脑瘫诊断的不确定性:澄清共识定义的机会。

IF 2.3 Q3 CLINICAL NEUROLOGY
Neurology. Clinical practice Pub Date : 2024-12-01 Epub Date: 2024-08-16 DOI:10.1212/CPJ.0000000000200353
Bhooma R Aravamuthan, Darcy L Fehlings, Iona Novak, Paul Gross, Noor Alyasiry, Ann H Tilton, Michael I Shevell, Michael C Fahey, Michael C Kruer
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引用次数: 0

摘要

背景和目的:我们已经证实,包括神经科医生在内的医生在使用 2006 年最新的脑瘫定义诊断脑瘫(CP)时存在差异。我们还知道,儿童神经学家和神经发育学家认为,基于他们的培训背景,他们最适合诊断 CP。因此,为了减少 CP 诊断中的变异性,我们的目标是阐明儿童神经学家和神经发育学家在实际应用 2006 年定义时可能存在的不确定性:我们在 2022 年儿童神经病学学会 (CNS) 年会的讨论研讨会上对儿童神经病学家和神经发育学家进行了横断面调查。研讨会向与会者提供了 2006 年的定义,并询问他们对该定义在 4 个假设临床案例中的实际应用是否有任何不确定性。随后,由国内外 CP 领导者组成的小组通过反复讨论对这些数据进行了处理,并提出了明确 2006 年定义的建议:在所有申请继续医学教育的参会者中,有 50%(202/401)参加了此次研讨会。在 164 名结束调查的受访者中,145 人(88%)对 2006 年定义的临床应用表示不确定。这些不确定性主要集中在:1)年龄,包括脑功能障碍或运动症状发病的最小和最大年龄(67/164,41%);2)对 "非进行性 "一词的解释(48/164,29%)。几乎所有的受访者(157/164,96%)都认为,我们应该修订 2006 年达成共识的 CP 定义:讨论:针对我们发现的最常见的 CP 诊断不确定性,我们共同建议对 2006 年的定义进行 4 点澄清:1) 运动症状/体征应在 2 岁之前出现;2) CP 可以且应该尽早诊断;3) 临床运动障碍表型在 5 岁之前应为非进行性;4) 如果运动障碍在 5 岁之前为进行性或不存在,则应重新评估 CP 诊断。我们预计,以这种方式澄清 2006 年的 CP 定义可以解决我们在儿童神经学家和神经发育学家中发现的不确定性,并减少目前存在的诊断变异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Uncertainties Regarding Cerebral Palsy Diagnosis: Opportunities to Clarify the Consensus Definition.

Background and objectives: We have established that physicians, including neurologists, variably diagnose cerebral palsy (CP) when using the most recent CP definition from 2006. We also know that child neurologists and neurodevelopmentalists view themselves to be optimally suited to diagnose CP based on their training backgrounds. Therefore, to reduce variability in CP diagnosis, our objective was to elucidate uncertainties child neurologists and neurodevelopmentalists may have regarding practical application of the 2006 definition.

Methods: We conducted a cross-sectional survey of child neurologists and neurodevelopmentalists built into a discussion seminar at the 2022 Child Neurology Society (CNS) Annual Meeting, the largest professional meeting of these specialists in North America. Seminar attendees were provided the 2006 definition and asked whether they had any uncertainties about the practical application of the definition across 4 hypothetical clinical vignettes. A group of national and international CP leaders then processed these data through iterative discussions to develop recommendations for clarifying the 2006 definition.

Results: The seminar was attended by 50% of all conference attendees claiming CME (202/401). Of the 164 closing survey respondents, 145 (88%) expressed uncertainty regarding the clinical application of the 2006 definition. These uncertainties focused on 1) age, both regarding the minimum and maximum ages of brain disturbance or motor symptom onset (67/164, 41%), and 2) interpretation of the term "nonprogressive" (48/164, 29%). Almost all respondents (157/164, 96%) felt that we should revise the 2006 consensus definition of CP.

Discussion: To address the most common CP diagnostic uncertainties we identified, we collectively propose 4 points of clarification to the 2006 definition: 1) motor symptoms/signs should be present by 2 years old; 2) CP can and should be diagnosed as early as possible; 3) the clinical motor disability phenotype should be nonprogressive through 5 years old; and 4) a CP diagnosis should be re-evaluated if motor disability is progressive or absent by 5 years old. We anticipate that clarifying the 2006 definition of CP in this manner could address the uncertainties we identified among child neurologists and neurodevelopmentalists and reduce the diagnostic variability that currently exists.

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来源期刊
Neurology. Clinical practice
Neurology. Clinical practice CLINICAL NEUROLOGY-
CiteScore
4.00
自引率
0.00%
发文量
77
期刊介绍: Neurology® Genetics is an online open access journal publishing peer-reviewed reports in the field of neurogenetics. The journal publishes original articles in all areas of neurogenetics including rare and common genetic variations, genotype-phenotype correlations, outlier phenotypes as a result of mutations in known disease genes, and genetic variations with a putative link to diseases. Articles include studies reporting on genetic disease risk, pharmacogenomics, and results of gene-based clinical trials (viral, ASO, etc.). Genetically engineered model systems are not a primary focus of Neurology® Genetics, but studies using model systems for treatment trials, including well-powered studies reporting negative results, are welcome.
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