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. 2020 Dec 17;156(2):61–64. doi: 10.1016/j.medcle.2020.08.004

Subjective evaluation of smell and taste dysfunction in patients with mild COVID-19 in Spain

Evaluación subjetiva de las alteraciones del olfato y del gusto en pacientes con afectación leve por COVID-19 en España

Elisabeth Ninchritz-Becerra a,b,, María Montserrat Soriano-Reixach a,b, Miguel Mayo-Yánez a,c, Christian Calvo-Henríquez a,d, Paula Martínez-Ruiz de Apodaca a,e, Carlos Saga-Gutiérrez a, Pablo Parente-Arias f, Itzhel María Villareal g, Jaime Viera-Artiles h, Daniel Poletti-Serafini i, Isam Alobid j, Tareck Ayad a,k, Sven Saussez a,l, Jerome R Lechien a,m, Carlos M Chiesa-Estomba a,b
PMCID: PMC7836722  PMID: 33521313

Abstract

Background

Has been described the loss of smell and taste as onset symptoms in SARS-CoV-2. The objective of this study was to investigate the prevalence in Spain.

Methods

Prospective study of COVID-19 confirmed patients through RT-PCR in Spain. Patients completed olfactory and gustatory questionnaires.

Results

A total of 1043 patients with mild COVID-19 disease. The mean age was 39 ± 12 years. 826 patients (79.2%) described smell disorder, 662 (63.4%) as a total loss and 164 (15.7%) partial. 718 patients (68.8%) noticed some grade of taste dysfunction. There was a significant association between both disorders (p < 0.001). The olfactory dysfunction was the first symptom in 17.1%. The sQOD-NS scores were significantly lower in patients with a total loss compare to normosmic or hyposmic individuals (p = 0.001). Female were significantly more affected by olfactory and gustatory dysfunctions (p < 0.001). The early olfactory recover in 462 clinically cured patients was 315 (68.2%), during the first 4 weeks.

Conclusion

The sudden onset smell and/or taste dysfunction should be considered highly suspicious for COVID-19 infection.

Keywords: COVID-19, SARS-CoV-2, Anosmia, Ageusia

Introduction

The clinical presentation of patients affected by COVID-19 in a mild-moderate way has consisted mainly of cough (46.6-83.3%), asthenia (63.3-72.9%), headache (60-71 %), anosmia (51.5-70.2%), nasal obstruction (58.6-67.8%) and taste dysfunctions (47.1-67.8%).1, 2, 3 Furthermore, the presence of comorbidities such as arterial hypertension, advanced age and obesity have been associated with a worse progression.

The main objective of this study was to investigate the prevalence of subjective smell (SSD) and taste (STD) dysfunction in patients with mild-moderate SARS-CoV-2 infection. The secondary objectives focused on evaluating the impact on quality of life resulting from these dysfunctions and the rate of recovery of both senses.

Patients and methods

This is a prospective study in which the patients included with mild-moderate COVID-19 responded to a questionnaire designed for the analysis of smell and/or taste dysfunction.

The inclusion and exclusion criteria used, as well as the clinical and/or subjective data, were obtained by completing an on-line questionnaire. These, as well as the study design are shown in Fig. 1 Fig. 1. All patients were asked to complete a short version of the olfactory dysfunction questionnaire (sQOD-NS).4 The rest of the questions about smell and taste were obtained from the North American National Health and Nutrition questionnaire.5

Fig. 1.

Fig. 1

The inclusion and exclusion criteria, as well as clinical and/or subjective data, were obtained through an on-line questionnaire.

The mean recovery of the sense of smell was evaluated between the days: 1–4; 5–8; 9–14 and >15. Referring to the studies that have shown that viral load drops significantly 14 days after the onset of symptoms.6

The Statistical Package for the Social Sciences (SPSS version 21.0; IBM Corp, Armonk, NY, USA) software was used to perform the statistical analyses. The normality contrast between the continuous variables was performed using the Shapiro-Wilk test. Potential associations between epidemiological, clinical, olfactory, and taste outcomes were evaluated by cross-tabulation between two variables (dichotomous or categorical variables) and the chi-square test. Incomplete responses were excluded from the analysis. Differences in the sQOD-NS in terms of olfactory dysfunctions between patients were analysed using the Kruskal-Wallis test. A multivariate logistic regression model was applied to estimate the association between smell and taste dysfunction with a group of independent variables (age, sex, symptoms, comorbidities). A value of p< 0.05 was determined to be statistically significant.

