Skip to main content
Health and Quality of Life Outcomes logoLink to Health and Quality of Life Outcomes
. 2011 May 12;9:32. doi: 10.1186/1477-7525-9-32

Evaluating oral health-related quality of life measure for children and preadolescents with temporomandibular disorder

Taís S Barbosa 1, Marina S Leme 1, Paula M Castelo 2, Maria Beatriz D Gavião 1,
PMCID: PMC3115836  PMID: 21569403

Abstract

Background

Oral health-related quality of life (OHRQoL) in children and adolescents with signs and symptoms of temporomandibular disorder (TMD) has not yet been measured. This study aimed to evaluate the validity and reliability of OHRQoL measure for use in children and preadolescents with signs and symptoms of TMD.

Methods

Five hundred and forty-seven students aged 8-14 years were recruited from public schools in Piracicaba, Brazil. Self-perceptions of QoL were measured using the Brazilian Portuguese versions of Child Perceptions Questionnaires (CPQ)8-10 (n = 247) and CPQ11-14 (n = 300). A single examiner, trained and calibrated for diagnosis according to the Axis I of the Research Diagnostic Criteria for TMD (RDC/TMD), examined the participants. A self-report questionnaire assessed subjective symptoms of TMD. Intraexaminer reliability was assessed for the RDC/TMD clinical examinations using Cohen's Kappa (κ) and intraclass correlation coefficient (ICC). Criterion validity was calculated using the Spearman's correlation, construct validity using the Spearman's correlation and the Mann-Whitney test, and the magnitude of the difference between groups using effect size (ES). Reliability was determined using Cronbach's alpha, alpha if the item was deleted and corrected item-total correlation.

Results

Intraexaminer reliability values ranged from regular (κ = 0.30) to excellent (κ = 0.96) for the categorical variables and from moderate (ICC = 0.49) to substantial (ICC = 0.74) for the continuous variables. Criterion validity was supported by significant associations between both CPQ scores and pain-related questions for the TMD groups. Mean CPQ8-10 scores were slightly higher for TMD children than control children (ES = 0.43). Preadolescents with TMD had moderately higher scores than the control ones (ES = 0.62; p < 0.0001). Significant correlation between the CPQ scores and global oral health, as well as overall well-being ratings (p < 0.001) occurred, supporting the construct validity. The Cronbach's alphas were 0.93 for CPQ8-10 and 0.94 for CPQ11-14. For the overall CPQ8-10 and CPQ11-14 scales, the corrected item-total correlation coefficients ranged from 0.39-0.76 and from 0.28-0.73, respectively. The alpha coefficients did not increase when any of the items were deleted in either CPQ samples.

Conclusions

The questionnaires are valid and reliable for use in children and preadolescents with signs and symptoms of temporomandibular disorder.

Introduction

Over the years, different theories of etiology and different emphases on the causative factors for the various signs and symptoms of temporomandibular disorder (TMD) have been proposed in the literature [1]. The current perspective regarding TMD is now multidimensional, with an appreciation that a combination of physical, psychological and social factors may contribute to the overall presentation of this disorder. Hence, today there is a preference for a biopsychosocial integrated approach [2]. Accordingly, TMD patients are a target population for quality of life (QoL) assessments because of the considerable psychosocial impact of orofacial pain [3]. TMD have generally been presumed to be conditions affecting only adults; however, epidemiological studies have reported signs and symptoms in children and adolescents to be as frequent as in adults [4] and the prevalence varies widely in the literature from 16% to 90%, due to the methodologies focusing largely on samples of patients seeking treatment or because they were conducted on convenience non-representative samples of the population. Brazilian studies have shown that in primary dentition 34% of the 99 children presented at least one sign and/or one symptom of TMD [5]. In the age of 12 years, 2.19% of the boys and 8.18% of the girls met the Research Diagnostic Criteria for TMD (RDC/TMD) when examined [6]. From 15 to 20 years-old 35.4% presented at least one symptom of TMD [7]. Signs and symptoms in childhood and adolescence have been indicating mild disorders, but these findings do not detract from the importance of early diagnosis to provide proper growth and development of the stomatognathic system [8]. Additionally the known fluctuation in signs and symptoms of musculoskeletal disorders in a time-dependent context might have been better addressed by carrying out repeated clinical recordings [4]. In addition, Dahlström and Carlsson [9], in a recent systematic review, observed a substantial negative impact on oral health-related quality of life (OHRQoL) in patients diagnosed with TMDs, being greater than other orofacial diseases/illnesses or conditions.

In this way, measuring health-related quality of life (HRQoL) in TMD patients with generic or condition-specific HRQoL instruments can complement efficacy measures, offering a complete picture of the impact of disease and treatment on overall well-being, as observed in adolescents with type 1 diabetes [10]. Jedel et al. [11] compared the HRQoL between children with TMD pain and a control group, using the Child health questionnaire-child form 87 (CHQ-CF87), a generic multidimensional instrument designed to assess physical and psychosocial impacts on children and adolescents aged 10-18 years. Although the results supported the use of generic instrument to measure health and to evaluate the efficacy of treatment in pediatric patients with TMD pain [11], other authors recommend the use of condition-specific instruments, which are more sensitive for detecting slight changes in specific conditions [12] and might allow a more detailed evaluation of the disability caused by TMD [13]. Accordingly, studies were conducted to evaluate the impact of TMD and associated pain on QoL in adult [3,12,14,15] and elderly [16] populations, using a condition-specific instruments, i.e., an OHRQoL measure (e.g., Oral Health Impact Profile and Geriatric Oral Health Assessment Index). The concepts in OHRQoL provide an opportunity to summarize a variety of possible psychosocial impacts in relation to specific oral diseases [14].

Measures have been developed specifically for assessing OHRQoL of children and adolescents [17-21]. The Child Perceptions Questionnaire (CPQ) is a measure applicable to children with a wide variety of oral and orofacial conditions, based on contemporary concepts of pediatric health and which can accommodate developmental differences among children across age ranges [17,18]. It consists of two age specific instruments for children aged 8-10 years (CPQ8-10) [18] and 11-14 years (CPQ11-14) [17]. A preliminary study has confirmed the validity and reliability of these measures for use in Brazilian children and adolescents [22]. Although these questionnaires are standardized and widely used for other oral conditions, they have not yet been tested in TMD samples.

Assessing the impact of TMD on children's QoL is important in many fronts. It provides an insight into the potential consequences of TMD to the day-to-day lives of children and thereby facilitates understanding of its importance in the provision of oral health care [23]. Moreover, identifying factors associated with the impact of TMD on children's QoL can influence management of such cases and inform best practice guidelines [24]. In this way, the present study aimed to test the validity and reliability of CPQ used in a population of Brazilian public school students aged 8-14 years to determine whether these measures are sensitive to clinical signs and subjective symptoms of TMD. An additional aim was to verify whether the presence and severity of signs and symptoms of TMD are sufficient to influence OHRQoL of this age-specific population.

Material and methods

This study was approved by the Research Ethics Committee of the Dental School of Piracicaba, State University of Campinas (protocol n°021/2006).

