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| 2010-22 |
| 22-1 |
ISSN (Print) 1013-9052
EISSN 1658-3558
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Temporomandibular disorders in Al-Ahsa province, KSA: An epidemiologic study
El-Fatih Ibrahim El-Amin*, BDS, MSc (London), FDSRCSI, AIMPT (London)
This one-year epidemiological study was designed to investigate TMD, among dental patients attending King Fahad Hospital, Hofuf. It is a retrospective case-control study of 72 Saudi TMD patients cross matched with 72 control subjects. The latter were randomly selected, interviewed and examined in the dental department. Subjects were assessed separately both by a dental specialist and a psychiatrist. Data were collected on a predesigned form, and was statistically analyzed using an Epi-Info 6.TMD cases among the attendants at the dental department were 4.8%. No significant associations (P>0.05) were found between socio-economic factors and the distribution of TMD cases. The mean opening extent of the mouth in the TMD patients was significantly lower than that in the controls (P<0.001). The study also showed that psychological problems were more prevalent among TMD patients. Anxiety-depression was 50% of the psychiatric disorders, while depression constituted 32.1%.This study also showed that patients with psychiatric problems were prone to TMD 4.5 times greater than those without and vice-versa. A liaison psychiatrist should be considered for TMD management. A simplified and valid psychiatric screening test is recommended to help dentists detect those TMD cases in need of psychiatric consultation.
Temporomandibular disorders (TMD) is a collective term embracing various clinical problems that involve the masticating musculature and the temporomandibular joint (TMJ). TMD problems are characterized by pain in the masticatory muscles, the temporomandibular joint and associated hard and soft tissues, limitations in jaw function and sounds in the TMJ.1 On the basis of some studies, recurrent headache was added to the list of major symptoms of TMD.2,3 The signature of TMD is pain provoked by function.4 Resting pain unrelated to jaw function is less common and should direct the clinician to consider alternative disorders.5 Epidemiolgic data relating to the type of individuals in whom TMD develop may be categorized broadly as demographic and etiologic.6 Demographic data describe definitive variables such as gender, age, nationality, marital status, years of education and occupation. Causal variables may include stress, depression, oral habits and occlusal scheme. This study aimed to assess the relationships among socio-economic factors (age, gender, marital status and education), psychological factors (anxiety and depression) and physical habits (bruxism, clenching, trauma, chewing gum, eating on one side and occlusal disharmony) in TMD subjects.
The study was conducted in the dental department of King Fahad Hospital, Hofuf (KFHH) in 1997. KFHH is located in Al-Ahsa province in the Eastern region of the Kingdom of Saudi Arabia. The study followed a case-control design, among the 673 TMD cases treated at the dental department.A sample of 72 patients (25 males & 47 females) with a confirmed diagnosis of TMD was chosen on a systematic random basis (2 cases/week). The TMD patients were cross-matched with a control group of 72 subjects who had dental problems other than TMD during the same period. In this study, a TMD diagnosis was established if the patient had pain and discomfort in the TMJ's, muscles of mastication and/or had masticatory dysfunction for a period exceeding 6 months.7 Then, all subjects were seen by a psychiatrist to diagnose possible psychiatric problems according to the WHO standards in the International Classification of Mental and Behavioral Disorders.8 Informed consent was obtained from all subjects according to ethical requirements. A form was designed to collect data from both TMD subjects and control group (Fig. 1). Data were statistically analyzed using an Epi-Info 6.9
Table 1 shows that the number of TMD cases (4.8%) was close to the figure for orthodontic cases (5.4%) among all cases treated in the dental department of KFHH in 1997. Non-significant associations (P>0.05) were found between socio-economic factors and the distribution of TMD subjects (Table 2). Table 2 also shows that the number of TMD females was approximately double that for males while the number of married TMD subjects was higher than that for single subjects. There were no significant variations in the mean ages the TMD subjects and the control group. The mean opening extent of the mouth in the TMD subjects was significantly less than that in the control group (P< 0.001, Table 3). Chewing on one side, clenching, bruxism, attrition and deflective contacts as well as psychological problems, were significantly more prevalent among theTMD subjects (Table 4). A large number (43.1%) of TMD subjects were in the habit of using one side for chewing (Table 4). Anxiety-depression disorders were 50% of the recorded psychiatric disorders, while depression constituted 32.1% (Table 5).
