TY - JOUR
T1 - Development of an International Odor Identification Test for Children
T2 - The Universal Sniff Test
AU - Schriever, Valentin A.
AU - Agosin, Eduardo
AU - Altundag, Aytug
AU - Avni, Hadas
AU - Cao Van, Helene
AU - Cornejo, Carlos
AU - de los Santos, Gonzalo
AU - Fishman, Gad
AU - Fragola, Claudio
AU - Guarneros, Marco
AU - Gupta, Neelima
AU - Hudson, Robyn
AU - Kamel, Reda
AU - Knaapila, Antti
AU - Konstantinidis, Iordanis
AU - Landis, Basile N.
AU - Larsson, Maria
AU - Lundström, Johan N.
AU - Macchi, Alberto
AU - Mariño-Sánchez, Franklin
AU - Martinec Nováková, Lenka
AU - Mori, Eri
AU - Mullol, Joaquim
AU - Nord, Marie
AU - Parma, Valentina
AU - Philpott, Carl
AU - Propst, Evan J.
AU - Rawan, Ahmed
AU - Sandell, Mari
AU - Sorokowska, Agnieszka
AU - Sorokowski, Piotr
AU - Sparing-Paschke, Lisa Marie
AU - Stetzler, Carolin
AU - Valder, Claudia
AU - Vodicka, Jan
AU - Hummel, Thomas
N1 - Publisher Copyright:
© 2018 Elsevier Inc.
PY - 2018/7
Y1 - 2018/7
N2 - Objective: To assess olfactory function in children and to create and validate an odor identification test to diagnose olfactory dysfunction in children, which we called the Universal Sniff (U-Sniff) test. Study design: This is a multicenter study involving 19 countries. The U-Sniff test was developed in 3 phases including 1760 children age 5-7 years. Phase 1: identification of potentially recognizable odors; phase 2: selection of odorants for the odor identification test; and phase 3: evaluation of the test and acquisition of normative data. Test—retest reliability was evaluated in a subgroup of children (n = 27), and the test was validated using children with congenital anosmia (n = 14). Results: Twelve odors were familiar to children and, therefore, included in the U-Sniff test. Children scored a mean ± SD of 9.88 ± 1.80 points out of 12. Normative data was obtained and reported for each country. The U-Sniff test demonstrated a high test—retest reliability (r 27 = 0.83, P <.001) and enabled discrimination between normosmia and children with congenital anosmia with a sensitivity of 100% and specificity of 86%. Conclusions: The U-Sniff is a valid and reliable method of testing olfaction in children and can be used internationally.
AB - Objective: To assess olfactory function in children and to create and validate an odor identification test to diagnose olfactory dysfunction in children, which we called the Universal Sniff (U-Sniff) test. Study design: This is a multicenter study involving 19 countries. The U-Sniff test was developed in 3 phases including 1760 children age 5-7 years. Phase 1: identification of potentially recognizable odors; phase 2: selection of odorants for the odor identification test; and phase 3: evaluation of the test and acquisition of normative data. Test—retest reliability was evaluated in a subgroup of children (n = 27), and the test was validated using children with congenital anosmia (n = 14). Results: Twelve odors were familiar to children and, therefore, included in the U-Sniff test. Children scored a mean ± SD of 9.88 ± 1.80 points out of 12. Normative data was obtained and reported for each country. The U-Sniff test demonstrated a high test—retest reliability (r 27 = 0.83, P <.001) and enabled discrimination between normosmia and children with congenital anosmia with a sensitivity of 100% and specificity of 86%. Conclusions: The U-Sniff is a valid and reliable method of testing olfaction in children and can be used internationally.
KW - Sniffin’ Sticks
KW - children
KW - olfaction
KW - olfactory dysfunction
KW - smell testing
UR - http://www.scopus.com/inward/record.url?scp=85046816309&partnerID=8YFLogxK
U2 - 10.1016/j.jpeds.2018.03.011
DO - 10.1016/j.jpeds.2018.03.011
M3 - Artículo
C2 - 29730147
AN - SCOPUS:85046816309
SN - 0022-3476
VL - 198
SP - 265-272.e3
JO - Journal of Pediatrics
JF - Journal of Pediatrics
ER -