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1.
J Craniofac Surg ; 34(6): 1756-1759, 2023 Sep 01.
Artigo em Inglês | MEDLINE | ID: mdl-37552130

RESUMO

PURPOSE: To assess the impact of 1 and 2-stage palatoplasty protocol on the dental arch relationships in unilateral cleft lip and palate (UCLP) in a single center. METHODS: Our study consisted of 349 individuals divided into 2 groups according to the palatoplasty protocol. Two-stage group comprised 169 subjects with UCLP (mean age: 6.9 y, 110 male and 59 female) who underwent lip, nasal ala, and anterior palate repair with vomer flap from 3 to 6 months (first surgery stage). Soft palate repair occurred from 12 to 18 months (second surgery stage). The one-stage group comprised 180 subjects with UCLP (mean age: 7.2 y, 108 male and 72 female) who underwent 1-stage palatoplasty. Dental models were evaluated by 3 experienced orthodontists applying Goslon Yardstick and the 5-year-old index (FYOI). The influence of the palatoplasty technique and surgeon factor on the interarch relationship was evaluated. The weighted Kappa was used to assess intraexaminer and interexaminer agreements for comparisons of dental arch relationships. Intergroup comparisons were conducted using the χ 2 test ( P <0.05). RESULTS: The intraexaminer reliability was very good (0.81 to 0.98) and interexaminer reliability varied from satisfactory to very good (0.56 to 0.83). The mean occlusal index of the 2-stage and 1-stage groups was 2.77 and 3.03, respectively. The variability of the mean index between surgeons varied from 2.38 to 3.2 in the 2-stage group and 2.91 to 3.2 in the 1-stage group. There were significant differences in the frequency of Goslon 5 index ( P =0.002) between groups, with the 2-stage group presenting less cases (1.18%) than the group 1-stage (11.11%). CONCLUSION: The interarch relationship was similar for both palate repair protocols. Two-stage palatoplasty showed a decreased prevalence of Goslon index 5.


Assuntos
Fenda Labial , Fissura Palatina , Masculino , Humanos , Feminino , Criança , Pré-Escolar , Fissura Palatina/cirurgia , Fenda Labial/cirurgia , Reprodutibilidade dos Testes , Arco Dental , Palato Mole/cirurgia , Resultado do Tratamento
2.
J Craniofac Surg ; 31(4): e356-e359, 2020 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-32217860

RESUMO

Robin sequence with cleft mandible and limb anomalies, known as Richieri-Costa-Pereira syndrome (RCPS), is an autosomal recessive acrofacial dysostosis characterized by mandibular cleft and other craniofacial anomalies and respiratory complications. The aim of this cross-sectional study was to describe the hyoid and head posture of 9 individuals with RCPS using cephalometric measurements and provide a discussion about its implications in obstructive sleep apnea syndrome (OSAS). The study was conducted on lateral cephalograms of patients with RCPS and 9 selected age-matched controls in tertiary cleft center in Brazil. The cephalograms were digitized and analyzed on a software to obtain the vertical and horizontal hyoid position, its relationship with the mandible and the relation of the cranial base and postvertebral line. The t test was used for analysis of means and Levene's test for equality of variances.Cephalometric measurements H-S (vertical distance between hyoid bone and sella) (Supplemental Digital Content, Figure 1, http://links.lww.com/SCS/B247) and H-C4lp (horizontal position of the hyoid in relation to the post-pharyngeal space) showed statistically significant difference compared to controls (P < 0.05). Therefore, the hyoid bone was more inferiorly and posteriorly positioned in the study group compared with the control group. The vertebrae measurements did not present differences compared to controls. The described position of hyoid bone could be involved in the severe OSAS of RCPS patients.


Assuntos
Pé Torto Equinovaro , Deformidades Congênitas da Mão , Cabeça , Osso Hioide , Síndrome de Pierre Robin , Postura , Adolescente , Cefalometria , Criança , Pé Torto Equinovaro/diagnóstico por imagem , Pé Torto Equinovaro/genética , Estudos Transversais , RNA Helicases DEAD-box/genética , Fator de Iniciação 4A em Eucariotos/genética , Deformidades Congênitas da Mão/diagnóstico por imagem , Deformidades Congênitas da Mão/genética , Humanos , Lactente , Masculino , Síndrome de Pierre Robin/diagnóstico por imagem , Síndrome de Pierre Robin/genética , Apneia Obstrutiva do Sono/etiologia
3.
Cleft Palate Craniofac J ; 56(10): 1366-1372, 2019 11.
Artigo em Inglês | MEDLINE | ID: mdl-31216877

