Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 20 de 68
Filtrar
1.
Hand Surg ; 20(2): 237-50, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26094485

RESUMO

The aim of this study is to introduce the classification of Swanson for congenital anomalies of upper limb modified by the Japanese Society for Surgery of the Hand (the JSSH modification) in English. The Swanson classification has been widely accepted by most hand surgeons. However, several authors have suggested that complex cases, particularly those involving the complex spectrum of cleft hand and symbrachydactyly, are difficult to classify into the classification schemes. In the JSSH modification, brachysyndactyly, so-called atypical cleft hand and transverse deficiency are included under the same concept of transverse deficiency. Cleft hand, central polydactyly, and syndactyly are included in the same category of abnormal induction of digital rays. We believe that the JSSH modification system is effective in providing hand surgeons with the clinical features and conditions for congenital anomalies.


Assuntos
Deformidades Congênitas da Mão/classificação , Deformidades Congênitas da Mão/cirurgia , Procedimentos Ortopédicos/métodos , Ortopedia , Sociedades Médicas , Humanos , Japão
2.
J Electromyogr Kinesiol ; 25(4): 689-96, 2015 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-25921817

RESUMO

In order to elucidate strict actions of the human wrist flexors, motion and force produced by electrical neuromuscular stimulation (ENS) to each of musculus (m.) flexsor carpi radialis (FCR) and m. flexsor carpi ulnaris (FCU) with the prone, semiprone, and supine forearm were studied in ten healthy human subjects. Abduction, extension, adduction, and flexion directions were represented by, respectively, 0°, 90°, 180°, and 270°. ENS to FCR and FCU produced motion in direction of, respectively, 273° (mean) and 265° with the prone, 249° and 232° with the semiprone, and 242° and 229° with the supine forearm to the maximal range. Direction/strength (Nm) of force by ENS to FCR and FCU were, respectively, 298°/1.16 and 239°/1.70 with the prone, 279°/1.30 and 241°/1.62 with the semiprone, and 267°/1.24 and 227°/2.04 with the supine forearm. ENS to FCR exhibited force of 20-29% of maximal flexion and 7-15% of maximal abduction or 1-4% of maximal adduction and that to FCU force of 24-28% of maximal flexion and 15-25% of maximal adduction. The force study results suggest that FCU is a flexor rather than an adductor with every forearm position. FCR should be a flexor rather than an abductor with the prone and semiprone and a flexor with the supine forearm. The action of FCR as the abductor should diminish with supinating the forearm.


Assuntos
Movimento/fisiologia , Amplitude de Movimento Articular/fisiologia , Articulação do Punho/fisiologia , Punho/fisiologia , Adulto , Estimulação Elétrica/métodos , Feminino , Antebraço/fisiologia , Humanos , Masculino , Pessoa de Meia-Idade , Músculo Esquelético/fisiologia , Estimulação Luminosa/métodos , Adulto Jovem
3.
Somatosens Mot Res ; 31(4): 214-20, 2014 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-25026240

RESUMO

Group I muscle afferents modulate the excitability of motor neurons through excitatory and inhibitory spinal reflexes. Spinal reflex relationships between various muscle pairs are well described in experimental animals but not in the human upper limb, which exhibits a fine control of movement. In the present study, spinal reflexes between the extensor carpi radialis (ECR) and pronator teres (PT) muscles were examined in healthy human subjects using a post-stimulus time histogram method. Electrical stimulation of low-threshold afferents of ECR nerves increased the motor neuron excitability in 31 of 76 PT motor units (MUs) in all eight subjects tested, while stimulation of low-threshold afferents of PT nerves increased the motor neuron excitability in 36 of 102 ECR MUs in all 10 subjects. The estimated central synaptic delay was almost equivalent to that of homonymous facilitation. Mechanical stimulation (MS) of ECR facilitated 16 of 30 PT MUs in all five subjects tested, while MS of PT facilitated 17 of 30 ECR MUs in all six subjects. These results suggest excitatory reflex (facilitation) between PT and ECR. Group I afferents should mediate the facilitation through a monosynaptic path.


