Literature DB >> 34664801

Risk Model Establishment of Endoscopic Sinus Surgery for Patients with Chronic Rhinosinusitis: a Multicenter Study in Korea.

Jin-Young Min1, Yong Min Kim2, Dae Woo Kim3, Jeong-Whun Kim4, Jin Kook Kim5, Ji-Hun Mo6, Jae-Min Shin7, Kyu-Sup Cho8, Sanggyu Kwak9, Seung-Heon Shin10.   

Abstract

BACKGROUND: Endoscopic sinus surgery (ESS) is the mainstay treatment for refractory chronic rhinosinusitis (CRS). Since various factors may contribute to the surgical outcome, it is challenging for physicians to predict surgical outcomes. The aim of study was to analyze the prognostic factors of postoperative outcomes and to establish the prediction model with the risk factors that impact the postoperative outcomes.
METHODS: Medical records of CRS patients who underwent ESS at 9 institutions in 2005, 2010, and 2016 were retrospectively reviewed. We classified the patients into 2 groups based on postoperative objective endoscopic outcomes. Demographics, nose-specific symptoms, olfactory function, eosinophil counts in blood (EoB) and nasal tissue (EoT), and Lund-Mackay CT score (LMS) were collected. Univariate and multivariate analyses were performed and established a prediction equation for postoperative endoscopic objective outcomes.
RESULTS: In total (n = 1,249), 27.0% were not satisfied under postoperative endoscopic examination. Of 10 variables, LMS (> 5), sinus dominancy (maxillary sinus and ethmoid sinus), EoB (> 210), and EoT (> 100) were statistically significant in univariate analysis (P < 0.05, all). In multivariate analysis, EoT (> 100) and LMS (> 5) were significantly associated with poor postoperative outcome. Furthermore, 5 significant variables were employed to establish the risk model of postoperative outcomes and P (the value of prediction probability) = 1 / (1 + exp [-0.392 + 1.088 × EoT (> 100) + 0.123 × mean LMS (> 5) - 0.366 × sinus dominancy (maxillary) + 0.064 × sinus dominancy (similar) + 0.200 × EoB (4%) + 0.344 × EoB (> 210)] was developed.
CONCLUSION: Tissue eosinophil count and radiographic severity predispose to a poorer outcome of ESS and the risk model established may be helpful to predict postoperative outcomes of ESS.
© 2021 The Korean Academy of Medical Sciences.

Entities:  

Keywords:  Chronic Rhinosinusitis; Computed Tomography; Endoscopic Sinus Surgery; Eosinophilia; Multicenter Study; Prognostic Factor

Mesh:

Year:  2021        PMID: 34664801      PMCID: PMC8524236          DOI: 10.3346/jkms.2021.36.e264

Source DB:  PubMed          Journal:  J Korean Med Sci        ISSN: 1011-8934            Impact factor:   2.153


INTRODUCTION

Chronic rhinosinusitis (CRS) is one of the common medical conditions around the world and is characterized by local inflammation of the sinonasal mucosa.12 Symptoms of CRS persist for at least 12 weeks, resulting in a profound impact on patients' quality of life.3 CRS is further classified into 2 clinical phenotypes: chronic rhinosinusitis with nasal polyps (CRSwNP) and CRS without nasal polyps.4 Regardless of clinical phenotypes, endoscopic sinus surgery (ESS) is the mainstay treatment option for refractory CRS.5 However, there is still a 20–50% recurrence rate after ESS.6 Surgical outcomes can be determined by subjective nose-specific symptoms as well as objective findings measured by endoscopic examination and/or radiographic imaging. Given these, clarification of the risk factors of poor subjective and/or objective outcomes of ESS and establishment of predictive models with the risk factors can be helpful for physicians to predict ESS outcomes. Many studies have reported the potential factors predicting ESS outcomes. One relatively well-studied factor is the presence of nasal polyps, unilateral or bilateral disease, and disease severity determined by computed tomography (CT) score and/or nasal endoscopic score.6 Additionally, comorbid diseases such as asthma, allergy, and gastroesophageal reflux disease, and demographic factors including age and gender, and previous history of ESS are also considered as risk factors.78910 Furthermore, recent studies have found that presence of osteitis involving bony paranasal sinuses, tissue eosinophilia and blood eosinophilia is significantly related to severity of CRS and poor postoperative outcomes.711121314 However, risk factors related to poor postoperative outcome are still controversial and remain unclear due to complicated pathophysiology of CRS. Moreover, risk factors related to poor ESS outcomes showed ethnic, geographic, and environmental differences and most studies were conducted in a single institution. In this study, we demonstrated clinical features of CRS during the last 12 years and analyzed the prognostic factors of postoperative outcomes in CRS in a multicenter study in South Korea. Furthermore, we sought to establish the prediction model of risk factors for postoperative outcomes in CRS.

