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1.
J Pediatr Orthop ; 40(8): 401-407, 2020 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-32379247

RESUMO

INTRODUCTION: Sprengel deformity (SD) is the most common congenital anomaly of the shoulder. Surgery is required for moderate and severe forms. The modified Woodward procedure is the most widely used procedure for the surgical treatment. METHODS: SD patients who applied to our institution between 2005 and 2018 were retrospectively reviewed. A modification of the Cavendish classification was used for preoperative and postoperative evaluations. RESULTS: Eighteen shoulders of 17 (mean age: 8.5 y, range: 2 to 18 y, 5 males and 12 females) patients were included. The right, left, and bilateral shoulders were affected in 9, 7, and 1 cases, respectively. The mean follow-up time was 62.9 months (12 to 161 mo). Preoperatively, 3 shoulders were type 2, 12 shoulders were type 3, and 3 shoulders were type 4 according to the Cavendish classification and 2 shoulders were type 0, 6 shoulders were type 1, and 10 shoulders were type 2 postoperatively. CONCLUSIONS: Periscapular congenital malformations play a significant role in range of motion limitation. The modified Woodward procedure is a viable alternative in the surgical treatment of SD and the proposed modification of Cavendish classification (grade 0) is functional.


Assuntos
Anormalidades Congênitas , Músculo Esquelético , Procedimentos Ortopédicos/métodos , Escápula/anormalidades , Articulação do Ombro/anormalidades , Articulação do Ombro/fisiopatologia , Ombro , Criança , Anormalidades Congênitas/classificação , Anormalidades Congênitas/diagnóstico , Anormalidades Congênitas/cirurgia , Feminino , Humanos , Masculino , Músculo Esquelético/anormalidades , Músculo Esquelético/cirurgia , Amplitude de Movimento Articular , Estudos Retrospectivos , Escápula/cirurgia , Ombro/anormalidades , Ombro/cirurgia , Articulação do Ombro/cirurgia , Resultado do Tratamento
2.
Occup Environ Med ; 76(6): 363-369, 2019 06.
Artigo em Inglês | MEDLINE | ID: mdl-30928906

RESUMO

OBJECTIVE: To examine the impact of a disabling non-traumatic shoulder lesion on work participation and working life expectancy. METHODS: From a 70% random sample of the Finnish population, we selected 30-59-year-old wage earners with prolonged sickness absence due to a shoulder lesion (n=7644). We followed the persons from 2006 to 2014 and calculated the proportion of time a person spent in different work participation statuses. The associations of potential determinants with a preterm exit from paid employment were tested using Cox regression. Years expected to be spent in different work participation statuses were estimated applying the Sullivan method for healthy life expectancy. RESULTS: During 9 years of follow-up time spent at work was reduced from 77.7% to 46.7%, and 15.8% of the persons were granted disability retirement, mostly due to shoulder and other musculoskeletal diseases. Compared with the general population persons with a disabling shoulder disease are expected to lose from 1.8 to 8.1 years of working life, depending on their age. Age, gender, education, duration of initial sickness absence due to the shoulder lesion, not being able to return to work sustainably and participation in vocational rehabilitation predicted preterm exit from work. Heavy lifting increased the risk of preterm exit marginally. CONCLUSIONS: Working life expectancy is markedly reduced in persons with a disabling shoulder lesion, mainly because of disability retirement due to musculoskeletal problems. Clinicians should consider interventions targeted at improving musculoskeletal functioning and necessary work modifications before shoulder problems become chronic or the persons develop disabling comorbid musculoskeletal conditions.


