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1.
J Arthroplasty ; 38(11): 2220-2225, 2023 11.
Artigo em Inglês | MEDLINE | ID: mdl-37172792

RESUMO

BACKGROUND: Racial and ethnic disparities have been suggested to be associated with poor outcomes after total knee arthroplasty (TKA). While socioeconomic disadvantage has been studied, analyses of race as the primary variable are lacking. Therefore, we examined the potential differences between Black and White TKA recipients. Specifically, we assessed 30-day and 90-day, as well as 1 year: (1) emergency department visits and readmissions; (2) total complications; (3) as well as risk factors for total complications. METHODS: A consecutive series of 1,641 primary TKAs from January 2015 to December 2021 at a tertiary health care system were reviewed. Patients were stratified according to race, Black (n = 1,003) and White (n = 638). Outcomes of interest were analyzed using bivariate Chi-square and multivariate regressions. Demographic variables such as sex, American Society of Anesthesiologists classification, diabetes, congestive heart failure, chronic pulmonary disease, and socioeconomic status based on Area Deprivation Index were controlled for across all patients. RESULTS: The unadjusted analyses found that Black patients had an increased likelihood of 30-day emergency department visits and readmissions (P < .001). However, in the adjusted analyses, Black race was demonstrated to be a risk factor for increased total complications at all-time points (P ≤ .0279). Area Deprivation Index was not a risk for cumulative complications at these time points (P ≥ .2455). CONCLUSION: Black patients undergoing TKA may be at increased risk for complications with more risk factors including higher body mass index, tobacco use, substance abuse, chronic obstructive pulmonary disease, congestive heart failure, hypertension, chronic kidney disease, and diabetes and were thus, "sicker" initially than the White cohort. Surgeons are often treating these patients at the later stages of their diseases when risk factors are less modifiable, which necessitates a shift to early, preventable public health measures. While higher socioeconomic disadvantage has been associated with higher rates of complications, the results of this study suggest that race may play a greater role than previously thought.


Assuntos
Artroplastia do Joelho , Negro ou Afro-Americano , Artropatias , Articulação do Joelho , Brancos , Humanos , Artroplastia do Joelho/efeitos adversos , Artroplastia do Joelho/estatística & dados numéricos , Negro ou Afro-Americano/estatística & dados numéricos , População Negra , Comorbidade , Diabetes Mellitus/epidemiologia , Diabetes Mellitus/etnologia , Insuficiência Cardíaca/epidemiologia , Insuficiência Cardíaca/etnologia , Artropatias/epidemiologia , Artropatias/etnologia , Artropatias/cirurgia , Articulação do Joelho/cirurgia , Complicações Pós-Operatórias/epidemiologia , Complicações Pós-Operatórias/etnologia , Complicações Pós-Operatórias/etiologia , Fatores Raciais , Estudos Retrospectivos , Fatores de Risco , Brancos/estatística & dados numéricos , Estados Unidos/epidemiologia
2.
Biosci Rep ; 40(6)2020 06 26.
Artigo em Inglês | MEDLINE | ID: mdl-32478388

RESUMO

Proximal symphalangism (SYM1) is an autosomal dominant disorder manifested by ankylosis of the proximal interphalangeal joints of fingers, carpal and tarsal bone fusion, and conductive hearing loss in some cases. Herein, we clinically diagnosed a Chinese patient with fusions of the bilateral proximal interphalangeal joints in the 2-5 digits without conductive hearing loss. Family history investigation revealed that his mother and grandfather also suffered from SYM1. Whole exome sequencing was performed to detect the genetic lesion of the family. The candidate gene variants were validated by Sanger sequencing. By data filtering, co-segregation analysis and bioinformatics analysis, we highly suspected that an unknown heterozygous frameshift variant (c.635_636insG, p.Q213Pfs*57) in NOG was responsible for the SYM1 in the family. This variant was predicted to be deleterious and resulted in a prolonged protein. This finding broadened the spectrum of NOG mutations associated with SYM1 and contributed to genetic diagnosis and counseling of families with SYM1.


Assuntos
Proteínas de Transporte/genética , Articulações dos Dedos/anormalidades , Mutação da Fase de Leitura , Artropatias/congênito , Povo Asiático , Criança , Análise Mutacional de DNA , Feminino , Predisposição Genética para Doença , Hereditariedade , Heterozigoto , Humanos , Artropatias/diagnóstico , Artropatias/etnologia , Artropatias/genética , Masculino , Linhagem , Fenótipo , Sequenciamento Completo do Genoma
3.
J Shoulder Elbow Surg ; 29(5): 886-892, 2020 May.
Artigo em Inglês | MEDLINE | ID: mdl-31767351