METHODS

Subjects

Adult CRS patients who received ESS were enrolled in this study. All CRS subjects met clinical criteria for CRS as defined by the EPOS guideline.1 The medical records were retrospectively analyzed at nine different medical institutions in 2005, 2010, and 2016. Patients who were younger than 18 years old and patients with antrochoanal polyp, postoperative cyst, mucocele, odontogenic sinusitis, and other benign or malignant tumors were excluded from this study. According to the postoperative patient's subjective satisfaction and physician's objective satisfaction, postoperative outcomes were defined as good, moderate, and poor group. If a patient had no sinonasal discomfort after ESS, the patient was considered as good group, while poor was defined as the sinonasal symptoms not having improved at all after ESS. Physician's objective satisfaction was determined by postoperative endoscopic evaluation. If the sinonasal mucosa showed no abnormal findings, it was determined to be good, while poor was defined as presence of mucosal scarring, crusting, edema, polyps, and discharge. Postoperative status was determined at least 6 months after ESS. Demographic factors including sex, age, smoking history, presence of atopy and asthma, nose-specific symptoms, and olfactory function were evaluated. Olfactory function including threshold, identification, and discrimination was assessed by the Korean version of the Sniffin' Stick test (KVSS II).15

CT severity

Severity of disease was determined by preoperative CT scans using the Lund-Mackay scoring system.16 Additionally, sinus dominancy was assessed by the ratio of the ethmoid sinus scores and maxillary sinus scores (E/M ratio). If the E/M ratio was lesser than 0.5, disease severity of the maxillary sinus was considered to be more severe than that of the ethmoid sinus. In contrast, if the E/M ratio was greater than 2, disease severity of the ethmoid sinus was considered to be more severe than that of the maxillary sinus. If E/M ratio is between 0.5 and 2, it was considered as “similar.”

Degree of eosinophilia in nasal tissue and peripheral blood

To assess the degree of eosinophilia in nasal tissue, nasal polyp tissues obtained during ESS were used. In the hematoxylin-and-eosin-stained tissue sections, the number of eosinophils in the submucosal area was counted in 5 high power field (HPF) by two independent physicians and the mean numbers of eosinophils were calculated. In addition, eosinophilia in peripheral blood was also determined and expressed as counts and/or percentage.

Statistical analysis

Summary for variables were performed using descriptive analysis, the values of mean and standard deviation presented for quantitative variables and the values of frequency and percent for qualitative variables. For univariate analysis, comparisons by post-operative subjective satisfaction variable (good vs. moderate vs. poor) and objective satisfaction (good vs. moderate vs. poor) were performed using one-way analysis of variance and χ2 test. And multiple comparison result was performed by Scheffe method. To obtain cut-off points for quantitative variables, a simulation algorithm was used. The simulation algorithm was performed with the following steps: 1) divide the interval from minimum value to maximum value into 100 points 2) analyze using 100 points and carry out whether it is significant or not 3) find all cut-off points which analysis was significant 4) among the significant points, determine the cut-off point closest to the median value. For multivariate analysis, the multinomial logistic regression model with forward conditional method was used and the good satisfaction category was used as reference value. The results were expressed by odds ratio (OR), 95% confidence interval (CI) and P value. Finally, to obtain a prediction equation for postoperative objective satisfaction (good vs. moderate and poor), the binary logistic regression model was used and the value of prediction probability was calculated. The range of prediction probability value from prediction equation is 0 to 1. When the prediction probability value is greater than 0.5, the patient will be predicted as a good satisfaction group. And if the prediction probability value is less than 0.5, the patient will be predicted as a moderate and poor satisfaction group. The data analysis was performed by a medical statistician. All statistical analyses were performed using the IBM SPSS software package for Windows (version 19.0, Chicago, IL, USA). And all tests were 2-sided and P values of less than 0.05 indicated statistical significance.

Ethics statement

The study was approved by the Institutional Review Board of each medical center (The Instututional Review Board of Daegu Catholic University Medical Center, CR-17-152). The informed consent was waived due to retrospective nature of the study.

