HOW THE SPEECH-LANGUAGE PATHOLOGIST INTERACTS WITH CYSTIC FIBROSIS PATIENTS? A SCOPING REVIEW
DOI:
https://doi.org/10.25110/arqsaude.v27i9.2023-003Palavras-chave:
Speech-Language Pathology, Cystic Fibrosis, Audiology, SleepResumo
Objective: The review describes the changes related to sleep-breathing disorders, communication and feeding processes in subjects with CF, through a scoping review. Methods: A scoping review based on the PRISMA protocol was carried out in Pubmed, Lilacs and Scopus databases, to investigate the possibility of including SLP in the treatment of patients with CF. The inclusion criteria included studies that addressed communication and eating processes and disorders related to CF. Studies with a sample that presented other comorbidities that would justify the worsening of the condition, or secondary studies, were excluded. There was no time or language delimitation. Results: The search found 1566 works, 27 Lilacs, 1009 Pubmed and 530 Scopus, by analysis of titles, abstract and reading in full. A total of 30 articles were selected for inclusion, 2 Lilacs, 22 Pubmed and 6 Scopus, all related to Speech-Language Pathology. Conclusion: It was observed that there is a poor sleep quality due to nocturnal desaturation, mild and moderate obstructive apnea. In studies related to hearing, individuals had sensorineural hearing loss. Speech-Language Pathology is of paramount importance in monitoring these subjects.
Referências
ATHANAZIO, R. A. et al. Diretrizes brasileiras de diagnóstico e tratamento da fibrose cística. Jornal brasileiro de pneumologia, v. 43, p. 219-245, 2017. ISSN 1806-3713.
BALBANI, A. P. S. et al. Fibrose cística, imunodeficiências e discinesia ciliar primária: causas de infecções de repetição das vias aéreas superiores. Arq Fund Otorrinolaringol, v. 2, n. 1, p. 31-6, 1998.
BLACHARSH, C. Dental aspects of patients with cystic fibrosis: a preliminary clinical study. Journal of the American Dental Association (1939), v. 95, n. 1, p. 106-110, 1977. ISSN 0002-8177.
CAUMO, D. et al. Hearing thresholds at high frequency in patients with cystic fibrosis: a systematic review☆. Brazilian journal of otorhinolaryngology, v. 83, p. 464-474, 2017. ISSN 1808-8694.
CHENG, A. G. et al. Sensorineural hearing loss in patients with cystic fibrosis. Otolaryngology—Head and Neck Surgery, v. 141, n. 1, p. 86-90, 2009. ISSN 0194-5998.
DE CÁSSIA FIRMIDA, M.; LOPES, A. J. Aspectos epidemiológicos da fibrose cística. Revista Hospital Universitário Pedro Ernesto (TÍTULO NÃO-CORRENTE), v. 10, n. 4, 2011. ISSN 1983-2567.
DOUMIT, M. et al. Diagnostic accuracy and distress associated with oropharyngeal suction in cystic fibrosis. Journal of Cystic Fibrosis, v. 15, n. 4, p. 473-478, 2016. ISSN 1569-1993.
DZIEKIEWICZ, M. A. et al. Gastroesophageal reflux disease in children with cystic fibrosis. In: (Ed.). Ventilatory Disorders: Springer, 2015. p.1-7.
FAUROUX, B. et al. Sleep quality and nocturnal hypoxaemia and hypercapnia in children and young adults with cystic fibrosis. Archives of disease in childhood, v. 97, n. 11, p. 960-966, 2012. ISSN 0003-9888.
FORCUCCI, R. A.; STARK, E. W. Hearing loss, speech-language, and cystic fibrosis. Archives of Otolaryngology, v. 96, n. 4, p. 361-364, 1972. ISSN 0003-9977.
FORMAN-FRANCO, B. et al. Cystic fibrosis and hearing loss. Archives of Otolaryngology, v. 105, n. 6, p. 338-342, 1979. ISSN 0003-9977.
FURLAN, L. L. et al. Variantes no gene da interleucina 8 e a resposta a broncodilatadores inalatórios na fibrose cística☆,☆☆. Jornal de Pediatria, v. 93, p. 639-648, 2017. ISSN 0021-7557.
GARINIS, A. C. et al. The cumulative effects of intravenous antibiotic treatments on hearing in patients with cystic fibrosis. Journal of Cystic Fibrosis, v. 16, n. 3, p. 401-409, 2017. ISSN 1569-1993.
