Best practice recommendations for the management of anxiety during the pegvaliase journey.

Anxiety Modified Delphi PKU Pegvaliase Phenylketonuria Recommendations

Journal

Molecular genetics and metabolism
ISSN: 1096-7206
Titre abrégé: Mol Genet Metab
Pays: United States
ID NLM: 9805456

Informations de publication

Date de publication:
22 Nov 2023
Historique:
received: 13 10 2023
revised: 16 11 2023
accepted: 16 11 2023
medline: 4 12 2023
pubmed: 4 12 2023
entrez: 3 12 2023
Statut: aheadofprint

Résumé

Pegvaliase, an enzyme substitution therapy, is a treatment option for phenylketonuria (PKU). Due to the neuropathophysiology and disease burden of PKU, individuals can experience baseline anxiety unrelated to pegvaliase therapy. In addition, there are aspects of pegvaliase therapy that may be anxiety-inducing for those considering or receiving treatment. The aim of this manuscript is to present best practice recommendations for the identification and management of anxiety symptoms that can occur along the pegvaliase journey. A modified Delphi approach was used to seek consensus among a multidisciplinary panel of experts. To this end, an in-person meeting was held that was preceded by a medical specialist- and patient-specific survey to develop preliminary recommendations on ways to address anxiety along the pegvaliase journey. After the meeting, an additional survey was conducted to rank the proposed solutions and mitigation strategies from which a set of recommendations was developed. All recommendations were voted on with the aim of consensus generation, defined as achieving ≥75% agreement among experts. The panel reached consensus on a total of 28 best practice recommendations for the management of anxiety during the pre-treatment, induction and titration, early maintenance (pre-efficacy), and late maintenance (post-efficacy) stages. The recommendations offer strategies to identify and address the most common causes of pegvaliase-related anxiety, including self-injection, side effects, the titration schedule, prescribed dietary changes, and variable time to efficacy. Overall, managing anxiety in those considering or receiving pegvaliase involves patient-centered communication, shared decision-making, and personalized treatment plans. The best practice recommendations described herein can guide healthcare providers in proactively addressing anxiety during the different stages of pegvaliase treatment, and support providers with initiating and managing pegvaliase in individuals who may experience baseline and treatment-related anxiety.

Sections du résumé

BACKGROUND BACKGROUND
Pegvaliase, an enzyme substitution therapy, is a treatment option for phenylketonuria (PKU). Due to the neuropathophysiology and disease burden of PKU, individuals can experience baseline anxiety unrelated to pegvaliase therapy. In addition, there are aspects of pegvaliase therapy that may be anxiety-inducing for those considering or receiving treatment. The aim of this manuscript is to present best practice recommendations for the identification and management of anxiety symptoms that can occur along the pegvaliase journey.
METHODS METHODS
A modified Delphi approach was used to seek consensus among a multidisciplinary panel of experts. To this end, an in-person meeting was held that was preceded by a medical specialist- and patient-specific survey to develop preliminary recommendations on ways to address anxiety along the pegvaliase journey. After the meeting, an additional survey was conducted to rank the proposed solutions and mitigation strategies from which a set of recommendations was developed. All recommendations were voted on with the aim of consensus generation, defined as achieving ≥75% agreement among experts.
RESULTS RESULTS
The panel reached consensus on a total of 28 best practice recommendations for the management of anxiety during the pre-treatment, induction and titration, early maintenance (pre-efficacy), and late maintenance (post-efficacy) stages. The recommendations offer strategies to identify and address the most common causes of pegvaliase-related anxiety, including self-injection, side effects, the titration schedule, prescribed dietary changes, and variable time to efficacy. Overall, managing anxiety in those considering or receiving pegvaliase involves patient-centered communication, shared decision-making, and personalized treatment plans.
CONCLUSIONS CONCLUSIONS
The best practice recommendations described herein can guide healthcare providers in proactively addressing anxiety during the different stages of pegvaliase treatment, and support providers with initiating and managing pegvaliase in individuals who may experience baseline and treatment-related anxiety.