A cross-sectional study with students of public schools of Piracicaba, Brazil, was developed. Piracicaba city has 368.843 scholars, with 50.187 enrolled in the elementary school system http://www.ibge.gov.br. The sample size was calculated by Epi info version 6.0.1 software. A standard error of 2%, a 95% confidence interval level and a 5.73% prevalence of TMD [25] were used for the calculation. The minimum sample size to satisfy the requirements was estimated at 513 subjects. A total of 547 students (235 boys and 312 girls), with no systemic diseases or communication and/or neuromuscular problems, participated in the study. The subjects ranged from 8 to 14 years of age, and were from nine public schools, which were randomly selected. All students obtained parental consent.

The exclusion criteria were conditions/children with facial traumatism, neurological or psychiatric disorders, use of dental prostheses, current use of medications (e.g., antidepressive, muscle relaxant, narcotic or non-steroidal anti-inflammatory), previous or present orthodontic treatment and other orofacial pain conditions, which could interfere with TMD diagnoses.

Data collection

Oral health-related quality of life evaluation

Data were collected using the Portuguese versions of the CPQ for individuals aged 8-10 years (CPQ8-10) and 11-14 years (CPQ11-14) [22]. These formed the components of the Child Oral Health Quality of Life Questionnaire that had been designed to assess the impact of oral conditions on the QoL of children and adolescents [17,18]. They were both self-completed. Items of the CPQ used Likert-type scales with response options of "Never" = 0; "Once or twice" = 1; "Sometimes" = 2; "Often" = 3; and "Very often" = 4. For the CPQ11-14, the recall period was three months, while for that of the CPQ8-10, it was four weeks. Items were grouped into four domains: oral symptoms, functional limitations, emotional well-being and social well-being.

Children and adolescents were also asked to give overall or global assessments of their oral health and the extent to which the oral or oro-facial condition affected their overall well-being. These questions preceded the multi-item scales in the questionnaires. A four-point response format, ranging from "Very good" = 0 to "Poor" and from "Not at all" = 0 to "A lot" = 3, was offered for these ratings in CPQ8-10. In CPQ11-14, these global ratings had a five-point response format ranging from "Excellent" = 0 to "Poor" = 5 for oral health and from "Not at all" = 0 to "Very much" = 5 for well-being.

Evaluation of signs and symptoms of TMD

Intraexaminer reliability

Prior to the clinical examinations, the dental examiner (TSB) participated in the calibration process, which was divided into theoretical discussions on codes and criteria for the study, as well as practical activities. Intra-examiner reliability was investigated by conducting replicated examinations on 20 individuals one week later to minimize recall bias as a result of the first test.

RDC/TMD

The RDC/TMD is a classification system composed by a dual-axis approach: Axis I (physical findings) and Axis II (pain-related disability and psychosocial status).

Subjective symptom interview

A self-report questionnaire was used to assess subjective symptoms according to Riolo et al. [26], regarding pain in the jaws when functioning (e.g., chewing), unusually frequent headaches (i.e., more than once a week and of unknown etiology), stiffness/tiredness in the jaws, difficulty opening one's mouth, grinding of the teeth and sounds from the TMJ. Each question could be answered with a "yes" or a "no."

Moreover, three specific questions (yes/no) of the RDC/TMD Axis II were considered for further TMD diagnosis [27,28]: (1) Have you had pain in the face, jaw, temple, in front of the ear or in the ear in the past month?; (2) Have you ever had your jaw lock or catch so that it won't open all the way?; (3) Was this limitation in jaw opening severe enough to interfere with your ability to eat? The other questions of Axis II were not included due to difficulty to understand or inappropriate for children.

Clinical signs evaluation

The clinical signs of TMD were assessed using the RDC/TMD criteria (Axis I) described as follows [28,29]:

Pain Site. To determine whether the present pain was ipsilateral to the pain provoked by the clinical examination of the masticatory muscles and during jaw function.

Mandibular Range of Motion (mm) and Associated Pain. Jaw-opening patterns. Corrected and uncorrected deviations in jaw excursions during vertical jaw opening. Vertical range of motion of the mandible. Extent of unassisted opening without pain, maximum unassisted opening and maximum assisted opening. Mandibular excursive movements. Extent of lateral and protrusive jaw excursions.

Temporomandibular Joint Sounds. Palpation of the TMJ for clicking, grating, and crepitus sounds during vertical, lateral and protrusive jaw excursions.

Muscle and Joint Palpation for Tenderness. Bilateral palpation of extraoral and intraoral masticatory and related muscles (n = 20 sites) and bilateral palpation of the TMJ (n = 4 joint sites).

The clinical evaluation selected individuals with at least one sign and one symptom of TMD [30], who were referred to as the TMD group in this present study. Subjects meeting the criteria for myofascial pain with or without limited opening (Axis I, Group 1a or 1b disorders) and/or for disc displacement with reduction, without reduction with limited opening or without reduction without limited opening (Axis I, Group 2a, 2b or 2c) or for arthralgia or arthritis (Axis I, Group 3a or 3b) were considered to have an RDC/TMD diagnosis (RDC/TMD diagnosis group) [28]. The control group consisted of individuals with no current signs or symptoms of TMD (supercontrols) or those without signs or symptoms of TMD (control group) [14,28]. This recruitment strategy was based on the principle that subjects belonging to different groups will almost certainly respond differently to the questionnaire [31]. If the questionnaire is valid, it must be sensitive to such differences.

Data analysis

Statistical analyses were performed using SPSS 9.0 (SPSS, Chicago, IL, USA) with a 5% significance level and normality was assessed using the Kolmogorov-Smirnov test. Since score distributions were asymmetrical, non-parametrical tests were used in the performed analyses.

Overall scores for each participant were calculated by summing the item codes, whereas the subscale scores were obtained by summing the codes for questions within the four health domains. Descriptive statistics were followed by bivariate analyses, which used (where appropriate) Chi-squared and Fisher's exact tests for a comparison of proportions and Mann-Whitney test for a comparison of the means of the continuous variables.

Intraexaminer reliability

Intraexaminer reliability calculations were performed on 20 individuals who participated in the Axis I assessment and the Axis II diagnosis interview. Only three questions (3, 14a, 14b) from the latter were used as required determinants for the Axis I diagnoses.

The two most commonly accepted methods for assessing the intraexaminer reliability were used [32]. When the clinical examination variable could be measured on a continuous scale, reliability was assessed by computing the intraclass correlation coefficient (ICC), using the one-way analysis of variance random effect parallel model [33]. The strength of the intra-examiner agreement was based on the following standards for ICC: < 0.2, poor; 0.21-0.40, fair; 0.41-0.60, moderate; 0.61-0.80, substantial and 0.81-1.0, excellent to perfect [34]. The Kappa statistic (Cohen's Kappa, κ) was computed to assess the reliability when variables were measured with a categorical rating scale (e.g., yes/no). Kappa values above 0.8 were considered excellent, from 0.61 to 0.8 good, 0.41 to 0.6 acceptable, 0.21 to 0.40 regular and below 0.20 fair [35].

Validity

The validity of a questionnaire represents the degree to which it measures what it is meant to measure. Criterion validity was calculated by comparing the correlations between CPQ scores and pain scores (obtained from Question 3 of the RDC/TMD Axis II), using the Spearman's correlation coefficient. As pain was considered a variable only in the TMD patients, the relevant correlation coefficients were calculated only for the TMD groups.

