Добавил:
kiopkiopkiop18@yandex.ru t.me/Prokururor I Вовсе не секретарь, но почту проверяю Опубликованный материал нарушает ваши авторские права? Сообщите нам.
Вуз: Предмет: Файл:

Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_4496_Библиотеки_им_академика_М_И_Перельмана

.pdf
Скачиваний:
0
Добавлен:
31.08.2026
Размер:
36 Мб
Скачать
18 Dental, Occlusal, andFunctional Evaluation ofPatients
https://t.me/medicina_free
Table 18.1 Validity of standard and exceptional caries detection tests
Caries detection test Sensitivity Specicity Source Visual examination 0.70 0.41 [41] Conventional bitewing radiograph (D-speed, invivo) 0.65 0.58 [41] Conventional bitewing radiograph (E-speed, invivo) 0.80 0.94 [41] Bitewing radiograph+computerized decision aid (in vitro) 0.67 0.83 [53] FOTI (in vitro) 0.97 0.50 [41] DIFOTI 0.97 0.50 [41] LF (DIAGNOdent 2095, KaVo, Biberach, Germany; invivo) 0.88 0.71 [41] LF (DIAGNOdent 2095, invitro) 0.75 0.76 [41] LF (DIAGNOdent pen 2190, invitro) 0.78 0.77 [41] QLF (proximal, |Fmax| cutoff=5.95, invivo) OCT (coronal plane, invitro) 0.81 1.00 [55]
0.74 0.73 [54]
243
light because enamel is very translucent to these wavelengths. The emitted, frequency-sweep laser light is coupled to the object and a refer­ence surface. The interference pattern is used to calculate an image. First results are promising as OCT showed better performance in detecting very early lesions than laser uorescence and QLF [52].
Although visual inspection, radiographic examination, and tactile test are available in every­day practice, inexpensive, reliable, and easily per­formed, the new techniques may improve caries diagnostics in future and be of special value in patients with craniofacial malformations.
Validity expressed in sensitivity and specic­ity values of standard and exceptional caries detection tests is listed in Table18.1.
Dental Pulp andPeriapical Status
Pulp sensitivity tests can be performed simply by applying a thermal or electrical stimulus to the cervical area [5659]. However, test results do not necessarily correlate with histologic nd­ings as a gold standard and are a questionable basis for further therapy in the case of oblitera­tion without infection [6062]. In patients who have undergone oral surgery, particularly man­dibular orthognathic operations, tooth pulp sen­sitivity to thermal or electrical stimuli may be
reduced even in the absence of pulp tissue dam­age [6365]. A reliable method for measuring dental pulp vitality is laser Doppler owmetry. A laser beam is directed at the tooth surface and passes through enamel and dentin to the pulp. There, circulating blood cells reect the laser beam, and cell movement alters the reected signal through the Doppler effect. Sensitivity and specicity of this test are reported to be high (0.82–100% sensitivity and 100% specic­ity) [66]. Dental pulp oximetry shows similar validity. However, pulp blood supply may be reduced without compromising tooth vitality, e.g., on the affected side of a cleft palate [67]. As a conclusion, in patients suffering from cra­niofacial malformations, particularly after orthognathic surgery, pulp sensitivity tests based on thermal or electrical stimuli should be inter­preted with caution. Comparison with the con­dition of the clinical crown and radiological ndings should be used before invasive end­odontic procedures are initiated.
If toxins from the dental pulp inltrate the periapical periodontal ligament, the affected tooth might be sensitive to pressure or touching. This condition can be examined by a percussion test [68].
Sensitivity and specicity values of standard and exceptional tests to evaluate pulp sensibility and periapical inammation are listed in Table18.2.
244
https://t.me/medicina_free
C. Runte
Table 18.2 Validity of standard and exceptional pulp sensibility and periapical status tests
Pulp sensibility and periapical status test Sensitivity Specicity Source
Cold stimulus 0.83 0.93 [18] Cold stimulus 0.916 0.896 [17] Warm stimulus 0.86 0.41 [18] Electric stimulus 0.72 0.93 [18] Electric stimulus 0.84 0.74 [17] Laser Doppler owmetry Pulse oximetry 0.81 0.95 [66] Periapical status Pain on tooth
percussion
0.82–1.00 1.00 [66]
0.72 0.41 [68]
Periodontal Examination
The basic examination procedures for periodon­tal disease are probing the depth of the periodon­tal sulcus, visual examination of bleeding on probing, and radiographic examination of attach­ment loss. Probing depth correlates to the further progression of periodontal disease and therefore is a valid diagnostic aid [69]. However, there is only limited knowledge about the periodontal health of patients with craniofacial malforma­tions. In syndromic craniosynostoses, tooth crowding, hypoplasia of the upper jaw, and gingi­val hyperplasia are suspected to contribute to plaque accumulation, and mouth breathing is also a factor discussed in this context [70]. Treatment of mandibular underdevelopment by distraction osteogenesis, e.g., in patients with hemifacial microsomia, might be a risk factor for juvenile paradental cysts, which have to be distinguished from lateral radicular inammatory cysts [71].
