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Turkish Archives of Otorhinolaryngology logoLink to Turkish Archives of Otorhinolaryngology
. 2019 Aug 14;58(1):24–29. doi: 10.5152/tao.2020.4685

Translation and Validation of Chronic Otitis Media Benefit Inventory (COMBI) in Turkish Language

Hakan Kara 1,, Can Doruk 1, Mehmet Çelik 1, Beldan Polat 1, Vedat Topsakal 2, Kadir Serkan Orhan 1
PMCID: PMC7162599  PMID: 32313891

Abstract

Objective

The aim of this study was to translate the Chronic Otitis Media Benefit Inventory (COMBI) into Turkish and evaluate the questionnaire’s reliability in assessing benefit outcomes in patients after ear surgery.

Methods

A total of 30 patients with chronic otitis media who underwent ear surgery were asked to fill out the translated Turkish version of the COMBI questionnaire six months after their surgery twice, 10 days apart. The patients were divided into two groups in two different ways based on surgical and audiological outcomes. These were surgical success (SS), surgical failure (SF), audiological success (AS), audiological failure (AF) groups. Student’s -t test was performed to show the differences in the COMBI scores of the groups. Cronbach’s alpha value was calculated to test internal consistency, Pearson’s correlation coefficient was measured to demonstrate test-retest reliability and factor analysis was run.

Results

The average score of the SS group was 51.08 and significantly higher than the score of the SF group (42.40) (p=0.012). There was, however, no statistically significant difference between the average scores of the AS and the AF groups (p=0.330). A Cronbach’s alpha value of 0.862 was found. Pearson’s r value was calculated 0.810. Factor analysis showed that a three-factor solution explained the 70.2% of the variance.

Conclusion

The Turkish version of the COMBI is a valid test with high test-retest reliability. It should be used with objective assessment tools for better understanding how patients benefit from the surgery.

Keywords: Otitis media, tympanoplasty, quality of life, reliability and validity, patient health questionnaire

Introduction

Chronic otitis media (COM) is a common health problem with a prevalence of <1% in high-income countries to up to 4% in developing countries (1). Along with chronic symptoms of ear drainage and hearing loss, chronic otitis may lead to devastating complications such as meningitis, labyrinthitis, facial nerve paralysis. Furthermore, COM deteriorates the quality of life (QoL) of the patients by affecting their social and work lives. Examples are malodorous ear drainage which causes patients to avoid getting involved in social activities, hearing loss which affects the home and work life of patients.

Measuring the Health-Related Quality of Life (HRQoL) scores of patients using the Patient-Reported Outcome Measures is a rapidly progressive field to assess patients’ symptoms and to determine personalized treatment (2). There are many QoL questionnaires available to assess COM, such as the Chronic Otitis Media Outcome Test-15 (3), the Chronic Otitis Media-5 (4) questionnaire, and the newest Chronic Otitis Media Questionnaire-12 (COMQ-12) developed by Phillips et al. (5).

Chronic Otitis Media Benefit Inventory (COMBI) is recently developed by Phillips et al. (6) to assess the changes in patient’s symptoms with treatment. Information about how patient’s quality of life measures are affected by surgical intervention can be determined with COMBI.

The aim of this study was to translate the COMBI into Turkish, evaluate the internal consistency, the test-retest reliability of the test, and to validate the adaptation to Turkish language for further use in studies.

Methods

Ethics Committee Approval for the study was taken from İstanbul University School of Medicine Ethics Committee for Scientific Research with file number 2019/50.

Study Design

Thirty patients that were older than 18 years of age, had COM and underwent ear surgery were enrolled in our prospective study. After a 6-month waiting period, which is considered to be the recovery period after surgical intervention, all patients were requested to fill out the COMBI questionnaire twice, 10 days apart. We excluded the patients who were not able to give their informed consent. Also, patients who had prior tympanoplasty or mastoidectomy were excluded from the study.

