FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2083485407> ?p ?o ?g. }

• W2083485407 endingPage "602" @default.
• W2083485407 startingPage "596" @default.
• W2083485407 abstract "Abstract We retrospectively reviewed our long-term experience with pediatric renal transplantation into a dysfunctional lower urinary tract to evaluate graft survival, function, and special urological complications. Between 1967 and March 2000, a total of 349 renal transplantations were performed in children younger than 18 years. Malformations of the lower urinary tract were the reasons for end-stage renal failure in 66 children (18.6%). The cause of urinary tract disorders included: meningomyelocele connected with neuropathic bladder (n= 4 transplantations); prune belly syndrome (n= 5 transplantations); VATER association (n= 2 transplantations); posterior urethral valves (n= 27 transplantations); and vesico-uretero-renal reflux (n= 28 transplantations). The majority of the patients underwent surgical interventions to preserve renal function or to prepare renal transplantation. The 1-and 5-year graft survival rate was evaluated with special reference to the underlying disease. The 1-year graft survival rate in all children with lower urinary tract malformations was 83.3%, compared with 88% for all children. In those children with ves-ico-ureteral reflux, it was 92.8% and in the children with Vater association and prune belly syndrome, it was 85.7%. One graft was lost in the children who had neurogenic bladder, so the 1-year graft survival rate was 75%. The worst 1-year graft survival rate was obtained for boys who had posterior urethral valves (1-year graft survival rate: 74%; 5-year graft survival rate: 62.9%). Concerning the 5-year graft survival rate, it was 70% for all children with malformations of the urinary tract. The best rate was obtained for children with reflux in the native kidneys (78.5%), followed by those with VATER association and prune bell syndrome. As an additional child with neurogenic bladder lost his graft, the 5-year graft survival rate was 50%. Pediatric renal transplantation into a dysfunctional bladder can be connected with high urological complication rates which may contribute to worse graft survival. The 1- and 5-year graft survival rate in children with malformations of the lower urinary tract is worse than in children without bladder dysfunction. We regarded a striking difference between graft survival and the urological disorders which led to renal insufficiency. We obtained the worst graft survival rates in children with posterior urethral valves which are usually connected with bladder emptying problems and dysfunctional voiding. Potential pediatric transplant recipients must be classified according to pathophysiological as well as anatomical abnormalities of the urinary tract and all urological problems have to be solved prior to transpalantation. At our center, living donors are favored to plan transpalantation of these children properly." @default.
• W2083485407 created "2016-06-24" @default.
• W2083485407 creator A5026875497 @default.
• W2083485407 creator A5057223629 @default.
• W2083485407 creator A5078759533 @default.
• W2083485407 date "2004-10-01" @default.
• W2083485407 modified "2023-10-16" @default.
• W2083485407 title "Pediatric renal transplantation and the dysfunctional bladder" @default.
• W2083485407 cites W157134127 @default.
• W2083485407 cites W1964432090 @default.
• W2083485407 cites W1976245886 @default.
• W2083485407 cites W1976309872 @default.
• W2083485407 cites W200112173 @default.
• W2083485407 cites W2015157750 @default.
• W2083485407 cites W2015321719 @default.
• W2083485407 cites W2017148696 @default.
• W2083485407 cites W2019001901 @default.
• W2083485407 cites W2020494530 @default.
• W2083485407 cites W2079458798 @default.
• W2083485407 cites W2094474992 @default.
• W2083485407 cites W2104232386 @default.
• W2083485407 cites W2113387680 @default.
• W2083485407 cites W2133650967 @default.
• W2083485407 cites W2135808145 @default.
• W2083485407 cites W2405393225 @default.
• W2083485407 cites W2414964676 @default.
• W2083485407 cites W2415359422 @default.
• W2083485407 cites W2439217044 @default.
• W2083485407 cites W2439623906 @default.
• W2083485407 cites W2472424339 @default.
• W2083485407 doi "https://doi.org/10.1007/s00147-004-0784-6" @default.