RESULTS

Subject demographics and clinical characteristics of CRS

Patients' demographics are shown in Table 1. Of a total of 1,249 patients, 301 CRS patients in 2005, 466 patients in 2010, and 482 patients in 2016 were enrolled in this study.
Table 1

Demographic and clinical profiles of the patients

Variables2005 (n = 301)2010 (n = 466)2016 (n = 482)P value
Sex0.069
Male173 (57.6)311 (66.7)295 (61.2)
Female128 (42.4)155 (33.3)187 (38.8)
Age, yr42.8 ± 15.244.7 ± 15.049.4 ± 15.70.000
Chief complaint0.236
Nasal obstruction195 (64.8)285 (61.2)265 (55.0)
Rhinorrhea44 (14.6)45 (9.6)55 (11.4)
Posterior nasal drip10 (3.2)37 (8.0)30 (6.3)
Facial pain/pressure11 (3.6)13 (2.7)33 (6.8)
Olfactory dysfunction14 (4.8)27 (5.7)41 (8.5)
Headache6 (2.0)22 (4.8)15 (3.1)
Foul odor4 (1.2)0 (0.0)7 (1.4)
Others17 (5.8)37 (8.0)36 (7.5)
Symptom duration, mon47.4 ± 65.444.4 ± 75.045.9 ± 80.30.899
History of smoking
Present83 (27.6)130 (27.8)145 (30.0)0.045
Past12 (4.0)5 (1.1)23 (4.8)
Non206 (68.4)331 (71.1)314 (65.2)
CT finding
Lund-Mackay score5.3 ± 3.25.2 ± 3.05.4 ± 2.80.576
Sinus dominancy0.021
Ethmoid > maxillary51 (16.9)62 (13.4)97 (20.1)
Ethmoid = maxillary113 (37.5)231 (49.4)206 (42.7)
Ethmoid < maxillary137 (45.5)173 (37.2)179 (37.2)
Olfactory function0.218
Anosmia90 (29.7)147 (31.6)111 (23.1)
Hyposmia92 (30.7)119 (25.5)145 (30.1)
Normosmia119 (39.6)200 (42.9)226 (46.8)
Atopic status0.078
Positive117 (39.0)156 (33.8)160 (42.1)
House dust mite83112137
Fungi71018
Tree pollen182434
Weed pollen303848
Bronchial asthma10 (3.4)14 (3.0)13 (2.7)0.718
Blood eosinophilia
Percentage, %3.6 ± 3.03.5 ± 2.73.6 ± 3.50.951
Count249.3 ± 244.5245.7 ± 238.6250.6 ± 261.80.983
Nasal polyp0.051
Presence157 (52.1)205 (44.0)251 (52.0)
Absence144 (47.9)261 (56.0)231 (48.0)
Tissue eosinophil count49.4 ± 77.642.8 ± 74.051.1 ± 96.80.640

Data are presented as number (%) or mean ± standard deviation.

CT = computed tomography.

Data are presented as number (%) or mean ± standard deviation. CT = computed tomography. Among the demographic factors evaluated in this study, there was a significant difference in the mean age of patients among 2005, 2010, and 2016 (42.8 ± 15.2, 44.7 ± 15.0, and 49.4 ± 15.7, respectively; P < 0.01). Additionally, history of smoking among 3 different years (P = 0.045, Table 1). Regarding disease severity determined by CT, there was no significant difference in Lund-Mackay score (LMS) among groups. Interestingly, we found a significantly different trend in sinus dominancy, showing more common ethmoid sinus dominancy in patients in 2016 compared to those in the other years (P = 0.021; Table 1). In addition, we couldn't find any significant difference in nose-specific symptoms, olfactory impairment, presence of asthma, and blood eosinophilia (Table 1).

