Literature DB >> 28162992

Adherence to clinic recommendations among patients with phenylketonuria in the United States.

E R Jurecki1, S Cederbaum2, J Kopesky3, K Perry4, F Rohr5, A Sanchez-Valle6, K S Viau7, M Y Sheinin4, J L Cohen-Pfeffer8.   

Abstract

OBJECTIVE: Assess current management practices of phenylketonuria (PKU) clinics across the United States (US) based on the key treatment metrics of blood phenylalanine (Phe) concentrations and blood Phe testing frequency, as well as patient adherence to their clinic's management practice recommendations.
METHODS: An online survey was conducted with medical professionals from PKU clinics across the US from July to September 2015. Forty-four clinics participated in the survey and account for approximately half of PKU patients currently followed in clinics in the US (Berry et al., 2013).
RESULTS: The majority of PKU clinics recommended target blood Phe concentrations to be between 120 and 360μM for all patients; the upper threshold was relaxed by some clinics for adult patients (from 360 to 600μM) and tightened for patients who are pregnant/planning to become pregnant (to 240μM). Patient adherence to these recommendations (percentage of patients with blood Phe below the upper recommended threshold) was age-dependent, decreasing from 88% in the 0-4years age group to 33% in adults 30+ years. Patient adherence to recommendations for blood testing frequency followed a similar trend. Higher staffing intensity (specialists per 100 PKU patients) was associated with better patient adherence to clinics' blood Phe concentrations recommendations.
CONCLUSION: Clinic recommendations of target blood Phe concentrations in the US are now stricter compared to prior years, and largely reflect recent guidelines by the American College of Medical Genetics and Genomics (Vockley et al., 2014). Adherence to recommended Phe concentrations remains suboptimal, especially in older patients. However, despite remaining above the guidelines, actual blood Phe concentrations in adolescents and adults are lower than those reported in the past (Walter et al., 2002; Freehauf et al., 2013). Continued education and support for PKU patients by healthcare professionals, including adequate clinic staffing, are needed to improve adherence. Future research is needed to understand how to improve adherence to reduce the number of patients lost to follow-up, as the findings of this and similar surveys do not address how to keep patients in clinic.
Copyright © 2017 The Authors. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  ACMG guidelines; Adherence; Adults; Blood phenylalanine; Phenylketonuria

Mesh:

Substances:

Year:  2017        PMID: 28162992     DOI: 10.1016/j.ymgme.2017.01.001

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  44 in total

1.  Extended Experience of Lower Dose Sapropterin in Irish Adults with Mild Phenylketonuria.

Authors:  S Doyle; M O'Regan; C Stenson; J Bracken; U Hendroff; A Agasarova; D Deverell; E P Treacy
Journal:  JIMD Rep       Date:  2017-10-14

2.  Domino liver transplant from a donor with maple syrup urine disease into a recipient with phenylketonuria.

Authors:  Vikram K Raghu; Steven F Dobrowolski; Rakesh Sindhi; Kevin A Strauss; George V Mazariegos; Jerry Vockley; Kyle Soltys
Journal:  Mol Genet Metab Rep       Date:  2022-04-21

3.  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

4.  PKU and COVID19: How the pandemic changed metabolic control.

Authors:  Valentina Rovelli; Juri Zuvadelli; Vittoria Ercoli; Chiara Montanari; Sabrina Paci; Alice Re Dionigi; Andrea Scopari; Elisabetta Salvatici; Graziella Cefalo; Giuseppe Banderali
Journal:  Mol Genet Metab Rep       Date:  2021-04-23

5.  Treatment adherence during childhood in individuals with phenylketonuria: Early signs of treatment discontinuation.

Authors:  María Ignacia García; Gabriela Araya; Soledad Coo; Susan E Waisbren; Alicia de la Parra
Journal:  Mol Genet Metab Rep       Date:  2017-04-28

6.  Long-term safety and efficacy of pegvaliase for the treatment of phenylketonuria in adults: combined phase 2 outcomes through PAL-003 extension study.

Authors:  Nicola Longo; Roberto Zori; Melissa P Wasserstein; Jerry Vockley; Barbara K Burton; Celeste Decker; Mingjin Li; Kelly Lau; Joy Jiang; Kevin Larimore; Janet A Thomas
Journal:  Orphanet J Rare Dis       Date:  2018-07-04       Impact factor: 4.123

7.  Development of a practical dietitian road map for the nutritional management of phenylketonuria (PKU) patients on pegvaliase.

Authors:  Júlio César Rocha; Heather Bausell; Amaya Bélanger-Quintana; Laurie Bernstein; Hülya Gökmen-Özel; Alexandra Jung; Anita MacDonald; Fran Rohr; Esther van Dam; Margret Heddrich-Ellerbrok
Journal:  Mol Genet Metab Rep       Date:  2021-05-25

8.  The Impact of the First 2020 COVID-19 Lockdown on the Metabolic Control of Patients with Phenylketonuria.

Authors:  Dariusz Walkowiak; Bożena Mikołuć; Renata Mozrzymas; Łukasz Kałużny; Bożena Didycz; Joanna Jaglowska; Danuta Kurylak; Jarosław Walkowiak
Journal:  Nutrients       Date:  2021-06-12       Impact factor: 5.717

Review 9.  Multiclinic Observations on the Simplified Diet in PKU.

Authors:  Laurie Bernstein; Casey Burns; Melissa Sailer-Hammons; Angela Kurtz; Frances Rohr
Journal:  J Nutr Metab       Date:  2017-09-13

10.  First 1.5 years of pegvaliase clinic: Experiences and outcomes.

Authors:  Stephanie Sacharow; Cassandra Papaleo; Kyla Almeida; Benjamin Goodlett; Amy Kritzer; Harvey Levy; Leslie Martell; Ann Wessel; Krista Viau
Journal:  Mol Genet Metab Rep       Date:  2020-05-25
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