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1.
Rev. Esp. Cir. Ortop. Traumatol. (Ed. Impr.) ; 59(5): 354-359, sept.-oct. 2015.
Artigo em Espanhol | IBECS | ID: ibc-140877

RESUMO

Objetivo. El propósito de este estudio es evaluar la validez interna de una prueba clínica descrita para el diagnóstico precoz de la capsulitis adhesiva de hombro: el Test de Distensión en Rotación Externa Pasiva (TDREP). Material y método. El TDREP se realiza con el paciente de pie, el brazo adducido y el codo flexionado a 90°. Desde esta posición, se inicia un movimiento suave de rotación externa pasiva, sosteniendo el brazo afectado con una mano del examinador en la muñeca y otra manteniendo el codo abducido hasta que se alcanza el punto máximo de rotación indolora. Desde este punto de máxima rotación externa con el brazo en aducción y sin dolor, se realiza un movimiento brusco de distensión, incrementando la rotación externa, causando dolor en el hombro si la prueba es positiva. Es test se realizó en un grupo de 155 pacientes con dolor de hombro de múltiples orígenes para analizar los valores predictivos, la sensibilidad, especificidad y razón de verosimilitud. Resultados. El TDREP mostró una sensibilidad de 100% (IC 95%, de 91,8 a 100%) y una especificidad del 90% (IC 95%, de 82,4 a 94,8%). El valor predictivo positivo fue de 0,62 y la razón de verosimilitud de 10,22 (IC 95%: 5,5 a 19,01). Los falsos positivos se encontraron solo en enfermos con tendinopatías del subescapular o con artrosis glenohumeral. Discusión. El TDREP tiene una alta sensibilidad para diagnosticar CA y cuando es negativo prácticamente la excluye. Los falsos positivos se pueden identificar fácilmente si existe una rotación externa sin limitación (tendinopatía subescapular) o con una radiografía simple de hombro (artrosis glenohumeral) (AU)


Objective. The aim of this study is to evaluate the internal validity of a clinical test for the early diagnosis of shoulder adhesive capsulitis, called the Distension Test in Passive External Rotation (DTPER). Material and method. The DTPER is performed with the patient standing up, the arm adducted, and the elbow bent at 90°. From this position, a smooth passive external rotation is started, the affected arm being supporting at the wrist with one hand of the examiner and the other maintaining the adducted elbow until the maximum painless point of the rotation is reached. From this point of maximum external rotation with the arm in adduction and with no pain, an abrupt distension movement is made, increasing the external rotation, causing pain in the shoulder if the test is positive. This term was performed on a group of patients with shoulder pain of many origins, in order to analyse the predictive values, sensitivity, specificity, and the likelihood ratio. Results. The DTPER showed a sensitivity of 100% (95% CI; 91.8 to 100%) and a specificity of 90% (95% CI; 82.4 to 94.8%). The positive predictive value was 0.62 and a likelihood ratio of 10.22 (95% CI; 5.5 to 19.01). False positives were only found in patients with subscapular tendinopathies or glenohumeral arthrosis. Discussion. The DTPER has a high sensitivity for the diagnosis of adhesive capsulitis, and is excluded when it is practically negative. False positives can easily be identified if there is external rotation with no limits (subscapular tendinopathy) or with a simple shoulder X-ray (glenohumeral arthrosis) (AU)


Assuntos
Bursite/complicações , Bursite/diagnóstico , Diagnóstico Precoce , Valor Preditivo dos Testes , Tendinopatia/complicações , Tendinopatia/diagnóstico , Ombro/patologia , Ombro/cirurgia , Ombro , Sensibilidade e Especificidade , Escápula/patologia , Articulação do Ombro/patologia , Articulação do Ombro , Imageamento por Ressonância Magnética/métodos
2.
Rev Esp Cir Ortop Traumatol ; 59(5): 354-9, 2015.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-25544715