Risk factors for postoperative subjective outcomes

In total patients, 61.6% (n = 769) of patients were satisfied, 32.3% (n = 404) moderate, and 6.1% (n = 76) not satisfied, subjectively. To identify the risk factors related to postoperative subjective satisfaction, univariate analysis was performed. In univariate analysis (Table 2), we found that risk factors included LMS, the presence of nasal polyp, blood eosinophil count, and tissue eosinophil count. When we determined the cutoff point for these risk factors, the mean LMS was 9, blood eosinophil count was 210, tissue eosinophil count was 100. The risk factors identified by univariate analysis were further introduced into a stepwise regression model to identify the independent risk factors for moderate and poor postoperative subjective outcomes. In the multivariate analysis, it has been revealed that tissue and blood eosinophilia, and LMS were independent risk factors for moderate postoperative subjective outcomes (Table 3). When tissue eosinophil count was > 100, its adjusted OR was 2.079 (95% CI, 1.071–4.033; P = 0.030). When blood eosinophil count was > 210, its adjusted OR was 1.939 (95% CI, 1.287–2.919; P = 0.002). When the LMS was > 9, its adjusted OR was 2.742 (95% CI, 1.520–4.945; P = 0.001). However, due to too small number of patients in poor group (n = 76), we could not find any statistically significant risk factors for poor postoperative subjective outcomes (Table 3).
Table 2

Risk factors related to postoperative subjective satisfaction: univariate analysis

VariablesGood (n = 769)Moderate (n = 404)Poor (n = 76)P value
Sex0.070
Male498 (64.8)262 (64.9)39 (51.4)
Female271 (35.2)142 (35.1)37 (48.6)
Age46.2 ± 15.145.3 ± 15.247.1 ± 16.20.490
History of smoking0.393
Present285 (37.0)136 (33.6)26 (33.8)
Past19 (2.5)16 (4.0)4 (5.6)
Non465 (60.4)252 (62.4)46 (60.6)
CT finding
Lund-Mackay score5.5 ± 2.65.7 ± 2.85.8 ± 2.50.270
Mean score ≤ 9703 (91.4)351 (86.8)72 (94.4)0.021
Mean score > 966 (8.6)53 (13.3)4 (5.6)
Sinus dominancy
Ethmoid > maxillary154 (20.0)82 (20.2)20 (25.7)0.133
Ethmoid = maxillary267 (34.7)165 (41.0)29 (38.6)
Ethmoid < maxillary348 (45.3)157 (38.8)27 (35.7)
Olfactory function0.480
Anosmia242 (31.5)120 (29.8)29 (37.7)
Hyposmia287 (37.3)141 (35.0)29 (37.7)
Normosmia240 (31.2)143 (35.3)18 (24.6)
Atopic status
Positive308 (40.0)167 (41.4)27 (34.9)0.607
Bronchial asthma35 (4.6)17 (4.2)4 (4.7)0.889
Blood eosinophilia
Percentage, %3.7 ± 3.34.0 ± 3.63.6 ± 3.20.376
Count200.5 ± 221.0250.9 ± 244.1218.1 ± 222.10.031
Nasal polyp0.027
Presence388 (50.4)237 (58.7)38 (50.0)
Absence381 (49.6)167 (41.3)38 (50.0)
Tissue eosinophil count50.1 ± 65.258.1 ± 98.558.8 ± 55.10.482
Mean count ≤ 100705 (91.7)346 (85.7)63 (82.8)0.044
Mean count > 10064 (8.3)58 (14.3)13 (17.2)

Data are presented as number (%) or mean ± standard deviation.

CT = computed tomography.

Table 3

Risk factors related to post-operative subjective satisfaction: multivariate logistic regression analysis

Subjective satisfactionVariablesOR (95% CI)P value
ModerateTissue eosinophil count
≤ 1001
> 1002.079 (1.071–4.033)0.030
PB eosinophil count
≤ 2101
> 2101.939 (1.287–2.919)0.002
LMS
≤ 91
> 92.742 (1.520–4.945)0.001
PoorTissue eosinophil count
≤ 1001
> 1001.951 (0.523–7.273)0.320
PB eosinophil count
≤ 2101
> 2101.050 (0.425–2.596)0.915
LMS
≤ 91
> 91.565 (0.429–51713)0.498

OR = odds ratio, CI = confidence interval, LMS = Lund-Mackay CT score, PB = peripheral blood.

Data are presented as number (%) or mean ± standard deviation. CT = computed tomography. OR = odds ratio, CI = confidence interval, LMS = Lund-Mackay CT score, PB = peripheral blood.

