Document Type : Research Paper

Authors

1 Department of Medicine, College of Medicine, University of Mosul, Mosul

2 The Rheumatology Outpatient Clinic, Ibn Sena Teaching Hospital, Mosul, Iraq

Abstract

Background: Self-reported questionnaires have become popular measures in assessing disability in patients with low back pain (LBP). Roland-Morris Questionnaire (RMQ) is one of the internationally accepted, self-reporting questionnaire which demonstrates good psychometric properties.
Objectives: The present study intended to evaluate a face to face interview applying Arabic version of the RMQ, and comparing it with a modified version of RMQ (RMQV), and whether the purely subjective RMQ scores correlate with symptoms and signs which have predictive or prognostic values.
Design: case-series study
Methods and materials: Case-series study conducted on seventy-two patients with chronic LBP at Ibn-Sina Teaching Hospital in Mosul city. Physical examination at rheumatology outpatient clinic performed for every patient, and the patients are allowed to answer the questions of RMQ through a direct investigator-patient Arabic conversation. The disability measured by the RMQ subdivided into: mild (0-8), moderate (9-16) and severe (17-24). An individualized literature review performed for clinical features which have predictive or prognostic values in LBP, and including these features in the clinical evaluation of patients in the current study.
Results: The results showed that the Arabic conversational RMQ have acceptable reliability and RMQV have excellent reliability (Cronbach’s alpha values=0.72 and 0.94 respectively). There was a significant direct correlation between these two questionnaires (r=0.861; p-value<0.001). However, we found a significant difference between them (p-value<0.01). The scores of the RMQ and RMQV correlate moderately with a score of the predictive features (r=0.503; p-value < 0.01 and 0.530; p-value Conclusion: The study found that the modified version (RMQV) has higher reliability than the original one. Also, the RMQV showed a better correlation with the narrow-angle straight leg raising test, and its mild and moderate subgroups have significant differences regarding the duration and pain intensity of the current episode of LBP. Other measured properties look similar between the two questionnaires.

Keywords

Main Subjects

INTRODUCTION

 

P

ain at lower back is a common problem in everyday practice that reported by the majority of adults during their lifetime and is the most frequent cause of disability for individuals younger than 45 years. It is the third leading cause of disability for those older than 45 years. 1, 2

   Acute LBP usually resolves spontaneously, but up to 10% progresses to chronic LBP resulting in temporary to permanent disability 3. Chronic nonspecific LBP and its resulting disability have become important epidemic health and a socioeconomic problem 4.

   LBP remains the most important occupational health problem in industrialized countries, accounting for about 20% to 30% of workers' compensation claims and up to 50% of all direct compensation costs 5.

   Disability encompasses impairments, limitations (on activity), and restrictions (to participation) that may occur in the presence of a health condition (disorder or disease)6. The LBP results in significant levels of disability, producing substantial restrictions on normal activities and participation, such as an inability to work 7. Also, the disability is considered as an excellent clinical assessment of severity in LBP 8. Several instruments or methods are used to measure disability in LBP. These measures improve our knowledge about the patient functions and the severity of his/her disorders and also can help in following the patient's course8,9. Self-reported questionnaires have become well-accepted measures in assessing disability in patients with LBP 10.

   The Roland-Morris Questionnaire (RMQ) has been frequently used to measure disability in patients with chronic LBP demonstrating good qualities11,12. The RMQ which is a self-reported instrument; its questions focus consistently on disabilities related to the back and the answers are dichotomous: yes/no13. The scores, therefore, range from zero (no disability) to 24 (maximum disability).  The questionnaire can complete in a maximum of 5 min, and an un-weighted score can calculate in less than 1 min. No sub-scoring reported, and the administration is straightforward. The questions deal with body functions (pain, sleeping, and appetite) as well as activities (self-care, walking, sitting, standing, lifting, dressing, stairs climbing, housework and resting) 14.

   The study aimed to evaluate the application of Roland-Morris Disability Questionnaire (RMQ) in its Arabic conversational version, look for correlations or disagreements between RMQ results and other clinical manifestations, particularly, features which can predict severity, and suggest modifications to improve the measurement.

 

METHODS

The protocol of this study was approved by the Scientific and regional research ethics committees at the College of Medicine in 2014 and by Directorate General of Neneveh Health Department. The study conducted at the rheumatology clinic of Ibn-Sina Teaching Hospital, Mosul, Iraq.

Study Design: Clinical case-series study.