Assuntos
Emprego/estatística & dados numéricos , Expectativa de Vida/tendências , Ombro/fisiopatologia , Absenteísmo , Adulto , Emprego/normas , Feminino , Finlândia/epidemiologia , Humanos , Estimativa de Kaplan-Meier , Masculino , Pessoa de Meia-Idade , Ombro/anormalidades , Avaliação da Capacidade de Trabalho
3.
Hum Mol Genet ; 22(3): 568-77, 2013 Feb 01.
Artigo em Inglês | MEDLINE | ID: mdl-23108159

RESUMO

Facioscapulohumeral muscular dystrophy (FSHD) is a common form of muscular dystrophy characterized by an asymmetric progressive weakness and wasting of the facial, shoulder and upper arm muscles, frequently accompanied by hearing loss and retinal vasculopathy. FSHD is an autosomal dominant disease linked to chromosome 4q35, but the causative gene remains controversial. DUX4 is a leading candidate gene as causative of FSHD. However, DUX4 expression is extremely low in FSHD muscle, and there is no DUX4 animal model that mirrors the pathology in human FSHD. Here, we show that the misexpression of very low levels of human DUX4 in zebrafish development recapitulates the phenotypes seen in human FSHD patients. Microinjection of small amounts of human full-length DUX4 (DUX4-fl) mRNA into fertilized zebrafish eggs caused asymmetric abnormalities such as less pigmentation of the eyes, altered morphology of ears, developmental abnormality of fin muscle, disorganization of facial musculature and/or degeneration of trunk muscle later in development. Moreover, DUX4-fl expression caused aberrant localization of myogenic cells marked with α-actin promoter-driven enhanced green fluorescent protein outside somite boundary, especially in head region. These abnormalities were rescued by coinjection of the short form of DUX4 (DUX4-s). Our results suggest that the misexpression of DUX4-fl, even at extremely low level, can recapitulate the phenotype observed in FSHD patients in a vertebrate model. These results strongly support the current hypothesis for a role of DUX4 in FSHD pathogenesis. We also propose that DUX4 expression during development is important for the pathogenesis of FSHD.


Assuntos
Proteínas de Homeodomínio/metabolismo , Distrofia Muscular Facioescapuloumeral/genética , Peixe-Zebra/genética , Actinas/genética , Actinas/metabolismo , Animais , Modelos Animais de Doenças , Regulação da Expressão Gênica no Desenvolvimento , Proteínas de Homeodomínio/genética , Humanos , Microscopia Eletrônica de Transmissão , Músculo Esquelético/anormalidades , Distrofia Muscular Facioescapuloumeral/patologia , Óvulo/crescimento & desenvolvimento , Fenótipo , Reação em Cadeia da Polimerase , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Ombro/anormalidades
4.
AJR Am J Roentgenol ; 203(3): 508-15, 2014 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-25148153

RESUMO

OBJECTIVE: The purpose of this article is to review frequently encountered pitfalls as they pertain to the biceps tendon, bursae and cysts around the shoulder, incidental findings, postsurgical findings, and frequently encountered imaging artifacts. CONCLUSION: Imaging pitfalls in and around the shoulder are not limited to normal anatomy and anatomic variants. Radiologists must be cognizant of the vast variability of structures in the shoulder and of the incidental and postsurgical findings and artifacts affecting them.


Assuntos
Artefatos , Cistos Ósseos/patologia , Bolsa Sinovial/patologia , Imageamento por Ressonância Magnética/métodos , Ombro/anormalidades , Ombro/patologia , Tendões/patologia , Bolsa Sinovial/anormalidades , Humanos , Aumento da Imagem/métodos , Achados Incidentais , Cuidados Pós-Operatórios , Tendões/anormalidades
5.
Aesthetic Plast Surg ; 38(2): 350-3, 2014 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-24643896

RESUMO

UNLABELLED: Brassiere strap grooves develop mostly on the shoulders of women with hypertrophied breasts. Varying degrees of the deformity are observed in such cases. To date, there is no universally accepted definition and classification for brassiere strap groove deformity. In this study, we aimed to define and classify the deformity in order to inform consultants and future surgeons. LEVEL OF EVIDENCE V: This journal requires that authors assign a level of evidence to each article. For a full description of these Evidence-Based Medicine ratings, please refer to the Table of Contents or the online Instructions to Authors www.springer.com/00266 .


