Open access peer-reviewed chapter

# Refractory Rhinosinusitis

By Yi-Tsen Lin and Te-Huei Yeh

Submitted: September 23rd 2018Reviewed: January 25th 2019Published: February 28th 2019

DOI: 10.5772/intechopen.84714

## Abstract

Various factors have been proposed to be related to refractory chronic rhinosinusitis (CRS). Treatment for refractory CRS is challenging for ear, nose, and throat (ENT) surgeons. The aim of the study was to determine the clinical features associated with the severity of CRS that may necessitate revision surgery by eliminating the bias of the surgeon’s technique using standardizing surgical procedures. Sinus wall thickness and blood eosinophilia, which may represent the depth of inflammation in CRS, are associated with the need for revision surgery. We found that, when the thickness of the posterolateral maxillary sinus wall is more than 3.03 mm, there is an increased probability for a need for revision surgery. CRS patients with thickened sinus walls were found to have poorer outcomes. Further research is needed in order to justify this type of surgical procedure for CRS.

### Keywords

• refractory
• chronic rhinosinusitis
• inflammation
• osteitis
• eosinophilia

## 1. Introduction

The sinonasal organ plays an important role in the human respiratory system, as this organ consistently encounters external irritants and is therefore one of the most frequently inflamed sites in the human body [1]. Inflammation may begin as an infectious process (acute rhinosinusitis), and, if the symptoms persist without resolution, it can lead to inflammatory consequences (chronic rhinosinusitis (CRS)) [2]. CRS is one of the most prevalent chronic diseases in modern society and is defined as the presence of more than one nasal symptom (mucopurulent drainage, nasal congestion, facial pain-pressure-fullness, and decreased sense of smell) and a documentation of inflammation for more than 12 weeks [3]. It is a heterogeneous, multifactorial disease with multiple distinct factors, including genetic, infectious, immune, anatomic, allergic, and inflammatory components [2]. The goal of CRS therapy is maximal medical treatment including oral and topical antibiotics, nasal steroids, systemic steroids, antihistamines, and saline irrigations. Functional endoscopic sinus surgery (FESS) is indicated if medical therapy fails [4].

The safety and efficacy of FESS for CRS have been strongly supported by meta-analyses from both large outcome studies and cohort studies. Improvement in both disease-specific and generic quality of life and objective measures have been demonstrated for the efficacy of FESS; however, across long-term follow-up, there is a 10–20% revision rate, which is considered to be refractory CRS [5]. Refractory CRS is defined by failure to stabilize after surgery and treatment with antibiotics, saline rinses, and topical steroid and has become a significant issue for ENT surgeons [6]. Predicting surgical outcome is crucial for evaluating the severity of CRS preoperatively, and the severity of CRS is usually defined by several factors. Temporally, the duration and frequency of symptoms and signs of CRS patients cannot be precisely correlated. Spatially, the Lund-Mackay (L-M) score, which is based on CT images, is the most frequently used method to evaluate the severity of CRS; nevertheless, the L-M score represents only a snapshot of the condition [7]. A swift change in mucosal swelling is frequently observed during the subacute stage of sinusitis. Other parameters should be considered in order to define the severity of CRS and more accurately predict its prognosis.

Various factors are related to refractory CRS, including mucociliary dysfunction, the presence of mucosal biofilm, peripheral eosinophil count, mucosal eosinophilia, acute postoperative infection, ASA triad, cystic fibrosis, osteitis, hyperreactive airway, inhaled allergen, and experience of the performing surgeon [8, 9, 10, 11, 12]. It is important to find a simple way to evaluate the severity of CRS in order to identify an accurate prognosis for patients and determine which patients may need long-term medical treatment. The aim of the study was to determine the clinical features related to the severity of CRS that would necessitate revision surgery, by carefully eliminating surgeon bias using standardizing surgical procedures.