Identifiants

pubmed: 38043481
pii: S1096-7192(23)00367-0
doi: 10.1016/j.ymgme.2023.107737
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

107737

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The expert panel was compensated for their participation in the in-person advisory board. In addition, KJB received consulting payments from BioMarin, Denali, Chiesi, and Sanofi and speaker fees as well as travel support from BioMarin, Chiesi, and Sanofi; CE received speaker fees from BioMarin; EE received consulting payments and speaker fees from BioMarin. SH received consulting payments from BioMarin, Cycle Therapeutics, PTC Therapeutics, Sanofi, and Vitaflo, speaker fees from Vitaflo, and participated as clinical trial investigator for BioMarin and PTC Therapeutics; BMH received consulting payments from BioMarin, Horizon Therapeutics, and Synlogic; MM received consulting payments from Horizon Therapeutics, BioMarin, Eton Pharmaceuticals, Acer Therapeutics, Ultragenyx, Applied Therapeutics, Jnana Therapeutics, BridgeBio, and Alexion, and participated as clinical trial investigator for Aeglea Biotherapeutics, Reneo Pharmaceuticals, PTC Therapeutics, Homology Medicines, Horizon Therapeutics, Arcturus Therapeutics, Jnana Therapeutics, Synlogic Therapeutics, and BioMarin; SM received consulting payments from Horizon Therapeutics; HN is a clinical trial investigator for BioMarin, Synlogic Therapeutics, Jnana Therapeutics, Sanofi, and PTC Therapeutics and received consulting fees from BioMarin, Synlogic Therapeutics, Jnana Therapeutics, and PTC as well as speakers fees from BioMarin; SS received consulting payments from BioMarin and travel support from BioMarin and NPKUA; LW received consulting payments from BioMarin and Cycle Pharmaceuticals; DAB received consulting payments from Synlogic Therapeutics, Encoded Therapeutics, and Taysha Gene Therapies as well as consulting payments and travel support from BioMarin. MR and MS have no conflicts of interest to declare. KL, SR, and BW are employees and shareholders of BioMarin Pharmaceutical Inc.

Auteurs

Kendra J Bjoraker (KJ)

3:1 Neuropsychology Consultants, PLLC, Minneapolis, MN, USA.

Caroline Eggerding (C)

Cooper University Health Care, Camden, NJ, USA.

Elisheva Ellenberg (E)

Children's Hospital of Michigan, Detroit, MI, USA.

Suzanne Hollander (S)

Department of Clinical Nutrition, Boston Children's Hospital, Boston, MA, USA; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, USA.

Brittany M Holmes (BM)

Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, USA.

Kristin Lindstrom (K)

BioMarin Pharmaceutical Inc., Novato, CA, USA.

Markey McNutt (M)

University of Texas Southwestern Medical Center, Dallas, TX, USA.

Suzanne Miller (S)

Program for Inherited Metabolic Diseases, Mount Sinai Health System, New York, NY, USA.

Hope Northrup (H)

Department of Pediatrics, McGovern Medical School at the University of Texas Health Science Center at Houston (UTHealth) and Children's Memorial Hermann Hospital, Houston, TX, USA.

Meaghan Rogers (M)

Individual with PKU, Pittsfield, MA, USA.

Sarah Rose (S)

BioMarin Pharmaceutical Inc., Novato, CA, USA. Electronic address: sarah.rose@bmrn.com.

Mia Scott (M)

Individual with PKU, Tucson, AZ, USA.

Soo Shim (S)

Ann and Robert H. Lurie Children's Hospital, Chicago, IL, USA.

Bridget Wardley (B)

BioMarin Pharmaceutical Inc., Novato, CA, USA.

Leah Wessenberg (L)

OHSU Doernbecher Children's Hospital, Portland, OR, USA.

Deborah A Bilder (DA)

Department of Psychiatry, University of Utah Huntsman Mental Health Institute, Salt Lake City, UT, USA.

Classifications MeSH