| Literature DB >> 32296471 |
Konstantinos Valsamidis1, Athanasia Printza1, Jannis Constantinidis1, Stefanos Triaridis1.
Abstract
Introduction Olfactory dysfunction may be present in patients with nasal obstruction and septal deviation. The impact of olfactory dysfunction on the psychological profile and quality of life (QoL) of these patients remains unexplored. Objective The present study aimed to investigate the emotional status and QoL of patients with olfactory dysfunction and septal deviation and to identify predictors associated with clinically significant improvement of psychological status and QoL, focusing mainly on the role of olfactory recovery after septoplasty. Methods The olfactory function was quantitatively assessed using the ''Sniffin' sticks'' test (Burghart Messtechnik GmbH, Wedel, Germany) in 60 patients and 25 controls enrolled in this prospective study. The participants completed validated questionnaires specific for general health (Short Form-36), nasal-symptom related QoL (SinoNasal Outcome Test-22), olfaction-associated QoL (Questionnaire of Olfactory Deficits) and for assessing their psychological state (Short Anxiety Screening Test and Beck Depression Inventory) preoperatively and 6 months postoperatively. The patients used the Glasgow Benefit Inventory to evaluate their personal benefit after septoplasty with. Results Septoplasty led to significantly improved olfactory function. Patients with olfactory impairment had significantly lower nasal-symptom related QoL, higher stress levels, and more depressive mood compared with normosmics and controls before and after septoplasty. Postoperatively, personal benefit from surgery was higher in normosmic patients. Improvement of nasal-symptom related QoL was significantly associated with higher likelihood of clinically significant improvement of patients' psychological profile and more personal benefit from surgery. Olfactory dysfunction was negatively correlated with the emotional status of the patients. Conclusion Olfactory dysfunction appears to significantly affect the psychological status of patients with nasal obstruction, and olfactory recovery improves the patients' perception of personal benefit from septoplasty.Entities:
Keywords: anxiety; emotional status; olfaction test; olfactory dysfunction; quality of life; septoplasty
Year: 2020 PMID: 32296471 PMCID: PMC7153923 DOI: 10.1055/s-0040-1701269
Source DB: PubMed Journal: Int Arch Otorhinolaryngol ISSN: 1809-4864
Olfactory function, questionnaires of quality of life and psychological status of the controls and the patient group (preoperatively and 6 months after surgery)
| Control | Patient group |
| ||
|---|---|---|---|---|
| preop | postop | |||
| Olfactory scores | ||||
| OT | 9.2 (2.19) |
|
| < 0.001 |
| OD | 13.12 (1.67) |
|
| 0.008 |
| OI | 13.32 (2.18) |
| 12.08 (1.97) | < 0.001 |
| TDI | 35.64 (2.62) |
|
| < 0.001 |
| QoL tools | ||||
| SF-36 | 83.48 (9.74) | 80.20 (15.45) | ||
| SNOT 22 | 12.9 (8.86) |
|
| < 0.001 |
| QOD | 6.92 (2.08) | 8.85 (5.11) | 7.91 (3.42) | 0.25 |
| Psychological tools | ||||
| SAST | 11.7 (6.39) |
|
| 0.05 |
| BDI | 6.85 (3.43) | 7.53 (5.76) | 7 (5.36) | 0.08 |
Abbreviations: BDI, Beck depression inventory; OD, olfactory discrimination; OI, olfactory identification; OT, olfactory threshold; QOD, questionnaire of olfactory disorders; QoL, quality of life; SAST, short anxiety screening test; SF-36, short form – 36; SNOT 22, SinoNasal outcome test 22; TDI, threshold discrimination identification.
Bold: Statistically significant difference compared with the control group, p -values: pre and posttreatment scores comparisons for the patient group—Wilcoxon Signed-Rank test for paired samples.
Data are expressed as mean values (standard deviation), preop: preoperatively, postop: postoperatively.
Nasal symptom related quality of life (QoL), olfaction related QoL, stress levels, depressive mood and general health status of controls, patients with olfactory deficits and normosmic patients, preoperatively
|
Controls (
|
Patients with olfactory deficits (
|
Normosmic Patients (
|
| |
|---|---|---|---|---|
| SNOT 22 | 12.9 (8.86) |
|
| 0.019 |
| QOD | 6.92 (2.08) |
| 8.9 (2.75) | 0.109 |
| SAST | 11.7 (6.39) |
|
| 0.222 |
| BDI | 4.65 (2.08) |
| 4.7 (2.7) | 0.029 |
| SF 36 | 83.48 (9.74) | 77.65 (13.34) | 81.2 (10.98) | 0.086 |
Abbreviations: BDI, Beck depression inventory; QOD, questionnaire of olfactory disorders; QoL, Quality of life; SAST, short anxiety screening test; SF-36, Short Form – 36; SNOT 22, SinoNasal outcome test 22.
