Publication: Continuous venovenous hemodiafiltration in the treatment of maple syrup urine disease
dc.contributor.coauthor | Sık, Güntülü | |
dc.contributor.coauthor | Topal, Nilüfer | |
dc.contributor.coauthor | Çitak, Agop | |
dc.contributor.coauthor | Zeybek, Çiğdem | |
dc.contributor.coauthor | Tüten, Abdulhamit | |
dc.contributor.department | School of Medicine | |
dc.contributor.kuauthor | Bilge, İlmay | |
dc.contributor.kuauthor | Demirkol, Demet | |
dc.contributor.schoolcollegeinstitute | SCHOOL OF MEDICINE | |
dc.date.accessioned | 2024-11-09T23:39:21Z | |
dc.date.issued | 2016 | |
dc.description.abstract | Background: The study aims to define the efficacy of continuous renal replacement therapy in acute metabolic decompensation treatment of maple syrup urine disease (MSUD). Methods: All the neonates, infants and children who have had life threatening conditions due to MSUD and were treated with continuous venovenous hemodiafiltration (CVVHDF) were analyzed retrospectively. Results: Fourteen patients underwent 15 sessions of CVVHDF (age range 15 days to 87 months, mean 40.8 +/- 31.4 months). One patient required additional CVVHDF 1 week after cessation of CVVHDF. Twenty seven percent (n = 4) of the patients were intubated and mechanically ventilated. Twelve patients responded to treatment and dramatic neurological improvement was observed within 24 h. Two of the 14 patients required 36 h of CVVHDF for neurological improvement. The mean duration of CVVHDF was 20.2 +/- 8.6 (9-36) h. The mean leucine level was 1,648 +/- 623.8 (714-2,768) mu mol/l before and was 256.5 +/- 150.6 (117-646) mu mol/l at the end of treatment. No mortality was observed. Conclusion: Continuous hemodiafiltration is an effective and safe method in correcting metabolic disturbances in MSUD. (C) 2016 S. Karger AG, Basel | |
dc.description.indexedby | WOS | |
dc.description.indexedby | Scopus | |
dc.description.issue | 1 | |
dc.description.openaccess | NO | |
dc.description.publisherscope | International | |
dc.description.sponsoredbyTubitakEu | N/A | |
dc.description.volume | 42 | |
dc.identifier.doi | 10.1159/000443783 | |
dc.identifier.eissn | 1421-9735 | |
dc.identifier.issn | 0253-5068 | |
dc.identifier.quartile | Q2 | |
dc.identifier.scopus | 2-s2.0-84961390738 | |
dc.identifier.uri | https://doi.org/10.1159/000443783 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14288/13097 | |
dc.identifier.wos | 377999600007 | |
dc.keywords | Maple syrup urine disease | |
dc.keywords | Continuous renal replacement therapy | |
dc.keywords | Hemodiafiltration | |
dc.keywords | Leucine | |
dc.keywords | Encephalopathy branched-chain amino | |
dc.keywords | Extracorporeal removal therapy | |
dc.keywords | Renal replacement therapy | |
dc.keywords | Inborn-errors | |
dc.keywords | Peritoneal-dialysis | |
dc.keywords | Acute-phase | |
dc.keywords | Hemodialysis | |
dc.keywords | Acids | |
dc.keywords | Hemofiltration | |
dc.keywords | Children | |
dc.language.iso | eng | |
dc.publisher | Karger | |
dc.relation.ispartof | Blood Purification | |
dc.subject | Hematology | |
dc.subject | Urology | |
dc.subject | Nephrology | |
dc.title | Continuous venovenous hemodiafiltration in the treatment of maple syrup urine disease | |
dc.type | Journal Article | |
dspace.entity.type | Publication | |
local.contributor.kuauthor | Demirkol, Demet | |
local.contributor.kuauthor | Bilge, İlmay | |
local.publication.orgunit1 | SCHOOL OF MEDICINE | |
local.publication.orgunit2 | School of Medicine | |
relation.isOrgUnitOfPublication | d02929e1-2a70-44f0-ae17-7819f587bedd | |
relation.isOrgUnitOfPublication.latestForDiscovery | d02929e1-2a70-44f0-ae17-7819f587bedd | |
relation.isParentOrgUnitOfPublication | 17f2dc8e-6e54-4fa8-b5e0-d6415123a93e | |
relation.isParentOrgUnitOfPublication.latestForDiscovery | 17f2dc8e-6e54-4fa8-b5e0-d6415123a93e |