Assuntos
Potenciais de Ação/fisiologia , Contração Muscular/fisiologia , Músculo Esquelético/inervação , Reflexo/fisiologia , Extremidade Superior/inervação , Adulto , Feminino , Humanos , Masculino , Condução Nervosa/fisiologia , Estimulação Física , Probabilidade , Tempo de Reação/fisiologia , Adulto Jovem
4.
Congenit Anom (Kyoto) ; 53(2): 78-82, 2013 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-23751041

RESUMO

We conducted a study of Kirner's deformity to investigate its radiologic features and consider its possible causes. Sixty-seven patients with Kirner's deformity, 41 in our series and 26 retrieved in a survey of the literature were investigated. We divided Kirner's deformity into three types according to the site of curvature: the epiphyseal line, diaphysis, and distal tip. Among our series, 12 hands were affected in males and 26 in females. The gender of the patients for the other three hands was unknown. Twelve cases occurred on the right side, five on the left side, and 24 on both sides. Radiographic data for 34 hands were available. The palmar surface of the distal phalanx was at a mean angle of 27.4 degrees to the long axis of the middle phalanx. Epiphyseal line curvature was seen in four hands (mean patient age, 11 years), diaphysis curvature in 10 (mean age, 12.4 years), and distal tip curvature in 20 (mean age, 26.5 years). Dorsal subluxation of the distal phalanx was noticed in six hands (18%). Radiographic data for 26 hands reported previously were analyzable. The differences between epiphyseal line or diaphysis curvature and distal tip curvature in terms of age were significant in both the present study and the literature.


Assuntos
Dedos/diagnóstico por imagem , Deformidades Congênitas da Mão/diagnóstico por imagem , Mãos/diagnóstico por imagem , Adolescente , Adulto , Criança , Feminino , Dedos/patologia , Mãos/fisiopatologia , Deformidades Congênitas da Mão/fisiopatologia , Humanos , Masculino , Radiografia , Adulto Jovem
5.
J Hand Surg Am ; 37(7): 1356-63, 2012 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-22721458

RESUMO

PURPOSE: To investigate the effects of platelet-rich plasma (PRP) with fibrin matrix on the healing of intrasynovial flexor tendons in a rabbit model in vivo. METHODS: We transected and repaired 156 toe flexors of 73 rabbits using the technique of Tsuge et al and a simple running epitendinous suture. We randomly assigned Repaired tendons to groups that recieved no additional treatment (control) or to which we applied PRP, fibrin (F), or PRP with fibrin matrix (PRP-F) at the repair site. We scored edema and adhesion at 2, 3, and 6 weeks after surgery, and linearly tested repaired tendons for load to failure. We also histologically evaluated tendons at 2 and 3 weeks. RESULTS: Edema scores and adhesion scores did not significantly differ among the 4 groups at any time point. Mean load to failure in the PRP-F group (14.7 N) was the highest among the 4 groups at 2 weeks after surgery, and was significantly higher than in the control group (10.0 N). Median histological scores in the PRP-F group (3.3 points) were significantly higher than in the control group (1.0 point). Mean load to failure in the PRP-F group (16.1 N) was highest, and median histological scores in the PRP-F group (3.5 points) were higher than in the control group (2.4 points) at 3 weeks, although there were no significant differences at 3 or 6 weeks. CONCLUSIONS: In a rabbit model of cut flexor tendons, PRP with fibrin matrix significantly increased healing strength within 2 weeks after surgery. Side effects such as increases in toe edema or adhesions around the tendons did not arise. CLINICAL RELEVANCE: Platelet-rich plasma with fibrin matrix might help reduce the risk of repeated rupture after flexor tendon surgery, and lead to early rehabilitation.


Assuntos
Adesivo Tecidual de Fibrina/uso terapêutico , Plasma Rico em Plaquetas , Tendões/metabolismo , Tendões/cirurgia , Cicatrização , Análise de Variância , Animais , Coelhos , Distribuição Aleatória , Estatísticas não Paramétricas , Estresse Mecânico , Técnicas de Sutura
6.
Am J Sports Med ; 40(7): 1583-90, 2012 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-22503809

RESUMO

BACKGROUND: Nonoperative treatment for humeral medial epicondylar fragmentation in baseball players, involving prohibition and limitation of throwing, has been reported to give good results. However, in some cases, such nonoperative treatment fails to yield an acceptable outcome. HYPOTHESIS: In nonoperative treatment for patients with medial epicondylar fragmentation, achievement of bone union of the fragmentation provides better clinical outcomes compared with those of patients with delayed bone union or nonunion. STUDY DESIGN: Cohort study; Level of evidence, 3. METHODS: Fifty-five young baseball players with medial epicondylar fragmentation before epiphyseal closure, aged between 9 and 13 years (mean, 11.0 years), participated in this study. They belonged to baseball teams in a youth league and underwent nonoperative treatment involving prohibition of throwing for an average of 2.0 months and subsequent limitation of throwing for an average of 1.8 months. We investigated whether achievement of bone union of the fragmentation was associated with better clinical outcomes. RESULTS: Bone union was achieved in 40 (73%) of 55 participants at 6 months after initial presentation, 31 (76%) of 41 participants at 1 year, and 32 (94%) of 34 participants at 2 years. Elbow pain was present in 7 participants (17%) at 1 year after initial presentation and in 6 participants (18%) at 2 years. At 1 year after initial presentation, statistical analysis showed that most participants with elbow pain had significant fragmentation (P = .0055). At 2 years after initial presentation, there was no significant relationship between elbow pain and medial epicondylar fragmentation (P = .32). Statistical analysis also showed that, at both 6 months and 1 year after initial presentation, bone union was significantly delayed in most participants who had not accepted nonoperative treatment and consequently resumed throwing vigorously before bone union. CONCLUSION: At 1 year after initial presentation, bone union of the medial epicondylar fragmentation was correlated with a decreased prevalence of elbow pain. At 6 months and 1 year after initial presentation, delayed bone union of the medial epicondylar fragmentation was associated with resumption of throwing at maximum strength before bone union had occurred.


