Rhinosinusitis (RS) may be sub-classified into several groups based on duration of symptoms, etiology, associated clinical history, and findings during endoscopic nasal examination. While one may dissect RS into several subgroups, the four major clinical categories are Recurrent Acute Rhinosinusitis (RARS), Chronic Rhinosinusitis without Nasal Polyps (CRSsNP), Chronic Rhinosinusitis with Nasal Polyps (CRSwNP), and Hyperplastic Rhinosinusitis (HRS).
Rhinosinusitis (RS) may be sub-classified into several groups based on duration of symptoms, etiology, associated clinical history, and findings during endoscopic nasal examination. While one may dissect RS into several subgroups, the four major clinical categories are Recurrent Acute Rhinosinusitis (RARS), Chronic Rhinosinusitis without Nasal Polyps (CRSsNP), Chronic Rhinosinusitis with Nasal Polyps (CRSwNP), and Hyperplastic Rhinosinusitis (HRS). The American academy of Otolaryngology defines RARS as 4 or more acute infections per year of acute bacterial rhinosinusitis [1] lasting < 12 weeks. CRS is an inflammatory condition requiring the presence of 2 or more symptoms; one of which should be nasal discharge or nasal obstruction/blockage/congestion, +/- facial pain, +/- reduced or absent sense of smell, for 12 weeks or more. In addition, endoscopic findings or CT images showing pathological changes in the middle meat us should be present. CRS may exist with Nasal Polyps (CRSwNP) or without Nasal Polyps (CRSsNP). Extensive nasal polyposis may also be driven by allergic fungal sinusitis or by aspirin sensitivity in a subset of patients with asthma and nasal polyposis (Samter’s triad) [2]. The latter two groups have been collectively referred to as Hyperplastic Rhinosinusitis (HRS) by Kennedy and Borish [3], and will be referred to as such for the purposes of this study.
The economic healthcare burden of RS is estimated to be in the region of $5.8 billion annually, while the Quality of Life (QoL) impact of RS is just as significant [4]. Studies have identified lower QoL scores in CRS patients compared to those with congestive heart failure, chronic back pain, and chronic obstructive pulmonary disease [5]. Furthermore, CRSwNP patients were identified as having a lighter QoL burden than CRSsNP, excluding congestion as a symptom [6]. Thus, one cannot predict the QoL impact associated with RS from imaging studies and endoscopic findings alone.
Indeed, the severity of disease on a pre-treatment CT scan can be a valid predictor of outcome following surgery for certain subsets of CRS [7], however, current diagnostic methods for evaluating sinonasal disease correlate poorly with QoL [8,9].
Along with the patient history and findings during nasal endoscopy, the Lund-Mackay (LM) CT scoring system is used to determine the sub-type of RS in a given patient. From a clinical, endoscopic, and radiologic standpoint, there are distinct clinical differences between the sub-types of RS as described herein, namely RARS, CRSsNP, CRSwNP, and HRS.
However, to our knowledge, there is currently no single published comparison between QoL and the main subtypes of rhinosinusitis. Zheng et al., have investigated the relationship between QoL and LM scores [10], and the correlation between different QoL instruments, but not the relationship between QoL scores and the main subgroups of RS. Thus, the aim of this paper is to explore the relationship between the pre-treatment QoL assessments in the major sub-categories of RS.
A cross-sectional, non-controlled study of consecutive patients presenting to a metropolitan rhinology practice over a 12-month period for evaluation of RS was undertaken. The patients underwent a full history, ENT/head and neck examination, including endoscopic assessment of the nasal cavity, and a CT of the nose and paranasal sinuses. According to their symptoms, radiological and endoscopic findings, each patient was classified into one of four groups - RARS, CRSwNP, CRSsNP and HRS - according to the criteria described above. The latter group is comprised of patients with Samter’s Triad and fungal sinusitis who have advanced hyperplastic sinusitis or pansinusitis that is medically and surgically challenging to control. While we appreciate that there are differences in etiology and medical management between the two latter groups, their general phenotype is similar, and it is the general phenotype of these disease categories that we believe are most relevant for such comparison [3]. Combining the hyperplastic subgroups also allows for better statistical comparison as the patient numbers in each of these categories alone would be insufficient.
The CT images were graded using the validated LM staging system, where each sinus and each osteomeatal complex is judged to be clear, partially opaque, or completely opaque, thereby yielding a numeric score between a minimum of 0 and a maximum of 24 [8].
