dc.contributor.author | Sanli, Deniz Esin Tekcan | |
dc.contributor.author | Altundag, Aytug | |
dc.contributor.author | Duz, Ozge Arici | |
dc.contributor.author | Saatci, Ozlem | |
dc.contributor.author | BATIOĞLU KARAALTIN, Ayşegül | |
dc.contributor.author | Kandemirli, Sedat Giray | |
dc.contributor.author | Temirbekov, Dastan | |
dc.contributor.author | Olmuscelik, Oktay | |
dc.contributor.author | Sanli, Ahmet Necati | |
dc.date.accessioned | 2021-03-02T16:19:20Z | |
dc.date.available | 2021-03-02T16:19:20Z | |
dc.identifier.citation | Altundag A., Saatci O., Sanli D. E. T. , Duz O. A. , Sanli A. N. , Olmuscelik O., Temirbekov D., Kandemirli S. G. , BATIOĞLU KARAALTIN A., "The temporal course of COVID-19 anosmia and relation to other clinical symptoms", EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY, 2020 | |
dc.identifier.issn | 0937-4477 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_e03fb6b0-a865-4ea3-83e0-cd938577a8d8 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/2853 | |
dc.identifier.uri | https://doi.org/10.1007/s00405-020-06496-5 | |
dc.description.abstract | Objective This study aimed to define the clinical course of anosmia in relation to other clinical symptoms. Methods 135 patients with COVID-19 were reached by phone and subsequently included in the study. Olfactory functions were evaluated using a questionnaire for assessment of self-reported olfactory function. Patients were divided into four subgroups according to the presence of olfactory symptoms and temporal relationship with the other symptoms: group1 had only olfactory complaints (isolated, sudden-onset loss of smell); group2 had sudden-onset loss of smell, followed by COVID-19 related complaints; group3 initially had COVID-19 related complaints, then gradually developed olfactory complaints; and group4 had no olfactory complaints. Results In total, 59.3% of the patients interviewed had olfactory complaints during the disease course. The olfactory dysfunction severity during COVID-19 infection was significantly higher in group1 compared to groups 2 and 3. In groups1-3, the odor scores after recovery from COVID-19 disease were significantly lower compared to the status prior to disease onset. The residual olfactory dysfunction was similar between groups1 and 2, but was more evident than group3. Mean duration for loss of smell was 7.8 +/- 3.1 (2-15) days. Duration of loss of smell was longer in groups1 and 2 than in group3. Odor scores completely returned back to the pre-disease values in 41 (51.2%) patients with olfactory dysfunction. Rate of complete olfactory dysfunction recovery was higher in group3 compared to groups1 and 2. Conclusion In isolated anosmia cases, anosmia is more severe, and complete recovery rates are lower compared to the patients who have other clinical symptoms. | |
dc.language.iso | eng | |
dc.subject | Klinik Tıp (MED) | |
dc.subject | Cerrahi Tıp Bilimleri | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Tıp | |
dc.subject | KULAK BURUN BOĞAZ | |
dc.subject | Klinik Tıp | |
dc.subject | Health Sciences | |
dc.subject | Speech and Hearing | |
dc.subject | Otorhinolaryngology | |
dc.subject | Kulak Burun Boğaz | |
dc.title | The temporal course of COVID-19 anosmia and relation to other clinical symptoms | |
dc.type | Makale | |
dc.relation.journal | EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY | |
dc.contributor.department | Biruni Üniversitesi , , | |
dc.contributor.firstauthorID | 2370883 | |