COMBI Questionnaire

The COMBI questionnaire contains 12 items that dynamically assesses the changes in the severity and the frequency of the symptoms and the QoL of the patients who underwent ear surgery for COM. The 5-point Likert scale was used to score each question in a descending order from 5 (much better) to 1 (much worse).

These 12 items were constructed by Phillips at al. (5) from the static assessment tool COMQ-12 which was translated into Turkish and validated in our previous study (7).

The first 7 items of the questionnaire inquire about the changes in the ear symptoms following surgical intervention. The next four items assess the effects of surgery on lifestyle, work and the use of healthcare services of the patient. The last item evaluates the changes in the overall well-being of the patients after the operation.

Translation and Back-Translation

An official permission was obtained from the main author to translate and validate the Turkish version of the COMBI questionnaire. Then, the COMBI was translated into Turkish by the second author and checked by the senior authors. Turkish questions were back-translated into English by a native English speaker after some adjustments were made. No differences were observed between the two versions of the questionnaire; hence, the adaptation was verified.

Subjects

Thirty COM patients that underwent ear surgery were enrolled in the study. All patients were native-Turkish speakers older than 18 years of age and operated on by the first two and the fourth authors. Patients who were able to give their informed consent for the study were asked to fill out the COMBI at the 6th month follow-up visit after their surgery. To understand test-retest reliability patients were asked to complete the questionnaire for a second time 10 days after their first responses.

Additional information about the study group were collected. These were demographic data of patients, otoscopic examination and pure-tone audiometry (PTA) (average of 0.5,2.0,4.0 kHz) status of the ears prior to and six months after the surgery and the type of surgery done.

Otoscopic findings prior to the surgery were classified into 5 groups: <1/4 dry perforation, >1/4 dry perforation, visible cholesteatoma (VC), retraction pocket without visible cholesteatoma (RPWVC) and wet ear.

Otoscopic findings after six months of the surgery were classified into 5 groups: 1) Intact tympanic membrane for tympanoplasty and dry cavity without recurrence of cholesteatoma for mastoidectomy was defined as “normal,” 2) <1/4 dry perforation 3) >1/4 dry perforation, 4) wet ear and 5) recurrence of cholesteatoma. Cases that did not fall under the “normal” definition at the postoperative 6th month were included in the surgical failure (SF) group, and patients with “normal” otoscopic results were included in the surgical success (SS) group.

Pre-and post-operative PTA were performed in all patients. Air and bone conduction (AC, BC) thresholds and air-bone gap (ABG) were measured. PTA statuses of the relevant ears were classified into two groups: Audiological failure (AF) and audiological success (AS). Achievement of 10 decibels (dB) or more improvement at the average of 0.5, 2.0, 4.0 kilohertz (kHz) on AC thresholds were classified as AS. A less then 10 dB decrease in AC thresholds and any increase in AC thresholds were classified as AF.

Statistical Analysis

IBM Statistical Package for the Social Sciences version 22.0 (IBM SPSS Corp.; Armonk, NY, USA) was used to perform the statistical analysis. A value of p<0.05 was considered statistically significant. Seven different tests were used:

  1. Descriptive analysis was made to report demographic data.

  2. Measurement of skewness and the Shapiro-Wilk test were used to evaluate the normality of the data.

  3. Parametric independent-samples t-test was used to compare the overall scores of the SF and SS groups and of the AF and AS groups. The validation of the questionnaire was made based on these comparisons.

  4. Cronbach’s alpha was calculated to assess inter-item correlation and internal consistency of the questionnaire. A coefficient of 0.70 or higher was considered reliable (8).

  5. Test-retest reliability was shown by using Pearson’s correlation coefficient. Correlation coefficients varied from 0 (no reliability) to 1 (perfect reliability). A value of >0.7 was considered acceptable reliability in the literature (9).

  6. Kaiser-Meyer-Olkin (KMO) and Bartlett’s tests were used to measure the adequacy of sampling for performing factor analysis. A value of >0.5 was considered acceptable in line with the literature (10).

  7. Factor analysis was performed using principal component extraction with varimax rotation. The factor loading coefficient was measured to show the correlation between the individual item and the underlying factor.

