Associação entre as alterações da via aérea superior e marcadores de progressão da doença em pacientes com fibrose cística

Detalhes bibliográficos
Autor(a) principal: Steffen, Luciane Mazzini
Data de Publicação: 2017
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Biblioteca Digital de Teses e Dissertações da PUC_RS
Texto Completo: http://tede2.pucrs.br/tede2/handle/tede/8211
Resumo: Introduction: Cystic Fibrosis is a disease characterized by recurrent infections and chronic inflammation of the respiratory system that lead to irreversible pulmonary complications. Infections are mainly caused by Staphilococcus aureos(SA) and Pseudomonas aeruginosa (PA). Early diagnosis for identification of colonizing germs is an important challenge. Guidelines suggest the use of swab cultures of the oropharynx or sputum. However, studies on molecular testing, or alternative methods of collection are still unconclusive. The involvement of the upper airway (nasopharynx and paranasal sinuses) has been cited as the primary source of infection. The present study aims to describe and compare the most frequent findings and pathogens in the nasal tract in patients with cystic fibrosis and to correlate findings with markers of severity and progression of lung disease. Methods: This is a retrospective study, which included patients with a diagnosis of Cystic Fibrosis (CF) who are followed up at the Multidisciplinary Outpatient Clinic of the Pediatric Pulmonology Unit of the Hospital São Lucas (Pontifical Catholic University of Rio Grande do Sul - PUCRS). Patients who have performed otorhinolaryngological evaluation (ENT) in the last two years (2015-2016) were included. The video naso endoscopy and nasal swab collection were part of the ENT evaluation. Results: 48 patients with CF were included, of which 30 (62.5%) were male. The mean age was 12.15 years ±6.60, and the mean predicted forced expiratory volume in the first second (FEV1%) was 83.36 ±30.04. When evaluating the presence and characteristic of nasal secretion, only 9 patients (18.7%) presented purulent secretion. Twenty-six patients (54.2%) presented grade 1 tonsils and 12 (25%) grade 2 or 3 patients. Nasal swab bacteriology was positive in 26 (54.1%) patients, from which 22 presented Staphylococcus aureos, 2 Pseudomonas aeruginosa, 1 Pseudomonas cepacea and 1 Stenotrophomonas maltophila (SM). In 22 patients (45.8%) the result of the culture was negative. In this study, patients who presented positive colonization by the traditional method (oropharynx / sputum) had a statistically significant chance of being identified also by nasal cavity culture (p<0.001). However, the association was not perfect, and showed a low correlation for the detection of gram negative germs. Nasal polyps were observed in 9 participants. When polyp is used as a marker of disease in nasal endoscopy, a strong association is observed between the presence of polyps and lower Shwachman-Kulczycki clinical score (p <0.001). Conclusions: the results of the culture obtained by collection of the nasal cavity were similar to those found by the standardized collection methods as markers of colonization of the inferior airway. In addition, nasal swabs is characterized as a non-invasive technique and showed to be sensitive to the identification of relevant pathogens in CF, especially SA. In addition, the presence of the polyp in the nasal cavity was shown to be associated with prognostic markers as Shwachman-Kulczycki clinical score.
