Observations from a nationwide vigilance program in medical care for spinal muscular atrophy patients in Chile

Detalhes bibliográficos
Autor(a) principal: ALVAREZ,Karin
Data de Publicação: 2019
Outros Autores: SUAREZ,Bernardita, PALOMINO,María Angélica, HERVIAS,Cecilia, CALCAGNO,Giancarlo, MARTÍNEZ-JALILIE,Maripaz, LOZANO-ARANGO,Andrés, LILLO,Susana, HARO,Mariana, CORTÉS,Fanny, PANTOJA,Samuel, CHAHIN,Andrés, ORELLANA,Paulina, BEVILACQUA,Jorge A, BERTINI,Enrico, CASTIGLIONI,Claudia
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Arquivos de neuro-psiquiatria (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2019000700470
Resumo: ABSTRACT Spinal muscular atrophy (SMA) has gained much attention in the last few years because of the approval of the first intrathecal treatment for this neurodegenerative disease. Latin America needs to develop the demographics of SMA, timely access to diagnosis, and appropriate following of the standards of care recommendations for patients. These are essential steps to guide health policies. Methods This was a descriptive study of a cohort of SMA patients from all over Chile. We analyzed the clinical, motor functional, and social data, as well as the care status of nutritional, respiratory and skeletal conditions. We also measured the SMN2 copy number in this population. Results We recruited 92 patients: 50 male; 23 SMA type-1, 36 SMA type-2 and 33 SMA type-3. The median age at genetic diagnosis was 5, 24 and 132 months. We evaluated the SMN2 copy number in 57 patients. The SMA type-1 patients were tracheostomized and fed by gastrostomy in a 69.6 % of cases, 65% of SMA type-2 patients received nocturnal noninvasive ventilation, and 37% of the whole cohort underwent scoliosis surgery. Conclusion Ventilatory care for SMA type-1 is still based mainly on tracheostomy. This Chilean cohort of SMA patients had timely access to genetic diagnosis, ventilatory assistance, nutritional support, and scoliosis surgery. In this series, SMA type-1 is underrepresented, probably due to restrictions in access to early diagnosis and the high and early mortality rate.
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spelling Observations from a nationwide vigilance program in medical care for spinal muscular atrophy patients in ChileSpinal muscular atrophyLatin AmericademographyStandard of careSMN1ABSTRACT Spinal muscular atrophy (SMA) has gained much attention in the last few years because of the approval of the first intrathecal treatment for this neurodegenerative disease. Latin America needs to develop the demographics of SMA, timely access to diagnosis, and appropriate following of the standards of care recommendations for patients. These are essential steps to guide health policies. Methods This was a descriptive study of a cohort of SMA patients from all over Chile. We analyzed the clinical, motor functional, and social data, as well as the care status of nutritional, respiratory and skeletal conditions. We also measured the SMN2 copy number in this population. Results We recruited 92 patients: 50 male; 23 SMA type-1, 36 SMA type-2 and 33 SMA type-3. The median age at genetic diagnosis was 5, 24 and 132 months. We evaluated the SMN2 copy number in 57 patients. The SMA type-1 patients were tracheostomized and fed by gastrostomy in a 69.6 % of cases, 65% of SMA type-2 patients received nocturnal noninvasive ventilation, and 37% of the whole cohort underwent scoliosis surgery. Conclusion Ventilatory care for SMA type-1 is still based mainly on tracheostomy. This Chilean cohort of SMA patients had timely access to genetic diagnosis, ventilatory assistance, nutritional support, and scoliosis surgery. In this series, SMA type-1 is underrepresented, probably due to restrictions in access to early diagnosis and the high and early mortality rate.Academia Brasileira de Neurologia - ABNEURO2019-07-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2019000700470Arquivos de Neuro-Psiquiatria v.77 n.7 2019reponame:Arquivos de neuro-psiquiatria (Online)instname:Academia Brasileira de Neurologiainstacron:ABNEURO10.1590/0004-282x20190073info:eu-repo/semantics/openAccessALVAREZ,KarinSUAREZ,BernarditaPALOMINO,María AngélicaHERVIAS,CeciliaCALCAGNO,GiancarloMARTÍNEZ-JALILIE,MaripazLOZANO-ARANGO,AndrésLILLO,SusanaHARO,MarianaCORTÉS,FannyPANTOJA,SamuelCHAHIN,AndrésORELLANA,PaulinaBEVILACQUA,Jorge ABERTINI,EnricoCASTIGLIONI,Claudiaeng2019-10-21T00:00:00Zoai:scielo:S0004-282X2019000700470Revistahttp://www.scielo.br/anphttps://old.scielo.br/oai/scielo-oai.php||revista.arquivos@abneuro.org1678-42270004-282Xopendoar:2019-10-21T00:00Arquivos de neuro-psiquiatria (Online) - Academia Brasileira de Neurologiafalse