GARINIS, A. C. et al. Chirp-evoked otoacoustic emissions and middle ear absorbance for monitoring ototoxicity in cystic fibrosis patients. Ear and hearing, v. 39, n. 1, p. 69, 2018.
GEYER, L. B. et al. High frequency hearing thresholds and product distortion otoacoustic emissions in cystic fibrosis patients☆,☆☆. Brazilian journal of otorhinolaryngology, v. 81, p. 589-597, 2015. ISSN 1808-8694.
HANDELSMAN, J. A. et al. Prevalence of hearing and vestibular loss in cystic fibrosis patients exposed to aminoglycosides. Pediatric pulmonology, v. 52, n. 9, p. 1157-1162, 2017. ISSN 8755-6863.
HAYES, D. et al. Polysomnographic differences associated with pulmonary hypertension in patients with advanced lung disease due to cystic fibrosis. Lung, v. 192, n. 3, p. 413-419, 2014. ISSN 0341-2040.
HELRIGLE, C.; PEREIRA, K. F.; LEMOS, V. S. O uso do oscilador oral de alta frequência Flutter®VRP1 na terapia respiratória. Arquivos de Ciências da Saúde da UNIPAR, v. 18, n. 1, p. 59-64, jan./abr. 2014.
HYPPOLITO, M. A.; OLIVEIRA, J. A. A. Ototoxicidade, otoproteção e autodefesa das células ciliadas da cóclea. Medicina (Ribeirão Preto), v. 38, n. 3/4, p. 279-289, 2005. ISSN 2176-7262.
ISAIAH, A. et al. Predictors of sleep hypoxemia in children with cystic fibrosis. Pediatric pulmonology, v. 54, n. 3, p. 273-279, 2019. ISSN 8755-6863.
ÍSCAR-URRUTIA, M. et al. Objective and subjective sleep efficiency in adult patients with cystic fibrosis and impact on quality of life. Lung, v. 196, n. 6, p. 761-767, 2018. ISSN 1432-1750.
JACOB, L. C. B. et al. Monitoramento auditivo na ototoxidade. Revista Brasileira de Otorrinolaringologia, v. 72, p. 836-844, 2006. ISSN 0034-7299.
JANKELOWITZ, L. et al. Cystic fibrosis patients have poor sleep quality despite normal sleep latency and efficiency. Chest, v. 127, n. 5, p. 1593-1599, 2005. ISSN 0012-3692.
KREICHER, K. L. et al. Audiometric assessment of pediatric patients with cystic fibrosis. Journal of Cystic Fibrosis, v. 17, n. 3, p. 383-390, 2018. ISSN 1569-1993.
LOURENÇO, B. M.; COSTA, K. M.; DA SILVA FILHO, M. Voice disorder in cystic fibrosis patients. PloS one, v. 9, n. 5, p. e96769, 2014. ISSN 1932-6203.
MARSON, A. et al. Efetividade da fonoterapia e proposta de intervenção breve em respiradores orais. Revista CEFAC, v. 14, p. 1153-1166, 2012. ISSN 1516-1846.
MARTINS, L. M. N. et al. Hearing loss in cystic fibrosis. International journal of pediatric otorhinolaryngology, v. 74, n. 5, p. 469-473, 2010. ISSN 0165-5876.
MCCORMICK, J. et al. Ivacaftor improves rhinologic, psychologic, and sleep‐related quality of life in G551D cystic fibrosis patients. 3: Wiley Online Library, 2019. p.292-297.
MILROSS, M. A. et al. Predicting sleep-disordered breathing in patients with cystic fibrosis. Chest, v. 120, n. 4, p. 1239-1245, 2001. ISSN 0012-3692.
MORALES-MÚNERA, O. L. et al. Utilidad de los criterios de Murray para el procesamiento de esputo en pacientes con fibrosis quística. Laboratorio de Infectados de la Universidad de Antioquia (Medellín/Colombia). Infectio, v. 24, n. 4, p. 229-233, 2020. ISSN 2422-3794.
MULHERAN, M. et al. Absence of cochleotoxicity measured by standard and high-frequency pure tone audiometry in a trial of once-versus three-times-daily tobramycin in cystic fibrosis patients. Antimicrobial agents and chemotherapy, v. 50, n. 7, p. 2293-2299, 2006. ISSN 0066-4804.