Assuntos
Beisebol/lesões , Fraturas do Úmero/terapia , Adolescente , Artralgia/etiologia , Criança , Articulação do Cotovelo/diagnóstico por imagem , Seguimentos , Consolidação da Fratura , Humanos , Fraturas do Úmero/diagnóstico por imagem , Imobilização , Cooperação do Paciente , Radiografia , Recuperação de Função Fisiológica
7.
J Hand Surg Am ; 37(4): 760-3, 2012 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-22397842

RESUMO

PURPOSE: The amputation of digits that occurs in association with congenital constriction band syndrome (CCBS) is often described as similar to that resulting from trauma. Some previous studies have suggested that no bone hypoplasia is present in the affected limb proximal to the amputated part. The purpose of this study was to report our series of patients with metacarpal hypoplasia in amputated digits associated with CCBS. METHODS: We reviewed a total of 37 hands of 24 patients diagnosed as having amputated fingers owing to CCBS and evaluated the clinical features of the metacarpal bone hypoplasia. RESULTS: We found coexistent metacarpal hypoplasia in 11 hands in 9 patients. Three of the patients were male and 6 were female. The average age at the time of examination was 9 years (range, 4-20 y). We observed metacarpal hypoplasia in cases of amputation at the level of the proximal phalanx and not at the level of the middle phalanx. CONCLUSIONS: We found metacarpal hypoplasia in 38% of patients and in 30% of hands with amputated digits owing to CCBS. TYPE OF STUDY/LEVEL OF EVIDENCE: Prognostic IV.


Assuntos
Síndrome de Bandas Amnióticas/complicações , Ossos Metacarpais/patologia , Adolescente , Adulto , Amputação Traumática , Criança , Pré-Escolar , Feminino , Humanos , Masculino , Ossos Metacarpais/diagnóstico por imagem , Radiografia , Síndrome , Adulto Jovem
8.
Clin Orthop Surg ; 4(1): 45-57, 2012 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-22379555

RESUMO

BACKGROUND: Free fat graft has been used for the treatment of congenital hand differences. However, there have been a few reports about the outcome of that treatment. In this study, the outcome of free fat grafts for congenital hand and foot differences was investigated. METHODS: Fourteen bones with longitudinal epiphyseal bracket, 3 wrists with Madelung deformity, and 5 cases of osseous syndactyly were treated with free fat graft with osteotomy, physiolysis, or separation of osseous syndactyly. Of the fourteen bones with longitudinal epiphyseal bracket, 9 were treated with open wedge osteotomy with free fat graft and 5 with physiolysis and free fat graft. The Madelung deformity was treated with physiolysis with free fat graft. For osseous syndactyly, syndactyly release with free fat graft was performed five times on four hands. RESULTS: In the fourteen cases with longitudinal epiphyseal bracket, lateral deviation improved in all except two cases after surgery. The average lateral deviation angle changed from 32.5 degrees before surgery to 15.2 degrees after surgery. The average improvement of the lateral deviation angle was 12.2 degrees in the osteotomy group and 20.6 degrees in the physiolysis group. The mean ratio of improvement of the lateral deviation angle to the lateral deviation angle before surgery was 39.4% in the osteotomy group and 51.2% in the physiolysis group. The Madelung deformity improved after surgery in two cases but there was no improvement in one case. For these conditions, the results were not good enough when surgery was done after age 13 or at age four for severely hypoplastic brachymesophalangy. Of the 5 cases of osseous syndactyly, reunion of the separated bones occurred in one case. The grafted free fat should be deep enough to cover the osteotomy site of the bones to prevent reunion of the separated bones. CONCLUSIONS: Physiolysis and free fat graft performed during the growth period can correct the deviation due to longitudinal epiphyseal bracket and Madelung deformity. Free fat graft is also useful to prevent reunion of the bones after separation of osseous syndcatyly, if the grafted fat is securely filled into the space between the separated bones.


