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[Spanish patients with central hypoventilation syndrome included in the European Registry. The 2015 data]. / Pacientes españoles con síndrome de hipoventilación central incluidos en el Registro europeo. Datos del 2015.
García Teresa, María Angeles; Porto Abal, Raquel; Rodríguez Torres, Silvia; García Urabayen, Diego; García Martínez, Silvia; Trang, Ha; Campos Barros, Angel; Llorente de la Fuente, Ana; Hernández González, Arturo; Bustinza Arriortua, Amaya; de la Cruz Moreno, Jesús; Pons Odena, Martí; Ventura Faci, Purificación; Rubio Ortega, Laura; Pérez Ruiz, Estela; Aguilar Fernández, Antonio; Pérez Ocón, Amaya; Osona, Borja; Delgado Pecellin, Isabel; Arroyo Carrera, Ignacio; Sayas Catalán, Javier; González Salas, Elvira; de Vicente, Carlos Martin.
Afiliación
  • García Teresa MA; Cuidados Intensivos Pediátricos, Hospital Niño Jesús, Madrid, España. Electronic address: angelesgarciateresa@gmail.com.
  • Porto Abal R; Pediatría, CS Villalva Pueblo, Madrid, España.
  • Rodríguez Torres S; Neumología Pediátrica, Hospital Sant Joan de Déu, Barcelona, Barcelona, España.
  • García Urabayen D; Cuidados Intensivos Pediátricos, Hospital de Cruces, Bilbao, Vizcaya, España.
  • García Martínez S; Hospitalización Domiciliaria Pediátrica, Hospital de la Arrixaca, Murcia, España.
  • Trang H; Centro de Referencia Francés de Hipoventilación Central, Hospital Robert Debré, Consorcio Europeo del Síndrome de Hipoventilación Central, París, Francia.
  • Campos Barros A; Instituto de Genética Médica y Molecular, IdiPAz, Hospital Universitario La Paz, CIBER de Enfermedades Raras, ISCIII, Madrid, España.
  • Llorente de la Fuente A; Cuidados Intensivos Pediátricos, Hospital Doce de Octubre, Madrid, España.
  • Hernández González A; Cuidados Intensivos Pediátricos, Hospital Puerta del Mar, Cádiz, España.
  • Bustinza Arriortua A; Cuidados Intensivos Pediátricos, Hospital Gregorio Marañón, Madrid, España.
  • de la Cruz Moreno J; Pediatría, Hospital Universitario Materno Infantil, Jaén, España.
  • Pons Odena M; Cuidados Intensivos Pediátricos, Hospital Sant Joan de Déu, Barcelona, España.
  • Ventura Faci P; Neonatología, Hospital Lozano Blesa, Zaragoza, España.
  • Rubio Ortega L; Hospitalización a Domicilio Pediátrica, Hospital General Universitario, Alicante, España.
  • Pérez Ruiz E; Neumología Infantil, Hospital Carlos Haya, Málaga, España.
  • Aguilar Fernández A; Neumología Pediátrica, Hospital Materno Infantil, Las Palmas, España.
  • Pérez Ocón A; Cuidados Intensivos Pediátricos, Complejo Hospitalario de Navarra, Pamplona, Navarra, España.
  • Osona B; Neumología Pediátrica, Hospital Son Espases, Palma de Mallorca, Islas Baleares, España.
  • Delgado Pecellin I; Neumología Pediátrica, Hospital Virgen del Rocío, Sevilla, España.
  • Arroyo Carrera I; Neonatología, Hospital San Pedro de Alcántara, Cáceres, España.
  • Sayas Catalán J; Neumología, Hospital Doce de Octubre, Madrid, España.
  • González Salas E; Cuidados Intensivos Pediátricos, Hospital Universitario de Salamanca, Salamanca, España.
  • de Vicente CM; Neumología Pediátrica, Hospital Miguel Servet, Zaragoza, España.
An Pediatr (Barc) ; 86(5): 255-263, 2017 May.
Article en Es | MEDLINE | ID: mdl-27377324
ABSTRACT

INTRODUCTION:

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.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Apnea Central del Sueño / Hipoventilación Tipo de estudio: Diagnostic_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male País/Región como asunto: Europa Idioma: Es Revista: An Pediatr (Barc) Asunto de la revista: PEDIATRIA Año: 2017 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Apnea Central del Sueño / Hipoventilación Tipo de estudio: Diagnostic_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male País/Región como asunto: Europa Idioma: Es Revista: An Pediatr (Barc) Asunto de la revista: PEDIATRIA Año: 2017 Tipo del documento: Article