The percent of TMD subjects (4.8%) shown in Table 1 may be far less than the actual prevalence in Al-Ahsa community for reasons discussed in previous studies.10,11 Females predominated among the TMD subjects with a ratio of 1.8:1 which was less than the previously reported ratios of 3.1: 1 and 4:1 respectively.4,12,13 This may be largely due to female interest in seeking medical treatment more routinely than males resulting in biased selection sampling.6 However, Bush et al14 in a TMD study, reported that personality, sensitivity to pain, symptoms presentation and pain relatedillness behavior did not vary significantly between males and females. Rugh and Solberg15 reviewed several studies that investigated the prevalence of TMD in the general population. Interestingly, TMD subjects in these studies showed a female to male ratio of 1:1, whereas TMD subjects actively seeking treatment had a 3:1 ratio of females to males. In this study, the mean age of TMD cases was 26.9 ± 7.6 years. Similarly, the peak age on presentation of TMD was reported to be between 20 and 30 years,16 but most cross-sectional epidemiological studies had shown higher prevalence figures for TMD namely between 20-40 year of age.17-19 The lowest prevalence figures were found among children, adolescents and elderly people.10,17,20,21 The cited age-related studies led many to conclude that TMD is a self-limiting condition that will resolve with time. TMD-age related findings contrasts sharply with that of chronic back pain individuals, in that the latter tends to persist and increase in frequency in the older age group.22 Klausner6 reported that the prevalence of TMJ pain decreased with age while the prevalence of face pain remained fairly constant in the population. Studies of the roles played by socio-economic factors in chronic pain have revealed an association among these variables.6 However, in our study, socio-economic factors (marital status, education and occupation) did not show significant differences between TMD subjects and the control subjects. Our different findings may be related to the differences in social and cultural backgrounds. However, these socio-economic factors may work together as risk factors. For example, while lower level of education alone may not be a direct risk factor, its consequential socio-economic status is reflected in the levels of income and education and occupation status. On the other hand, Franks23 stated that certain personality traits were more likely to be affected by TMD conditions and that there was an indication of a greater prevalence in the higher social classes. It seems likely that life stress may play an important role in some aspects of TMD. Beaton et al24 and Niemi et al25 had reported a higher level of stress symptoms among TMD subjects when compared to a control group. It has been suggested that some TMD patients may have problems in coping with increased life stress and daily hassles.26 Consequently they tend to respond with eleva-ted muscle tension.24,25,27 All these factors have led workers to recognize the importance of psy-chophysiology factors in the etiology of TMD.27-29 This study proved a significant relationship between psychologic problems and TMD cases (P<0.001). This agreed with other studies that related psychological problems to TMD condition.24,25,30 Those with psychiatric problems in this study were 4.5 times more prone to TMD than those without psychiatric problems (Table 4) or vice versa, as it was not clear which condition developed first. However, Juniper11 believed that most cases of depression associated with TMD were the result of chronic pain and not the cause of it. TMD represents a curious combination of psychological and somatic manifestation, yet the inclusion criteria for the case definition are dependent on physical findings. Therefore the magnitude and quality of mandibular movements are usually the best objective indicators of TMJ and masticatory muscle status.31 Active range of motion (AROM) is the opening of mouth under voluntary effort. It may show hypomobility (restriction) associated with pain, TMJ internal derangement or neuromuscular disorder. Or it can be hypermobility (excessive movement) caused by joint laxity and