Assuntos
Tecido Adiposo/transplante , Dedos/anormalidades , Deformidades Congênitas da Mão/cirurgia , Sindactilia/cirurgia , Adolescente , Criança , Pré-Escolar , Feminino , Dedos/cirurgia , Deformidades Congênitas do Pé/cirurgia , Hallux Varus/cirurgia , Humanos , Masculino , Osteotomia , Estatísticas não Paramétricas , Resultado do Tratamento
9.
Arthroscopy ; 28(2): 255-63, 2012 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-22119291

RESUMO

PURPOSE: The purpose of this study was to investigate the in vivo effects of gelatin hydrogels (GHs) incorporating fibroblast growth factor 2 (FGF-2) on meniscus repair in a rabbit model. METHODS: FGF-2 was biologically stabilized by incorporation into GHs. This system enables FGF-2 to be released with its biologic activity intact. A total of 64 skeletally mature female Japanese white rabbits were used. A horizontal tear was made in the medial meniscus, and these tears were divided into 4 groups: GH-FGF, GH-no FGF, FGF (FGF-2 alone), and no treatment. The meniscus was evaluated histologically at 2, 4, 8, and 12 weeks after surgery. Cell density and the percentages of proliferating cell nuclear antigen-positive cells and terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling-positive cells were measured, and a scoring system ranging from 5 points (complete healing) to 0 points (no evidence of healing) was used. RESULTS: Cell density was significantly higher in the GH-FGF group than in the other 3 groups at 2, 4, 8, and 12 weeks (P < .01). The percentage of proliferating cell nuclear antigen-positive cells was significantly higher whereas the percentage of terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling-positive cells was significantly lower in the GH-FGF group at 2 and 4 weeks after surgery (P < .05). At 4, 8, and 12 weeks after surgery, healing scores were significantly higher in the GH-FGF group (2.5 points, 2.7 points, and 3.0 points, respectively) than in the GH-no FGF group (1.3 points, 1.4 points, and 2.0 points, respectively) (P < .05). CONCLUSIONS: GHs incorporating FGF-2 significantly stimulated proliferation and inhibited the death of meniscal cells until 4 weeks, thereby increasing meniscal cell density and enhancing meniscal repair in a rabbit model. CLINICAL RELEVANCE: GHs incorporating FGF-2 are able to enhance the healing of meniscal injury.


Assuntos
Portadores de Fármacos , Fator 2 de Crescimento de Fibroblastos/farmacologia , Gelatina , Hidrogéis , Lesões do Menisco Tibial , Cicatrização/efeitos dos fármacos , Animais , Apoptose , Contagem de Células , Feminino , Marcação In Situ das Extremidades Cortadas , Meniscos Tibiais/metabolismo , Meniscos Tibiais/patologia , Antígeno Nuclear de Célula em Proliferação/metabolismo , Coelhos
10.
PLoS Genet ; 7(4): e1002050, 2011 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-21533187

RESUMO

Metachondromatosis (MC) is a rare, autosomal dominant, incompletely penetrant combined exostosis and enchondromatosis tumor syndrome. MC is clinically distinct from other multiple exostosis or multiple enchondromatosis syndromes and is unlinked to EXT1 and EXT2, the genes responsible for autosomal dominant multiple osteochondromas (MO). To identify a gene for MC, we performed linkage analysis with high-density SNP arrays in a single family, used a targeted array to capture exons and promoter sequences from the linked interval in 16 participants from 11 MC families, and sequenced the captured DNA using high-throughput parallel sequencing technologies. DNA capture and parallel sequencing identified heterozygous putative loss-of-function mutations in PTPN11 in 4 of the 11 families. Sanger sequence analysis of PTPN11 coding regions in a total of 17 MC families identified mutations in 10 of them (5 frameshift, 2 nonsense, and 3 splice-site mutations). Copy number analysis of sequencing reads from a second targeted capture that included the entire PTPN11 gene identified an additional family with a 15 kb deletion spanning exon 7 of PTPN11. Microdissected MC lesions from two patients with PTPN11 mutations demonstrated loss-of-heterozygosity for the wild-type allele. We next sequenced PTPN11 in DNA samples from 54 patients with the multiple enchondromatosis disorders Ollier disease or Maffucci syndrome, but found no coding sequence PTPN11 mutations. We conclude that heterozygous loss-of-function mutations in PTPN11 are a frequent cause of MC, that lesions in patients with MC appear to arise following a "second hit," that MC may be locus heterogeneous since 1 familial and 5 sporadically occurring cases lacked obvious disease-causing PTPN11 mutations, and that PTPN11 mutations are not a common cause of Ollier disease or Maffucci syndrome.