Assuntos
Mama/anormalidades , Vestuário/efeitos adversos , Hipertrofia/complicações , Ombro/anormalidades , Anormalidades Congênitas/classificação , Medicina Baseada em Evidências , Feminino , Humanos
6.
Am J Med Genet A ; 161A(12): 3161-5, 2013 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-24039145

RESUMO

Cousin syndrome, also called pelviscapular dysplasia (OMIM 260660), is characterized by short stature, craniofacial dysmorphism, and multiple skeletal anomalies. Following its description in two sibs in 1982, no new cases have been observed until the observation of two unrelated cases in 2008 who were homozygous for frameshift mutations in TBX15. We investigated an adult individual with short stature, a complex craniofacial dysmorphism, malformed and rotated ears, short neck, elbow contractures, hypoacusis, and hypoplasia of scapula and pelvis on radiographs. We identified homozygosity for a novel nonsense mutation (c.841C>T) in TBX15 predicted to cause a premature stop (p.Arg281*) with truncation of the protein. This observation confirms that Cousin syndrome is a consistent and clinically recognizable phenotype caused by loss of function of TBX15.


Assuntos
Anormalidades Múltiplas/genética , Disostoses/congênito , Pelve/anormalidades , Ombro/anormalidades , Proteínas com Domínio T/genética , Anormalidades Múltiplas/fisiopatologia , Adulto , Códon sem Sentido , Nanismo , Disostoses/complicações , Disostoses/diagnóstico por imagem , Disostoses/genética , Disostoses/fisiopatologia , Feminino , Homozigoto , Humanos , Mutação , Linhagem , Pelve/diagnóstico por imagem , Pelve/fisiopatologia , Fenótipo , Radiografia , Ombro/diagnóstico por imagem , Ombro/fisiopatologia
7.
Surg Radiol Anat ; 34(7): 655-9, 2012 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-22314797

RESUMO

METHOD: During the routine dissection of a male cadaver for teaching undergraduate medical students, a variation was seen in the morphology of coracobrachialis muscle. RESULTS: The presence of an anomalous head of coracobrachialis muscle which had muscular origin from an abnormal site on coracoid process and thin tendinous insertion at the junction of brachialis and triceps muscle in common with insertion of coracobrachialis muscle to the medial surface of the middle of the shaft of the humerus. CONCLUSION: Coracobrachialis muscle can have variant origin related to its embryogenesis with its clinical and surgical significance.


Assuntos
Braço/anormalidades , Músculo Esquelético/anormalidades , Cadáver , Humanos , Masculino , Nervo Musculocutâneo/anormalidades , Ombro/anormalidades
8.
Muscle Nerve ; 41(2): 262-4, 2010 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-20082410

RESUMO

Sprengel's deformity is the most common congenital deformity of the shoulder. A known complication of correcting this deformity is brachial plexus palsy. In this study we used somatosensory evoked potential (SSEP) monitoring during correction of a Sprengel's deformity and identified an early iatrogenic brachial plexus injury. The operation was modified, and permanent nerve injury was avoided. We recommend that SSEP monitoring be considered in procedures to correct Sprengel's deformity.


Assuntos
Plexo Braquial/fisiologia , Potenciais Somatossensoriais Evocados/fisiologia , Monitorização Intraoperatória/métodos , Osteotomia/métodos , Ombro/anormalidades , Ombro/cirurgia , Plexo Braquial/lesões , Pré-Escolar , Humanos , Masculino , Osteotomia/efeitos adversos , Resultado do Tratamento
9.
J Rehabil Med ; 52(6): jrm00068, 2020 Jun 11.
Artigo em Inglês | MEDLINE | ID: mdl-32451555

RESUMO

Botulinum toxins, such as abobotulinumtoxinA, are used to treat spasticity (muscle overactivity) in arm muscles. Spasticity in shoulder muscles occurs in many patients following a stroke. Shoulder spasticity can be painful and limit limb movement. This paper compares the results from patients who did and those who did not receive abobotulinumtoxinA injections in shoulder muscles (among other arm muscles) in 2 studies. In both studies, the results showed that more patients receiving treatment in shoulder muscles chose pain as a key goal for treatment and had reduced pain following treatment compared with patients not treated in the shoulder. In addition, patients receiving shoulder injections showed further improvement in arm movement compared with those not receiving shoulder injections. Overall, these results suggest that abobotulinumtoxinA treatment in shoulder muscles may improve outcomes for patients with arm spasticity involving the shoulder.