Methods and materials: This study conducted on seventy-two patients after taking their consent to participate in the study with an age range between (18 – 60) years who suffered from low back pain (LBP) ± lumbar root symptoms for more than three months.

Exclusion criteria included: Suspicion of neoplastic or infective spinal conditions, compression fractures, chronic inflammatory joint/spinal diseases, organ failure (cardiovascular, respiratory, renal and hepatic), specific neurological problems (stroke, multiple sclerosis, peripheral neuropathy) and pregnancy.Materials included:Mechanical weight and height scale (Fazzini), tape measure, 128 Hz tuning fork, neurological (reflex) hammer, examination couch, plumb-bob (plummet), electronic stop-watch, and plastic goniometer.

   Face to face interviews were performed for patients participated in the study. Demographic, clinical, and other relevant data obtained. The focusing was mainly on the crucial features that have predictive values and included the following:

Buttock pain, below knee pain, the sitting difficulty, Stress pain15-21, a history of sciatica longer than three months, decreased lumbar lordosis, painful side bending 22,23,24 as well as painful forward flexion, positive quadrant test, extension test, neurological deficit of the legs (decreased sensation & /or power & /or reflexes), decreased vibration sense at the big toe,scoliosis, limited forward flexion, and limited lateral bending. 25-29

   The pain intensity of the initial episode measured retrospectively on global visual analog scale (VAS) of (0 – 100) divisions where zero means no pain and 100 means the worst pain, then; this pain intensity subdivided into three subgroups: mild (0-33), moderate (34-66) and severe (67-100). Pain intensity of the current episode is also measured on VAS and also divided into three subgroups: mild (0-33), moderate (34-66) and severe (67-100).

   The presence of scoliosis was assessed by using plumb-bob with the tip of the string placed at the spinous process of the first thoracic vertebra and the weight allowed to hang down to reach the buttock of the patient, if any deviation of the weight from the mid-gluteal cleft observed then the patient reported as having scoliosis 30.

   Flexion of the spine was evaluated by Schober's test 31. Any increase in the distance of less than 5 cm considers abnormal. The lateral flexion was assessed using a finger to fibula test, in which the patient asked to bend to one side as much as he can (without any bending forward). The test is considering abnormal if the distance between the tip of the third finger and the head of the fibula was more than 5 cm, then the test repeated on the other side 32. The extension test is done by asking the patient to actively extend his back as far as tolerated with the examiner providing support for balance, the position held for 30 seconds and the test considered positive if the patient reports pain in the low back area or the lower limb24. While in the quadrant test the patient actively moves into lateral bending, extension, and rotation to the same side as far as tolerated, the examiner guides the patient in this motion and provides overpressure if no pain is reported with this movement.

   The test considered positive if the patient reports pain or numbness in the area of the back or lower extremities 25.

   The angle of the SLR test was measured for each patient by the plastic goniometer and subdivided into 3 subgroups: patients with narrow -angle SLR (0-45 degree), patients with wide angle SLR (46-70 degree) and patients with negative SLR (more than 70 degree).

   Vibration sense as part of the neurological examination for both lower limbs was assessed using a 128 Hz tuning fork on the medial malleolus and the big toe.

   Following a physical examination, the process of answering the twenty-four questions of the Roland-Morris Questionnaire (RMQ) was started. Because the level of illiteracy in our community is relatively high, a direct, conversational method was chosen. In this method, the questions of RMQ have answered through face to face investigator-patient Arabic conversation. The disability measured by the RMQ subdivided into mild (0-8), moderate (9-16) and severe (17-24).

   After filling the RMQ in its original form, another investigator-patient Arabic conversation started to answer the questions of RMQ in a modified method (RMQV). In this method the answer for each item is obtained on a global visual analogue scales (VAS) of zero to 100 subdivisions. The patient was asked to determine how much his/her various activities (daily living, duties, recreation, and vitality feeling) were affected by each particular question due to the LBP, with zero means no any effect on these activities while 100 indicates the worst outcome that the patient can think of. The disability measured by the RMQV also subdivided into three subgroups: mild (0-30), moderate (31-60) and severe (61-100).

 

RESULTS

Seventy-two patients with the history of chronic LBP for more than three months duration participated in this study. Male to female percentage was 41.7: 58.3. As shown in the Table 1, the mean age and BMI of the studied group were 37.23 ±9.14 and 29.3± 4.46 respectively.

   Table 2 demonstrates the mean duration of LBP (50.31±52.42 months), initial episode duration (in days), and the initial episode duration (29.16 ±37.23 days).

