Literature DB >> 28705085

International Survey of ALS Experts about Critical Questions for Assessing Patients with ALS.

Mamede De Carvalho1,2, Adam Ryczkowski3, Peter Andersen4, Marta Gromicho1, Julian Grosskreutz5, Magdalena Kuźma-Kozakiewicz6,7, Susanne Petri8, Maria Piotrkiewicz3, Gabriel Miltenberger Miltenyi1.   

Abstract

OBJECTIVE: To define an applicable dataset for ALS patient registries we weighted specific clinical items as scored by worldwide ALS experts.
METHODS: Sixty participants were invited based on relevant clinical work, publications and personal acquaintance. They rated 160 clinical items consensually agreed by the members of our project, incorporating specialists from five European Centres. Scoring scheme was defined as: 1 - essential; 2 - important; 3 - not very important. A mixed effect model was applied to rank items and to find possible correlations with geographical region (Europe vs. outside Europe).
RESULTS: We received 40 responses, 20 from Europe and 20 from outside; 42/160 data were scored as essential by >50% of the respondents, including: date of birth, gender, date of disease onset, date of diagnosis, ethnicity, region of onset, predominant upper neuron (UMN) or lower motor neuron (LMN) impairment, proximal versus distal weakness, respiratory symptoms, dysarthria, weight loss, signs of LMN/UMN involvement, emotional incontinence, cognitive changes, respiratory signs, neck weakness, body mass index, ALSFRS-R at entry, ALSFRS-R subscores at entry, timing and pattern of spreading and staging, electromyography, spirometry, MRI, CK level, riluzole intake, genetic background, history of physical exercise and previous and current main occupation. Four components were scored as non-relevant, including place of birth, blood pressure and pain at onset. There was no significant difference between regions (European vs. non-European countries).
CONCLUSIONS: Our study identified a consensual set of clinical data with 42 specific items that can be used as a minimal data set for patient registers and for clinical trials.

Entities:  

Keywords:  Amyotrophic lateral sclerosis; hierarchy; signals; survey; symptoms

Mesh:

Year:  2017        PMID: 28705085     DOI: 10.1080/21678421.2017.1349150

Source DB:  PubMed          Journal:  Amyotroph Lateral Scler Frontotemporal Degener        ISSN: 2167-8421            Impact factor:   4.092


  2 in total

1.  Spreading in ALS: The relative impact of upper and lower motor neuron involvement.

Authors:  Marta Gromicho; Manuel Figueiral; Hilmi Uysal; Julian Grosskreutz; Magdalena Kuzma-Kozakiewicz; Susana Pinto; Susanne Petri; Sara Madeira; Michael Swash; Mamede de Carvalho
Journal:  Ann Clin Transl Neurol       Date:  2020-06-18       Impact factor: 4.511

2.  Analysis of routine blood parameters in patients with amyotrophic lateral sclerosis and evaluation of a possible correlation with disease progression-a multicenter study.

Authors:  Nora Hertel; Magdalena Kuzma-Kozakiewicz; Marta Gromicho; Julian Grosskreutz; Mamede de Carvalho; Hilmi Uysal; Reinhard Dengler; Susanne Petri; Sonja Körner
Journal:  Front Neurol       Date:  2022-07-27       Impact factor: 4.086

  2 in total

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