RESUMO

OBJECTIVE: To compare the cephalometric characteristics of patients with and without Opitz G/BBB syndrome type I. DESIGN: Cross-sectional, case-control study. SETTING: Tertiary cleft center in Brazil. PARTICIPANTS: Eighteen individuals with Opitz G/BBB syndrome with complete bilateral cleft lip and palate (BCLP), compared to 18 individuals with nonsyndromic complete cleft lip and palate and 18 individuals without malformations, matched for gender and age. INTERVENTIONS: Pretreatment lateral cephalograms of all patients were manually traced and digitized for achievement of linear and angular measurements. MAIN OUTCOME MEASURES: Analysis of variance or Kruskal-Wallis followed by Tukey tests were used for intergroup comparisons at a significance level of P < .05. RESULTS: Individuals with Opitz G/BBB syndrome exhibited alterations in SNGn, P-Co, and N'-Pr/Po-Or that were not attributable to BCLP. Co-Go, Sella-Nasion-Supramentale, ANB (maxillo-mandibular relationship), and anterior nasal spine-posterior nasal spine (ANS-PNS)/U1A-U1T were significantly different in both G/BBB and BCLP groups compared to control, but not different between G/BBB and BCLP groups. Anterior nasal spine-posterior nasal spine/Go-Gn, ANS-PNS, V-Upper pharyngeal wall, and U-lower pharyngeal wall were different in nonsyndromic BLCP compared to nonsyndromic controls and Opitz G/BBB group. CONCLUSION: Patients with Opitz G/BBB syndrome exhibited some unique cephalometric alterations compared to patients with nonsyndromic complete BCLP and controls.


Assuntos
Fenda Labial , Fissura Palatina , Brasil , Estudos de Casos e Controles , Cefalometria , Estudos Transversais , Humanos , Masculino
4.
J Craniofac Surg ; 29(6): 1518-1521, 2018 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-29944557

RESUMO

OBJECTIVE: To compare the efficacy of dental plaque removal between manual and powered toothbrushes in individuals with syndactyly. MATERIAL AND METHODS: Seventeen patients with Apert syndrome aged 11 to 30 years. The efficacy of toothbrushing was evaluated by the O'Leary plaque index at 2 periods: initial (before toothbrushing) and final (immediately after toothbrushing), using manual toothbrush (Colgate Twister) and powered toothbrush (Colgate Actibrush). Means were compared by the ANOVA test at a significance level of 5%. RESULTS: The reduction in the plaque index was different for each type of toothbrush (interaction factor between manual and powered toothbrushes and initial and final periods, P = 0.026). The powered toothbrush provided greater reduction of dental plaque than the manual toothbrush. CONCLUSION: In individuals with syndactyly, both manual and powered toothbrushes allowed significant plaque reduction on tooth surfaces; however, the powered toothbrush exhibited greater efficacy of plaque removal compared with the manual toothbrush.


Assuntos
Placa Dentária/prevenção & controle , Sindactilia , Escovação Dentária , Adolescente , Adulto , Criança , Humanos , Escovação Dentária/instrumentação , Escovação Dentária/métodos , Escovação Dentária/estatística & dados numéricos , Adulto Jovem
5.
J Craniofac Surg ; 29(6): 1596-1600, 2018 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-29863549

RESUMO

The Richieri-Costa-Pereira syndrome (RCPS) is an autosomal-recessive acrofacial dysostosis caused by mutations in EIF4A3, characterized by mandibular cleft comprising other craniofacial anomalies and limb defects such as cleft palate/Robin Sequence, microstomia, absence of mandibular central incisors, minor ear anomalies, clubfeet and first and 5 ray defects. The findings from this study are useful for better understanding the morphological consequences of disorders of EIF4A3, and having a better picture of the anatomic characteristics of the syndrome for a better therapeutic planning. Twenty-four angular and linear variables were measured to assess anteroposterior and vertical (superior-inferior) position of the cranial base, maxilla, mandible, and facial profile. The cephalometric radiographic analysis was performed on 9 individuals with RCPS, obtained at a mean age of 10.3 years, and compared with randomly selected age-matched 9 controls, without clefts and with well-balanced faces, with mean age of 10.6 years (both groups range 8.1 to 13.7 years). t test was used for analysis of means and Levene test for equality of variances. The syndrome group presented severe mandibular hypoplasia and retrognathism (P = 0.009, P = 0.001), greater facial convexity (N'PnPog and N'SnPog, P < 0.05) in syndrome group compared with the control group (P = 0.003, P = 0.004). In conclusion, in the RCPS group, most craniofacial defects affect the lower facial third, considering the severely affected mandible.