A common but invasive and time-consuming method to assess the periodontal health status is measuring the periodontal pocket depth by prob­ing. In combination, bleeding on probing (BOP) and presence of plaque and calculus or defective crown margins can be assessed. As a full exami­nation of these parameters, e.g., in the Community Periodontal Index for Treatment Need (CPITN), takes a lot of time and is not comfortable to the patient, reduced screening procedures were pro­posed, e.g., the partial CPITN using only ten
index teeth with limited inuence on sensitivity and specicity values (0.58 and 0.81 for full CPITN and 0.50 and 0.87 for partial CPITN, respectively) [72]. The CPITN was modied to the Periodontal Screening and Recording Index (PSR) to reduce examination time [73].
With the Periotest® device (Gulden, Modautal, Germany), periodontal reaction to an impulse induced to the crown surface can be measured. Correlation with bone loss has been reported to be strong [74].
As gingival bleeding is a frequent symptom of periodontitis, saliva hemoglobin levels have been evaluated for their suitability to detect this dis­ease without probing the pocket depth. In combi­nation with a self-report questionnaire, a sensitivity of 0.7 and specicity >0.75 have been reported [75]. A simple, also noninvasive screen­ing method for periodontitis using saliva hemo­globin and saliva lactate dehydrogenase levels in combination was introduced by Nomura [76]. Using both values has been reported to have a positive predictive value of 91.7%. Other peri­odontal diagnostic tests, e.g., for microbiome [7779] or interleukin-1 genotype [77, 78, 80,
81], should be interpreted with care in general
[82] and have not been evaluated for their appli­cation in craniofacial malformation patients yet. An inuence of the underlying genetic variation on test results cannot be ruled out at present; for example, it has been reported that Apert patients exhibit a higher interleukin-1 receptor antagonist level [83] and altered extracellular matrix pro­teins [84].
Dental Misalignment, Temporomandibular Disorders, andMalocclusion
Pronounced underdevelopments of the midface (especially in conjunction with a cleft) or the mandible in patients with craniofacial malforma­tions almost necessarily lead to misalignment and malocclusion of the dental arches. Especially malformations of the temporomandibular joints (up to complete aplasia of the condyle) lead to a position and function deviating from the physio-
18 Dental, Occlusal, andFunctional Evaluation ofPatients
https://t.me/medicina_free
245
logic situation. In these cases, temporomandibu­lar joint dysfunction and malocclusion are frequently present. However, craniofacial mal­formations might or might not be associated with (painful) temporomandibular disorders (TMDs). Temporomandibular disorders are dened as “conditions producing abnormal, incomplete, or impaired function of the temporomandibular joint(s) and/or the muscles of mastication” [85].
The Diagnostic Criteria for Temporomandibular Disorders (DC/TMD) have been developed from the former Research Diagnostic Criteria and proven to be a reliable diagnostic tool [86]. The screening tool consists of two axes. With axis I, pain history (within the preceding 30days; mas­seter and temporal muscles, other orofacial mus­cles, and headache, with or without referral) and physical function and condition of the temporo­mandibular joints are assessed. Axis II refers to the psychosocial status. DC/TMD protocol is evi­dence based, valid, and applicable in clinical and research settings. However, not every single item might be applicable in patients with craniofacial malformations; for example, in complete condylar aplasia, anterior disc displacement is probably hard to dene. In patients with craniofacial mal­formations, a lot of diagnostic information is already available and should be evaluated with respect to TMD.As De Boever etal. (2000) stated: “The diagnosis should be based on sound judge­ment of a careful medical and dental history, detailed clinical examination, and some optional modalities, such as radiographs of the jaws and imaging of the TMJs” [87].
Frequently used parameters of misalignment and malocclusion in orthodontic and orthogna­thic examination are overbite, overjet, crossbite, dental crowding, congenital missing teeth, and midline deviation [88].
Kobayashi etal. found anterior open bite (i.e., overbite <4mm) in 6 out of 7 cases of Apert, and 2 out of 12 cases in Crouzon syndrome, respectively. Posterior crossbite was found in every subject of both craniofacial malformations. Severe dental crowding (i.e., arch length discrep­ancy >10mm) in the upper jaw was present in 6 of 7 Apert syndrome and 2 of 12 Crouzon syn­drome patients. The corresponding numbers of
the mandibular arch are 3 out of 7 and 1 out of 12, respectively. Due to sagittal underdevelopment of the midface, patients had an average overjet of
8.2mm in case of Apert and 5.3mm in case of Crouzon syndrome [6].
Malformations from the craniofacial microso­mia complex arise from the rst and second pha­ryngeal arches, and underdevelopment of the mandible is a typical consequence [89, 90]. This frequently leads to an Angle class II malocclu­sion [32]. Again, anterior open bite is a frequent condition, caused by a shortened posterior verti­cal height of the mandible [91].
Thorough orthodontic and cephalometric examination is essential for successful treatment outcome, and regular follow-up examinations are mandatory as long-term relapse is possible [92].
