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Pretransplant biopsy in expanded criteria donors: do we really need it?

dc.contributor.authorTavares da Silva, E
dc.contributor.authorOliveira, R
dc.contributor.authorCastelo, D
dc.contributor.authorMarques, V
dc.contributor.authorSousa, V
dc.contributor.authorMoreira, P
dc.contributor.authorSimões, P
dc.contributor.authorBastos, C
dc.contributor.authorFigueiredo, A
dc.contributor.authorMota, A
dc.date.accessioned2016-12-12T15:43:01Z
dc.date.available2016-12-12T15:43:01Z
dc.date.issued2014-12
dc.description.abstractAbstract INTRODUCTION: Renal transplantation is the best treatment for end-stage renal disease, including when using expanded criteria donors (ECD) kidneys. However, these suboptimal kidneys should be evaluated rigorously to meet their usefulness. Opinions differ about the best way to evaluate them. MATERIALS AND METHODS: We retrospectively reviewed kidneys from ECD harvested by a single academic institution between January 2008 and September 2013. Needle biopsies were performed at the time of the harvest when considered relevant by the transplant team. Two pathologists where responsible for their analysis; the Remuzzi classification has been used in all cases. RESULTS: We evaluated 560 ECD kidneys. Biopsies were made in 197 (35.2%) organs, 20 of which were considered not usable and 36 good only for double transplantation. Sixty-three kidneys (11.3%) were discarded by the transplant team based on the biopsy result and clinical criteria. Donors who underwent a biopsy were older (P < .001) and had a worse glomerular filtration rate (GFR; P = .001). Comparing donors approved and rejected by the biopsy, the rejected donors were heavier (P = .003) and had a lower GFR (P = .002). Cold ischemia time was longer for the biopsy group (P < .001). Regarding graft function, the biopsy overall score correlated with the transplant outcome in the short and long term. Separately, glomeruli and interstitium scores were correlated with recipient's GFR in the earlier periods (3 months; P = .025 and .037), and the arteries and tubules correlated with GFR in the longer term (at 3 years P = .004 and .010). CONCLUSION: The decision on the usability of ECD grafts is complex. At our center, we chose a mixed approach based on donor risk. Low-risk ECD do not require biopsy. In more complex situations, especially older donors or those with a lower GFR, prompted a pretransplant biopsy. The biopsy results proved to be useful as they relate to subsequent transplant outcomes, thereby allowing us to exclude grafts whose function would most probably be less than optimal.pt_PT
dc.identifier.citationTransplant Proc. 2014 Dec;46(10):3330-4.pt_PT
dc.identifier.doi10.1016/j.transproceed.2014.10.026pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.4/1992
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.subjectTransplantação de Rimpt_PT
dc.subjectBiopsiapt_PT
dc.subjectPeríodo Pré-Operatóriopt_PT
dc.subjectSobrevivência de Enxertopt_PT
dc.titlePretransplant biopsy in expanded criteria donors: do we really need it?pt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage3334pt_PT
oaire.citation.issue10pt_PT
oaire.citation.startPage3330-4pt_PT
oaire.citation.volume46pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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