## 2. Standardization of surgical procedure and treatment protocol

The first consideration of this study was to select appropriate patients in order to exclude the congenitally influential factor of heterogeneity of CRS. The next consideration was to standardize the preoperative treatment, surgical procedure, and postoperative follow-up protocol. Over the past 10 years, we have developed a standardized surgical procedure and treatment protocol. Preoperatively, the referral doctor administers optimal medical treatment to the patient; if that does not occur, our clinics will administer the treatment. If treatment fails, surgery is suggested. Preoperative medication is not given for at least 2 weeks, if acute exacerbation was not noted before surgery. Some patients are given a loose schedule of intranasal steroid spray, but oral antibiotics are not given regularly.

Other information are also collected during the preoperative visit: age, gender, asthma, nasal polyps, allergic rhinitis, obstructive sleep apnea, diabetes, smoking status, gastroesophageal reflux disease, prior FESS history, and Samter’s triad. For the surgical procedure, the objects of FESS include several folds: to clear out the occluded ostium by correcting the anatomical flaw of bottleneck of draining pathway for diseased sinus, to decrease inflammatory load by removing developed polyps or swollen mucosa which was filled with inflammatory milieu, and to clean out entrapped discharge from deep-seated recess which contained inflammation-inducing materials. Based on the principles described above, we developed eight complete steps to perform standard FESS:

1. Middle turbinate trimming: This procedure is used instead of medial fracture in order to expose the posterior margin of uncinate process and hiatus semilunaris.

2. Uncinectomy: The first step of ethmoidectomy is to properly remove the uncinate process. It can be antegrade, with a sickle knife, or retrograde, by using backbiting forceps, until the superiorly agger nasi cell, and frontal recess and inferiorly the natural ostium of maxillary sinus are identified.

3. Enlargement of the natural ostium of maxillary sinus: By removing the mucosa of posterior fontanelle, the accessory ostium can be identified during this step. Pathologic tissue in the maxillary sinus is removed, and irrigation by normal saline is frequently applied.

4. Removal of the bony wall of the ethmoid bulla: Identifying the basal lamella of the middle turbinate. The retrobullar recess and suprabullar cells are exposed. It is important to expose and identify lamina papyracea in order to delineate the lateral margin of the ethmoid cavity.

5. Removal of the basal lamella at the medial inferior site: In order to enter posterior ethmoid sinus space safely, the middle turbinate insertion is not destabilized. When entering posterior ethmoid space, the superior turbinate and skull base are identified by carefully removing the ethmoid bony septum of the posterior ethmoid sinuses.

6. Opening of the sphenoid sinus, if necessary: The sphenoid sinus is not frequently involved in CRS. If necessary, remove the inferior third of superior turbinate in order to easily find the natural ostium of sphenoid sinus. Irrigation or removing polypoid mucosa surround the ostium is sufficient for most patients.

7. Removal of the bony partitions along the skull base: After identifying the skull base at the posterior ethmoid roof, its is safe to remove the partitions anteriorly to reach the bony indentation of the anterior ethmoid artery (AEA), which is the most important landmark to manage frontal recess. The AEA is a landmark (“Nike” logo-shaped curve) and may be buried inside a bony canal in patients with well-pneumatized anterior ethmoid sinuses; it could be mesenteric. This space is complicated by various possible suprabullar or frontobullar cells and is a challenging step for beginners.

8. Cleaning frontal sinus-draining route: Using the 45-degree endoscope, mark the anatomic landmark of AEA posteriorly and agger nasi or frontoethmoid cells anteriorly; the frontal sinus-draining route is frequently buried in the complicated anterior ethmoid cell system. There may be anteriorly, posteriorly, medially, and laterally located ethmoid air cells; it is important to identify the boundary of ethmoid cavity laterally to the lamina papyracea, medially to the middle turbinate concha, and superiorly along the skull base. The frontal sinus will be safely opened.

Postoperative care includes regularly follow-up for at least 6 months using optimal antibiotic treatment, including low-dose macrolide for 2 months and nasal steroids, as well as routine saline nasal douching plus adjuvant of gentamicin for at least 3 months.

