Literature DB >> 23748994

Qualitative analysis of factors affecting adherence to the phenylketonuria diet in adolescents.

Rachael Sharman1, Kate Mulgrew, Mary Katsikitis.   

Abstract

PURPOSE/
OBJECTIVE: Phenylketonuria (PKU) is an inborn error of metabolism that is primarily treated with a severely restricted, low-protein diet to prevent permanent neurological damage. Despite the recognition of the importance of strict dietary adherence in the prevention of intellectual impairment in individuals with PKU, apathy and attrition from diet, especially during adolescence, remain a threat to normal development in this population. This study's aim was to examine adolescents' perception of factors that encourage or inhibit their dietary adherence.
DESIGN: This was a qualitative study, with the authors using thematic analysis to interpret the findings.
SETTING: The study was conducted as part of a Metabolic Disorders Association conference. SAMPLE: Eight adolescents with PKU were recruited through convenience sampling.
METHODS: A focus group was conducted with the adolescents to gather information about factors that encourage and discourage dietary adherence.
FINDINGS: Thematic analysis revealed that the adolescents encountered problems explaining the nature and food requirements of their condition to other people. Friends, family, and wanting to maintain "normal" cognitive abilities were identified as factors that encouraged dietary adherence.
CONCLUSION: Adolescents with PKU appear to share several barriers and incentives for maintaining the strict dietary regimen. IMPLICATIONS: Considering such perceptions may aid future interventions aiming to reduce diet attrition rates among adolescents.

Entities:  

Mesh:

Year:  2013        PMID: 23748994     DOI: 10.1097/NUR.0b013e31829555d5

Source DB:  PubMed          Journal:  Clin Nurse Spec        ISSN: 0887-6274            Impact factor:   1.067


  7 in total

1.  Living with Intoxication-Type Inborn Errors of Metabolism: A Qualitative Analysis of Interviews with Paediatric Patients and Their Parents.

Authors:  Nina A Zeltner; Markus A Landolt; Matthias R Baumgartner; Sarah Lageder; Julia Quitmann; Rachel Sommer; Daniela Karall; Chris Mühlhausen; Andrea Schlune; Sabine Scholl-Bürgi; Martina Huemer
Journal:  JIMD Rep       Date:  2016-08-13

2.  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

3.  Phenylketonuria patients' and their parents' acceptance of the disease: multi-centre study.

Authors:  Ewa Witalis; Bożena Mikoluc; Radoslaw Motkowski; Justyna Szyszko; Agnieszka Chrobot; Bozena Didycz; Agata Lange; Renata Mozrzymas; Andrzej Milanowski; Maria Nowacka; Mariola Piotrowska-Depta; Hanna Romanowska; Ewa Starostecka; Jolanta Wierzba; Magdalena Skorniewska; Barbara Iwona Wojcicka-Bartlomiejczyk; Maria Gizewska
Journal:  Qual Life Res       Date:  2016-05-31       Impact factor: 4.147

4.  Phenylketonuria patients' and their parents' knowledge and attitudes to the daily diet - multi-centre study.

Authors:  Ewa Witalis; Bozena Mikoluc; Radoslaw Motkowski; Jolanta Sawicka-Powierza; Agnieszka Chrobot; Bozena Didycz; Agata Lange; Renata Mozrzymas; Andrzej Milanowski; Maria Nowacka; Mariola Piotrowska-Depta; Hanna Romanowska; Ewa Starostecka; Jolanta Wierzba; Magdalena Skorniewska; Barbara Iwona Wojcicka-Bartlomiejczyk; Maria Gizewska; Halina Car
Journal:  Nutr Metab (Lond)       Date:  2017-08-17       Impact factor: 4.169

5.  Nutritional management of phenylalanine hydroxylase (PAH) deficiency in pediatric patients in Canada: a survey of dietitians' current practices.

Authors:  Nataliya Yuskiv; Beth K Potter; Sylvia Stockler; Keiko Ueda; Alette Giezen; Barbara Cheng; Erica Langley; Suzanne Ratko; Valerie Austin; Maggie Chapman; Pranesh Chakraborty; Jean Paul Collet; Amy Pender
Journal:  Orphanet J Rare Dis       Date:  2019-01-08       Impact factor: 4.123

6.  Development of an inventory to assess perceived barriers related to PKU treatment.

Authors:  Katia Irie Teruya; Eduardo Remor; Ida Vanessa Doederlein Schwartz
Journal:  J Patient Rep Outcomes       Date:  2020-05-01

7.  Large neutral amino acid status in association with P:T ratio and diet in adult and pediatric patients with phenylketonuria.

Authors:  Teresa D Douglas; Anita M Nucci; Ann M Berry; Sarah T Henes; Rani H Singh
Journal:  JIMD Rep       Date:  2019-09-16
  7 in total

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