Cargando…

Volumetric capnography versus spirometry for the evaluation of pulmonary function in cystic fibrosis and allergic asthma()()

OBJECTIVE: To compare the values of the markers for volumetric capnography and spirometry and their ability to classify children and adolescents with asthma, cystic fibrosis (CF), and healthy controls. METHODS: This was a cross-sectional study that included 103 patients with controlled persistent al...

Descripción completa

Detalles Bibliográficos
Autores principales:	Almeida-Junior, Armando, Marson, Fernando Augusto Lima, Almeida, Celize Cruz Bresciani, Ribeiro, Maria Ângela Gonçalves Oliveira, Paschoal, Ilma Aparecida, Moreira, Marcos Mello, Ribeiro, José Dirceu
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Elsevier 2018
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9432330/ https://www.ncbi.nlm.nih.gov/pubmed/30529075 http://dx.doi.org/10.1016/j.jped.2018.10.008

Ejemplares similares

Volumetric capnography for the evaluation of chronic airways diseases
por: Veronez, Liliani, et al.
Publicado: (2014)

Ventilatory abnormalities in patients with cystic fibrosis undergoing the submaximal treadmill exercise test
por: Parazzi, Paloma Lopes Francisco, et al.
Publicado: (2015)

Respiratory evaluation through volumetric capnography among grade III obese and eutrophic individuals: a comparative study
por: Modena, Débora Aparecida Oliveira, et al.
Publicado: (2018)

Saliva as a potential tool for cystic fibrosis diagnosis
por: Gonçalves, Aline Cristina, et al.
Publicado: (2013)

Volumetric capnography: In the diagnostic work-up of chronic thromboembolic disease
por: Moreira, Marcos Mello, et al.
Publicado: (2010)

Novel volumetric capnography indices measure ventilation inhomogeneity in cystic fibrosis
por: Fouzas, Sotirios, et al.
Publicado: (2022)

Volumetric capnography and chronic obstructive pulmonary disease staging
por: Romero, Pablo V, et al.
Publicado: (2007)

The relationship between physical functional capacity and lung function in obese children and adolescents
por: Ferreira, Mariana Simões, et al.
Publicado: (2014)

Screening for F508del as a first step in the molecular diagnosis of cystic fibrosis,
por: Marson, Fernando Augusto de Lima, et al.
Publicado: (2013)

Volumetric capnography: lessons from the past and current clinical applications
por: Verscheure, Sara, et al.
Publicado: (2016)

Current methodological and technical limitations of time and volumetric capnography in newborns
por: Schmalisch, Gerd
Publicado: (2016)

Polymorphisms in the glutathione pathway modulate cystic fibrosis severity: a cross-sectional study
por: Marson, Fernando Augusto de Lima, et al.
Publicado: (2014)

Genetic interaction of GSH metabolic pathway genes in cystic fibrosis
por: Marson, Fernando Augusto de Lima, et al.
Publicado: (2013)

Cystic fibrosis transmembrane conductance regulator mutations at a referral center for cystic fibrosis
por: Coutinho, Cyntia Arivabeni de Araújo Correia, et al.
Publicado: (2013)

Sweat test and cystic fibrosis: overview of test performance at public and private centers in the state of São Paulo, Brazil
por: Servidoni, Maria Fátima, et al.
Publicado: (2017)

Diagnostic value of volumetric capnography in patients with chronic cough variant asthma
por: Sun, Xiaoli, et al.
Publicado: (2020)

Lung function and stress echocardiography in pulmonary arterial hypertension: a cross-sectional study
por: de Almeida, Guilherme Casagrande, et al.
Publicado: (2021)

Volumetric but Not Time Capnography Detects Ventilation/Perfusion Mismatch in Injured Rabbit Lung
por: Tolnai, József, et al.
Publicado: (2018)

Volumetric capnography pre- and post-surfactant during initial resuscitation of premature infants
por: Williams, Emma E., et al.
Publicado: (2021)

Quality of sweat test (ST) based on the proportion of sweat sodium (Na) and sweat chloride (Cl) as diagnostic parameter of cystic fibrosis: are we on the right way?
por: Faria, Alethéa Guimarães, et al.
Publicado: (2016)

Can continuous glucose monitoring predict cystic fibrosis-related diabetes and worse clinical outcome?
por: Zorron, Mariana, et al.
Publicado: (2022)

Erratum to: Quality of sweat test (ST) based on the proportion of sweat sodium (Na) and sweat chloride (Cl) as diagnostic parameter of cystic fibrosis: are we on the right way?
por: Faria, Alethéa Guimarães, et al.
Publicado: (2017)

Nasal Potential Difference in Cystic Fibrosis considering Severe CFTR Mutations
por: Ng, Ronny Tah Yen, et al.
Publicado: (2015)

Evaluation of continuous constant current and continuous pulsed current in sweat induction for cystic fibrosis diagnosis
por: Gomez, Carla Cristina Souza, et al.
Publicado: (2018)

IMPULSE OSCILLOMETRY AND SPIROMETRY IN SCHOOLERS SUBMITTED TO THE SIX-MINUTE WALK TEST
por: de Assumpção, Maíra Seabra, et al.
Publicado: (2018)

Volumetric capnography and return of spontaneous circulation in an experimental model of pediatric asphyxial cardiac arrest
por: de la Mata Navazo, Sara, et al.
Publicado: (2023)

Demographic, clinical, and laboratory parameters of cystic fibrosis during the last two decades: a comparative analysis
por: Marson, Fernando Augusto de Lima, et al.
Publicado: (2015)

The Efficiency Index (EFFi), based on volumetric capnography, may allow for simple diagnosis and grading of COPD
por: Jarenbäck, Linnea, et al.
Publicado: (2018)

Retrospective validation of a new volumetric capnography parameter for the exclusion of pulmonary embolism at the emergency department
por: Fabius, Timon M., et al.
Publicado: (2018)

Home Spirometry in Children with Cystic Fibrosis
por: Berlinski, Ariel, et al.
Publicado: (2023)

Spirometry Outside the Hospital
por: Morais-Almeida, Mário, et al.
Publicado: (2021)

Spirometry Outside the Hospital
por: Morais-Almeida, Mário, et al.
Publicado: (2021)

Lung ultrasound assessment of response to antibiotic therapy in cystic fibrosis exacerbations: a study of two cases
por: Peixoto, Andressa Oliveira, et al.
Publicado: (2019)

Combined multi-channel intraluminal impedance measurement and pHmetry in the detection of gastroesophageal reflux disease in children with cystic fibrosis
por: Gonçalves, Emília da Silva, et al.
Publicado: (2022)

Factors impacting the growth and nutritional status of cystic fibrosis patients younger than 10 years of age who did not undergo neonatal screening
por: Hortencio, Taís Daiene Russo, et al.
Publicado: (2015)

Near-fatal pulmonary embolism: capnographic perspective
por: Moreira, Marcos Mello, et al.
Publicado: (2018)

Bronchiectasis associated with severe COPD: Clinical, functional, microbiological and tomographic features
por: Doria da Silva, Silvia Maria, et al.
Publicado: (2022)

Epidemiological aspects of and risk factors for wheezing in the first year of life
por: Fogaça, Hamilton Rosendo, et al.
Publicado: (2014)

Routine spirometry in cystic fibrosis patients: impact on pulmonary exacerbation diagnosis and FEV(1) decline
por: de Aquino, Carolina Silva Barboza, et al.
Publicado: (2022)

Effects of home-based inspiratory muscle training on sickle cell disease (SCD) patients
por: Galvão, Fábio, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_k68ea5all512bstcruf868kgt8