Sensitivity to change of the Quebec Back Pain Disability Scale and the Dallas Pain Questionnaire




Abstract


Objective


To study and compare the sensitivities to change of the French versions of the Quebec Back Pain Disability Scale (QBPDS) and the Dallas Pain Questionnaire (DPQ).


Method


A retrospective study of the medical records of 30 chronic low back pain (LBP) outpatients undergoing a 4-week functional training program in a physical medicine and rehabilitation unit. Physical data (a visual analogue pain scale, the Schöber index, Sorensen and Shirado tests and the finger-to-floor distance) and functional status (QBPDS and DPQ scores) were measured at D0 and D25. Sensitivity to change was assessed in terms of the standardized response mean (SRM) and the effect size (ES).


Results


With the exception of the DPQ’s “social interest” domain, all QBPDS and DPQ scores improved significantly over the course of the rehabilitation programme. Sensitivity to change was high for the QBPDS (SRM = 0.80; ES = 0.62) but only moderate for the DPQ (SRM = 0.59; ES = 0.61).


Discussion-Conclusion


Our results show that the QBPDS was more sensitive to clinical change than the DPQ in a sample of chronic LBP sufferers. It would be interesting to assess this sensitivity in a population of acute LBP patients and to evaluate the long-term effects of a functional rehabilitation program on the DPQ’s “social interest” domain.


Résumé


Objectif


Étudier la sensibilité au changement de l’échelle de Québec (QBPDS) et la comparer à celle du questionnaire de Dallas (DPQ), en langue française.


Méthode


Étude rétrospective à partir de 30 dossiers de patients lombalgiques chroniques pris en charge lors d’un programme de réentraînement à l’effort sur une période de quatre semaines ; analyse à j0 et j25 du programme, de données cliniques physiques (échelle visuelle analogique, indice de Schöber, test de Sorensen et de Shirado, distance mains-sol), et fonctionnelles avec l’échelle de Québec et le questionnaire de Dallas. L’étude de la sensibilité au changement est effectuée par l’indice de réponse standardisée moyenne (SRM) et par l’effet taille ( effect size [ES]).


Résultats


Il existe une amélioration significative du score total et des sous-chelles du QBPDS et du DPQ sauf la dimension « comportements sociaux ». On retrouve une bonne sensibilité au changement du QBPDS (SRM = 0,80 ; ES = 0,62) et modérée pour DPQ (SRM = 0,59 ; ES = 0,61).


Discussion-Conclusion


Les résultats de cette étude montre une sensibilité au changement clinique du QBPDS plus satisfaisante que le DPQ dans le cas de la lombalgie chronique. Il serait utile d’évaluer cette sensibilité dans le cas de la lombalgie aiguë ou sub-aiguë, et à distance d’un programme pour déterminer la sensibilité des dimensions « comportements sociaux » du DPQ.



English Version



Introduction


Many functional disability scales have been prompted by research and medical care in the field of low back pain (LBP) in general and its chronic form in particular . The Oswestry Disability Questionnaire, the Quebec Back Pain Disability Scale (QBPDS), the Roland-Morris Disability Questionnaire and the Dallas Pain Questionnaire (DPQ) are the best known tools but none has prevailed as the “gold standard” – notably in terms of the metrological criteria (reliability, validity, feasibility, etc.) needed to justify the choice of a measurement scale.


However, the two most recently developed tools (the QBPDS and the DPQ ) have been shown to be both reliable and valid. The LBP-specific QBPDS self-questionnaire for functional evaluation was developed and validated by Kopec in English and in Canadian French. It takes account of pain-related functional limitations and monitors changes over time in LBP patients participating in rehabilitation programmes. This scale has proven metrological properties (i.e. reliability, reproducibility and validity of construction) in LBP patients and is considered to be suitable for measuring different levels of functional disability. The QBPDS is also very easy and rapid to complete (3 to 5 min) and is appropriate for use in France, despite the presence of a few terms that are more characteristic of Canadian French . However, the QBPDS’s sensitivity to change, the predictive validity of the initial scores and its usefulness in longitudinal evaluations remain to be described (notably for the French-language version) .


