Early identification of transplant glomerulopathy in pediatric kidney transplant biopsies: A single‐center experience with electron microscopy analysis
Banff 2013 criteria recommend performing ultrastructural studies with electron microscopy (EM) in kidney transplant biopsies if the technology is available. We sought to determine the impact of EM on enhancing diagnostic findings in pediatric kidney transplant biopsies and the prognostic information...
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Veröffentlicht in: | Pediatric transplantation 2019-08, Vol.23 (5), p.e13459-n/a |
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description | Banff 2013 criteria recommend performing ultrastructural studies with electron microscopy (EM) in kidney transplant biopsies if the technology is available. We sought to determine the impact of EM on enhancing diagnostic findings in pediatric kidney transplant biopsies and the prognostic information gained from the additional findings. All kidney transplant biopsies since routine EM use started on June 1, 2014, until October 31, 2016, were reviewed. Primary outcome measures included the positive yield frequency of EM use defined as an upgraded diagnosis based on EM findings relative to light microscopy, and 12‐month kidney allograft outcome of progression to ESRD or doubling of serum creatinine stratified by transplant glomerulopathy (TG) status on EM. Eighty unique kidney transplant biopsies were reviewed. EM studies were completed for 61 biopsies (76%). Complication rate was low (3.7%). In 61 biopsies where EM was completed, EM findings included foot process fusion (62%), endothelial cell swelling (38%), subendothelial lucencies (31%), and glomerular basement membrane duplication (41%). EM confirmed FSGS recurrence in three cases. In the remaining 58 cases, there was a positive yield of 31% where 18 biopsies were upgraded to a worse category after TG identification on EM. Kidney allograft outcome was poor regardless whether TG was detected early on EM or advanced on LM. Routine EM use in analyzing pediatric kidney transplant biopsies proved safe and provided valuable additional diagnostic information in almost one‐third of cases. Additional studies are needed to determine if clinical interventions for early TG identified on EM can improve long‐term outcomes. |
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We sought to determine the impact of EM on enhancing diagnostic findings in pediatric kidney transplant biopsies and the prognostic information gained from the additional findings. All kidney transplant biopsies since routine EM use started on June 1, 2014, until October 31, 2016, were reviewed. Primary outcome measures included the positive yield frequency of EM use defined as an upgraded diagnosis based on EM findings relative to light microscopy, and 12‐month kidney allograft outcome of progression to ESRD or doubling of serum creatinine stratified by transplant glomerulopathy (TG) status on EM. Eighty unique kidney transplant biopsies were reviewed. EM studies were completed for 61 biopsies (76%). Complication rate was low (3.7%). In 61 biopsies where EM was completed, EM findings included foot process fusion (62%), endothelial cell swelling (38%), subendothelial lucencies (31%), and glomerular basement membrane duplication (41%). EM confirmed FSGS recurrence in three cases. In the remaining 58 cases, there was a positive yield of 31% where 18 biopsies were upgraded to a worse category after TG identification on EM. Kidney allograft outcome was poor regardless whether TG was detected early on EM or advanced on LM. Routine EM use in analyzing pediatric kidney transplant biopsies proved safe and provided valuable additional diagnostic information in almost one‐third of cases. Additional studies are needed to determine if clinical interventions for early TG identified on EM can improve long‐term outcomes.</description><identifier>ISSN: 1397-3142</identifier><identifier>EISSN: 1399-3046</identifier><identifier>DOI: 10.1111/petr.13459</identifier><identifier>PMID: 31062922</identifier><language>eng</language><publisher>Denmark: Wiley Subscription Services, Inc</publisher><subject>Adolescent ; Biopsy ; Cell fusion ; Cell size ; Creatinine ; Disease Progression ; Electron microscopy ; Endothelial cells ; Female ; Graft Rejection - pathology ; Humans ; Kidney Glomerulus - pathology ; kidney transplant ; Kidney Transplantation ; Kidney transplants ; Male ; Microscopy ; Microscopy, Electron ; Pediatrics ; Postoperative Complications - pathology ; Prognosis ; Retrospective Studies ; Reviews ; transplant glomerulopathy</subject><ispartof>Pediatric transplantation, 2019-08, Vol.23 (5), p.e13459-n/a</ispartof><rights>2019 Wiley Periodicals, Inc.