Assuntos
Inibidores da Liberação da Acetilcolina/uso terapêutico , Toxinas Botulínicas Tipo A/uso terapêutico , Espasticidade Muscular/tratamento farmacológico , Fármacos Neuromusculares/uso terapêutico , Ombro/anormalidades , Inibidores da Liberação da Acetilcolina/farmacologia , Adulto , Toxinas Botulínicas Tipo A/farmacologia , Feminino , Humanos , Injeções , Masculino , Pessoa de Meia-Idade , Fármacos Neuromusculares/farmacologia , Resultado do Tratamento
10.
Medicine (Baltimore) ; 99(46): e23299, 2020 Nov 13.
Artigo em Inglês | MEDLINE | ID: mdl-33181720

RESUMO

Calcific tendinitis (CT) of the shoulder is a painful disorder usually identified in individuals aged 40 and 60 years. The estimated global prevalence of CT is 2.7% to 36%. We examined the association of hyperlipidemia and sex with CT of the shoulder using Taiwan Biobank (TWB) and the National Health Insurance Research Database (NHIRD).Data were available for 9903 TWB participants who were recruited between 2008 and 2015. We used multiple logistic regression analysis to estimate the odds ratios (OR) and 95% confidence intervals (CI) for CT of the shoulder.Overall, 1564 women, and 1491 men were identified with hyperlipidemia. Women, compared to men, had higher odds of CT of the shoulder (OR, 1.53; 95% CI, 1.08-2.16). Hyperlipidemia, compared to no hyperlipidemia, was associated with an increased risk of CT (OR, 1.40; 95% CI, 1.02-1.93). The test for interaction was significant for sex and hyperlipidemia (P = .006). After stratification, the odds ratio for CT was 1.95 (95% CI, 1.30-2.92) in women and 0.82 (95% CI, 0.48-1.39) in men, respectively. Compared to men with no hyperlipidemia, the odds ratio was 0.86 (95% CI, 0.53-1.38) for men with hyperlipidemia and 2.00 (95% CI, 1.29-3.10) for women with hyperlipidemia.Importantly, our findings indicated that the risk for CT of the shoulder was higher among Taiwanese women with hyperlipidemia. However, CT risk among their male counterparts with hyperlipidemia was not significant.


Assuntos
Calcinose/etiologia , Hiperlipidemias/complicações , Artropatias/etiologia , Fatores Sexuais , Ombro/anormalidades , Tendinopatia/etiologia , Doenças Vasculares/etiologia , Adulto , Idoso , Calcinose/epidemiologia , Calcinose/fisiopatologia , Feminino , Humanos , Hiperlipidemias/epidemiologia , Hiperlipidemias/fisiopatologia , Artropatias/epidemiologia , Artropatias/fisiopatologia , Modelos Logísticos , Masculino , Pessoa de Meia-Idade , Razão de Chances , Prevalência , Ombro/fisiopatologia , Taiwan/epidemiologia , Tendinopatia/epidemiologia , Tendinopatia/fisiopatologia , Doenças Vasculares/epidemiologia , Doenças Vasculares/fisiopatologia
11.
Mil Med ; 174(5): 548-50, 2009 May.
Artigo em Inglês | MEDLINE | ID: mdl-20731291

RESUMO

Congenital absence of the long head of the biceps (LHB) tendon is a rare condition. The literature describes unilateral cases, associations with other congenital developmental anomalies, and associations with shoulder instability and SLAP tears. We present a case with bilateral absent LHB tendons and subacromial impingement pathology in a patient without a history of trauma or other congenital developmental abnormalities.