RESUMO

BACKGROUND: Although prior studies have reported health disparities in total knee and hip arthroplasty, few have evaluated the effect of race/ethnicity on total shoulder arthroplasty, particularly in a setting in which patients have uniform access to care. Because the procedural volume of shoulder arthroplasty has increased dramatically over the past decade, evaluating the association between race/ethnicity and postoperative outcomes is warranted. We sought to evaluate racial/ethnic disparities in adverse postoperative events within a universally insured shoulder arthroplasty cohort in an integrated health care system. METHODS: An integrated health care system's registry was used to identify patients who underwent elective primary (total or reverse) shoulder arthroplasty from 2005 to 2016. Four mutually exclusive race/ethnicity groups were investigated: white, Asian, black, and Hispanic. Racial differences were evaluated using Cox proportional hazards regression for all-cause revision and conditional logistic regression for 90-day unplanned readmissions and 90-day emergency department (ED) visits while adjusting for confounders. RESULTS: Of the 8360 shoulder procedures, 2% were performed in Asian patients; 5%, black patients; 9%, Hispanic patients; and 84%, white patients. Compared with white patients, Hispanic patients had a 44% lower revision risk (hazard ratio, 0.56; 95% confidence interval, 0.33-0.97). Black patients had a 45% higher likelihood of a 90-day ED visit (odds ratio, 1.45; 95% confidence interval, 1.12-1.89). CONCLUSION: We found minority groups to have revision and unplanned readmission risks that were similar to or lower than those of white patients. However, black patients had a higher likelihood of ED visits. Further investigation is needed to determine the reasons for this disparity and identify interventions to mitigate unnecessary ED visits.


Assuntos
Artroplastia do Ombro/efeitos adversos , Etnicidade/estatística & dados numéricos , Disparidades nos Níveis de Saúde , Disparidades em Assistência à Saúde/etnologia , Artropatias/etnologia , Complicações Pós-Operatórias/etnologia , Adulto , Idoso , Idoso de 80 Anos ou mais , Artroplastia do Ombro/estatística & dados numéricos , Procedimentos Cirúrgicos Eletivos , Serviço Hospitalar de Emergência , Feminino , Humanos , Artropatias/diagnóstico , Artropatias/cirurgia , Masculino , Pessoa de Meia-Idade , Sistema de Registros , Estudos Retrospectivos , Fatores Socioeconômicos
4.
BMC Med Genet ; 20(1): 53, 2019 03 29.
Artigo em Inglês | MEDLINE | ID: mdl-30922245

RESUMO

BACKGROUND: Progressive pseudorheumatoid dysplasia (PPRD) is a rare autosomal-recessive, non-inflammatory arthropathy, shown to be caused by mutations in the WNT1-inducible signaling pathway protein 3 (WISP3) gene. Although several hundred cases were reported worldwide, the diagnosis remains challenging. Subsequently, the syndrome is often unrecognized and misdiagnosed (for instance, as Juvenile Idiopathic Arthritis), leading to unnecessary procedures and treatments. The objective of the current study was to identify the molecular basis in a family with PPRD and describe their phenotype and course of illness. PATIENTS AND METHODS: We present here a multiply affected consanguineous family of Iraqi-Jewish descent with PPRD. The proband, a 6.5 years old girl, presented with bilateral symmetric bony enlargements of the 1st interphalangeal joints of the hands, without signs of synovitis. Molecular analysis of the family was pursued using Whole Exome Sequencing (WES) and homozygosity mapping. RESULTS: WES analysis brought to the identification of a novel homozygous missense mutation (c.257G > T, p.C86F) in the WISP3 gene. Following this diagnosis, an additional 53 years old affected family member was found to harbor the mutation. Two other individuals in the family were reported to have had similar involvement however both had died of unrelated causes. CONCLUSION: The reported family underscores the importance of recognition of this unique skeletal dysplasia by clinicians, and especially by pediatric rheumatologists and orthopedic surgeons.


Assuntos
Proteínas de Sinalização Intercelular CCN/genética , Sequenciamento do Exoma/métodos , Artropatias/congênito , Mutação de Sentido Incorreto , Criança , Consanguinidade , Diagnóstico Precoce , Feminino , Predisposição Genética para Doença , Sequenciamento de Nucleotídeos em Larga Escala/métodos , Humanos , Iraque/etnologia , Judeus/genética , Artropatias/diagnóstico , Artropatias/etnologia , Artropatias/genética , Masculino , Pessoa de Meia-Idade , Linhagem , Fenótipo , Literatura de Revisão como Assunto
5.
J Orthop Sci ; 24(4): 624-630, 2019 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-30579647