Results

Of the total 1411 patients with positive RT-PCR for COVID-19 infection, 1043 patients completed the study. Regarding sex, 663 (63.6%) were women and 380 (36.4%) were men. The mean age was 39 ± 12 years (range 19−78). The most common comorbidities are listed in Table 1 , Table 1. 42% of the patients were in the acute phase of the infection.

Table 1.

Clinical and demographic variables.

Variable N % p
Sex:
 Female 663 63.6 0.294
 Male 380 36.4
Mean Age 39 ± 12 years (range 19−78),
Ethnicity:
 European 859 82.4
 Latin American 173 16.6
 North American 6 0.6
 North African 3 0.3
 Sub-Saharan Africa 2 0.2
Comorbidities
 Diabetes mellitus 20 1.9 0.921
 Arterial hypertension 68 6.5 0.892
 WP or NP rhinosinusitis 22 2.1 0.339
 Autoimmune disease (SLE, RA, etc.) 36 3.5 0.066
 Hypothyroidism in treatment 59 5.7 0.535
 Hypothyroidism without treatment 6 0.6 0.671
 Allergic rhinitis 192 18.4 0.661
 Renal failure 11 1.1 0.902
 Liver failure 16 1.5 0.116
 COPD 8 0.8 0.947
 Asthma 63 6 0.454
 Cardiac pathology 20 1.9 0.076
 Neurodegenerative disease 9 0.9 0.917
 Depression 46 4.4 0.381
 Cancer in treatment 3 0.3 0.663
 Cancer pending treatment 2 0.2 0.095
 Extrinsic allergies (pollen, grass, etc.) 264 25.3 0.053
Smoking habit
 Non-smoker 914 87.6 0.337
 0-10 cigarettes-day 101 9.7 0.115
 11-20 cigarettes-day 26 2.5 0.077
 >20 cigarettes a day 2 0.2 0.965
Symptoms associated with COVID-19
 Fever > 38° 391 37.5 0.027
 Dry cough 570 54.7 0.038
 Loss of appetite 595 57 0.078
 Bronchial mucus-expectoration 207 19.8 0.087
 Arthralgia 517 49.6 0.998
 Myalgia 719 68.9 0.709
 Diarrhoea 419 40.2 0.009
 Abdominal pain 210 20.1 0.763
 Headache 782 75 0.540
Mean time onset of disease/evaluation 10.4 ° ±  5.7 days (range 4-13)

RA : rheumatoid arthritis; WP : with polyps; COPD : chronic obstructive pulmonary disease; SLE : systemic lupus erythematosus; NP : without polyps.

Regarding SSD, 826 patients (79.2%) described some type of loss related to the infection. Of these, 662 described their dysfunction as total and 164 as partial. Furthermore, 16.6% associated changes suggestive of dysosmia, and 18.2% phantosmia. SSD appeared before (17.1%), after (47.8%) or at the same time as the rest of the general and/or otolaryngological symptoms (23.9%).

The recovery rate of smell evaluated in 462 cured patients after 4 weeks revealed that 315 (68.2%) showed a partial or total recovery. 57.5% recovered olfactory function in the first 7 days after the resolution of the disease with an overall mean of 9 ± 6 days (range 5–29).

Regarding the impact of SSD on quality of life, patients who perceived a total loss of smell had a significantly lower score (sQOD-NS) compared to those individuals with a partial loss (p = 0.001) or who did not notice any dysfunction of smell (p = 0.001) (Appendix B supplementary material).

Regarding STD, 718 patients (68.8%) reported taste disorders. STD consisted of a reduced (48%) or distorted (22.9%) ability to perceive flavours. Of the 286 patients without taste dysfunction, 52 (5%) did not have olfactory dysfunction, while 194 (18.6%) had a total dysfunction of smell and 40 (3.8%) a partial one.

Multivariate analysis showed that women (OR = 0.924; 95% CI: 0.876–1.69) or those over 60 years of age (OR = 0.980; 95% CI: 0.723–1.113) had a higher risk of suffering from SSD or STD. In addition, a significant correlation between the presence of fever (OR = 0.981; 95% CI: 0.434–1.396) or headache (OR = 1,160; 95% CI: 0.917–1.313) and SSD or STD was observed. While we did not find a correlation between otolaryngological symptoms and the presence of comorbidities with the occurrence of sensory dysfunctions (Table 2 ).

Table 2.

Multivariate analysis of characteristics associated with loss of smell and taste in patients affected by COVID-19.