 

Table 1: Demographic features of the patients.

Demographic features (No.= 72)

Gender

Male

Female

 

30 (41.7%)

42 (58.3%)

Age:

range/Mean/ (±SD) years

 

19 - 60/37.23 (±9.14)

BMI: range/Mean (±SD)

20.9 – 42.91/29.3 (±4.46)

 

Table 2: Different duration categories of LBP and number of the prior episodes.

Categories

Mean (±SD)

Categories

Mean (±SD)

LBP duration in months

50.31 (±52.42)

Current episode duration  in days

22.26 (±22.49)

Initial episode duration  in days

29.16 (±37.23)

No. of prior episodes of LBP

11.52 (±11.69)

SD = Standard deviation

   Table 3 shows the range and mean of the pain intensity for the initial episode of LBP measured on VAS retrospectively and current episodes of LBP measured on VAS. Also range and mean for both RMQ and RMQV are shown.

    Table 4 shows the different subgroups of LBP. In RMQ, we can see that the highest percentage of patients (48.6%) lie within the moderate subgroup followed by the severe subgroup (26.4%) and the lowest percentage for the mild subgroup (25%). In contrast, the distribution of patients within the severity subgroups of RMQV is clearly different, most of the patients lie within the mild subgroup (76.4%), a small number of patients within the moderate subgroup (19.4%) and only few number of patients lie within the severe subgroup (4.2%).

   Some of the important clinical features of the patients are shown in the Table 5, including the number and percentage of patients having each particular feature. These clinical features were chosen because they have predictive values.

 

Table 3: Total pain intensity of initial and current episodes and disability scores.

Pain intensity of the initial episode measured on VAS: range/mean(±SD)

10 - 100 / 71.52 (±23.05)

Pain intensity of the current episode measured on VAS: range/mean(±SD)

20 - 100 / 59.58 (±15.42)

RMQ score: range/mean (±SD)

2 - 22 / 12.38 (±5.47)

RMQV score: range/mean (±SD)

0 - 66.67 / 21.71 (±17.26)

 

Table 4: Severity subgroups of LBP.

Severity subgroups

No. of patients (%)

Pain intensity of first episode measured by VAS

Mild

4/72(5.6)

Moderate

20/72 (27.8)

Severe

48/72 (66.7)

Pain intensity of current episode measured by VAS

Mild

1/72 (1.4)

Moderate

53/72 (73.6)

Severe

18/72 (25)

SLR test subgroups

Narrow angle

15/72 (20.8)

Wide angle

23/72 (31.9)

Negative test

34/72 (47.2)

RMQ subgroups

Mild

18/72 (25)

Moderate

35/72 (48.6)

severe

19/72 (26.4)

RMQV subgroups

Mild

55/72 (76.4)

Moderate

14/72 (19.4)

severe

3/72 (4.2)

VAS = Visual Analogue Scale.

 

Table 5: Some of the essential clinical features of the patients.

Features

No. of patients (%)

Features

No. of patients (%)

Pain site

Lumbar pain

72 / 72 (100)

Painful forward flexion

47 / 72 (65.3)

Gluteal pain

33 / 72 (45.8)

Limited lateral bending

10 / 72 (13.9)

Below knee pain

29 / 72 (40.3)

Painful lateral bending

41 / 72 (56.9)

Stress pain

34 / 72 (47.2)

Positive extension test

45 / 72 (62.5)

Difficulty in sitting

49 / 72 (68.1)

Positive quadrant test

49 / 72 (68.1)

History of sciatica > 3 months

9 / 72 (12.5)

Positive SLR

38 / 72 (52.8)

Scoliosis

9 / 72 (12.5)

Neurological deficit of leg

35 / 72 (48.6)

Decreased lordosis

7 / 72 (9.7)

Decreased big toe vibration

19 / 72 (26.4)

Limited forward flexion

9 / 72 (12.5)

 

 

 

 

   The total number of positive clinical features with predictive values (16 features) for each patient was estimated and, the resulting total score of these predictive features (which ranged from 0-16) was compared with that of the RMQ and RMQV separately. The range and mean of this predictive features-score were (0-15) and 6.43±2.83 respectively. Table 6 shows the correlation between the predictive features score and each of RMQ and RMQV.

   Table 7 compares between the means for RMQ and RMQV questionnaires according to Pearson correlation coefficient and independent samples t-test. Both of them were significant.