RESUMO

BACKGROUND: Asians generally have smaller stature than Europeans and Americans, and currently available implants used in reverse shoulder arthroplasty might not fit smaller bony anatomies. However, few articles have reported glenoid geometry in the Asian population. The purpose of this study was to measure the dimensions and orientations of the glenoid from three-dimensional computed tomography reconstructions of elderly Japanese subjects. METHODS: This study included 100 shoulders (50 males and 50 females with >50 years of age). The mean age was 67 ± 7 years for both sexes, and the mean height was 167 ± 7 cm for males and 154 ± 6 cm for females. Three-dimensional scapular models were created from computed tomographic images, and the glenoid height, glenoid width, glenoid version, glenoid inclination, vault depth, and vault width were measured. RESULTS: The mean glenoid height and width were 38.6 and 29.4 mm for males and 33.1 and 24.4 mm for females, respectively. Both retroversion and superior inclination were approximately 3° in both sexes. The glenoid vault was deeper in the posterior region with the maximum depth of 26.1 and 23.6 mm in males and females. The vault width was narrower in the anterior region with the anterior width of 2.5 mm at 15 mm medial from the glenoid face in females. CONCLUSION: Glenoids of Japanese females are small compared to currently available baseplates for reverse shoulder arthroplasty. These results may be helpful to aid design in smaller baseplates that better fit the anatomic geometry of the Asian glenoid.


Assuntos
Povo Asiático , Cavidade Glenoide/diagnóstico por imagem , Cavidade Glenoide/patologia , Artropatias/diagnóstico por imagem , Articulação do Ombro/diagnóstico por imagem , Articulação do Ombro/patologia , Idoso , Artroplastia do Ombro , Pesos e Medidas Corporais , Feminino , Humanos , Imageamento Tridimensional , Japão , Artropatias/etnologia , Artropatias/patologia , Prótese Articular , Masculino , Pessoa de Meia-Idade , Fatores Sexuais , Tomografia Computadorizada por Raios X
6.
Clin Orthop Relat Res ; 474(9): 1986-95, 2016 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-27278675

RESUMO

BACKGROUND: Race is an important predictor of TKA outcomes in the United States; however, analyses of race can be confounded by socioeconomic factors, which can result in difficulty determining the root cause of disparate outcomes after TKA. QUESTIONS/PURPOSES: We asked: (1) Are race and socioeconomic factors at the individual level associated with patient-reported pain and function 2 years after TKA? (2) What is the interaction between race and community poverty and patient-reported pain and function 2 years after TKA? METHODS: We identified all patients undergoing TKA enrolled in a hospital-based registry between 2007 and 2011 who provided 2-year outcomes and lived in New York, Connecticut, or New Jersey. Of patients approached to participate in the registry, more than 82% consented and provided baseline data, and of these patients, 72% provided 2-year data. Proportions of patients with complete followup at 2 years were lower among blacks (57%) than whites (74%), among patients with Medicaid insurance (51%) compared with patients without Medicaid insurance (72%), and among patients without a college education (67%) compared with those with a college education (71%). Our final study cohort consisted of 4035 patients, 3841 (95%) of whom were white and 194 (5%) of whom were black. Using geocoding, we linked individual-level registry data to US census tracts data through patient addresses. We constructed a multivariate linear mixed-effect model in multilevel frameworks to assess the interaction between race and census tract poverty on WOMAC pain and function scores 2 years after TKA. We defined a clinically important effect as 10 points on the WOMAC (which is scaled from 1 to 100 points, with higher scores being better). RESULTS: Race, education, patient expectations, and baseline WOMAC scores are all associated with 2-year WOMAC pain and function; however, the effect sizes were small, and below the threshold of clinical importance. Whites and blacks from census tracts with less than 10% poverty have similar levels of pain and function 2 years after TKA (WOMAC pain, 1.01 ± 1.59 points lower for blacks than for whites, p = 0.53; WOMAC function, 2.32 ± 1.56 lower for blacks than for whites, p = 0.14). WOMAC pain and function scores 2 years after TKA worsen with increasing levels of community poverty, but do so to a greater extent among blacks than whites. Disparities in pain and function between blacks and whites are evident only in the poorest communities; decreasing in a linear fashion as poverty increases. In census tracts with greater than 40% poverty, blacks score 6 ± 3 points lower (worse) than whites for WOMAC pain (p = 0.03) and 7 ± 3 points lower than whites for WOMAC function (p = 0.01). CONCLUSIONS: Blacks and whites living in communities with little poverty have similar patient-reported TKA outcomes, whereas in communities with high levels of poverty, there are important racial disparities. Efforts to improve TKA outcomes among blacks will need to address individual- and community-level socioeconomic factors. LEVEL OF EVIDENCE: Level III, therapeutic study.