Discriminant construct validity was evaluated by comparing the mean scale scores between TMD and control groups using the Mann-Whitney test. The magnitude of the difference between groups was assessed using the effect size (ES). This was derived from the mean difference in scores between the groups divided by the pooled SD of scores: a value of 0.2 was taken to be small, 0.5 to be moderate and 0.8 to be large [36]. Discriminant construct validity was also assessed by verifying the difference between RDC/TMD diagnosis (individuals in Group I, II or III diagnosis) and "supercontrol" groups (individuals with no current sign and symptom of TMD). Correlational construct validity was assessed by comparing the mean scores and global ratings of oral health and overall well-being using Spearman's correlation coefficient.

Internal reliability

Reliability can be defined as a measure of the internal consistency or homogeneity of the items. Two measures were used for the analysis of internal reliability; the corrected item total correlation and the Cronbach's alpha coefficient [37]. Values above 0.2 for the former and 0.7 for the latter can be acceptable [38]. Alphas were also calculated with each item deleted.

Results

Descriptive statistics

A sample distribution of the evaluated characteristics (e.g., age, gender, TMD groups and CPQ scores) is shown in Additional file 1. Female children and preadolescents were more prevalent in TMD groups. Muscle tenderness and headaches were the most frequent signs and symptoms of TMD found in children and preadolescents, being observed more significantly in girls than in boys (Chi-squared test).

Intraexaminer reliability

Among the 20 subjects for the reliability study, there were 14 girls and 6 boys with an average age of 10.30 ± 1.78 years. Fourteen of the subjects complained of symptoms suggestive of TMD, while six were asymptomatic. In almost all subjects (n = 19), at least one sign of TMD was observed. The frequency of individuals with RDC/TMD diagnosis was 10% for muscle tenderness and 5% for disc displacements, respectively.

Table 1 shows the intraexaminer reliability for the clinical examinations and diagnostic questions of RDC/TMD. The ICC and Kappa values for the former ranged from 0.49 to 0.74, indicating a moderate to substantial agreement and from 0.30 to 0.96, indicating a regular to excellent agreement, respectively. High levels of reliability were found for all three questions of the Axis II, with kappa values ranging from 0.70 to 0.81.

Table 1.

Intraexaminer reliability of diagnostic questions and clinical examinations of the RDC/TMD criteria (n = 20)

Reliability

RDC/TMD criteria Statistical tests Interpretation
Sign of TMD - Axis I
Muscle tenderness
 Extraoral myofascial sites (4-category variable) 0.74 Substantial agreement
 Intraoral myofascial sites (4-category variable) 0.53 Moderate agreement
 Jaw movements* 0.46 Acceptable agreement
Joint pain
 Palpation (4-category variable) 0.67 Substantial agreement
 Jaw movements* 0.96 Excellent agreement
Range of motion
 Vertical dimension (mm) 0.68 Substantial agreement
 Jaw excursions (mm) 0.49 Moderate agreement
 Jaw-opening pattern* 0.30 Regular agreement
Joint sounds
 Sound on jaw movement* 0.84 Excellent agreement

(Question) Symptom of TMD - Axis II*
 (3) Pain in facial area, the jaws or the jaw joint 0.81 Excellent agreement
 (14a) Limitation in jaw opening 0.70 Good agreement
 (14b) Diet restriction due to limitation in jaw opening 0.80 Good agreement

RDC/TMD, research diagnostic criteria for temporomandibular disorder

* Cohen's Kappa

† Intraclass correlation coefficient

Criterion validity

Table 2 shows the correlations between the scores of the different subscales and variable pain, which was the sum of the positive responses to question number 3 of the RDC/TMD Axis II, "Have you had pain in the face, jaw, temple, in front of the ear or in the ear in the past month?" There were positive correlations between the CPQ11-14 total scores and variable pain (r = 0.32, p < 0.0001). Positive correlations were also observed between all of the domains of CPQ11-14 and pain scores. There were no significant correlations observed between the scale and subscale CPQ8-10 scores and variable pain, with the exception of the functional limitation subscale (r = 0.18, p < 0.05).

Table 2.

Criterion validity: correlations between the CPQ scores and variable pain (Question 3, RDC/TMD Axis II) for TMD groups

TMD groups Pain variable

ra P
CPQ8-10 Total scale 0.14 0.089
n = 141 Subscales
 Oral symptoms 0.13 0.106
 Functional limitations 0.18 0.024
 Emotional well-being 0.06 0.476
 Social well-being 0.09 0.278

CPQ11-14 Total scale 0.32 < 0.0001
n = 176 Subscales
 Oral symptoms 0.33 < 0.0001
 Functional limitations 0.26 0.000
 Emotional well-being 0.24 0.001
 Social well-being 0.27 0.000

TMD, temporomandibular disorder; CPQ, child perceptions questionnaire

a Spearman's correlation coefficient

Discriminant construct validity

Children with signs and symptoms of TMD reported, on average, worse OHRQoL than the control group, as indicated by the mean overall scores of 20.6 versus 13.5, respectively (Table 3). The effect size of 0.43 indicated that the difference between the groups was moderate (p < 0.0001). The CPQ8-10 scores for the TMD group were also higher than in all subscales. When expressed as effect size, the magnitude of the mean differences was small to moderate. The mean score in the RDC/TMD diagnosis group (25.6 ± 22.3) was moderately higher than in the "supercontrol" group (7.5 ± 7.8) (Table 4). There were also significant differences between the groups for all the domains, with effect sizes ranging from moderate for functional (ES = 0.58), emotional (ES = 0.50) and social (ES = 0.54) domains to large for the oral symptom subscale (ES = 0.87).

Table 3.

Discriminant construct validity: a comparison between the CPQ mean scores of the TMD and control groups

TMD group (n = 141) Control group (n = 106)

Mean (SD) Mean (SD) P* ES
CPQ8-10 Overall scale [0-100] 20.6 (17.7) 13.5 (15.4) < 0.0001 0.43
Subscales
 Oral symptoms [0-20] 7.2 (4.0) 5.2 (3.9) < 0.0001 0.55
 Functional limitations [0-20] 3.8 (4.2) 2.6 (3.8) 0.001 0.36
 Emotional well-being [0-20] 4.6 (4.7) 2.6 (4.1) < 0.0001 0.52
 Social well-being [0-40] 5.5 (7.4) 3.1 (5.9) 0.009 0.39

TMD group (n = 176) Control group (n = 124)

Mean (SD) Mean (SD) P* ES

CPQ11-14 Overall scale [0-148] 27.6 (20.7) 16.3 (14.8) < 0.0001 0.62
Subscales
 Oral symptoms [0-24] 7.0 (4.7) 5.2 (3.5) < 0.0001 0.46
 Functional limitations [0-26] 6.5 (5.6) 3.6 (4.2) < 0.0001 0.62
 Emotional well-being [0-36] 7.9 (7.6) 4.5 (5.6) < 0.0001 0.53
 Social well-being [0-52] 5.9 (6.7) 2.9 (4.0) < 0.0001 0.56

TMD, temporomandibular disorder; CPQ, child perceptions questionnaire

Values in square brackets indicate range of possible scores

* P-values obtained from Mann-Whitney test

† ES = Effect sizes, difference in group means/pooled SD

Table 4.