id P_RS_e587a07e42939cb9a794054056f9903b
oai_identifier_str oai:tede2.pucrs.br:tede/8211
network_acronym_str P_RS
network_name_str Biblioteca Digital de Teses e Dissertações da PUC_RS
repository_id_str
spelling Pinto, Leonardo Araújohttp://lattes.cnpq.br/5296343733640465http://lattes.cnpq.br/6900341721328176Steffen, Luciane Mazzini2018-07-17T11:32:31Z2017-03-22http://tede2.pucrs.br/tede2/handle/tede/8211Introduction: Cystic Fibrosis is a disease characterized by recurrent infections and chronic inflammation of the respiratory system that lead to irreversible pulmonary complications. Infections are mainly caused by Staphilococcus aureos(SA) and Pseudomonas aeruginosa (PA). Early diagnosis for identification of colonizing germs is an important challenge. Guidelines suggest the use of swab cultures of the oropharynx or sputum. However, studies on molecular testing, or alternative methods of collection are still unconclusive. The involvement of the upper airway (nasopharynx and paranasal sinuses) has been cited as the primary source of infection. The present study aims to describe and compare the most frequent findings and pathogens in the nasal tract in patients with cystic fibrosis and to correlate findings with markers of severity and progression of lung disease. Methods: This is a retrospective study, which included patients with a diagnosis of Cystic Fibrosis (CF) who are followed up at the Multidisciplinary Outpatient Clinic of the Pediatric Pulmonology Unit of the Hospital São Lucas (Pontifical Catholic University of Rio Grande do Sul - PUCRS). Patients who have performed otorhinolaryngological evaluation (ENT) in the last two years (2015-2016) were included. The video naso endoscopy and nasal swab collection were part of the ENT evaluation. Results: 48 patients with CF were included, of which 30 (62.5%) were male. The mean age was 12.15 years ±6.60, and the mean predicted forced expiratory volume in the first second (FEV1%) was 83.36 ±30.04. When evaluating the presence and characteristic of nasal secretion, only 9 patients (18.7%) presented purulent secretion. Twenty-six patients (54.2%) presented grade 1 tonsils and 12 (25%) grade 2 or 3 patients. Nasal swab bacteriology was positive in 26 (54.1%) patients, from which 22 presented Staphylococcus aureos, 2 Pseudomonas aeruginosa, 1 Pseudomonas cepacea and 1 Stenotrophomonas maltophila (SM). In 22 patients (45.8%) the result of the culture was negative. In this study, patients who presented positive colonization by the traditional method (oropharynx / sputum) had a statistically significant chance of being identified also by nasal cavity culture (p<0.001). However, the association was not perfect, and showed a low correlation for the detection of gram negative germs. Nasal polyps were observed in 9 participants. When polyp is used as a marker of disease in nasal endoscopy, a strong association is observed between the presence of polyps and lower Shwachman-Kulczycki clinical score (p <0.001). Conclusions: the results of the culture obtained by collection of the nasal cavity were similar to those found by the standardized collection methods as markers of colonization of the inferior airway. In addition, nasal swabs is characterized as a non-invasive technique and showed to be sensitive to the identification of relevant pathogens in CF, especially SA. In addition, the presence of the polyp in the nasal cavity was shown to be associated with prognostic markers as Shwachman-Kulczycki clinical score.Introdução: a fibrose cística é uma patologia caracterizada por infecções recorrentes e inflamação crônica do sistema respiratório que levam a complicações pulmonares, por vezes, irreversíveis. As infecções são causadas, principalmente pelos microorganismos Staphilococcusaureos(SA) e Pseudomonas aeruginosa(PA). O diagnóstico precoce para identificação dos germes colonizadores é ainda um desafio. Consensos sugerem o uso de culturas de swab da orofaringe ou escarro. No entanto, pesquisa por testes moleculares como opção, ou formas alternativas de coleta ainda são inconclusivos. O comprometimento da via aérea superior (nasofaringe e seios paranasais) tem sido citada como fonte primária de infecção. O presente estudo tem por objetivo descrever e comparar as alterações e os patógenos mais frequentes no trato nasal em pacientes