oru.sePublikasjoner
Endre søk
RefereraExporteraLink to record
Permanent link

Direct link
Referera
Referensformat
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Annet format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annet språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf
The highest mortality rates in childhood dilated cardiomyopathy occur during the first year after diagnosis
Department of Paediatrics, Örebro University Hospital, Örebro, Sweden.
The Queen Silvia Children`s Hospital, Institution of Clinical Sciences, Sahlgrenska University Hospital, Gothenburg University, Gothenburg, Sweden.
Örebro universitet, Institutionen för medicinska vetenskaper. (Clinical Epidemiology and Biostatistics)ORCID-id: 0000-0002-3649-2639
Örebro universitet, Institutionen för medicinska vetenskaper. Region Örebro län. Unit of Biostatistics, Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden. (Clinical Epidemiology and Biostatistics)ORCID-id: 0000-0002-3552-9153
Vise andre og tillknytning
2018 (engelsk)Inngår i: Acta Paediatrica, ISSN 0803-5253, E-ISSN 1651-2227, Vol. 107, nr 4, s. 672-677Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

AIM: The aim of the study was to assess the incidence, mortality and morbidity of dilated cardiomyopathy (DCM) and non-compaction of the left ventricle (LVNC) in Swedish children.

METHODS: We reviewed hospital records of all children with dilated cardiomyopathy (DCM) or left ventricular non-compaction cardiomyopathy (LVNC) up to the age of 18 in the healthcare region of western Sweden from 1991 to 2015.

RESULTS: In total, 69 cases (61% males) were identified. The combined incidence of DCM and LVNC was 0.77 (95% CI 0.59-0.96) per 100,000 person years. Children were divided into six groups and their outcomes were analysed depending on their aetiology. Idiopathic DCM was reported in 43% and familial dilated and left ventricular non-compaction aetiology was present in 32%. DCM due to various diseases occurred in 8%. DCM associated with neuromuscular diseases was present in 16%. The overall risk of death or receiving transplants in children with idiopathic and familial DCM was 30% over the study period and 21% died in the first year after diagnosis.

CONCLUSION: The combined incidence of DCM and LVNC was similar to previous reports. Most children with idiopathic DCM presented during infancy and mortality was highest during the first year after diagnosis.

sted, utgiver, år, opplag, sider
John Wiley & Sons, 2018. Vol. 107, nr 4, s. 672-677
Emneord [en]
Cardiomyopathy, cohort study, dilated cardiomyopathy, incidence mortality
HSV kategori
Identifikatorer
URN: urn:nbn:se:oru:diva-63447DOI: 10.1111/apa.14183ISI: 000427002500023PubMedID: 29224255Scopus ID: 2-s2.0-85038892042OAI: oai:DiVA.org:oru-63447DiVA, id: diva2:1167874
Merknad

Funding Agencies:

Örebro County Research Committee  OLL-524371 

Sahlgrenska University Hospital  

Tilgjengelig fra: 2017-12-19 Laget: 2017-12-19 Sist oppdatert: 2018-08-16bibliografisk kontrollert

Open Access i DiVA

Fulltekst mangler i DiVA

Andre lenker

Forlagets fulltekstPubMedScopus

Personposter BETA

Fall, KatjaCao, Yang

Søk i DiVA

Av forfatter/redaktør
Fall, KatjaCao, Yang
Av organisasjonen
I samme tidsskrift
Acta Paediatrica

Søk utenfor DiVA

GoogleGoogle Scholar

doi
pubmed
urn-nbn

Altmetric

doi
pubmed
urn-nbn
Totalt: 203 treff
RefereraExporteraLink to record
Permanent link

Direct link
Referera
Referensformat
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Annet format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annet språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf