Literature DB >> 26382660

Quality of Life and Anxiety in Parents of Children with an Anorectal Malformation or Hirschsprung Disease: The First Year after Diagnosis.

Marieke J Witvliet1, Roel Bakx1, Sander Zwaveling2, Tonnis H van Dijk3, Alida F W van der Steeg1.   

Abstract

INTRODUCTION: In 2012, we started the KLANKbord-study. A quality of life (QoL) study that follows patients with an anorectal malformation (ARM) or Hirschsprung disease (HD) and their parents from diagnosis till the age of 18 years. We hypothesized that the diagnosis of ARM or HD initially has a negative influence on QoL and anxiety levels of parents, but that this influence will diminish over time. The aim of this study is to see whether QoL and anxiety levels of parents change within the first year after the diagnosis.
METHODS: Parents of all children born with ARM or HD, were eligible for this study. Within 3 months after the diagnosis ARM or HD, parents received a set of validated QoL questionnaires (measurement 1). Measurement 2 was 12 months after the first questionnaire. MAIN
RESULTS: During measurement 1 mothers (n = 20) scored significantly higher on the social (p value, 0.01; 95% confidence interval [CI], 0.3946-3.1528) and environmental domain (p value, 0.01; 95% CI, 0.4449-2.2851) of the World Health Organization Quality of Life-BREF (WHOQOL-BREF) compared with the known reference values. Fathers (n = 19) scored significantly higher on the physical (p value, 0.01; 95% CI, 0.2964-1.8072), psychological (p value, 0.001; 95% CI, 0.7697-2.4757), and environmental domain (p value, 0.003; 95% CI, 0.5586-2.4214) than the reference values. Comparison of all domains of the WHOQOL-BREF for mothers and fathers between measurements did not show a significant difference. Anxiety levels of mothers were lower during measurement 2 compared with measurement 1. Anxiety levels of fathers were higher during measurement 2 compared with measurement 1. These differences are not significant. Anxiety levels of mothers were significantly higher than anxiety levels of fathers during measurement 1 (p value, 0.002; 95% CI, 0.808-2,956). During measurement 2 this difference in anxiety of mothers versus fathers did not exist (p value, 0.373; 95% CI, -1.157 to 2.922).
CONCLUSION: A negative influence on the QoL of parents having a child with ARM or HD, compared with the reference population was not seen in this population. QoL did not change significantly during the first year for both fathers and mothers. Anxiety levels of mothers did decline during this first year. The number of parents included in this study is still small, which might influence our results. Therefore, we will continue the KLANKbord-study indefinitely. Georg Thieme Verlag KG Stuttgart · New York.

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Year:  2015        PMID: 26382660     DOI: 10.1055/s-0035-1559885

Source DB:  PubMed          Journal:  Eur J Pediatr Surg        ISSN: 0939-7248            Impact factor:   2.191


  6 in total

1.  High Levels of Interest in Reproductive Genetic Information in Parents of Children and Adults With Hirschsprung Disease.

Authors:  Courtney D Berrios; Aravinda Chakravarti; Barbara B Biesecker
Journal:  J Pediatr Gastroenterol Nutr       Date:  2019-09       Impact factor: 2.839

2.  Current status of Hirschsprung's disease: based on a nationwide survey of Japan.

Authors:  Tomoaki Taguchi; Satoshi Obata; Satoshi Ieiri
Journal:  Pediatr Surg Int       Date:  2017-01-05       Impact factor: 1.827

Review 3.  Quality of life of parents with children with congenital abnormalities: a systematic review with meta-analysis of assessment methods and levels of quality of life.

Authors:  Marisa Garcia Rodrigues; Matilde Monteiro Soares; José Daniel Rodrigues; Luís Filipe Azevedo; Pedro Pereira Rodrigues; José Carlos Areias; Maria Emília Areias
Journal:  Qual Life Res       Date:  2021-09-05       Impact factor: 4.147

4.  Generic and disease-specific health-related quality of life in patients with Hirschsprung disease: A systematic review and meta-analysis.

Authors:  Veerle Huizer; Naveen Wijekoon; Daniëlle Roorda; Jaap Oosterlaan; Marc A Benninga; Lw Ernest van Heurn; Shaman Rajindrajith; Joep Pm Derikx
Journal:  World J Gastroenterol       Date:  2022-04-07       Impact factor: 5.374

5.  Distress and post-traumatic stress in parents of patients with congenital gastrointestinal malformations: a cross-sectional cohort study.

Authors:  D Roorda; A F W van der Steeg; M van Dijk; J P M Derikx; R R Gorter; J Rotteveel; J B van Goudoever; L W E van Heurn; J Oosterlaan; L Haverman
Journal:  Orphanet J Rare Dis       Date:  2022-09-11       Impact factor: 4.303

Review 6.  Being the Pillar for Children with Rare Diseases-A Systematic Review on Parental Quality of Life.

Authors:  Johannes Boettcher; Michael Boettcher; Silke Wiegand-Grefe; Holger Zapf
Journal:  Int J Environ Res Public Health       Date:  2021-05-08       Impact factor: 3.390

  6 in total

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