Assuntos
Pé Torto Equinovaro/diagnóstico por imagem , Deformidades Congênitas da Mão/diagnóstico por imagem , Anormalidades Maxilomandibulares/diagnóstico por imagem , Síndrome de Pierre Robin/diagnóstico por imagem , Crânio/diagnóstico por imagem , Adolescente , Estudos de Casos e Controles , Cefalometria , Criança , Pé Torto Equinovaro/patologia , Feminino , Deformidades Congênitas da Mão/patologia , Humanos , Anormalidades Maxilomandibulares/patologia , Masculino , Síndrome de Pierre Robin/patologia , Crânio/patologia
6.
Rev Esc Enferm USP ; 48(6): 993-8, 2014 Dec.
Artigo em Português | MEDLINE | ID: mdl-25626497

RESUMO

OBJECTIVE: To identify the main doubts of caregivers of children with cleft lip and palate on postoperative care after cheiloplasty and palatoplasty. METHOD: Cross-sectional study carried out in a reference hospital, between September and November 2012. The sample was composed of 50 individuals divided in two groups, of which 25 caregivers of children submitted to cheiloplasty, and 25 of children submitted to palatoplasty. The doubts were identified by an interview applied during the preoperative nursing consultation and were then categorized by similarity. Descriptive statistics was used for analysis of the outcomes. RESULTS: Concerning cheiloplasty, the doubts were related to feeding (36%), hygiene and healing (24% each), pain and infection (8% each). With regard to palatoplasty, the doubts were related to feeding (48%), hygiene (24%), pain (16%), bleeding (8%) and infection (4%). CONCLUSION: The study evidenced the concern of caregivers in relation to feeding and care of the postoperative wound.


Assuntos
Cuidadores/psicologia , Fenda Labial/cirurgia , Fissura Palatina/cirurgia , Conhecimentos, Atitudes e Prática em Saúde , Cuidados Pós-Operatórios/enfermagem , Adulto , Criança , Fenda Labial/enfermagem , Fissura Palatina/enfermagem , Estudos Transversais , Métodos de Alimentação/enfermagem , Humanos , Hemorragia Pós-Operatória/enfermagem , Infecção da Ferida Cirúrgica/enfermagem , Cicatrização , Adulto Jovem
7.
J Appl Oral Sci ; 31: e20220478, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-37132668

RESUMO

The prevalence of impaction of the permanent canine on the cleft side (PCCS) ranges from 12-35% after alveolar bone grafting (ABG). PCCSs usually develop above other permanent teeth in the alveolar process, gradually becoming vertical until they reach the occlusal plane. The type of cleft, hypodontia of lateral incisor on the cleft side, slower PCCS root development, and genetic factors are predictors of impaction and/or its ectopic eruption. To compare the behavior of PCCS in individuals with complete unilateral cleft lip and palate (UCLP) subjected to secondary alveolar grafting (SAG) with different materials. This retrospective longitudinal study analyzed 120 individuals undergoing SAG with iliac crest bone, rhBMP-2, and mandibular symphysis. The individuals were selected at a single center and equally divided into three groups. Panoramic radiographs were analyzed by the Dolphin Imaging 11.95 software to measure PCCS angulation and PCCS height from the occlusal plane at two different timepoints. No statistical significance was found between grafting materials (P=0.416). At T1, the PCCS height from the occlusal plane was greater for rhBMP-2 and mandibular symphysis compared to iliac crest bone. The lateral incisor on the cleft side was not related to success or lack of eruption of PCCS (P=0.870). Impaction rates of PCCS were similar for the materials studied. Absence of the lateral incisor on the cleft side did not prevent spontaneous eruption of PCCSs.


Assuntos
Fenda Labial , Fissura Palatina , Dente Impactado , Humanos , Fenda Labial/cirurgia , Fissura Palatina/cirurgia , Estudos Retrospectivos , Estudos Longitudinais , Dente Canino
8.
Cleft Palate Craniofac J ; 47(3): 241-6, 2010 May.
Artigo em Inglês | MEDLINE | ID: mdl-20426673

RESUMO

OBJECTIVE: To compare cephalometric measurements of patients with and without velocardiofacial syndrome. DESIGN: Cross-sectional. SETTING: Public tertiary craniofacial center. SUBJECTS: Lateral cephalograms of 18 patients with velocardiofacial syndrome and 18 controls without morphofunctional alterations, matched for gender and age; all cephalograms were obtained before orthodontic intervention. MAIN OUTCOME MEASURES: The cephalograms were manually traced and digitized for the achievement of linear and angular measurements. RESULTS: Individuals with velocardiofacial syndrome presented a reduced length of the skull base, retrusion of nasal bones, reduced posterior height of the maxilla, increased gonial angle, increased interincisal angle, greater lingual inclination of the mandibular incisors, reduced nasolabial angle, and reduced nasal depth compared with the control group. CONCLUSIONS: Patients with velocardiofacial syndrome presented morphological differences compared with individuals without morphofunctional alterations, which might be considered in the evaluation of patients with suspected diagnosis of the syndrome, as well as for the establishment of treatment protocols adequate to their needs. The present findings did not support the hypothesis of differences in pharyngeal dimensions mentioned by other authors, suggesting that the velopharyngeal insufficiency in these patients may be caused by functional alterations rather than by anatomical differences.