Discriminant construct validity: CPQ overall and domain scores by the RDC/TMD diagnosis and "supercontrol" groups

RDC/TMD Diagnosis Group (n = 32) Supercontrol Group (n = 28)

Mean (SD) Mean (SD) P* ES
CPQ8-10 Overall scale [0-100] 25.6 (22.3) 7.5 (7.8) < 0.0001 0.61
Subscales
 Oral symptoms [0-20] 8.7 (4.6) 3.5 (3.4) < 0.0001 0.87
 Functional limitations [0-20] 4.8 (4.7) 1.3 (1.9) < 0.0001 0.58
 Emotional well-being [0-20] 4.7 (5.2) 1.1 (1.7) 0.000 0.50
 Social well-being [0-40] 7.4 (9.6) 1.7 (3.1) 0.006 0.54

RDC/TMD Diagnosis Group (n = 69) Supercontrol Group (n = 29)

Mean (SD) Mean (SD) P* ES

CPQ11-14 Overall scale [0-148] 35.0 (24.1) 11.7 (9.6) < 0.0001 0.88
Subscales
 Oral symptoms [0-24] 8.7 (5.8) 4.2 (2.1) < 0.0001 0.74
 Functional limitations [0-26] 8.8 (7.0) 2.2 (2.9) < 0.0001 0.89
 Emotional well-being [0-36] 10.0 (8.9) 3.1 (4.1) < 0.0001 0.73
 Social well-being [0-52] 7.5 (6.8) 2.1 (3.4) < 0.0001 0.82

TMD, temporomandibular disorder; CPQ, child perceptions questionnaire

Values in square brackets indicate range of possible scores

* P-values obtained from Mann-Whitney test

† ES = Effect sizes, difference in group means/pooled SD

Preadolescents in the TMD group had, on average, higher overall scores than in the control group (27.6 vs. 16.3; p < 0.0001) (Table 3). The same difference was observed in all domains, with the mean functional and social well-being score being two times higher in the former than in the latter patient group: 6.5 vs. 3.6 (p < 0.0001) and 5.9 vs. 2.9 (p < 0.0001). The magnitude of the differences between the clinical groups was moderate, ranging from 0.46 in the oral symptoms domain to 0.62 in the functional limitations domain. When the scores for the RDC/TMD diagnosis groups were examined, preadolescents diagnosed with TMD had significantly higher scores than the "supercontrol" group for all total and subscale CPQ11-14 scores (Mann-Whitney U test) (Table 4).

Correlational construct validity

As an index of construct validity, Spearman's correlation was highly significant at the 0.0001 level in both global ratings for CPQ8-10 total scales in the TMD group (Table 5). Positive correlations were also observed between all the CPQ8-10 subscale scores and global oral health ratings, as well as overall well-being.

Table 5.

Correlational construct validity: correlations between CPQ scores and global ratings of oral health and overall well-being (TMD groups)

TMD groups CPQ8-10 (n = 141) CPQ11-14 (n = 176)

Oral Health Overall Well-being Oral Health Overall Well-being

Ra Pb Ra Pb Ra Pb Ra Pb
Total scale 0.36 < 0.0001 0.41 < 0.0001 0.37 < 0.0001 0.62 < 0.0001
Subscales
 Oral symptoms 0.37 < 0.0001 0.39 < 0.0001 0.36 < 0.0001 0.42 < 0.0001
 Functional limitations 0.25 0.002 0.41 < 0.0001 0.28 0.000 0.48 < 0.0001
 Emotional well-being 0.44 < 0.0001 0.38 < 0.0001 0.34 < 0.0001 0.57 < 0.0001
 Social well-being 0.28 0.000 0.36 < 0.0001 0.26 0.000 0.53 < 0.0001

TMD, temporomandibular disorder; CPQ, child perceptions questionnaire

The TMD group showed significant correlations between overall CPQ11-14 scores and global oral health ratings (p < 0.0001) and overall well-being (p < 0.0001). Significant correlations were also observed between the scores for all CPQ11-14 subscale scores and both global ratings (Table 5).

Reliability

Internal consistency reliability was assessed for the TMD samples using Cronbach's alpha (Table 6). This was 0.93 for the total CPQ8-10 and ranged from 0.68 to 0.90 for the subscales, indicating an acceptable to good level of internal consistency. For the overall CPQ8-10 scale, the corrected item-total correlation coefficients were from 0.39 to 0.76 and for the domains the same coefficients ranged from 0.37 to 0.77. The alpha coefficients did not increase when any of the items were deleted.

Table 6.

Internal consistency reliability: Cronbach's alpha, Alpha if item deleted and Corrected item-total correlation (TMD groups)

TMD groups Number of items Cronbach's alpha Range of α's if items deleted Range of corrected item total correlations
CPQ8-10 Total scale 25 0.93 (0.93-0.93) (0.39-0.76)
n = 141 Subscales
 Oral symptoms 5 0.68 (0.61-0.66) (0.37-0.48)
 Functional limitations 5 0.78 (0.70-0.75) (0.51-0.67)
 Emotional well-being 5 0.85 (0.81-0.83) (0.60-0.71)
 Social well-being 10 0.90 (0.88-0.90) (0.52-0.77)

CPQ11-14 Total scale 37 0.94 (0.93-0.94) (0.28-0.73)
n = 176 Subscales
 Oral symptoms 6 0.69 (0.62-0.68) (0.33-0.51)
 Functional limitations 9 0.79 (0.76-0.78) (0.40-0.57)
 Emotional well-being 9 0.90 (0.88-0.89) (0.59-0.76)
 Social well-being 13 0.87 (0.85-0.87) (0.28-0.67)

TMD, temporomandibular disorder; CPQ, child perceptions questionnaire

A total of 176 TMD individuals were used to test the internal reliability of the CPQ11-14 (Table 6). Cronbach's alpha for CPQ11-14, as a whole, was excellent (0.94). For the domains of the CPQ11-14, the coefficients ranged from 0.69 for oral symptoms to 0.90 for emotional well-being, indicating an acceptable to good levels of internal consistency reliability. The corrected item-total correlations for the total CPQ11-14 scale ranged from 0.28 to 0.73. For the CPQ11-14 subscales, the corrected item-total correlation coefficients ranged from 0.28, which represented the lower coefficient for the social well-being domain, to 0.76 for emotional well-being. The alpha was not higher when any item was deleted.

Discussion

This study was undertaken to provide evidence of the reliability and validity of the CPQ8-10 and CPQ11-14 in children and preadolescents with signs and symptoms of TMD. Our previous study had indicated that these measures were able to discriminate between children and preadolescents with different levels of severity of dental caries, malocclusion, fluorosis and gingivitis [22]. According to Locker et al. [39], the process of evaluating HRQoL measures consists of two stages; the first involves an assessment of the reliability and validity and the second consists of on-going evaluations of the performance in different populations and the various contexts for which it was intended. Furthermore, the linguistic and cultural context in which a measure is used can have a bearing on the validity, as can the intended purpose of the measure; thus prior validity and reliability tests, the instruments must be translated, back-translated, and cross culturally adapted in order to ensure their conceptual and functional equivalences [22,27,31].

The RDC/TMD had been the best and most used classification system to date for epidemiological studies that sought to understand TMD etiology and mechanisms [40]. Together, Axis I and Axis II assessments constitute a comprehensive evaluation consistent with the biopsychosocial health model [2]. In this study, only three specific items for the latter were included, since they were more appropriate for the age sample. Accordingly, a questionnaire containing items regarding self-reported pain and associated symptoms of TMD [26] was used to replace the pain-related disability approach of RDC/TMD Axis II [41].