Results

A total of 30 patients (19 females, 11 males) completed the COMBI questionnaire and the retest. The mean age of the patients + standard deviation (SD) was 36.8+12.5 years (range: 18 to 59 years). Descriptive analysis is shown in Table 1.

Table 1.

Descriptive analysis of COMBI scores, AC thresholds, age and sex of patients

Total (n=30) SS Group (n=25) SF Group (n=5) AS Group (n=19) AF Group (n=11)
COMBI Score 49.63±7.25 (31–60) 51.08±6.36 (39–60)* 42.4±7.77 (31–51)* 50.63±8.09 (31–60)+ 47.91±5.43 (39–55)+
Preop AC th (dB) 42.6±17.4 41.48±16.63 48.2±22.11 42.58±18.97 42.64±15.17
Postop AC th (dB) 30.3±20.9 30.24±21.78 30.6±17.91 22.37±16.41 44±21.35
Age 36.8 (18–59) 34.84 (18–59) 47 (36–59) 36.42 (18–59) 37.64 (18–59)
Sex
Female 19 14 5 13 6
Male 11 11 0 6 5

Data are presented as Mean+Standard deviation (minimum-maximum values).

*

p value for difference between groups is 0.012.

+

p value for difference between groups is 0.330.

SS: surgical success; SF: surgical failure; AS: audiological success; AF: audiological failure; SD: standard deviation, AC th: air-conduction threshold

Tympanoplasty was performed in 20 patients. Of these, 15 had >1/4 dry perforation, three had <1/4 perforation and the remaining two had RPWVC before the surgery. Two of the patients underwent ossicular chain reconstruction (OCR). Tympanostomy tube was inserted in one patient. Four patients were included in the SF group because they had <1/4 perforation in the 6th month of their operations. Sixteen patients were considered as SS due to normal otoscopy after the surgery. An improvement of 10 dB or more in AC thresholds were achieved in 15 patients, and the remaining five patients were included in the AF group.

Canal wall down (CWD) mastoidectomy + tympanoplasty was done in five patients. One of them had wet ear prior to the surgery. One patient had VC. One patient had >1/4 dry perforation and tympanosclerosis. The remaining two patients had RPWVC. OCR was only performed in the patient with >1/4 dry perforation and tympanosclerosis. All patients had normal otoscopy after surgery, and they were included in the SS group. Three of five patients showed 10 dB or more improvement in AC thresholds and were included in the AS group.

CWD mastoidectomy without tympanoplasty was performed in two patients. Both of these patients had VC prior to surgery. Both of these patients were included in the SS group, but at the same time in the AF group because of their increase in AC thresholds.

Canal wall up (CWU) mastoidectomy + tympanoplasty was performed in two patients. One had VC. The other had RPWVC and cholesterol granuloma was seen during the operation. Both received OCR. The patient with VC had wet ear six months after the surgery and included in the SF group, but also in the AS group since she had a 15 dB decrease in AC threshold. The other patient had normal otoscopy, but a 12 dB increase in AC threshold after the surgery and was included in the AF group.

Only one patient who had VC prior to surgery underwent atticotomy + tympanoplasty + OCR. She was included in the SS group since she had no abnormal otoscopic findings, but in the AF group because of an 8 dB gain in AC threshold.

As a result, only five patients were evaluated in the SF group and 11 patients in the AF group. Only one patient met the criteria of both surgical and audiological failure (Table 2).

Table 2.