   Table 8 shows the proportions of patients for each particular clinical feature within the severity subgroups of the RMQV. The comparison between the percentages of patients having each particular clinical feature within the mild and moderate subgroups of the RMQV has been studied using the two-proportion test. If the number of patients for a specific clinical feature was zero in the mild and/or the moderate subgroups, then the percentage of patients for this feature is not compared. Statistical analysis of the severe subset of the RMQV was omitted because of the small number of patients in this subgroup (3 patients only).

  

Table 6: Correlation (Pearson’s coefficient r) between predictive features score and the disability scores (RMQV and RMQ).

Predictive features score

Pearson’s coefficient ( r )

RMQV

RMQ

0.530

0.503

P-value

< 0.01

< 0.01

 

 

 

 

Table 7: The Cronbach’s alpha, Pearson's correlation coefficient (r) and comparison between the means for both RMQ and RMQV.

Disability score

Independent samples t-test

Pearson's correlation coefficient (r)

Cronbach’s alpha

RMQ

P < 0.01

0.861

(P < 0.001)

0.72 (acceptable reliability)

RMQV

0.94 (excellent reliability)

  

Table 8: Numbers and percentages of patients having some particular clinical features within RMQV subgroups.

Clinical features

Mild 55/72 (%)

Moderate 14/72 (%)

p-value

Pain intensity of the current episode

Mild

 

Moderate

 

Severe

1 (1.8)

 

47 (85.5)

 

7 (12.7)

0

 

6 (42.9)

 

8 (57.1)

NC

 

0.002

 

0.001

Buttock pain

21 (38.2)

9 (64.3)

NS

Below knee pain

22 (40)

5 (35.7)

NS

Stress pain

19 (34.5)

12 (85.7)

<0.001

Difficulty in sitting

36 (65.5)

10 (71.4)

NS

Prior sciatica > 3 months

7 (12.7)

1 (7.1)

NS

Scoliotic posture

5 (9.1)

2 (14.3)

NS

Decreased lordosis

4 (7.3)

2 (14.3)

NS

Limited forward flexion

4 (7.3)

3 (21.4)

NS

Painful forward flexion

34 (61.8)

11 (78.6)

NS

Limited lateral bending

6 (10.9)

1 (7.1)

NS

Painful lateral bending

27 (49.1)

11 (78.6)

0.022

Positive quadrant test

36 (65.5)

10 (71.4)

NS

Positive extension test

33 (60)

10 (71.4)

NS

Positive SLR

26 (47.3)

10 (71.4)

NS

Neurological deficit of leg

24 (43.6)

8 (57.1)

NS

Decreased big toe vibration

13 (23.6)

4 (28.6)

NS

         

NC = No comparison has been done; NS = Not significant (p >0.05) according to two-proportion z-test.

   Table 9 shows the proportions of patients for each particular clinical feature within the severity subgroups of the RMQ. The comparisons between the percentages of patients having each particular clinical feature within the mild and moderate subgroups of the RMQ have been studied using the two-proportions z-test. If the number of patients for a particular clinical feature was found to be zero in the mild and/or the moderate subgroups, then the percentage of patients for that feature has not been compared. A comparison with the severe subgroup was not performed as it has not been performed in that of the RMQV one (the preceding table).

   Table 10 shows the different duration categories of LBP for each severity subgroup of the RMQV and RMQ. Statistical analysis between the severe subgroups of the RMQ and RMQV was omitted because of the small number of patients in the severe subgroup of RMQV (3 patients only).

 

Table 9: Numbers and percentages of patients having some particular clinical features within RMQ subgroups.

Clinical features

Mild 18/72 (%)

Moderate

35/72 (%)

p-value

Pain intensity of the current episode

Mild

Moderate

Severe

1 (5.6)

17 (94.4)

0

0

29 (82.9)

6 (17.1)

NC

NS

NC

Buttock pain

5 (27.8)

16 (45.7)

NS

Below knee pain

7 (38.9)

14 (40)

NS

Stress pain

3 (16.7)

15 (42.9)

0.031

Difficulties in sitting

9 (50)

24 (68.6)

NS

Prior sciatica > 3 months

1 (5.6)

5 (14.3)

NS

Scoliotic posture

1(5.6)

5(14.3)

NS

Decreased lordosis

1(5.6)

2(5.7)

NS

Limited forward flexion

3(16.7)

1(2.9)

NS

Painful forward flexion

11(61.1)

21(60)

NS

Limited lateral bending

1(5.6)

4(11.4)

NS

Painful lateral bending

4(22.2)

21(60)

0.003

Positive quadrant test

9(50)

24(68.6)

NS

Positive extension test

8(44.4)

22(62.8)

NS

Positive SLR

9(50)

16(45.7)

NS

Neurological deficit of leg

5(27.8)

16(45.7)

NS

Decreased big toe vibration

3(16.7)

10(28.6)

NS

         

NC = No comparison has been done; NS = Not significant test (p >0.05). According to two-proportions z-test.

