Minimizing the Diagnostic Delay in Amyotrophic Lateral Sclerosis: The Role of Nonneurologist Practitioners.

IF 1.7 Q4 NEUROSCIENCES Neurology Research International Pub Date : 2020-05-11 eCollection Date: 2020-01-01 DOI:10.1155/2020/1473981
Martin Matharan, Stéphane Mathis, Sarah Bonabaud, Louis Carla, Antoine Soulages, Gwendal Le Masson
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引用次数: 12

Abstract

Introduction: Amyotrophic lateral sclerosis (ALS), usually fatal in a few years, is a neurodegenerative disorder where the diagnostic delay, although variable according to the studies, remains too long. The main objective of this study was to determine the average time to diagnose ALS and the role of each physician, general practitioner (GP), or specialist (neurologist or not) involved in the management of these patients. The secondary objective was to propose some simple schemes to quickly identify an ALS suspicion with the aim to reduce this delay. Patients and Methods. This retrospective study evaluated the diagnostic delay (and other intermediate delays) of 90 ALS patients registered in the ALS Center of Bordeaux (France) in 2013. The main clinical signs encountered (and their order of appearance) were studied.

Results: The average diagnostic delay was 17 months, with a median diagnostic delay of 12 months. The average diagnostic delay was 2.7 months between the first symptoms and the first complaint to GP, followed by an additional 6.5 month delay before the patient's first visit to a neurologist. This period could be shortened, especially if GP performed additional tests quickly (p=0.01), as the time spent consulting various specialists often extends this crucial step. Overall, diagnostic delay accounted for 40% of the total duration of the disease progression.

Conclusion: In relation to total survival time, the diagnostic delay of ALS appears to be proportionately very long, sometimes longer than that observed in previous studies (because it also included the total delay to diagnostic or treatment initiation). The rapid execution of useful additional tests by the first medical doctor, often GP (with the help of a neurologist), considerably reduces the diagnostic delay. The central role of GP seems to be crucial in the management of patients with ALS. The main objective is, of course, to initiate appropriate treatment and care as soon as possible. Finally, based on our results, we also provide a short practical diagram to help nonneurologist practitioners to quickly discuss the diagnosis of ALS in case of some specific symptoms ("red flags").

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最大限度地减少肌萎缩侧索硬化症的诊断延迟:非神经科医生的作用。
简介:肌萎缩性侧索硬化症(ALS)是一种神经退行性疾病,虽然根据研究的不同,但诊断延迟仍然太长,通常在几年内致命。本研究的主要目的是确定诊断ALS的平均时间以及每位医生、全科医生(GP)或专科医生(神经科医生或非神经科医生)在这些患者管理中的作用。次要目标是提出一些简单的方案来快速识别ALS的怀疑,目的是减少这种延迟。患者和方法。本回顾性研究评估了2013年在法国波尔多ALS中心登记的90例ALS患者的诊断延迟(和其他中间延迟)。研究了所遇到的主要临床症状(及其出现顺序)。结果:平均诊断延迟为17个月,中位诊断延迟为12个月。首次出现症状和首次向全科医生投诉之间的平均诊断延迟为2.7个月,其次是患者首次访问神经科医生之前的额外6.5个月。这段时间可以缩短,特别是如果全科医生快速进行额外的检查(p=0.01),因为咨询各种专家的时间通常会延长这一关键步骤。总体而言,诊断延迟占疾病进展总持续时间的40%。结论:与总生存时间相关,ALS的诊断延迟似乎成比例地非常长,有时比先前研究中观察到的更长(因为它还包括诊断或治疗开始的总延迟)。由第一个医生,通常是全科医生(在神经科医生的帮助下)快速执行有用的附加检查,大大减少了诊断延误。全科医生的核心作用似乎是至关重要的管理与ALS患者。当然,主要目标是尽快开始适当的治疗和护理。最后,根据我们的研究结果,我们还提供了一个简短的实用图表,以帮助非神经科医生在出现某些特定症状(“危险信号”)的情况下快速讨论ALS的诊断。
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来源期刊
CiteScore
3.50
自引率
0.00%
发文量
10
审稿时长
17 weeks
期刊介绍: Neurology Research International is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies focusing on diseases of the nervous system, as well as normal neurological functioning. The journal will consider basic, translational, and clinical research, including animal models and clinical trials.
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