The DPQ is a self-questionnaire based on a cognitive and behavioural conception of chronic pain. It was designed to evaluate the impact of LBP on everyday life ; its field of investigation goes beyond physical disability and addresses the social interest domain. The DPQ’s metrological properties (reliability, reproducibility, validity of content, validity of construction, discriminant power and predictive validity) have been confirmed in LBP sufferers . However, the original American English version has not been investigated in terms of sensitivity to change. In the French-language version , sensitivity to change has been demonstrated for the “daily living”, “work-leisure”, and “anxiety/depression” domains but not for the “social interest” domain .


In the present study, we set out to evaluate the QBPDS’s sensitivity to change (and to compare it with that of the DPQ) in a population of LBP sufferers participating in a functional rehabilitation programme.



Methods



Population


Male or female LBP sufferers aged between 18 to 60 inclusive, regardless of the aetiology of the lesions (discopathy, facet joint arthritis, etc.) and the medicinal, orthopaedic or surgical treatments administered.



Method


Retrospective examination of the medical records of LBP outpatients participating in a 4-week functional training programme in a physical medicine and rehabilitation department (with five sessions per week, i.e. 20 sessions).



Clinical and functional evaluation


Performed on the first day (D1) and last day (D25) of the 4-week training programme.



General data


Age, gender, time since LBP onset, prior treatments (analgesics, anti-inflammatories, antidepressants, muscle relaxants, infiltrations, surgical or orthopaedic treatments, rehabilitation, etc.).



Clinical data


Clinical data are as follows:




  • pain evaluation: a 10 cm visual analogue scale (VAS);



  • evaluation of sub- and suprapelvic flexibility: the finger-to-floor distance (FFD) (in centimetre) and the Schöber-MacRae test (SMRT, in centimetre);



  • the Shirado test: measurement of the time during which the subject can hold his/her head and trunk off the ground (as far as the shoulder blades), while lying on his/her back on the floor with the thighs vertical and the calves resting on a bench;



  • the Sorensen test: measurement of the time during which the subject can maintain his/her prone, unsupported upper body (from the hip joint upwards and with the hands held behind the head) in a horizontal, pain-free position while his/her legs are held on the table.




Functional disability


Functional disability are:




  • the French-language version of the QBPDS includes 20 items grouped into six categories: rest/bed, sitting/standing, walking, body movements, bending down and carrying/moving objects; each activity is scored from 0 to 5 according to the difficulty experienced. An overall score (maximum: 100) and a category score (a maximum of 15 for the first four categories and 20 for the last two) are thus established and expressed as absolute values: the highest scores correspond to the most severe physical disability;



  • the French-language version of the DPQ includes 16 items in four domains: daily living, work/leisure, anxiety/depression and social interest. After each question has been scored, the values in each domain are summed and then multiplied by a constant. The overall score corresponds to the mean of the four subscores.




Statistics


Parameters are reported as the mean ± standard deviation. Depending on the sample size and the variable in question, Mann-Whitney or Wilcoxon tests were used to compare the results. The significance threshold was set to p < 0.05. Assessment of the tools’ sensitivity to change was based on two indices: the standardized response mean (SRM) and the effect size (ES) calculated according to Cohen . Sensitivity to change is small if the SRM or ES is below 0.50, moderate for values between 0.51 and 0.80 and high for values above 0.80.



Results



Population


We examined 30 sets of medical records (selected due to the lack of missing data). The study population comprised 19 men and 11 women (mean age: 41.6; range: 29 to 59). The LBP was due to a variety of mechanisms: arthritis, herniated disc, other disc conditions, etc. All the subjects have received the usual drug treatments (various classes of analgesics, non-steroidal anti-inflammatories, myorelaxants, etc.) and physiotherapy sessions. Ten patients had received foraminal or facet joint infiltrations, six had undergone orthopaedic treatment with a corset and five had been treated for a herniated disc.