All patients’ pre- and post-operative otoscopic examination and PTA status

N Age Sex Operation Side Preop otoscopy Postop otoscopy Preop AC th Postop AC th AC th change Preop ABG Postop ABG ABG change Score test Score retest Surg outcome Audiol outcome
1 26 F AT+TP+OCR L CHOLESTEATOMA N 36 28 8 35 15 20 43 55 SS AF
2 59 M CWD M R CHOLESTEATOMA N 70 80 −10 43 26 17 50 51 SS AF
3 34 M CWD M R CHOLESTEATOMA N 52 58 −6 30 40 −10 55 55 SS AF
4 47 F CWD M+TP L RPWVC N 80 65 15 45 35 10 44 45 SS AS
5 45 F CWD M+TP L WET EAR N 60 55 5 45 37 8 53 54 SS AF
6 37 F CWD M+TP L RPWVC N 48 71 −23 43 66 −23 45 46 SS AF
7 45 F CWD M+TP R CHOLESTEATOMA N 73 43 30 36 10 26 56 56 SS AS
8 52 F CWD M+TP+OCR R >1/4 DRY PERFORATION+ TYMPANOSCLEROSIS N 40 22 18 27 5 22 50 50 SS AS
9 59 F CWU M+TP+OCR R RPWVC WET EAR 65 50 15 35 25 10 31 31 SF AS
10 30 M CWU M+TP+OCR L CHOLESTEATOMA N 43 55 −12 31 42 −11 46 46 SS AF
11 24 F TP L RPWVC N 35 15 20 34 10 24 59 60 SS AS
12 45 M TP L <1/4 DRY PERFORATION N 36 17 19 31 7 24 60 60 SS AS
13 46 F TP L >1/4 DRY PERFORATION <1/4 DRY PERFORATION 75 47 28 40 9 31 40 31 SF AS
14 32 M TP L >1/4 DRY PERFORATION N 43 36 7 31 28 3 41 48 SS AF
15 18 M TP L >1/4 DRY PERFORATION N 15 10 5 10 5 5 50 56 SS AF
16 34 F TP L >1/4 DRY PERFORATION N 45 11 34 28 8 20 60 59 SS AS
17 34 F TP L <1/4 DRY PERFORATION N 26 25 1 26 22 4 54 46 SS AF
18 45 F TP L >1/4 DRY PERFORATION N 40 36 4 30 20 10 39 50 SS AF
19 24 F TP L >1/4 DRY PERFORATION N 38 15 23 38 15 23 48 51 SS AS
20 39 M TP L >1/4 DRY PERFORATION N 40 23 17 29 13 16 48 45 SS AS
21 18 F TP R >1/4 DRY PERFORATION N 35 15 20 30 10 20 49 51 SS AS
22 40 F TP R >1/4 DRY PERFORATION <1/4 DRY PERFORATION 45 16 29 35 13 22 48 53 SF AS
23 37 M TP R >1/4 DRY PERFORATION N 22 6 16 9 6 3 60 56 SS AS
24 54 F TP R >1/4 DRY PERFORATION <1/4 DRY PERFORATION 36 30 6 30 22 8 51 55 SF AF
25 36 F TP R <1/4 DRY PERFORATION <1/4 DRY PERFORATION 20 10 10 20 10 10 42 48 SF AS
26 38 M TP R >1/4 DRY PERFORATION N 25 13 12 24 8 16 59 59 SS AS
27 18 M TP R >1/4 DRY PERFORATION N 20 10 10 20 10 10 45 45 SS AS
28 53 F TP+OCR L >1/4 DRY PERFORATION N 58 22 36 33 12 21 59 59 SS AS
29 18 M TP+OCR L >1/4 DRY PERFORATION N 27 15 12 17 5 12 52 52 SS AS
30 19 F TP+TUBE INS. L RPWVC N 30 10 20 27 7 20 52 52 SS AS

TP: tympanoplasty; AT: atticotomy; CWD: canal wall down; CWU: canal wall up; M: mastoidectomy; OCR: ossicular chain reconstruction; L: left; R: right; RPWVC: retraction pocket without visible cholesteatoma; SS: surgical success; SF: surgical failure; AS: audiological success; AF: audiological failure; AC th: air-conduction threshold; ABG: air-bone gap; Surg: surgical, Audiol: audiological

Mean preoperative and postoperative AC thresholds were 42.6+17.4 dB and 30.3+20.9 dB, respectively. While mean ABG prior to surgery was 30.4+9.05, it was 18.03+14.2 after the 6-month recovery period.

Average scores for the first test and the retest of the COMBI questionnaire were 49.6+7.2 and 50.8+7.1, respectively.