Assuntos
Artroplastia de Quadril , Negro ou Afro-Americano , Disparidades em Assistência à Saúde , Articulação do Quadril/cirurgia , Hispânico ou Latino , Artropatias/cirurgia , Pobreza , População Branca , Idoso , Artroplastia de Quadril/efeitos adversos , Artroplastia de Quadril/economia , Censos , Distribuição de Qui-Quadrado , Fatores de Confusão Epidemiológicos , Feminino , Disparidades em Assistência à Saúde/economia , Disparidades em Assistência à Saúde/etnologia , Articulação do Quadril/fisiopatologia , Humanos , Artropatias/economia , Artropatias/etnologia , Artropatias/fisiopatologia , Modelos Lineares , Masculino , Medicaid/economia , Pessoa de Meia-Idade , Análise Multivariada , Medição da Dor , Dor Pós-Operatória/economia , Dor Pós-Operatória/etnologia , Medidas de Resultados Relatados pelo Paciente , Pobreza/economia , Pobreza/etnologia , Recuperação de Função Fisiológica , Sistema de Registros , Estudos Retrospectivos , Medição de Risco , Fatores de Risco , Fatores de Tempo , Resultado do Tratamento , Estados Unidos/epidemiologia
7.
Sci Rep ; 6: 27684, 2016 06 13.
Artigo em Inglês | MEDLINE | ID: mdl-27291587

RESUMO

We report identification and genetic characterization of a rare skeletal disorder that remained unidentified for decades in a village of Jammu and Kashmir, India. The population residing in this region is highly consanguineous and a lack of understanding of the disorder has hindered clinical management and genetic counseling for the many affected individuals in the region. We collected familial information and identified two large extended multiplex pedigrees displaying apparent autosomal recessive inheritance of an uncharacterized skeletal dysplasia. Whole exome sequencing (WES) in members of one pedigree revealed a rare mutation in WISP3:c.156C > A (NP_003871.1:p.Cys52Ter), that perfectly segregated with the disease in the family. To our surprise, Sanger sequencing the WISP3 gene in the second family identified a distinct, novel splice site mutation c.643 + 1G > A, that perfectly segregated with the disease. Combining our next generation sequencing data with careful clinical documentation (familial histories, genetic data, clinical and radiological findings), we have diagnosed the families with Progressive Pseudorheumatoid Dysplasia (PPD). Our results underscore the utility of WES in arriving at definitive diagnoses for rare skeletal dysplasias. This genetic characterization will aid in genetic counseling and management, critically required to curb this rare disorder in the families.


Assuntos
Proteínas de Sinalização Intercelular CCN/genética , Exoma , Artropatias/congênito , Adulto , Criança , Consanguinidade , Feminino , Genes Recessivos , Sequenciamento de Nucleotídeos em Larga Escala , Humanos , Índia , Artropatias/etnologia , Artropatias/genética , Masculino , Pessoa de Meia-Idade , Mutação , Linhagem , Fenótipo , Adulto Jovem
9.
J Arthroplasty ; 29(1): 71-4, 2014 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-23706908

RESUMO

The purpose of this study was to evaluate how the gender specific or morphological specific total knee prostheses improve the component fit in the distal femur of the Chinese population. The data showed that the perfect fit rate of the femoral component remarkably increased in both the male and female subjects when using the gender specific (Nexgen-LPS GSF, Zimmer) or morphological specific (Advance Stature Knee, Wright Medical Technology) knee prostheses, compared to their standard counterparts. The highest femoral component perfect fit rate was achieved when both the standard and the corresponding gender or morphological specific knee prostheses were available for selection. Additionally, the percentage of the gender or morphological specific prosthesis selection in the females was significantly higher than the males.


Assuntos
Artroplastia do Joelho , Fêmur/anatomia & histologia , Artropatias/etnologia , Articulação do Joelho/anatomia & histologia , Prótese do Joelho , Desenho de Prótese , Adulto , Povo Asiático , Feminino , Fêmur/diagnóstico por imagem , Humanos , Artropatias/cirurgia , Articulação do Joelho/diagnóstico por imagem , Masculino , Pessoa de Meia-Idade , Fatores Sexuais , Tomografia Computadorizada Espiral
11.
Clin Orthop Relat Res ; 471(5): 1472-83, 2013 May.
Artigo em Inglês | MEDLINE | ID: mdl-23011845