Assuntos
Síndrome de DiGeorge/diagnóstico por imagem , Síndrome de DiGeorge/fisiopatologia , Cefalometria , Anormalidades Craniofaciais/diagnóstico por imagem , Anormalidades Craniofaciais/fisiopatologia , Estudos Transversais , Feminino , Humanos , Masculino , Desenvolvimento Maxilofacial , Radiografia
9.
Braz. j. oral sci ; 23: e241330, 2024. tab
Artigo em Inglês | LILACS, BBO | ID: biblio-1553491

RESUMO

Aim: This study aimed to investigate the occurrence of enamelin gene (ENAM) single nucleotide polymorphisms (SNP) and ENAM polymorphism association with dental anomalies (DA) in individuals with unilateral or bilateral cleft lip and palate (CLP). Methods: Saliva samples were collected from 147 individuals aged between 6 and 15 years-old, both genders, and divided into 4 groups: Group 1 (G1) - CLP and DA; Group 2 (G2) - CLP without DA; Group 3 (G3) - without CLP with DA; Group 4 (G4) - without CLP and DA. The genomic DNA was extracted from saliva samples and the following ENAM SNPs markers were genotyped: rs3796703, rs3796704, rs3796705, rs7671281, rs2609428, and rs35951442. Fisher exact and Pearson's Chi-square tests statistically analyzed the results (α=5%). Results: Individuals without CLP with DA (Group 3 - 19.2%) showed statistically higher prevalence of SNP rs2609428 heterozygotes (p=0.006) than individuals with CLP and DA (Group 1 - 0%). Individuals without CLP (10%) exhibited statistically higher prevalence of mutated heterozygotes/homozygous (p=0.028) than in individuals with CLP (1.3%). Conclusion: SNP rs2609428 marker of ENAM gene may be associated with dental anomalies in individuals without cleft lip and palate


Assuntos
Humanos , Masculino , Feminino , Criança , Adolescente , Anormalidades Dentárias , Proteínas da Matriz Extracelular , Fenda Labial , Fissura Palatina , Polimorfismo de Nucleotídeo Único
10.
Hematol Transfus Cell Ther ; 40(4): 354-357, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-30370413

RESUMO

BACKGROUND: This study investigated the association of Robin Sequence with ABO and RhD blood group phenotypes. METHODS: A retrospective cross-sectional study was performed of a cohort of Robin Sequence patients of the Hospital de Reabilitação de Anomalias Craniofaciais - Universidade de São Paulo (USP), Brazil. The study group was composed of 339 individuals of both genders with Robin Sequence referred for specific treatment. A control group was composed of 1780 individuals without syndromes. The groups were compared using the Pearson' chi-square test (χ 2) with statistical significance being defined for an alpha error of 5% (p-value < 0.05). RESULTS: A comparison of gender found a significant difference for the AB phenotype between groups (p-value = 0.007). Comparing blood type by gender there was no significant difference within the same group (p-value = 0.117 and 0.388 respectively, for Robin Sequence and the control group). When comparing the AB blood type between groups, there was no difference for females (p-value = 0.577), but there was a significant difference for males (p-value = 0.0029). CONCLUSIONS: This study showed that the population with Robin Sequence had different patterns related to gender concerning the phenotypic distribution of ABO and RhD blood group phenotypes. Robin Sequence is more common among females. The AB phenotype was significantly higher in males with Robin Sequence than in males of the Control Group. The prevalence of the RhD-negative phenotype is higher in individuals with Robin Sequence. This result suggests a possible association of ABO and RhD phenotypes with Robin Sequence that should be better investigated by molecular studies, as it deserves greater attention.

