1. Pediatric Barcelona Olfactory Test ̶ 6 (pBOT-6): Validation of a Combined Odor Identification and Threshold Screening Test in Healthy Spanish Children and Adolescents
- Author
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Claudio Fragola, A Aguirre, M J Rojas Lechuga, J Valero, G de Los Santos, Ignacio Cobeta, Isam Alobid, Meritxell Valls-Mateus, Jordi Alonso, J Mullol, Amparo Santamaría, and Franklin Mariño-Sánchez
- Subjects
Male ,Olfactometria ,medicine.medical_specialty ,Adolescent ,Screening test ,Intraclass correlation ,Immunology ,Olfaction ,Audiology ,Sensitivity and Specificity ,Reference Values ,Olfactometry ,medicine ,Humans ,Immunology and Allergy ,In patient ,Child ,Children ,Diagnostic Tests, Routine ,Two-alternative forced choice ,business.industry ,Age Factors ,Reproducibility of Results ,Healthy Volunteers ,Test (assessment) ,Smell ,Odor ,Spain ,Sensory Thresholds ,Odorants ,Female ,business ,Infants ,Pediatric population - Abstract
Background: Few odor tests have been developed for children. Objectives: The aim of the present study was to develop and validate a simple and quick olfactory test to evaluate odor identification and threshold in a Spanish pediatric population. Methods: The Pediatric Barcelona Olfactory Test-6 (pBOT-6) consisted of a set of 6 odorants for a forced choice identification test and a 6-dilution phenyl ethyl alcohol geometric series for the threshold test. The pBOT-6 was compared with the Universal Sniff test (a validated international pediatric smell test) in 131 healthy Spanish volunteers aged 6-17 years. A Bland-Altman plot was used to determine the agreement between the 2 tests. Reliability was analyzed in 15 volunteers using the intraclass correlation coefficient. Normative data were obtained, and 8 children diagnosed with subjective loss of smell were tested for validation. Results: The Bland-Altman analysis demonstrated a minimal bias of –1.71% with upper and lower limits of agreement of –31.1% and 27.6%, respectively. The intraclass correlation coefficient was 0.83 (95%CI, 0.6-0.96) for the identification test and 0.73 (95%CI, 0.36-0.9) for the threshold test, with excellent and good consistency between measurements over time. Mean pBOT-6 scores were significantly higher in healthy volunteers than in patients with loss of smell. Discrimination between normosmia and loss of smell was achieved with a sensitivity of 96.9% and a specificity of 100%. Conclusions: pBOT-6 offers an effective and fast method that is useful in clinical routine to distinguish, with high sensitivity and specificity, between pediatric patients with normosmia and those with loss of smell.
- Published
- 2020