RESUMO

BACKGROUND: Coronal alignment is considered key to the function and longevity of a TKA. However, most studies do not consider femoral and tibial anatomical features such as lateral femoral bowing and the effects of these features and subsequent alignment on function after TKA are unclear. QUESTIONS/PURPOSES: We therefore determined (1) the prevalence of lateral femoral bowing, varus femoral condylar orientation, and severe tibia plateau inclination in female Koreans undergoing TKA; (2) whether postoperative alignments are affected by these anatomical features and improved by the use of navigation; and (3) whether postoperative coronal alignments are associated with function. METHODS: We measured alignment in 367 knees that underwent TKA and 60 sex- and age-matched normal knees (control group). We determined patterns and degrees of femoral bowing angle, femoral condylar orientation, and tibial plateau inclination on preoperative full-limb radiographs. Postoperatively, coronal alignment of limbs and of femoral and tibial components was measured. We compared American Knee Society scores, WOMAC scores, and SF-36 scores in aligned knees and outliers (beyond ± 3° or ± 2°) at 1 year. RESULTS: The prevalence of lateral femoral bowing was 88% in the TKA group and 77% in the control group. Mean femoral condylar orientation angle was varus 2.6° in the TKA group and valgus 1.1° in the control group, and mean tibial plateau inclination was varus 8.3° in the TKA group and varus 5.4° in the control group. Femoral lateral bowing and varus femoral condylar orientation were associated with postoperative alignments. Several clinical outcome scales were inferior in the outliers in mechanical tibiofemoral angle, anatomical tibiofemoral angle, and tibial coronal alignment but not in femoral coronal alignment outliers. CONCLUSIONS: Lateral femoral bowing, varus condylar orientation, and severe varus inclination of the tibia plateau should be considered when performing TKA in Korean patients or patients with otherwise similar anatomical features.


Assuntos
Artroplastia do Joelho , Povo Asiático , Fêmur/cirurgia , Artropatias/cirurgia , Articulação do Joelho/cirurgia , Tíbia/cirurgia , Idoso , Idoso de 80 Anos ou mais , Artroplastia do Joelho/efeitos adversos , Fenômenos Biomecânicos , Avaliação da Deficiência , Feminino , Fêmur/diagnóstico por imagem , Fêmur/fisiopatologia , Humanos , Artropatias/diagnóstico por imagem , Artropatias/etnologia , Artropatias/fisiopatologia , Articulação do Joelho/diagnóstico por imagem , Articulação do Joelho/fisiopatologia , Pessoa de Meia-Idade , Prevalência , Radiografia , Recuperação de Função Fisiológica , República da Coreia/epidemiologia , Estudos Retrospectivos , Tíbia/diagnóstico por imagem , Tíbia/fisiopatologia , Resultado do Tratamento
12.
Surg Radiol Anat ; 34(1): 65-71, 2012 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-21626275

RESUMO

PURPOSE: To explore the anatomic features of the fabella and its relationship with the common peroneal nerve and the fabellofibular ligament, so as to provide anatomical evidence for clinical diagnosis and treatment of fabella diseases in a Chinese population. METHODS: Sixty-one formalin-fixed knee specimens were obtained for anatomic dissection. Structural features of the fabella were investigated by radiological and histological tests. RESULTS: There were 53 cases (86.89%) with fabellae in the lateral head of the gastrocnemius muscle, including 34 bony ones (55.74%), whereas only 6 cases had fabellae in the medial head (9.84%). The fabellae were accompanied by common peroneal nerves on their surfaces in 11 cases (20.8%), and the presence of the fabella was not generally predictive of a fabellofibular ligament. As much as 57.9% of the cartilage fabellae were not visualized on radiograph. The structure of the ossified fabella is similar to a typical long bone. CONCLUSIONS: Fabellae were mainly present in the lateral head of the gastrocnemius muscle in a large proportion of the Chinese population. More than half of the cartilage fabellae were not visualized on radiograph. Its clinical significance could not be ignored by physicians and anatomists.


Assuntos
Artropatias/etnologia , Articulação do Joelho/anatomia & histologia , Músculo Esquelético/anatomia & histologia , Ossos Sesamoides/anatomia & histologia , Idoso , Idoso de 80 Anos ou mais , Povo Asiático , Cadáver , Dissecação , Feminino , Humanos , Artropatias/diagnóstico por imagem , Artropatias/cirurgia , Ligamentos Articulares/anatomia & histologia , Masculino , Pessoa de Meia-Idade , Músculo Esquelético/diagnóstico por imagem , Nervo Fibular/anatomia & histologia , Radiografia , Ossos Sesamoides/diagnóstico por imagem
13.
Am J Phys Anthropol ; 146(1): 94-103, 2011 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-21766284

RESUMO

Using the protocol outlined in The Backbone of History: Health and Nutrition in the Western Hemisphere (BBH) (Steckel and Rose. 2002a. The backbone of history: health and nutrition in the Western Hemisphere. Cambridge: Cambridge University Press), this project compares the Mark I Health Index (MIHI) scores of the Ipiutak (n = 76; 100BCE-500CE) and Tigara (n = 298; 1200-1700CE), two samples of North American Arctic Eskimos excavated from Point Hope, Alaska. Macroscopic examination of skeletal remains for evidence of anemia, linear enamel hypoplasias (LEH), infection, trauma, dental health, and degenerative joint disease (DJD) was conducted to assess differences in health status resulting from a major economic shift at Point Hope. These data demonstrate that despite differences in settlement pattern, economic system, and dietary composition, the MIHI scores for the Ipiutak (82.1) and Tigara (84.6) are essentially equal. However, their component scores differ considerably. The Ipiutak component scores are suggestive of increased prevalence of chronic metabolic and biomechanical stresses, represented by high prevalence of nonspecific infection and high frequencies of DJD in the hip/knee, thoracic vertebrae, and wrists. The Tigara experienced more acute stress, evidenced by higher prevalence of LEH and trauma. Comparison of overall health index scores with those published in BBH shows the MIHI score for the Ipiutak and Tigara falling just above the average for sites in the Western Hemisphere, adding support to the argument that the human capacity for cultural amelioration of environmental hardships is quite significant.