11.
J. appl. oral sci ; 31: e20220478, 2023. tab, graf
Artigo em Inglês | LILACS-Express | LILACS | ID: biblio-1440409

RESUMO

Abstract The prevalence of impaction of the permanent canine on the cleft side (PCCS) ranges from 12-35% after alveolar bone grafting (ABG). PCCSs usually develop above other permanent teeth in the alveolar process, gradually becoming vertical until they reach the occlusal plane. The type of cleft, hypodontia of lateral incisor on the cleft side, slower PCCS root development, and genetic factors are predictors of impaction and/or its ectopic eruption. Objective: To compare the behavior of PCCS in individuals with complete unilateral cleft lip and palate (UCLP) subjected to secondary alveolar grafting (SAG) with different materials. Methodology: This retrospective longitudinal study analyzed 120 individuals undergoing SAG with iliac crest bone, rhBMP-2, and mandibular symphysis. The individuals were selected at a single center and equally divided into three groups. Panoramic radiographs were analyzed by the Dolphin Imaging 11.95 software to measure PCCS angulation and PCCS height from the occlusal plane at two different timepoints. Results: No statistical significance was found between grafting materials (P=0.416). At T1, the PCCS height from the occlusal plane was greater for rhBMP-2 and mandibular symphysis compared to iliac crest bone. The lateral incisor on the cleft side was not related to success or lack of eruption of PCCS (P=0.870). Conclusion: Impaction rates of PCCS were similar for the materials studied. Absence of the lateral incisor on the cleft side did not prevent spontaneous eruption of PCCSs.

12.
Braz. j. oral sci ; 22: e239097, Jan.-Dec. 2023. tab
Artigo em Inglês | LILACS, BBO | ID: biblio-1509447

RESUMO

Aim: to verify the relation between endodontic treatment of teeth adjacent to the cleft area and the rehabilitation of patients with unilateral cleft lip and palate, at the Hospital for Rehabilitation of Craniofacial Anomalies. Methods: the present split-mouth study was composed of 406 individuals with complete unilateral cleft lip and palate who had completed the rehabilitation process in a single tertiary cleft center (55.9% males). The information was collected from the dental history on the patients' records and radiographs. The frequency of endodontic treatment in the upper incisors and canines was calculated for the cleft and non-cleft sides. The comparison between sides was performed by the chi-square test (p <0.05). Results: endodontic treatment was more frequent in teeth adjacent to the cleft than in contralateral teeth. The frequency of endodontic treatment in at least one tooth adjacent to the cleft was 18.97%, and 11.6% on the contralateral side. It was observed that endodontic treatment was necessary in 63.5% of patients who had been submitted to orthodontic treatment, 42.4% of those rehabilitated with fixed partial dentures and 12.0% of patients who underwent dental reshaping of teeth adjacent to the cleft. The treatments performed included vital pulp therapy (46.1%), non-vital pulp therapy (46.8%) and endodontic retreatment (7.1%). Conclusion: in individuals with complete cleft lip and palate, teeth close to the bone defect area and used for rehabilitation treatment presented greater need of endodontic intervention


Assuntos
Humanos , Masculino , Feminino , Fenda Labial , Fissura Palatina , Diagnóstico , Endodontia
13.
J Appl Oral Sci ; 26: e20170125, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-29742253

RESUMO

Objective This study analyzed the maintenance of lateral incisors in the dental rehabilitation of individuals with cleft lip and palate. Material and Methods The study was conducted on a tertiary craniofacial center and comprised retrospective analysis of panoramic and periapical radiographs of Caucasoid individuals with non-syndromic complete unilateral cleft lip and palate, analyzing all radiographs available on the records of each individual, from the first to the last up to 12 years of age. Overall, 2,826 records were reviewed to achieve a sample of 1,000 individuals. Among these, 487 individuals presented the permanent lateral incisors on both cleft and non-cleft sides, which were included in this study. Results The results were evaluated in percentages and by descriptive statistics. The association between maintenance of the lateral incisor and timing of alveolar bone graft were analyzed by the t test. Among the 487 individuals, 265 had not completed treatment, 62 presented insufficient information, and 44 concluded the treatment elsewhere. Among the remaining 116 individuals, the lateral incisor was extracted from 88 (75.86%) of them on the cleft side (CS) and from 23 (19.83%) people on the non-cleft side (NCS). The age at accomplishment of alveolar bone graft was significantly associated with maintenance of the lateral incisor on the cleft side (p<0.01). Most extractions were indicated because of the inadequate positioning on the CS and for midline correction on the NCS. Rehabilitation was primarily completed by orthodontic movement (53 individuals on the CS and 13 individuals on the NCS). Conclusion In conclusion, the lateral incisor on the cleft side was not maintained in most individuals. Positive relationship was observed between extraction of the lateral incisor and age at accomplishment of the alveolar bone graft, suggesting the need to anticipate the initial radiographic evaluation to enhance its maintenance and reduce the procedures required for rehabilitation.