Risk factors for postoperative objective outcomes

In terms of objective postoperative satisfaction, 73.0% (n = 912) of patients were satisfied, 23.8% (n = 297) moderate, and 3.2% (n = 40) not satisfied subjectively. In univariate analysis (Table 4), we found that risk factors included LMS (mean score > 5), sinus dominancy (ethmoid sinus > maxillary sinus), blood eosinophilia (mean % > 4 and mean count > 210), and tissue eosinophil count (mean count > 100). The risk factors that proved significant in the univariate analysis were included in the multivariate analysis. As a result, the maximum contribution for moderate postoperative objective outcome was tissue eosinophilia (OR, 2.952; 95% CI, 1.534–5.678; P = 0.001), followed by LMS (OR, 1.719; 95% CI, 1.134–2.607; P = 0.011). However, like subjective outcomes, we could not find any statistically significant risk factors for poor postoperative objective outcomes due to the small number of patients in the poor group (n = 40; Table 5).
Table 4

Risk factors related to endoscopic objective satisfaction: univariate analysis

VariablesGood (n = 912)Moderate (n = 297)Poor (n = 40)P value
Sex0.075
Male569 (62.4)202 (68.0)21 (52.5)
Female343 (37.6)95 (32.0)19 (47.5)
Age46.4 ± 15.644.8 ± 14.546.3 ± 15.50.319
History of smoking0.075
Present323 (35.5)109 (36.6)14 (35.0)
Past32 (3.4)10 (3.5)2 (5.0)
Non557 (61.1)178 (59.9)24 (60.0)
CT finding
Lund-Mackay score5.5 ± 2.56.1 ± 2.96.5 ± 2.00.000
Mean score ≤ 5463 (50.8)133 (44.8)12 (30.0)0.011
Mean score > 5449 (49.2)164 (55.2)28 (70.0)
Sinus dominancy0.000
Ethmoid > maxillary175 (19.2)61 (20.6)16 (40.0)
Ethmoid = maxillary315 (34.6)132 (44.3)13 (32.5)
Ethmoid < maxillary422 (46.4)104 (35.1)11 (27.5)
Olfactory function0.110
Anosmia275 (30.1)92 (31.1)20 (50.0)
Hyposmia345 (37.8)97 (32.6)12 (30.0)
Normosmia292 (32.0)108 (36.3)8 (20.0)
Atopic status
Positive372 (40.8)116 (39.2)17 (43.2)0.841
Bronchial asthma42 (4.6)13 (4.2)2 (4.7)0.873
Blood eosinophilia
Percentage, %3.5 ± 3.24.3 ± 3.84.0 ± 3.80.410
Mean % ≤ 4627 (68.7)178 (59.8)26 (64.1)0.010
Mean % > 4285 (31.3)119 (40.2)14 (35.9)
Count207.1 ± 215.7242.7 ± 251.7235.7 ± 233.40.042
Mean count ≤ 210596 (65.4)172 (57.8)32 (81.0)0.039
Mean count > 210316 (34.6)125 (42.3)8 (19.0)
Nasal polyp0.053
Presence444 (48.7)159 (53.6)24 (60.7)
Absence468 (51.3)138 (46.4)16 (39.3)
Tissue eosinophil count45.4 ± 60.367.7 ± 87.046.9 ± 50.70.053
Mean count ≤ 100842 (92.3)246 (82.7)36 (88.9)0.005
Mean count > 10070 (7.7)51 (17.3)4 (11.1)

Data are presented as number (%) or mean ± standard deviation.

CT = computed tomography.

Table 5

Risk factors related to endoscopic objective satisfaction: multivariate logistic regression analysis

Objective satisfactionVariableOR (95% CI)P value
ModerateTissue eosinophil count
≤ 1001
> 1002.952 (1.534–5.678)0.001
PB eosinophil %
≤ 41
> 41.176 (0.707–1.958)0.532
PB eosinophil count
≤ 2101
> 2101.279 (0.777–2.107)0.334
LMS
≤ 51
> 51.719 (1.134–2.607)0.011
Sinus dominancy
Ethmoid > maxillary1
Ethmoid = maxillary1.645 (0.670–2.212)0.519
Ethmoid < maxillary1.217 (0.941–2.876)0.081
PoorTissue eosinophil count
≤ 1001
> 1002.304 (0.456–11.674)0.313
PB eosinophil %
≤ 41
> 42.777 (0.734–10.507)0.132
PB eosinophil count
≤ 2101
> 2100.322 (0.078–1.324)0.116
LMS
≤ 51
> 53.243 (0.947–11.104)0.061
Sinus dominancy
Ethmoid > maxillary1
Ethmoid = maxillary0.425 (0.067–2.647)0.359
Ethmoid < maxillary1.316 (0.356–4.869)0.681

OR = odds ratio, CI = confidence interval, PB = peripheral blood, LMS = Lund-Mackay CT score.

