Loading…

Heart Retransplantation for Coronary Allograft Vasculopathy in Children: 25 Years of Single-Center Experience

Pediatric end-stage heart disease is surgically managed by heart transplantation. A major complication of primary transplantation (PTx) is coronary allograft vasculopathy (CAV), a form of accelerated atherosclerosis. Retransplantation (RTx) has been the management of CAV; however, there is limited c...

Full description

Saved in:
Bibliographic Details
Published in:Transplantation proceedings 2020-06, Vol.52 (5), p.1394-1396
Main Authors: Azeka, Estela, Walker, Thomas, Siqueira, Adailson Wagner da Silva, Penha, Juliano, Miana, Leonardo, Caneo, Luiz Fernando, Massoti, Maria Raquel, Tanamati, Carla, Miura, Nana, Jatene, Marcelo Biscegli
Format: Article
Language:English
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c380t-82a136d4964a67bba692a171ed69dd269ddc7eb4205a0a464dd9f4b9d1c8f7983
cites cdi_FETCH-LOGICAL-c380t-82a136d4964a67bba692a171ed69dd269ddc7eb4205a0a464dd9f4b9d1c8f7983
container_end_page 1396
container_issue 5
container_start_page 1394
container_title Transplantation proceedings
container_volume 52
creator Azeka, Estela
Walker, Thomas
Siqueira, Adailson Wagner da Silva
Penha, Juliano
Miana, Leonardo
Caneo, Luiz Fernando
Massoti, Maria Raquel
Tanamati, Carla
Miura, Nana
Jatene, Marcelo Biscegli
description Pediatric end-stage heart disease is surgically managed by heart transplantation. A major complication of primary transplantation (PTx) is coronary allograft vasculopathy (CAV), a form of accelerated atherosclerosis. Retransplantation (RTx) has been the management of CAV; however, there is limited comprehensive literature on this subject. Here we report 25 years of single-center experience in managing CAV with RTx and place it in the context of recent studies. A retrospective cohort study was undertaken on patients who underwent PTx 
doi_str_mv 10.1016/j.transproceed.2020.03.012
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2401115478</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0041134520303122</els_id><sourcerecordid>2401115478</sourcerecordid><originalsourceid>FETCH-LOGICAL-c380t-82a136d4964a67bba692a171ed69dd269ddc7eb4205a0a464dd9f4b9d1c8f7983</originalsourceid><addsrcrecordid>eNqNkE1PGzEQhi1URELKX0BWT73s4q_sBze0UEBCQgJaqSfLa8-Co42d2k5F_j0OCRJHLh555p139D4I_aCkpIRWZ4syBeXiKngNYEpGGCkJLwllB2hKm5oXrGL8G5oSImhBuZhP0HGMC5L_TPAjNOGMNzVp6BQtb0CFhB9gZzkql1Sy3uHBB9z54J0KG3wxjv45qCHhPyrq9ehXKr1ssHW4e7GjCeDOMZvjv9krYj_gR-ueRyg6cAkCvnpdQbDgNHxHh4MaI5zs6wz9_nX11N0Ud_fXt93FXaF5Q1LRMEV5ZURbCVXVfa-qNndqCqZqjWHbR9fQC0bmiihRCWPaQfStoboZ6rbhM_Rz55sZ_VtDTHJpo4YxxwO_jpIJQimdi3orPd9JdfAxBhjkKthlDi0pkVvcciE_45Zb3JJwmXHn5dP9nXW_zLOP1Q--WXC5E0BO-99CkFG_kzA2gE7SePuVO291VZk_</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2401115478</pqid></control><display><type>article</type><title>Heart Retransplantation for Coronary Allograft Vasculopathy in Children: 25 Years of Single-Center Experience</title><source>ScienceDirect Freedom Collection</source><creator>Azeka, Estela ; Walker, Thomas ; Siqueira, Adailson Wagner da Silva ; Penha, Juliano ; Miana, Leonardo ; Caneo, Luiz Fernando ; Massoti, Maria Raquel ; Tanamati, Carla ; Miura, Nana ; Jatene, Marcelo Biscegli</creator><creatorcontrib>Azeka, Estela ; Walker, Thomas ; Siqueira, Adailson Wagner da Silva ; Penha, Juliano ; Miana, Leonardo ; Caneo, Luiz Fernando ; Massoti, Maria Raquel ; Tanamati, Carla ; Miura, Nana ; Jatene, Marcelo Biscegli</creatorcontrib><description>Pediatric end-stage heart disease is surgically managed by heart transplantation. A major complication of primary transplantation (PTx) is coronary allograft vasculopathy (CAV), a form of accelerated atherosclerosis. Retransplantation (RTx) has been the management of CAV; however, there is limited comprehensive literature on this subject. Here we report 25 years of single-center experience in managing CAV with RTx and place it in the context of recent studies. A retrospective cohort study was undertaken on patients who underwent PTx &lt;18 years old and subsequent RTx due to CAV at the Heart Institute (InCor) University of São Paulo Medical School between 1992 and 2018. The maintenance immunosuppression protocol was double immunosuppression. For both PTx and RTx, quantitative and qualitative analyses were conducted for transplantation indication, donor/recipient demographics, post-transplant survival, rejection, infection, and immunosuppression. Between 1992 and 2018, 200 children underwent heart transplantation. Ten re-transplantations were performed, for which 7 (70%) were for CAV. Ages at RTx ranged from 11.5 to 29.3 years (19.1 ± 5.68 years; median 18.2 years). The mean time between PTx and RTx was 12.9 ± 3.4 years (median 13.4 years). The Kaplan-Meier survival rate at 1 month, 3 years, and 5 years was 85.7%, 71.5%, and 47.6%, respectively. Cardiac RTx can be a management option for CAV in patients who have undergone PTx in childhood with double immunosuppression therapy.