Reliability and validity are the basic underpinnings of any scientific measure. The reliability of a diagnostic instrument sets the upper limit for its validity [42]. Several studies evaluating the reliability of clinical findings have shown that the experiences and calibration of the examiners are crucial for accuracy of the results [32,43,44], as done in the present study. Individuals with most common TMD conditions as well as asymptomatic controls were included in the reliability assessment (n = 20) to ensure that a broad spectrum, ranging from none to severe findings, was present [32,45]. It provided a more realistically simulated actual clinical and research conditions, wherein patients and subjects who were both symptomatic and asymptomatic for TMD might actually appear to undergo RDC/TMD diagnostic examinations [46]. Other influencing factors included the feasibility of conducting such examinations in an acceptable time frame [46-48].

Considering the minimum acceptable level for agreement at 0.40 (kappa) for categorical measures and at 0.70 (ICC) for continuous variables [49], inconsistency was found in some RDC/TMD measurements, mainly in the pain scores and in the ranges of motion. However, the overall reliability results were still good. The poor intraoral muscle reliability found in the present study and by others [43,47] could be explained by the low specificity of muscle palpation [50,51]. Moreover, a low reproducibility for the pain scores is not unusual because pain intensities do vary over even short periods of time [52] partly due to poor memory recall for pain [53]. Only a moderate level of reproducibility was found for jaw excursions, compared with other studies where more agreement was observed [43,47]. In addition, differences in reliability findings may reflect variations in the methodology, such as differences in subject samples, numbers of examiners, study designs, statistical analyses, as well as prevalence and sampling variability [43,46,54].

Muscle tenderness was the most frequent clinical sign, found in 77.3% of children and 67% of preadolescents, agreeing with Tuerlings and Limme [55]. However, these results must be carefully considered given the low specificity of muscle palpation [50,51]. The prevalence of joint pain was substantial, being the second most frequent sign observed in 48.9% of the children and 44.9% of the preadolescents, higher than values observed in adolescents by Bonjardim et al. [41] (7.83%-10.6%). The less prevalent sign of TMD were TMJ sounds, found in just 5% of the children and 8% of the preadolescents and even lower than those observed in previous studies [41,56,57]. The difference in findings may reflect variations in the tools being used. The high sensitivity of RDC/TMD classification for TMJ sounds, which is based on reproducible clicks on two of three trials, contributes to the elimination of indistinct or temporary clicking sounds [32], decreasing the probability of false positive results.

In TMD groups, the presence of headaches was higher in children than in preadolescents, as previously observed [41,56,58]. There was no gender difference in the symptomatic children, but among preadolescents, the prevalence of headaches associated with TMD was higher in girls than in boys. In line with these findings, previous studies found an increasing of this association with age among adolescents, especially in females [59,60]. Similarly, the higher prevalence of the clinical signs of TMD, mainly painful signs among females, was consistent with some previous findings [57,58,61], whereas others found no gender-linked relationships [41,62]. The difference between genders could probably be explained by the fact that girls may be more sensitive to tenderness and pain on palpation of the TMJ and adjacent muscles [63] mainly in older age due to hormonal changes [56,61].

Ideally, criterion validity would be measured relative to a "gold standard." As no such standard exists for oral health status measures, criterion validity was evaluated by correlating the CPQ scores with a score corresponding to the sum of the answers to the item investigating pain (Question 3, RDC/TMD Axis II). This approach is consistent with literature reports that suggest the use of external criteria to test criterion validity [31]. Subjects with pain-associated conditions presented higher impacts on daily function in this study and in others performed in adult [3,12] and elderly [10] populations. Accordingly, the patients' well-being decreased as a function of pain duration and increased in pain intensity, frequency and number of pain sites [12,31]. In the only study to address this issue in youth patients, Jedel et al. [11] found that children and adolescents with TMD pain more than once a week were associated with higher impacts on physical functioning, emotional roles and behavioral roles, resulting in limitations on physical activities, school work and activities with friends. Similarly, positive correlations were observed between all the domains of CPQ11-14 and pain scores for preadolescents. Although a substantial prevalence of pain symptoms existed in the CPQ8-10 sample (36.2%), only the functional domain was associated with this variable. It is likely that reporting symptoms of minor severity or of fleeting nature resulted in such a high prevalence. Less severe pain and sensations may be responsible for less impaired OHRQoL in children reporting TMD. In fact, patients with TMD initially display functional limitations. These are followed by psychological discomfort, social disability and handicap and finally chronic pain [31]. This progression can also explain the different discriminant construct validity results, which compared the controls with both TMD groups and with the advanced cases.

The discriminant construct validity of the questionnaires was supported by their ability to detect differences in the impact on QoL, evidenced by the highest scores being seen in children and preadolescents with signs and symptoms of TMD. However, although the difference in scores supported the validity of the measures, the magnitude of these differences was only low to moderate. According to Reissmann et al. [14], the magnitude of TMD impact depends on the definition of the comparison group without TMD diagnoses. Although patients in the general population are the most plausible choice for comparison (which was chosen in the present study), they may have some signs and symptoms of TMD; these are insufficient to warrant an RDC/TMD diagnosis but sufficient to influence QoL. This is consistent with the findings by Reissmann et al. [14], where subjects without diagnosis had a more than 50% higher OHRQoL impact levels compared to subjects without any TMD sign or symptom. Other authors suggest that differences in scores of QoL measures can be properly interpreted only after minimally important differences have been recognized [64]. The minimum important difference is defined as the smallest difference in scores that patients perceive as being important, which would suggest a change in the patient's management [65]. This score can be determined only following longitudinal studies in which some individuals changed and some did not, either as the result of therapy or natural fluctuations in the disorder. This evaluation has yet to be undertaken with respect to the measures used in this study.

Evidence that the higher scores of the TMD individuals may be important was found in the responses of the advanced cases when compared to the "supercontrol" reports. Analyses of the scores derived from both questionnaires indicated that the QoL of children and preadolescents diagnosed with TMD was markedly worse than that of individuals with no current signs or symptoms of TMD. These results were consistent with the higher impact found in adults diagnosed with TMD when compared with control groups in the study by Rener-Sitar et al. [15], which suggested that diagnoses associated with pain (e.g., myofascial pain, arthralgia) have a higher impact than non-pain-related diagnoses (e.g., disc displacement with reduction). Considering that muscle tenderness was the most frequent diagnosis observed among the evaluated TMD sample, greater impact on QoL was expected for these subjects.

The construct validity was further supported when the CPQ scores were assessed for the TMD groups against the global questions, as high correlations between them suggest that they are measuring the same construct. Moreover, these associations showed that the reported issues and concerns of the TMD groups extend beyond oral health and are of sufficient magnitude to have some effect on their life as a whole. It means that the questionnaires actually measured as originally intended [38].

Accepted minimal standards for internal reliability coefficients are 0.70 for group comparisons and 0.90-0.95 for individual comparisons [66]. Accordingly, the reliability coefficients for both CPQ total and subscales exceeded standards for group and individual level comparisons [67], except for oral symptoms domains, which were slightly lower at 0.68 for CPQ8-10 and at 0.69 for CPQ11-14. However, these values can be acceptable, as they are far greater than 0.50, an indicative level for non-homogeneous scales [68]. According to Gherunpong et al. [59], alpha is not a perfect indicator of reliability, as it tends to underestimate the reliability of multidimensional scales and because lower values can be expected from health-related measures. All item-total correlations were above the minimum recommended level of 0.20 [19] and alpha did not increase when an item was deleted.