Data are presented as number (%) or mean ± standard deviation. CT = computed tomography. OR = odds ratio, CI = confidence interval, PB = peripheral blood, LMS = Lund-Mackay CT score.

Prediction model for postoperative outcomes

To establish a risk model of postoperative objective outcome, we combined the moderate and poor group of patients and risk factors shown from the multivariate analysis were used. Based on logistic regression equation, multivariate logistic regression predictive model that calculated the risk of post-operative objective satisfaction after ESS for CRS was developed. The value of prediction probability (P) is P = 1 / (1 + A), where A = exp [−0.392 + 1.088 × tissue eosinophil count (> 100) + 0.123 × mean LMS (> 5) −0.366 × sinus dominancy (maxillary) + 0.064 × sinus dominancy (similar) + 0.200 × PB eosinophil % (4%) + 0.344 × PB eosinophil count (> 210)]. When the prediction probability value is greater than 0.5, the patient will be predicted as a good satisfaction group. And when the prediction probability value is less than 0.5, the patient will be predicted as a moderate/poor satisfaction group. To test the model if it had the ability to predict postoperative satisfaction, an alpha value of 5% was considered as the threshold for significance. Applying training samples showed that the accuracy, sensitivity, specificity, positive predictive value and negative predictive value was 70.30%, 76.19%, 42.13%, 86.29%, and 27.00%, respectively.

DISCUSSION

In this study, we demonstrated clinical features of CRS during the last 12 years, showing recent patients who underwent ESS in 2016 shows significant difference in age, ethmoid sinus dominancy, and smoking status, compared to those in the other years (all, P < 0.05; Table 1). Although we collected data from three different years (2005, 2010, and 2016) and four different seasons (spring: April, summer: July, autumn: October, and winter; January), the year and season of ESS performed did not influence the results of ESS (data not shown). Furthermore, we found that tissue eosinophilia, and LMS were significant independent risk factors for poor postoperative subjective and objective outcomes (Tables 3 and 5). Additionally, blood eosinophilia also contributed to poor subjective post ESS outcomes. Finally, with these risk factors, we established a prediction model for poor prognosis of ESS in patients with CRS. To our knowledge, this is the first study to comprehensively analyze the prognostic factors in multiple centers in Korea. Consistent with our study, previous studies have found that preoperative disease extents determined by CT and the presence of nasal polyps could be related to poor prognosis of ESS.1017 Grgic et al.17 reported that patients with a worse preoperative CT score showed less improvement postoperatively while they did not find a correlation between preoperative endoscopic score and postoperative recurrence. In another recent study, high CT score was recognized as an independent risk factor for poorly controlled CRS after ESS in Chinese population.10 Furthermore, it has been demonstrated that preoperative CT score of the olfactory cleft is predictive for worse olfactory outcome.18 In contrast, there are several studies showing that CT scores are not significantly related to revision surgery after ESS as well as subjective outcomes.919 In addition to severity of CRS determined by total CT score, it has been demonstrated that ethmoid-dominant characteristics in CT scans are likely to be a risk factor for poor prognosis after surgery.710 In our study, we found the predominance of ethmoid sinusitis in CT scans in patients with poor postoperative objective outcome in univariate analysis, but not in multivariate analysis. Thus, future studies are warranted to confirm these discrepancies. Another factor that significantly influenced postoperative outcome was eosinophilia especially in nasal tissue. We found that tissue eosinophil count (mean count > 100) was significantly related to poor postoperative outcomes both subjectively and objectively. Furthermore, in multivariate analysis, tissue eosinophilia was the most important contributor for poor objective outcome, showing adjusted OR 2.952. Clinical implication of tissue eosinophilia has been emphasized in numerous studies, especially in Western population.2021 The presence of eosinophilia in nasal tissue from CRSwNP patients is known to be related to disease severity, less improvement in both nose-specific and general quality of life, and higher recurrence rate of nasal polyp.2021 Even though definition of tissue eosinophilia is not defined yet, degree of eosinophilic infiltration may represent the distinct endotype of CRS, showing difference in not only histologic appearance but also in genetic and protein expression patterns of inflammatory mediators.22 It is widely accepted that CRSwNP is frequently associated with type 2 inflammation and tissue eosinophilia especially in Western countries.23 However, recent studies have revealed that the percentage of type 2 signature disease in patients with CRS is dramatically increasing in Asian countries including Korea, Japan, and China over the last 20 years.724 Supporting our results, Tokunaga et al.7 showed that tissue eosinophilia of 70 or higher eosinophils/HPF was significantly correlated with recurrence after ESS. Altogether, since the implication of tissue eosinophilia on disease course of CRS as well as prognosis of treatment outcome in Asia is rising, further studies identifying the role of tissue eosinophilia is warranted for Asian CRS patients. In addition, we also found that blood eosinophilia is closely related to subjective postoperative satisfaction, showing adjusted OR as 1.939. Similar to the results of the present study, it has been shown that blood eosinophilia over 5% was associated with poor postoperative outcomes in Japanese population.7 Aslan et al.25 also reported that mucosal and peripheral eosinophilia can be used as a marker to predict disease severity in nasal polyps and Kountakis et al.21 found a correlation between peripheral eosinophil count and preoperative CT scores as well as endoscopic scores. Although we found statistical significance in univariate analysis for the risk factors for objective postoperative outcome, we couldn't find statistical significance in multivariate analysis. Further studies are warranted to confirm whether peripheral blood eosinophilia is one of the risk factors for poor prognosis of ESS. Lastly, in this study, we established the prediction equation for poor prognosis of ESS by using potential risk factors identified from univariate and multivariate analysis including tissue eosinophil count (> 100), blood eosinophil count (> 210), blood eosinophil % (> 4%), LMS (> 5), and sinus dominancy. Since the prediction model is based on routine preoperative blood test, preoperative CT scan, and intraoperative pathology specimen, an otolaryngologist could easily predict the prognosis of ESS with tests that are required for CRS patients who underwent surgery and further tests are not necessary. Of note, our prediction model might provide useful clinical information for physicians to predict patients who needs strict postoperative management after ESS. Though prediction equation was not established as shown in our study, a recent study demonstrated prediction models for uncontrolled CRS after surgical treatment in Chinese population.10 Supporting our results, 2 separate models have been generated in their study, showing a pathologic model based on tissue eosinophil ratio > 0.206 and CT scores and a clinical model based on combination of blood eosinophil ratio > 0.025 and CT scores. This study has several limitations. First, the number of patients who were classified as poor postoperative outcome subjectively and objectively was too small. Future studies including enough number of patients will provide definite risk factors to distinguish moderate and poor postoperative outcomes. Second, preoperative and postoperative information was retrospectively obtained from medical records of 9 different tertiary medical centers. Therefore, there was no standardized patient care protocol and information about tissue collecting site could not be gathered. Future prospective studies are required to improve accuracy. Another possible limitation is that since all of the patients were recruited from tertiary medical centers, more severe patients with CRS could be included in this study. Further research will be helpful to generalize our findings.
  25 in total

