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Parental Burden and Quality of Life in 5q-SMA Diagnosed by Newborn Screening

Bibliographic Data

ID15716822
AuthorsHeike Kölbel (0000-0001-9629-7053, University of Duisburg-Essen, corresponding author), Laura Modler (University of Duisburg-Essen), Astrid Blaschek (0000-0003-2918-0159, University of Duisburg-Essen), Ulrike Schara‐Schmidt (0000-0001-5833-2751, University of Duisburg-Essen), Ulrike Schara-Schmidt (Centre for Neuromuscular Disorders, Center for Translational Neuro and Behavioral Sciences, Department of Pediatric Neurology, University Duisburg-Essen, 45147 Essen, Germany), Katharina Vill (0000-0003-1925-7538, Ludwig-Maximilians-Universität München), Oliver Schwartz (University Hospital Münster), Wolfgang Müller‐Felber (0000-0001-9916-5048, University of Duisburg-Essen), Wolfgang Müller-Felber (Centre for Neuromuscular Disorders, Center for Translational Neuro and Behavioral Sciences, Department of Pediatric Neurology, University Duisburg-Essen, 45147 Essen, Germany)
Year2022
Volume9
Issue12
Pages1829-1829
Publication date2022-11-26
Open AccessYes
TypeARTICLE
VenueChildren (JOURNAL)
Journal identifiersISSN: 2227-9067 • E-ISSN: 2227-9067
PublisherMultidisciplinary Digital Publishing Institute (PUBLISHER • CH)
DOI10.3390/children9121829
PMID36553273
OpenAlexW4310213141
LanguageEN
Citations received1
References cited36

The aim of this study was to assess the psychosocial burden in parents of children with spinal muscular atrophy (SMA), detected by newborn screening (NBS), for which first pilot projects started in January 2018 in Germany. The survey, performed 1-2 years after children's diagnosis of SMA via NBS, included 3 parent-related questionnaires to evaluate the psychosocial burden, quality of life (QoL)/satisfaction and work productivity and activity impairment in the families. 42/44 families, detected between January 2018 and February 2020, could be investigated. Interestingly, statistical analysis revealed a significant difference between families with children that received SMN-targeted therapy vs. children with a wait-and-see strategy as to social burden ( p = 0.016) and personal strain/worries about the future ( p = 0.02). However, the evaluation of QoL showed no significant differences between treated vs. untreated children. Fathers of treated children felt more negative impact regarding their productivities at work ( p = 0.005) and more negative effects on daily activities ( p = 0.022) than fathers of untreated children. Thus, NBS in SMA has a psychosocial impact on families, not only in terms of diagnosis but especially in terms of treatment, and triggers concerns about the future, emphasizing the need for comprehensive multidisciplinary care. Understanding the parents' perspective allows genetic counselors and NBS programs to proactively develop a care plan for parents during the challenging time of uncertainty, anxiety, frustration, and fear of the unknown

Anxiety · Caregiver burden · Disease · Multidisciplinary approach · Psychiatry · Psychosocial · Quality of life (healthcare · SMA · Spinal muscular atrophy · Clinical Psychology · Congenital Anomalies and Fetal Surgery · Medicine · Neurogenetic and Muscular Disorders Research · Nursing · Prenatal Screening and Diagnostics · Psychology · Gerontology · Internal Medicine · Pediatrics

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    Open Access•Maja Brandt, Joenna Driemeyer et al.•BMC Psychology•2024

  • The Validity and Reproducibility of a Work Productivity and Activity Impairment Instrument

    Open Access•Margaret C Reilly, Arthur S Zbrozek et al.•PharmacoEconomics•1993

  • Diseases Costs and Impact of the Caring Role on Informal Carers of Children with Neuromuscular Disease

    Open Access•Alicia Aurora Rodríguez, Óscar Martinez et al.•International Journal of…•2021

  • Quality of Life in Families of Children with Congenital Heart Disease

    Open Access•Lutz Goldbeck, Juliane Melches•Quality of Life Research•2005

  • The impact of newly diagnosed chronic paediatric conditions on parental quality of life

    Open Access•Lutz Goldbeck•Quality of Life Research•2006

  • The Development of an Impact-on-Family Scale

    Ruths E K Stein, Catherine Kohler Riessman•Medical Care•1980

Citations per year0.5
Citation span2024 - 2024 (1)
Highly citedNo

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