## 3. Patient selection, radiographic evaluation, and statistical analyses

We reviewed the medical records of 243 patients who received bilateral FESS in our department by the same senior surgeon of a tertiary referral hospital from September 2010 to August 2011. Computed tomography (CT) of paranasal sinuses was performed in all patients at most 2 months prior to surgery. Other preoperative evaluations included hematologic examination the day before surgery. Patients with known systemic diseases or malignancies were excluded, such as diabetes mellitus, asthma, or other immunocompromised diseases. Forty-eight CRS patients who received revised sinus surgery during this period were recruited; 21 of these patients received surgery by the same surgeon, and the other 27 patients received surgery from different surgeons. Among the 21 patients, patients with no previous sinus CT scan available for comparison were excluded. Among the 27 patients, we excluded the patients who received previous Caldwell-Luc procedures. Nine patients were assigned to Group A (primary and revised surgery by the same senior surgeon), 17 patients were assigned to Group B (previously operated on by other surgeons), and 30 control patients were assigned to Group C who received primary FESS surgery during the same period and were followed up for at least 3 years without revision surgery. Group D included 30 control patients with head and neck CT scan from parotid surgery without notified sinonasal problems. Hematologic examination was evaluated for Group D patients 1 day prior to surgery. The flow chart of patient selection is shown in Figure 1. The clinical information including the result of bacterial culture and pathology to evaluate eosinophilic rhinosinusitis, with or without asthma and ImmunoCAP Specific IgE blood test, were also collected for further analysis.

The extent of paranasal sinus mucosal disease was evaluated by using the L-M staging system [7]. Sinus wall thickness was measured in coronal view of the sinus CT. The posterolateral wall of maxillary sinus, para-crista galli level (around the lateral lamella) of the ethmoid sinus, and the anterior clinoid level of sphenoid sinus were measured as the representative thickness of each sinus wall (Figure 2). All CT studies were performed by 64 multidetector-row CTs (LightSpeed VCT, GE Medical Systems). Contiguous axial 1.2-mm-thick slices were obtained through the maxillofacial bones, and images were reconstructed with soft tissue and bone reconstruction algorithms; 3.0-mm-thick coronal and sagittal reformatted images were obtained per our institutional protocol. All CT measurements were made on bone algorithm reconstructed and bone-windowed images (W:2000, L:500) using an independent workstation. The measurements were repeated by two independent otolaryngologists. In detail, maxillary sinus wall thickness is measured at the posterolateral region where the first cut is shown when the zygoma is separated from the maxillary sinus wall, measuring the thickest part. The ethmoid sinus wall thickness is measured at the para-crista galli region around the lateral lamella, also the thickest part. The sphenoid sinus wall thickness is measured at the first cut showing the anterior clinoid, the thickest part. At the lateral sphenoid wall, the carotid canal and optic nerve may introduce measurement confusion, and it is the reason why we choose the anterior clinoid level instead of the lateral sphenoid wall for wall thickness measurement where more constant sinus wall thickness could be measured. Frontal sinus wall was excluded due to its high variation of pneumatization in normal population.

We assessed gender, age, hemoglobin (Hb) levels, white blood cell (WBC) count, eosinophilic count, L-M score, bony wall thickness of maxillary/ethmoid/sphenoid sinus, and mean recurrence time of CRS. Comparisons between groups were performed by analysis of variance (ANOVA) tests for normally distributed variables and Kruskal-Wallis test for nonparametric variables, as required. Chi-square tests for categorical variables. Multiple logistic regression analysis was performed between Groups A and C against various parameters including age, gender and maxillary sinus wall thickness, LM score, Hb, and eosinophil count. Receiver-operating characteristic (ROC) curves were constructed to define cutoff value for potential refractory CRS. Linear regression was used to determine the relationship between scalar variables. All statistical analyses were performed using SPSS software. p < 0.05 was considered to be statistically significant.