Assuntos
Enxerto de Osso Alveolar/métodos , Fenda Labial/reabilitação , Fissura Palatina/reabilitação , Incisivo , Adolescente , Adulto , Criança , Pré-Escolar , Fenda Labial/diagnóstico por imagem , Fenda Labial/cirurgia , Fissura Palatina/diagnóstico por imagem , Fissura Palatina/cirurgia , Feminino , Humanos , Incisivo/diagnóstico por imagem , Lactente , Masculino , Maxila , Radiografia Panorâmica , Estudos Retrospectivos , Fatores de Tempo , Extração Dentária/métodos , Técnicas de Movimentação Dentária/métodos , Resultado do Tratamento , Adulto Jovem
14.
J Appl Oral Sci ; 26: e20170244, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-29742256

RESUMO

The repair of bone defects raises the interest of investigators in several health specialties. Grafting techniques with bone substitutes and laser therapies have been investigated to replace autogenous bone and accelerate the bone healing process. Objective To evaluate the effect of photobiomodulation therapy (PBMT) associated with guided bone regeneration (GBR) in critical size defects. Material and Methods The study was conducted on 80 male rats (Rattus norvegicus albinus, Wistar) submitted to surgical creation of a critical size defect on the calvaria, divided into eight study groups: group C (control - only blood clot); group M (collagen membrane); group PBMT (photobiomodulation therapy); group AB (autogenous bone); group AB+PBMT; group AB+M; group PBMT+M; group AB+PBMT+M. The animals were killed 30 days postoperatively. After tissue processing, bone regeneration was evaluated by histomorphometric analysis and statistical analyses were performed (Tukey test, p<0.05). Results All groups had greater area of newly formed bone compared to group C (9.96±4.49%). The group PBMT+M (achieved the greater quantity of new bone (64.09±7.62%), followed by groups PBMT (47.67±8.66%), M (47.43±15.73%), AB+PBMT (39.15±16.72%) and AB+PBMT+M (35.82±7.68%). After group C, the groups AB (25.10±16.59%) and AB+M (22.72±13.83%) had the smallest quantities of newly formed bone. The area of remaining particles did not have statistically significant difference between groups AB+M (14.93±8.92%) and AB+PBMT+M (14.76±6.58%). Conclusion The PBMT utilization may be effective for bone repair, when associated with bone regeneration techniques.


Assuntos
Regeneração Óssea/efeitos da radiação , Regeneração Tecidual Guiada/métodos , Terapia com Luz de Baixa Intensidade/métodos , Animais , Autoenxertos , Regeneração Óssea/fisiologia , Colágeno/análise , Masculino , Osteogênese/fisiologia , Osteogênese/efeitos da radiação , Distribuição Aleatória , Ratos Wistar , Valores de Referência , Reprodutibilidade dos Testes , Crânio/fisiologia , Crânio/efeitos da radiação , Crânio/cirurgia , Resultado do Tratamento , Cicatrização/fisiologia , Cicatrização/efeitos da radiação
15.
Oral Health Prev Dent ; 4(3): 173-9, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-16961025

RESUMO

OBJECTIVE: To gain more information on the oral health status of subjects with syndromic craniosynostosis. DESIGN: A cross-sectional study. MATERIALS AND METHODS: The present study took place at the Hospital for Rehabilitation of Craniofacial Anomalies of University of São Paulo (HRAC-USP). The sample was 19 patients with syndromic craniosynostosis (10 Apert, 5 Crouzon, 2 Pfeiffer and 2 Saethre-Chotzen), aged 5 to 15 years. An assessment of plaque, caries and gingival indices, and evaluation of the efficacy of toothbrushing was carried out. The measurements included PHP index, dmft and DMFT indices, gingival index, comparison of PHP before and after non-supervised toothbrushing and between individuals with and without severe syndactyly. RESULTS: The patients displayed high plaque index and poor efficacy of toothbrushing, regardless of the presence of severe syndactyly; despite the plaque accumulation, the gingival index was not proportionally high. There was predominance of the D component for the DMFT index, which combined with the need for restorative treatment in 42.1% of the patients indicates poor access to dental care by these patients. CONCLUSIONS: The results show the need for a dental follow-up programme for these patients. Carers should be informed of the importance in aiding these patients during accomplishment of oral hygiene at home.


Assuntos
Craniossinostoses/complicações , Cárie Dentária/complicações , Placa Dentária/complicações , Nível de Saúde , Saúde Bucal , Acrocefalossindactilia/complicações , Adolescente , Criança , Pré-Escolar , Disostose Craniofacial/complicações , Métodos Epidemiológicos , Feminino , Humanos , Masculino , Fotografia Dentária , Síndrome , Escovação Dentária
16.
Braz. dent. sci ; 24(4): 1-7, 2021. tab
Artigo em Inglês | LILACS, BBO | ID: biblio-1293148