   Table 11 shows the correlations between the severity subgroups of both (RMQ and RMQV) and the pain intensity of the current episode of LBP (Pearson’s correlation), and between the severity subgroups of both RMQ and RMQV, and the SLR test subgroups (Spearman’s rank correlation).

 

Table 10: Different duration categories for each severity subgroups of RMQ & RMQV.

Severity subgroups

Duration since onset in months: mean (±SD)

Initial episode duration  in days: mean (±SD)

Current episode duration  in days: mean (±SD)

Mild RMQV

49.34

(±53.01)

 

NS

24.58

(±28.41)

 

NS

18.56

(±18.2)

 

S**

Moderate RMQV

44.35

(±41.57)

34.28

(±25.3)

39.78

(±30.8)

Mild RMQ

44.94

(±63.38)

 

NS

30.94

(±41.05)

 

NS

17.88

(±16.82)

 

NS

Moderate RMQ

51.34

(±49.1)

18.94

(±16.79)

15.97

(±15.28)

Severe RMQ

53.52 (±49.5)

46.31 (±53.18)

38 (±30.47)

S** = significant difference at p-value <0.01; NS = not significant (using independent samples t-test (>0.05).

 

Table 11: Correlations between subgroups of pain intensity and SLR test with that of RMQV and RMQ.

Features

RMQV subgroups

RMQ subgroups

Pain intensity subgroups

0.634** (r)

0.625** (r)

SLR degree subgroups

0.262* (rho)

0.154 (rho)

* = P-value

rho = Spearman’s rank correlation coefficient.

 

DISCUSSION

The self-reported questionnaires of disability are of great relevance in assessing the severity of low back pain (LBP). The Roland-Morris Questionnaire (RMQ) is considered one of the most commonly studied self-reported disability measures 8, 33. This questionnaire is considered thoroughly validated, have acceptable reliability and is recommended and referred to as a tool of choice in the assessment of the severity of disability caused by LBP 34.Also, it is quickly completed, easy to be understood and scored, and broadly consistent with the WHO ICF definition of activity limitation.

   But among the weakening points of this questionnaire are: being purely subjective and lack any physical signs, dichotomous responses only with no ability to rate the degree of limitation for a given functional activity, providing equal marks to mild and severe symptoms, patients rate limitation just in last 24 hours, depends mainly on daily living activities rather than duties and work activities (such as lifting, carrying, pushing or pulling objects) 35, 36. Moreover, the high levels of illiteracy in many countries make the completion of such self-reported questionnaire by the patient alone very difficult. Therefore in this study, an Arabic conversational version of the RMQ was chosen, which has been adapted in the rheumatology unit of Ibn-Sina teaching hospital.

   The mean age of seventy-two participated patients was 37.23 years, and this is within the range of age considered to have the highest frequency of LBP 37. Their mean BMI was also high (29.3 kg/m2) and the high BMI is considered as a risk factor for chronicization of acute and subacute LBP 20. The mean duration of LBP since its initial onset was 50.31 months and the mean duration of the initial episode of LBP was 29.16 days; whereas the mean duration of the current episode of LBP was 22.26 days. All the patients were having a history of more than one previous episode of LBP with the mean number equal to 11.52 episodes.

   The mean intensity of the pain for initial episodes measured on global VAS scale (0-100 scores) was (71.52/out of 100 scores) and, there were 4 patients (5.6%) having mild pain, 20 patients (27.8%) having moderate pain and, 48 patients (66.7%) having severe pain. The mean intensity of the current episode pain which also measured on global VAS scale was 59.58 and, there was only one patient (1.4%) having mild pain, 53 patients (73.6%) having moderate pain and 18 patients (25%) having severe pain. The range and mean for RMQ were 2- 22 and 12.38 respectively; and there were 18 patients (25%) lie within its mild subgroup, 35 patient (48.6%) within its moderate subgroup, and nineteen patients (26.4%) within the severe subgroup. While for RMQV the range and mean were 0 - 66.67 and 21.71 respectively; and there were 55 patients (76.4%) lie within its mild subgroup, 14 patients (19.4%) within its moderate subgroup, and only 3 patients (4.2%) within the severe subgroups. The mean scores for the RMQ reflect a moderate level of disability while that for the RMQV reflect a mild degree of disability.