dc.title.none.fl_str_mv Observations from a nationwide vigilance program in medical care for spinal muscular atrophy patients in Chile
title Observations from a nationwide vigilance program in medical care for spinal muscular atrophy patients in Chile
spellingShingle Observations from a nationwide vigilance program in medical care for spinal muscular atrophy patients in Chile
ALVAREZ,Karin
Spinal muscular atrophy
Latin America
demography
Standard of care
SMN1
title_short Observations from a nationwide vigilance program in medical care for spinal muscular atrophy patients in Chile
title_full Observations from a nationwide vigilance program in medical care for spinal muscular atrophy patients in Chile
title_fullStr Observations from a nationwide vigilance program in medical care for spinal muscular atrophy patients in Chile
title_full_unstemmed Observations from a nationwide vigilance program in medical care for spinal muscular atrophy patients in Chile
title_sort Observations from a nationwide vigilance program in medical care for spinal muscular atrophy patients in Chile
author ALVAREZ,Karin
author_facet ALVAREZ,Karin
SUAREZ,Bernardita
PALOMINO,María Angélica
HERVIAS,Cecilia
CALCAGNO,Giancarlo
MARTÍNEZ-JALILIE,Maripaz
LOZANO-ARANGO,Andrés
LILLO,Susana
HARO,Mariana
CORTÉS,Fanny
PANTOJA,Samuel
CHAHIN,Andrés
ORELLANA,Paulina
BEVILACQUA,Jorge A
BERTINI,Enrico
CASTIGLIONI,Claudia
author_role author
author2 SUAREZ,Bernardita
PALOMINO,María Angélica
HERVIAS,Cecilia
CALCAGNO,Giancarlo
MARTÍNEZ-JALILIE,Maripaz
LOZANO-ARANGO,Andrés
LILLO,Susana
HARO,Mariana
CORTÉS,Fanny
PANTOJA,Samuel
CHAHIN,Andrés
ORELLANA,Paulina
BEVILACQUA,Jorge A
BERTINI,Enrico
CASTIGLIONI,Claudia
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv ALVAREZ,Karin
SUAREZ,Bernardita
PALOMINO,María Angélica
HERVIAS,Cecilia
CALCAGNO,Giancarlo
MARTÍNEZ-JALILIE,Maripaz
LOZANO-ARANGO,Andrés
LILLO,Susana
HARO,Mariana
CORTÉS,Fanny
PANTOJA,Samuel
CHAHIN,Andrés
ORELLANA,Paulina
BEVILACQUA,Jorge A
BERTINI,Enrico
CASTIGLIONI,Claudia
dc.subject.por.fl_str_mv Spinal muscular atrophy
Latin America
demography
Standard of care
SMN1
topic Spinal muscular atrophy
Latin America
demography
Standard of care
SMN1
description ABSTRACT Spinal muscular atrophy (SMA) has gained much attention in the last few years because of the approval of the first intrathecal treatment for this neurodegenerative disease. Latin America needs to develop the demographics of SMA, timely access to diagnosis, and appropriate following of the standards of care recommendations for patients. These are essential steps to guide health policies. Methods This was a descriptive study of a cohort of SMA patients from all over Chile. We analyzed the clinical, motor functional, and social data, as well as the care status of nutritional, respiratory and skeletal conditions. We also measured the SMN2 copy number in this population. Results We recruited 92 patients: 50 male; 23 SMA type-1, 36 SMA type-2 and 33 SMA type-3. The median age at genetic diagnosis was 5, 24 and 132 months. We evaluated the SMN2 copy number in 57 patients. The SMA type-1 patients were tracheostomized and fed by gastrostomy in a 69.6 % of cases, 65% of SMA type-2 patients received nocturnal noninvasive ventilation, and 37% of the whole cohort underwent scoliosis surgery. Conclusion Ventilatory care for SMA type-1 is still based mainly on tracheostomy. This Chilean cohort of SMA patients had timely access to genetic diagnosis, ventilatory assistance, nutritional support, and scoliosis surgery. In this series, SMA type-1 is underrepresented, probably due to restrictions in access to early diagnosis and the high and early mortality rate.
publishDate 2019
dc.date.none.fl_str_mv 2019-07-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2019000700470
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2019000700470
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/0004-282x20190073
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
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dc.publisher.none.fl_str_mv Academia Brasileira de Neurologia - ABNEURO
publisher.none.fl_str_mv Academia Brasileira de Neurologia - ABNEURO
dc.source.none.fl_str_mv Arquivos de Neuro-Psiquiatria v.77 n.7 2019
reponame:Arquivos de neuro-psiquiatria (Online)
instname:Academia Brasileira de Neurologia
instacron:ABNEURO
instname_str Academia Brasileira de Neurologia
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reponame_str Arquivos de neuro-psiquiatria (Online)
collection Arquivos de neuro-psiquiatria (Online)
repository.name.fl_str_mv Arquivos de neuro-psiquiatria (Online) - Academia Brasileira de Neurologia
repository.mail.fl_str_mv ||revista.arquivos@abneuro.org
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