Effect of the functional rehabilitation programme



Physical parameters


The results evidenced a significant clinical improvement for all parameters: VAS ( p = 0.0005), SMRT ( p = 0.001), Sorensen ( p < 0.0001), Shirado ( p = 0.003) and FFD ( p = 0.005) ( Table 1 ).



Table 1

Values and comparative analysis of the physical data on D1 and D25.














































VAS SMRT FFD Sorensen Shirado
n D1 27 30 30 28 29
Mean D1 3.4 (± 1.5) 3.8 (± 1.0) 23.1 (± 13.6) 52.9 (± 40.1) 30.4 (± 26.1)
n D25 21 29 29 27 27
Mean D25 2.2 (± 2.0) 4.5 (± 1.3) 7.7 (± 10.6) 72.1 (± 49.4) 50.0 (± 34.3)
p 0.0005 0.001 < 0.0001 0.003 0.005



Functional disability


The QBPDS results showed a significant improvement in all six category scores and in the overall score ( p = 0.0001) ( Table 2 ).



Table 2

Comparative analysis of the Quebec Back Pain Disability Scale scores on D1 and D25 and analysis of the sensitivity to change.


























































Quebec 1 Quebec 2 Quebec 3 Quebec 4 Quebec 5 Quebec 6 Quebec T
Mean D1 6.0 (± 2.4) 7.4 (± 2.8) 4.2 (± 3.1) 5.1 (± 2.7) 7.2 (± 3.3) 8.6 (± 4.3) 38.4 (± 13.3)
Mean D25 4.8 (± 2.5) 5.9 (± 3.0) 3.0 (± 2.5) 4.0 (± 2.9) 5.8 (± 3.5) 6.7 (± 4.1) 30.2 (± 14.5)
p 0.01 0.001 0.006 0.006 0.01 0.0003 0.0001
SRM 0.48 0.64 0.54 0.54 0.49 0.75 0.80
ES 0.51 0.53 0.37 0.40 0.41 0.45 0.62

Quebec 1: items 1 to 3, “rest/bed”; Quebec 2: items 4 to 6, “sitting”; Quebec 3: items 7 to 9, “walking”; Quebec 4: items 10 to 12, “body movements”; Quebec 5: items 13 to 16, “bending over”; Quebec 6: items 17 to 20, “carrying/moving objects”; Quebec T: total Quebec Back Pain Disability Scale scale score; SRM: standardized response mean; ES: effect size.


The DPQ results showed a significant improvement in the first three dimensions of this questionnaire and in the overall score ( p = 0.003) but there was no significant change in the “social interest” domain ( Table 3 ).



Table 3

Comparative analysis of the Dallas Pain Questionnaire scores on D1 and D25 and analysis of the sensitivity to change.
















































Dallas 1 Dallas 2 Dallas 3 Dallas 4 Dallas T
Mean D1 60.9 (± 15.1) 68.8 (± 20.7) 57.7 (± 23.6) 47.0 (± 25.1) 58.6 (± 17.6)
Mean D25 50.9 (± 19) 55.2 (± 23.8) 42.7 (± 26.1) 48.8 (± 43.0) 47.8 (± 20.8)
p 0.003 0.004 0.003 0.81 0.003
SRM 0.60 0.57 0.68 −0.04 0.59
ES 0.66 0.66 0.64 −0.07 0.61

Dallas 1: responses 1 to 7 (as a %), the “daily living” subscale; Dallas 2: responses 8 to 10 (as a %), the “work and leisure” subscale; Dallas 3: responses 11 to 13 (as a %), the “anxiety/depression” subscale; Dallas 4: responses 14 to 16 (as a %), the “social interest” subscale; Dallas T: total Dallas Pain Questionnaire score, expressed as a percentage; SRM: standardized response mean; ES: effect size.