The greatest strenght of this study is the use of the standardized OHRQoL questionnaires and also the standardized assessment of the level of impairment of different anatomical structures that constitute a stomatognathic system according to the RDC/TMD protocol [15]. Besides that, the recruitment strategy of sample allowed for a spectrum of participants, which provided a valid estimation of the differences between individuals with variety levels of severity of the same clinical condition, so that a judgement could safely be made concerning the generalisation of the results to that population [31]. On the other hand, it is also important to recognize the limitations of the work performed in terms of the methodology and analytic strategies used [69]. Given the cross-sectional nature of the data study, the observed finding could address only the descriptive and discriminative potential of OHRQoL measures in relation to TMD condition. Further research is required to determine whether or not these instruments discriminated between groups of children and adolescents with different clinical conditions. Studies should also include the measurement of factors that may account for the variation in OHRQoL observed in TMD patients, as well as, for other oral conditions. Finally, longitudinal studies are required to demonstrate OHRQoL responsiveness to change prior to using it in a context where change is expected, desired or possible [70].

Conclusions

The results of this study emphasize the importance of perceived health status and QoL assessment for evaluating TMD patients, since signs and symptoms of TMD can have a substantial functional, emotional and psychologic impact, negatively affecting the QoL of children and preadolescents. Comparisons between individuals with different levels of the same condition clearly indicated the progressive aspects of the pathology that appear in advanced cases. Sufficient descriptive and discriminative psychometric properties of CPQ in TMD populations make these instruments suitable for assessing OHRQoL in cross-sectional studies. Finally, further studies are required to confirm the evaluative potential of these measures in this clinical and age-specific population.

Abreviattions

(CPQ): Child Perceptions Questionnaire; (CPQ8-10): Child Perceptions Questionnaire 8-10 years; (CPQ11-14): Child Perceptions Questionnaire 11-14 years; (κ): Cohen's Kappa; (ES): Effect size; (HRQoL): Health-related quality of life; (ICC): Intraclass correlation coefficient; (OHRQoL): Oral health-related quality of life; (QoL): Quality of life; (RDC/TMD): Research Diagnostic Criteria for temporomandibular disorder; (TMD): Temporomandibular disorder

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

TSB participated in conception and design of the study, data analysis and interpretation, acquisition of data and drafting the manuscript. MSL contributed to the data collection. PMC made critical comments on the manuscript. MBDG participated in the conception and design of the study and critical revision of manuscript. All authors read and approved the final manuscript.

Supplementary Material

Additional file 1

Sample distribution in accordance with the evaluated characteristics - number of children (%). The data provided represent the distribution of the age-specific samples according to clinical groups, signs and symptoms of TMD and perception of oral health.

Click here for file (97.1KB, PDF)

Contributor Information

Taís S Barbosa, Email: tais_sb@yahoo.com.

Marina S Leme, Email: ma_leme@terra.com.br.

Paula M Castelo, Email: pcasteloferrua@hotmail.com.

Maria Beatriz D Gavião, Email: mbgaviao@fop.unicamp.br.

Acknowledgements

The authors gratefully acknowledge the financial support from the State of São Paulo Research Foundation (FAPESP, SP, Brazil, n. 2008/00325-9).