Due to the severity of malocclusion, occlusal adjustment is achieved by craniofacial and orthognathic surgery, orthodontic treatment, and, nally, other measures like selective occlusal substance removal or augmentation, e.g., by bonded composite restorations, veneers, crowns, and, in some cases, occlusal splints or xed or removable partial dentures.
During these treatment procedures, instru­mental centric relation records might be advan­tageous for treatment planning and to evaluate the treatment outcome. However, common facebows might not always be suitable for cra­niofacial malformation patients. For example, facebows using earplugs for xation like the ARCUS/ARCUSevo® (KaVo, Biberach, Germany), Artex® (Amann Girrbach, Koblach, Austria), DENAR® Slidematic® (Whip Mix, Louisville, KY, USA), and SAM® AXIOQuick III® (SAM Praezisionstechnik, Gauting, Germany) have one drawback in common: they need both external ear canals in their physio­logical position to be properly xed. In cranio­facial malformations, one or both external ear canals might not be present or be ectopic. However, facebows still might be helpful: In reversal of its intended purpose, the use of a facebow to support the positioning of bilateral auricular prostheses was demonstrated using the example of a patient with Crouzon syn­drome [93]. Facebows and articulators also
246
https://t.me/medicina_free
C. Runte
might not be adjustable to an individual posi­tion of the occlusal plane far away from the average. In cases with condylar aplasia, man­dibular movements may become irregular and simulation with a mechanical articulator impossible. With the possibility of movement tracking using intraoral scanners, mandibular movements can be simulated digitally without mechanical limitations [94].
In the future, a newly developed technique could make it possible to draw the hinge axis and sagittal condylar pathway on the patient’s skin and integrate them with the three-dimen­sional patient data using a face scan [95].
Conclusions
Patients with craniofacial malformations require particularly careful, regular dental examinations. New technologies in caries detection and peri­odontitis diagnosis as well as intraoral scanning may facilitate the examination procedure and registration of irregular mandibular movements. However, the underlying disease and conse­quences of orthognathic surgery may have an inuence on some of the test results.
References
1. Da Dalben GS, Costa B, Gomide MR.Oral health sta­tus of children with syndromic craniosynostosis. Oral Health Prev Dent. 2006;4(3):173–9.
2. Surman TL, Logan RM, Townsend GC, Anderson PJ. Oral features in Apert syndrome: a histological investigation. Orthod Craniofac Res. 2010;13(1):61–7.
3. Vilan Xavier AC, Pinto Silva LC, Oliveira P, Villamarim Soares R, de Almeida Cruz R. A review and dental management of persons with craniosynosto­sis anomalies. Spec Care Dentist. 2008;28(3):96–100.
4. Shin K, Moreno-Uribe LM, Allareddy V, Burton RG, Menezes AH, Fisher MD, et al. Multidisciplinary care for a patient with syndromic craniosynostosis: a case report with 20 years of special care. Spec Care Dentist. 2020;40(1):127–33.
5. Reitsma JH, Ongkosuwito EM, van Wijk AJ, Prahl­Andersen B.Patterns of tooth agenesis in patients with Crouzon or apert syndrome. Cleft Palate Craniofac J. 2014;51(2):178–83.
6. Kobayashi Y, Ogura K, Hikita R, Tsuji M, Moriyama K. Craniofacial, oral, and cervical morphologi-
cal characteristics in Japanese patients with Apert syndrome or Crouzon syndrome. Eur J Orthod. 2021;43(1):36–44.
7. Rynearson RD. Case report: orthodontic and dento­facial orthopedic considerations in Apert’s syndrome. Angle Orthod. 2000;70(3):247–52.
8. Ahluwalia M, Brailsford SR, Tarelli E, Gilbert SC, Clark DT, Barnard K, etal. Dental caries, oral hygiene, and oral clearance in children with craniofa­cial disorders. J Dent Res. 2004;83(2):175–9.
9. Prado HV, Carneiro NCR, Perazzo MF, de Abreu MHNG, Martins CC, Bor-ges-Oliveira AC.Assessing a possible vulnerability to dental caries in individu­als with rare genetic diseases that affect the skeletal development. Orphanet J Rare Dis. 2019;14(1):145.
10. Allam KA. Hemifacial microsomia: clinical fea­tures and associated anomalies. J Craniofac Surg. 2021;32(4):1483–6.
11. Galea CJ, Dashow JE, Woerner JE. Congenital abnormalities of the temporomandibular joint. Oral Maxillofac Surg Clin North Am. 2018;30(1):71–82.
12. Khawaja SN, Crow H, Gonzalez Y. Goldenhar syn­drome and pain-related temporomandibular disorders. A case report. N Y State Dent J 2016; 82(3):21–24.
13. Desai V. Oculo-auriculo-vertebral spectrum with radial defects, a bid condyle and taurodontism: a case report. Dent Med Probl. 2019;56(4):427–31.
14. Sjögreen L, Andersson-Norinder J, Bratel J. Oral health and oromotor function in rare diseases—a data­base study. Swed Dent J. 2015;39(1):23–37.
15. Letra A, de Almeida ALPF, Kaizer R, Esper LA, Sgarbosa S, Granjeiro JM. Intraoral features of Apert’s syndrome. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2007;103(5):e38–41.