</rights><rights>2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3169-946eaec71f8425a6df82164f7be65854137a2646de69c73893f3522587f1f9243</cites><orcidid>0000-0003-0539-4021</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fpetr.13459$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fpetr.13459$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31062922$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Grodsky, Jacob D.</creatorcontrib><creatorcontrib>Craver, Randall D.</creatorcontrib><creatorcontrib>Ashoor, Isa F.</creatorcontrib><title>Early identification of transplant glomerulopathy in pediatric kidney transplant biopsies: A single‐center experience with electron microscopy analysis</title><title>Pediatric transplantation</title><addtitle>Pediatr Transplant</addtitle><description>Banff 2013 criteria recommend performing ultrastructural studies with electron microscopy (EM) in kidney transplant biopsies if the technology is available. We sought to determine the impact of EM on enhancing diagnostic findings in pediatric kidney transplant biopsies and the prognostic information gained from the additional findings. All kidney transplant biopsies since routine EM use started on June 1, 2014, until October 31, 2016, were reviewed. Primary outcome measures included the positive yield frequency of EM use defined as an upgraded diagnosis based on EM findings relative to light microscopy, and 12‐month kidney allograft outcome of progression to ESRD or doubling of serum creatinine stratified by transplant glomerulopathy (TG) status on EM. Eighty unique kidney transplant biopsies were reviewed. EM studies were completed for 61 biopsies (76%). Complication rate was low (3.7%). In 61 biopsies where EM was completed, EM findings included foot process fusion (62%), endothelial cell swelling (38%), subendothelial lucencies (31%), and glomerular basement membrane duplication (41%). EM confirmed FSGS recurrence in three cases. In the remaining 58 cases, there was a positive yield of 31% where 18 biopsies were upgraded to a worse category after TG identification on EM. Kidney allograft outcome was poor regardless whether TG was detected early on EM or advanced on LM. Routine EM use in analyzing pediatric kidney transplant biopsies proved safe and provided valuable additional diagnostic information in almost one‐third of cases. Additional studies are needed to determine if clinical interventions for early TG identified on EM can improve long‐term outcomes.</description><subject>Adolescent</subject><subject>Biopsy</subject><subject>Cell fusion</subject><subject>Cell size</subject><subject>Creatinine</subject><subject>Disease Progression</subject><subject>Electron microscopy</subject><subject>Endothelial cells</subject><subject>Female</subject><subject>Graft Rejection - pathology</subject><subject>Humans</subject><subject>Kidney Glomerulus - pathology</subject><subject>kidney transplant</subject><subject>Kidney Transplantation</subject><subject>Kidney transplants</subject><subject>Male</subject><subject>Microscopy</subject><subject>Microscopy, Electron</subject><subject>Pediatrics</subject><subject>Postoperative Complications - pathology</subject><subject>Prognosis</subject><subject>Retrospective Studies</subject><subject>Reviews</subject><subject>transplant glomerulopathy</subject><issn>1397-3142</issn><issn>1399-3046</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp90c1qFTEYBuAgiq3VjRcgATdFmDr5mczEXSnHHygoUtdDTuZLm5pJYpKhzs5LcOvteSXm9FQRF2bzZfHwJh8vQk9Je0LqeRmhpBPCeCfvoUPCpGxYy8X923vfMMLpAXqU83XbEsEH_hAdMNIKKik9RD82KrkV2wl8scZqVWzwOBhckvI5OuULvnRhhrS4EFW5qtbjCJNVJVmNP9vJw_q33toQs4X8Cp_ibP2lg5_fvusaDwnD1wjJgteAb2y5wuBAl1QfnK1OIesQV6y8cmu2-TF6YJTL8ORuHqFPrzcXZ2-b8_dv3p2dnjeaESEbyQUo0D0xA6edEpMZaF3T9FsQ3dBxwnpFBRcTCKl7NkhmWEdpN_SGGEk5O0LH-9yYwpcFchlnmzW4ugyEJY-UMkpY2w2i0uf_0OuwpPrfnRKiJ2LoZVUv9mq3Uk5gxpjsrNI6knbcFTbuChtvC6v42V3ksp1h-kN_N1QB2YMb62D9T9T4YXPxcR_6C3eVpLM</recordid><startdate>201908</startdate><enddate>201908</enddate><creator>Grodsky, Jacob D.</creator><creator>Craver, Randall D.</creator><creator>Ashoor, Isa F.