   It appears that the differences in the distribution of patients within the severity subgroups of RMQ and RMQV are remarkable. Most patients lie within the mild subgroup of the RMQV and a minimal number within the severe one, while most of the patients lie in the moderate subgroup of RMQ followed by the severe, then the mild ones. These may indicate that a high percentage of the patients who considered to have moderate or severe disabilities according to the RMQ was really only mildly disabled according to the RMQV. Therefore these two questionnaires are different from each other, and this difference was confirmed by comparing the means for both questionnaires using independent samples t-test which showed a significant difference between them (p-value< 0.01). Yet they were found to have a strong direct correlation with each other (r=0.861; p-value< 0.001). The reliability for the Arabic conversational version of the RMQ was estimated using Cronbach’s alpha, and it was 0.73, and for the RMQV the reliability was higher (Cronbach’s alpha = 0.94).

   What we call them predictive features are actually predict various aspects in LBP, like unresponsiveness to physical medicine modalities 17,18,38,chronicity19,20,23, poor or unfavorable outcome 21,24,25,28, severity 26,29,30, and the presence of underlying nerve root compression or disc protrusion22,32.     

   Collectively, these predictive features have an impact on the management of patients with LBP.

A set of clinical features (16 features) with predictive and prognostic values was used for comparison with both RMQ & RMQV separately. The total numbers of positive predictive features were estimated for each patient, and the final score was used to compare it with that of RMQ and RMQV for the same patient.

   The correlation between these predictive features score and each of the RMQ and RMQV were found to be moderate and significant (r=0.503, p-value < 0.01 and r=0.530, p-value < 0.01 respectively). The number and percentages of patients having each particular clinical feature in each severity subgroup of the RMQ and RMQV were estimated. The two-proportion test was used to compare the percentages of patients having each of these clinical features in the mild subgroup and those having the same clinical features in the moderate subgroup of the RMQV. The same comparisons also performed for the patients within the mild and moderate subgroups of the RMQ. The results revealed that there were significant differences between the mild and moderate subgroups of RMQV in the frequency of stress pain and painful lateral bending (p-value

   The mean duration of LBP since its onset was found to be longer in the mild subgroup (49.34 months) than the moderate subgroup (44.35 months) of the RMQV, while it was longer in the moderate (51.34 months) than the mild subgroups (44.94 months) of the RMQ. The mean duration of the initial episodes was found to be longer in the moderate subgroup (34.28 days) than in the mild one (24.58 days) in the RMQV, while it was longer in the mild (30.94 days) than the moderate subgroups (18.94 days) of the RMQ. In case of the current episode, its mean duration was found to be longer in the moderate subgroups (39.78 days) than in the mild one (18.56 days). Also, its mean duration was longer in the mild (17.88 days) than the moderate subgroups (15.97 days) of the RMQ. These differences in the duration categories were found to be significant only for the mean duration of the current episode of LBP between the severity subgroups of RMQV with p-value < 0.01 (using independent samples t-test).

   Furthermore, the intensity of the LBP was found to have strong correlations with RMQ and RMQV (r=0.625 at p-value < 0.01 and r=0.634 at p-value < 0.01 respectively). The pain intensity of the LBP considered having predictive values such as being a predictor of short-term outcome after lumbar discectomy 39, also it is considered to be correlated with greater disability in patients with lumbar spinal stenosis 40.

   A narrow angle SLR test also has predictive values such as being a predictor of poor outcome after lumbar disc herniation surgery 41. Spearman’s rank correlation was used to compare the severity subgroups of both the RMQ and RMQV with the SLR test subgroups, a significant moderate correlation was found between the SLR test subgroups and the RMQV subgroups (rho= 0.262 at p-value<0.05), whereas the relationship between the SLR test subgroups and the RMQ subgroups was weak and not significant (rho = 0.154).

 

CONCLUSIONS

Arabic translation and face to face interview instead of the original patient report can maintain the excellent internal consistency of the questionnaires.

   The differences between the original RMQ and the VAS-graded modification (RMQV) are prominent in that the RMQV have better reliability, better correlation with the narrow-angle straight leg raising test, and its mild and moderate subgroups have significant differences regarding the duration and pain intensity of the current episode of low back pain.

   The scores of the two versions RMQ correlated somewhat moderately with the predictive and prognostic clinical feature.