16. Soancă A, Dudea D, Gocan H, Roman A, Culic B.Oral manifestations in Apert syndrome: case pre­sentation and a brief review of the literature. Rom J Morphol Embryol. 2010;51(3):581–4.
17. Jespersen JJ, Hellstein J, Williamson A, Johnson WT, Qian F.Evaluation of dental pulp sensibility tests in a clinical setting. J Endod. 2014;40(3):351–4.
18. Petersson K, Söderström C, Kiani-Anaraki M, Lévy G.Evaluation of the ability of thermal and electrical tests to register pulp vitality. Endod Dent Traumatol. 1999;15(3):127–31.
19. Hausen H. Caries prediction—state of the art. Community Dent Oral Epidemiol. 1997;25(1):87–96.
20. Bader JD, Shugars DA, Bonito AJ.Systematic reviews of selected dental caries diagnostic and management methods. J Dent Educ. 2001;65(10):960–8.
21. Marinelli G, Inchingolo AD, Inchingolo AM, Malcangi G, Limongelli L, Montenegro V, etal. White spot lesions in orthodontics: prevention and treatment. A descriptive review. J Biol Regul Homeost Agents. 2021;35(2 Suppl. 1):227–40.
22. Côrtes DF, Ellwood RP, Ekstrand KR. An in vitro comparison of a combined FOTI/visual examination of occlusal caries with other caries diagnostic meth­ods and the effect of stain on their diagnostic perfor­mance. Caries Res. 2003;37(1):8–16.
18 Dental, Occlusal, andFunctional Evaluation ofPatients
https://t.me/medicina_free
247
23. Braga MM, Morais CC, Nakama RCS, Leamari VM, Siqueira WL, Mendes FM. In vitro performance of methods of approximal caries detection in primary molars. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2009;108(4):e35–41.
24. Ekstrand KR, Ricketts DN, Kidd EA. Do occlu­sal carious lesions spread laterally at the enamel­dentin junction? A histopathological study. Clin Oral Investig. 1998;2(1):15–20.
25. Pitts NB. The use of bitewing radiographs in the management of dental caries: scientic and prac­tical considerations. Dentomaxillofac Radiol. 1996;25(1):5–16.
26. Lith A. Frequency of radiographic caries examina­tions and development of dental caries. Swed Dent J Suppl. 2001;(147):1–72.
27. Moles DR, Downer MC.Optimum bitewing examina­tion recall intervals assessed by computer simulation. Community Dent Health. 2000;17(1):14–9.
28. Lucas VS, Gupta R, Ololade O, Gelbier M, Roberts GJ.Dental health indices and caries associated micro­ora in children with unilateral cleft lip and palate. Cleft Palate Craniofac J. 2000;37(5):447–52.
29. Mustafa D, Lucas VS, Junod P, Evans R, Mason C, Roberts GJ. The dental health and caries-related microora in children with craniosynostosis. Cleft Palate Craniofac J. 2001;38(6):629–35.
30. Sundell AL, Ullbro C, Marcusson A, Twetman S.Comparing caries risk proles between 5- and 10­year-old children with cleft lip and/or palate and non­cleft controls. BMC Oral Health. 2015;15:85.
31. Worth V, Perry R, Ireland T, Wills AK, Sandy J, Ness A.Are people with an orofacial cleft at a higher risk of dental caries? A systematic review and meta- analysis. Br Dent J. 2017;223(1):37–47.
32. Cabanillas-Aquino AG, Rojas-Yauri MC, Atoche­Socola KJ, Arriola-Guillén LE. Assessment of cra­niofacial and dental characteristics in individuals with Treacher Collins syndrome. A review. J Stomatol Oral Maxillofac Surg. 2020;122:511.
33. Mariath AAS, Casagrande L, de Araujo FB.Grey lev­els and radiolucent lesion depth as cavity predictors for approximal dentin caries lesions in primary teeth. Dentomaxillofac Radiol. 2007;36(7):377–81.
34. Bin-Shuwaish M, Dennison JB, Yaman P, Neiva G.Estimation of clinical axial extension of Class II caries lesions with ultraspeed and digital radiographs: an in-vivo study. Oper Dent. 2008;33(6):613–21.
35. Wenzel A. Radiographic display of carious lesions and cavitation in approximal surfaces: advantages and drawbacks of conventional and advanced modalities. Acta Odontol Scand. 2014;72(4):251–64.
36. Wenzel A.Radiographic modalities for diagnosis of caries in a historical perspective: from lm to machine­intelligence supported systems. Dentomaxillofac Radiol. 2021;50(5):20210010.
37. Lee S, Oh S-I, Jo J, Kang S, Shin Y, Park J-W.Deep learning for early dental caries detection in bitewing radiographs. Sci Rep. 2021;11(1):16807.
38. Kühnisch J, Söchtig F, Pitchika V, Laubender R, Neuhaus KW, Lussi A, et al. In vivo validation of near-infrared light transillumination for inter­proximal dentin caries detection. Clin Oral Investig. 2016;20(4):821–9.
