Prática fisioterapêutica no tratamento da fibrose cística

Carolina Lazzarim de Conto, Cintia Teixeira Vieira, Kelen Nunes Fernandes, Laís Machado Jorge, Gabriela da Silva Cândido, Rafael Inácio Barbosa, Rafael Cypriano Dutra

Resumo


A fibrose cística (FC), denominada também de mucoviscidose, é uma doença genética do tipo autossômica recessiva que acomete principalmente crianças e indivíduos de raça branca. O objetivo deste estudo foi propiciar uma visão sobre a FC, assim como as possíveis formas de tratamento fisioterapêutico. A pesquisa da literatura foi realizada nas bases de dados SciELO e PubMed, no período de abril de 2002 a março de 2013, através da seleção de artigos científicos referentes à FC, utilizando como palavras-chave: “fibrose cística”, “fisioterapia em fibrose cística” e “fisioterapia respiratória”. Por meio desta revisão, pôde-se observar que, apesar da complexidade da doença, a prática fisioterapêutica, com o uso das técnicas: tapotagem, vibração, drenagem postural (DP), huffing, oscilação oral de alta frequência (OOAF), drenagem autógena (DA) e o ciclo ativo da respiração (CAR), apresenta eficácia tanto no tratamento como na manutenção da qualidade de vida dos pacientes com FC.


Palavras-chave


fibrose cística; fisioterapia; muco

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Referências


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DOI: https://doi.org/10.7322/abcshs.v39i2.629

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Direitos autorais 2014 Carolina Lazzarim de Conto, Cintia Teixeira Vieira, Kelen Nunes Fernandes, Laís Machado Jorge, Gabriela da Silva Cândido, Rafael Inácio Barbosa, Rafael Cypriano Dutra