com fibrose cística e correlacionar os achados com marcadores de gravidade e progressão da doença pulmonar. Métodos: este é um estudo retrospectivo, que incluiu pacientes com diagnóstico de Fibrose Cística (FC) que são acompanhados no Ambulatório Multidisciplinar de FC do Serviço de Pneumologia Pediátrica do Hospital São Lucas da Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS), e que tenham realizado avaliação otorrinolarigológica (ORL) entre os anos de 2015 e 2016. A videonasoendoscopia e a coleta de material da fossa nasal com o uso do swab fizeram parte da avaliação ORL. Os marcadores de gravidade e progressão da doença foram: índice de massa corporal (IMC), volume expiratório forçado no primeiro segundo(VEF1%) e o escore clínico de Shwachman-Kulczycki(S-K). Resultados: foram incluídos 48 pacientes com FC, sendo 30 (62,5%) do gênero masculino. A média de idade foi 12,15 anos ± 6,60, e a média do percentual do valor previsto de volume expiratório forçado no primeiro segundo (VEF1%) foi de 83,36 ± 30,04. Ao avaliar a presença e característica da secreção nasal, apenas 9 pacientes (18,7%) apresentavam secreção purulenta. Com relação as tonsilas faríngeas, 26 pacientes (54,2%) apresentavam tonsilas grau 1 e 12 pacientes (25%) grau 2 ou 3. A bacteriologia do swab nasal foi positiva em 26 (54,1%) pacientes, onde 22 apresentavam Staphylococcus aureos, 2 Pseudomonas aeruginosa, 1 Pseudomonas cepacea e 1 Stenotrophomonas maltophila(SM). Em 22 pacientes (45,8%) o resultado da cultura foi negativo. Neste estudo, os pacientes que apresentavam colonização positiva pelo método tradicional (orofaringe/escarro), tinham uma chance estatisticamente significativa de serem identificados também pela cultura da cavidade nasal (p<0,001). Porém a associação não é perfeita, e demonstrou baixa correlação para detecção de germes gram negativos. Foram observados pólipos nasais em 9 participantes. Quando utilizada a presença de pólipo como marcador de doença na endoscopia nasal, observa-se uma forte associação entre a presença de pólipos e o redução dos valores no escore clínico de Shwachman-Kulczycki (p<0,001). Conclusões: os resultados da cultura obtidos pela coleta da fossa nasal foram semelhantes aos encontrados pelos métodos de coleta padronizados como marcadores de colonização da via aérea inferior. Além de caracterizar-se como uma técnica pouco invasiva, o swab nasal mostra-se sensível à identificação de patógenos relevantes na FC, especialmente SA. Além disso, a presença do pólipo na cavidade nasal mostrou ser um dado associado a marcadores de prognóstico medido pelo escore clínico de Shwachman-Kulczycki.Submitted by PPG Pediatria e Saúde da Criança (pediatria-pg@pucrs.br) on 2018-07-12T11:24:06Z No. of bitstreams: 1 DissertaçãoLu SteffenVersãoFinal.pdf: 1086203 bytes, checksum: 9b8f206613da0e87460cd6110bcec5ac (MD5)Approved for entry into archive by Sheila Dias (sheila.dias@pucrs.br) on 2018-07-17T11:24:05Z (GMT) No. of bitstreams: 1 DissertaçãoLu SteffenVersãoFinal.pdf: 1086203 bytes, checksum: 9b8f206613da0e87460cd6110bcec5ac (MD5)Made available in DSpace on 2018-07-17T11:32:31Z (GMT). No. of bitstreams: 1 DissertaçãoLu SteffenVersãoFinal.pdf: 1086203 bytes, checksum: 9b8f206613da0e87460cd6110bcec5ac (MD5) Previous issue date: 2017-03-22Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESapplication/pdfhttp://tede2.pucrs.br:80/tede2/retrieve/172837/DIS_LUCIANE_MAZINI_STEFFEN_CONFIDENCIAL.pdf.jpghttps://tede2.pucrs.br/tede2/retrieve/188517/DIS_LUCIANE_MAZINI_STEFFEN_COMPLETO.pdf.jpgporPontifícia Universidade Católica do Rio Grande do SulPrograma de Pós-Graduação em Medicina/Pediatria e Saúde da CriançaPUCRSBrasilEscola de MedicinaFibrose CísticaVia Aérea InferiorBacteriologiaPólipo NasalCystic FibrosisRespiratory Tract InfectionsBacteriologyNasal PolypsCIENCIAS DA SAUDE::MEDICINAAssociação entre as alterações da via aérea superior e marcadores de progressão da doença em pacientes com fibrose císticainfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisTrabalho será publicado como artigo ou livro60 meses17/07/20233098206005268432148500500500600-224747486637135387-9693694523087866272075167498588264571info:eu-repo/semantics/openAccessreponame:Biblioteca Digital de Teses e Dissertações da