Assuntos
Encondromatose/genética , Exostose Múltipla Hereditária/genética , Proteína Tirosina Fosfatase não Receptora Tipo 11/genética , Cromossomos Humanos/genética , Variações do Número de Cópias de DNA , Encondromatose/patologia , Éxons , Deleção de Genes , Ligação Genética , Sequenciamento de Nucleotídeos em Larga Escala , Humanos , Perda de Heterozigosidade , Mutação , Linhagem , Polimorfismo de Nucleotídeo Único , Proteína Tirosina Fosfatase não Receptora Tipo 11/metabolismo , Análise de Sequência de DNA
11.
J Orthop Res ; 29(7): 984-92, 2011 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-21308757

RESUMO

Macrophages phagocytose metallic wear particles and produce mediators, which can induce cellular host response and aseptic implant loosening. Lipopolysaccharide (LPS) on the wear debris can stimulate macrophages via Toll-like receptor 4 (TLR4) and enhance the response. However, the precise functional role and interaction of TLRs and their adaptor molecules is still unclear. Rat bone marrow macrophages were stimulated with titanium particle (Ti) coated by LPS (Ti/LPS+) and LPS-free Ti (Ti/LPS-). mRNA levels of cytokines, TLRs and their adaptor molecules were measured using real time PCR. mRNA levels of TNF-α, IL-1ß, and IL-6 increased in Ti/LPS+ than Ti/LPS-. In contrast, mRNA levels of TLR4, TLR5, and TLR9 decreased in Ti/LPS+ compared to Ti/LPS-. mRNA levels of MyD88, IRAK1, IRAK4 decreased gradually, and TRAF6 underwent an initial transient increase, followed by suppression in Ti/LPS+. However, mRNA levels of TLR2 and IRAK2 increased after phagocytosis of Ti/LPS+ than Ti/LPS-. The increased expressions of proinflammatory cytokines found in Ti/LPS+ indicated that their productions cytokines could be enhanced by phagocytosis of LPS-coated particles. Subsequent down-regulation of TLR4, TLR5, TLR9, MyD88, IRAK1, and IRAK4 suggests that self-protective mechanisms to regulate excessive host responses are activated in macrophages. Increase of TLR2 and IRAK2 and a transient increase of TRAF6 in Ti/LPS+ suggest that another possible pathway to modulate TLR-mediated cellular response to prolong inflammatory response in foreign body reaction of aseptic loosening. This down- and/or up-regulation of the potential TLR-mediated responses to LPS-coated particles reflects the proactive behavior of effector cells.


Assuntos
Lipopolissacarídeos/imunologia , Macrófagos/efeitos dos fármacos , Falha de Prótese/etiologia , Titânio/imunologia , Receptores Toll-Like/imunologia , Animais , Artroplastia de Substituição/efeitos adversos , Células da Medula Óssea/citologia , Células da Medula Óssea/efeitos dos fármacos , Células da Medula Óssea/imunologia , Células Cultivadas , Quinases Associadas a Receptores de Interleucina-1/genética , Quinases Associadas a Receptores de Interleucina-1/imunologia , Quinases Associadas a Receptores de Interleucina-1/metabolismo , Lipopolissacarídeos/farmacocinética , Macrófagos/citologia , Macrófagos/imunologia , Fator 88 de Diferenciação Mieloide/genética , Fator 88 de Diferenciação Mieloide/imunologia , Fator 88 de Diferenciação Mieloide/metabolismo , Fagocitose/efeitos dos fármacos , Fagocitose/imunologia , Ratos , Ratos Wistar , Titânio/farmacocinética , Receptor 4 Toll-Like/genética , Receptor 4 Toll-Like/imunologia , Receptor 4 Toll-Like/metabolismo , Receptor 5 Toll-Like/genética , Receptor 5 Toll-Like/imunologia , Receptor 5 Toll-Like/metabolismo , Receptor Toll-Like 9/genética , Receptor Toll-Like 9/imunologia , Receptor Toll-Like 9/metabolismo , Receptores Toll-Like/genética , Receptores Toll-Like/metabolismo
12.
J Hand Surg Am ; 35(9): 1497-501, 2010 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-20807627

RESUMO

PURPOSE: To describe radial longitudinal deficiency with hypoplastic or absent thumb and cutaneous syndactyly between the most radial digits. In addition, to discuss the clinical relevance and unique treatment decisions involved in optimizing functional outcomes in these patients. METHODS: A total of 163 extremities of 122 patients with radial longitudinal deficiencies were reviewed. We reviewed radiographs and clinical images that were available, with most radial hypoplastic digit and cutaneous syndactyly to the adjacent finger. RESULTS: There were 7 hands with this type of deformity. Four cases had a hypoplastic thumb associated with cutaneous syndactyly between the thumb and index finger. Three cases had a deformity in which the thumb was absent and the hypoplastic index finger was syndactylized to the long finger. Proximal and distal radioulnar synostoses were associated with these deformities in 3 patients. CONCLUSIONS: Because the most radial digit is severely hypoplastic in this type of deformity, pollicization is usually indicated. However, the pollicization procedure must be modified due to associated syndactyly with different degrees of hypoplasia or absence of the intrinsic muscles. This type of deformity should be distinguished from hypoplastic thumb without syndactyly. TYPE OF STUDY/LEVEL OF EVIDENCE: Therapeutic IV.