RESUMO

Objective: Congenital defects, including cleft lip and palate, increase the morbidity and mortality in the affected population. This study aimed to determine the prevalence of cleft lip and palate in the city of Bauru, Brazil, by evaluation of registry in the Brazilian Livebirth Certificate (DNV) and the Information System on Livebirths (SINASC), and analyzed the concordance of diagnosis compared with registries of the Hospital for Rehabilitation of Craniofacial Anomalies (HRAC/USP), located in the same city. Material and Methods: This retrospective observational study comprised analysis of all DNVs and identification of individuals with clefts born and living in Bauru, comparing with data from HRAC/USP. The prevalence was calculated by dividing the number of children born with clefts in the study period by the total number of livebirths registered. The reporting of different types of clefts was compared by the chi-square test. Results: Overall, 50,898 DNV were evaluated, among which there were 25 reported cases of cleft lip and/or palate. In the same period, HRAC/USP registered 77 cases born in Bauru, representing 67.5% of underreporting of the occurrence of clefts. Cleft palate was the most prevalent (34.9%), followed by cleft lip and palate (31.7%) and cleft lip (30.2%), mostly affecting males (58.5%). The reporting of cleft palate (16.12%) was lower compared to cleft lip (43.75%) and cleft lip and palate (54.54%). Conclusion: The study revealed predominance of cleft palate, with significant underreporting of clefts in the public health system, especially for cleft palate as compared to cleft lip and cleft lip and palate (AU)


Objetivo: Os defeitos congênitos, incluindo fenda labial e palatina, aumentam a morbidade e mortalidade na população afetada. Este estudo teve como objetivo determinar a prevalência de fissura labiopalatina na cidade de Bauru, Brasil, por meio da avaliação do registro na Certidão de Nascimento de Vivos (DNV) e no Sistema de Informação de Nascidos Vivos (SINASC), e analisar a concordância do diagnóstico em comparação com registros do Hospital de Reabilitação de Anomalias Craniofaciais (HRAC / USP), localizado na mesma cidade. Material e Métodos: Este estudo observacional retrospectivo compreendeu a análise de todas as DNVs e a identificação dos indivíduos com fissuras nascidos e residentes em Bauru, comparando com os dados do HRAC / USP. A prevalência foi calculada dividindo-se o número de filhos nascidos com fissura no período do estudo pelo total de nascidos vivos registrados. O relato de diferentes tipos de fissuras foi comparado pelo teste do qui-quadrado. Resultados: No geral, foram avaliadas 50.898 DNV, entre as quais houve 25 casos notificados de fenda labial e / ou palatina. No mesmo período, o HRAC / USP registrou 77 casos nascidos em Bauru, representando 67,5% de subnotificação da ocorrência de fissuras. A fenda palatina foi a mais prevalente (34,9%), seguida da fenda labiopalatina (31,7%) e fenda labial (30,2%), ocorrendo principalmente no sexo masculino (58,5%). O relato de fissura palatina (16,12%) foi menor em comparação com fissura labial (43,75%) e fissura labiopalatina (54,54%). Conclusão: O estudo revelou predomínio de fissura palatina, com subnotificação significativa de fissuras no sistema público de saúde, principalmente para fenda palatina em relação à fenda labial e labiopalatina. (AU)


Assuntos
Humanos , Masculino , Feminino , Epidemiologia , Prevalência , Fenda Labial , Fissura Palatina
17.
Braz Oral Res ; 28 Spec No: 1-8, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25118803

RESUMO

This text begins by reflecting on health promotion and equity/ inequity. In health, inequity is understood as a political concept that has moral implications and that is committed to social justice. A discussion follows on some issues regarding the risk and prevention of diseases, still considered a hegemonic practice, and lack of experience in oral health-care, bearing in mind the concept of vulnerability. The risk is probabilistic and involves the mathematical chances of acquiring a disease in a certain group, whereas vulnerability addresses the potential of acquiring or not acquiring a disease in a certain environment. The need for systematic studies on determinants is stressed, with the ultimate goal of improving health and reducing inequities, and with the concern and political intention of including health equity in governmental policies.


Assuntos
Cárie Dentária/prevenção & controle , Promoção da Saúde/tendências , Acessibilidade aos Serviços de Saúde/tendências , Saúde Bucal/tendências , Brasil , Criança , Humanos , Prevenção Primária , Fatores de Risco , Fatores Socioeconômicos
18.
Dent. press endod ; 9(1): 21-25, jan.-mar. 2019. tab, Ilus
Artigo em Português | BBO, LILACS | ID: biblio-1000053