39. Pretty IA.Caries detection and diagnosis: novel tech­nologies. J Dent. 2006;34(10):727–39.
40. Young DA. New caries detection technologies and modern caries management: merging the strategies. Gen Dent. 2002;50(4):320–31.
41. Kapor S, Rankovic MJ, Khazaei Y, Crispin A, Schüler I, Krause F, etal. Systematic review and meta- analysis of diagnostic methods for occlusal surface caries. Clin Oral Investig. 2021;25(8):4801–15.
42. Virajsilp V, Thearmontree A, Aryatawong S, Paiboonwarachat D. Comparison of proximal car­ies detection in primary teeth between laser uo­rescence and bitewing radiography. Pediatr Dent. 2005;27(6):493–9.
43. Ko H-Y, Kang S-M, Kim HE, Kwon H-K, Kim B-I. Validation of quantitative light-induced uorescence- digital (QLF-D) for the detection of approximal caries invitro. J Dent. 2015;43(5):568–75.
44. Macey R, Walsh T, Riley P, Glenny A-M, Worthington HV, Fee PA, etal. Fluorescence devices for the detec­tion of dental caries. Cochrane Database Syst Rev. 2020;12:CD013811.
45. Park K-J, Schneider H, Ziebolz D, Krause F, Haak R.Optical coherence tomography to evaluate variance in the extent of carious lesions in depth. Lasers Med Sci. 2018;33(7):1573–9.
46. Shimada Y, Yoshiyama M, Tagami J, Sumi Y. Evaluation of dental caries, tooth crack, and age-related changes in tooth structure using opti­cal coherence tomography. Jpn Dent Sci Rev. 2020;56(1):109–18.
47. Macey R, Walsh T, Riley P, Glenny A-M, Worthington HV, Clarkson JE, etal. Electrical conductance for the detection of dental caries. Cochrane Database Syst Rev. 2021;3:CD014547.
48. Antipoviene A, Girijotaite M, Bendoraitiene EA. Assessment of the depth of clinically detected approximal caries lesions using digital imaging ber­optic transillumination in comparison to periapical radiographs. J Oral Maxillofac Res. 2020;11(1):e3.
49. König K, Flemming G, Hibst R.Laser-induced auto­uorescence spectroscopy of dental caries. Cell Mol Biol. 1998;44(8):1293–300.
50. Lussi A, Hellwig E.Performance of a new laser uo­rescence device for the detection of occlusal caries invitro. J Dent. 2006;34(7):467–71.
51. Pretty IA, Pender N, Edgar WM, Higham SM.The in vitro detection of early enamel de- and re­mineralization adjacent to bonded orthodontic cleats using quantitative light-induced uorescence. Eur J Orthod. 2003;25(3):217–23.
52. Park K-J, Voigt A, Schneider H, Ziebolz D, Haak R. Light-based diagnostic methods for the in vivo assessment of initial caries lesions: laser uores-
248
https://t.me/medicina_free
C. Runte
cence, QLF and OCT.Photodiagnosis Photodyn Ther. 2021;34:102270.
53. Mileman PA, van den Hout WB.Improving treatment decisions from radiographs: effect of a decision aid. Int J Comput Assist Radiol Surg. 2009;4(4):367–73.
54. Oh SH, Lee SR, Choi JY, Choi YS, Kim SH, Yoon HC, etal. Detection of dental caries and cracks with quantitative light-induced uorescence in comparison to radiographic and visual examination: a retrospec­tive case study. Sensors (Basel). 2021;21(5):1741.
55. Xing H, Eckert GJ, Ando M.Detection and analyzing plane of non-cavitated approximal caries by cross­polarized optical coherence tomography (CP-OCT). J Dent. 2021;110:103679.
56. Balevi B.Cold pulp testing is the simplest and most accurate of all dental pulp sensibility tests. Evid Based Dent. 2019;20(1):22–3.
57. Alghaithy RA, Qualtrough AJE. Pulp sensibil­ity and vitality tests for diagnosing pulpal health in permanent teeth: a critical review. Int Endod J. 2017;50(2):135–42.
58. Castillo-Silva BE, Alegría-Torres JA, Martínez­Castañón GA, Medina-Solís CE, Zavala-Alonso NV, Niño-Martínez N, et al. Diagnostic accuracy of three placement sites for the cold test in subjects amongst different age groups. BMC Oral Health. 2019;19(1):189.
59. Sui H, Lv Y, Xiao M, Zhou L, Qiao F, Zheng J, etal. Relationship between the difference in electric pulp test values and the diagnostic type of pulpitis. BMC Oral Health. 2021;21(1):339.
60. Bastos JV, de Souza Côrtes MI. Pulp canal oblitera­tion after traumatic injuries in permanent teeth—sci­entic fact or ction? Braz Oral Res. 2018;32(suppl
1):e75.
61. Chen E, Abbott PV.Evaluation of accuracy, reliabil­ity, and repeatability of ve dental pulp tests. J Endod. 2011;37(12):1619–23.
62. Weisleder R, Yamauchi S, Caplan DJ, Trope M, Teixeira FB. The validity of pulp testing: a clinical study. J Am Dent Assoc. 2009;140(8):1013–7.