RESUMO

OBJECTIVE: The aim of this study is to evaluate the internal validity of a clinical test for the early diagnosis of shoulder adhesive capsulitis, called the Distension Test in Passive External Rotation (DTPER). MATERIAL AND METHOD: The DTPER is performed with the patient standing up, the arm adducted, and the elbow bent at 90°. From this position, a smooth passive external rotation is started, the affected arm being supporting at the wrist with one hand of the examiner and the other maintaining the adducted elbow until the maximum painless point of the rotation is reached. From this point of maximum external rotation with the arm in adduction and with no pain, an abrupt distension movement is made, increasing the external rotation, causing pain in the shoulder if the test is positive. This term was performed on a group of patients with shoulder pain of many origins, in order to analyse the predictive values, sensitivity, specificity, and the likelihood ratio. RESULTS: The DTPER showed a sensitivity of 100% (95% CI; 91.8 to 100%) and a specificity of 90% (95% CI; 82.4 to 94.8%). The positive predictive value was 0.62 and a likelihood ratio of 10.22 (95% CI; 5.5 to 19.01). False positives were only found in patients with subscapular tendinopathies or glenohumeral arthrosis. DISCUSSION: The DTPER has a high sensitivity for the diagnosis of adhesive capsulitis, and is excluded when it is practically negative. False positives can easily be identified if there is external rotation with no limits (subscapular tendinopathy) or with a simple shoulder X-ray (glenohumeral arthrosis).


Assuntos
Bursite/diagnóstico , Amplitude de Movimento Articular , Rotação , Articulação do Ombro/fisiopatologia , Adulto , Idoso , Bursite/fisiopatologia , Diagnóstico Precoce , Reações Falso-Positivas , Feminino , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , Sensibilidade e Especificidade
3.
Rev. esp. enferm. metab. óseas (Ed. impr.) ; 17(4): 71-75, jul. 2008. ilus, tab
Artigo em Es | IBECS | ID: ibc-67076

RESUMO

En enfermedades asintomáticas como la osteoporosis es especialmente importante que las pacientes conozcan la enfermedad, sus tratamientos y las pautas de vidanecesarias para prevenir de ese modo las posibles fracturas y sus consecuencias. En un estudio observacional, prospectivo, multicéntrico, comparativo y abierto de 12 meses de duración para evaluar el cumplimiento, como objetivo secundario del estudio se analizó el grado de conocimiento de la enfermedad mediante la prueba de Batalla, modificada para la osteoporosis. Los resultaron mostraron que, globalmente, el 49,3% de las pacientes tenía un conocimientoaceptable de la enfermedad, el 14,3% medianamente aceptable y en un 36,5% era inaceptable. Por tanto, si bien el grado de conocimiento de la osteoporosisen mujeres posmenopáusicas españolas fue aceptable, el conocimiento de esta enfermedad es todavía deficiente en más del 50%, por lo que es necesario continuaraumentando el conocimiento de la enfermedad en esta población


In asymptomatic diseases such as osteoporosis, it is especially important for the patients to know about the disease, its treatment and the life guidelines necessaryto prevent this method of possible fractures and their consequences. In an observational, prospective, multicenter, comparative and open label 12 monthlong study to evaluate compliance, as a secondary objective of the study, grade of knowledge of the disease was evaluated to study compliance using theBatalla test, modified for osteoporosis. The results showed that, overall, 49.3% of the patients had acceptable knowledge about the disease, 14.3% somewhatacceptable and 36.5% unacceptable knowledge. Thus, although the grade of knowledge on osteoporosis in postmenopausal Spanish women was accepted,knowledge on osteoporosis is still deficient in more than 50%. Thus, it is necessary to continue to increase knowledge about the disease in this population


Assuntos
Humanos , Feminino , Pessoa de Meia-Idade , Idoso , Osteoporose Pós-Menopausa/epidemiologia , Conhecimentos, Atitudes e Prática em Saúde , Cooperação do Paciente , Educação de Pacientes como Assunto/tendências , Osteoporose Pós-Menopausa/tratamento farmacológico , Cloridrato de Raloxifeno/uso terapêutico , Pós-Menopausa
4.
J Surg Oncol ; 93(7): 585-92, 2006 Jun 01.
Artigo em Inglês | MEDLINE | ID: mdl-16705732

RESUMO

Tamoxifen is the established adjuvant treatment for postmenopausal women with hormone-sensitive early breast cancer. However, the side-effects associated with tamoxifen therapy have prompted a search for safer and potentially more effective endocrine agents. Results from randomized trials of the third-generation aromatase inhibitors, anastrozole, letrozole and exemestane, demonstrating improved efficacy compared with tamoxifen and favorable tolerability profiles, are discussed in this review.


