Lessons learned from 5 years of pegvaliase in US clinics: A case series.

IF 1.8 4区 医学 Q3 GENETICS & HEREDITY Molecular Genetics and Metabolism Reports Pub Date : 2024-12-26 eCollection Date: 2025-03-01 DOI:10.1016/j.ymgmr.2024.101181
Erin Cooney, Zineb Ammous, Tricia Bender, Gillian E Clague, Marilyn Clifford, Angela Crutcher, Laura Davis-Keppen, Kirsten Havens, Melissa Lah, Stephanie Sacharow, Amarilis Sanchez-Valle, Erika Vucko, Bridget Wardley, Leah Wessenberg, Hans C Andersson
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引用次数: 0

Abstract

Objective: To provide insights and strategies for pegvaliase management in challenging cases with phenylketonuria (PKU) based on the first 5 years of experience with pegvaliase in real-world clinical practice.

Methods: Twelve PKU experts gathered during a one-day, in-person meeting to discuss clinical cases illustrating important lessons from their experiences treating patients with pegvaliase in real-world clinical practice. Challenges with pegvaliase experienced prior to and during treatment and corresponding strategies to overcome them were discussed.

Results: Twelve cases of adults with PKU (eight females and four males, aged 18 to 68 years) receiving pegvaliase were reviewed and discussed. Challenges of the cases included medical or mental health comorbidities, executive function deficits, challenging social or socioeconomic situations, logistical or geographic barriers, or a combination of these; one was considering pregnancy. Despite challenges, pegvaliase was initiated successfully in most cases. Strategies to overcome barriers included individualized education, including side effect action plans, help from support organizations, collaboration with local providers, and use of telemedicine. Recommendations from the clinicians included that comorbid conditions should be monitored closely after treatment initiation and may require collaboration with other healthcare providers. A collaborative relationship with the clinic, ongoing education, and supportive relatives or friends can help individuals to remain adherent to pegvaliase. Suboptimal adherence may be addressed by a daily reminder system, telemedicine, in-home support, or a modified titration plan. Treated individuals with eating disorders require additional follow-up and support to achieve a healthy relationship with food. In most cases, including late-diagnosed individuals, reduced blood Phe levels resulted in improved PKU-related symptoms, including neurological issues.

Conclusion: Experience from the presented cases and 5 years of expert experience with pegvaliase in the real-world setting provide insight and guidance for healthcare professionals initiating and managing pegvaliase treatment in complex PKU cases. These cases demonstrate that, through comprehensive assessment and addressing barriers, pegvaliase treatment can be successful in adults with PKU, regardless of prior treatment success, age, socioeconomic, cognitive, or executive function challenges, as well as in those with comorbidities or considering pregnancy. Ongoing documentation of clinical experience is crucial for advancing the management of individuals receiving this treatment.

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美国诊所5年pegvaliase的经验教训:一个病例系列。
目的:基于在现实世界的临床实践中使用pegvaliase的前5年经验,为具有挑战性的苯丙酮尿症(PKU)患者提供pegvaliase管理的见解和策略。方法:12位PKU专家在为期一天的面对面会议中聚集在一起,讨论临床病例,说明他们在实际临床实践中治疗pegvaliase患者的重要经验教训。讨论了在治疗前和治疗期间pegvaliase所遇到的挑战以及克服这些挑战的相应策略。结果:回顾和讨论了12例成人PKU(8女4男,年龄18 ~ 68岁)接受pegvaliase治疗的病例。这些病例面临的挑战包括医疗或精神健康合并症、执行功能缺陷、具有挑战性的社会或社会经济状况、后勤或地理障碍,或这些因素的组合;其中一个正在考虑怀孕。尽管存在挑战,pegvaliase在大多数情况下都成功启动。克服障碍的战略包括个体化教育,包括副作用行动计划、支助组织的帮助、与当地提供者合作以及使用远程医疗。临床医生的建议包括,在治疗开始后应密切监测合并症,并可能需要与其他医疗保健提供者合作。与诊所的合作关系,持续的教育和支持的亲戚或朋友可以帮助个人保持对pegvaliase的坚持。不理想的依从性可以通过每日提醒系统、远程医疗、家庭支持或修改滴定计划来解决。治疗过的饮食失调患者需要额外的随访和支持,以实现与食物的健康关系。在大多数情况下,包括晚期诊断的个体,血液Phe水平的降低导致pku相关症状的改善,包括神经问题。结论:本文病例的经验和在现实世界中使用pegvaliase的5年专家经验为医疗保健专业人员在复杂的PKU病例中启动和管理pegvaliase治疗提供了见解和指导。这些病例表明,通过综合评估和解决障碍,pegvaliase治疗对于PKU成人患者是成功的,无论先前的治疗是否成功,年龄,社会经济,认知或执行功能的挑战,以及那些有合并症或考虑怀孕的患者。临床经验的持续记录对于推进接受这种治疗的个体的管理至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports Biochemistry, Genetics and Molecular Biology-Endocrinology
CiteScore
4.00
自引率
5.30%
发文量
105
审稿时长
33 days
期刊介绍: Molecular Genetics and Metabolism Reports is an open access journal that publishes molecular and metabolic reports describing investigations that use the tools of biochemistry and molecular biology for studies of normal and diseased states. In addition to original research articles, sequence reports, brief communication reports and letters to the editor are considered.
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