Review 1.  International Consensus Statement on Allergy and Rhinology: Rhinosinusitis.

Authors:  Richard R Orlandi; Todd T Kingdom; Peter H Hwang; Timothy L Smith; Jeremiah A Alt; Fuad M Baroody; Pete S Batra; Manuel Bernal-Sprekelsen; Neil Bhattacharyya; Rakesh K Chandra; Alexander Chiu; Martin J Citardi; Noam A Cohen; John DelGaudio; Martin Desrosiers; Hun-Jong Dhong; Richard Douglas; Berrylin Ferguson; Wytske J Fokkens; Christos Georgalas; Andrew Goldberg; Jan Gosepath; Daniel L Hamilos; Joseph K Han; Richard Harvey; Peter Hellings; Claire Hopkins; Roger Jankowski; Amin R Javer; Robert Kern; Stilianos Kountakis; Marek L Kowalski; Andrew Lane; Donald C Lanza; Richard Lebowitz; Heung-Man Lee; Sandra Y Lin; Valerie Lund; Amber Luong; Wolf Mann; Bradley F Marple; Kevin C McMains; Ralph Metson; Robert Naclerio; Jayakar V Nayak; Nobuyoshi Otori; James N Palmer; Sanjay R Parikh; Desiderio Passali; Anju Peters; Jay Piccirillo; David M Poetker; Alkis J Psaltis; Hassan H Ramadan; Vijay R Ramakrishnan; Herbert Riechelmann; Hwan-Jung Roh; Luke Rudmik; Raymond Sacks; Rodney J Schlosser; Brent A Senior; Raj Sindwani; James A Stankiewicz; Michael Stewart; Bruce K Tan; Elina Toskala; Richard Voegels; De Yun Wang; Erik K Weitzel; Sarah Wise; Bradford A Woodworth; Peter-John Wormald; Erin D Wright; Bing Zhou; David W Kennedy
Journal:  Int Forum Allergy Rhinol       Date:  2016-02       Impact factor: 3.858

