Validation of the Korean version of the walking impairment questionnaire in patients with peripheral arterial disease

Abstract

Purpose

Intermittent claudication is the most common early symptom of peripheral arterial occlusive disease. Walking impairment questionnaire (WIQ) is a short, inexpensive, easy-to-complete questionnaire to assess intermittent claudication and can provide data of usual walking. The purpose of this study is to validate the new Korean version of WIQ.

Methods

Total 51 patients with claudication were enrolled. While 4 patients were dropped out, 47 patients with claudication into were divided groups based on the treatment received: surgery (n = 33) and medication (n = 14). The surgery group was subdivided into the bypass (n = 13) and intervention (n = 20) groups. WIQ score, ankle-brachial index (ABI), and treadmill test scores were assessed initially and after 12 weeks.

Results

The WIQ scores were significantly correlated with ABI and pain-free walking distance (PFWD) and maximum walking distance (MWD) in all groups (except for MWD in the intervention group). Speed and stair-climb scores (2 WIQ domains) were well correlated with ABI, PFWD, and MWD. Distance scores were mostly correlated with ABI, PFWD, and MWD in all groups except ABI in the bypass and intervention groups and MWD in the bypass group. Reproducibility was observed in all groups (intraclass correlation coefficient > 0.8).

Conclusion

The Korean version of the WIQ is valid and reproducible, and can be effectively used to assess Korean patients with intermittent claudication.

INTRODUCTION

Intermittent claudication (IC) is a walking-related impairment involving specific ischemic pain of the lower extremity, as a result of peripheral arterial occlusive disease (PAD). This PAD symptom specifically worsens after exercise such as walking or stair-climbing, although it usually disappears after a short rest period [1,2]. Assessments of the walking ability of PAD patients are important both during daily life and in the hospital. Hence, there is a need for a measurement method that can be easily used by patients to determine whether the disease severity has worsened [3,4,5,6,7,8,9].

The conventional test for IC usually involves the treadmill exercise test, wherein the distance of walking is measured until the initiation of pain or pain intolerance develops. This treadmill test is considered to be one of the most important objective tests [10]. However, it does not represent the walking ability of patients during daily life, and is impossible to perform without treadmill equipment or medical professionals. Moreover, this test is not practical in epidemiologic research. Therefore, Regensteiner, Hiatt, and others developed the walking impairment questionnaire (WIQ), which makes it simple and easy for patients to self-assess their walking ability [11,12].

The WIQ measures walking distance, speed, and the ability to climb stairs. The WIQ can objectively measure PAD symptoms, and its use has been recommended in the Trans-Atlantic Inter-Society Consensus [13]. The WIQ has been translated into several languages, including Dutch, German, Italian, Spanish, Swedish, Japanese, and Chinese, and is used worldwide [14,15,16,17,18,19,20]. Translation of this questionnaire into the native language of the patients is essential for accurate assessment. Hence, a Korean version of the WIQ is important to evaluate Korean PAD patients. In the present study, we aimed to develop the Korean version of the WIQ and to validate its use among Korean PAD patients.

METHODS

Patient enrollment

We consecutively enrolled Korean patients diagnosed with PAD at 3 hospitals in 1 medical college. The inclusion criteria were as follows: age of 19–80 years; chronic symptoms of IC; ankle-brachial index (ABI) of <0.9; if ABI was abnormally high (>1.3), then toe-brachial index of <0.7; ability to perform treadmill test involving 12% gradient and 2.4-km/hr speed; informed consent for participating in the study. The exclusion criteria were as follows: critical limb ischemia with pain at rest or ischemic ulcers; ankle blood pressure <40 mmHg; claudication induced by other causes such as spinal stenosis, arthritis, or cerebrovascular disease; high risk of acute coronary syndrome during the treadmill test; and anticipated noncompliance. The patients were treated either by medication, endovascular intervention, or open bypass based on the decision of the vascular surgeons. All participants eligible and willing to attend gave their written informed consent prior to their enrollment.

This study was approved by the Institutional Review Board of the Seoul National University Hospital (approval number: 1207-025-416).

Korean version of the WIQ

The WIQ was translated in compliance with Beaton's guidelines while respecting “the process of cross-cultural adaptation of self-report measures” [21]. First, the original English questionnaire was translated to the Korean version by three Korean bilingual translators. Thereafter, the translated Korean version was translated back to the English version by another three bilingual translators whose native language was English. After discussion among the authors, the final Korean version was selected. Examples of scoring and samples of main questions that were used in this version of the WIQ are presented in Supplementary material 1.

Study design for validation of WIQ

We aimed to validate the Korean version of WIQ, by determining the reproducibility of the WIQ scores and its correlation with other objective indices such as ABI or treadmill test scores. The enrolled patients were divided into groups according to the treatment received: surgery and medication group. The surgery group was further divided into the bypass and intervention groups, for subgroup analysis. The objective indices of the patients included ABI, initial claudication distance, and maximum walking distance (MWD). All components of WIQ, including distance, speed, and stairclimbing scores were also analysed.