PUC_RSinstname:Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS)instacron:PUC_RSORIGINALDIS_LUCIANE_MAZZINI_STEFFEN_COMPLETO.pdfDIS_LUCIANE_MAZZINI_STEFFEN_COMPLETO.pdfapplication/pdf1086203https://tede2.pucrs.br/tede2/bitstream/tede/8211/8/DIS_LUCIANE_MAZZINI_STEFFEN_COMPLETO.pdf9b8f206613da0e87460cd6110bcec5acMD58THUMBNAILDIS_LUCIANE_MAZZINI_STEFFEN_COMPLETO.pdf.jpgDIS_LUCIANE_MAZZINI_STEFFEN_COMPLETO.pdf.jpgimage/jpeg6320https://tede2.pucrs.br/tede2/bitstream/tede/8211/7/DIS_LUCIANE_MAZZINI_STEFFEN_COMPLETO.pdf.jpgbdbd748f0032938429e475c094139355MD57TEXTDIS_LUCIANE_MAZZINI_STEFFEN_COMPLETO.pdf.txtDIS_LUCIANE_MAZZINI_STEFFEN_COMPLETO.pdf.txttext/plain73893https://tede2.pucrs.br/tede2/bitstream/tede/8211/6/DIS_LUCIANE_MAZZINI_STEFFEN_COMPLETO.pdf.txt8da6fc231e484b12af78ab6de31f0b92MD56LICENSElicense.txtlicense.txttext/plain; charset=utf-8610https://tede2.pucrs.br/tede2/bitstream/tede/8211/1/license.txt5a9d6006225b368ef605ba16b4f6d1beMD51tede/82112023-07-24 18:32:45.272oai:tede2.pucrs.br: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Biblioteca Digital de Teses e Dissertaçõeshttp://tede2.pucrs.br/tede2/PRIhttps://tede2.pucrs.br/oai/requestbiblioteca.central@pucrs.br||opendoar:2023-07-24T21:32:45Biblioteca Digital de Teses e Dissertações da PUC_RS - Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS)false
dc.title.por.fl_str_mv Associação entre as alterações da via aérea superior e marcadores de progressão da doença em pacientes com fibrose cística
title Associação entre as alterações da via aérea superior e marcadores de progressão da doença em pacientes com fibrose cística
spellingShingle Associação entre as alterações da via aérea superior e marcadores de progressão da doença em pacientes com fibrose cística
Steffen, Luciane Mazzini
Fibrose Cística
Via Aérea Inferior
Bacteriologia
Pólipo Nasal
Cystic Fibrosis
Respiratory Tract Infections
Bacteriology
Nasal Polyps
CIENCIAS DA SAUDE::MEDICINA
title_short Associação entre as alterações da via aérea superior e marcadores de progressão da doença em pacientes com fibrose cística
title_full Associação entre as alterações da via aérea superior e marcadores de progressão da doença em pacientes com fibrose cística
title_fullStr Associação entre as alterações da via aérea superior e marcadores de progressão da doença em pacientes com fibrose cística
title_full_unstemmed Associação entre as alterações da via aérea superior e marcadores de progressão da doença em pacientes com fibrose cística
title_sort Associação entre as alterações da via aérea superior e marcadores de progressão da doença em pacientes com fibrose cística
author Steffen, Luciane Mazzini
author_facet Steffen, Luciane Mazzini
author_role author
dc.contributor.advisor1.fl_str_mv Pinto, Leonardo Araújo
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/5296343733640465
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/6900341721328176
dc.contributor.author.fl_str_mv Steffen, Luciane Mazzini
contributor_str_mv Pinto, Leonardo Araújo
dc.subject.por.fl_str_mv Fibrose Cística
Via Aérea Inferior
Bacteriologia
Pólipo Nasal
topic Fibrose Cística
Via Aérea Inferior
Bacteriologia
Pólipo Nasal
Cystic Fibrosis
Respiratory Tract Infections
Bacteriology
Nasal Polyps
CIENCIAS DA SAUDE::MEDICINA
dc.subject.eng.fl_str_mv Cystic Fibrosis
Respiratory Tract Infections
Bacteriology
Nasal Polyps
dc.subject.cnpq.fl_str_mv CIENCIAS DA SAUDE::MEDICINA
description Introduction: Cystic Fibrosis is a disease characterized by recurrent infections and chronic inflammation of the respiratory system that lead to irreversible pulmonary complications. Infections are mainly caused by Staphilococcus aureos(SA) and Pseudomonas aeruginosa (PA). Early diagnosis for identification of colonizing germs is an important challenge. Guidelines suggest the use of swab cultures of the oropharynx or sputum. However, studies on molecular testing, or alternative methods of collection are still unconclusive. The involvement of the upper airway (nasopharynx and paranasal sinuses) has been cited as the primary source of infection. The present study aims to describe and compare the most frequent findings and pathogens in the nasal tract in patients with cystic fibrosis and to correlate findings with markers of severity and progression of lung disease. Methods: This is a retrospective study, which included patients with a diagnosis of Cystic Fibrosis (CF) who are followed up at