2.  The incidence of concurrent osteitis in patients with chronic rhinosinusitis: a clinicopathological study.

Authors:  Jivianne T Lee; David W Kennedy; James N Palmer; Michael Feldman; Alexander G Chiu
Journal:  Am J Rhinol       Date:  2006 May-Jun

3.  The status of the olfactory cleft may predict postoperative olfactory function in chronic rhinosinusitis with nasal polyposis.

Authors:  Dae Woo Kim; Jin-Young Kim; Sea-Yuong Jeon
Journal:  Am J Rhinol Allergy       Date:  2011 Mar-Apr       Impact factor: 2.467

4.  Surgical treatment for nasal polyposis: predictors of outcome.

Authors:  Marko Velimir Grgić; Hrvoje Ćupić; Livije Kalogjera; Tomislav Baudoin
Journal:  Eur Arch Otorhinolaryngol       Date:  2015-01-30       Impact factor: 2.503

Review 5.  Pathogenesis of chronic rhinosinusitis: inflammation.

Authors:  Koen Van Crombruggen; Nan Zhang; Philippe Gevaert; Peter Tomassen; Claus Bachert
Journal:  J Allergy Clin Immunol       Date:  2011-08-24       Impact factor: 10.793

6.  Measurement and comparison of health utility assessments in chronic rhinosinusitis.

Authors:  Elisabeth H Ference; Vanessa Stubbs; Alcina K Lidder; Rakesh K Chandra; David Conley; Pedro C Avila; Annemarie G Hirsch; Jin-Young Min; Stephanie Shintani Smith; Robert C Kern; Bruce K Tan
Journal:  Int Forum Allergy Rhinol       Date:  2015-06-16       Impact factor: 3.858

7.  JESREC score and mucosal eosinophilia can predict endotypes of chronic rhinosinusitis with nasal polyps.

Authors:  Tsuguhisa Nakayama; Naoki Sugimoto; Naoko Okada; Tadao Tsurumoto; Ryoto Mitsuyoshi; Shinya Takaishi; Daiya Asaka; Hiromi Kojima; Mamoru Yoshikawa; Yasuhiro Tanaka; Shin-Ichi Haruna
Journal:  Auris Nasus Larynx       Date:  2018-09-19       Impact factor: 1.863

8.  Categorization and clinicopathological features of chronic rhinosinusitis with eosinophilic mucin in a korean population.

Authors:  Suk-Ho Lee; Hak-Jun Kim; Jin-Woo Lee; Young-Hoon Yoon; Yong-Min Kim; Ki-Sang Rha
Journal:  Clin Exp Otorhinolaryngol       Date:  2015-02-03       Impact factor: 3.372

9.  Enhanced Type 2 Immune Reactions by Increased IL-22/IL-22Ra1 Signaling in Chronic Rhinosinusitis With Nasal Polyps.

Authors:  Dong Kyu Kim; Ara Jo; Hee Suk Lim; Jin Youp Kim; Kyoung Mi Eun; Jayoung Oh; Joon Kon Kim; Seong Ho Cho; Dae Woo Kim
Journal:  Allergy Asthma Immunol Res       Date:  2020-11       Impact factor: 5.764

10.  Comparison Between Signature Cytokines of Nasal Tissues in Subtypes of Chronic Rhinosinusitis.

Authors:  Dong Kyu Kim; Kyoung Mi Eun; Min Kyung Kim; Deuktae Cho; Sun A Han; Sang Yoon Han; Yuju Seo; Dong Han Lee; Seong Ho Cho; Dae Woo Kim
Journal:  Allergy Asthma Immunol Res       Date:  2019-03       Impact factor: 5.764

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Review 1.  Managing Chronic Rhinosinusitis with Nasal Polyps in the Elderly: Challenges and Solutions.

Authors:  Tyler Merrill; Alissa Kanaan
Journal:  Clin Interv Aging       Date:  2022-05-02       Impact factor: 3.829

  1 in total

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