</description><identifier>ISSN: 0041-1345</identifier><identifier>EISSN: 1873-2623</identifier><identifier>DOI: 10.1016/j.transproceed.2020.03.012</identifier><identifier>PMID: 32387081</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><ispartof>Transplantation proceedings, 2020-06, Vol.52 (5), p.1394-1396</ispartof><rights>2020 Elsevier Inc.</rights><rights>Copyright © 2020 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c380t-82a136d4964a67bba692a171ed69dd269ddc7eb4205a0a464dd9f4b9d1c8f7983</citedby><cites>FETCH-LOGICAL-c380t-82a136d4964a67bba692a171ed69dd269ddc7eb4205a0a464dd9f4b9d1c8f7983</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27915,27916</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32387081$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Azeka, Estela</creatorcontrib><creatorcontrib>Walker, Thomas</creatorcontrib><creatorcontrib>Siqueira, Adailson Wagner da Silva</creatorcontrib><creatorcontrib>Penha, Juliano</creatorcontrib><creatorcontrib>Miana, Leonardo</creatorcontrib><creatorcontrib>Caneo, Luiz Fernando</creatorcontrib><creatorcontrib>Massoti, Maria Raquel</creatorcontrib><creatorcontrib>Tanamati, Carla</creatorcontrib><creatorcontrib>Miura, Nana</creatorcontrib><creatorcontrib>Jatene, Marcelo Biscegli</creatorcontrib><title>Heart Retransplantation for Coronary Allograft Vasculopathy in Children: 25 Years of Single-Center Experience</title><title>Transplantation proceedings</title><addtitle>Transplant Proc</addtitle><description>Pediatric end-stage heart disease is surgically managed by heart transplantation. A major complication of primary transplantation (PTx) is coronary allograft vasculopathy (CAV), a form of accelerated atherosclerosis. Retransplantation (RTx) has been the management of CAV; however, there is limited comprehensive literature on this subject. Here we report 25 years of single-center experience in managing CAV with RTx and place it in the context of recent studies. A retrospective cohort study was undertaken on patients who underwent PTx &lt;18 years old and subsequent RTx due to CAV at the Heart Institute (InCor) University of São Paulo Medical School between 1992 and 2018. The maintenance immunosuppression protocol was double immunosuppression. For both PTx and RTx, quantitative and qualitative analyses were conducted for transplantation indication, donor/recipient demographics, post-transplant survival, rejection, infection, and immunosuppression. Between 1992 and 2018, 200 children underwent heart transplantation. Ten re-transplantations were performed, for which 7 (70%) were for CAV. Ages at RTx ranged from 11.5 to 29.3 years (19.1 ± 5.68 years; median 18.2 years). The mean time between PTx and RTx was 12.9 ± 3.4 years (median 13.4 years). The Kaplan-Meier survival rate at 1 month, 3 years, and 5 years was 85.7%, 71.5%, and 47.6%, respectively. Cardiac RTx can be a management option for CAV in patients who have undergone PTx in childhood with double immunosuppression therapy.</description><issn>0041-1345</issn><issn>1873-2623</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqNkE1PGzEQhi1URELKX0BWT73s4q_sBze0UEBCQgJaqSfLa8-Co42d2k5F_j0OCRJHLh555p139D4I_aCkpIRWZ4syBeXiKngNYEpGGCkJLwllB2hKm5oXrGL8G5oSImhBuZhP0HGMC5L_TPAjNOGMNzVp6BQtb0CFhB9gZzkql1Sy3uHBB9z54J0KG3wxjv45qCHhPyrq9ehXKr1ssHW4e7GjCeDOMZvjv9krYj_gR-ueRyg6cAkCvnpdQbDgNHxHh4MaI5zs6wz9_nX11N0Ud_fXt93FXaF5Q1LRMEV5ZURbCVXVfa-qNndqCqZqjWHbR9fQC0bmiihRCWPaQfStoboZ6rbhM_Rz55sZ_VtDTHJpo4YxxwO_jpIJQimdi3orPd9JdfAxBhjkKthlDi0pkVvcciE_45Zb3JJwmXHn5dP9nXW_zLOP1Q--WXC5E0BO-99CkFG_kzA2gE7SePuVO291VZk_</recordid><startdate>20200601</startdate><enddate>20200601</enddate><creator>Azeka, Estela</creator><creator>Walker, Thomas</creator><creator>Siqueira, Adailson Wagner da Silva</creator><creator>Penha, Juliano</creator><creator>Miana, Leonardo</creator><creator>Caneo, Luiz Fernando</creator><creator>Massoti, Maria Raquel</creator><creator>Tanamati, Carla</creator><creator>Miura, Nana</creator><creator>Jatene, Marcelo Biscegli</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20200601</creationdate><title>Heart Retransplantation for Coronary