The Shapiro-Wilk test was used to assess the distribution of the data. P-values for the overall scores of the first test of COMBI were 0.232 and 0.814 for the SS and the SF groups, respectively. Skew values for the same groups were −0.086 and −0.608, respectively.

In addition, the p-values for the overall scores of the AS and the AF groups for the first test of COMBI were 0.101 and 0.546, respectively. Skew values were −0.651 and −0.324, respectively. Since all p-values were >0.05, and all skew values were between +1 and −1, the distribution of the data was considered as normal. Therefore, parametric tests were chosen for further analysis.

The COMBI score of the SS group (51.08+6.35) was significantly higher than that of the SF group (42.40+7.76), with a mean difference value of 8.68 (p=0.012).

However, there was no statistically significant difference between the COMBI scores of the AS group (50.63+8.09) and the AF group (47.91+5.43) (p=0.330).

Cronbach’s alpha value was 0.862 and since higher than 0.70, indicated high inter-item correlation and the internal consistency for the questionnaire.

Pearson’s correlation between the total score of first test and the total score of the retest was calculated as r=0.810 at a significance level of 0.01. This shows that the test and retest scores were correlated; hence, test-retest reliability was considered high.

The KMO measure of sample adequacy showed a ratio of 0.550 with a significance of less than 0.001 using Bartlett’s test of sphericity. Thus, sample adequacy was considered sufficient to run factor analysis. Factor analysis using principal component extraction with varimax rotation produced a three-factor solution that explained 70.2% of the variances. Factor loading coefficients were higher than 0.5 for all items, which show the correlation between an individual item and its underlying factor (Table 3).

Table 3.

Factor loading coefficients

COMBI question Factor (rotated component matrix) PC
1 (Impact on patient’s life) 2 (Hearing status) 3 (Ear status)
1 0.909 0.900
2 0.843 0.735
3 0.718 0.362 0.656
4 0.629 0.534
5 0.788 0.716
6 0.778 0.763
7 0.823 0.753
8 0.581 0.427 0.562
9 0.704 0.523
10 0.863 0.785
11 0.845 0.839
12 0.614 0.386 0.369 0.662

PC: principal component analysis

Discussion

This study is the first to validate the Turkish adaptation of the recognized and validated English HRQoL questionnaire that was developed for COM patients undergoing ear surgery. To date, the questionnaire has been translated only into Dutch (11).

Although patients with COM have similar pathophysiologic causes, the effects of the disease on patients show great variety. While some patients are asymptomatic and the condition is identified during routine check-up, in others the disease can severely deteriorate QoL. Hence, several questionnaires that evaluate HRQoL in COM patients have been developed. These questionnaires, however, determine the need for treatment and the expected benefits from an intervention. Patient-reported outcome measures mostly evaluate the impact of the intervention on patient’s life. The Glasgow Benefit Index is a commonly used dynamic assessment tool for otolaryngology surgeries, is, however, not specific to ear surgery (12). Therefore, the COMBI questionnaire was created to combine HRQoL and patient-reported outcome measures for COM.

In our prospective study, the patients were divided into two different groups twice according to their surgical and hearing outcomes. By doing so, our main goal was to validate the Turkish version of the COMBI whilst showing the differences in the COMBI scores of the success and the failure groups. The average score of the SS group was 51.08+6.36. This average score was higher than that of the SF group, which was 42.40+7.77, and statistically significant (p<0.05). However, patients 22 and 24, i.e., 2 of the 5 patients in the SF group, had a total score of 48 and 51, respectively. Their total scores of the questionnaire were close to the average score of the SS group. These unexpectedly high scores may be explained in two ways. Patient 22 showed 29 dB improvement in AC threshold and ABG after surgery. Whereas the patient’s tympanic membrane perforation remained after the surgery, the size of the perforation had decreased sufficiently enough to prevent symptoms of recurrent drainage. Patient 24 was the only one included in both the SF and the AF groups. The patient also had a minimal failure and ear symptoms were recovered after surgery. Her hearing outcome was also considered as failure because she showed only 6 dB decrease in AC threshold and 8 dB in ABG. Nevertheless, some individuals can discriminate even minor differences in hearing and can score higher than expected, as was the case of this patient. These kinds of diversities bring forth the importance of patient-based assessment tools.