Assuntos
Síndrome de Colisão do Ombro/patologia , Ombro/anormalidades , Tendões/anormalidades , Adulto , Diagnóstico Diferencial , Humanos , Masculino , Síndrome de Colisão do Ombro/diagnóstico , Síndrome de Colisão do Ombro/cirurgia
12.
J Zoo Wildl Med ; 40(3): 453-7, 2009 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-19746859

RESUMO

A radiographic study documented shoulder dysplasia (n = 43), with varying degrees of malformation of the supraglenoid and infraglenoid tubercles and the coracoid process, shallowing or loss of the glenoid cavity, flattening or loss of the humeral head, malformation of the greater and lesser tubercles, loss of the intertubercle groove, and humeral diaphyseal abnormalities, in northern koalas (Phascolarctos cinereus) in the San Diego Zoo (San Diego, California, USA) colony. Retrospectively, historic radiographs (n = 38) were examined where available. Prospectively, three standard views (lateral extended arm, ventrodorsal cranially positioned arms, and ventrodorsal caudally positioned arms) were imaged (n = 25). In all radiographs, shoulders were graded as normal, or mildly, moderately, or severely dysplastic. Although affected koalas typically do not exhibit clinical signs, degenerative joint disease may develop and clinical signs treated with nonsteroidal anti-inflammatory drugs. Where shoulder and hip radiographs were both available (n = 60), 92% of individuals had correlation between the degree of shoulder and hip dysplasia.


Assuntos
Doenças do Desenvolvimento Ósseo/veterinária , Instabilidade Articular/veterinária , Phascolarctidae , Ombro/anormalidades , Animais , Animais de Zoológico , Doenças do Desenvolvimento Ósseo/diagnóstico por imagem , Doenças do Desenvolvimento Ósseo/patologia , California , Feminino , Masculino , Radiografia , Estudos Retrospectivos , Índice de Gravidade de Doença , Ombro/diagnóstico por imagem , Articulação do Ombro/diagnóstico por imagem , Articulação do Ombro/patologia
13.
BMJ Open ; 9(9): e032901, 2019 09 30.
Artigo em Inglês | MEDLINE | ID: mdl-31575585

RESUMO

INTRODUCTION: In children with brachial plexus birth injury (BPBI), denervation of the shoulder muscles leads to bony deformity in the first months of life, reducing active and passive range of motion (ROM) and causing activity limitation. The aim of this multicentre randomised controlled trial is to evaluate the effectiveness of botulinum toxin injections (BTI) in the shoulder internal rotator muscles of 12-month-old babies in limiting the progression of posterior subluxation of the glenohumeral joint, compared with a sham procedure mimicking BTI. The secondary aims are to evaluate the effectiveness of BTI in (1) limiting the progression of glenoid retroversion and three-dimensional (3D) deformity and (2) improving shoulder ROM and upper limb function, as well as to confirm the tolerance of BTI. METHODS AND ANALYSIS: Sixty-two babies with unilateral BPBI and a risk of posterior humeral head subluxation will be included. Only those with at least 7% posterior subluxation of the humeral head compared with the contralateral shoulder on the MRI will be randomised to one of two groups: 'BTI' and 'Sham'. The BTI group will receive BOTOX injections at the age of 12 months in the internal shoulder rotator muscles (8 UI/kg). The sham group will undergo a sham BTI procedure. Both groups will undergo repeated shoulder MRI at 18 months of age to quantify changes in the percentage of posterior migration of the humeral head (primary outcome), glenoid version and 3D bone deformity. Clinical evaluations (passive shoulder ROM, active movement scale) will be carried out at baseline and 15 and 18 months of age. The mini-assisting hand assessment will be rated between 10 and 11 months and at 18 months of age. Adverse events will be recorded at least monthly for each child. ETHICS AND DISSEMINATION: Full ethical approval for this study has been obtained. The findings will be disseminated in peer-reviewed publications. TRIAL REGISTRATION NUMBER: EudraCT: 2015-001402-34 in European Clinical Trial database; NCT03198702 in Clinical Trial database; Pre-results.


Assuntos
Traumatismos do Nascimento/complicações , Toxinas Botulínicas/uso terapêutico , Plexo Braquial/lesões , Ombro/anormalidades , Toxinas Botulínicas/administração & dosagem , Toxinas Botulínicas/efeitos adversos , Plexo Braquial/diagnóstico por imagem , Método Duplo-Cego , Estudos de Equivalência como Asunto , Feminino , Humanos , Lactente , Injeções Intramusculares , Imageamento por Ressonância Magnética , Masculino , Estudos Multicêntricos como Assunto , Ensaios Clínicos Controlados Aleatórios como Assunto , Ombro/diagnóstico por imagem , Resultado do Tratamento
14.
Orthopedics ; 31(3): 226, 2008 03.
Artigo em Inglês | MEDLINE | ID: mdl-19292248

