From Crisis to Continuum: Redefining Survivorship in Neurometabolic Care

IF 2.1 3区 医学 Q2 CLINICAL NEUROLOGY
Bharatendu Chandra MBBS , Madelyn Klemmensen BS , Brian J. Shayota MD, MPH , Andrea L. Gropman MD
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引用次数: 0

Abstract

Advances in newborn screening, molecular diagnostics, and targeted therapies have markedly improved survival for individuals with inborn errors of metabolism (IEM), allowing many to live well into adulthood. While some may remain asymptomatic, their underlying metabolic vulnerabilities persist and can be unmasked by illness, stress, or other triggers. As a result, a growing population of adults with IEM now faces unique and evolving challenges related to long-term disease management, continuity of care, and quality of life. Despite these shifting demographics, there remains limited literature directly comparing pediatric and adult treatment outcomes, and emerging data suggest that therapeutic effectiveness in childhood may not always extend into adulthood. Survivorship in IEM spans a wide range of medical, neurodevelopmental, and psychosocial domains. These include maintaining metabolic stability, managing complex dietary needs, monitoring for progressive organ dysfunction, addressing neurocognitive outcomes, and navigating socioeconomic and mental health challenges. Compounding these issues are barriers such as limited access to specialized adult care, inconsistent insurance coverage for medical foods and therapies, and a lack of established adult-specific treatment protocols. This review explores the critical components of survivorship in IEM, including emerging therapies and the increasing importance of multidisciplinary care models. It underscores the necessity of well-coordinated transition programs that support adolescents and young adults as they shift from pediatric to adult healthcare systems. In addition, it highlights the need for expanded education and research efforts aimed at understanding and addressing the distinct and evolving needs of adults with IEM. By highlighting the lived experience, gaps in education, and complex care requirements of this growing patient population, this invited manuscript aims to inform tailored, lifespan-focused management strategies that reflect the realities of aging with a rare metabolic disorder.
从危机到连续:重新定义神经代谢护理的生存期。
新生儿筛查、分子诊断和靶向治疗的进步显著提高了先天性代谢错误(IEM)患者的生存率,使许多人能够健康地活到成年。虽然有些人可能没有症状,但他们潜在的代谢脆弱性持续存在,并可能被疾病、压力或其他触发因素所掩盖。因此,越来越多的成年IEM患者现在面临着与长期疾病管理、护理连续性和生活质量相关的独特和不断变化的挑战。尽管人口结构发生了变化,但直接比较儿童和成人治疗结果的文献仍然有限,而且新出现的数据表明,儿童的治疗效果可能并不总是延伸到成年期。IEM的幸存者跨越了广泛的医学、神经发育和社会心理领域。这些包括维持代谢稳定,管理复杂的饮食需求,监测进行性器官功能障碍,解决神经认知结果,以及应对社会经济和心理健康挑战。使这些问题更加复杂的是一些障碍,例如获得专门成人护理的机会有限,医疗食品和疗法的保险范围不一致,以及缺乏既定的针对成人的治疗方案。这篇综述探讨了IEM存活的关键组成部分,包括新兴疗法和多学科护理模式的日益重要性。它强调了协调良好的过渡规划的必要性,以支持青少年和年轻人从儿科转向成人医疗保健系统。此外,它还强调需要扩大教育和研究工作,以了解和解决患有IEM的成年人的独特和不断变化的需求。通过强调生活经验、教育差距和日益增长的患者群体的复杂护理需求,本特邀手稿旨在告知量身定制的、以寿命为中心的管理策略,这些策略反映了罕见代谢紊乱的衰老现实。
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来源期刊
Pediatric neurology
Pediatric neurology 医学-临床神经学
CiteScore
4.80
自引率
2.60%
发文量
176
审稿时长
78 days
期刊介绍: Pediatric Neurology publishes timely peer-reviewed clinical and research articles covering all aspects of the developing nervous system. Pediatric Neurology features up-to-the-minute publication of the latest advances in the diagnosis, management, and treatment of pediatric neurologic disorders. The journal''s editor, E. Steve Roach, in conjunction with the team of Associate Editors, heads an internationally recognized editorial board, ensuring the most authoritative and extensive coverage of the field. Among the topics covered are: epilepsy, mitochondrial diseases, congenital malformations, chromosomopathies, peripheral neuropathies, perinatal and childhood stroke, cerebral palsy, as well as other diseases affecting the developing nervous system.
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