Assuntos
Osso e Ossos/patologia , Indicadores Básicos de Saúde , Estado Nutricional/fisiologia , Paleopatologia , Dente/patologia , Adolescente , Adulto , Alaska , Anemia/etnologia , Anemia/história , Doenças Ósseas Infecciosas/etnologia , Doenças Ósseas Infecciosas/história , Distribuição de Qui-Quadrado , Criança , Pré-Escolar , Hipoplasia do Esmalte Dentário/etnologia , Hipoplasia do Esmalte Dentário/história , Feminino , História do Século XV , História do Século XVI , História do Século XVII , História Antiga , História Medieval , Humanos , Lactente , Inuíte/história , Inuíte/estatística & dados numéricos , Artropatias/etnologia , Artropatias/história , Masculino , Pessoa de Meia-Idade , Ferimentos e Lesões/etnologia , Ferimentos e Lesões/história
14.
Hip Int ; 21(3): 311-6, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21698580

RESUMO

There is sometimes uncertainty concerning the correct socket position prior to total hip arthroplasty (THA). We conducted a study to determine the hip centre in Japanese women in order to define the true anatomical position of the acetabulum. The study involved 200 consecutive female patients in whom the contralateral hip joint was normal or was prearthritic and who underwent unilateral THA. The 'normal' group comprised 100 hip joints with no acetabular hip dysplasia, and the prearthritis group comprised 100 hip joints with Crowe type I dysplasia. The length of a perpendicular line drawn under the teardrop (interteardrop line) connecting both inferior edges of the teardrop with the centre of the femoral head was recorded as the vertical distance, and the distance from the intersection of the perpendicular line and interteardrop line up to the teardrop was recorded as the horizontal distance. We measured these distances on the femoral head of the side that did not undergo THA. The mean vertical distances in the 'normal' and prearthritis groups were 14.6 ± 2.8 mm and 16.8 ± 2.7 mm, respectively, and the mean horizontal distances were 30.2 ± 2.8 mm and 32.5 ± 2.7 mm, respectively. We therefore determined the mean centre of the hips to lie at a vertical distance of 11 to 22 mm and a horizontal distance of 27 to 38 mm. These values can serve as a useful index for socket positioning in THA.


Assuntos
Acetábulo/diagnóstico por imagem , Povo Asiático , Artropatias/diagnóstico por imagem , Artropatias/etnologia , Adulto , Idoso , Idoso de 80 Anos ou mais , Artroplastia de Quadril , Estatura , Índice de Massa Corporal , Estudos de Coortes , Feminino , Prótese de Quadril , Humanos , Japão , Artropatias/cirurgia , Pessoa de Meia-Idade , Radiografia , Amplitude de Movimento Articular
15.
Clin Orthop Relat Res ; 469(7): 1817-23, 2011 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-21468785

RESUMO

BACKGROUND: For minority populations in the United States, especially African Americans, Hispanics, and Native Americans, healthcare disparities are a serious problem. The literature documents racial and ethnic utilization disparities with regard to THA and TKA. QUESTIONS/PURPOSES: We therefore (1) defined utilization disparities for total joint arthroplasty in racial and ethnic minorities, (2) delineated patient and provider factors contributing to the lower total joint arthroplasty utilization, and (3) discussed potential interventions and future research that may increase total joint arthroplasty utilization by racial and ethnic minorities. METHODS: We searched the MEDLINE database and identified 67 articles, 21 of which we excluded. By searching Google and Google Scholar and reference lists of the included articles, we identified 40 articles for this review. Utilization disparities were defined by documented lower utilization of THA or TKA in specific racial or ethnic groups. RESULTS: Lower utilization of THA and TKA among some racial and ethnic minority groups (African Americans, Hispanics) is not explained by decreased disease prevalence or disability. At least some utilization disparities are independent of income, geographic location, education, and insurance status. Causal factors related to racial and ethnic disparities may be related in part to patient factors such as health literacy, trust, and preferences. Provider unconscious or conscious biases or beliefs also play a role in at least some healthcare disparities. CONCLUSIONS: Racial and ethnic THA and TKA utilization disparities exist. These disparities are not explained by lower disease prevalence. The existing data suggest patient education, improved health literacy regarding THA and TKA, and a patient-provider relationship leading to improved trust would be beneficial. Research providing a better understanding of the root causes of these disparities is needed.