The ABI and treadmill tests, along with WIQ questionnaire scoring, were performed at baseline (Fig. 1). These tests and the questionnaire were again administered after 3 months. At initial stage of the study, it is planned that the data of the surgery group, including the bypass and intervention groups, would be analysed as one group like the medication group by using the paired t-test. Thereafter, the surgery group was split into the bypass and the intervention groups due to different severity of surgical site pain in early stage between the open surgery and the minimal invasive intervention. To test for reproducibility, patients were again administered the WIQ questionnaire at 1 month after treatment. A period of 1 month was considered to be sufficient time for the patients to forget the initial questionnaire data, but was not believed to be sufficient to exhibit the results of medication. However, in the surgery group, major clinical changes may be evident during the first month itself, and hence, 1- and 3-month data were used to determine reproducibility. The intraclass correlation test was used to assess reproducibility. An intraclass correlation coefficient (ICC) between 0.8 and 1, between 0.6 and 0.79, and <0.6 was considered to very reliable, moderately reliable, and not reliable, respectively. Sample size was set as size in previous study with other language [22] and using G^*Power software (version 3.0.10, Faul et al., Germany) that calculated required sample size was 34 in 2 tailed t-test with effect size 0.5, alpha error 0.05, and power (1-beta error) 0.8. Statistical computations were performed using SAS 9.3 (SAS Institute Inc., Cary, NC, USA), for the 1-way analysis of variance, paired t, repeated-measures analysis of variance, and Pearson correlation tests, as well as the IBM SPSS Statistics ver. 20.0 (IBM Co., Armonk, NY, USA) for the intraclass correlation test.

Fig. 1. Study flowchart for testing for validity and reproducibility. ABI, ankle-brachial index; WIQ, walking impairment questionnaire.

RESULTS

Study population

From March 2013 to May 2014, we enrolled 51 Korean PAD patients (Fig. 2). Four patients were excluded from the study after enrollment; the reasons included treatment for angina pectoris in 1 patient and loss to follow-up in 3 patients; 2 of these patients were from the intervention group, and the other 2 were from the medication group. Finally, a total of 47 patients (13 from the bypass group, 20 from the intervention group, and 14 from the medication group) completed the follow-up. The patient demographics are summarised in Table 1. The mean age of the patients was 65.9 ± 10.1 years, and did not significantly differ among the 3 treatment groups (P = 0.665). Male sex was dominant in all the groups. The affected sites were determined during initial radiologic imaging. In the surgery group, the disease was more often occlusive and involved an aorto-iliac lesion, as compared to the medication group, although this did not significantly differ (P = 0.210).

Fig. 2. Consort diagram. The enrolled subjects were assigned to the surgery and medication groups; the surgery group was further subdivided into the bypass and intervention groups.

Table 1. Patient demographics.

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

The ABI and treadmill test scores were obtained as objective data, whereas the initial WIQ scores were obtained as subjective data at baseline after informed consent was obtained (Table 2). There were no differences throughout the baseline data among the treatment groups. The degree of crural and hip pain was recorded initially and was also assessed along with the conventional WIQ score in order to reduce bias based on disease location and to represent the subjective symptoms that directly influence claudication but do not correspond with the radiologic results. Hip pain did not differ among the treatment groups, and all the patients experienced greater pain at the crural site than at the hip during the claudication period. Only the degree of crural pain exhibited a significant difference among groups (P < 0.001).

Table 2. Baseline data.

Values are presented as mean ± standard deviation.

ABI, ankle-brachial index; PFWD, pain-free walking distance; MWD, maximum walking distance; WIQ, walking impairment questionnaire.

^a)One-way analysis of variance test.

Assessment of validity using correlation

Correlations between the objective indices (ABI, initial PFWD, and MWD) and the WIQ score are presented using a scatter plot (Fig. 3). The WIQ score was significantly correlated with the objective indices in all the treatment groups, except with MWD in the intervention group. However, the MWD score in the surgery group was well correlated with the objective indices.

Fig. 3. Correlation analysis between the objective indices and walking impairment questionnaire scores. ^a)Pearson correlation efficient (r) and P-value. ^b)The surgery group included the bypass and intervention groups. ABI, ankle-brachial index; PFWD, pain-free walking distance; MWD, maximum walking distance.

The WIQ score included fragmentary scores, which were determined via detailed questions in the questionnaire. These fragmentary scores can also reflect the objective indices in each treatment group. The speed and stair-climbing scores showed a greater correlation with the objective indices (Table 3). Moreover, the distance score was correlated with all the objective indices, except with ABI in bypass and intervention groups and with MWD in the bypass group. The distance score was significantly correlated with ABI in the surgery group.