RESUMO

UNLABELLED: This prospective study of 367 consecutive shoulder arthroscopies assessed variants of the anterosuperior glenoid labrum and associated shoulder pathology. Thirty-three shoulders were excluded because of prior surgery, septic arthritis, or adhesive capsulitis. Anterosuperior glenoid variants were classified as: type I, cordlike middle glenohumeral ligament without sublabral foramen; type II, sublabral foramen without a cordlike middle glenohumeral ligament; type III, sublabral foramen with a cordlike middle glenohumeral ligament; and type IV, absent anterosuperior labrum with the anterior aspect of the superior labrum continuous with a cordlike middle glenohumeral ligament. The presence of these variants was correlated with the incidence of shoulder pathology found on arthroscopic inspection. Of 334 shoulders, 118 (35.3%) had variants of the anterosuperior glenoid labrum. Of these, 32 (27.1%) were type I, 27 (22.9%) were type II, 34 (28.8%) were type III, and 25 (21.2%) were type IV. The incidence of advanced superior labrum anterior-posterior lesions in the 86 shoulders displaying a type II, III, or IV variant was significantly higher than in shoulders with no anterosuperior variant (48.8% versus 23.6%, P<.001). Other pathologic findings were not significantly increased in shoulders with variants compared to those without. LEVEL OF EVIDENCE: Level 1.


Assuntos
Ligamentos/anormalidades , Ligamentos/patologia , Articulação do Ombro/anormalidades , Articulação do Ombro/patologia , Ombro/anormalidades , Ombro/patologia , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Reprodutibilidade dos Testes , Sensibilidade e Especificidade , Adulto Jovem
15.
Mil Med ; 183(1-2): e134-e137, 2018 01 01.
Artigo em Inglês | MEDLINE | ID: mdl-29401341

RESUMO

Introduction: Stabilizing surgery of the shoulder with a coracoid graft according to Latarjet is a recognized surgical treatment for anterior instability of the shoulder. This pathology frequently affects soldiers. Postoperatively, the potential risk of recurrence or of secondary shoulder arthritis can limit the practitioner in their ability assessment. The aim of this study is to analyze the long-term outcomes of this surgery in a military population, in order to assess the possible implications for French soldiers' medical ability. Material and Methods: Twenty soldiers operated on the shoulder by Latarjet procedure by the same surgeon were retrospectively reviewed after more than 15 yr. All of them did regular physical activity for leisure or competitions. None had preoperative osteoarthritis injuries. The number of dislocation recurrences, the functional score, and the rate of radiographic osteoarthritis were assessed. Results: After more than 16.3 yr (extremes: 15-24 yr), none displayed a dislocation recurrence. The average Rowe's score was 91.8 ± 9.9. The average subjective shoulder value was 89.2 ± 9.7. All patients had resumed sport. Three of them developed level 1 or 2 radiological signs of osteoarthritis according to Samilson. No level 3 or 4 osteoarthritis was found. Among all the patients, 14 still did regular physical activity. Discussion: In view of our results and of those from the literature, the results of treatment for anterior shoulder instability with the Latarjet procedure are good, even very good in the long term. These data must be considered to favor this procedure for soldiers with shoulder instability and from a medico-administrative viewpoint for military patients in order to pursue their careers without any job restrictions.


Assuntos
Artroplastia/normas , Instabilidade Articular/cirurgia , Resultado do Tratamento , Adulto , Artroplastia/instrumentação , Artroplastia/métodos , Feminino , Seguimentos , Humanos , Instabilidade Articular/epidemiologia , Masculino , Pessoa de Meia-Idade , Militares/estatística & dados numéricos , Projetos de Pesquisa , Estudos Retrospectivos , Ombro/anormalidades , Ombro/cirurgia
16.
Rev. Bras. Ortop. (Online) ; 58(4): 625-631, July-Aug. 2023. tab, graf
Artigo em Inglês | LILACS | ID: biblio-1521790