No statistically significant difference was found between the average scores of the AF and the AS groups. Ten of the 11 patients in the AF group had successful surgical outcomes. All 11 patients had neither a draining ear nor bad smell in the operated ear. Only three of the 11 patients showed deterioration in AC threshold. The remaining eight patients had a decrease of less than 10 dB in their AC threshold. All of these causes can explain why the groups (AS and AF) had similar scores.

These results may indicate that COM patients are mostly satisfied with the surgical outcomes. Assessing the results of a procedure only by objective methods may lead to the under- or over-assessment of subjective (patient’s point of view) outcomes. Therefore, it is very important to integrate self-assessment QoL questionnaires, such as otoscopic examination and PTA status into objective tools, as we have done in our study.

We also calculated a reliable Cronbach’s alpha value of 0.862, which is similar to that of the original English study (0.911) (6). Pearson’s correlation r value (0.810) demonstrated that test and retest reliability was consistent. Two patients (numbers 1 and 18), however, showed more than 10 points of difference in their COMBI scores for test and retest reliability. This may be due to test-retest variability.

Furthermore, factor analysis showed a three-factor solution that explained 70.2% of the variances in our study, which is similar to that of the original study. Phillips et al. (6) named these factors as changes in hearing, in ear symptoms and in healthcare use. In their study, questions 3, 4, 8 and 9 were loaded onto factor 1 about hearing which assess the changes in hearing at home and in a group, in problems when performing daily activities, and in fear of water exposure, respectively. Questions 1, 2, 5, 6 were loaded onto factor 2 (ear symptoms) corresponding to the changes in ear discharge, bad smell in ear, ear discomfort, and dizziness, respectively. Questions about the changes in general practitioner attendance (Question 10) and in requirement for drugs (Question 11) were loaded onto factor 3 (healthcare use).

In our study, questions 8, 9, 10, 11, 12 were loaded onto factor 1 which is about the effects on patient life, and questions 3, 4, 5, 7 were loaded onto factor 2 (hearing status). Questions 1, 2, 6 were loaded onto factor 3 (ear status).

Conclusion

Our study demonstrated the Turkish version of the COMBI questionnaire (appendix) to be a reliable and valid test for assessing QoL after ear surgery in patients with COM. It is appropriate to be used with objective assessment tools to better understand the outcomes of ear surgeries and their effects on the QoL of Turkish speaking patients.

While objective assessment tools should be used to show the benefits of the surgeries performed, self-assessment tools like QoL questionnaires should be added in order to better estimate the changes in the QoL of patients. Self-assessment tools can help doctors and healthcare providers to understand patients’ feelings and thoughts about the intervention they have undergone.

Appendix. Turkish version of COMBI Questionnaire

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Footnotes

Ethics Committee Approval: Ethics committee approval was received for this study from the Scientific Research Ethics Committee of İstanbul University School of Medicine (2019/50).

Informed Consent: Written informed consent was obtained from the patients who participated in this study.

Peer-review: Externally peer-reviewed.

Conflict of Interest: The authors have no conflicts of interest to declare.

Author Contributions: Concept - H.K., C.D., M.Ç., B.P., V.T., K.S.O.; Design - H.K., C.D., M.Ç., B.P., V.T., K.S.O.; Supervision - H.K., C.D., M.Ç., B.P., V.T., K.S.O.; Fundings - B.P., V.T., K.S.O.; Data Collection and/or Processing - H.K., C.D., B.P.; Analysis and/or Interpretation - H.K., B.P., C.D.; Literature Review - H.K., B.P., C.D.; Writing - H.K., C.D., M.Ç., B.P., V.T., K.S.O.; Critical Reviews - H.K., C.D., M.Ç., B.P., V.T., K.S.O.

Financial Disclosure: The authors declared that this study has received no financial support.

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