References

  1. Suvinen TI, Reade PC, Kemppainen P, Könönen M, Dworkin SF. Review of aetiological concepts of temporomandibular pain disorder: towards a biopsychosocial model for integration of physical disorder factors with psychological and psychosocial illness impact factors. Eur J Pain. 2005;9:613–633. doi: 10.1016/j.ejpain.2005.01.012. [DOI] [PubMed] [Google Scholar]
  2. Gatchel RJ, Peng YB, Peters ML, Fuchs PN, Turk DC. The biopsychosocial approach to chronic pain: scientific advances and future directions. Psychol Bull. 2007;133:581–624. doi: 10.1037/0033-2909.133.4.581. [DOI] [PubMed] [Google Scholar]
  3. Barros de VM, Seraidarian PI, Côrtes MI, de Paula LV. The impact of orofacial pain on the quality of life of patients with temporomandibular disorder. J Orofac Pain. 2009;23:28–37. [PubMed] [Google Scholar]
  4. Barbosa S Tde, Miyakoda LS, Pocztaruk L Rde, Rocha CP, Gavião MB. Temporomandibular disorders and bruxism in childhood and adolescence: review of the literature. Int J Pediatr Otorhinolaryngol. 2008;72:299–314. doi: 10.1016/j.ijporl.2007.11.006. [DOI] [PubMed] [Google Scholar]
  5. Castelo PM, Gavião MB, Pereira LJ, Bonjardim LR. Relationship between oral parafunctional/nutritive sucking habits and temporomandibular joint dysfunction in primary dentition. Int J Paediatr Dent. 2005;15:29–36. doi: 10.1111/j.1365-263X.2005.00608.x. [DOI] [PubMed] [Google Scholar]
  6. Pereira LJ, Pereira-Cenci T, Del Bel Cury AA, Pereira SM, Pereira AC, Ambosano GM, Gavião MB. Risk indicators of temporomandibular disorder incidences in early adolescence. Pediatr Dent. 2010;32:324–328. [PubMed] [Google Scholar]
  7. Gonçalves DA, Dal Fabbro AL, Campos JA, Bigal ME, Speciali JG. Symptoms of temporomandibular disorders in the population: an epidemiological study. J Orofac Pain. 2010;24:270–278. [PubMed] [Google Scholar]
  8. Farsi N, Alamoudi N, Feteih R, El-Kateb M. Association between temporo mandibular disorders and oral parafunctions in Saudi children. Odontostomatol Trop. 2004;27:9–14. [PubMed] [Google Scholar]
  9. Dahlström L, Carlsson GE. Temporomandibular disorders and oral health-related quality of life. A systematic review. Acta Odontol Scand. 2010;68:80–85. doi: 10.3109/00016350903431118. [DOI] [PubMed] [Google Scholar]
  10. Graue M, Wentzel-Larsen T, Hanestad BR, Båtsvik B, Søvik O. Measuring self-reported, health-related, quality of life in adolescents with type 1 diabetes using both generic and disease-specific instruments. Acta Paediatr. 2003;92:1190–1196. doi: 10.1111/j.1651-2227.2003.tb02483.x. [DOI] [PubMed] [Google Scholar]
  11. Jedel E, Carlsson J, Stener-Victorin E. Health-related quality of life in child patients with temporomandibular disorder pain. Eur J Pain. 2007;11:557–563. doi: 10.1016/j.ejpain.2006.07.007. [DOI] [PubMed] [Google Scholar]
  12. Murray H, Locker D, Mock D, Tenenbaum HC. Pain and the quality of life in patients referred to a craniofacial pain unit. J Orofac Pain. 1996;10:316–323. [PubMed] [Google Scholar]
  13. Locker D, Grushka M. The impact of dental and facial pain. J Dent Res. 1987;66:1414–1417. doi: 10.1177/00220345870660090101. [DOI] [PubMed] [Google Scholar]
  14. Reissmann DR, John MT, Schierz O, Wassell RW. Functional and psychosocial impact related to specific temporomandibular disorder diagnoses. J Dent. 2007;35:643–650. doi: 10.1016/j.jdent.2007.04.010. [DOI] [PubMed] [Google Scholar]
  15. Rener-Sitar K, Celebić A, Stipetić J, Marion L, Petricević N, Zaletel-Kragelj L. Oral health related quality of life in Slovenian patients with craniomandibular disorder. Coll Antropol. 2008;32:513–517. [PubMed] [Google Scholar]
  16. Luo Y, McMillan AS, Wong MC, Zheng J, Lam CL. Orofacial pain conditions and impact on quality of life in community-dwelling elderly people in Hong Kong. J Orofac Pain. 2007;21:63–71. [PubMed] [Google Scholar]
  17. Jokovic A, Locker D, Stephens M, Kenny D, Tompson B, Guyatt G. Validity and reliability of a questionnaire for measuring child oral-health-related quality of life. J Dent Res. 2002;81:459–463. doi: 10.1177/154405910208100705. [DOI] [PubMed] [Google Scholar]
  18. Jokovic A, Locker D, Tompson B, Guyatt G. Questionnaire for measuring oral health-related quality of life in eight- to ten year- old children. Pediatr Dent. 2004;26:512–518. [PubMed] [Google Scholar]
  19. Gherunpong S, Tsakos G, Sheiham A. Developing and evaluating an oral health-related quality of life index for children; The CHILD-OIDP. Community Dental Health. 2004;21:161–169. [PubMed] [Google Scholar]
  20. Pahel BT, Rozier RG, Slade GD. Parental perceptions of children's oral health: the Early Childhood Oral Health Impact Scale (ECOHIS) Health Qual Life Outcomes. 2007;5:6. doi: 10.1186/1477-7525-5-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Broder HL, Wilson-Genderson M. Reliability and convergent and discriminant validity of the Child Oral Health Impact Profile (COHIP Child's version) Community Dent Oral Epidemiol. 2007;35:20–31. doi: 10.1111/j.1600-0528.2007.0002.x. [DOI] [PubMed] [Google Scholar]
  22. Barbosa TS, Tureli MCM, Gavião MBD. Validity and reliability of the Child Perceptions Questionnaires applied in Brazilian children. BMC Oral Health. 2009;9:13. doi: 10.1186/1472-6831-9-13. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Sheiham A, Maizels JE, Cushing AM. The concept of need in dental care. Int Dent J. 1982;32:265–270. [PubMed] [Google Scholar]
  24. Locker D. Health outcomes of oral disorders. Int J Epidemiol. 1995;24:85–89. doi: 10.1093/ije/24.supplement_1.s85. [DOI] [PubMed] [Google Scholar]
  25. Pereira LJ, Pereira-Cenci T, Pereira SM, Cury AA, Ambrosano GM, Pereira AC, Gavião MB. Psychological factors and the incidence of temporomandibular disorder in early adolescence. Braz Oral Res. 2009;23:155–160. doi: 10.1590/S1806-83242009000200011. [DOI] [PubMed] [Google Scholar]
  26. Riolo ML, Brandt D, TenHave TR. Associations between occlusal characteristics and signs and symptoms of TMJ dysfunction in children and young adults. Am J Orthod Dentofacial Orthop. 1987;92:467–477. doi: 10.1016/0889-5406(87)90228-9. [DOI] [PubMed] [Google Scholar]
  27. de Lucena LB, Kosminsky M, da Costa LJ, de Góes PS. Validation of the Portuguese version of the RDC/TMD Axis II questionnaire. Braz Oral Res. 2006;20:312–317. doi: 10.1590/S1806-83242006000400006. [DOI] [PubMed] [Google Scholar]
  28. Dworkin SF, LeResche L. Research diagnostic criteria for temporomandibular disorder: review, criteria, examinations and specifications, critique. J Craniomandib Disord. 1992;6:301–355. [PubMed] [Google Scholar]
  29. Pereira FJ, Favilla EE, Dworkin SF, Huggins KH. Critérios de diagnóstico para pesquisa das desordens temporomandibulares RDC/TMD. http://www.rdc-tmdinternational.org/OtherResources/TranslationGuidelines.aspx
  30. Bonjardim LR, Gaviao MB, Carmagnani FG, Pereira LJ, Castelo PM. Signs and symptoms of temporomandibular joint dysfunction in children with primary dentition. J Clin Pediatr Dent. 2003;28:53–58. doi: 10.17796/jcpd.28.1.0772w75g91963670. [DOI] [PubMed] [Google Scholar]
  31. Segù M, Collesano V, Lobbia S, Rezzani C. Cross-cultural validation of a short form of the Oral Health Impact Profile for temporomandibular disorder. Community Dent Oral Epidemiol. 2005;33:125–130. doi: 10.1111/j.1600-0528.2005.00215.x. [DOI] [PubMed] [Google Scholar]
  32. Dworkin SF, LeResche L, DeRouen T, Von Korff M. Assessing clinical signs of temporomandibular disorder: reliability of clinical examiners. J Prosthet Dent. 1990;63:574–579. doi: 10.1016/0022-3913(90)90079-R. [DOI] [PubMed] [Google Scholar]
  33. Shrout PE, Fleiss JL. Intraclass correlation: uses in assessing rater reliability. Psych Bull. 1979;86:420–428. doi: 10.1037//0033-2909.86.2.420. [DOI] [PubMed] [Google Scholar]
  34. Kramer MS, Feinstein AR. The biostatistics of concordance. Clin Pharmacol Ther. 1981;29:111–123. doi: 10.1038/clpt.1981.18. [DOI] [PubMed] [Google Scholar]
  35. Cohen J. A coefficient of agreement for nominal scales. Educ Psychol Measurement. 1960;20:37–46. doi: 10.1177/001316446002000104. [DOI] [Google Scholar]