instability in disc-condyle complex and capsule. Men open more widely than women.32 But the distribution of (AROM) is relatively constant from the early teens to the old age.32 A 40-mm inter-incisor opening is a realistic lower limit for person from 10-70 years of age.31 In the present study, the mean opening extent of the mouth in TMD cases (35.6±11.5 mm) was significantly lower than that in the controls (43.8 ± 4.8 mm, Table 3). A number of occlusal factors have been linked with TMD. They include loss of occlusal vertical dimension, occlusal interferences and deflective occlusal contacts. The way in which occlusal factors may initiate TMD condition has spawned many speculations. Some propose that posterior tooth loss can predispose to overloading of the TMJ's particularly in the presence of parafunction.33 On the other hand, the mode of action of the occlusal interference and deflective occlusal contacts can produce TMD. This may be explained by either inducing a subject to parafunction (bruxism and clenching ),34 or by the fact that functional movements (during mastication, speech and swallowing) and mandibular posture are adversely affected due to the subconscious avoidance of the aberrant tooth contact.35 Both explanations acknowledge that psychological stress may combine with an unfavorable occlusion to produce TMD. It is apparent that most patients exhibit some form of occlusal discrepancy, but only a small proportion present with TMD. Even in the TMD cases, occlusal variables have no significant statistical relationship with the severity of their signs and symptoms.36 In this study, occlusal interferences have shown a significant relationship to TMD cases in contrast to deflective occlusal contacts. This finding gives an impression that occlusal interferences may induce a strong overexertion effect on the muscles of mastication, resulting in increased loading on the TMJ's. Hence, this leads to TMD development in high risk patients (Table 4). Chewing on one side, bruxism, clenching and teeth attrition were found to be significantly correlated to TMD subjects (Table 4). Attrition which is the physical wear caused by movement of one tooth against another, is directly related to both bruxism and clenching and also has an effect in reducing the occlusal vertical dimension. TMD patients chewing on one side (43.1%) were mostly not aware that they had this habit earlier before or after the TMD condition. If it was present before the TMD condition, it may be considered as a provocative factor for symptoms if it developed after. The TMD on set, it may be considered as a preventive habit in order to avoid pain on the affected side. Based upon the findings of this study, the following conclusions are drawn: 2.Psychological consultations should beconsidered in the team management of TMD. 3.A simplified and valid psychological/psychiatric screening test is needed.
1.Okeson JP (ed). Orofacial pain: Guidelines for assessment,diagnosis and management. Chicago: Quintessence, 1996. 2.Magnusson T and Carlsson GE. Recurrent headaches in relation to tempo-romandibular joint pain dysfunction. Acta Odont Scand 1978; 36:333-338. 3.Forsell H and Kangansiemi P. Correlation of thefrequency and intensity of headache to mandibulardysfunction in headache patients. Proc Finn Dent Soc 1984; 80: 223-226. 4.Solberg WK. Temporomandibular disorders: Background and the clinical problems. Br Dent J1985; 160: 157-161. 5.Bell WE. Clinical management of temporomandi- bular disorders. Chicago: Yearbook Medical Publishers, 1982. 6.Klausner JJ. Epidemiological studies reveal trends intemporomandibular pain and dysfunction. J Mass Dent Soc 1995; 44 (I): 21-25. 7.Bell WE. President's conference on the examination,diagnosis and management of temporomandibular disorders. American Dental Association 1982; 24-25. 8.WHO. The ICD-10 Classification of mental and behavioral disorders. Diagnostic criteria forresearch. New York: Oxford University Press, 1993. 9.WHO. Epi Info 6. A World Processing database statistical program for public health version 6.02-Geneva, Switzerland. October 1994. 10. Dworkin SF, Huggins KH, Le Resche L,Von Korff M, Howard J and Truelove E et al. Epidemiology of signs and symptoms in temporomandibular disorders: Clinical signs in cases and Controls. J Am Dent Assoc 1990; 120:239-244. 