## 4. Clinical features associated with the severity of CRS

### 4.1 Patient demographics

Group A included 8 males and 1 female (mean age, 49.1 ± 15.1 years), Group B included 11 males and 6 females (mean age, 47.8 ± 15.6 years), Group C included 23 males and 7 females (mean age, 41.9 ± 11.3 years), and Group D included 10 males and 20 females (mean age, 50 ± 14.9 years). There was no significantly difference across age (unpaired t-test, p > 0.05). The gender distribution was significantly different with obvious male preponderance in Groups A, B, and C (Kruskal-Wallis test, p < 0.05; Table 1). The information including bacteriology, eosinophilic rhinosinusitis, asthma, or ImmunoCAP Specific IgE blood test were shown in Table 1. The bacteriological data indicated Staphylococcus aureus was the major bacterial species found. The main infiltrative inflammatory cells according to pathologic slides were lymphoplasma cells and, occasionally, neutrophil infiltration. Eosinophilic rhinosinusitis was defined as average eosinophil count >10/high power field in ten randomly selected fields (X 400) under H&E staining from our previous publication [13]. Aspirin intolerance and bronchial asthma were very scarce (only one case in Groups A and C, respectively).

GroupN=AgeGender*Bacteriology#Eosinophilic rhinosinusitis$Aspirin intolerance or asthma A949.1 ± 15.18M1F (1)&311 B1747.8 ± 15.611M6F (3)311 C3041.9 ± 11.323M7F (4)210 D3044.7 ± 13.610M20FNANANA ### Table 1. Patients’ demographic data. p < 0.05 (Kruskal-Wallis test). Other than normal flora, there are Staphylococcus aureus (n = 5), MRSA (n = 1), Citrobacter koseri (n = 1), and Haemophilus influenzae (n = 1). Average eosinophil count >10/high power field in ten randomly selected fields (X 400) under H&E staining13. Number of patient with positive ImmunoCAP test. Group A: Revision group (same surgeon). Group B: Revision group (different surgeons). Group C: Primary FESS group. Group D: Normal control group. ### 4.2 Hematologic examination There was no statistically significant difference in hematologic examination results between groups (unpaired t-test, p > 0.05). The absolute peripheral eosinophil counts in Group A were significantly higher than in Group D (Table 2). GroupHematologic exam HemoglobinWBC count (k/μl)Eos. (%)Peripheral eos. count (k/μl)Sugar (g/dL) A14.58 ± 0.676333.3 ± 1494.54.48 ± 3.82303.09 ± 297.48*91.2 ± 8.3 B14.34 ± 1.296119.4 ± 1781.62.91 ± 2.03181.45 ± 179.3193.1 ± 14.3 C14.29 ± 1.536994.3 ± 1637.03.66 ± 3.03249.48 ± 240.4990.1 ± 9.2 D14.00 ± 1.236146.7 ± 1598.43.50 ± 2.51164.29 ± 204.1596.4 ± 21.6 ### Table 2. Hematologic examination result in different groups. p < 0.05, compared with group D. Group A: Revision group (same surgeon). Group B: Revision group (different surgeons). Group C: Primary FESS group. Group D: Normal control group. ### 4.3 L-M score and sinus wall thickness The average L-M score of Group A was 16.7 ± 8.0 and of Group C was 12.9 ± 5.1; there was no significant difference between these groups (unpaired t-test, p > 0.05, Table 3). GroupL-M scoreSinus wall thickness (mm) MaxillaryEthmoidSphenoid A16.7 ± 8.04.25 ± 1.661.83 ± 0.371.89 ± 0.66 B12.9 ± 6.6$2.43 ± 0.831.49 ± 0.281.49 ± 0.59
C12.9 ± 5.12.06 ± 0.491.46 ± 0.241.34 ± 0.28
D0.23 ± 0.431.97 ± 0.42,#1.44 ± 0.331.39 ± 0.34

### Table 3.

L-M score and sinus wall thickness result in different groups.

p < 0.05, compared with group A.

p < 0.05, compared with group B.