Assuntos
Artroplastia de Quadril/estatística & dados numéricos , Artroplastia do Joelho/estatística & dados numéricos , Etnicidade/estatística & dados numéricos , Disparidades em Assistência à Saúde/estatística & dados numéricos , Artropatias/cirurgia , Humanos , Artropatias/etnologia , Grupos Minoritários , Saúde das Minorias , Estados Unidos/etnologia
16.
Clin Orthop Relat Res ; 469(7): 1886-90, 2011 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-21503786

RESUMO

BACKGROUND: Many authors report racial and ethnic disparities in total joint arthroplasty. The extent and implications, however, are not fully understood. QUESTIONS/PURPOSES: Our purposes in this breakout session were to (1) define "Where are we now?"; (2) outline "Where do we need to go?"; and (3) generate a plan for "How do we get there?" in addressing issues of racial disparity and total joint arthroplasty. WHERE ARE WE NOW?: Blacks and some other ethnic minorities have a greater incidence of arthritis and chronic disability than the population in general. Blacks have a lower use of total joint arthroplasty for a variety of reasons, including patient trust, perceived limited satisfaction with results by peers, varying knowledge about total joint arthroplasty, and concerns about pain associated with these procedures. Current data, however, are insufficient to clearly define the magnitude and nature of musculoskeletal disparities. WHERE DO WE NEED TO GO?: We need to better define the magnitude and nature of racial disparities to best design and implement research questions and studies and target areas for improvement. We should define geographic and provider variation that lead to the differences in use that has been observed in total joint arthroplasty. HOW DO WE GET THERE?: A profession-wide emphasis and focus on disparities needs to be developed with other medical specialties and national organizations to advocate for changes to better define and address racial disparities. Partnerships with organizations and/or investigators that can gain access to relevant databases should be encouraged. Special attention to disparities and manuscript reviewing and editing is essential.


Assuntos
Artroplastia do Joelho , Etnicidade , Disparidades em Assistência à Saúde/etnologia , Artropatias , Grupos Minoritários , Saúde das Minorias/etnologia , Atitude Frente a Saúde , Conhecimentos, Atitudes e Prática em Saúde , Nível de Saúde , Disparidades em Assistência à Saúde/estatística & dados numéricos , Humanos , Artropatias/etnologia , Artropatias/fisiopatologia , Artropatias/cirurgia , Dor/psicologia , Aceitação pelo Paciente de Cuidados de Saúde/psicologia , Preconceito
17.
Acta Med Okayama ; 65(1): 41-8, 2011 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-21339795

RESUMO

This study aimed to determine whether there was any association between the regional climate and the proportion of people with joint pain. Regional climate data between 1971 and 2000 were obtained from the Japan Meteorological Agency. The variables used in the cluster analysis included sunlight hours, amount of precipitation, number of days with precipitation, and temperature. The regional proportion of people with joint pain was obtained from the National Survey for Health in 2001. After performing a cluster analysis, one-way ANOVA and Welch's test were used to determine whether the climate characteristics of the clusters were significantly different. Within each cluster, stepwise multiple linear regression analyses were performed. We found that sunlight hours showed a direct, negative association with the proportion of people with joint pain (adjusted R2=0.532, p=0.016) in cluster 1, which was characterized as the region with the fewest total hours of sunlight, less precipitation, a modest number of rainy days, and low temperature. In the other clusters, the regional female population rate (cluster 2) and the senior population rate (cluster 3, 4) were the primary predictors. We concluded that the degree of exposure to sunlight may play a crucial role in prevention of joint pain. This finding should encourage people to set aside some time for staying outdoors in their daily lives.


Assuntos
Clima , Artropatias/etnologia , Conceitos Meteorológicos , Dor/etnologia , Adulto , Idoso , Análise por Conglomerados , Emprego , Feminino , Humanos , Japão/epidemiologia , Masculino , Pessoa de Meia-Idade , Fotoperíodo , Valor Preditivo dos Testes , Chuva , Fatores de Risco , Luz Solar
18.
Spat Spatiotemporal Epidemiol ; 1(2-3): 133-41, 2010 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-20563237

RESUMO

Human papillomavirus (HPV) infection is an established causal agent for cervical cancer and a subset of oropharyngeal cancers. It is hypothesized that orogenital transmission results in oral cavity infection. In this paper we explore the geographical association between cervical and male oropharyngeal cancer incidence in blacks and whites in South Carolina using Bayesian joint disease mapping models fit to publicly available data. Our results suggest weak evidence for county-level association between the diseases, and different patterns of joint disease behavior for blacks and whites.