Each patient also completed a Sinonasal Outcome Test-20 (SNOT-20) questionnaire (Table 1) to assess the QoL impact of their condition. The SNOT-20 is a frequently utilized and validated disease specific questionnaire (Table 1) [11]. It is based on 20 questions divided into five subgroups (nasal symptoms, paranasal symptoms, sleep-related symptoms, and social and emotional impairment), with the severity of the symptoms rated on a 6-point likert scale. Statistical analysis using post-hoc pair wise T-tests and ANOVA was performed using Graphpad Prism Inc., version 6.
|
No Problem |
Very Mild Problem |
Mild or Slight Problem |
Moderate Problem |
Severe Problem |
Problem as Bad as it can be |
1. Need to blow nose |
0 |
1 |
2 |
3 |
4 |
5 |
2. Sneezing |
0 |
1 |
2 |
3 |
4 |
5 |
3. Runny nose |
0 |
1 |
2 |
3 |
4 |
5 |
4. Cough |
0 |
1 |
2 |
3 |
4 |
5 |
5. Postnasal discharge |
0 |
1 |
2 |
3 |
4 |
5 |
6. Thick nasal discharge |
0 |
1 |
2 |
3 |
4 |
5 |
7. Ear fullness |
0 |
1 |
2 |
3 |
4 |
5 |
8. Dizziness |
0 |
1 |
2 |
3 |
4 |
5 |
9. Ear pain |
0 |
1 |
2 |
3 |
4 |
5 |
10. Facial pain/pressure |
0 |
1 |
2 |
3 |
4 |
5 |
11. Difficulty falling asleep |
0 |
1 |
2 |
3 |
4 |
5 |
12. Wake up at night |
0 |
1 |
2 |
3 |
4 |
5 |
13. Lack of a good night’s sleep |
0 |
1 |
2 |
3 |
4 |
5 |
14. Wake up tired |
0 |
1 |
2 |
3 |
4 |
5 |
15. Fatigue |
0 |
1 |
2 |
3 |
4 |
5 |
16. Reduced productivity |
0 |
1 |
2 |
3 |
4 |
5 |
17. Reduced concentration |
0 |
1 |
2 |
3 |
4 |
5 |
18. Frustrated/ restless / irritable |
0 |
1 |
2 |
3 |
4 |
5 |
19. Sad |
0 |
1 |
2 |
3 |
4 |
5 |
20. Embarrassed |
0 |
1 |
2 |
3 |
4 |
5 |
Table 1: Sinonasal outcome test (SNOT-20).
Ninety patients were included in the study, comprising the four subgroups: RARS (n=25), CRSsNP (n=25), CRSwNP (n=19), and HRS (n=21). The mean age of each group was 37.9, 42.4, 44.4 and 48.3 years, with females accounting for 68, 62, 39 and 56% of each group, respectively. The mean SNOT-20 scores in each group were 35.6, 45.8, 48 and 54.3, respectively (Figure 1). Statistical analysis showed the SNOT-20 scores differed significantly between the HRS and RARS subgroups, but no other pair-wise differences were identified between the 4 subgroups. Interestingly, the mean SNOT-20 scores for each of the 4 subgroups was higher in female patients than in males (Table 2).
Figure 1: Mean pre-operative SNOT-20 scores in each subgroup.
|
SNOT-20 (male) |
SNOT-20 (female) |
CRSwNP |
43.6 |
57.5 |
CRSsNP |
40.75 |
48.2 |
HRS |
53 |
55.25 |
RARS |
33.75 |
36.5 |
Table 2: Mean pre-operative SNOT-20 scores by sex in each subgroup.
The mean LM scores were 12.6, 5.0, 17.6 and 6 in the CRSwNP, CRSsNP, HRS and RARS groups, respectively (Figure 2). Using ANOVA and post-hoc pairwise T-test analysis (with Bonferroni adjustment) to compare each subgroup, the LM scores differed significantly between each subgroup, with the exception of the CRSsNP and RARS subgroups.
Figure 2: Mean pre-operative Lund-Mackay score in each subgroup.
The purpose of this cross-sectional study was to investigate the relationship in patient baseline QoL scores between the four main subgroups of RS. Our results only show a statistically significant difference in QoL scores between patients with RARS and HRS. Furthermore, a statistically significant difference in baseline LM scores was seen between all groups with the exception of the RARS and CRSsNP subgroups. The rationale for the study is based on our understanding that RS is adebilitating, chronic condition for many patients, and one which imparts a significant impact on the quality of life. The impact that any condition has on QoL is an individualized, unique perspective at the time of symptoms and is influenced by several factors. For example, it is known that RS can disturb the sleep cycle [12]; is associated with a higher risk of depression than that observed in the general population [13]; is associated with sexual and olfactory dysfunction [14,15]; and can also result in considerable absence from work and school. Many of these factors improve significantly with medical and surgical treatment of RS.
The SNOT-20 score is a disease-specific questionnaire, originally devised as a condensed version of the Rhinosinusitis Outcome Measure (RSOM-31) that was developed by Piccirillo in 1995 [16]. While it fails to address nasal obstruction and olfactory dysfunction (which were subsequently added to make the SNOT-22 questionnaire), historically, most of the published studies relating to QoL in RS use the SNOT-20 instrument, and for this reason it was chosen as the QoL measure in our patients instead of the SNOT-22.
