Literature DB >> 27344649

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

Keiko Yamaguchi1, Rie Wakimizu2, Mitsuru Kubota3.   

Abstract

To assess the quality of life (QoL) of children in Japan with inborn errors of metabolism (IEM) as well as of their parents, we reviewed 23 previous studies published in Japanese and 1 published in English, focusing on the difficulties they encounter in daily life, the factors associated with these difficulties, and their QoL. We divided the difficulties and associated factors into three developmental stages. At the infant stage, individuals with IEM tend to be at high risk of hypercatabolism. Their parents suffered anxiety and distress because of the child's diet therapy and regarded the parents' support group as an essential presence, particularly given that IEM is a rare disease. At the school-age stage, as their sphere of social relationships expanded, children with IEM became nervous about being compared with healthy children of their own age because of their diet therapy. At the adolescence-to-adulthood stage, the children suffered medically, economically, and socially. Even in the absence of any IEM symptoms, the children's QoL was affected by the demands associated with the metabolic disorder, such as diet and treatment. The psychological health of their caregivers was also poor. To improve the QoL of children with IEM and of their parents, future comprehensive quantitative and qualitative studies of their QoL and of their subjective support needs are required. Additionally, the specific factors related to the QoL of such individuals need to be explored in large population-based statistical studies.

Entities:  

Year:  2016        PMID: 27344649      PMCID: PMC5413451          DOI: 10.1007/8904_2016_573

Source DB:  PubMed          Journal:  JIMD Rep        ISSN: 2192-8304


  12 in total

1.  Cultural aspects in the management of inborn errors of metabolism.

Authors:  Sylvia Stockler; Dorothea Moeslinger; Marion Herle; Banu Wimmer; Osman S Ipsiroglu
Journal:  J Inherit Metab Dis       Date:  2012-02-23       Impact factor: 4.982

2.  Treatment of a citrin-deficient patient at the early stage of adult-onset type II citrullinaemia with arginine and sodium pyruvate.

Authors:  K Mutoh; K Kurokawa; K Kobayashi; T Saheki
Journal:  J Inherit Metab Dis       Date:  2008-10-29       Impact factor: 4.982

3.  Fatigue and quality of life in citrin deficiency during adaptation and compensation stage.

Authors:  Yoshiyuki Okano; Kyoko Kobayashi; Kenji Ihara; Tetsuya Ito; Makoto Yoshino; Yoriko Watanabe; Shunsaku Kaji; Toshihiro Ohura; Masayoshi Nagao; Atsuko Noguchi; Sotaro Mushiake; Naohiro Hohashi; Tomoko Hashimoto-Tamaoki
Journal:  Mol Genet Metab       Date:  2013-02-09       Impact factor: 4.797

Review 4.  [Phenylketonuria--toward a better carry-over care].

Authors:  Makoto Yoshino; Yoriko Watanabe; Tomoko Ohira; Naomi Harada
Journal:  Nihon Rinsho       Date:  2010-01

5.  Quality of life in children treated with restrictive diet for inherited metabolic disease.

Authors:  Tuba F Eminoglu; Sebnem A Soysal; Leyla Tumer; Ilyas Okur; Alev Hasanoglu
Journal:  Pediatr Int       Date:  2013-05-30       Impact factor: 1.524

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

Authors:  Gwendolyn Gramer; Gisela Haege; Esther M Glahn; Georg F Hoffmann; Martin Lindner; Peter Burgard
Journal:  J Inherit Metab Dis       Date:  2013-08-16       Impact factor: 4.982

7.  Assessment of the impact of phenylketonuria and its treatment on quality of life of patients and parents from seven European countries.

Authors:  Annet M Bosch; Alberto Burlina; Amy Cunningham; Esther Bettiol; Flavie Moreau-Stucker; Ekaterina Koledova; Khadra Benmedjahed; Antoine Regnault
Journal:  Orphanet J Rare Dis       Date:  2015-06-18       Impact factor: 4.123

8.  Quality of Life (QoL) assessment in a cohort of patients with phenylketonuria.

Authors:  Chiara Cazzorla; Luca Cegolon; Alessandro P Burlina; Andrea Celato; Pamela Massa; Laura Giordano; Giulia Polo; Aurora Daniele; Francesco Salvatore; Alberto B Burlina
Journal:  BMC Public Health       Date:  2014-12-04       Impact factor: 3.295

Review 9.  Quality of life, psychological adjustment, and adaptive functioning of patients with intoxication-type inborn errors of metabolism - a systematic review.

Authors:  Nina A Zeltner; Martina Huemer; Matthias R Baumgartner; Markus A Landolt
Journal:  Orphanet J Rare Dis       Date:  2014-10-25       Impact factor: 4.123

10.  Evaluation of quality of life and description of the sociodemographic state in adolescent and young adult patients with phenylketonuria (PKU).

Authors:  Eva Simon; Martin Schwarz; Judith Roos; Nico Dragano; Max Geraedts; Johannes Siegrist; Gudrun Kamp; Udo Wendel
Journal:  Health Qual Life Outcomes       Date:  2008-03-26       Impact factor: 3.186

View more
  1 in total

1.  Relationship of familial cytochrome P450 4V2 gene mutation with liver cirrhosis: A case report and review of the literature.

Authors:  Jin-Lian Jiang; Jiang-Fu Qian; De-Hui Xiao; Xia Liu; Fang Zhu; Jie Wang; Zhou-Xiong Xing; De-Lin Xu; Yuan Xue; Yi-Huai He
Journal:  World J Clin Cases       Date:  2022-10-06       Impact factor: 1.534

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.