Assuntos
Antineoplásicos Hormonais/uso terapêutico , Inibidores da Aromatase/uso terapêutico , Neoplasias da Mama/tratamento farmacológico , Tamoxifeno/uso terapêutico , Anastrozol , Androstadienos/uso terapêutico , Neoplasias da Mama/cirurgia , Quimioterapia Adjuvante , Ensaios Clínicos como Assunto , Feminino , Humanos , Letrozol , Nitrilas/uso terapêutico , Pós-Menopausa , Ensaios Clínicos Controlados Aleatórios como Assunto , Triazóis/uso terapêutico
5.
Artigo em Es | IBECS | ID: ibc-394

RESUMO

Las infiltraciones esteroideas son un procedimiento terapéutico muy extendido en Cirugía Ortopédica y Traumatología. Sin embargo, en la cara dorso-radial de la muñeca la utilización de estas infiltraciones para el tratamiento de patología tendinosa y osteo-articular pueden provocar atrofias cutáneas dolorosas incapacitantes y de difícil tratamiento. Se presenta una técnica no descrita de tratamiento de una atrofia cutánea dolorosa post-infiltración esteroidea por una enfermedad de De Quervain mediante expansión tisular. Se realizó una expansión cutánea progresiva del dorso de la muñeca, trasladándose la piel expandida para cubrir el defecto creado tras la resección de la zona patológica atrófica. Se detallan las indicaciones y la técnica operatoria utilizada. El resultado de la paciente intervenida, tanto funcional como estético, ha sido excelente (AU)


Assuntos
Atrofia/cirurgia , Traumatismos do Punho , Punho/patologia , Dermatopatias/cirurgia
8.
JAMA ; 277(18): 1467-74, 1997 May 14.
Artigo em Inglês | MEDLINE | ID: mdl-9145720

RESUMO

OBJECTIVE: To provide guidance on informed consent to clinicians offering cancer susceptibility testing. PARTICIPANTS: The Task Force on Informed Consent is part of the Cancer Genetics Studies Consortium (CGSC), whose members were recipients of National Institutes of Health grants to assess the implications of cancer susceptibility testing. The 10 task force members represent a range of relevant backgrounds, including various medical specialties, social science, genetic counseling, and consumer advocacy. EVIDENCE: The CGSC held 3 public meetings from 1994 to 1996. At its first meeting, the task force jointly established a list of topics. The cochairs (G.G. and J.R.B) then developed an outline and assigned each topic to an appropriate writer and reviewer. Writers summarized the literature on their topics and drafted recommendations, which were then revised by the reviewers. The cochairs compiled and edited the entire manuscript. All members were involved in writing this report. CONSENSUS PROCESS: The first draft was distributed to task force members, after which a meeting was held to discuss its content and organization. Consensus was reached by voting. A subsequent draft was presented to the entire CGSC at its third meeting, and comments were incorporated. CONCLUSIONS: The task force recommends that informed consent for cancer susceptibility testing be an ongoing process of education and counseling in which (1) providers elicit participant, family, and community values and disclose their own, (2) decision making is shared, (3) the style of information disclosure is individualized, and (4) specific content areas are discussed.


Assuntos
Revelação , Testes Genéticos , Consentimento Livre e Esclarecido , Neoplasias/genética , Adaptação Psicológica , Comitês Consultivos , Compreensão , Confidencialidade , Termos de Consentimento , Cultura , Bases de Dados de Ácidos Nucleicos , Tomada de Decisões , Predisposição Genética para Doença , Privacidade Genética , Humanos , Disseminação de Informação , Seguro Saúde , Educação de Pacientes como Assunto , Medição de Risco , Preservação de Tecido
9.
Bone Marrow Transplant ; 19(3): 221-6, 1997 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-9028549

