Frequency of NMOSD misdiagnosis in a cohort from Latin America: Impact and evaluation of different contributors

Author:

Carnero Contentti Edgar1ORCID,López Pablo A1,Criniti Juan2,Alonso Ricardo3ORCID,Silva Berenice4ORCID,Luetic Geraldine5ORCID,Correa-Díaz Edgar Patricio6ORCID,Galleguillos Lorna7ORCID,Navas Carlos8,Soto de Castillo Ibis9ORCID,Hamuy Fernando Diaz de Bedoya10,Gracia Fernando11,Tkachuk Verónica12,Weinshenker Brian G13,Rojas Juan Ignacio14

Affiliation:

1. Neuroimmunology Unit, Department of Neuroscience, Hospital Alemán, Buenos Aires, Argentina

2. Department of Internal Medicine, Hospital Alemán, Buenos Aires, Argentina

3. Neurology Department, Hospital J.M. Ramos Mejía, University of Buenos Aires, Buenos Aires, Argentina

4. Neurology Department, Hospital J.M. Ramos Mejía, University of Buenos Aires, Buenos Aires, Argentina/Sección Enfermedades Desmielinizantes, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina

5. Instituto de Neurociencias de Rosario, Santa Fe, Argentina

6. Neurology Department, Hospital Carlos Andrade Marin, Universidad Central del Ecuador, Quito, Ecuador

7. Clínica Alemana de Santiago, Santiago, Chile; Universidad del Desarrollo, Santiago, Chile

8. Clínica Enfermedad Desmielinizante, Clinica Universitaria Colombia, Bogotá, Colombia

9. Neurology Department, Hospital Universitario de Maracaibo, Maracaibo, Venezuela

10. Centro Nacional de Esclerosis Multiple, Asuncion, Paraguay

11. Hospital Santo Tomas, Universidad Interamericana de Panamá, Panama City, Panamá

12. Neuroimmunology Section, Department of Neurology, Hospital de Clínicas “José de San Martín,” Buenos Aires, Argentina

13. Department of Neurology, University of Virginia, Charlottesville, VA, USA

14. Centro de Esclerosis Múltiple de Buenos Aires (CEMBA), Buenos Aires, Argentina

Abstract

Background: Neuromyelitis optica spectrum disorder (NMOSD) misdiagnosis (i.e. the incorrect diagnosis of patients who truly have NMOSD) remains an issue in clinical practice. We determined the frequency and factors associated with NMOSD misdiagnosis in patients evaluated in a cohort from Latin America. Methods: We retrospectively reviewed the medical records of patients with NMOSD, according to the 2015 diagnostic criteria, from referral clinics in six Latin American countries (Argentina, Chile, Paraguay, Colombia, Ecuador, and Venezuela). Diagnoses prior to NMOSD and ultimate diagnoses, demographic, clinical and paraclinical data, and treatment schemes were evaluated. Results: A total of 469 patients presented with an established diagnosis of NMOSD (73.2% seropositive) and after evaluation, we determined that 56 (12%) patients had been initially misdiagnosed with a disease other than NMOSD. The most frequent alternative diagnoses were multiple sclerosis (MS; 66.1%), clinically isolated syndrome (17.9%), and cerebrovascular disease (3.6%). NMOSD misdiagnosis was determined by MS/NMOSD specialists in 33.9% of cases. An atypical MS syndrome was found in 86% of misdiagnosed patients, 50% had NMOSD red flags in brain and/or spinal magnetic resonance imaging (MRI), and 71.5% were prescribed disease-modifying drugs. Conclusions: NMOSD misdiagnosis is relatively frequent in Latin America (12%). Misapplication and misinterpretation of clinical and neuroradiological findings are relevant factors associated with misdiagnosis.

Funder

LACTRIMS support

Publisher

SAGE Publications

Subject

Neurology (clinical),Neurology

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