the Multidisciplinary Outpatient Clinic of the Pediatric Pulmonology Unit of the Hospital São Lucas (Pontifical Catholic University of Rio Grande do Sul - PUCRS). Patients who have performed otorhinolaryngological evaluation (ENT) in the last two years (2015-2016) were included. The video naso endoscopy and nasal swab collection were part of the ENT evaluation. Results: 48 patients with CF were included, of which 30 (62.5%) were male. The mean age was 12.15 years ±6.60, and the mean predicted forced expiratory volume in the first second (FEV1%) was 83.36 ±30.04. When evaluating the presence and characteristic of nasal secretion, only 9 patients (18.7%) presented purulent secretion. Twenty-six patients (54.2%) presented grade 1 tonsils and 12 (25%) grade 2 or 3 patients. Nasal swab bacteriology was positive in 26 (54.1%) patients, from which 22 presented Staphylococcus aureos, 2 Pseudomonas aeruginosa, 1 Pseudomonas cepacea and 1 Stenotrophomonas maltophila (SM). In 22 patients (45.8%) the result of the culture was negative. In this study, patients who presented positive colonization by the traditional method (oropharynx / sputum) had a statistically significant chance of being identified also by nasal cavity culture (p<0.001). However, the association was not perfect, and showed a low correlation for the detection of gram negative germs. Nasal polyps were observed in 9 participants. When polyp is used as a marker of disease in nasal endoscopy, a strong association is observed between the presence of polyps and lower Shwachman-Kulczycki clinical score (p <0.001). Conclusions: the results of the culture obtained by collection of the nasal cavity were similar to those found by the standardized collection methods as markers of colonization of the inferior airway. In addition, nasal swabs is characterized as a non-invasive technique and showed to be sensitive to the identification of relevant pathogens in CF, especially SA. In addition, the presence of the polyp in the nasal cavity was shown to be associated with prognostic markers as Shwachman-Kulczycki clinical score.
publishDate 2017
dc.date.issued.fl_str_mv 2017-03-22
dc.date.accessioned.fl_str_mv 2018-07-17T11:32:31Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
format masterThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://tede2.pucrs.br/tede2/handle/tede/8211
url http://tede2.pucrs.br/tede2/handle/tede/8211
dc.language.iso.fl_str_mv por
language por
dc.relation.program.fl_str_mv 3098206005268432148
dc.relation.confidence.fl_str_mv 500
500
500
600
dc.relation.department.fl_str_mv -224747486637135387
dc.relation.cnpq.fl_str_mv -969369452308786627
dc.relation.sponsorship.fl_str_mv 2075167498588264571
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Pontifícia Universidade Católica do Rio Grande do Sul
dc.publisher.program.fl_str_mv Programa de Pós-Graduação em Medicina/Pediatria e Saúde da Criança
dc.publisher.initials.fl_str_mv PUCRS
dc.publisher.country.fl_str_mv Brasil
dc.publisher.department.fl_str_mv Escola de Medicina
publisher.none.fl_str_mv Pontifícia Universidade Católica do Rio Grande do Sul
dc.source.none.fl_str_mv reponame:Biblioteca Digital de Teses e Dissertações da PUC_RS
instname:Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS)
instacron:PUC_RS
instname_str Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS)
instacron_str PUC_RS
institution PUC_RS
reponame_str Biblioteca Digital de Teses e Dissertações da PUC_RS
collection Biblioteca Digital de Teses e Dissertações da PUC_RS
bitstream.url.fl_str_mv https://tede2.pucrs.br/tede2/bitstream/tede/8211/8/DIS_LUCIANE_MAZZINI_STEFFEN_COMPLETO.pdf
https://tede2.pucrs.br/tede2/bitstream/tede/8211/7/DIS_LUCIANE_MAZZINI_STEFFEN_COMPLETO.pdf.jpg
https://tede2.pucrs.br/tede2/bitstream/tede/8211/6/DIS_LUCIANE_MAZZINI_STEFFEN_COMPLETO.pdf.txt
https://tede2.pucrs.br/tede2/bitstream/tede/8211/1/license.txt
bitstream.checksum.fl_str_mv 9b8f206613da0e87460cd6110bcec5ac
bdbd748f0032938429e475c094139355
8da6fc231e484b12af78ab6de31f0b92
5a9d6006225b368ef605ba16b4f6d1be
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
MD5
MD5
repository.name.fl_str_mv Biblioteca Digital de Teses e Dissertações da PUC_RS - Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS)
repository.mail.fl_str_mv biblioteca.central@pucrs.br||
_version_ 1799765334866001920