NAQVI, S. K. et al. Sleep architecture in children and adolescents with cystic fibrosis and the association with severity of lung disease. Sleep and Breathing, v. 12, n. 1, p. 77-83, 2008. ISSN 1522-1709.
NELSON, J. et al. Pulmonary aspiration of sinus secretions in patients with cystic fibrosis. 3: Wiley Online Library, 2018. p.385-388.
PERIN, C. et al. Sleep findings and predictors of sleep desaturation in adult cystic fibrosis patients. Sleep and Breathing, v. 16, n. 4, p. 1041-1048, 2012. ISSN 1522-1709.
PILTCHER, O. B. et al. The prevalence of neurosensorial hearing loss among cystic fibrosis patients from Hospital de Clınicas de Porto Alegre. International journal of pediatric otorhinolaryngology, v. 67, n. 9, p. 939-941, 2003. ISSN 0165-5876.
RAMOS, R. T. T. et al. Arquitetura do sono e perfil respiratório polissonográfico de crianças e adolescentes com fibrose cística. Jornal de Pediatria, v. 87, p. 63-69, 2011. ISSN 0021-7557.
RAMOS, R. T. T. et al. Evaluation of the upper airway in children and adolescents with cystic fibrosis and obstructive sleep apnea syndrome. International journal of pediatric otorhinolaryngology, v. 73, n. 12, p. 1780-1785, 2009. ISSN 0165-5876.
RIBEIRO, J. D.; RIBEIRO, M. Â. G. D. O.; RIBEIRO, A. F. Controvérsias na fibrose cística: do pediatra ao especialista. Jornal de pediatria, v. 78, p. 171-186, 2002. ISSN 0021-7557.
SABATI, A. A. et al. Characteristics of gastroesophageal reflux in adults with cystic fibrosis. Journal of Cystic Fibrosis, v. 9, n. 5, p. 365-370, 2010. ISSN 1569-1993.
SHAKKOTTAI, A. et al. Sleep disturbances and their impact in pediatric cystic fibrosis. Sleep medicine reviews, v. 42, p. 100-110, 2018. ISSN 1087-0792.
SPICUZZA, L. et al. Early occurrence of obstructive sleep apnea in infants and children with cystic fibrosis. Archives of pediatrics & adolescent medicine, v. 166, n. 12, p. 1165-1169, 2012. ISSN 1072-4710.
STAVROULAKI, P. et al. Otoacoustic emissions for monitoring aminoglycoside-induced ototoxicity in children with cystic fibrosis. Archives of Otolaryngology–Head & Neck Surgery, v. 128, n. 2, p. 150-155, 2002. ISSN 0886-4470.
TOGEIRO, S. M. G. P.; SMITH, A. K. Métodos diagnósticos nos distúrbios do sono. Brazilian Journal of Psychiatry, v. 27, p. 8-15, 2005. ISSN 1516-4446.
TRICCO, A. C. et al. PRISMA Extension for Scoping Reviews (PRISMA-ScR): Checklist and Explanation. Ann Intern Med, v. 169, n. 7, p. 467-473, Oct 2 2018. ISSN 0003-4819.
VERONEZI, J. et al. Sleep-disordered breathing in patients with cystic fibrosis. Jornal Brasileiro de Pneumologia, v. 41, p. 351-357, 2015. ISSN 1806-3756.
VIJAYASINGAM, A. et al. Tablet and web-based audiometry to screen for hearing loss in adults with cystic fibrosis. Thorax, v. 75, n. 8, p. 632-639, 2020. ISSN 0040-6376.
Downloads
Publicado
Como Citar
Edição
Seção
Licença
Este trabalho está licenciado sob uma licença Creative Commons Attribution 4.0 International License.
Os Direitos Autorais para artigos publicados são de direito da revista. Em virtude da aparecerem nesta revista de acesso público, os artigos são de uso gratuito, com Creative Commons Attribution 4.0 International License.
A revista se reserva o direito de efetuar, nos originais, alterações de ordem normativa, ortográfica e gramatical, com vistas a manter o padrão culto da língua e a credibilidade do veículo. Respeitará, no entanto, o estilo de escrever dos autores.
Alterações, correções ou sugestões de ordem conceitual serão encaminhadas aos autores, quando necessário. Nesses casos, os artigos, depois de adequados, deverão ser submetidos a nova apreciação.
As opiniões emitidas pelos autores dos artigos são de sua exclusiva responsabilidade.