Covid19
Conditions
Keywords
flavor, smell, flavor test, hyposmia, retro-nasal olfaction
Brief summary
The Flavor test has been developed and validated by our group to assess retro-nasal olfactory performances. The original flavor test has been simplified, with the great advantage to be self-administrable for COVID-19 patients in isolation, without any risk to health professionals.
Detailed description
Smell and taste dysfunctions (STDs) are symptoms associated with COVID-19 syndrome, even if their incidence is still uncertain and variable. In this study, the effects of SARS-CoV-2 infection on chemosensory function have been investigated using both a self-reporting questionnaire on smell and flavor perception, and a simplified flavor test. A total of 111 subjects (19 hospitalized \[HOS\] and 37 home-isolated \[HI\] COVID-19 patients, and 55 healthy controls \[CTRL\]) were enrolled in the study. The flavor test used consists in the self-administration of four solution with a pure olfactory stimulus (coffee), a mixed olfactory-trigeminal stimulus (peppermint), and a complex chemical mixture (banana). After SARS-CoV-2 infection, HOS and HI patients reported similar frequency of STDs, with a significant reduction of both smell and flavor self-estimated perception. The aromas of the Flavor test were recognized by HI and HOS COVID-19 patients similarly to CTRL, however the intensity of the perceived aromas was significantly lower in patients compared to controls. This suggests that a chemosensory impairment is present after SARS-CoV-2 infection, and the modified flavor test could be a novel self-administering objective screening test to assess STDs in COVID-19 patients.
Interventions
A simplified self-administrable flavor test has been proposted to all the enrolled subjects
Questionnaire to score subjective chemosensory function (smell and flavor) before and after COVID-19 using a 0-10 scale with 0 corresponding to no smell/flavor perception and 10 corresponding to excellent smell/flavor perception.
Sponsors
Study design
Eligibility
Inclusion criteria
* Adults (≥18 years of age) that gave their written informed consent to the study * Diagnosis of COVID-19 was confirmed by PCR of nasopharyngeal swab (HI or HOS) * Negative COVID-19 nasopharyngeal swab (CTRL) * Subjects with no critical conditions and able to understand the protocol
Exclusion criteria
* nasal obstruction or previous nasal diseases
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Flavor perception | Apr, 2020- Jan, 2021 | To assess qualitative flavor perception |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Flavor perception intensity | Apr, 2020- Jan, 2021 | To assess quantitative flavor perception |
Other
| Measure | Time frame | Description |
|---|---|---|
| Comparison with self-estimated flavor perception | Apr, 2020- Jan, 2021 | To compare results of the test with self-assessed flavor and smell perception |
Countries
Italy