With primary CT; n = 8.

Group A: Revision group (same surgeon). Group B: Revision group (different surgeons). Group C: Primary FESS group. Group D: Normal control group.

The assessments of sinus wall thickness between the independent otolaryngologists were very close. The average intraclass correlation coefficient between two assessors was 0.833 (95% confidence interval, 0.782–0.872). In terms of individual sinuses, the closest interrater agreement was found for sphenoid sinuses (0.821, 0.932), followed by the ethmoid sinuses (0.631, 0.851) and the maxillary sinuses (0.576, 0.825). In Group A, the mean sinus wall thickness of the maxillary, ethmoid, and sphenoid sinuses were 4.25 ± 1.66 mm, 1.83 ± 0.37 mm, and 1.89 ± 0.66 mm, respectively. Group B had a mean thickness of 2.43 ± 0.83 mm, 1.49 ± 0.28 mm, and 1.49 ± 0.59 mm in the maxillary, ethmoid, and sphenoid sinuses. In Group C, the sinus wall thickness was as follows: maxillary sinus, 2.06 ± 0.49 mm; ethmoid sinus, 1.46 ± 0.24 mm; and sphenoid sinus, 1.34 ± 0.28 mm. In Group D, the measured sinus wall mean thickness of the maxillary, ethmoid, and sphenoid sinuses were 1.97 ± 0.42 mm, 1.44 ± 0.33 mm, and 1.39 ± 0.34 mm, respectively.

The sinus wall thickness of Group A was significantly higher than Groups C and D; in Group B, only the maxillary sinus wall thickness was significantly different compared to Group D (unpaired t-test, p < 0.05; Table 3). Multiple logistic regression analysis was performed between Groups A and C against various parameters including age, gender and maxillary sinus wall thickness, LM score, Hb, and eosinophil count. Eventually, maxillary sinus wall thickness was an independent significant factor noted (p = 0.037; Table 4).

P valueOdds ratio95% CI
Age0.6481.0390.881–1.226
Gender0.7110.0010.026–8.020
Maxillary thickness0.03719.4421.192–317.181
L-M score0.9580.9940.800–1.235
Hb0.6481.4000.330–5.951
Eosinophil count0.8270.9990.989–1.009

### Table 4.

Multiple logistic regression between Groups A and C.

Group A: Revision group (same surgeon). Group C: Primary FESS group.

### 4.4 Mean recurrence time

Average recurrence time of Group A was 28.7 ± 13.9 months. There was no significant correlation between the mean recurrence time and preoperative L-M score (Figure 3) or sinus wall thickness (linear regression, p > 0.05; Figure 4).

### 4.5 The cutoff values of sinus wall thickness for the prediction of recalcitrant CRS

The cutoff value of sinus wall thickness in prediction of refractory CRS who needs revision surgery differed across sinuses. The sensitivity and specificity for prediction also varied. Using 3.03 mm as a cutoff value for the maxillary sinus, the sensitivity was 88.9% and the specificity was 90%. Using 1.63 mm as cutoff value for ethmoid sinus, the sensitivity and specificity were 77.8 and 80.0%, respectively. Using 1.75 mm as a cutoff value for the sphenoid sinus, the sensitivity was 44.4% and the specificity was 80.0%.

Different sinus wall thicknesses showed areas under ROC curve (AUC) of 0.94, 0.72, and 0.63, for maxillary, ethmoid, and sphenoid sinuses, respectively. The AUC of maxillary sinus wall thickness reached statistical significance (ROC curve, p < 0.05; Figure 5).

## 5. Sinus wall thickness and blood eosinophilia as the indicators for revision surgeries

The success of FESS for CRS is still variable, ranging from 76 to 98% [4]. Although the exact predictive factors are still controversial, several risk factors, such as nasal polyps, allergic rhinitis, aspirin intolerance, and bacterial resistance, can result in unfavorable treatment outcomes for CRS patients. In this study, we found that the presence of thickened maxillary sinus walls of more than 3.03 mm and increased peripheral blood eosinophil count are good predictors of unfavorable outcomes from FESS. In addition to the classical L-M scoring system, a two-dimensional parameter, we suggest that these two factors may represent another three-dimensional parameter that may indicate the depth of inflammation in CRS in order to evaluate its severity.