1. Dunn KM, Croft PR. Epidemiology and natural history of low back pain. Eur med phys 2004;40:9-13.
2. Wildstein MS and Carragee EJ. Low Back Pain. In: Firestein GS, Budd RC, Harris Jr ED, Mclnnes IB, Ruddy S, Sergent JS (eds) Kelley’s Textbook of Rheumatology, eighth edition. 2009. Sunders Elsever. Philadelphia, p 617.
3. Whiteman HH, Clauw DJ, Beary JF. Low Back Pain. In: Paget SA, Gibofsky A, Beary JF, Sculco TB (eds) Hospital for Special Surgery Manual of Rheumatology and Outpatient Orthopedic Disorders: Diagnosis and Therapy, fifth edition. 2006. Lippincott Williams & Wilkins. Philadelphia, p 145-147.
4. Smeets RJ, Vlaeyen JW, Hidding A, Kester AD, van der Heijden GJ, Knottnerus JA . Chronic low back pain: physical training, graded activity with problem solving training, or both? The one-year post-treatment results of a randomized controlled trial. Pain 2008;134:263-276.
5. Kerr MS, Frank JW, Shannon HS, Norman RW, Wells RP, Neumann WP, et al. Biomechanical and psychosocial risk factors for low back pain at work. Am J Public Health 2001;91(7):1069-75.
6. Rondinelli RD. Disability Determination. In: Delisa JA, Gans BM, Walsh NE, Bockenek WL, Frontera WR, Geiringer SR, et al. (eds) Physical Medicine & Rehabilitation: Principles and Practice, fourth edition. 2005. Lippincott Williams & Wilkins, p 170-171.
7. Louw QA, Morris LD, Grimmer-Somers K. The prevalence of low back pain in Africa: a systematic review. BMC Musculoskelet Disord. 2007; 8:105.
8. Mannion AF, Dvorak J, Müntener M, Grob D. A prospective study of the interrelationship between subjective and objective measures of disability before and 2 months after lumbar decompression surgery for disc herniation. Eur Spine J. 2005;14(5):454-65.
9. Stratford PW, Binkley JM. Applying the results of self-report measures to individual patients: an example using the Roland-Morris Questionnaire. J Orthop Sports Phys Ther. 1999;29(4):232-9.
10. Cai C, Pua YH, Lim KC. Correlates of self-reported disability in patients with low back pain: the role of fear-avoidance beliefs. Ann Acad Med Singapore 2007; 36(12):1013-20.
11. Beurskens AJ, de Ver HC, Koke AJ, van der Heijden GJ, Knipschild PG. Measuring the functional status of patients with low back pain. Assessment of the quality of four disease-specific questionnaires. Spine (Phila pa 1976), 1995;20(9):1017-28.
12. Calmels P, Bethoux F, Condemine A, Fayolle-Minon I. Low back pain disability assessment tools. Ann Readapt Med Phys. 2005;48(6):288-97.
13. Roland M, Morris R. A study of the natural history of back pain. Part I: development of a reliable and sensitive measure of disability in low-back pain. Spine (Phila Pa 1976), 1983; 8(2):141-4.
14. Muller U, Duetz MS, Roeder C, Greenough CG. Condition-specific outcome measures for low back pain Part 1: Validation. Eur Spine J 2004 a ;13(4):301-313.
15. Fritz JM, Whitman JM, Flynn TW, Wainner RS, Childs JD. Factors related to the inability of individuals with low back pain to improve with a spinal manipulation. Phys Ther. 2004;84(2):173-90.
16. Childs JD, Fritz JM, Flynn TW, Irrgang JJ, Johnson KK, Majkowski GR. A clinical prediction rule to identify patients with low back pain most likely to benefit from spinal manipulation: a validation study. Ann Intern Med. 2004;141(12):920-8.
17. Valat JP, Goupille P, Védere V. Low back pain: risk factors for chronicity. Rev Rhum Engl Ed 1997; 64(3): 189-94. (abstract)
18. Negrini S, Fusco C, Atanasio S, Romano M, Zaina F. low back pain: state of art. European Journal of Pain Supplements 2008;2:52–56.
19. Vroomen PC, de Krom MC, Knottnerus JA. Predicting the outcome of sciatica at short-term follow-up. Br J Gen Pract 2002 a; 52(475):119-23.
20. Vroomen PC, de Krom MC, Wilmink JT, Kester AD, Knottnerus JA. Diagnostic value of history and physical examination in patients suspected of lumbosacral nerve root compression. J Neurol Neurosurg Psychiatry 2002 b; 72(5):630-4.
