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dc.contributor.author Plotnicki L
dc.contributor.author Kohl CD
dc.contributor.author Hocker B
dc.contributor.author Krupka K
dc.contributor.author Rahmel A
dc.contributor.author Pape L
dc.contributor.author Hoyer P
dc.contributor.author Marks SD
dc.contributor.author Webb NJ
dc.contributor.author Soylemezoglu O
dc.contributor.author Topaloglu R
dc.contributor.author Szabó, Attila
dc.contributor.author Seeman T
dc.contributor.author Marlies Cornelissen EA
dc.contributor.author Knops N
dc.contributor.author Grenda R
dc.contributor.author Tonshoff B
dc.date.accessioned 2016-11-23T15:45:44Z
dc.date.available 2016-11-23T15:45:44Z
dc.date.issued 2013
dc.identifier 84878583986
dc.identifier.citation pagination=1414-1417; journalVolume=45; journalIssueNumber=4; journalTitle=TRANSPLANTATION PROCEEDINGS;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/2690
dc.identifier.uri doi:10.1016/j.transproceed.2013.01.007
dc.description.abstract BACKGROUND: The results of pediatric renal transplantation have improved markedly in the last decade. However, a number of relevant clinical problems remain, such as organ damage caused by chronic rejection, long-term toxicity of immunosuppressive therapy, difficulty in developing tolerance-inducing protocols, secondary cardiovascular comorbidity, post-transplantation lymphoproliferative disease, suboptimal longitudinal growth, quality of life, adherence to immunosuppressive medication, and structured transition programs to adult care. These unmet clinical needs require intense collaborative and interdisciplinary clinical research. We recently founded the Cooperative European Paediatric Renal TransplAnt INitiative (CERTAIN; www.certain-registry.eu) as a research network and platform built on a novel, web-based registry. RESULTS: The registry's dataset provides essential information on generic kidney transplantation-related topics and also captures pediatric-specific topics, such as growth, physical and psychosocial development, and adherence. Due to its flexibility the system can be used as follows: (1) as a registry capturing a minimal or an extended dataset; (2) as a center and/or country-specific transplantation database; or (3) as a patient-specific electronic transplantation chart. The data can be exported directly from the CERTAIN web application into statistical software packages for scientific analyses. The rights regarding data ownership, evaluation, and publications are regulated in the registry's rules of procedure. Data quality is ensured by automatic software validation and a manual data review process. To avoid redundant data entry, CERTAIN has established interfaces for data change with Eurotransplant, the Collaborative Transplant Study (CTS), and the registry of the European Society of Pediatric Nephrology (ESPN) and European Renal Association - European Dialysis and Transplant Association (ERA-EDTA) (ESPN/ERA-EDTA registry). CERTAIN fulfils all regulatory and ethical requirements of the European Union and Germany, in particular, regarding patients' data privacy and security. CONCLUSION: Using modern information technology, the recently established multinational CERTAIN Registry fills a gap in Europe for collaborative 5research and quality assurance in the field of pediatric renal transplantation.
dc.relation.ispartof urn:issn:0041-1345
dc.title The CERTAIN Registry: A Novel, Web-Based Registry and Research Platform for Pediatric Renal Transplantation in Europe
dc.type Journal Article
dc.date.updated 2015-11-25T09:23:16Z
dc.language.rfc3066 en
dc.identifier.mtmt 2333379
dc.identifier.wos 000320627500033
dc.identifier.pubmed 23726585
dc.contributor.department SE/AOK/K/I. Sz. Gyermekgyógyászati Klinika
dc.contributor.institution Semmelweis Egyetem


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