Correlation analysis


Analysis of correlations between the physical indices and the functional disability measurements showed a significant relationship between the pain VAS on one hand and each of the disability questionnaires on the other. There was also a correlation between the two disability scales (0.0032 < p < 0.0226) ( Table 4 ).



Table 4

Correlation analysis between the overall scores on the Quebec and Dallas scales and the physical parameters used, on D1 and D25.























































































































Correlation Number p
Quebec T J 1/VAS D1 0.434 27 0.0226
Quebec T J 1/Schober D1 −0.026 30 0.8915
Quebec T J 1/Sorensen D1 −0.144 28 0.4681
Quebec T J 1/ Shirado D1 −0.121 29 0.5341
Quebec T J 1/FFD D1 −0.229 30 0.2258
Dallas T J 1/VAS D1 0.491 27 0.0085
Dallas T J 1/Schober D1 0.055 30 0.7763
Dallas T J 1/Sorensen D1 0.042 28 0.8331
Dallas T J 1/ Shirado D1 0.199 29 0.3026
Dallas T J 1/FFD D1 0.031 30 0.8720
Quebec T J 1/Dallas T D1 0.437 30 0.0150
Quebec T J 25/VAS D25 0.425 21 0.054
Quebec T J 25/Schober D25 −0.046 29 0.8152
Quebec T J 25/Sorensen D25 −0.170 27 0.4005
Quebec T J 25/ Shirado D25 −0.243 27 0.2238
Quebec T J 25/FFD D25 0.083 29 0.6722
Dallas T J 25/VAS D25 0.544 21 0.0098
Dallas T J 25/Schober D25 −0.253 29 0.1865
Dallas T J 25/Sorensen D25 −0.088 27 0.6666
Dallas T J 25/ Shirado D25 −0.127 27 0.5318
Dallas T J 25/FFD D25 0.109 29 0.5768
Quebec T J 25/Dallas T D25 0.513 30 0.0032



Sensitivity to change


Calculation of the SRM showed that the overall QBPDS score displayed high sensitivity to change (0.80). In contrast, analysis of the individual domains indicated only moderate-to-low sensitivity to change. On the whole, calculation of the ES confirmed these results for the overall QBPDS score (0.62) and the category scores ( Table 2 ). The overall DPQ score’s sensitivity to change was considered to be moderate for the overall score and the daily living, work/leisure and anxiety/depression domains (but not the social interest domain) when considering either the SRM or the ES ( Table 3 ).



Discussion


Our retrospective study on a sample of 30 chronic LBP subjects evaluated before and after a back functional rehabilitation programme showed that the QBPDS displayed high sensitivity to change, whereas that of the DPQ was moderate. However, our study had a number of limitations: the population (30 subjects) was quite small and our analysis was based on the retrospective examination of medical records filled out by physicians and physiotherapists, with some data loss. Some sets of records were not fully exploitable. On the methodological level, it would have been interesting to calculate the minimum clinical change ; however, this would have required a different methodology (i.e. a prospective study).


In contrast, our population was characteristic of a “hospital population” on whom chronic LBP had a significant socioprofessional impact; 22 of the 30 patients were off work (sick leave, workplace accident, invalidity, etc.).


