Publication:
Continuous venovenous hemodiafiltration in the treatment of maple syrup urine disease

dc.contributor.coauthorŞık, Güntülü
dc.contributor.coauthorTopal, Nilüfer
dc.contributor.coauthorÇıtak, Agop
dc.contributor.coauthorZeybek, Çigdem
dc.contributor.coauthorTüten, Abdülhamit
dc.contributor.departmentSchool of Medicine
dc.contributor.facultymemberYes
dc.contributor.kuauthorDemirkol, Demet
dc.contributor.kuauthorBilge, İlmay
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-09T23:39:21Z
dc.date.issued2016
dc.description.abstractBackground: 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) μmol/l before and was 256.5 ± 150.6 (117-646) μmol/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.
dc.description.fulltextNo
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.openaccessNO
dc.description.peerreviewstatusN/A
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.studentonlypublicationNo
dc.description.studentpublicationNo
dc.description.versionN/A
dc.identifier.WoSQuartileQ2
dc.identifier.doi10.1159/000443783
dc.identifier.eissn1421-9735
dc.identifier.embargoN/A
dc.identifier.endpage32
dc.identifier.issn0253-5068
dc.identifier.issue1
dc.identifier.pubmed26998605
dc.identifier.scopus2-s2.0-84961390738
dc.identifier.startpage27
dc.identifier.urihttps://doi.org/10.1159/000443783
dc.identifier.urihttps://hdl.handle.net/20.500.14288/13097
dc.identifier.volume42
dc.identifier.wos000377999600007
dc.keywordsMaple syrup urine disease
dc.keywordsContinuous renal replacement therapy
dc.keywordsHemodiafiltration
dc.keywordsLeucine
dc.keywordsEncephalopathy
dc.language.isoeng
dc.publisherKarger
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofBlood Purification
dc.relation.openaccessN/A
dc.rightsN/A
dc.subjectPediatric intensive care
dc.subjectNephrology
dc.subjectInherited metabolic disorders
dc.titleContinuous venovenous hemodiafiltration in the treatment of maple syrup urine disease
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorDemirkol, Demet
local.contributor.kuauthorBilge, İlmay
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relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
relation.isParentOrgUnitOfPublication.latestForDiscovery17f2dc8e-6e54-4fa8-b5e0-d6415123a93e

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