Psychophysical Olfactory Tests and Detection of COVID-19 in Patients With Sudden Onset Olfactory Dysfunction: A Prospective Study

Objective: To investigate the coronavirus disease 2019 (COVID-19) status of patients with initial sudden olfactory anosmia (ISOA) through nasopharyngeal swabs for reverse transcription–polymerase chain reaction (RT-PCR) analysis and to explore their olfactory dysfunctions with psychophysical olfacto...

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Veröffentlicht in:Ear, nose, & throat journal nose, & throat journal, 2020-11, Vol.99 (9), p.579-583
Hauptverfasser: Lechien, Jerome R., Cabaraux, Pierre, Chiesa-Estomba, Carlos M., Khalife, Mohamad, Plzak, Jan, Hans, Stéphane, Martiny, Delphine, Calvo-Henriquez, Christian, Barillari, Maria R., Hopkins, Claire, Saussez, Sven
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container_end_page 583
container_issue 9
container_start_page 579
container_title Ear, nose, & throat journal
container_volume 99
creator Lechien, Jerome R.
Cabaraux, Pierre
Chiesa-Estomba, Carlos M.
Khalife, Mohamad
Plzak, Jan
Hans, Stéphane
Martiny, Delphine
Calvo-Henriquez, Christian
Barillari, Maria R.
Hopkins, Claire
Saussez, Sven
description Objective: To investigate the coronavirus disease 2019 (COVID-19) status of patients with initial sudden olfactory anosmia (ISOA) through nasopharyngeal swabs for reverse transcription–polymerase chain reaction (RT-PCR) analysis and to explore their olfactory dysfunctions with psychophysical olfactory evaluation. Methods: A total of 78 ISOA patients were recruited from April 6, 2020, to April 10, 2020, through a public call of University of Mons (Mons, Belgium). Patients benefited from nasopharyngeal swabs and fulfilled the patient-reported outcome questionnaire. Among them, 46 patients performed psychophysical olfactory evaluation using olfactory identification testing. Based on the duration of the ISOA, 2 groups of patients were compared: patients with olfactory dysfunction duration ≤12 days (group 1) and those with duration >12 days (group 2). Results: In group 1, 42 patients (87.5%) had a positive viral load determined by RT-PCR and 6 patients (12.5%) were negative. In group 2, 7 patients (23%) had a positive viral load and 23 patients (77%) were negative. The psychophysical olfactory evaluation reported that anosmia and hyposmia occurred in 24 (52%) and 11 (24%) patients, respectively. Eleven patients were normosmic. The viral load was significantly higher in patients of group 1 compared with those of group 2. Conclusions: Coronavirus disease 2019 was detected in a high proportion of ISOA patients, especially over the first 12 days of olfactory dysfunction. Anosmia is an important symptom to consider in the detection of COVID-19 infection.
doi_str_mv 10.1177/0145561320929169
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Methods: A total of 78 ISOA patients were recruited from April 6, 2020, to April 10, 2020, through a public call of University of Mons (Mons, Belgium). Patients benefited from nasopharyngeal swabs and fulfilled the patient-reported outcome questionnaire. Among them, 46 patients performed psychophysical olfactory evaluation using olfactory identification testing. Based on the duration of the ISOA, 2 groups of patients were compared: patients with olfactory dysfunction duration ≤12 days (group 1) and those with duration &gt;12 days (group 2). Results: In group 1, 42 patients (87.5%) had a positive viral load determined by RT-PCR and 6 patients (12.5%) were negative. In group 2, 7 patients (23%) had a positive viral load and 23 patients (77%) were negative. The psychophysical olfactory evaluation reported that anosmia and hyposmia occurred in 24 (52%) and 11 (24%) patients, respectively. Eleven patients were normosmic. The viral load was significantly higher in patients of group 1 compared with those of group 2. Conclusions: Coronavirus disease 2019 was detected in a high proportion of ISOA patients, especially over the first 12 days of olfactory dysfunction. 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The viral load was significantly higher in patients of group 1 compared with those of group 2. Conclusions: Coronavirus disease 2019 was detected in a high proportion of ISOA patients, especially over the first 12 days of olfactory dysfunction. 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subjects Adult
Aged
Belgium
Betacoronavirus
Case-Control Studies
Clinical Laboratory Techniques
Coronavirus Infections - complications
Coronavirus Infections - diagnosis
Coronaviruses
COVID-19
COVID-19 Testing
Diagnostic Techniques, Respiratory System
Diagnostic tests
Dysgeusia
Female
Humans
Life Sciences
Male
Medical diagnosis
Middle Aged
Nasal Obstruction
Odorants
Olfaction disorders
Olfaction Disorders - complications
Olfaction Disorders - diagnosis
Otolaryngology
Pandemics
Patient Reported Outcome Measures
Physical Stimulation
Pneumonia, Viral - complications
Pneumonia, Viral - diagnosis
Prospective Studies
Reverse Transcriptase Polymerase Chain Reaction
SARS-CoV-2
Smell
Young Adult
title Psychophysical Olfactory Tests and Detection of COVID-19 in Patients With Sudden Onset Olfactory Dysfunction: A Prospective Study
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