Allograft Vasculopathy in Children: 25 Years of Single-Center Experience</title><author>Azeka, Estela ; Walker, Thomas ; Siqueira, Adailson Wagner da Silva ; Penha, Juliano ; Miana, Leonardo ; Caneo, Luiz Fernando ; Massoti, Maria Raquel ; Tanamati, Carla ; Miura, Nana ; Jatene, Marcelo Biscegli</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c380t-82a136d4964a67bba692a171ed69dd269ddc7eb4205a0a464dd9f4b9d1c8f7983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Azeka, Estela</creatorcontrib><creatorcontrib>Walker, Thomas</creatorcontrib><creatorcontrib>Siqueira, Adailson Wagner da Silva</creatorcontrib><creatorcontrib>Penha, Juliano</creatorcontrib><creatorcontrib>Miana, Leonardo</creatorcontrib><creatorcontrib>Caneo, Luiz Fernando</creatorcontrib><creatorcontrib>Massoti, Maria Raquel</creatorcontrib><creatorcontrib>Tanamati, Carla</creatorcontrib><creatorcontrib>Miura, Nana</creatorcontrib><creatorcontrib>Jatene, Marcelo Biscegli</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Transplantation proceedings</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Azeka, Estela</au><au>Walker, Thomas</au><au>Siqueira, Adailson Wagner da Silva</au><au>Penha, Juliano</au><au>Miana, Leonardo</au><au>Caneo, Luiz Fernando</au><au>Massoti, Maria Raquel</au><au>Tanamati, Carla</au><au>Miura, Nana</au><au>Jatene, Marcelo Biscegli</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Heart Retransplantation for Coronary Allograft Vasculopathy in Children: 25 Years of Single-Center Experience</atitle><jtitle>Transplantation proceedings</jtitle><addtitle>Transplant Proc</addtitle><date>2020-06-01</date><risdate>2020</risdate><volume>52</volume><issue>5</issue><spage>1394</spage><epage>1396</epage><pages>1394-1396</pages><issn>0041-1345</issn><eissn>1873-2623</eissn><abstract>Pediatric end-stage heart disease is surgically managed by heart transplantation. A major complication of primary transplantation (PTx) is coronary allograft vasculopathy (CAV), a form of accelerated atherosclerosis. Retransplantation (RTx) has been the management of CAV; however, there is limited comprehensive literature on this subject. Here we report 25 years of single-center experience in managing CAV with RTx and place it in the context of recent studies. A retrospective cohort study was undertaken on patients who underwent PTx &lt;18 years old and subsequent RTx due to CAV at the Heart Institute (InCor) University of São Paulo Medical School between 1992 and 2018. The maintenance immunosuppression protocol was double immunosuppression. For both PTx and RTx, quantitative and qualitative analyses were conducted for transplantation indication, donor/recipient demographics, post-transplant survival, rejection, infection, and immunosuppression. Between 1992 and 2018, 200 children underwent heart transplantation. Ten re-transplantations were performed, for which 7 (70%) were for CAV. Ages at RTx ranged from 11.5 to 29.3 years (19.1 ± 5.68 years; median 18.2 years). The mean time between PTx and RTx was 12.9 ± 3.4 years (median 13.4 years). The Kaplan-Meier survival rate at 1 month, 3 years, and 5 years was 85.7%, 71.5%, and 47.6%, respectively. Cardiac RTx can be a management option for CAV in patients who have undergone PTx in childhood with double immunosuppression therapy.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>32387081</pmid><doi>10.1016/j.transproceed.2020.03.012</doi><tpages>3</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0041-1345
ispartof Transplantation proceedings, 2020-06, Vol.52 (5), p.1394-1396
issn 0041-1345
1873-2623
language eng
recordid cdi_proquest_miscellaneous_2401115478
source ScienceDirect Freedom Collection
title Heart Retransplantation for Coronary Allograft Vasculopathy in Children: 25 Years of Single-Center Experience
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-15T06%3A32%3A56IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Heart%20Retransplantation%20for%20Coronary%20Allograft%20Vasculopathy%20in%20Children:%2025%20Years%20of%20Single-Center%20Experience&rft.jtitle=Transplantation%20proceedings&rft.au=Azeka,%20Estela&rft.date=2020-06-01&rft.volume=52&rft.issue=5&rft.spage=1394&rft.epage=1396&rft.pages=1394-1396&rft.issn=0041-1345&rft.eissn=1873-2623&rft_id=info:doi/10.1016/j.transproceed.2020.03.012&rft_dat=%3Cproquest_cross%3E2401115478%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c380t-82a136d4964a67bba692a171ed69dd269ddc7eb4205a0a464dd9f4b9d1c8f7983%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2401115478&rft_id=info:pmid/32387081&rfr_iscdi=true