Table 3. Correlation analysis between the objective indices and each domain score of the WIQ.

WIQ, walking impairment questionnaire; ABI, ankle-brachial index; PFWD, pain-free walking distance; MWD, maximum walking distance.

^*Pearson correlation efficient (r) and P-value. ^a)The surgery group included the bypass and intervention groups.

Reproducibility

The ICCs between the 1- and 3-month WIQ scores of the bypass and intervention groups were 0.82 (P = 0.003) and 0.90 (P < 0.001), respectively. The ICC between the baseline and 1-month scores of the medication group was 0.84 (P = 0.001). Based on the abovementioned definitions of reliability, it appeared that this version of the WIQ was reproducible, regardless of the treatment type, and that it is very reliable.

DISCUSSION

In the present study, we aimed to compare the usefulness of the WIQ in different clinical settings, including patients who received medication alone or those who underwent surgery including open bypass or interventional treatment. As the patients who received bypass surgery tended to complain about greater difficulty in walking during the early postoperative period, compared to patients who received interventional treatment, we subdivided the surgery group patients into the bypass and intervention groups. However, the bypass and intervention groups did not show any significant difference in the change in WIQ score according to time (P = 0.380 in repeated-measures analysis of variance test); moreover, the baseline data was not significantly different between these groups (Table 2).

All treatments led to clinical improvements in WIQ scores, ABI, PFWD, and MWD during the follow-up period. Between baseline and 3 months after treatment, the WIQ score improved by 0.43 ± 0.20 in the bypass group (P < 0.001), 0.42 ± 0.26 in the intervention group (P < 0.001), and 0.24 ± 0.22 in the medication group (P = 0.002), each by paired t-test. The improvement in the WIQ score was significantly higher in the surgery group than in the medication group (P = 0.045). The objective indices—including ABI, PFWD, and MWD—were also significantly improved in surgery group as compared to the medication group (P < 0.001, P = 0.036, and P = 0.019 for ABI, PFWD, and MWD, respectively). The WIQ score was well correlated with the objective indices in all treatment groups. Although improvements in walking ability as a result of each treatment were evident, our main focus was to verify whether the WIQ score could reflect the objective indices at each timepoint, not the effects comparison among the treatments. Importantly, this study validated the value of Korean version of the WIQ in Korean PAD patients. We noted that the WIQ could objectively and effectively indicate the patient's status throughout the study period in different clinical settings. These results suggest that the Korean WIQ can be used as an alternative test, instead of other objective examinations such as ABI or treadmill tests. Moreover, the WIQ effectively reflects the patient's daily walking ability. Thus, it offers considerable benefit in the outpatient clinic for physicians or surgeons in terms of its cost-effective and time-saving nature. Hence, the treadmill test can be performed in only selected patients.

This study has some unique characteristics as compared to previous studies on questionnaires in PAD patients. First, the Korean WIQ is reproducible and reliable in various treatment groups, including patients receiving medication, intervention, or bypass treatments. Hence, this Korean WIQ can be used in PAD patients in various clinical settings. Second, in another Korean version of a peripheral artery questionnaire suggested by Lee et al. [23], the questions were mainly focused on the patient's satisfaction with treatment, discomfort, or mood change due to the disease, whereas validity was assessed by identifying associations with other questionnaires. The method of validation, involving comparisons with other type of questionnaires, has often been used in other language versions of the WIQ [14,17]. However, in the present study, we directly compared the questionnaire with objective tests such as the ABI or treadmill tests. Finally, we observed that the domain scores of the Korean WIQ also reflected the ABI and the treadmill test scores. Thus, not only the total score, but also the domain scores of distance, speed, and stair climbing, of this Korean WIQ are reliable.

This study has certain limitations. First, the sample size was small due to limitations of time and funding. However, in most of the groups, we could confirm the presence of significant correlations. Second, this study did not include other PAD lesions including Buerger's disease. Third, we did not compare the WIQ with other previously developed questionnaires that often target the emotional aspects of the patients. However, we focused on whether the patient self-reported questionnaire could reflect the objective indices. Finally, this study included native Korean PAD patients only, and hence, these results may differ from those with a different ethnic background.

In conclusion, the Korean version of the WIQ appears to be valid and reproducible. These results suggest that our Korean WIQ could be effectively used to assess Korean patients with peripheral arterial disease. Therefore the WIQ can be easy and simple alternative test of the conventional tests like ABI or treadmill test for Korean IC patients and is also expected to represent the walking ability of patient's daily life more effectively.

SUPPLEMENTARY MATERIAL

Supplementary material can be found via https://astr.or.kr/src/sm/astr-93-103-s002.pdf

Supplementary Material 1

Scoring of the Korean version of the walking impairment questionnaire (WIQ)