Variable OR 95% confidence interval p
Sex (female) 0.924 0.876 to 1.369 0.020
Age (> 60 years) 0.980 0.723 to 1.113 0.023
Comorbidities
 Diabetes mellitus 0.460 −2.308 to 0.756 0.321
 Arterial hypertension 0.626 −1.290 to 0.852 0.263
 WP or NP rhinosinusitis 0.692 −0.054 to 1.035 0.163
 Autoimmune disease (SLE, RA, etc.) 0.659 −1.571 to 0.737 0.479
 Hypothyroidism in treatment 0.525 −0.333 to 0.777 0.273
 Hypothyroidism without treatment 0.173 −0.460 to 0.449 0.268
 Allergic rhinitis 0.331 −0.199 to 0.455 0.790
 Renal failure 0.243 −0.188 to 0.356 0.281
 Liver failure 1.317 −0.070 to 1.468 0.064
 COPD 0.722 −0.236 to 0.932 0.394
 Asthma 1.200 −0.587 to 1.952 0.642
 Cardiac pathology 0.930 −0.522 to 1.837 0.275
 Neurodegenerative disease 0.144 −0.528 to 0.658 0.144
 Depression 0.611 −0.360 to 1.314 0.264
 Extrinsic allergies (pollen, grass, etc.) 0.532 −0.032 to 0.885 0.068
 Smoker 0.371 −0.674 to 0.615 0.929
Symptoms associated with COVID-19
 Fever > 38° 0.981 0.434 to 1.396 0.008
 Dry cough 1.202 −0.377 to 1.744 0.521
 Loss of appetite 0.482 −0.027 to 0.814 0.067
 Bronchial mucus-expectoration 0.978 −0.513 to 1.468 0.929
 Arthralgia 0.835 0.642 to 1.281 0.443
 Myalgia 1.038 0.449 to 1.524 0.123
 Diarrhoea 1.092 −0.321 to 1.497 0.673
 Abdominal pain 0.657 0.213 to 0.769 0.268
 Headache 1.160 0.917 to 1.313 0.021
ENT symptoms
 Nasal Congestion 0.997 0.145 to 1.139 0.967
 Rhinorrhoea 0.816 0.376 to -1.031 0.531
 Postnasal drip 1.019 0.425 to 1.163 0.799
 MF 1.007 0.546 to 0.160 0.931
 CF pain 1.240 0.376 to 1.354 0.102
 Earache 0.909 0.681 to 0.990 0.311
 Dysphagia 0.972 0.431 to 1.174 0.781
 Dyspnoea 0.951 0.605 to 1.104 0.521

RA: rheumatoid arthritis; WP : with polyps; COPD : chronic obstructive pulmonary disease; SLE : lupus erythematosus; OR : odds ratio; NP : without polyps.

Discussion

After the expansion of SARS-CoV-2 in Europe, multiple authors have described the high incidence of SSD and STD in patients with COVID-19, even as the only clinical manifestation.7

Several studies have observed a high rate of recovery of smell within 1–2 weeks after the onset of anosmia or hyposmia, and a recovery of taste between the second and third week after the onset of ageusia or hypogeusia.6 As well as a higher prevalence of SSD and STD in women, young and with mild or asymptomatic symptoms.3

Identification and isolation of patients with SARS-CoV-2 is the most important strategy to slow the spread of the disease. Given the scarcity of diagnostic tests, it is important to determine which are the most common initial symptoms for early isolation. Within our population, we have especially investigated mild-moderate cases and we have confirmed the presence of anosmia or dysgeusia in a high percentage of patients.

We highlight as strengths of this study the size of the sample and the reproducibility of the questionnaire. Despite being a study with a reduced follow-up time (maximum one month), we consider that the findings are valuable insofar as they can define early prevention attitudes while helping to define lines of work for future studies. While the main limitation of this study corresponds to the use of a questionnaire by telematic means, which we can tend to underestimate the olfactory threshold.

Conclusion

At present, multiple publications have found a relationship between SARS-CoV-2 infection (COVID-19) and smell and/or taste dysfunction. These data suggest that there is a significant association between viral infection and olfactory or gustatory dysfunction, and that this information could help in the early diagnosis of SARS-CoV-2 disease.

Conflict of interests

The authors declare no conflict of interest.

Footnotes

Please cite this article as: Ninchritz-Becerra E, Soriano-Reixach MM, Mayo-Yánez M, Calvo-Henríquez C, Martínez-Ruiz de Apodaca P, Saga-Gutiérrez C, et al. Evaluación subjetiva de las alteraciones del olfato y del gusto en pacientes con afectación leve por COVID-19 en España. Med Clin (Barc). 2021;156:61–64.

Appendix A

Supplementary material related to this article can be found, in the online version, at doi:https://doi.org/10.1016/j.medcli.2020.08.004.

Appendix A. Supplementary data

The following are Supplementary data to this article:

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