The sinonasal organ is an expanding air-filled space that grows in a random pattern proven by using a simple computerized equation [14]. The sinus pneumatization process may be considered as using limited material ballooning to occupy the space among the eyeballs, brain, and mouth. This expanding process creates one frontal, maxillary, and sphenoid sinus cell on each side and, more importantly, the complexity of the ethmoid cell system. The bony sinus wall, which confines this sinonasal cavity, represents the boundary and most peripheral lining of this organ. If it is involved in the inflammatory process, it might be considered as one of the dimensions of the depth of disease extent, indicating a more severe form of sinonasal disease. One study showed that CRS patients had smaller maxillary sinuses than normal controls. These authors proposed that the increased bone thickness in the maxillary sinus itself might be related to the size of the sinus [15]. Accordingly, we demonstrated that maxillary sinus wall thickness is an indicator of poor surgical outcome.

The success rate of surgical outcomes for CRS patients across surgeons varies. The experience and technique of the surgeon are important factors related to the successfulness of treatment. Surgical studies contain congenital bias, that is, procedures or interventions are not executed in a uniform way; there is also a lack of patient-blinding to the surgical intervention and performance bias, which is also the case between different surgeons. Therefore, it is crucial to establish a standard surgical protocol in order to avoid the impact of the confounding effect of surgical techniques on patient outcomes. Therefore, over the past 10 years, we have made an effort to standardize surgical procedures in order to eliminate differences among surgeons. The standard eight-step FESS procedure is based on Stammberger and Kennedy’s methods, which sequentially remove the obstruction of the drainage pathway anterior to posterior to reach the sphenoid sinus ostium; then, it is moved from posterior back to anterior along the identified skull base until the AEA is identified and the frontal sinus is opened. If the diseased sinuses are limited, the surgical procedure can be tailored so that the normal sinus mucosa and draining pathway are exposed and identified; this is also a way to educate beginners to understand FESS in an organized method.

In 1992, it was first suggested that chronic inflammation of the bony framework of paranasal sinuses plays a pivotal role in the pathophysiology of CRS; this hypothesis was further confirmed by subsequent animal studies [16]. Georgalas et al. proposed a global osteitis scoring scale as an indicator of revised sinus surgery [17]. Snidvongs et al. proposed that the osteitic sinus bone is a surrogate of tissue or serum eosinophilia in CRS patients [18]. Osteitis changes in the sinus bone are present in heterogeneous, irregular bone in areas of growth and destruction. Some studies have proposed that bone thickness can predict the severity of osteitis [19, 20]. Recently, sinus osteitis and subsequent bony remodeling were also suggested as a contributing factor to refractory CRS. At a microscopic level, osteitis is associated with eosinophilic inflammation and may represent a method to predict patients with P-glycoprotein overexpression by using an epithelial-to-background staining ratio; increased osteitis burden is associated with increased P-glycoprotein membranous expression in CRS [21, 22, 23]. In our study, the sinus bony walls in Group A were significantly thicker than those in Groups C and D; in Group B, only the maxillary sinus wall was significantly thicker than that of the control group. These results reflect the importance of the role of a surgeon in evaluating surgical outcomes. Our data also suggest that a posterolateral maxillary sinus wall thickness of 3.03 mm should be the cutoff value in order to predict refractory CRS.