Assuntos
Anormalidades Múltiplas/diagnóstico , Deformidades Congênitas da Mão/epidemiologia , Rádio (Anatomia)/anormalidades , Sindactilia/diagnóstico , Polegar/anormalidades , Anormalidades Múltiplas/epidemiologia , Anormalidades Múltiplas/cirurgia , Pré-Escolar , Estudos de Coortes , Feminino , Seguimentos , Deformidades Congênitas da Mão/diagnóstico por imagem , Deformidades Congênitas da Mão/cirurgia , Humanos , Incidência , Lactente , Masculino , Radiografia , Procedimentos de Cirurgia Plástica/métodos , Estudos Retrospectivos , Medição de Risco , Sindactilia/epidemiologia , Sindactilia/cirurgia , Sinostose/diagnóstico por imagem , Sinostose/epidemiologia , Sinostose/cirurgia , Polegar/diagnóstico por imagem , Polegar/cirurgia , Resultado do Tratamento
13.
J Electromyogr Kinesiol ; 20(6): 1178-85, 2010 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-20638861

RESUMO

Motion and force produced by electrical neuromuscular stimulation (ENS) to each of the extensor carpi radialis longus (ECRL) and brevis (ECRB), and extensor carpi ulnaris (ECU) with the prone (P), semiprone (SP), and supine forearm (S) were studied in ten normal human subjects. Abduction (AB), extension (E), adduction (AD), and flexion (F) directions were represented by, respectively, 0°, 90°, 180°, and 270°. ENS to ECRL, ECRB, and ECU produced motion in direction of, respectively, 60° (mean), 87°, and 205° with P, 66°, 83°, and 166° with SP, and 47°, 66°, and 116° with S to maximal range. Direction/strength (Nm) of force by ENS to ECRL, ECRB, and ECU were, respectively, 54°/1.75, 74°/1.78, and 184°/1.49 with P, 34°/1.65, 63°/1.66, and 152°/1.43 with SP, and 32°/1.66, 70°/1.49, and 147°/1.25 with S. ENS to ECRL exhibited force of 15-20% of maximal E (15-20%Max-E) and 19-29%Max-AB, that to ECRB 24-32%Max-E, and that to ECU 17-30%Max-AD. The force study results suggest that ECRL is an abductor and extensor and ECRB is an extensor rather than an abductor. ECU should be an adductor rather than an extensor with SP and S and an adductor with P. The data must contribute to reconstruct motor functions of paralyzed hands.


Assuntos
Estimulação Elétrica , Punho/fisiologia , Feminino , Humanos , Masculino , Músculo Esquelético/inervação , Músculo Esquelético/fisiologia , Postura
14.
J Orthop Trauma ; 24(6): 387-8, 2010 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-20502224

RESUMO

Digital tourniquets have been used worldwide in finger and toe surgery. Digital tourniquets of various types have been used, and a rolled glove technique provides a simple and quick method. We have modified a rolled glove technique to prevent iatrogenic complications associated with digital tourniquets being inadvertently left in place after surgery.


Assuntos
Dedos/cirurgia , Erros Médicos/prevenção & controle , Torniquetes , Desenho de Equipamento , Luvas Cirúrgicas , Humanos
15.
J Hand Surg Am ; 35(6): 981-5, 2010 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-20456870

RESUMO

An 11-year-old boy with congenital radial head dislocation experienced painful snapping of his left elbow upon movement. He had no previous history of trauma. A plain radiograph of his left elbow showed anterior dislocation of the radial head and flexion deformity of the hypoplastic radial neck. Arthroscopy showed that the snapping of the elbow occurred between the annular ligament and the dislocated radial head during elbow flexion and extension. After the annular ligament was released, the snapping immediately disappeared. Five years after the surgery, the patient has no pain or snapping upon elbow movement.