Bold: Statistically significant difference compared with control group, p value: comparisons between normosmics and patients with olfactory dysfunction, all groups comparisons: Mann-Whitney U test for independent samples.
Data are expressed as mean values (standard deviation). n: number of patients.
Nasal symptom-related quality of life (QoL), olfaction-related QoL, stress levels, depressive mood and patient's satisfaction with the surgical procedure of patients with olfactory deficits and normosmic patients, 6 months after surgery
|
Controls (
|
Patients with olfactory deficits (
|
Normosmic patients (
|
| |
|---|---|---|---|---|
| SNOT 22 | 12.9 (8.86) |
|
| 0.014 |
| QOD | 6.92 (2.08) | 8.27 (4.33) | 7.02 (3.4) | 0.14 |
| SAST | 11.7 (6.39) |
| 15.57 (5.76) | 0.045 |
| BDI | 4.65 (2.08) |
| 4.63 (0.61) | 0.028 |
| GBI | 5.35 (2.18) | 18.05 (3.51) | 0.002 |
Abbreviations: BDI, Beck depression inventory; GBI, Glasgow benefit inventory; QOD, questionnaire of olfactory disorders; QoL, quality of life; SAST, short anxiety screening test; SNOT 22: SinoNasal outcome test 22.
Bold: Statistically significant difference compared with control group, p -value: comparisons between normosmic patients and patients with olfactory dysfunction, all groups comparisons: Mann-Whitney U test for independent samples.
Data are expressed as mean values (standard deviation). n: number of patients.
Clinically significant improvement of questionnaire of olfactory disorders and positive change of Glasgow benefit inventory in relation to the demographic and clinical characteristics of the patients
| Clinically improved QOD (n, %) | OR (95% CI) |
| Positive change GBI (n, %) | OR (95% CI) |
| |
|---|---|---|---|---|---|---|
|
| 0.39 | 0.55 | ||||
| ≤ 30 years | 9 (30%) | Ref. | 15 (50%) | Ref. | ||
| > 30 years | 13 (43.3%) | 1.02 (0.97–1.06) | 17 (56.7%) | 1.01 (0.97–1.05) | ||
|
| 0.429 | 0.944 | ||||
| Males | 12 (35.2%) | Ref. | 18 (52.9%) | Ref. | ||
| Females | 10 (38.4%) | 1.53 (0.53–4.42) | 14 (53.8%) | 1.03 (0.37–2.88) | ||
|
| 0.85 | 0.855 | ||||
| No | 15(37.5%) | Ref. | 22 (55%) | Ref. | ||
| Yes | 7 (35%) | 0.46 (0.36–1.21) | 10 (50%) | 0.9 (0.3–2.65) | ||
|
| 0.285 | 0.804 | ||||
| Low | 4 (28.5%) | Ref. | 7 (50%) | Ref. | ||
| Medium | 8 (33.3%) | 1.26 (0.56–2.07) | 13 (54.1%) | 1.02 (0.66–2.25) | ||
| High | 10 (45.4%) | 1.47 (0.72–2.98) | 12 (54.5%) | 1.08 (0.56–2.11) | ||
|
| 0.009 | < 0.001 | ||||
| No | 9 (20%) | Ref. | 4 (9%) | Ref. | ||
| Yes | 13 (63.3%) | 4.57 (1.45–14.38) | 28 (88%) | 11 (3.29–36.75) | ||
|
| 0.022 | 0.001 | ||||
| No | 7 (22.5%) | Ref. | 10 (26.2%) | Ref. | ||
| Yes | 15 (51.7%) | 3.67 (1.2–11.18) | 22 (81.3%) | 6.6 (2.12–20.55) | ||
|
| 0.024 | 0.302 | ||||
| No | 17 (46.3%) | Ref. | 22 (53.6%) | Ref. | ||
| Yes | 5 (26.3%) | 0.27 (0.18–0.96) | 10 (52.6%) | 0.97 (0.6–2.29) |
Abbreviations: CI, confidence intervals; GBI, Glasgow benefit inventory; NOSE, nasal obstruction symptom evaluation; OR, odds ratio; p -values, univariate linear regression; QOD, questionnaire of olfactory disorders; SNOT 22, SinoNasal outcome test 22.
