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接受酶替代疗法的苯丙酮尿症(PKU)患者的管理:意大利模式(专家意见)。

Management of patients with phenylketonuria (PKU) under enzyme replacement therapy: An Italian model (expert opinion).

作者信息

Scala Iris, Brodosi Lucia, Rovelli Valentina, Noto Davide, Burlina Alberto

机构信息

Clinical Genetics Unit, Department of Maternal and Child Health, "Federico II" University Hospital, Naples, Italy.

Department of Medical and Surgical Sciences, "Alma Mater" University, Sant'Orsola-Malpighi Hospital, Bologna, Italy.

出版信息

Mol Genet Metab Rep. 2024 Feb 22;39:101065. doi: 10.1016/j.ymgmr.2024.101065. eCollection 2024 Jun.

Abstract

OBJECTIVE

Phenylketonuria (PKU) is a metabolic disorder necessitating lifelong management to prevent severe neurological impairments. This paper synthesises clinical practices from Italian specialist centres to delineate a unified approach for administering pegvaliase, a novel enzyme replacement therapy for PKU.

METHODS

Virtual meetings convened in September 2022, gathering a steering committee (SC) of experts from five Italian centres specialising in PKU. The SC reviewed, and discussed clinical practices, and formulated recommendations for pegvaliase treatment.

RESULTS

The SC outlined a comprehensive treatment roadmap for PKU management with pegvaliase, emphasising the importance of multidisciplinary care teams, patient selection, pre-treatment evaluation, and education. Recommendations include initial hospital-based pegvaliase administration, regular monitoring of phenylalanine and tyrosine levels, dietary adjustments, and management of adverse events. A consensus was reached on the need for a digital database to manage treatment plans and enhance communication between healthcare professionals and patients.

CONCLUSION

The expert panel's consensus highlights the complexity of PKU management and the necessity for a coordinated, patient-centred approach. The recommendations aim to standardise care across Italian centres and provide a framework for integrating pegvaliase therapy into clinical practice, potentially informing international guidelines. Further research is warranted to evaluate the long-term impact of these practices on patient outcomes and quality of life.

摘要

目的

苯丙酮尿症(PKU)是一种代谢紊乱疾病,需要终身管理以预防严重的神经损伤。本文综合了意大利各专科中心的临床实践,以勾勒出一种统一的方法来管理培格瓦酶,这是一种用于PKU的新型酶替代疗法。

方法

2022年9月召开了虚拟会议,召集了来自意大利五个PKU专科中心的专家指导委员会(SC)。该指导委员会审查并讨论了临床实践,并制定了培格瓦酶治疗的建议。

结果

指导委员会概述了使用培格瓦酶进行PKU管理的全面治疗路线图,强调了多学科护理团队、患者选择、治疗前评估和教育的重要性。建议包括最初在医院进行培格瓦酶给药、定期监测苯丙氨酸和酪氨酸水平、饮食调整以及不良事件的管理。就需要一个数字数据库来管理治疗计划并加强医疗保健专业人员与患者之间的沟通达成了共识。

结论

专家小组的共识突出了PKU管理的复杂性以及采取以患者为中心的协调方法的必要性。这些建议旨在使意大利各中心的护理标准化,并提供一个将培格瓦酶疗法纳入临床实践的框架,可能为国际指南提供参考。有必要进行进一步研究,以评估这些实践对患者结局和生活质量的长期影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59c7/10899016/3fb342499d60/gr1.jpg

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