subject>Living Donors</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Nervous system (semeiology, syndromes)</subject><subject>Neurology</subject><subject>Retrospective Studies</subject><subject>Survival Rate - trends</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><issn>0918-2918</issn><issn>1349-7235</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc1u1DAUhSMEokPhFZA3sMtgO3Z-2FWl5UcjDYthwSq6cW46rhw72A4wb9FHroeJWgnB5tqyv3vu0T1ZRhhdc1Y277SN6C2YEXuttMW1EGvGJHuSrVghmrzihXyarWjD6pyncpa9COGW0qKuGv48O2NlISsh-Sq726El3xF8IG4gV78n9BqtQvJLxz3Z6J_oyc6DDZMBGyFqZ8ngPLmGURsNhlyMB-N0T746c7A4ezdB3B-ItuQLTGDfk-0clRvxj37S0_aGfHA2SfxTPLzMng1gAr5azvPs2_XV7vJTvtl-_Hx5scmVlDLmWNFCio5WRbp1zVByRiWnAArVoOpe8PQ0YNcLFAAdrYGKmvV91yjOUYniPHt70p28-zFjiO2og0KTnKCbQ1vWdVNXskpgfQKVdyF4HNrJ6xH8oWW0PabR_p1GK0R7TCO1vl5mzF36fGxc1p-ANwsAQYEZ0i6UDo9cJUTJyjpx2xN3GyLc4AMAPmpl8D8Olnq08kCqPfgWbXEPG5y5cQ</recordid><startdate>20051101</startdate><enddate>20051101</enddate><creator>TAKEI, Yo-ichi</creator><creator>IKEDA, Shu-ichi</creator><creator>IKEGAMI, Toshihiko</creator><creator>HASHIKURA, Yasuhiko</creator><creator>MIYAGAWA, Shin-ichi</creator><creator>ANDO, Yukio</creator><general>The Japanese Society of Internal Medicine</general><general>Japanese Society of Internal Medicine</general><scope>IQODW</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></search><sort><creationdate>20051101</creationdate><title>Ten Years of Experience with Liver Transplantation for Familial Amyloid Polyneuropathy in Japan: Outcomes of Living Donor Liver Transplantations</title><author>TAKEI, Yo-ichi ; IKEDA, Shu-ichi ; IKEGAMI, Toshihiko ; HASHIKURA, Yasuhiko ; MIYAGAWA, Shin-ichi ; ANDO, Yukio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c555t-e70354b073e70b9f6210520aacecfc8d42f62febd4e4aab08a0481ddb9c22ec43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Adult</topic><topic>Amyloid Neuropathies, Familial - mortality</topic><topic>Amyloid Neuropathies, Familial - surgery</topic><topic>Biological and medical sciences</topic><topic>Cranial nerves. Spinal roots. Peripheral nerves. Autonomic nervous system. Gustation. Olfaction</topic><topic>familial amyloid polyneuropathy</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>General aspects</topic><topic>Humans</topic><topic>Japan</topic><topic>Japan - epidemiology</topic><topic>Liver Transplantation - methods</topic><topic>Liver Transplantation - mortality</topic><topic>living donor liver transplantation</topic><topic>Living Donors</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Nervous system (semeiology, syndromes)</topic><topic>Neurology</topic><topic>Retrospective Studies</topic><topic>Survival Rate - trends</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>TAKEI, Yo-ichi</creatorcontrib><creatorcontrib>IKEDA, Shu-ichi</creatorcontrib><creatorcontrib>IKEGAMI, Toshihiko</creatorcontrib><creatorcontrib>HASHIKURA, Yasuhiko</creatorcontrib><creatorcontrib>MIYAGAWA, Shin-ichi</creatorcontrib><creatorcontrib>ANDO, Yukio</creatorcontrib><creatorcontrib>Japanese Liver Transplantation Society</creatorcontrib><collection>Pascal-Francis</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><jtitle>Internal Medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>TAKEI, Yo-ichi</au><au>IKEDA, Shu-ichi</au><au>IKEGAMI, Toshihiko</au><au>HASHIKURA, Yasuhiko</au><au>MIYAGAWA, Shin-ichi</au><au>ANDO, Yukio</au><aucorp>Japanese Liver Transplantation Society</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ten Years of Experience with Liver Transplantation for Familial Amyloid Polyneuropathy in Japan: Outcomes of Living Donor Liver Transplantations</atitle><jtitle>Internal Medicine</jtitle><addtitle>Intern. Med.</addtitle><date>2005-11-01</date><risdate>2005</risdate><volume>44</volume><issue>11</issue><spage>1151</spage><epage>1156</epage><pages>1151-1156</pages><issn>0918-2918</issn><eissn>1349-7235</eissn><abstract>Object We summarize 10 years of experience with liver transplantation for FAP patients in Japan and review the current opinions regarding this treatment for FAP. Methods and Patients All basic report data on patients at the time of transplantation were registered with the Japanese Liver Transplantation Society (JLTS). Based on the JLST report data, more detailed information on FAP patients was requested from each center. Results Living donor liver transplantation (LDLT) for FAP patients was first performed in Japan in 1993. LDLT has since been performed in 41 FAP patients, including nine cases of temporary auxiliary partial orthotopic liver transplantation (APOLT). Orthotopic liver transplantation (OLT) from cadaveric donors for FAP patients began in 1999, but only one FAP patient has subsequently undergone this procedure. Of these total of 43 FAP patients, 36 are currently alive: the one-year survival rate of patients after transplantation was 93%, and the five-year survival rate of these cases was 77%. Preoperative clinical severity and the nutritional status of patients are correlated with their outcome after liver transplantation. Domino (sequential) liver transplantation has been carried out in 20 domino recipients with end-stage liver diseases. Of the 20 domino recipients, 12 are currently alive. Conclusion For FAP patients, these outcomes after the operation were very similar to those of OLT from cadaveric donors reported in other countries. Therefore, we concluded that for the treatment of FAP, LDLT from a living donor is equally effective as OLT from a cadaveric donor.</abstract><cop>Tokyo</cop><pub>The Japanese Society of Internal Medicine</pub><pmid>16357452</pmid><doi>10.2169/internalmedicine.44.1151</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; J-STAGE (Japan Science & Technology Information Aggregator, Electronic) Freely Available Titles - Japanese
subjects Adult
Amyloid Neuropathies, Familial - mortality
Amyloid Neuropathies, Familial - surgery
Biological and medical sciences
Cranial nerves. Spinal roots. Peripheral nerves. Autonomic nervous system. Gustation. Olfaction
familial amyloid polyneuropathy
Female
Follow-Up Studies
General aspects
Humans
Japan
Japan - epidemiology
Liver Transplantation - methods
Liver Transplantation - mortality
living donor liver transplantation
Living Donors
Male
Medical sciences
Middle Aged
Nervous system (semeiology, syndromes)
Neurology
Retrospective Studies
Survival Rate - trends
Time Factors
Treatment Outcome
title Ten Years of Experience with Liver Transplantation for Familial Amyloid Polyneuropathy in Japan: Outcomes of Living Donor Liver Transplantations
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