RESUMO

Abstract Objective The present study aims to analyze the use of shoulder imbalance as a parameter for scoliosis screening as well as its relationship with other parameters of physical examination. Methods This study assesses a smartphone application that analyzes several parameters of the physical examination in adolescent idiopathic scoliosis. Medical and non-medical examiners applied the screening tool in students in a public school and in a private sports club. After data collection, interobserver correlation was done to verify shoulder imbalance and to compare shoulder imbalance with Adam's bending test and with trunk rotation. Results Eighty-nine participants were examined, 18 of whom were women and 71 of whom were men. Two subjects were excluded from the analysis. The mean age of subjects from the public school was 11.30 years and, for those from the sports club, it was 11.92 years. The examiners had poor-to-slight interobserver concordance on shoulder asymmetry in the anterior and posterior view. No significant statistical correlation was found between shoulder asymmetry and positive Adam's forward bending test. Conclusion Our preliminary study shows that the shoulder asymmetry has a poor correlation with the Adam's forward bending test and measuring trunk rotation using a scoliometer. Therefore, the use of shoulder imbalance might not be useful for idiopathic scoliosis screening. Level of Evidence III; Diagnostic Study


Resumo Objetivo O objetivo deste estudo é analisar o uso da assimetria de ombros como parâmetro para a triagem de escoliose e sua relação a outros parâmetros do exame físico. Métodos Este estudo avalia um aplicativo para smartphone que analisa diversos parâmetros do exame físico de adolescentes com escoliose idiopática. Examinadores médicos e não médicos utilizaram o instrumento de triagem em alunos de uma escola pública e de um clube esportivo privado. Após a coleta de dados, a correlação interobservador foi determinada para verificar a assimetria de ombros e compará-la ao teste de inclinação de Adam e à medição da rotação do tronco. Resultados Oitenta e nove participantes foram examinados, sendo 18 do sexo feminino e 71 do sexo masculino. Dois indivíduos foram excluídos da análise. A média de idade dos participantes da escola pública foi de 11,30 anos e do clube esportivo, 11,92 anos. Os examinadores apresentaram concordância interobservador baixa a branda quanto à assimetria de ombros em incidência anterior e posterior. Não houve correlação estatística significativa entre a assimetria de ombros e o resultado positivo no teste de inclinação do tronco de Adam. Conclusão Nosso estudo preliminar mostra que a assimetria de ombros tem baixa correlação com o teste de inclinação de Adam e assim como com a medição de rotação do tronco com escoliômetro. Portanto, o uso da assimetria de ombros pode não ser útil na triagem da escoliose idiopática. Nível de Evidência III; Estudo Diagnóstico


Assuntos
Humanos , Masculino , Feminino , Criança , Adolescente , Escoliose , Ombro/anormalidades , Anormalidades Congênitas , Programas de Rastreamento , Incidência
17.
Clin Spine Surg ; 30(4): E351-E357, 2017 05.
Artigo em Inglês | MEDLINE | ID: mdl-28437337

RESUMO

STUDY DESIGN: Prospective observational study. OBJECTIVE: To study axial plane deformation of the shoulder in adolescent idiopathic scoliosis (AIS) and try to correlate it with curve type and surgical correction. SUMMARY OF BACKGROUND DATA: It is established that AIS is a 3-dimensional deformity. The rib hump is the most common manifestation of axial plane deformations; the least common manifestation seems to be upper trunk and shoulder rotation, which has been hitherto undescribed. METHODS: Fourteen consecutive, operated cases of AIS were analyzed prospectively. Preoperative and postoperative x-rays of the spine and clinical photographs were studied. Clinical photographs (top view) were taken with patients in the sitting position, to show shoulder level in relation to the axis of the head and pelvis. Chest computed tomography scans were also studied to determine the direction of apical vertebra and trunk torsion. RESULTS: All 14 patients in this series had their right shoulders anteriorly rotated preoperatively (anticlockwise). The direction of rotation seemed unrelated to the curve type and shoulder elevation, although most had rib humps on the right. This shoulder rotation was corrected postoperatively by routine maneuvers done for scoliosis correction. Minor residual rotation was seen in 6 patients who also had minimal persisting rib hump. In 1 case the axial plane rotation worsened, although the shoulder level and trunk symmetry improved significantly. The apical vertebral rotation on computed tomography had little bearing on the direction of shoulder rotation. CONCLUSIONS: Axial plane rotation of the shoulder is a hitherto un-described dimension of AIS deformity complex. Much of it corrects spontaneously with correction of the thoracic spinal deformity.