RESUMO

Objetivo: avaliar, radiograficamente, a prevalência, extensão e severidade da reabsorção dentária em dentes adjacentes à área de fissura após enxerto ósseo alveolar. Métodos: radiografias de 200 indivíduos com fissura unilateral e bilateral, alveolar e palatina, foram analisadas para se investigar a presença de reabsorção dentária relacionada com o enxerto ósseo. No total, 1.315 radiografias foram analisadas (periapical, oclusal e radiografias panorâmicas), obtidas a partir de 200 indivíduos com fissura labiopalatina unilateral e bilateral completa ubmetidos a cirurgia de enxerto, disponíveis a partir dos arquivos da Seção de Radiologia do HRAC-USP. Resultados: entre os 200 indivíduos, 33 tinham reabsorções dentárias externas. Dessas, 15 estavam presentes nas radiografias pré-operatórias e 18 só depois do enxerto ósseo. No geral, 30 reabsorções localizaram- se no terço apical da raiz e 3 no terço cervical; o incisivo central esquerdo foi o mais afetado. Não foram observadas reabsorções dentárias no terço médio da raiz e nenhuma reabsorção afetou mais de um terço. Não existiu diferença estatisticamente significativa entre a idade do paciente durante a cirurgia de enxerto ósseo e a presença de reabsorção dentária externa. Conclusões: a prevalência da reabsorção dentária em dentes adjacentes à área da fissura em indivíduos submetidos a enxerto ósseo foi baixa (16,5%). O terço apical da raiz foi o local mais frequente de reabsorção radicular externa, e não houve reabsorções afetando mais de um terço da raiz. (AU)


Assuntos
Humanos , Masculino , Feminino , Perda do Osso Alveolar/diagnóstico por imagem , Fenda Labial/cirurgia , Fissura Palatina/cirurgia , Enxerto de Osso Alveolar/métodos , Reabsorção de Dente , Distribuição de Qui-Quadrado
19.
Hematol., Transfus. Cell Ther. (Impr.) ; 40(4): 354-357, Oct.-Dec. 2018. tab
Artigo em Inglês | LILACS | ID: biblio-984495

RESUMO

ABSTRACT Background: This study investigated the association of Robin Sequence with ABO and RhD blood group phenotypes. Methods: A retrospective cross-sectional study was performed of a cohort of Robin Sequence patients of the Hospital de Reabilitação de Anomalias Craniofaciais - Universidade de São Paulo (USP), Brazil. The study group was composed of 339 individuals of both genders with Robin Sequence referred for specific treatment. A control group was composed of 1780 individuals without syndromes. The groups were compared using the Pearson' chi-square test (χ 2) with statistical significance being defined for an alpha error of 5% (p-value < 0.05). Results: A comparison of gender found a significant difference for the AB phenotype between groups (p-value = 0.007). Comparing blood type by gender there was no significant difference within the same group (p-value = 0.117 and 0.388 respectively, for Robin Sequence and the control group). When comparing the AB blood type between groups, there was no difference for females (p-value = 0.577), but there was a significant difference for males (p-value = 0.0029). Conclusions: This study showed that the population with Robin Sequence had different patterns related to gender concerning the phenotypic distribution of ABO and RhD blood group phenotypes. Robin Sequence is more common among females. The AB phenotype was significantly higher in males with Robin Sequence than in males of the Control Group. The prevalence of the RhD-negative phenotype is higher in individuals with Robin Sequence. This result suggests a possible association of ABO and RhD phenotypes with Robin Sequence that should be better investigated by molecular studies, as it deserves greater attention.


Assuntos
Humanos , Masculino , Feminino , Síndrome de Pierre Robin , Sistema do Grupo Sanguíneo Rh-Hr , Sistema ABO de Grupos Sanguíneos
20.
Ear Nose Throat J ; 92(3): E10-4, 2013 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-23532654

RESUMO

We report the case of a 9-year-old girl who presented with a complaint of a malodorous bloody discharge from the left naris. The patient had previously undergone a complete repair of left-sided cleft lip and palate. Clinical examination revealed hyperplasia of the nasal mucosa on the left side. X-ray examination of the nasal cavity demonstrated a radiopaque structure that resembled a tooth and a radiopaque mass similar to an odontoma that was adherent to the root of the suspected tooth. With the patient under general anesthesia, the structure was removed. On gross inspection, the structure was identified as a tooth with a rhinolith attached to the surface of its root. Microscopic examination revealed normal dentin and pulp tissue. A nonspecific inflammatory infiltrate was observed around the rhinolith, and areas of regular and irregular mineralization were seen. Some mineralized areas exhibited melanin-like brownish pigmentation. Areas of mucus with deposits of mineral salts were also observed. Rare cases of an intranasal tooth associated with a rhinolith have been described in the literature. We believe that this case represents only the second published report of an intranasal tooth associated with a rhinolith in a patient with cleft lip and palate.


Assuntos
Calcinose/complicações , Coristoma/complicações , Fenda Labial/complicações , Fissura Palatina/complicações , Doenças Nasais/complicações , Dente , Criança , Feminino , Humanos
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