The overall results of the functional rehabilitation programme were similar to those reported in the literature. However, the goal of the present study was not to evaluate the efficacy of this programme, even though knowledge of the outcome was important for describing our results on the scales’ sensitivity to change. Even though many authors have underlined the generally positive effects of functional rehabilitation programmes, there is no consensus on this matter and the conclusions vary according to the parameters evaluated. Most studies have reported an improvement in clinical variables (pain intensity, mobility and muscle strength) and a functional enhancement that enables the patient to return to work . Bontoux et al. studied a population of 87 chronic LBP sufferers (mean age: 40.9; range: 18 to 53) with major problems at work and reported a significant improvement in pain intensity and physical test results at the end of the training programme and then six and 12 months afterwards. After four weeks of training, the latter authors also reported a significant decrease in the overall DPQ score (from 174.6 ± 73.3 to 91.9 ± 68.8 out of 400 for the absolute scores) and the four domain scores. There was also a significant improvement in the QBPDS score, which fell from 32 ± 5.1 to 18.8 ± 14.5 after four weeks . Verfaille et al. reported similar results for a sample of 26 chronic LBP patients (mean age: 44.7; range: 26 to 53) in terms of the VAS, SMRT, Shirado test and FFD. These authors also observed a significant improvement in the DPQ overall score and the four domain scores 11 months after the end of the treatment. In a population of 60 chronic LBP patients (mean age: 44 ± 9.8; range: 26 to 65), Genet et al. reported an improvement in all the physical parameters (except for the Sorensen test) at five weeks and at three months. In contrast, this improvement was no longer significant at 12 months, regardless of the physical parameter considered. The QBPDS score was significantly better at five weeks ( p = 0.007) but not at later time points. Lastly, Chaory et al. reported an improvement in pain and physical parameters (except for the SMRT) in a multicentre study of 70 chronic LBP patients (mean age: 42.5 ± 9.2). The authors also observed an improvement in the total QBPDS score (from 40.7 ± 15.7 to 28.1 ± 18.2) after a 5- or 6-week programme. The sensitivity to change (0.80 and 0.78 for the ES and the SRM, respectively) was similar to that found in the present work.


Our study confirmed these results on the clinical and functional levels. For the DPQ, we observed a significant improvement in the “daily living”, “work/leisure” and “anxiety/depression” domains. In contrast, we did not observe any change in the “social interest” domain. This difference may be related to the type of patient management used in the rehabilitation programme, which focuses essentially on the physical and functional domains of LBP and far less on the psychological domain. It can also be explained by the early evaluation (performed at the end of programme, after only four weeks), whereas the effects on the “social interest” domain become apparent later (as shown by Verfaille et al.’s observations after 11 months ). Likewise, Bontoux et al. showed that all the domains are improved after five weeks of a functional rehabilitation programme. In contrast, after six and 12 months, there was a drop off in the level of benefit provided by the programme for all domains. For the QBPDS score (which does not take into account psychosocial aspects), we observed significant improvements in all categories and in the overall score. These benefits were correlated with improvements in the physical tests (particularly the VAS).


Concerning the sensitivity to change, we noted a greater value for the QBPDS than for the DPQ when considering the SRM (0.80 and 0.59, respectively, for the overall score). In contrast, the QBPDS and DPQ’s sensitivities to change were similar when considering the ES (0.62 and 0.61, respectively). We also noted higher sensitivity for the QBPDS’s overall score, relative to its different categories. This can be explained by the overall score’s greater amplitude of variation (from 0 to 100), compared with that of the category scores (from 0 to 15 or 20). However, our results also show that each category was sensitive to change.


The difference in sensitivity between the two tools is probably related to their respective designs and the content of their items . In fact, the QBPDS only takes account of the patient’s functional limitations, whereas the DPQ evaluates cognitive and behavioural aspects and includes more subjective data (such as pain, anxiety/depression status and social relationships). However, in chronic LBP, the absence of a correlation between physical disability and the functional and psychological impact is well established . These various domains probably change over longer time scales and so the “social interest” domain is less likely to improve in just four weeks. Although the physical improvement prompted by the functional rehabilitation programme has a direct impact on physical and functional parameters, this is less true for psychosocial components which depend on other (notably environmental) factors.



Conclusion


This retrospective study of 30 LBP outpatients undergoing a 4-week functional rehabilitation programme showed that the QBPDS’s sensitivity to change (for the overall score and for the four constituent category scores) is satisfactory in this context and is greater than that of the DPQ. Indeed, the Dallas questionnaire appears to be less sensitive to change – notably for the “social interest” domain, although the latter may need to be evaluated further beyond the end of the functional rehabilitation programme.


