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MMCUP – a secondary prevention follow-up program in spina bifida and hydrocephalus.

Josenby, Annika Lundkvist and Westbom, Lena LU (2015) European Academy of Childhood Disabilities, Köpenhamn In Developmental Medicine & Child Neurology 57(Suppl 4). p.52-52
Abstract
In persons born with myelomeningocele (MMC) secondaryprevention measures are important to survive and to retainfunction. Swedish guidelines in MMC have been developedand a follow-up programme is linked to a quality of care reg-istry, internet-based since 2012. The rationale for creation ofthis registry were to avoid complications in MMC by provid-ing a medical and health overview, facilitate the coordinationof services, improve quality of care, learn more about MMC,health and social care management. Professionals and patientsfill in internet-based registration forms. InterdisciplinaryMMCUP-teams in each of the six tertiary health care regionsin Sweden run the program. One team includes the registryholder to create, update and quality... (More)
In persons born with myelomeningocele (MMC) secondaryprevention measures are important to survive and to retainfunction. Swedish guidelines in MMC have been developedand a follow-up programme is linked to a quality of care reg-istry, internet-based since 2012. The rationale for creation ofthis registry were to avoid complications in MMC by provid-ing a medical and health overview, facilitate the coordinationof services, improve quality of care, learn more about MMC,health and social care management. Professionals and patientsfill in internet-based registration forms. InterdisciplinaryMMCUP-teams in each of the six tertiary health care regionsin Sweden run the program. One team includes the registryholder to create, update and quality check the internet registryat a national registry competence centre, ERCSYD. 91 chil-dren born with MMC or lipo-MMC from 2007–2012 lived inSweden 1 Jan 2013, seven were born abroad. There were morefemales (n=50) than males among the 84 children born in Swe-den; total incidence 1.26/10000, 1/3 of the celes was closed. Ofthe prospectively reported children 1 Jan 2013 (n=86), two werenot operated on; the remaining 84 children, 4 months–5.9 yearsof age, had 302 operations, of which 202 neurosurgical. Updatedresults will be presented. An unselected total population bornwith MMC is followed, to date including about 100 children0–7 years of age. The high proportion of closed celes, and ahigher incidence in females in this population are preliminaryfindings that contrast to earlier studies. (Less)
Please use this url to cite or link to this publication:
author
and
organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Developmental Medicine & Child Neurology
volume
57
issue
Suppl 4
article number
PO75-94996
pages
52 - 52
publisher
John Wiley & Sons Inc.
conference name
European Academy of Childhood Disabilities, Köpenhamn
conference location
Köpenhamn, Denmark
conference dates
2015-05-27 - 2015-05-30
ISSN
0012-1622
language
English
LU publication?
yes
id
437357a5-1ecf-42ad-8a80-7dd5ad32d29f
alternative location
https://onlinelibrary.wiley.com/doi/epdf/10.1111/dmcn.12780_74
date added to LUP
2017-03-17 09:45:26
date last changed
2021-12-27 12:18:19
@misc{437357a5-1ecf-42ad-8a80-7dd5ad32d29f,
  abstract     = {{In persons born with myelomeningocele (MMC) secondaryprevention measures are important to survive and to retainfunction. Swedish guidelines in MMC have been developedand a follow-up programme is linked to a quality of care reg-istry, internet-based since 2012. The rationale for creation ofthis registry were to avoid complications in MMC by provid-ing a medical and health overview, facilitate the coordinationof services, improve quality of care, learn more about MMC,health and social care management. Professionals and patientsfill  in  internet-based  registration  forms.  InterdisciplinaryMMCUP-teams in each of the six tertiary health care regionsin Sweden run the program. One team includes the registryholder to create, update and quality check the internet registryat a national registry competence centre, ERCSYD. 91 chil-dren born with MMC or lipo-MMC from 2007–2012 lived inSweden 1 Jan 2013, seven were born abroad. There were morefemales (n=50) than males among the 84 children born in Swe-den; total incidence 1.26/10000, 1/3 of the celes was closed. Ofthe prospectively reported children 1 Jan 2013 (n=86), two werenot operated on; the remaining 84 children, 4 months–5.9 yearsof age, had 302 operations, of which 202 neurosurgical. Updatedresults will be presented. An unselected total population bornwith MMC is followed, to date including about 100 children0–7 years of age. The high proportion of closed celes, and ahigher incidence in females in this population are preliminaryfindings that contrast to earlier studies.}},
  author       = {{Josenby, Annika Lundkvist and Westbom, Lena}},
  issn         = {{0012-1622}},
  language     = {{eng}},
  note         = {{Conference Abstract}},
  number       = {{Suppl 4}},
  pages        = {{52--52}},
  publisher    = {{John Wiley & Sons Inc.}},
  series       = {{Developmental Medicine & Child Neurology}},
  title        = {{MMCUP – a secondary prevention follow-up program in spina bifida and hydrocephalus.}},
  url          = {{https://onlinelibrary.wiley.com/doi/epdf/10.1111/dmcn.12780_74}},
  volume       = {{57}},
  year         = {{2015}},
}