• W2083485407 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/15517166" @default.
• W2083485407 hasPublicationYear "2004" @default.
• W2083485407 type Work @default.
• W2083485407 sameAs 2083485407 @default.
• W2083485407 citedByCount "29" @default.
• W2083485407 countsByYear W20834854072012 @default.
• W2083485407 countsByYear W20834854072013 @default.
• W2083485407 countsByYear W20834854072014 @default.
• W2083485407 countsByYear W20834854072015 @default.
• W2083485407 countsByYear W20834854072018 @default.
• W2083485407 countsByYear W20834854072019 @default.
• W2083485407 countsByYear W20834854072021 @default.
• W2083485407 countsByYear W20834854072022 @default.
• W2083485407 countsByYear W20834854072023 @default.
• W2083485407 crossrefType "journal-article" @default.
• W2083485407 hasAuthorship W2083485407A5026875497 @default.
• W2083485407 hasAuthorship W2083485407A5057223629 @default.
• W2083485407 hasAuthorship W2083485407A5078759533 @default.
• W2083485407 hasConcept C126322002 @default.
• W2083485407 hasConcept C126894567 @default.
• W2083485407 hasConcept C141071460 @default.
• W2083485407 hasConcept C159641895 @default.
• W2083485407 hasConcept C2776283816 @default.
• W2083485407 hasConcept C2776729220 @default.
• W2083485407 hasConcept C2776953683 @default.
• W2083485407 hasConcept C2778702563 @default.
• W2083485407 hasConcept C2779134260 @default.
• W2083485407 hasConcept C2779762690 @default.
• W2083485407 hasConcept C2911091166 @default.
• W2083485407 hasConcept C43270747 @default.
• W2083485407 hasConcept C71924100 @default.
• W2083485407 hasConcept C77411442 @default.
• W2083485407 hasConceptScore W2083485407C126322002 @default.
• W2083485407 hasConceptScore W2083485407C126894567 @default.
• W2083485407 hasConceptScore W2083485407C141071460 @default.
• W2083485407 hasConceptScore W2083485407C159641895 @default.
• W2083485407 hasConceptScore W2083485407C2776283816 @default.
• W2083485407 hasConceptScore W2083485407C2776729220 @default.
• W2083485407 hasConceptScore W2083485407C2776953683 @default.
• W2083485407 hasConceptScore W2083485407C2778702563 @default.
• W2083485407 hasConceptScore W2083485407C2779134260 @default.
• W2083485407 hasConceptScore W2083485407C2779762690 @default.
• W2083485407 hasConceptScore W2083485407C2911091166 @default.
• W2083485407 hasConceptScore W2083485407C43270747 @default.
• W2083485407 hasConceptScore W2083485407C71924100 @default.
• W2083485407 hasConceptScore W2083485407C77411442 @default.
• W2083485407 hasIssue "10" @default.
• W2083485407 hasLocation W20834854071 @default.
• W2083485407 hasLocation W20834854072 @default.
• W2083485407 hasOpenAccess W2083485407 @default.
• W2083485407 hasPrimaryLocation W20834854071 @default.
• W2083485407 hasRelatedWork W1976944473 @default.
• W2083485407 hasRelatedWork W1985412339 @default.
• W2083485407 hasRelatedWork W2000117684 @default.
• W2083485407 hasRelatedWork W2016556358 @default.
• W2083485407 hasRelatedWork W2083485407 @default.
• W2083485407 hasRelatedWork W2128010086 @default.
• W2083485407 hasRelatedWork W2399770488 @default.
• W2083485407 hasRelatedWork W2411706116 @default.
• W2083485407 hasRelatedWork W2415039327 @default.
• W2083485407 hasRelatedWork W4234808054 @default.
• W2083485407 hasVolume "17" @default.
• W2083485407 isParatext "false" @default.
• W2083485407 isRetracted "false" @default.
• W2083485407 magId "2083485407" @default.
• W2083485407 workType "article" @default.