Sensitivity to change influences a tool’s qualities and its suitability for particular purposes. However, the sensitivity evaluation must be designed according to the scale’s target population. In fact, we believe that the sensitivity of the QBPDS and the DPQ needs to be evaluated at different stages of acute, sub-acute and chronic LBP, in order to judge the impact of different treatments on the scales’ various domains.





Version française



Introduction


De nombreuses échelles d’incapacité fonctionnelle ont été développées dans le cadre de la lombalgie, particulièrement dans sa forme chronique . Les échelles d’Oswestry et de Québec, les questionnaires de Roland-Morris et de Dallas en sont les plus connus, mais aucun ne constitue l’outil gold standard , en regard notamment des critères métrologiques (fiabilité, validité, faisabilité, etc.) qui justifient le choix d’un outil de mesure.


Les deux outils les plus récents, le Quebec Back Pain Disability Scale (QBPDS), ou échelle de Québec , et le Dallas Pain Questionnaire (DPQ), ou questionnaire de Dallas , ont bénéficié d’études démontrant leur fiabilité et leur validité.


Le QBPDS, autoquestionnaire d’évaluation fonctionnelle spécifique de la lombalgie, a été développé et validé parallèlement en anglais et en français du Québec (Canada) par Kopec . Il prend en compte les limitations fonctionnelles liées à la douleur, dans le but de suivre l’évolution de sujets lombalgiques engagés dans des programmes de réadaptation. Cette échelle a fait la preuve de propriétés métrologiques satisfaisantes chez les lombalgiques : fiabilité, reproductibilité, validité de construit. Elle est considérée comme adaptée aux différents niveaux d’incapacité fonctionnelle. Elle est aussi d’une acceptabilité très satisfaisante et d’un temps de passation court (3 à 5 min) . Son utilisation en France est adaptée, malgré quelques termes plus habituels au français québécois . Sa sensibilité au changement, la validité prédictive des scores initiaux et son utilité dans les évaluations longitudinales restent cependant à préciser, notamment en langue française .


Le DPQ est un autoquestionnaire anglo-saxon basé sur une conception cognitivocomportementale de la douleur chronique et conçu pour évaluer le retentissement de la douleur lombaire dans la vie quotidienne . Son champ d’investigation dépasse l’incapacité physique pour s’intéresser aux activités sociales. Ses propriétés métrologiques (fiabilité, reproductibilité, validité de contenu, validité de construit, pouvoir discriminant, validité prédictive) sont établies chez des sujets lombalgiques chroniques . La version originale américaine n’a toutefois pas étudié la sensibilité au changement. Dans la version française du questionnaire de Dallas , la sensibilité au changement a été reconnue pour les dimensions « activités quotidiennes », « travail/loisirs » et « anxiété/dépression » mais pas pour la dimension « comportement social » .


Dans cette étude, nous proposons d’évaluer la sensibilité au changement de l’échelle de Québec et de la comparer à celle du questionnaire de Dallas, sur une population de sujets lombalgiques intégrés à un programme de restauration fonctionnelle du rachis.



Méthodologie



Population


Sujets âgés de 18 à 60 ans, de sexe masculin et féminin, ayant une lombalgie chronique commune quels qu’en soient les mécanismes lésionnels (discopathie, arthrose articulaire postérieure) et les traitements médicaux, orthopédiques ou chirurgicaux proposés.



Méthode


Étude rétrospective sur dossiers de patients pris en charge en hospitalisation de jour pour un programme de restauration fonctionnelle du rachis (RRF) d’une durée de quatre semaines dans un service de médecine physique et réadaptation, à raison de cinq séances par semaine, soit 20 jours au total.



Évaluation clinique et fonctionnelle


Réalisée au premier jour (j1) et au dernier jour du programme (j25), c’est-à-dire à la fin de la quatrième semaine.



Données générales


Âge, sexe, durée d’évolution de la lombalgie, traitements suivis avant ce programme (antalgiques, anti-inflammatoires, antidépresseurs, myorelaxants, infiltrations, traitements chirurgicaux, ou orthopédiques, rééducation).