21. Thomas E, Silman AJ, Croft PR, Papageorgiou AC, Jayson MI, Macfarlane GJ. Predicting who develops chronic low back pain in primary care: a prospective study. BMJ 1999;318(7199):1662-7.
22. Schoeggl A, Maier H, Saringer W, Reddy M, Matula C. Outcome after chronic sciatica as the only reason for lumbar microdiscectomy. J Spinal Disord Tech 2002; 15(5):415-9.
23. Nykvist F, Alaranta H, Hurme M, Karppi SL. Clinical findings as outcome predictors in rehabilitation of patients with sciatica. Int J Rehabil Res 1991;14(2):131-44.
24. Katz JN, Dalgas M, Stucki G, Katz NP, Bayley J, Fossel AH et al. Degenerative lumbar spinal stenosis. Diagnostic value of the history and physical examination. Arthritis Rheum. 1995;38(9):1236-41.
25. Lyle MA, Manes S, McGuinness M, Ziaei S, Iversen MD. Relationship of physical examination findings and self-reported symptom severity and physical function in patients with degenerative lumbar conditions. Phys Ther. 2005;85(2):120-33.
26. Grotle M, Brox JI, Veierød MB, Glomsrød B, Lønn JH, Vøllestad NK. Clinical course and prognostic factors in acute low back pain: patients consulting primary care for the first time. Spine (Phila Pa 1976). 2005;30(8):976-82.
27. Lin SI, Lin RM. Disability and walking capacity in patients with lumbar spinal stenosis: association with sensorimotor function, balance, and functional performance. J Orthop Sports Phys Ther 2005; 35(4):220-6.
28. Michel A, Kohlmann T, Raspe H. The association between clinical findings on physical examination and self-reported severity in back pain. Results of a population-based study. Spine (Phila Pa 1976), 1997; 22(3): 296-303.
29. Kerr RS, Cadoux-Hudson TA, Adams CB. The value of accurate clinical assessment in the surgical management of the lumbar disc protrusion. J Neurol Neurosurg Psychiatry. 1988;51(2):169-73.
30. Levine DB, Leipzig JM. The Painful Back. In: McCarty DJ, Koopman WJ (eds). Arthritis and Allied Conditions. A Textbook of Rheumatology, twelfth edition. 1993. Lee & Febiger. London, p 1586.
31. Schober's test – Wikipedia. Found in: https://en.wikipedia.org/wiki/Schober%27s_test.
32. Schned ES. Ankylosing Spondylitis. In: (eds) Hospital for Special Surgery Manual of Rheumatology and Outpatient Orthopedic Disorders: Diagnosis and Therapy, fifth edition. 2006. Lippincott Williams & Wilkins. Philadelphia, p 309.
33. Riddle DL, Stratford PW, Binkley JM. Sensitivity to change of the Roland-Morris Back Pain Questionnaire: part 2. Phys Ther 1998;78(11):1197-207.
34. Björklund M, Hamberg J, Heiden M, Barnekow-Bergkvist M. The assessment of symptoms and functional limitations in low back pain patients: validity and reliability of a new questionnaire. Eur Spine J. 2007;16 (11):1799-811.
35. Peat G. PPA recommendation for low back pain-related functional limitation outcome measures. The Chartered Society of Physiotherapy. 2004. Found in: https://www.csp.org.uk.
36. Davidson M. Rasch analysis of 24-, 18- and 11-item versions of the Roland-Morris Disability Questionnaire. Qual Life Res. 2009;18 (4):473-81.
37. Manchikanti L. Epidemiology of Low Back Pain. Pain Physician 2000;3(2)167-192.
38. Hicks GE, Fritz JM, Delitto A, McGill SM. Preliminary development of a clinical prediction rule for determining which patients with low back pain will respond to a stabilization exercise program. Arch Phys Med Rehabil. 2005;86(9):1753-62.
39. Moranjkic M, Ercegovic Z, Hodzic M, Brkic H. Outcome Prediction in Lumbar Disc Herniation Surgery. Acta Medica Saliniana 2010;39(2):75-80.
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
40. Lin SI, Lin RM, Huang LW. Disability in patients with degenerative lumbar spinal stenosis. Arch Phys Med Rehabil. 2006;87(9):1250-6.
41. Jönsson B, Strömqvist B. The straight leg raising test and the severity of symptoms in lumbar disc herniation. A preoperative evaluation.Spine. 1995; 20(1):27-30.