Assuntos
Escoliose/patologia , Ombro/anormalidades , Adolescente , Criança , Feminino , Humanos , Masculino , Tomografia Computadorizada por Raios X , Adulto Jovem
18.
Am J Sports Med ; 45(4): 775-781, 2017 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-28298065

RESUMO

BACKGROUND: Diagnosing superior labrum anterior and posterior (SLAP) lesions through physical examination remains challenging. The dynamic labral shear test (DLST) has been shown to have likelihood ratios (LRs) of 31.6 and 1.1 for diagnosing SLAP lesions. PURPOSE: To determine the clinical utility of the DLST for diagnosing SLAP lesions. STUDY DESIGN: Cohort study (diagnosis); Level of evidence, 2. METHODS: This prospective, consecutive case series included 774 patients who underwent diagnostic arthroscopy and a preoperative DLST between 2007 and 2013. Patients were divided into 3 groups: 610 control patients with no SLAP lesion but with other abnormalities, 9 patients with isolated SLAP lesion (ISL), and 155 patients with concomitant SLAP lesion (CSL), who had a SLAP lesion and another shoulder abnormality. We determined sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), odds ratio (OR), and diagnostic accuracy (DA) of the DLST with and without other tests. RESULTS: The DLST was positive for 242 of 610 controls (40%), 7 of 9 patients (78%) in the ISL group, and 88 of 155 patients (57%) in the CSL group. In the ISL group, the DLST had a sensitivity of 78%, specificity of 51%, PPV of 2%, NPV of 100%, OR of 3.58, and DA of 51%. In comparison, the ORs were 1.09 for the active compression test, 1.30 for the lift-off test, and 1.53 for the relocation test, which were not significantly different from each other. For diagnosing a SLAP lesion existing in a joint with other associated injury, the DLST had a sensitivity of 57%, specificity of 52%, PPV of 23%, NPV of 83%, OR of 1.4, and DA of 53%. Combining all 4 tests did not improve the OR for detecting ISLs or CSLs. CONCLUSION: The DLST is sensitive but not specific for detecting ISLs. With an OR of 3.58, the DLST is useful for diagnosing ISLs. However, in patients who have CSLs, the DLST is not as useful for diagnosing SLAP lesions.


Assuntos
Exame Físico/métodos , Lesões do Ombro/diagnóstico , Articulação do Ombro/fisiopatologia , Adulto , Artroscopia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Razão de Chances , Valor Preditivo dos Testes , Estudos Prospectivos , Amplitude de Movimento Articular , Sensibilidade e Especificidade , Ombro/anormalidades , Lesões do Ombro/fisiopatologia , Adulto Jovem
19.
J Pediatr Orthop B ; 26(3): 266-269, 2017 May.
Artigo em Inglês | MEDLINE | ID: mdl-28079744

RESUMO

Sprengel deformity (SD) results in a limitation of movement of the shoulder girdle and produces an esthetic defect. Our aim is to assess the feasibility and advantages of a minimally invasive endoscopic approach for SD correction. A 4-year-old boy with a Cavendish grade III right SD. The patient underwent an endoscopic Woodward procedure with access through two small incisions at the level of the upper and lower angles of the scapula. Near-symmetrical shoulder elevation was achieved, with an excellent cosmetic result. The endoscopic Woodward procedure is a feasible, effective, and minimally invasive technique in the treatment of SD. LEVEL OF EVIDENCE: V.


Assuntos
Anormalidades Congênitas/diagnóstico por imagem , Anormalidades Congênitas/terapia , Endoscopia/métodos , Procedimentos Ortopédicos/métodos , Escápula/anormalidades , Articulação do Ombro/anormalidades , Pré-Escolar , Humanos , Masculino , Escápula/diagnóstico por imagem , Ombro/anormalidades , Articulação do Ombro/diagnóstico por imagem
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