RESUMO

In an effort to decrease the relapse rate following autologous bone marrow transplantation for non-Hodgkin's lymphoma, patients were given cyclosporine and interferon following autologous marrow transplantation. Forty patients with intermediate grade non-Hodgkin's lymphoma that was relapsed or refractory to standard chemotherapy underwent autologous marrow transplantation. The preparative regimen consisted of cyclophosphamide 6.8 g/m2, etoposide 1600 mg/m2, and carmustine 400 mg/m2 over 4 days followed by reinfusion of bone marrow. Intravenous cyclosporine was started on day -1 as a 16 mg/kg loading dose followed by 3.6 mg/kg/day for 28 days after transplant. Patients were begun on alpha-interferon (starting dose, 0.5 million units s.c. every other day) following platelet engraftment (median day 24 post-transplant) and continued on 1.5 million units s.c. daily for 2 years. Regimen-related toxicities resulted in four (10%) deaths. Twenty-one (53%) patients developed marked erythema of the palms, soles, and arms. Biopsies of the erythema were consistent with grade I GVHD. Patients who did not develop rashes were not biopsied. The erythema persisted for a median of 10 days and resolved in all cases without treatment. Visceral GVHD was not apparent. All patients have been followed for a median of 24 months (range 12-54 months). To date, only five patients (13%) have relapsed after bone marrow transplant. Multivariant analysis could not identify risk factors for relapse post-transplant. Disease-free survival of all patients is 77% (95% confidence interval, 67-93%). The results of this pilot study suggest that the administration of cyclosporine and interferon may decrease the relapse rate of relapsed/refractory non-Hodgkin's lymphoma following autologous bone marrow transplantation.


Assuntos
Protocolos de Quimioterapia Combinada Antineoplásica/uso terapêutico , Transplante de Medula Óssea , Ciclosporina/administração & dosagem , Rejeição de Enxerto/prevenção & controle , Imunossupressores/administração & dosagem , Interferon-alfa/administração & dosagem , Linfoma não Hodgkin/terapia , Adolescente , Adulto , Idoso , Terapia Combinada , Feminino , Humanos , Infusões Intravenosas , Linfoma não Hodgkin/patologia , Masculino , Pessoa de Meia-Idade , Recidiva , Transplante Autólogo
10.
Cancer Res ; 57(24): 5480-4, 1997 Dec 15.
Artigo em Inglês | MEDLINE | ID: mdl-9407954

RESUMO

An increased incidence of colorectal cancer has been observed in breast and breast-ovarian cancer syndrome families, including those of Ashkenazi origin. Recently, a germ-line missense mutation in the APC gene, I1307K, was identified that may indirectly cause colorectal cancer in Ashkenazi Jews. To determine whether the excess of colon cancer in some breast-ovarian cancer families is related to the I1307K mutation, we evaluated 264 Ashkenazi Jews from 158 families. Most of these individuals had either a personal or a family history of breast and/or ovarian cancer, and 19.3% (51 of 264) carried one of the recurrent BRCA1 (185delAG or 5382 insC) or BRCA2 (6174delT) mutations. We detected the APC I1307K mutation in 7% (11 of 158) of the Ashkenazi Jewish families and in 4.5% (12 of 264) of the individuals participating in these studies. Of the families studied, 26.6% (42 of 158) had at least one case of colorectal cancer in a first-, second-, or third-degree relative of the proband. Significantly, of the 12 individuals who possessed the I1307K mutation, none was diagnosed with colorectal cancer and none had a known first-, second-, or third-degree relative diagnosed with colon cancer. The results suggest that factors other than the I1307K mutation contribute to the increased incidence of colon cancer in Ashkenazi breast-ovarian cancer families. Our results emphasize that only a subset of Ashkenazi Jewish individuals with a family history of colorectal cancer should be viewed as candidates for genetic susceptibility testing for the I1307K APC mutation.