</creator><general>Wiley Subscription Services, Inc</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>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0539-4021</orcidid></search><sort><creationdate>201908</creationdate><title>Early identification of transplant glomerulopathy in pediatric kidney transplant biopsies: A single‐center experience with electron microscopy analysis</title><author>Grodsky, Jacob D. ; Craver, Randall D. ; Ashoor, Isa F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3169-946eaec71f8425a6df82164f7be65854137a2646de69c73893f3522587f1f9243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adolescent</topic><topic>Biopsy</topic><topic>Cell fusion</topic><topic>Cell size</topic><topic>Creatinine</topic><topic>Disease Progression</topic><topic>Electron microscopy</topic><topic>Endothelial cells</topic><topic>Female</topic><topic>Graft Rejection - pathology</topic><topic>Humans</topic><topic>Kidney Glomerulus - pathology</topic><topic>kidney transplant</topic><topic>Kidney Transplantation</topic><topic>Kidney transplants</topic><topic>Male</topic><topic>Microscopy</topic><topic>Microscopy, Electron</topic><topic>Pediatrics</topic><topic>Postoperative Complications - pathology</topic><topic>Prognosis</topic><topic>Retrospective Studies</topic><topic>Reviews</topic><topic>transplant glomerulopathy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Grodsky, Jacob D.</creatorcontrib><creatorcontrib>Craver, Randall D.</creatorcontrib><creatorcontrib>Ashoor, Isa F.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Pediatric transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Grodsky, Jacob D.</au><au>Craver, Randall D.</au><au>Ashoor, Isa F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Early identification of transplant glomerulopathy in pediatric kidney transplant biopsies: A single‐center experience with electron microscopy analysis</atitle><jtitle>Pediatric transplantation</jtitle><addtitle>Pediatr Transplant</addtitle><date>2019-08</date><risdate>2019</risdate><volume>23</volume><issue>5</issue><spage>e13459</spage><epage>n/a</epage><pages>e13459-n/a</pages><issn>1397-3142</issn><eissn>1399-3046</eissn><abstract>Banff 2013 criteria recommend performing ultrastructural studies with electron microscopy (EM) in kidney transplant biopsies if the technology is available. We sought to determine the impact of EM on enhancing diagnostic findings in pediatric kidney transplant biopsies and the prognostic information gained from the additional findings. All kidney transplant biopsies since routine EM use started on June 1, 2014, until October 31, 2016, were reviewed. Primary outcome measures included the positive yield frequency of EM use defined as an upgraded diagnosis based on EM findings relative to light microscopy, and 12‐month kidney allograft outcome of progression to ESRD or doubling of serum creatinine stratified by transplant glomerulopathy (TG) status on EM. Eighty unique kidney transplant biopsies were reviewed. EM studies were completed for 61 biopsies (76%). Complication rate was low (3.7%). In 61 biopsies where EM was completed, EM findings included foot process fusion (62%), endothelial cell swelling (38%), subendothelial lucencies (31%), and glomerular basement membrane duplication (41%). EM confirmed FSGS recurrence in three cases. In the remaining 58 cases, there was a positive yield of 31% where 18 biopsies were upgraded to a worse category after TG identification on EM. Kidney allograft outcome was poor regardless whether TG was detected early on EM or advanced on LM. Routine EM use in analyzing pediatric kidney transplant biopsies proved safe and provided valuable additional diagnostic information in almost one‐third of cases. Additional studies are needed to determine if clinical interventions for early TG identified on EM can improve long‐term outcomes.</abstract><cop>Denmark</cop><pub>Wiley Subscription Services, Inc</pub><pmid>31062922</pmid><doi>10.1111/petr.13459</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-0539-4021</orcidid></addata></record> |
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subjects | Adolescent Biopsy Cell fusion Cell size Creatinine Disease Progression Electron microscopy Endothelial cells Female Graft Rejection - pathology Humans Kidney Glomerulus - pathology kidney transplant Kidney Transplantation Kidney transplants Male Microscopy Microscopy, Electron Pediatrics Postoperative Complications - pathology Prognosis Retrospective Studies Reviews transplant glomerulopathy |
title | Early identification of transplant glomerulopathy in pediatric kidney transplant biopsies: A single‐center experience with electron microscopy analysis |
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