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Sökning: id:"swepub:oai:lup.lub.lu.se:f7e65790-be18-4df3-9123-b5f161c695a3" > Diagnosis and manag...

Diagnosis and management of individuals with Fetal Valproate Spectrum Disorder; A consensus statement from the European Reference Network for Congenital Malformations and Intellectual Disability

Clayton-Smith, Jill (författare)
Manchester Centre for Genomic Medicine,University of Manchester
Bromley, Rebecca (författare)
University of Manchester,Royal Manchester Children's Hospital
Dean, John (författare)
Aberdeen Royal Infirmary
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Journel, Hubert (författare)
Centre Hospitalier Bretagne Atlantique
Odent, Sylvie (författare)
CHU Hôpital Sud, Rennes
Wood, Amanda (författare)
Aston University,Murdoch Children's Research Institute
Williams, Janet (författare)
The Fetal Anti-Convulsant Trust (FACT)
Cuthbert, Verna (författare)
Royal Manchester Children's Hospital
Hackett, Latha (författare)
Royal Manchester Children's Hospital
Aslam, Neelo (författare)
Royal Manchester Children's Hospital
Malm, Heli (författare)
Helsinki University Central Hospital,University of Helsinki
James, Gregory (författare)
University College London,National Hospital for Neurology and Neurosurgery,Great Ormond Street Hospital
Westbom, Lena (författare)
Lund University,Lunds universitet,Pediatrik, Lund,Sektion V,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Paediatrics (Lund),Section V,Department of Clinical Sciences, Lund,Faculty of Medicine,Skåne University Hospital
Day, Ruth (författare)
Guardian Medical Centre
Ladusans, Edmund (författare)
Royal Manchester Children's Hospital
Jackson, Adam (författare)
Salford Royal NHS Foundation Trust
Bruce, Iain (författare)
Royal Manchester Children's Hospital
Walker, Robert (författare)
Royal Manchester Children's Hospital
Sidhu, Sangeet (författare)
Royal Manchester Children's Hospital
Dyer, Catrina (författare)
Royal Manchester Children's Hospital
Ashworth, Jane (författare)
University Hospital of South Manchester NHS Foundation Trust
Hindley, Daniel (författare)
Breightmet Health Centre
DIaz, Gemma Arca (författare)
Hospital Clínic of Barcelona
Rawson, Myfanwy (författare)
Manchester Centre for Genomic Medicine
Turnpenny, Peter (författare)
Royal Devon & Exeter Hospital
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 (creator_code:org_t)
2019-07-19
2019
Engelska.
Ingår i: Orphanet Journal of Rare Diseases. - : Springer Science and Business Media LLC. - 1750-1172. ; 14:1
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Background: A pattern of major and minor congenital anomalies, facial dysmorphic features, and neurodevelopmental difficulties, including cognitive and social impairments has been reported in some children exposed to sodium valproate (VPA) during pregnancy. Recognition of the increased risks of in utero exposure to VPA for congenital malformations, and for the neurodevelopmental effects in particular, has taken many years but these are now acknowledged following the publication of the outcomes of several prospective studies and registries. As with other teratogens, exposure to VPA can have variable effects, ranging from a characteristic pattern of major malformations and significant intellectual disability to the other end of the continuum, characterised by facial dysmorphism which is often difficult to discern and a more moderate effect on neurodevelopment and general health. It has become clear that some individuals with FVSD have complex needs requiring multidisciplinary care but information regarding management is currently lacking in the medical literature. Methods: An expert group was convened by ERN-ITHACA, the European Reference Network for Congenital Malformations and Intellectual Disability comprised of professionals involved in the care of individuals with FVSD and with patient representation. Review of published and unpublished literature concerning management of FVSD was undertaken and the level of evidence from these sources graded. Management recommendations were made based on strength of evidence and consensus expert opinion, in the setting of an expert consensus meeting. These were then refined using an iterative process and wider consultation. Results: Whilst there was strong evidence regarding the increase in risk for major congenital malformations and neurodevelopmental difficulties there was a lack of high level evidence in other areas and in particular in terms of optimal clinical management. The expert consensus approach facilitated the formulation of management recommendations, based on literature evidence and best practice. The outcome of the review and group discussions leads us to propose the term Fetal Valproate Spectrum Disorder (FVSD) as we feel this better encompasses the broad range of effects seen following VPA exposure in utero. Conclusion: The expert consensus approach can be used to define the best available clinical guidance for the diagnosis and management of rare disorders such as FVSD. FVSD can have medical, developmental and neuropsychological impacts with life-long consequences and affected individuals benefit from the input of a number of different health professionals.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Hälsovetenskap -- Hälso- och sjukvårdsorganisation, hälsopolitik och hälsoekonomi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Health Sciences -- Health Care Service and Management, Health Policy and Services and Health Economy (hsv//eng)

Nyckelord

Antiepileptic drug
Expert consensus
Fetal valproate syndrome
Guideline
Management
Teratogen

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