Assuntos
Neoplasias da Mama/genética , Neoplasias Colorretais/genética , Genes APC , Judeus/genética , Mutação , Neoplasias Ovarianas/genética , Idoso , Idoso de 80 Anos ou mais , Neoplasias da Mama/sangue , Neoplasias Colorretais/sangue , DNA/sangue , DNA/genética , DNA de Neoplasias/sangue , DNA de Neoplasias/genética , Suscetibilidade a Doenças , Saúde da Família , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Neoplasias Ovarianas/sangue , Linhagem
12.
Cancer Res ; 56(15): 3409-14, 1996 Aug 01.
Artigo em Inglês | MEDLINE | ID: mdl-8758903

RESUMO

Recent studies have identified mutations in the breast and (ovarian cancer susceptibility gene 2 (BRCA2), one which has been found in the germline of several males and one female affected with breast cancer. To establish the carrier frequency of this mutation in a large population of individuals affected with cancer, we evaluated constitutional DNA isolated from 83 individuals diagnosed with breast cancer and 93 diagnosed with ovarian cancer at any age, 42 of whom reported a family history of cancer. Using a simple allele-specific PCR-based nonradioactive method, we detected a total of eight individuals (4.5%) carrying a 1-bp deletion at nucleotide 6174 of the BRCA2 gene (6174delT). The age of disease onset in the mutant allele carriers was highly variable and typically late onset (41-72 years for breast cancer and 48-73 years for ovarian cancer). Evaluation of family histories for the eight mutant allele carriers revealed that several individuals had significant cancer histories that included, in addition to breast and/or ovarian cancer, an increased incidence of colon, esophageal, pancreatic, stomach, and hematopoietic cancers. Interestingly, seven of the eight individuals were of Ashkenazi Jewish descent. Haplotype data for the mutant allele carriers using markers spanning the region of the BRCA2 gene on chromosome 13ql2-ql3 suggest that only two of the confirmed Jewish Ashkenazi individuals share a single common ancestry, indicating several independent origins for this mutation. These data provide evidence for the presence of a specific BRCA2 mutation which has its origins in both Jewish Ashkenazi and non-Jewish populations. The observed overrepresentation of specific mutations within a subgroup of the general population may eventually help contribute to the development of inexpensive and routine tests such as the one described in our study.


Assuntos
Neoplasias da Mama Masculina/genética , Neoplasias da Mama/genética , Judeus/genética , Mutação , Proteínas de Neoplasias/genética , Neoplasias Ovarianas/genética , Fatores de Transcrição/genética , Adulto , Idoso , Alelos , Proteína BRCA2 , Sequência de Bases , DNA de Neoplasias/genética , DNA de Neoplasias/isolamento & purificação , Suscetibilidade a Doenças , Saúde da Família , Feminino , Testes Genéticos , Haplótipos , Heterozigoto , Humanos , Masculino , Pessoa de Meia-Idade , Dados de Sequência Molecular , Reação em Cadeia da Polimerase , Fatores de Risco
13.
Curr Probl Cancer ; 18(1): 6-79, 1994.
Artigo em Inglês | MEDLINE | ID: mdl-8005001

RESUMO

Chemoprevention is a strategy used to block the development of cancers in human beings. This emerging field has broad potential for influencing cancer incidence rates in defined high-risk groups and the general population. In this review, we define some of the mechanisms of carcinogenesis, describe some of the genetic markers of carcinogenesis, and list possible biomarkers that may serve as surrogate end points in chemoprevention studies. A major component of this review is a description of the agents that are currently under investigation in animal systems or in human trials. They are grouped according to the agents that block or suppress mutation, such as oltipraz, selenium, vitamin C and the flavones, or according to agents that block promotion and proliferation, such as difluoromethylornithine, tamoxifen, nonsteroidal antiinflammatory drugs, and the vitamin A derivatives. We describe the issues that are considered in the design of chemoprevention trials and in the phase I, II, and III components of these trials. The following national trials are discussed: the Breast Cancer Prevention Trial, which uses tamoxifen; the Prostate Cancer Prevention Trial, which uses finasteride; and a Lung Cancer Prevention Trial, which uses 13-cis-retinoic acid. The review ends with some insights about future studies in chemoprevention.


