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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Sleep, lung function, and quality of life in patients with myasthenia gravis: A cross-sectional study

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Oliveira, Ezequiel Fernandes ; Nacif, Sergio Roberto ; Urbane, Jessica Julioti ; Silva, Anderson Soares ; Oliveira, Claudia Santos ; Perez, Eduardo Araujo ; Polaro, Melissa Nunes ; Oliveira Valerio, Berenice Cataldo ; Stirbulov, Roberto ; Insalaco, Giuseppe ; Bulle Oliveira, Acary Sousa ; Franco Oliveira, Luis Vicente
Número total de Autores: 12
Tipo de documento: Artigo Científico
Fonte: Neuromuscular Disorders; v. 27, n. 2, p. 120-127, FEB 2017.
Citações Web of Science: 6
Resumo

The purpose of this study was to investigate the physiological variables of lung function, respiratory muscle strength, and sleep in clinically stable patients with myasthenia gravis. This was a prospective cross-sectional study conducted in accordance with the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement. Patients adhering to the eligibility criteria were consecutively recruited from the Research Department of Neuromuscular Diseases at the Federal University of Sao Paulo and the Department of Neurology at Santa Casa de Misericordia of Sao Paulo and were referred to the Nove de Julho University Sleep Laboratory (Sao Paulo, Brazil). The study included 25 patients (21 female) with a mean age of 45.28 +/- 12.33 years. Only one patient exhibited a restrictive ventilatory pattern. The maximum ventilatory pressures observed were considerably reduced in most patients as compared to reference values. In sleep studies, the patients exhibited significantly reduced oxygen saturation, reduced rapid eye movement sleep time, increased non-rapid eye movement stage 3 sleep, and considerable apnoea/hypopnoea indexes. Clinically stable patients with myasthenia gravis exhibit a high prevalence of sleep-disordered breathing, significant reductions in maximum ventilatory pressures, and impairment of health-related quality of life. (C) 2016 Elsevier B.V. All rights reserved. (AU)

Processo FAPESP: 15/11738-6 - Estudo do sono, função pulmonar, força muscular ventilatória e validação de dois instrumentos de evolução clínica em pacientes com miastenia gravis: Quantitative Myasthenia gravis testing form e MG Composite Scale.
Beneficiário:Ezequiel Fernandes de Oliveira
Modalidade de apoio: Bolsas no Brasil - Doutorado