63. Nardi P, Guarducci M, Cervino M.Chirurgia ortogna­tica. Studio sulle lesioni nervose. Minerva Stomatol. 2002;51(11–12):461–71.
64. Chen E, Goonewardene M, Abbott P.Monitoring den­tal pulp sensibility and blood ow in patients receiv­ing mandibular orthognathic surgery. Int Endod J. 2012;45(3):215–23.
65. Ruiz Valero CA, Gómez-Delgado A, Henao-Moreno N.Postoperative neurosensory impairment perception using ultrasonic BoneScalpel and conventional rotary instruments after bilateral split sagittal osteotomy. Oral Maxillofac Surg. 2021;25:495.
66. Ghouth N, Duggal MS, BaniHani A, Nazzal H.The diagnostic accuracy of laser Doppler owmetry in assessing pulp blood ow in permanent teeth: a sys­tematic review. Dent Traumatol. 2018;34(5):311–9.
67. Khademi AA, Shahtouri MM, Attar BM, Rikhtegaran N. Pulp vitality of maxillary canines after alveolar
cleft bone grafting: pulse oximetry versus electric pulp test versus cold test. J Craniofac Surg. 2017;32:e314.
68. Pigg M, Nixdorf DR, Nguyen RHN, Law AS.Validity of preoperative clinical ndings to identify dental pulp status: a National Dental Practice-Based Research Network Study. J Endod. 2016;42(6):935–42.
69. Renvert S, Persson GR.A systematic review on the use of residual probing depth, bleeding on prob­ing and furcation status following initial periodontal therapy to predict further attachment and tooth loss. J Clin Periodontol. 2002;29(Suppl 3):82–9; discussion 90–1.
70. Múfalo PS, de Oliveira Fortes Kaizer R, da Silva Dalben G, de Almeida ALPF. Comparison of peri­odontal parameters in individuals with syndromic craniosynostosis. J Appl Oral Sci. 2009;17(1):13–20.
71. Korolenkova MV.Juvenile paradental cysts in chil­dren after mandible distraction: case-control study and clinical cases presentation. Stomatologiia (Mosk). 2015;94(6):36–40.
72. Bassani DG, Da Silva CM, Oppermann RV.Validity of the “community periodontal index of treatment needs” (CPITN) for population periodontitis screen­ing. Cad Saude Publica. 2006;22(2):277–83.
73. Rams TE, Loesche WJ. Relationship between peri­odontal screening and recording index scores and need for periodontal access surgery. J Periodontol. 2017;88(10):1042–50.
74. Schulte W, d'Hoedt B, Lukas D, Maunz M, Steppeler M. Periotest for measuring periodontal character­istics—correlation with periodontal bone loss. J Periodontal Res. 1992;27(3):184–90.
75. Nam S-H, Jung H-I, Kang S-M, Inaba D, Kwon H-K, Kim B-I. Validity of screening methods for peri­odontitis using salivary hemoglobin level and self­report questionnaires in people with disabilities. J Periodontol. 2015;86(4):536–45.
76. Nomura Y, Okada A, Kakuta E, Gunji T, Kajiura S, Hanada N. A new screening method for periodonti­tis: an alternative to the community periodontal index. BMC Oral Health. 2016;16(1):64.
77. Montenegro SCL, Retamal-Valdes B, Bueno-Silva B, Duarte PM, Faveri M, Figueiredo LC, etal. Do patients with aggressive and chronic periodontitis exhibit specic differences in the subgingival micro­bial composition? A systematic review. J Periodontol. 2020;91(11):1503–20.
78. Atieh MA. Accuracy of real-time polymerase chain reaction versus anaerobic culture in detec­tion of Aggregatibacter actinomycetemcomitans and Porphyromonas gingivalis: a meta-analysis. J Periodontol. 2008;79(9):1620–9.
79. Sanz M, Lau L, Herrera D, Morillo JM, Silva A. Methods of detection of Actinobacillus acti­nomycetemcomitans, Porphyromonas gingiva­lis and Tannerella forsythensis in periodontal microbiology, with special emphasis on advanced molecular techniques: a review. J Clin Periodontol. 2004;31(12):1034–47.
18 Dental, Occlusal, andFunctional Evaluation ofPatients
https://t.me/medicina_free
249
80. Brodzikowska A, Górska R, Kowalski J.Interleukin-1 genotype in periodontitis. Arch Immunol Ther Exp. 2019;67(6):367–73.
81. Huynh-Ba G, Lang NP, Tonetti MS, Zwahlen M, Salvi GE.Association of the composite IL-1 genotype with peri-implantitis: a systematic review. Clin Oral Implants Res. 2008;19(11):1154–62.
82. Mombelli A, Casagni F, Madianos PN. Can pres­ence or absence of periodontal pathogens distinguish between subjects with chronic and aggressive peri­odontitis? A systematic review. J Clin Periodontol. 2002;29(Suppl 3):10–21; discussion 37–8.
83. Bodo M, Carinci F, Baroni T, Becchetti E, Bellucci C, Giammarioli M, etal. Interleukin pattern of Apert broblasts invitro. Eur J Cell Biol. 1998;75(4):383–8.