Assuntos
Lesões no Cotovelo , Luxações Articulares/congênito , Luxações Articulares/cirurgia , Artroscopia , Criança , Articulação do Cotovelo/diagnóstico por imagem , Articulação do Cotovelo/fisiopatologia , Antebraço/diagnóstico por imagem , Humanos , Luxações Articulares/fisiopatologia , Ligamentos Articulares/cirurgia , Imageamento por Ressonância Magnética , Masculino , Movimento/fisiologia , Osteotomia , Radiografia
16.
J Shoulder Elbow Surg ; 19(4): 502-7, 2010 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-20189835

RESUMO

HYPOTHESIS: There are some risk factors that could predispose a young baseball player to elbow injuries. MATERIALS AND METHODS: Study participants were 294 baseball players aged 9 to 12 years old. A questionnaire, physical examination, and ultrasound imaging to investigate elbow injuries were performed. Data for the groups with and without elbow injuries were analyzed statistically using multivariate logistic regression models. RESULTS: Ultrasound imaging showed that 60 participants had elbow injuries, including medial epicondylar fragmentation in 58 and osteochondritis dissecans of the capitellum in 2. The odds ratio (95% confidence interval) of the risk factors that statistical analysis showed were significant were age older than 11 years, 2.82 (1.30-6.10); height exceeding 150 cm, 2.02 (1.07-3.82); pitching, 4.50 (2.42-8.37); daily training, 1.96 (1.02-3.79); range of motion (ROM) of external rotation of the shoulder below 130 degrees , 1.98 (1.01-3.87); muscle strength (MS) of external rotation of the shoulder exceeding 80 N, 4.11 (1.47-11.55); and MS of internal rotation of the shoulder exceeding 100 N, 2.04 (1.08-3.90). DISCUSSION: Risk factors for elbow injuries are age, height, pitcher, days of training, grip strength, range of motion of external rotation of the shoulder, and muscle strength of the shoulder. CONCLUSION: As new information, our results suggest that decrease of ROM of external rotation of the shoulder and increase of MS of external and internal rotation of the shoulder predispose elbow injuries.


Assuntos
Beisebol/lesões , Lesões no Cotovelo , Traumatismos da Mão/epidemiologia , Fatores Etários , Criança , Intervalos de Confiança , Articulação do Cotovelo/fisiopatologia , Seguimentos , Traumatismos da Mão/etiologia , Traumatismos da Mão/fisiopatologia , Humanos , Incidência , Japão/epidemiologia , Razão de Chances , Prognóstico , Estudos Prospectivos , Amplitude de Movimento Articular , Fatores de Risco , Inquéritos e Questionários
17.
Congenit Anom (Kyoto) ; 50(2): 133-8, 2010 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-20214671

RESUMO

Five patients were reported in our congenital anomaly registry who had six hands in total with muscular hyperplasia, aberrant muscles, ulnar drift of the fingers in the metacarpophalangeal (MP) joints, flexion contractures of the MP joints, and enlargement of the metacarpal spaces. Thirty patients with unilateral involvement of this condition have been reported previously. We reviewed these cases and found that the condition varied in severity and that it was reported using different names. However, this condition seems different from true macrodactyly and multiple camptodactyly, including windblown hand, and seems to be an isolated entity of congenital upper limb anomaly. The authors recommend 'aberrant muscle syndrome' or 'accessory muscle syndrome' as a diagnostic name, because this seems to be the most common pathological finding in this condition.


Assuntos
Deformidades Congênitas da Mão/patologia , Doenças Musculares/congênito , Deformidades Congênitas das Extremidades Superiores/complicações , Adolescente , Pré-Escolar , Feminino , Dedos/anormalidades , Humanos , Hipertrofia/patologia , Masculino , Músculo Esquelético/anormalidades , Doenças Musculares/complicações , Síndrome
18.
Mod Rheumatol ; 20(2): 147-53, 2010 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-20012459

RESUMO

This study aimed to evaluate joint-preserving procedures by a modified Mann method for rheumatoid forefoot deformities and their functional outcomes in the mid-term. Eleven feet in seven patients underwent forefoot surgery using a modified Mann method for the big toe, combined with offset osteotomy or resection arthroplasty of the lesser toes. The mean follow-up period was 3.6 years. The mean score on the Japanese Society for Surgery of the Foot scale for rheumatoid arthritis foot and ankle joints improved from 44.0 to 72.0. The mean hallux valgus angle improved from 39.4 degrees to 20.5 degrees and the mean M1M5 angle improved from 31.1 degrees to 25.8 degrees . However, deformities involving a hallux valgus angle of more than 25.0 degrees recurred in three feet at the latest follow-up, although the patients did not complain of any symptoms from the recurrence. Improvement in the Sharp score for joint space narrowing was observed in the big toe, indicating better congruity of the metatarsophalangeal joint. For restraint of rheumatoid forefoot deformities, a modified Mann method, combined with offset osteotomy or resection arthroplasty, was satisfactory for not only improving the foot function, but also preserving the metatarsophalangeal joint mobility.