Assuntos
Anticarcinógenos/farmacologia , Neoplasias/prevenção & controle , Adulto , Idoso , Anti-Inflamatórios não Esteroides/farmacologia , Anticarcinógenos/uso terapêutico , Ácido Ascórbico/farmacologia , Biomarcadores Tumorais/análise , Neoplasias da Mama/prevenção & controle , Cálcio/farmacologia , Ensaios Clínicos como Assunto , Eflornitina/farmacologia , Ácido Elágico/farmacologia , Feminino , Finasterida/uso terapêutico , Marcadores Genéticos , Humanos , Neoplasias Pulmonares/prevenção & controle , Masculino , Pessoa de Meia-Idade , Mutagênese/efeitos dos fármacos , Neoplasias/genética , Neoplasias/patologia , Neoplasias da Próstata/prevenção & controle , Pirazinas/farmacologia , Selênio/farmacologia , Tamoxifeno/uso terapêutico , Tionas , Tiofenos , Tretinoína/uso terapêutico , Vitamina A/farmacologia , Vitamina E/farmacologia
15.
Arterioscler Thromb ; 12(4): 430-6, 1992 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-1558834

RESUMO

Clopidogrel, like the homologous thienopyridine derivative ticlopidine, selectively inhibits platelet aggregation induced by ADP. We have previously described two nucleotide-binding sites on platelets related to ADP-mediated platelet responses. The first is a high-affinity binding site for 2-methylthio-ADP (2-MeSADP) that is linked to the inhibition of stimulated adenylate cyclase. The second is the 100-kd exofacial membrane protein aggregin, which is labeled by the reactive ADP analogue 5'-p-fluorosulfonylbenzoyl adenosine (FSBA) that is related to shape change and aggregation. We set out to determine if either of these sites is blocked in vivo by clopidogrel or its active metabolite. Six subjects were given clopidogrel (75 mg/day for 10 days) in a double-blind crossover experiment. All of the subjects developed prolonged bleeding times while taking the drug. The rate of onset of the effect on bleeding time varied among subjects. Platelet aggregation induced by ADP or thrombin was significantly impaired by the drug treatment, but no effect was detected on shape change. The incorporation of [3H]FSBA into aggregin was also unaffected. Inhibition of adenylate cyclase by ADP or by 2-MeSADP was greatly reduced in all subjects, and in the case of 2-MeSADP, there was evidence for a noncompetitive effect. Inhibition of adenylate cyclase by epinephrine was unaffected. In the three subjects for whom binding measurements were made, the number of binding sites for [32P]2-MeSADP was reduced from 534 +/- 44 molecules per platelet during control and placebo periods (11 determinations) to 199 +/- 78 molecules per platelet during drug treatment (three determinations). There was no consistent change in the binding affinity.(ABSTRACT TRUNCATED AT 250 WORDS)


Assuntos
Difosfato de Adenosina/análogos & derivados , Inibidores de Adenilil Ciclases , Plaquetas/enzimologia , Receptores Purinérgicos/efeitos dos fármacos , Ticlopidina/análogos & derivados , Adenosina/análogos & derivados , Adenosina/metabolismo , Difosfato de Adenosina/metabolismo , Difosfato de Adenosina/farmacologia , Adulto , Sítios de Ligação , Clopidogrel , Humanos , Masculino , Agregação Plaquetária/efeitos dos fármacos , Inibidores da Agregação Plaquetária/farmacologia , Glicoproteínas da Membrana de Plaquetas/metabolismo , Receptores Purinérgicos/metabolismo , Tionucleotídeos/metabolismo , Trombina/farmacologia , Ticlopidina/farmacologia
17.
Acta Eur Fertil ; 22(3): 177-9, 1991.
Artigo em Inglês | MEDLINE | ID: mdl-1839483

RESUMO

The activity of the blocking factor (BF) was studied in 88 patients affected by recurrent abortion syndrome (RAS) by means of the determination of lymphocyte proliferation rate (LPR) in one-way mixed maternal-paternal lymphocyte cultures (MLC). Forty patients (45.5%) showed inadequate blocking activity (LPR greater than 80%). Pearson's correlation did not reveal any link between patient age and LPR (m2 = 0.031), or between LPR and number of aborted pregnancy (m20.058). Fifteen of the 88 patients had had only two consecutive abortions, but Pearson's correlation did not result in any particular differences in the link between LPR and number of abortions in this group; we therefore felt perfectly justified in extending the study to these subjects.


Assuntos
Aborto Habitual/etiologia , Antígenos de Neoplasias/sangue , Adulto , Feminino , Idade Gestacional , Humanos , Teste de Cultura Mista de Linfócitos , Idade Materna , Gravidez
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