Literature DB >> 23949009

Living with an inborn error of metabolism detected by newborn screening-parents' perspectives on child development and impact on family life.

Gwendolyn Gramer1, Gisela Haege, Esther M Glahn, Georg F Hoffmann, Martin Lindner, Peter Burgard.   

Abstract

BACKGROUND: Newborn screening for inborn errors of metabolism is regarded as highly successful by health professionals. Little is known about parents' perspectives on child development and social impact on families.
METHODS: Parents of 187 patients with metabolic disorders detected by newborn screening rated child development, perceived burdens on child and family, and future expectations on a questionnaire with standardized answers. Parental ratings were compared with standardized psychometric test results. Regression analysis was performed to identify factors associated with extent of perceived burden.
RESULTS: In 26.2% of patients, parents perceived delays in global development and/or specific developmental domains (physical, social, intellectual, language). Parents expected normal future development in 95.7%, and an independent adult life for their child in 94.6%. Comparison with psychometric test results showed that parents of children with cognitive impairments tended to overrate their child's abilities. Mild/medium burden posed on the family (child) by the metabolic disorder was stated by 56.1% (48.9%) of parents, severe/very severe burden by 19.3% (8.6%). One third of families reported financial burden due to the metabolic disorder. Dietary treatment and diagnoses with risk for metabolic decompensation despite treatment were associated with higher perceived burden for the family. Disorders rated as potentially very burdensome by experts were not rated accordingly by parents, demonstrating different perspectives of professionals and parents.
CONCLUSION: Although newborn screening leads to favourable physical and cognitive outcome, living with a metabolic disorder may cause considerable stress on patients and families, emphasizing the need for comprehensive multidisciplinary care including psychological and social support.

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Mesh:

Year:  2013        PMID: 23949009     DOI: 10.1007/s10545-013-9639-6

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  22 in total

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  13 in total

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Review 2.  Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision.

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3.  Difficulties in Daily Life and Associated Factors, and QoL of Children with Inherited Metabolic Disease and Their Parents in Japan: A Literature Review.

Authors:  Keiko Yamaguchi; Rie Wakimizu; Mitsuru Kubota
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4.  Parent Coping and the Behavioural and Social Outcomes of Children Diagnosed with Inherited Metabolic Disorders.

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6.  Experiences of caregivers of children with inherited metabolic diseases: a qualitative study.

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8.  What are the information needs of parents caring for a child with Glutaric aciduria type 1?

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9.  Screening for organic acidurias and aminoacidopathies in high-risk Brazilian patients: Eleven-year experience of a reference center.

Authors:  Moacir Wajner; Angela Sitta; Aline Kayser; Marion Deon; Ana C Groehs; Daniella M Coelho; Carmen R Vargas
Journal:  Genet Mol Biol       Date:  2019-04-11       Impact factor: 1.771

10.  Parental Experiences of Raising a Child With Medium Chain Acyl-CoA Dehydrogenase Deficiency.

Authors:  Hilary Piercy; Katarzyna Machaczek; Parveen Ali; Sufin Yap
Journal:  Glob Qual Nurs Res       Date:  2017-05-03
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