The existence of bacterial biofilms (BBF) has also been proposed to be associated with osteitis in CRS [10]. Biofilm formation might reflect the severity, chronicity, or both of sinus infection; therefore, the release of inflammatory mediators would stimulate osteoblast activity, inducing bony remodeling and osteitis. Osteitis may further spread the pathogen either via the Haversian canal system hematogenously or from direct local invasion [24]. Intraepithelial bacteria are also found in CRS patients [25]. Considering the histology of sinus mucosa, these factors represent the depth of involvement of inflammatory process and indicate a prolonged treatment course. Although it did not reach statistical significance, maxillary sinus wall thickness is also related to shortened time to recurrence (Figures 3 and 4); therefore, compared to L-M scores of sinus CT, sinus wall thickness may represent greater proximity for the chronicity of CRS. At present, the mainstay of sinus surgery still focuses on restoring ventilation, yet no specific surgical method has been proven to be effective in treating osteitis associated with CRS. Instead, long-term or topical antibiotic treatment is administrated in cases of sinus osteitis and refractory sinusitis [26].

It has previously been reported that eosinophilic inflammation in the sinonasal tissues is correlated with the advanced severity of CRS and the poor outcomes associated with FESS [12]. Recent evidence has shown that eosinophilic inflammation in Caucasians CRS patients with polyps does not affect Asian to the same extent. A study from Thailand indicated a time-shifting migration of neutrophilic inflammation to eosinophilic inflammation, and a study from Korea suggested that eosinophilic inflammation might not be related to surgical outcome in Korean CRS patients [27, 28]. In our study, increased peripheral eosinophil numbers had a limited impact on surgical outcomes, suggesting that the clinical implication of eosinophilic inflammation might be different in Asian patients. Nevertheless, our study strengthens the hypothesis that increased eosinophil numbers are a poor indicator of CRS outcomes. Blood eosinophilia is induced from proliferation of eosinophil progenitor from bone marrow (myeloproliferative) or clonal expansion of peripheral eosinophil in the blood stream [29, 30]. The proposal that refractory CRS represents a local manifestation of systemic inflammatory disease is supported by our results. Our study suggested that, for those patients with obvious sinus wall thickening, more detailed preoperative consultation and laboratory tests and more aggressive postoperative medical treatment are needed.

There are several limitations of this study. First, we had small case numbers. Second, there are individual differences in the tolerance of sinusitis, as revision surgery was used as the judgment for refractory sinusitis. Despite the limitations, the knowledge gained in our study provides crucial information to guide surgical selection in CRS patients.

In summary, a variety of factors lead to refractory CRS. As a result, treatment for refractory CRS is a great challenge for ENT surgeons. Thickness of posterolateral maxillary sinus wall of more than 3.03 mm indicates possibility for revised surgery. For those CRS patients with thickened sinus wall in which we expect poor outcomes, further research is needed in order to justify the surgical procedure in such a probable systemic inflammatory disease.

## 6. Conclusions

In this study of subjects of chronic rhinosinusitis (CRS) undergoing functional endoscopic sinus surgery (FESS), we determined which clinical features are associated with higher possibility for revised surgery. We have developed an eight-step standard procedure to perform FESS in order to eliminate the bias of surgical technique. Sinus wall thickness and blood eosinophilia are associated with the need for revision surgery. Thickness of posterolateral sinus wall of more than 3.03 mm in maxillary sinus indicates the higher possibility for revised surgery. Also, CRS patients with thickened sinus walls were found to have poorer outcomes.

## Acknowledgments

This study was supported by a grant (100-2314-B-002-044) from the Ministry of Science and Technology (MOST) of the Republic of China.

## Conflict of interest

There are no financial or other relationships that could lead to a conflict of interest.

## Appendices and nomenclature

CRS

Chronic rhinosinusitis

FESS

Functional endoscopic sinus surgery

## More

© 2019 The Author(s). Licensee IntechOpen. This chapter is distributed under the terms of the Creative Commons Attribution 3.0 License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Yi-Tsen Lin and Te-Huei Yeh (February 28th 2019). Refractory Rhinosinusitis, Rhinosinusitis, Balwant Singh Gendeh and Mirjana Turkalj, IntechOpen, DOI: 10.5772/intechopen.84714. Available from:

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