Données cliniques


Les données cliniques sont :




  • l’évaluation de la douleur : échelle visuelle analogique (EVA) de 10 cm ;



  • l’évaluation de la souplesse sous- et sus-pelvienne par la distance doigts-sol (en centimètre) et l’indice de Schöber-Mac Rae (ISMR, en centimètre) ;



  • le test de Shirado : mesure du temps pendant lequel le sujet, installé en décubitus dorsal au sol, mains au niveau des oreilles, cuisses verticales et jambes posées sur un banc suédois, maintient l’enroulement de la tête et le décollement du tronc jusqu’à la pointe des omoplates en gardant les coudes écartés ;



  • le test de Sorensen : mesure du temps pendant lequel le sujet peut maintenir le dos en position horizontale, sans douleur, alors qu’il est couché à plat ventre, membres inférieurs maintenus par un tiers, le tronc dépassant du bord au niveau du pli de flexion de hanche, les mains placées au niveau des oreilles.




Incapacité fonctionnelle


L’incapacité fonctionnelle :




  • l’échelle de Québec (version française) : elle comporte 20 items regroupés en six catégories : repos/lit, assis/debout, locomotion, mobilité du corps, se pencher, porter/déplacer les objets ; chaque activité est cotée de 0 à 5 selon la difficulté ressentie pour la mener à bien ; un score global (maxima à 100) et un score catégoriel (maxima à 15 pour les quatre premières catégories et à 20 pour les deux dernières) sont ainsi établis et exprimés en valeur absolue ; les scores les plus élevés correspondent aux incapacités physiques les plus sévères ;



  • questionnaire de Dallas (version française) : il comporte 16 items explorant quatre dimensions : activités quotidiennes, travail/loisirs, anxiété/dépression et comportements sociaux ; l’évaluation est chiffrée pour chaque question, ces valeurs sont additionnées et multipliées par un facteur constant ; le score global correspond à la moyenne des quatre sous-scores.




Statistiques


Les moyennes et écarts-types sont établis pour les différentes variables étudiées pour l’ensemble de la population. Les tests statistiques de Mann-Whitney et de Wilcoxon sont utilisés pour la comparaison des résultats, compte tenu des effectifs et des variables analysées, avec un seuil de significativité p < 0,05. L’étude de la sensibilité au changement a utilisé deux indices : réponse standardisée moyenne (RSM) et effet taille (ET) . Notre interprétation de la valeur de ces indices a suivi le classement de Cohen : la sensibilité au changement est médiocre si RSM ou ET inférieur à 0,50, modérée si compris entre 0,51 et 0, 80 et importante si supérieur à 0,80.



Résultats



Population


L’étude a porté sur 30 dossiers, retenus car complets sur l’évaluation. La population est constituée de 19 hommes et 11 femmes, d’un âge moyen de 41,6 ans (extrêmes : 29 à 59 ans). Divers mécanismes lésionnels sont rapportés à l’origine des douleurs lombaires : hernie discale, arthrose, discopathie. Les traitements médicamenteux habituels ont le plus souvent été proposés à l’ensemble des patients (antalgiques de divers paliers, anti-inflammatoires non stéroïdiens, myorelaxants), ainsi que des séances de kinésithérapie ; dix patients ont bénéficié d’une infiltration locale (foraminale ou articulaire postérieure), six d’un traitement orthopédique avec corset et cinq d’une cure de hernie discale.



Effet du programme de RFR



Indices physiques


Les résultats montrent une amélioration clinique significative pour l’ensemble des indices : EVA ( p = 0,0005), ISMR ( p = 0,001), Sorensen ( p < 0,0001), Shirado ( p = 0,003) et distance main sol ( p = 0,005) ( Tableau 1 ).


Apr 23, 2017 | Posted by in PHYSICAL MEDICINE & REHABILITATION | Comments Off on Sensitivity to change of the Quebec Back Pain Disability Scale and the Dallas Pain Questionnaire

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