84. Bodo M, Carinci F, Baroni T, Giammarioli M, Bellucci C, Bosi G, et al. Apert’s syndrome: differ­ential in vitro production of matrix macromolecules and its regulation by interleukins. Eur J Clin Invest. 1997;27(1):36–42.
85. The glossary of prosthodontic terms: ninth edition. J Prosthet Dent. 2017;117(5S):e1–e105.
86. Schiffman E, Ohrbach R, Truelove E, Look J, Anderson G, Goulet J-P, etal. Diagnostic criteria for temporomandibular disorders (DC/TMD) for clinical and research applications: recommendations of the International RDC/TMD Consortium Network* and Orofacial Pain Special Interest Group†. J Oral Facial Pain Headache. 2014;28(1):6–27.
87. de Boever JA, Carlsson GE, Klineberg IJ. Need for occlusal therapy and prosthodontic treatment in the management of temporomandibular disorders. Part II: tooth loss and prosthodontic treatment. J Oral Rehabil. 2000;27(8):647–59.
88. Akram A, McKnight MM, Bellardie H, Beale V, Evans RD.Craniofacial malformations and the ortho­dontist. Br Dent J. 2015;218(3):129–41.
89. Passos-Bueno MR, Ornelas CC, Fanganiello RD. Syndromes of the rst and second pha­ryngeal arches: a review. Am J Med Genet A. 2009;149A(8):1853–9.
90. Birgfeld C, Heike C.Craniofacial microsomia. Clin Plast Surg. 2019;46(2):207–21.
91. Nguyen PD, Caro MC, Smith DM, Tompson B, Forrest CR, Phillips JH.Long-term orthognathic sur­gical outcomes in Treacher Collins patients. J Plast Reconstr Aesthet Surg. 2016;69(3):402–8.
92. Solano-Hernández B, Antonarakis GS, Scolozzi P, Kiliaridis S. Combined orthodontic and orthogna­thic surgical treatment for the correction of skel­etal anterior open-bite malocclusion: a systematic review on vertical stability. J Oral Maxillofac Surg. 2013;71(1):98–109.
93. Rathee M, Tamrakar AK, Kundu R, Yunus N.Three­dimensional precise orientation of bilateral auricu­lar trial prosthesis using a facebow for a young adult with Crouzon syndrome. BMJ Case Rep. 2014;2014:bcr2013203248.
94. Hong S-J, Choi Y, Park M, Paek J, Pae A, Kim H-S, et al. Setting the sagittal condylar inclination on a virtual articulator using intraoral scan of protrusive interoc­clusal position and cone beam computed tomography. J Prosthodont. 2020;29(2):185–9.
95. Yang S, Feng N, Li D, Wu Y, Yue L, Yuan Q. A Novel Technique to Align the Intraoral Scans to the Virtual Articulator and Set the Patient-Specic Sagittal Condylar Inclination. J Prosthodont. 2022;31(1): 79–84. PMID: 34170604
Stereoscopic Imaging
https://t.me/medicina_free
ofCraniofacial Malformations
ChristophRunte, MarkusDeki, andDieterDirksen
19
Introduction
Stereoscopic vision allows spatial recognition of three-dimensional objects. Spatial perception of anatomical structures is a fundamental prerequi­site especially for performing surgical interven­tions. Unsurprisingly, surgeons show high-level competence in stereoacuity [1]. In a recent meta­analysis, Bogomolova et al. [2] showed an enhanced learning effect for anatomical content, if stereoscopic imaging was used in an interactive environment. “Interaction” included the ability to rotate the object. Rotating the object means add­ing different perspectives, which means that in this kind of interaction, other important clues for spatial recognition were presented along with stereoscopic viewing. However, comparing inter­active stereoscopic 3D models to interactive monoscopic 3D models still showed a positive effect of stereoscopic presentation [2].
Spatial Perception
linear perspective, shadow position, illumination by close light sources, color saturation and brightness, and stereopsis. Stereoscopic viewing is most effective in spatial recognition of close objects. Theoretically, triangulation allows a very precise determination of distance. However, human stereoscopic perception is subject to two systematic errors: visuospatial compression and depth underconstancy [3]. “Visuospatial com­pression” refers to the fact that the distance of near objects is overestimated and that of far objects is underestimated. “Depth undercon­stancy” means that objects appear atter and at­ter with increasing distance from the viewer. At very close distances, parallax angle to back­ground objects gets too large, and at greater dis­tances, parallax is too small to perceive distance. Spatial perception therefore should be regarded as a process based on different sensations, with stereopsis being one of the most important. It was shown that even if all other depth cues were elim­inated, binocular depth perception of visual stim­uli is still possible [4].
If we are looking at a three-dimensional scenery, we can estimate the relative distance of objects by several clues, e.g., perceived size of the object, movements, partial occlusion by other objects,
C. Runte (*) · M. Dekiff · D. Dirksen Department of Prosthodontics, University of Muenster, Muenster, Germany e-mail: crunte@uni-muenster.de
© Springer Nature Switzerland AG 2023 U. Meyer (ed.), Fundamentals of Craniofacial Malformations,
https://doi.org/10.1007/978-3-031-28069-6_19
Production andAlignment ofStereoscopic Images
Stereoscopic images of craniofacial malforma­tions can be obtained from already available 3D data (e.g., from CT scans, MRI, or facial surface scans) or taken by stereoscopic camera systems.
