Paediatric Barcelona Olfactory Test-6 (pBOT-6): Validation of a Combined Odour Identification and Threshold Screening Test in Healthy Spanish Children and Adolescents

dc.contributor.authorMariño-Sánchez, Franklin Santiago
dc.contributor.authorValls Mateus, Meritxell
dc.contributor.authorFragola, C.
dc.contributor.authorSantos, G. de los
dc.contributor.authorAguirre, A.
dc.contributor.authorAlonso, J.
dc.contributor.authorValero, J.
dc.contributor.authorSantamaría, A.
dc.contributor.authorRojas Lechuga, María Jesús
dc.contributor.authorCobeta, I.
dc.contributor.authorAlobid, Isam
dc.contributor.authorMullol i Miret, Joaquim
dc.date.accessioned2020-05-04T17:20:46Z
dc.date.available2020-05-04T17:20:46Z
dc.date.issued2019-01-01
dc.date.updated2020-02-28T10:37:41Z
dc.description.abstractBackground: Few odour tests have been created for children. Objectives: The aim of the present study was to develop and validate a simple and quick olfactory test, suitable for the evaluation of odour identification and threshold in a Spanish paediatric population, the paediatric Barcelona Olfactory Test-6 (pBOT-6).The pBOT-6 consisted in a set of 6 odorants for a forced-choice identification test (IT), and a 6 dilutions phenyl ethyl alcohol geometric series for the threshold test (TT). The pBOT-6 was compared with the U-sniff test (a validated international paediatric smell test) in 131 Spanish healthy volunteers aged 6-17 years. A Bland-Altman plot was used to determine the agreement between two tests. Reliability was analyzed in fifteenvolunteers using the intraclass correlation coefficient (ICC). Normative data was obtained and 8 children diagnosed with subjective smell loss were tested for validation.Bland-Altman analysis demonstrated a minimal bias of -1.71% with upper and lower limit of agreement of -31.1% and 27.6%, respectively. The ICC was 0.83 (95% CI 0.6-0.96) for the IT and 0.73 (95% CI 0.36-0.9) for the TT, showing excellent and good consistency between measurements over time. Mean pBOT-6 scores were significantly higher in healthy volunteers compared with patients with smell loss. Discrimination between normosmia and smell loss was achieved with a sensitivity of 96.9% and a specificity of 100%.The pBOT-6 offers an effectiveand fast method useful in clinical routine to distinguish, with high sensitivity and specificity, between paediatric patients with normosmia and those with smell dysfunction.
dc.format.extent24 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idimarina5882134
dc.identifier.urihttps://hdl.handle.net/2445/158592
dc.language.isoeng
dc.publisherEsmon Publicidad S.A.
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.18176/jiaci.0451
dc.relation.ispartofJournal of Investigational Allergology and Clinical Immunology, 2019, vol. 30, num. 6
dc.relation.urihttps://doi.org/10.18176/jiaci.0451
dc.rights(c) Esmon Publicidad S.A., 2019
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.sourceArticles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)
dc.subject.classificationInfants
dc.subject.classificationOlfactometria
dc.subject.otherChildren
dc.subject.otherOlfactometry
dc.titlePaediatric Barcelona Olfactory Test-6 (pBOT-6): Validation of a Combined Odour Identification and Threshold Screening Test in Healthy Spanish Children and Adolescents
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/acceptedVersion

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