Literature DB >> 30656971

Predictors of diagnostic delay in amyotrophic lateral sclerosis: a cohort study based on administrative and electronic medical records data.

Francesca Palese1, Arianna Sartori2, Giancarlo Logroscino3,4, Federica Edith Pisa5.   

Abstract

Objectives: To characterize the timing and pathway of amyotrophic lateral sclerosis (ALS) diagnosis and to identify predictors of delayed diagnosis in a retrospective cohort.
Methods: The cohort included all patients with incident ALS between 2010 and 2014 in Friuli-Venezia Giulia (FVG) region, Italy, admitted to two University Hospitals. Information on demographics, clinical presentation, and healthcare use was obtained from health databases and electronic medical records (EMRs). Total diagnostic time (TDT), the interval between ALS symptoms onset and diagnosis, was compared between patient groups through Wilcoxon-Mann-Whitney test. The adjusted odds ratio (aOR), with 95% confidence interval (95% CI), of having a TDT ≥12 months was estimated using unconditional logistic regression.
Results: Among 134 patients, median TDT (interquartile range [IQR]) was 11.5 months (7.1-18.3), shorter in those aged <60 years vs. ≥60 years (8.1; 5.1-11.1 vs. 12.4; 7.4-21.5; p = 0.0064), first referred to a neurologist vs. other specialist (10.2; 6.1-16.3 vs. 13.2; 8.1-24.5; p = 0.0386) and without neurologic comorbidities (11.1; 7.1-16.5 vs. 19.7; 8.8-33.7; p = 0.0243). TDT was ≥12 months in 64 (48.5%) patients and was predicted by male sex (aOR: 2.47; 95% CI: 1.06-5.75), age at onset ≥60 years (11.46; 3.13-41.9), spinal onset (2.04; 1.00-5.93), and prior therapies or first referral to a non-neurologist (3.15; 1.36-7.29). Conclusions: In this cohort, delayed diagnosis was common, particularly in older patients and in those with neurological comorbidities. Timely referral to a neurologist may improve diagnostic timing.

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Year:  2019        PMID: 30656971     DOI: 10.1080/21678421.2018.1550517

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


  6 in total

1.  Diagnostic Process in Rare Diseases: Determinants Associated with Diagnostic Delay.

Authors:  Juan Benito-Lozano; Greta Arias-Merino; Mario Gómez-Martínez; Alba Ancochea-Díaz; Aitor Aparicio-García; Manuel Posada de la Paz; Verónica Alonso-Ferreira
Journal:  Int J Environ Res Public Health       Date:  2022-05-26       Impact factor: 4.614

2.  Pain in amyotrophic lateral sclerosis: a narrative review.

Authors:  Soyoung Kwak
Journal:  J Yeungnam Med Sci       Date:  2022-06-08

3.  Early and progressive dysfunction revealed by in vivo neurite imaging in the rNLS8 TDP-43 mouse model of ALS.

Authors:  Akram Zamani; Adam K Walker; Ben Rollo; Katie L Ayers; Raysha Farah; Terence J O'Brien; David K Wright
Journal:  Neuroimage Clin       Date:  2022-04-22       Impact factor: 4.891

Review 4.  The Cure VCP Scientific Conference 2021: Molecular and clinical insights into neurodegeneration and myopathy linked to multisystem proteinopathy-1 (MSP-1).

Authors:  Michelle A Johnson; Jacob A Klickstein; Richa Khanna; Yunzi Gou; Malavika Raman
Journal:  Neurobiol Dis       Date:  2022-04-08       Impact factor: 7.046

5.  Amyotrophic lateral sclerosis care and research in the United States during the COVID-19 pandemic: Challenges and opportunities.

Authors:  Jinsy A Andrews; James D Berry; Robert H Baloh; Nathan Carberry; Merit E Cudkowicz; Brixhilda Dedi; Jonathan Glass; Nicholas J Maragakis; Timothy M Miller; Sabrina Paganoni; Jeffrey D Rothstein; Jeremy M Shefner; Zachary Simmons; Michael D Weiss; Richard S Bedlack
Journal:  Muscle Nerve       Date:  2020-06-05       Impact factor: 3.852

6.  TDP-43 Cytoplasmic Translocation in the Skin Fibroblasts of ALS Patients.

Authors:  Miguel A Rubio; Mireia Herrando-Grabulosa; Roser Velasco; Israel Blasco; Monica Povedano; Xavier Navarro
Journal:  Cells       Date:  2022-01-08       Impact factor: 6.600

  6 in total

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