Our study of the four main subgroups of RS demonstrated the HRS group to be the most symptomatic and RARS, the least symptomatic, according to pre-operative SNOT-20 evaluations (54.3 and 35.6, respectively), with a statistically significant difference between the two. The CRSwNP group had an elevated mean SNOT-20 over the CRSsNP group (48 and 45.8, respectively), but was less symptomatic than the HRS group (54.3).
Previous studies have also demonstrated significantly worse symptoms and signs using both the SNOT-20 and an endoscopic scoring system in patients with HRS over CRSwNP [17]. Bhattacharyya and Lee found that the sinus symptoms in RARS and CRS (wNP and sNP) were similar in magnitude [18]. The mean preoperative SNOT-20 score in our HRS subgroup was higher at 54.3 versus 48 for the CRSwNP subgroup. These scores are both higher when compared with scores reported in the literature of 31.1 and 22.1, respectively [17]. This may be related to the different environment and weather patterns existing in the Northeast, in comparison to that of Augusta, Georgia, where the prior study was performed.
Interestingly, the mean SNOT-20 scores for each of the 4 subgroups was higher in female patients than in males (Table 2), indicating that females are more symptomatic overall. This is contrary to other studies [19,20] that have not demonstrated a gender difference in pre-treatment SNOT-20 scores, and is the first study to suggest that RS may impact the QoL differently in males and females.
The decision to operate on patients for RS is based on a combination of history, clinical examination, response to medications, and radiological imaging findings. The treatment offered the patients in this study is beyond the scope and intent of this investigation. Our study was focused on differences in baseline QoL between patients with different sub-types of RS.
A non-contrast CT of the nose and paranasal sinuses allows a privileged view of the nasal cavity, sinuses, and osteomeatal complex which may be difficult to appreciate with endoscopic assessment alone (e.g., Haller cells, concha bullosa, intra-sinus disease). The LM scoring system was developed to allow the interpretation of the CT of the nose and paranasal sinuses to confirm and quantify the degree of inflammation present in an unambiguous manner. To this end, it has demonstrated high inter-observer reliability. The mean LM scores of 12.6, 5.0, 17.6 and 6 in the CRSwNP, CRSsNP, HRS, and RARS groups, respectively, are also notably higher than those documented for similar subgroups in other studies. Elsewhere, the mean LM score reported in CRS patients was 9.8 [21], and in RARS 3.8 [22]. Our analysis showed the LM scores differed significantly between each subgroup in our study, with the exception of the RARS and CRSsNP groups. Contrary to what was anticipated, the RARS group actually had a higher mean LM score than the CRSsNP group.
The discrepancies existing between the RARS and CRSsNP groups in relation to their Symptoms (SNOT-20) and imaging (LM scores) are noteworthy. In our study, the RARS group was the less symptomatic, but had more changes on CT imaging when compared with the CRSsNP group. Patients with RARS, by definition, are thought to have clear ‘normal’ imaging between attacks of RS, and perhaps the ease with which patients can access our office and obtain immediate CT imaging for real-time review may explain a higher mean LM score of 6 compared with 3.8 in a prior study [21].
As Lund identified previously, the results of diagnostic studies for CRS do not correlate well with the patient’s perception of their QoL [9]. This raises an important question - do we rely more on CT findings, or on the patient’s subjective complaints as indications for treatment? Upon comparing the SNOT-20 and LM scores for each subgroup, a non-significant correlation between the two scores was demonstrated. In patients who had imaging performed for non-rhinological symptoms, the “normal” LM score was found to be 4.3 [21]. Some advocate a LM score of at least 4.0 as an indication for endoscopic sinus surgery [8], while others suggest a score ranging from 0 to 5 to be within the incidentally ‘normal’ range [22]. Currently, there is no pre-operative SNOT-20 score that is generally accepted as an indicator of whether or not a patient would benefit from sinus surgery. However, comparing pre - and post-operative scores, Piccirillo et al., believed a SNOT-20 standardized response mean (calculated by mean change score divided by its standard deviation) of >0.8 to be a “clinically significant” improvement between pre and post-op SNOT-20 scores [11].
As mentioned earlier, Zheng et al., investigated the correlation between three QoL instruments, and the relationship between these questionnaires and the patient’s corresponding LM scores [10]. They found very good correlation between the SNOT-20, SF-36, and Visual Analog Scale, however, there was no correlation between any of the QoL metrics and corresponding LM scores. As in our study, they did find a higher and statistically significant difference in CT stage between patients with CRSwNP vs CRSsNP, but the QoL scores were better in their CRSwNP subgroup vs the CRSsNP subgroup. In our study, the QoL scores between these 2 subgroups were similar with the SNOT-20 scores for the CRSwNP subgroup slightly worse than the CRSsNP subgroup (48 vs 46, respectively). Both studies used the SNOT-20 as opposed to the SNOT-22 QoL instrument, and the differences in findings between studies highlights the complexity in assessing subjective symptoms across heterogenous populations having the same clinical diagnosis.