Data are expressed as number of patients (n) and percentages (%).
Based on TDI score.
Clinically significant improvement of short anxiety screening test and Beck depression inventory in relation to the demographic and clinical characteristics of the patients
| Clinically improved SAST (n, %) | OR (95% CI) |
| Clinically improved BDI (n, %) | OR (95% CI) |
| |
|---|---|---|---|---|---|---|
|
| 0.143 | 0.114 | ||||
| ≤ 30 years | 17 (56.7%) | Ref. | 10 (33.3%) | Ref. | ||
| > 30 years | 15 (50%) | 0.33 (0.18–1.08) | 8 (26.7%) | 0.87 (0.69–1.08) | ||
|
| 0.944 | 0.309 | ||||
| Male | 17 (50%) | Ref. | 11 (32.3%) | Ref. | ||
| Female | 15 (58%) | 1.76 (0.34–2.68) | 7 (27%) | 0.55 (0.17–1.74) | ||
|
| 0.204 | 0.238 | ||||
| No | 20 (50%) | Ref. | 7 (35%) | Ref. | ||
| Yes | 12 (45%) | 0.25 (0.17–2.32) | 11 (27.5%) | 0.24 (0.17–4.7) | ||
|
| 0.443 | 0.825 | ||||
| Low | 7 (50%) | Ref. | 5 (21.7%) | Ref. | ||
| Medium | 13 (54.1%) | 1.02 (0.43–2.12) | 7 (25.1%) | 1.03 (0.24–1.98) | ||
| High | 12 (54.5%) | 1.3 (0.66–2.54) | 6 (29.2%) | 1.08 (0.52–2.24) | ||
|
| 0.011 | 0.029 | ||||
| No | 7 (23.3%) | Ref. | 6 (24%) | Ref. | ||
| Yes | 25 (83.3%) | 4.03 (1.37–11.83) | 12 (68%) | 3.82 (1.15–12.71) | ||
|
| 0.001 | 0.019 | ||||
| No | 9 (15%) | Ref. | 5 (21.3%) | Ref. | ||
| Yes | 23 (79.3%) | 6.39 (2.07–19.68) | 13 (72.4%) | 4.22 (1.26–14.09) | ||
|
| 0.941 | 0.012 | ||||
| No | 22 (53.6%) | Ref. | 12 (65.7%) | Ref. | ||
| Yes | 10 (52.6%) | 0.94 (0.35–3.1) | 6 (17.2%) | 0.28 (0.14–0.68) |
Abbreviations: BDI, Beck depression inventory; CI, confidence intervals; NOSE, nasal obstruction symptom evaluation; OR, odds ratio; p -values, univariate linear regression; SAST, short anxiety screening test; SNOT 22, SinoNasal outcome test 22.
Data are expressed as number of patients (n) and percentages (%).
Based on TDI score.
Multivariate logistic regression analysis between predictor variables and clinically significant improvement of QOD, SAST and BDI scores and positive change of GBI scores
| OR (95% CI) |
| |
|---|---|---|
|
| ||
| Clinically improved NOSE | 3.51 (1.02–12.04) | 0.046 |
| Clinically improved SNOT-22 | 3.79 (1.11–12.88) | 0.033 |
| Olfactory Dysfunction postoperatively | 0.23 (0.16–1.8) | 0.204 |
|
| ||
| Clinically improved NOSE | 3.82 (1.16–12.51) | 0.027 |
| Clinically improved SNOT-22 | 6.14 (1.87–20.07) | 0.003 |
|
| ||
| Clinically improved NOSE | 2.67 (0.69–10.39) | 0.154 |
| Clinically improved SNOT 22 | 5.61 (1.35–23.15) | 0.017 |
| Olfactory Dysfunction postoperatively | 0.56 (0.13–0.76) | 0.021 |
|
| ||
| Clinically improved NOSE | 14 (3.32–58.95) | < 0.001 |
| Clinically improved SNOT-22 | 8.75 (2.07–36.93) | 0.003 |
Abbreviations: BDI, Beck depression inventory; GBI, Glasgow benefit inventory; NOSE, nasal obstruction symptom evaluation; QOD, questionnaire of olfactory disorders; SAST, short anxiety screening test; SNOT-22, SinoNasal outcome test-22.
Data are expressed as odds ratios (OR) with their 95% confidence intervals (CI). Only variables with statistical significance during univariate linear regression analysis are included. p values: Multivariate logistic regression analysis.