251
252
https://t.me/medicina_free
C. Runte et al.
With existing 3D data, common 3D programs can be used to create a pair of images from two perspectives shifted in parallel and to save them using the export or screenshot function of the program. In doing so, a vertical offset or rotation of the virtual camera’s position must be avoided. With programs such as “StereoPhoto Maker” (http://stereo.jpn.org/eng/stphmkr/index.html), correct adjustment of the image pairs and export to various formats are possible.
Stereo photographic images of the facial sur­face will probably be less helpful in examination and diagnosis, as they only show what can also be seen. In stereoscopic photographs, interactive rota­tion of the images is not possible, but nevertheless they might be helpful in education and easier at hand in comparison to a 3D surface scan.
Some equipment for stereo photography are depicted in Fig.19.1. Digital stereoscopic cameras such as the FinePix Real 3D W1 and W3 (Fujilm, Tokyo, Japan) have been available; however, in most cases, production has ceased. They usually had a xed stereoscopic baseline (distance between the two camera lenses) similar to human eye dis­tance. However, such a stereoscopic baseline should not be used for close-up images, as it would lead to a large stereoscopic disparity. The closest and farthest objects in a stereoscopic image pair should have a parallax angle below 70′ [1, 5]. As a simple rule of thumb, when adjusting an image pair to the far point, the deviation of the left and right far point can be set to 1/30 to 1/40 of the picture width. Objects at the distance of the stereo window (= the frame around each image of the
Fig. 19.1 Digital stereo camera FinePix Real 3D W3® (upper left); digital SLR camera (Nikon D100, Nikon Corp., Tokyo, Japan) with stereoscopic macro lens (De Wijs apparatenbouw, Houten, the Netherlands; upper right); digital SLR camera (Nikon D100) with medical Nikkor Makro Lens (Nikon Corp., Tokyo, Japan), mounted on a Manfrotto micro-positioning sliding plate
(Manfrotto, Cassola, Italy) and with additional Traumieger twin ashes (Traumieger Fotographics, Wedel, Germany; lower left); and light eld camera Lytro Illum light eld camera (lower right) with an LED ring light (Walimex universal ring light, Studioexpress GmbH, Wiernsheim, Germany)
19 Stereoscopic Imaging ofCraniofacial Malformations
https://t.me/medicina_free
253
pair that is perceived as a window at a certain dis­tance through which the image pair is seen) have no stereoscopic disparity in the adjusted image pair. The closest point should usually not be located in front of the stereo window. If a close object is cut by the frame of the stereo window, it will be perceived as partially occluded by the frame. This would be contradictory to a perceived closer distance to the observer. Only elements in the picture center might be located closer to the observer than the stereo window [6].
Immobile objects may be photographed from two perspectives one after the other, which allows also to use small stereoscopic baselines, e.g., by a positioning sliding plate for the camera. However, in this case, external, immobile ashlights or dif­fusors should be used in order to avoid different shadows in the stereoscopic images.
Light eld cameras, especially the Lytro Illum camera (Lytro Inc., Mountain View, USA), also offer the possibility to produce stereoscopic image pairs. Since the possible stereoscopic baseline is very small, close-up recordings are possible. The camera is easy to use, but the result­ing images have a comparatively low resolution, and depth information is of limited precision. Sales of the camera were discontinued in 2018.
Presentation ofStereoscopic Images
The need for special equipment for comfortable stereoscopic viewing seems to be the main obsta­cle to its application. Therefore, 3D technology was mainly used by few enthusiasts for a long time. When from around the year 2000 onwards, the equipment in the cinemas of large operator chains was upgraded to digital technology; this was an opportunity to re-establish 3D technology in cinemas at the same time (after earlier, rather short-lived approaches and specialized theatres such as IMAX 3D [7]). In 2009, several 3D mov­ies, e.g., “Avatar” by James Cameron (USA,
2009), were released [8]. As a result, the demand for stereoscopic equipment in the private sector also increased and stereoscopic devices, for example stereoscopic monitors with shutter glasses and autostereoscopic displays for stereo cameras, became available.
For interactive stereoscopic display of 3D data, powerful computers and graphic cards as well as special software are necessary due to the high data volume and calculation time (Fig.19.2).
Noninteractive presentation is possible by using image pairs instead of 3D data. Possible
Fig. 19.2 Interactive presentation software DView® (unpublished, by Prof. Dr. D.Dirksen, Münster, Germany). Display is set to anaglyph; shutter and lenticular displays are also possible. The user can interactively rotate and scale the 3D object (volume tomography of an oculo-
auriculo- vertebral dysplasia patient, data used with kind permission of Prof. Dr. Dr. U.Meyer). With the clip box activated, sections in any directions can be made by shift­ing the spherical marks. Data format was .stl