11. Juniper RP. Temporomandibular dysfunction: facts and fallacies. Dent Update 1984; 479-490. 12. Kuttila M, Niemi PM, Kuttila S, AlanenP and Le Bell Y. TMD Treatment need in relation to age, gender, stress, and diagnostic subgroup. J Orofacial Pain1998; 12 (1): 67-74. 13. Conti PC, Ferreira PM, Pegoraro LF, Conti JV andSalvador MCG. Across-sectional study of prevalence and etiology of signs and symptoms of temporomandibular disorders in high school and university students. J Orofacial Pain 1996; 10: 254- 262. 14. Bush FM, Harkins SW, Harrington WG and Price DD. Analysis of gender effects on pain perception andsymptom presentation in temporomandibular pain. Pain 1993; 53:73-80. 15. Rugh JD and Solberg WK. Oral health status in the United States; temporomandibular disorders. J Dent 1985; 49:398-405. 16. Heloe B and HelÖe A. Characteristics of a group of patients with temporomandibular joint disorders. Community Dent Oral Epidemiol 1975; 3:72-79. 17. Salonen L, Helldén L and Carlsson GE. Prevalence of signs and symptoms of dysfunction in the masticatory system: An epidemiolgic study in adult Swedish population. J Craniomandib Disord FacialOral Pain 1990; 4:241-250. 18. Agerberg G and Bergenholz A. Craniomandibular disorders in adult populations of West Bothnia, Sweden. Acta Odontol Scand 1989: 47:129-140. 19. De Leeuw JR, Steenks MH, Ros WJG, Bosman F,Winnubst JAM and Lobbezoo-Scholte AM. Psychosocial aspects of Craniomandibular dysfunction. An assessment of clinical andcommunity findings. J Oral Rehab 1994; 21:127-143. 20. Magnusson T, Carlsson GE and Egermark-Eriksson I.An evaluation of the need and demand for treatment of craniomandibular disorders in a young Swedish population. J Craniomandib Disord FacialOral Pain 1991; 5: 57-63. 21. Kononen M and NystrÖm M. A longitudinal study ofcraniomandibular disorders in Finnish adolescents. J Orofacial Pain 1993; 329-336. 22. Deyo RA and Tsui-Wu YJ. Descriptive epidemiology oflow back pain and its related medical care in the United States. Spine 1987; 12: 264-268. 23. Franks AST. The social character of temporoman- dibular joint dysfunction. Dent Practit 1964; 15: 94- 100. 24. Beaton RD, Egon KJ, Nakagawa-Kogan H and Morrison KN. Self-reported symptoms of stress with temporomandibular disorders: Comparison tohealthy men and women. J Prosthet Dent 1991;65:289-293. 25. Niemi P, Le Bell Y and Koskinen-Moffett L. Self-reported symptoms of stress in Finnish patients withcraniomandibular disorders. J Orofacial Pain 1993;7:354-358. 26. Stockstill JW and Callahan CD. Personality hardiness,anxiety and depression as constructs of interest inthe study of temporomandibular disorders. J Craniomandib Disord Facial Oral Pain 1991;5:129-134. 27. Marbach JJ and Dworkin SF. Chronic MPD, grouptherapy andpsychodynamics. J Am Dent Assoc 1975; 90: 827-833. 28. Franks AST. Masticatory muscle hyperactivity andtemporomandibular joint dysfunction. J Prosthet Dent 1965; 15:1122-1131. 29. Lupton DE. Psychological aspects of temporoman-dibular joint dysfunction. J Am Dent Assoc 1969; 79: 131-136. 30. Farsi NM. Temporomandibular dysfunction and the emotional status of 6-14 years old Saudi female children. SDJ 1999;11(3):114-119. 31. Solberg WK. Temporomandibular disorders: physical tests in diagnosis. Br Dent J 1986; 160: 273-277. 32. Solberg WK, Woo MS and Houston JB. Prevalence ofmandibular dysfunction in young adults. J Am Dent Assoc 1979, 98:25-34. 33. Wassell RW. Do occlusal factors play a part in tem- poromandibular dysfunction. J Dent 1989; 17:101-110. 34. Ramfjord SP and Ash MM. Occlusion. 3rd ed. Phila- delphia, W.B. Saunders, 1983. 35. Dawson P. Temporomandibular joint pain dysfunction problems can be solved. J Prosthet Dent 1973; 29:100-112. 36. Droukas B, Linder C and Carlsson GE. Relationshipbetween occlusal factors and signs and symptoms ofmandibular dysfunction -A clinical study of 48 dental students. Acta Odont Scand 1984; 42: 277-283. Address reprint requests to: Dr. El Fatih I. El-Amin Consultant Prosthodontist Acting Director, Al-Ahsa Dental Center Al-Ahsa Directorate of Health P.O. Box 5161 Al-Ahsa 31982 Saudi Arabia
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