Assuntos
Artrite Reumatoide/complicações , Hallux Valgus/cirurgia , Articulação Metatarsofalângica/cirurgia , Procedimentos Ortopédicos/métodos , Feminino , Hallux Valgus/etiologia , Humanos , Pessoa de Meia-Idade , Qualidade de Vida , Recuperação de Função Fisiológica
19.
J Orthop Sci ; 14(6): 704-10, 2009 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-19997816

RESUMO

BACKGROUND: Periprosthetic infection is one of the serious complications after total hip arthroplasty (THA). This study analyzed the perioperative and postoperative status of patients who underwent antibiotics-impregnated cement spacer technique in the first step of the two-stage revision. METHODS: Ten joints of the nine patients (mean age, 65 years; seven women, two men) received two-stage revision as a result of infection that appeared after primary THAs in seven joints, aseptic revision in one, and recurrent type in two. An antibiotics-impregnated cement spacer made by a mold system was applied in the femoral side of all joints. An acetabular spacer was made by hand using a cup gauge in eight joints with extensive tissue loss. RESULTS: The change of leg length after the first stage was -2.2 mm, and range of hip flexion was 72 degrees on average, respectively. Patients could walk with crutches after the first stage, except one patient with simultaneous infections of both hips and one with fracture of the cement spacer. One fracture of femoral cement spacer, and one dislocation of femoral spacer accompanied by fracture of acetabular cement spacer and curable recurrent infection, were found. In all cases of the second-stage procedure, the acetabular side was reconstructed with allogeneic bone graft with cross plate and that of the femur was by impaction bone grafting method. In the latest follow-up, reconstructed implants were stable. Seven patients could walk without any supportive devices and two could walk with the support of a T-cane. CONCLUSIONS: An antibiotics-impregnated cement spacer in the first step of the two-stage revision was effective not only to compensate tissue loss after removal of the implants and to minimize discrepancy of leg length, but also to contribute to improvement of perioperative and postoperative daily activities of the patient's life as well as treatment of the infection.


Assuntos
Antibacterianos/administração & dosagem , Artroplastia de Quadril/efeitos adversos , Cimentos Ósseos/uso terapêutico , Desenho de Prótese , Infecções Relacionadas à Prótese/tratamento farmacológico , Idoso , Idoso de 80 Anos ou mais , Implantes de Medicamento , Feminino , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , Infecções Relacionadas à Prótese/cirurgia , Recuperação de Função Fisiológica , Reoperação/métodos , Reoperação/reabilitação
20.
Spine (Phila Pa 1976) ; 34(25): E911-7, 2009 Dec 01.
Artigo em Inglês | MEDLINE | ID: mdl-19940720

RESUMO

STUDY DESIGN: A study of the histologic changes of the intervertebral discs (IVDs) in biglycan (Bgn)-deficient mice. OBJECTIVE: In this study, we investigate whether the absence of Bgn accelerates the degenerative process in mouse intervertebral disc (IVD). SUMMARY OF BACKGROUND DATA: Proteoglycans and collagen fibrils are major components in the extracellular matrix (ECM) composition of IVD. The ECM of IVD contains several members of the small leucine repeat proteoglycans (SLRPs) family. Bgn is one member of SLRPs family, and showed a unique expression with age and degeneration in the human IVD. To date, there have been no in vivo studies to see whether SLRPs have a role in maintaining the structural integrity of IVD. To explore the functions of Bgn in the IVD, we examined discs in Bgn-deficient mice. METHODS: A total of 30 spine specimens were harvested from wild-type (WT) and Bgn-deficient mice. Five specimens for each genotype at 4-, 6-, and 9-month old were examined in the experiments. Histologic analysis of the IVD was performed. Histologic gradings were performed separately on nucleus pulposus, anulus fibrosus, and endplate according to the classification system proposed by Boos et al. RESULTS: We found that Bgn-deficient mice developed an early onset of disc degeneration compared with WT mice. The degenerative scores of Bgn-deficient mice were significantly higher than those of WT mice at 4- and 9-month-old. High scores for nucleus pulposus and anulus fibrosus in Bgn-deficient mice significantly affected the difference in total degenerative scores at 9 months of age. CONCLUSION: Bgn deficiency significantly accelerated disc degeneration.


Assuntos
Progressão da Doença , Proteínas da Matriz Extracelular/deficiência , Degeneração do Disco Intervertebral/metabolismo , Disco Intervertebral/metabolismo , Proteoglicanas/deficiência , Envelhecimento/metabolismo , Envelhecimento/patologia , Animais , Biglicano , Modelos Animais de Doenças , Proteínas da Matriz Extracelular/genética , Proteínas da Matriz Extracelular/metabolismo , Disco Intervertebral/patologia , Degeneração do Disco Intervertebral/patologia , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Knockout , Proteoglicanas/genética , Proteoglicanas/metabolismo
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...