Spanish patients with central hypoventilation syndrome included in the European Registry. The 2015 data

dc.contributor.authorTeresa, Maria Angeles Garcia
dc.contributor.authorAbal, Raquel Porto
dc.contributor.authorTorres, Silvia Rodriguez
dc.contributor.authorUrabayen, Diego Garcia
dc.contributor.authorMartinez, Silvia Garcia
dc.contributor.authorTrang, Ha
dc.contributor.authorBarros, Angel Campos
dc.contributor.authorGrupo Espanol de Trabajo del SHCC
dc.contributor.authoraffiliation[Teresa, Maria Angeles Garcia] Hosp Nino Jesus, Cuidados Intensivos Pediat, Madrid, Spain
dc.contributor.authoraffiliation[Abal, Raquel Porto] CS Villalva Pueblo, Pediat, Madrid, Spain
dc.contributor.authoraffiliation[Torres, Silvia Rodriguez] Hosp St Joan de Deu, Neumol Pediat, Barcelona, Spain
dc.contributor.authoraffiliation[Urabayen, Diego Garcia] Hosp Cruces, Cuidados Intensivos Pediat, Bilbao, Vizcaya, Spain
dc.contributor.authoraffiliation[Martinez, Silvia Garcia] Hosp Arrixaca, Hospitalizac Domiciliaria Pediat, Murcia, Spain
dc.contributor.authoraffiliation[Trang, Ha] Hosp Robert Debre, Consorcio Europeo Sindrome Hipoventilac Cent, Ctr Referencia Frances Hipoventilac Cent, Paris, France
dc.contributor.authoraffiliation[Barros, Angel Campos] Hosp Univ La Paz, ISCIII, CIBER Enfermedades Raras, Inst Genet Med & Mol,IdiPAz, Madrid, Spain
dc.date.accessioned2025-01-07T12:50:52Z
dc.date.available2025-01-07T12:50:52Z
dc.date.issued2017-05-01
dc.description.abstractIntroduction: Congenital Central Hypoventilation Syndrome (CCHS) is a very rare genetic disease. In 2012 the European Central Hypoventilation Syndrome (EuCHS) Consortium created an online patient registry in order to improve care.Aim: To determine the characteristics and outcomes of Spanish patients with CCHS, and detect clinical areas for improvement.Materials and method: An assessment was made on the data from Spanish patients in the European Registry, updated on December 2015.Results: The Registry contained 38 patients, born between 1987 and 2013, in 18 hospitals. Thirteen (34.2%) were older than 18 years. Three patients had died. Genetic analysis identified PHOX2B mutations in 32 (86.5%) out of 37 patients assessed. The 20/25, 20/26 and 20/27 polyalanine repeat mutations (PARMs) represented 84.3% of all mutations. Longer PARMs had more, as well as more severe, autonomic dysfunctions. Eye diseases were present in 47%, with 16% having Hirschsprung disease, 13% with hypoglycaemia, and 5% with tumours. Thirty patients (79%) required ventilation from the neonatal period onwards, and 8 (21%) later on in life (late onset/presentation). Eight children (21%) were using mask ventilation at the first home discharge. Five of them were infants with neonatal onset, two of them, both having a severe mutation, were switched to tracheostomy after cardiorespiratory arrest at home. Approximately one-third (34.3%) of patients were de-cannulated and switched to mask ventilation at a mean age of 13.7 years. Educational reinforcement was required in 29.4% of children attending school.Conclusion: The implementation of the EuCHS Registry in Spain has identified some relevant issues for optimising healthcare, such as the importance of genetic study for diagnosis and assessment of severity, the high frequency of eye disease and educational reinforcement, as well as some limitations in ventilatory techniques. (C) 2016 Asociacion Espanola de Pediatria. Published by Elsevier Espana, S.L.U. All rights reserved.
dc.identifier.doi10.1016/j.anpedi.2016.05.008
dc.identifier.essn1696-4608
dc.identifier.issn1695-4033
dc.identifier.pmid27377324
dc.identifier.unpaywallURLhttps://doi.org/10.1016/j.anpedi.2016.05.008
dc.identifier.urihttps://hdl.handle.net/10668/24988
dc.identifier.wosID401496800004
dc.issue.number5
dc.journal.titleAnales de pediatria
dc.journal.titleabbreviationAn. pediatr.
dc.language.isoes
dc.organizationSAS - Hospital Universitario Torrecárdenas
dc.organizationSAS - Hospital Universitario de Jaén
dc.organizationSAS - Hospital Universitario Regional de Málaga
dc.page.number255-263
dc.publisherEdiciones doyma s a
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectCongenital central hypoventilation syndrome
dc.subjectRegistry
dc.subjectHealth care
dc.subjectRare disease
dc.subjectPHOX2B
dc.subjectOnset central hypoventilation
dc.subjectPositive-pressure ventilation
dc.subjectHypothalamic dysfunction
dc.subjectAutomatic-control
dc.subjectOndines-curse
dc.subjectPhox2b gene
dc.subjectChildren
dc.subjectMutations
dc.subjectPhenotype
dc.subjectFailure
dc.titleSpanish patients with central hypoventilation syndrome included in the European Registry. The 2015 data
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number86
dc.wostypeArticle

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