Assuntos
População Negra/estatística & dados numéricos , Papillomavirus Humano 16/isolamento & purificação , Artropatias/etnologia , Neoplasias Orofaríngeas/etnologia , Infecções por Papillomavirus/etnologia , Neoplasias do Colo do Útero/etnologia , População Branca/estatística & dados numéricos , Teorema de Bayes , Causalidade , Comorbidade , Feminino , Humanos , Incidência , Artropatias/diagnóstico , Masculino , Neoplasias Orofaríngeas/virologia , Infecções por Papillomavirus/diagnóstico , Infecções por Papillomavirus/transmissão , Distribuição de Poisson , Medição de Risco , South Carolina/epidemiologia , Topografia Médica , Neoplasias do Colo do Útero/virologia
19.
Joint Bone Spine ; 77(4): 355-7, 2010 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-20462779

RESUMO

Authors trace an ochronotic Hungarian family, which moved from Slovakia to Hungary 300 years ago. As the family members lived in a relatively close village community the gene mutation had been survived silently for ages before the clinical symptoms developed. Family tree analysis could detect with the use of allele specific PCR amplification-the p.G161R mutation of the homogentisic acid 1,2-dioxygenase (HGD) gene, which resulted in a specific genotype appearing in the Slovak population. We found a heterozygote member of this family who has children with an alkaptonuria-homozygote and known-heterozygote genotypes so there would be a high risk of alkaptonuria in their offsprings. Therefore genetic counselling is highly recommended to minimize the risk factors.


Assuntos
Homogentisato 1,2-Dioxigenase/genética , Artropatias/genética , Mutação/genética , Ocronose/genética , Feminino , Predisposição Genética para Doença , Genótipo , Humanos , Hungria , Artropatias/etnologia , Masculino , Ocronose/etnologia , Linhagem , Eslováquia/etnologia
20.
West Indian med. j ; 58(6): 506-511, Dec. 2009. tab
Artigo em Inglês | LILACS | ID: lil-672533

RESUMO

OBJECTIVE: This study is designed to further characterize Limited Joint Mobility (LJM) of the hand using quantitative goniometric measurements among Black Africans with Type 2 diabetes mellitus and non-diabetes. METHODS: Seventy-six patients with Type 2 diabetes and 63 normal controls matched for age and gender were purposively selected. Visual clinical examination and quantitative goniometric assessment of patients with DM and non-DM controls were done. The LJM was graded using the criteria of Silverstein et al. Glycaemic control and proteinuria were also assessed. RESULTS: Prevalence of LJM among Type 2 DM patients was 26.3% compared with 4.8% in normal controls. Subjects with LJM within the control group were significantly older than those with LJM within the DM group (p < 0.05). Prayer sign was 11.8% in DM patients compared with 4.8% of control. The flattening sign demonstrated by the inability to flatten their hands on a flat surface was more in patients with DM (10.5%) compared with 4.8% in the control group. Stage II LJM with 18.4% prevalence was the commonest followed by Stage III (7.9%) among patients with DM. Poor glycaemic control was found in 85%, using fasting plasma glucose and 70%, using 2-hour postprandial blood glucose (2 hpp). CONCLUSION: We conclude that Black Africans with Type 2 DM only have moderately severe cases of LJM.


OBJETIVO: Este estudio fue diseñado para caracterizar más a fondo la limitación de la movilidad articular (LMA) de la mano, usando mediciones goniométricas entre africanos. MÉTODOS: Setenta y seis pacientes con diabetes mellitus tipo 2 y 63 controles normales pareados por edad y género fueron seleccionados para este propósito. Se realizó un examen clínico visual y una evaluación goniométrica cuantitativa de los pacientes con DM y controles no DM. La LMA fue graduada usando los criterios de Silverstein et al. También se evaluaron el control glicérico y la proteinuria. RESULTADOS: La prevalencia de LMA entre pacientes con DM tipo 2 fue de 26.3% comparada con 4.8% en los controles normales. Los sujetos con LMA en el grupo de control fueron significativamente mayores en edad que aquellos con LMA en el grupo con DM (p < 0.05). La signo de las manos en oración fue 11.8% en los pacientes con DM comparado con el 4.8% del control. El signo de aplanamiento demostrado por la incapacidad de los pacientes de poner sus manos totalmente planas sobre una superficie, fue mayor en aquellos con DM (10.5%) en comparación con el 4.8% del grupo control. La LMA de la segunda etapa con una prevalencia de 18.4%, fue la más común seguida por la de etapa III (7.9%) entre pacientes con DM. Un control glicémico pobre fue hallado en 85%, usando glucosa plasmática en ayunas. CONCLUSIÓN: Concluimos que los africanos negros con DM tipo 2 presentan sólo casos moderadamente severos de LMA.


Assuntos
Adulto , Idoso , Idoso de 80 Anos ou mais , Humanos , Masculino , Pessoa de Meia-Idade , População Negra , /complicações , /etnologia , Artropatias/etnologia , Amplitude de Movimento Articular , Glicemia/metabolismo , Estudos de Casos e Controles , /sangue , Nigéria , Estudos Prospectivos
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