Child Neurology and Psychiatric Unit-Presidio Ospedaliero Santa Maria Nuova -AUSL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.
Department of Paediatric Neuropsychiatry, Università La Sapienza, Rome, Italy.
Ital J Pediatr. 2021 Jan 21;47(1):13. doi: 10.1186/s13052-021-00954-4.
Aromatic L-amino acid decarboxylase (AADC) deficiency is a rare and underdiagnosed neurometabolic disorder resulting in a complex neurological and non-neurological phenotype, posing diagnostic challenges resulting in diagnostic delay. Due to the low number of patients, gathering high-quality scientific evidence on diagnosis and treatment is difficult. Additionally, based on the estimated prevalence, the number of undiagnosed patients is likely to be high.
Italian experts in AADC deficiency formed a steering committee to engage clinicians in a modified Delphi consensus to promote discussion, and support research, dissemination and awareness on this disorder. Five experts in the field elaborated six main topics, each subdivided into 4 statements and invited 13 clinicians to give their anonymous feedback.
100% of the statements were answered and a consensus was reached at the first round. This enabled the steering committee to acknowledge high rates of agreement between experts on clinical presentation, phenotypes, diagnostic work-up and treatment strategies. A research gap was identified in the lack of standardized cognitive and motor outcome data. The need for setting up an Italian working group and a patients' association, together with the dissemination of knowledge inside and outside scientific societies in multiple medical disciplines were recognized as critical lines of intervention.
The panel expressed consensus with high rates of agreement on a series of statements paving the way to disseminate clear messages concerning disease presentation, diagnosis and treatment and strategic interventions to disseminate knowledge at different levels. Future lines of research were also identified.
芳香族 L-氨基酸脱羧酶(AADC)缺乏症是一种罕见且诊断不足的神经代谢疾病,导致复杂的神经和非神经表型,诊断具有挑战性,导致诊断延迟。由于患者数量较少,因此难以收集关于诊断和治疗的高质量科学证据。此外,根据估计的患病率,未确诊患者的数量可能很高。
意大利 AADC 缺乏症专家组成了一个指导委员会,让临床医生参与修改后的 Delphi 共识,以促进对该疾病的讨论,并支持研究、传播和认识。该领域的五位专家详细阐述了六个主要主题,每个主题又分为 4 个陈述,并邀请了 13 位临床医生提供匿名反馈。
100%的陈述都得到了回答,并在第一轮就达成了共识。这使指导委员会能够承认专家对临床表现、表型、诊断方法和治疗策略的高度一致。专家们认识到认知和运动功能结果数据缺乏标准化是一个研究空白。确定了需要建立一个意大利工作组和一个患者协会,并在多个医学学科的科学协会内外传播知识,这被认为是关键的干预措施。
专家小组对一系列陈述表示一致同意,这些陈述为传播有关疾病表现、诊断和治疗的明确信息以及在不同层面传播知识的战略干预措施铺平了道路。还确定了未来的研究方向。