Literature DB >> 29110168

Caregiver Quality of Life with Tyrosinemia Type 1.

Hailey Campbell1, Rani H Singh1, Eric Hall2, Nadia Ali3.   

Abstract

Tyrosinemia type I (HT1) is an inborn error of metabolism (IEM). Current management guidelines include lifelong specialized diet and use of the orphan drug, nitisinone. This study explores the quality of life (QOL) of caregivers of children with HT1. Caregivers for 26 children with HT1 completed a questionnaire (TYR-QOL) adapted to this patient population from an existing validated QOL questionnaire (PKU-QOL). Responses were analyzed via domain scores, based on predetermined scoring guidelines. Results suggest HT1 has a moderate overall impact on caregiver QOL, with emotional aspects of the disease having the greatest impact. HT1 diet and specialized formula also had an impact on caregiver QOL, with the vast majority feeling guilt if their child's diet and specialized formula plan were not followed. Management of nitisinone did not impact caregiver QOL. Results were compared to the phenylketonuria (PKU) population. Domain scores for the emotional, practical, social, and overall impact on QOL were higher for HT1 than for mild PKU, indicating a greater impact on QOL. Domain scores for practical and social aspects were similarly higher for HT1 than for classic PKU, though emotional and overall impacts were comparable. This is the first questionnaire to assess QOL in caregivers of children with HT1. Results can be used to better understand psychosocial implications of HT1 and assist healthcare professionals in addressing treatment issues.

Entities:  

Keywords:  HT1; Inborn errors of metabolism; PKU-QOL; Quality of life; TYR-QOL; Tyrosinemia type 1

Mesh:

Year:  2017        PMID: 29110168     DOI: 10.1007/s10897-017-0157-9

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  16 in total

1.  Incidence of inborn errors of metabolism in British Columbia, 1969-1996.

Authors:  D A Applegarth; J R Toone; R B Lowry
Journal:  Pediatrics       Date:  2000-01       Impact factor: 7.124

2.  Novel and recurrent mutations in the TAT gene in Tunisian families affected with Richner-Hanhart syndrome.

Authors:  Yosra Bouyacoub; Hela Zribi; Hatem Azzouz; Fehmi Nasrallah; Rim Ben Abdelaziz; Monia Kacem; Ben Rekaya; Olfa Messaoud; Lilia Romdhane; Cherine Charfeddine; Mustapha Bouziri; Sonia Bouziri; Neji Tebib; Mourad Mokni; Naziha Kaabachi; Samir Boubaker; Sonia Abdelhak
Journal:  Gene       Date:  2013-08-13       Impact factor: 3.688

3.  Nitisinone in the treatment of hereditary tyrosinaemia type 1.

Authors:  Patrick J McKiernan
Journal:  Drugs       Date:  2006       Impact factor: 9.546

4.  Sapropterin treatment does not enhance the health-related quality of life of patients with phenylketonuria and their parents.

Authors:  Reinhold Feldmann; Eva Wolfgart; Josef Weglage; Frank Rutsch
Journal:  Acta Paediatr       Date:  2017-03-19       Impact factor: 2.299

5.  Tyrosinemia Type III detected via neonatal screening: management and outcome.

Authors:  Evelyne Heylen; Gerd Scherer; Marie-Françoise Vincent; Sandrine Marie; Judith Fischer; Marie-Cécile Nassogne
Journal:  Mol Genet Metab       Date:  2012-09-07       Impact factor: 4.797

6.  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

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.  Development and psychometric validation of measures to assess the impact of phenylketonuria and its dietary treatment on patients' and parents' quality of life: the phenylketonuria - quality of life (PKU-QOL) questionnaires.

Authors:  Antoine Regnault; Alberto Burlina; Amy Cunningham; Esther Bettiol; Flavie Moreau-Stucker; Khadra Benmedjahed; Annet M Bosch
Journal:  Orphanet J Rare Dis       Date:  2015-05-10       Impact factor: 4.123

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.  Child and family experiences with inborn errors of metabolism: a qualitative interview study with representatives of patient groups.

Authors:  Sara D Khangura; Kylie Tingley; Pranesh Chakraborty; Doug Coyle; Jonathan B Kronick; Anne-Marie Laberge; Julian Little; Fiona A Miller; John J Mitchell; Chitra Prasad; Shabnaz Siddiq; Komudi Siriwardena; Rebecca Sparkes; Kathy N Speechley; Sylvia Stockler; Yannis Trakadis; Brenda J Wilson; Kumanan Wilson; Beth K Potter
Journal:  J Inherit Metab Dis       Date:  2015-07-25       Impact factor: 4.982

View more
  3 in total

1.  Exploring the Barriers and Motivators to Dietary Adherence among Caregivers of Children with Disorders of Amino Acid Metabolism (AAMDs): A Qualitative Study.

Authors:  Jing Ying Lim; Roslee Rajikan; Noh Amit; Nazlena Mohamad Ali; Haslina Abdul Hamid; Huey Yin Leong; Maslina Mohamad; Bi Qi Koh; Aini Musa
Journal:  Nutrients       Date:  2022-06-18       Impact factor: 6.706

2.  Families' healthcare experiences for children with inherited metabolic diseases: protocol for a mixed methods cohort study.

Authors:  Andrea J Chow; Ryan Iverson; Monica Lamoureux; Kylie Tingley; Isabel Jordan; Nicole Pallone; Maureen Smith; Zobaida Al-Baldawi; Pranesh Chakraborty; Jamie Brehaut; Alicia Chan; Eyal Cohen; Sarah Dyack; Lisa Jane Gillis; Sharan Goobie; Ian D Graham; Cheryl R Greenberg; Jeremy M Grimshaw; Robin Z Hayeems; Shailly Jain-Ghai; Ann Jolly; Sara Khangura; Jennifer J MacKenzie; Nathalie Major; John J Mitchell; Stuart G Nicholls; Amy Pender; Murray Potter; Chitra Prasad; Lisa A Prosser; Andreas Schulze; Komudi Siriwardena; Rebecca Sparkes; Kathy Speechley; Sylvia Stockler; Monica Taljaard; Mari Teitelbaum; Yannis Trakadis; Clara van Karnebeek; Jagdeep S Walia; Brenda J Wilson; Kumanan Wilson; Beth K Potter
Journal:  BMJ Open       Date:  2022-02-22       Impact factor: 2.692

Review 3.  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

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.