  36. Cohen J. Statistical Power Analysis for the Behavioural Sciences. Hillside, NJ: Lawrence Erlbaum Associates; 1988. [Google Scholar]
  37. Cronbach LJ. Coefficient alpha and the internal structure of tests. Psychometrika. 1951;16:297–334. doi: 10.1007/BF02310555. [DOI] [Google Scholar]
  38. Streiner DL, Norman GR. A practical guide to their development and use. New York: Oxford University Press; 2000. Health measurement scales. [Google Scholar]
  39. Locker D, Jokovic A, Tompson B, Prakash P. Is the Child Perceptions Questionnaire for 11-14 year olds sensitive to clinical and self-perceived variations in orthodontic status? Community Dent Oral Epidemiol. 2007;35:179–185. doi: 10.1111/j.1600-0528.2006.00324.x. [DOI] [PubMed] [Google Scholar]
  40. International Consortium for RDC/TMD-based Research. http://www.rdc-tmdinternational.org
  41. Bonjardim LR, Gavião MB, Pereira LJ, Castelo PM, Garcia RC. Signs and symptoms of temporomandibular disorder in adolescents. Braz Oral Res. 2005;19:93–98. doi: 10.1590/S1806-83242005000200004. [DOI] [PubMed] [Google Scholar]
  42. Smith TW. In: Foundations of Health Psychology. Friedman HS, Silver RC, editor. New York: Oxford University; 2007. Measurement in health psychology research; pp. 19–51. [Google Scholar]
  43. List T, John MT, Dworkin SF, Svensson P. Recalibration improves inter-examiner reliability of TMD examination. Acta Odontol Scand. 2006;64:146–152. doi: 10.1080/00016350500483137. [DOI] [PubMed] [Google Scholar]
  44. Steenks MH, de Wijer A. Validity of the Research Diagnostic Criteria for Temporomandibular Disorder Axis I in clinical and research settings. J Orofac Pain. 2009;23:9–16. [PubMed] [Google Scholar]
  45. Lobbezoo F, van Selms MK, John MT, Huggins K, Ohrbach R, Visscher CM, van der Zaag J, van der Meulen MJ, Naeije M, Dworkin SF. Use of the Research Diagnostic Criteria for Temporomandibular Disorder for multinational research: translation efforts and reliability assessments in The Netherlands. J Orofac Pain. 2005;19:301–308. [PubMed] [Google Scholar]
  46. John MT, Dworkin SF, Mancl LA. Reliability of clinical temporomandibular disorder diagnoses. Pain. 2005;118:61–9. doi: 10.1016/j.pain.2005.07.018. [DOI] [PubMed] [Google Scholar]
  47. Wahlund K, List T, Dworkin SF. Temporomandibular disorder in children and adolescents: reliability of a questionnaire, clinical examination, and diagnosis. J Orofac Pain. 1998;12:42–51. [PubMed] [Google Scholar]
  48. White P, Lewith G, Prescott P. The core outcomes for neck pain: validation of a new outcome measure. Spine. 2004;29:1923–1930. doi: 10.1097/01.brs.0000137066.50291.da. [DOI] [PubMed] [Google Scholar]
  49. Look JO, John MT, Tai F, Huggins KH, Lenton PA, Truelove EL, Ohrbach R, Anderson GC, Shiffman EL. The Research Diagnostic Criteria For Temporomandibular Disorder. II: reliability of Axis I diagnoses and selected clinical measures. J Orofac Pain. 2010;24:25–34. [PMC free article] [PubMed] [Google Scholar]
  50. Stratmann U, Mokrys K, Meyer U, Kleinheinz J, Joos U, Dirksen D, Bollmann F. Clinical anatomy and palpability of the inferior lateral pterygoid muscle. J Prosthet Dent. 2000;83:548–554. doi: 10.1016/S0022-3913(00)70013-8. [DOI] [PubMed] [Google Scholar]
  51. Türp JC, Minagi S. Palpation of the lateral pterygoid region in TMD - where is the evidence? J Dent. 2001;29:475–483. doi: 10.1016/S0300-5712(01)00042-2. [DOI] [PubMed] [Google Scholar]
  52. Ohrbach R, Turner JA, Sherman JJ, Mancl LA, Truelove EL, Schiffman EL, Dworkin SF. The Research Diagnostic Criteria for Temporomandibular Disorder. IV: evaluation of psychometric properties of the Axis II measures. J Orofac Pain. 2010;24:48–62. [PMC free article] [PubMed] [Google Scholar]
  53. Jamison RN, Sbrocco T, Parris WC. The influence of physical and psychosocial factors on accuracy of memory for pain in chronic pain patients. Pain. 1989;37:289–294. doi: 10.1016/0304-3959(89)90193-0. [DOI] [PubMed] [Google Scholar]
  54. Sousa LM, Nagamine HM, Chaves TC, Grossi DB, Regalo SC, Oliveira AS. Evaluation of mandibular range of motion in Brazilian children and its correlation to age, height, weight, and gender. Braz Oral Res. 2008;22:61–66. doi: 10.1590/S1806-83242008000100011. [DOI] [PubMed] [Google Scholar]
  55. Tuerlings V, Limme M. The prevalence of temporomandibular joint dysfunction in the mixed dentition. Eur J Orthod. 2004;26:311–320. doi: 10.1093/ejo/26.3.311. [DOI] [PubMed] [Google Scholar]
  56. Farsi NM. Symptoms and signs of temporomandibular disorder and oral parafunctions among Saudi children. J Oral Rehabil. 2003;30:1200–1208. doi: 10.1111/j.1365-2842.2003.01187.x. [DOI] [PubMed] [Google Scholar]
  57. Sönmez H, Sari S, Oksak G Oray, Camdeviren H. Prevalence of temporomandibular dysfunction in Turkish children with mixed and permanent dentition. J Oral Rehabil. 2001;28:280–285. doi: 10.1111/j.1365-2842.2001.tb01678.x. [DOI] [PubMed] [Google Scholar]
  58. Thilander B, Rubio G, Pena L, de Mayorga C. Prevalence of temporomandibular dysfunction and its association with malocclusion in children and adolescents: an epidemiologic study related to specified stages of dental development. Angle Orthod. 2002;72:146–154. doi: 10.1043/0003-3219(2002)072<0146:POTDAI>2.0.CO;2. [DOI] [PubMed] [Google Scholar]
  59. LeResche L, Mancl LA, Drangsholt MT, Saunders K, Korff MV. Relationship of pain and symptoms to pubertal development in adolescents. Pain. 2005;118:201–209. doi: 10.1016/j.pain.2005.08.011. [DOI] [PubMed] [Google Scholar]
  60. Nilsson IM, List T, Drangsholt M. Prevalence of temporomandibular pain and subsequent dental treatment in Swedish adolescents. J Orofac Pain. 2005;19:144–150. [PubMed] [Google Scholar]
  61. List T, Wahlund K, Wenneberg B, Dworkin SF. TMD in children and adolescents: prevalence of pain, gender differences, and perceived treatment need. J Orofac Pain. 1999;13:9–20. [PubMed] [Google Scholar]
  62. Nilsson IM, Drangsholt M, List T. Impact of temporomandibular disorder pain in adolescents: differences by age and gender. J Orofac Pain. 2009;23:115–122. [PubMed] [Google Scholar]
  63. Dao TT, LeResche L. Gender differences in pain. J Orofac Pain. 2000;14:169–184. [PubMed] [Google Scholar]
  64. Juniper G, Guyatt G, Willan A, Griffith L. Determining a minimal important change in a disease-specific quality of life questionnaire. J Clin Epidemiol. 1994;47:81–87. doi: 10.1016/0895-4356(94)90036-1. [DOI] [PubMed] [Google Scholar]
  65. Jaeschke R, Singer J, Guyatt G. Measurement of health status: ascertaining the minimal clinically important difference. Controlled Clin Trials. 1989;10:407–415. doi: 10.1016/0197-2456(89)90005-6. [DOI] [PubMed] [Google Scholar]
  66. Scientific Advisory Committee of the Medical Outcomes Trust. Assessing health status and quality-of-life instruments: attributes and review criteria. Qual Life Res. 2002;11:193–205. doi: 10.1023/A:1015291021312. [DOI] [PubMed] [Google Scholar]
  67. Norman GR, Streiner DL. PDQ statistics. Louis: Mosby; 1996. [Google Scholar]
  68. Bowling A. Research Methods in Health: Investigating Health and Health Services. Buckingham: Open University Press; 1997. [Google Scholar]
  69. Li S, Veronneau J, Allison PJ. Validation of a French language version of the Early Childhood Oral Health Impact Scale (ECOHIS) Health Qual Life Outcomes. 2008;6:9. doi: 10.1186/1477-7525-6-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  70. Li S, Malkinson S, Veronneau J, Allison PJ. Testing responsiveness to change for the early childhood oral health impact scale (ECOHIS) Community Dent Oral Epidemiol. 2008;36:542–548. doi: 10.1111/j.1600-0528.2008.00434.x. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Additional file 1

Sample distribution in accordance with the evaluated characteristics - number of children (%). The data provided represent the distribution of the age-specific samples according to clinical groups, signs and symptoms of TMD and perception of oral health.

Click here for file (97.1KB, PDF)

Articles from Health and Quality of Life Outcomes are provided here courtesy of BMC

RESOURCES