RESUMEN
BACKGROUND: Health libraries contribute to many activities of a health care organisation. Impact assessment needs to capture that range of contributions. OBJECTIVES: To develop and pilot a generic impact questionnaire that: (1) could be used routinely across all English NHS libraries; (2) built on previous impact surveys; and (3) was reliable and robust. METHODS: This collaborative project involved: (1) literature search; (2) analysis of current best practice and baseline survey of use of current tools and requirements; (3) drafting and piloting the questionnaire; and (4) analysis of the results, revision and plans for roll out. FINDINGS: The framework selected was the International Standard Methods And Procedures For Assessing The Impact Of Libraries (ISO 16439). The baseline survey (n = 136 library managers) showed that existing tools were not used, and impact assessment was variable. The generic questionnaire developed used a Critical Incident Technique. Analysis of the findings (n = 214 health staff and students), plus comparisons with previous impact studies indicated that the questionnaire should capture the impact for all types of health libraries. CONCLUSIONS: The collaborative project successfully piloted a generic impact questionnaire that, subject to further validation, should apply to many types of health library and information services.
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Benchmarking/métodos , Práctica Clínica Basada en la Evidencia/métodos , Bibliotecas Médicas , Garantía de la Calidad de Atención de Salud , Humanos , Servicios de Información , Encuestas y Cuestionarios , Reino UnidoAsunto(s)
Crizotinib/administración & dosificación , Pulmón , Orquiectomía/métodos , Neoplasias Testiculares , Testículo , Adenocarcinoma del Pulmón/tratamiento farmacológico , Adenocarcinoma del Pulmón/patología , Adenocarcinoma Mucinoso/tratamiento farmacológico , Adenocarcinoma Mucinoso/patología , Adulto , Antineoplásicos/administración & dosificación , Humanos , Pulmón/diagnóstico por imagen , Pulmón/patología , Masculino , Estadificación de Neoplasias , Neoplasias Testiculares/patología , Neoplasias Testiculares/secundario , Neoplasias Testiculares/cirugía , Testículo/diagnóstico por imagen , Testículo/patología , Tomografía Computarizada por Rayos X/métodos , Resultado del Tratamiento , Ultrasonografía/métodosRESUMEN
Marginal zone lymphoma (MZL) is the third most common subtype of B-cell non-Hodgkin lymphoma. Here we perform a two-stage GWAS of 1,281 MZL cases and 7,127 controls of European ancestry and identify two independent loci near BTNL2 (rs9461741, P=3.95 × 10(-15)) and HLA-B (rs2922994, P=2.43 × 10(-9)) in the HLA region significantly associated with MZL risk. This is the first evidence that genetic variation in the major histocompatibility complex influences MZL susceptibility.
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Linfoma de Células B de la Zona Marginal/genética , Complejo Mayor de Histocompatibilidad/genética , Glicoproteínas de Membrana/genética , Polimorfismo de Nucleótido Simple/genética , Población Blanca/genética , Butirofilinas , Biología Computacional , Estudio de Asociación del Genoma Completo , Genotipo , HumanosRESUMEN
Chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids (CLIPPERS) is an inflammatory disease of the central nervous system that predominantly involves the pons and cerebellum and that improves with immunosuppressive treatment. Only recently described, the etiology is unknown, diagnosis is difficult and long-term neurological sequelae may occur without aggressive treatment. Herein, we describe a 59-year-old woman who presented with subcutaneous nodules affecting her face, trunk, limbs and an indurated annular erythematous lesion on her forearm. This was associated with marked dysesthesia of her skin, refractory to treatment. There was a 4-year history of dysequilibrium, vertigo, truncal and gait ataxia with progressive neurological symptoms. Skin biopsy of the annular nodular lesion showed a lymphohistiocytic infiltrate in dermis and subcutis with a striking lymphocyte-dominant infiltrate that was perineural and formed a nodular collection extending along a prominent subcutaneous nerve. Immunophenotyping indicated a marked predominance of T cells that were CD3 positive with a 2 : 1 CD4 : CD8 ratio. Scattered histiocytes were present but no well-formed granulomas or vasculitis. Magnetic resonance imaging studies showed changes in the pontine, brain stem and cerebellar region, which subsequently were defined as characteristic for CLIPPERS, but no brain biopsy was pursued. The marked neural skin symptoms and the cutaneous histopathological findings indicate that the skin may be an additional target organ in CLIPPERS, and the immune response may be directed against a common neural antigen. In radiologically typical CLIPPERS, identification of clinical skin lesions particularly subcutaneous nodules and biopsy may potentially form a basis for tissue diagnosis in this syndrome.
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Encefalitis/patología , Inflamación/patología , Linfocitosis/patología , Enfermedades de la Piel/patología , Linfocitos T/patología , Tronco Encefálico/patología , Cerebelo/patología , Femenino , Humanos , Imagen por Resonancia Magnética , Persona de Mediana Edad , Puente/patologíaRESUMEN
There is inconsistent evidence that increasing birth order may be associated with risk of non-Hodgkin lymphoma (NHL). The authors examined the association between birth order and related variables and NHL risk in a pooled analysis (1983-2005) of 13,535 cases and 16,427 controls from 18 case-control studies within the International Lymphoma Epidemiology Consortium (InterLymph). Overall, the authors found no significant association between increasing birth order and risk of NHL (P-trend = 0.082) and significant heterogeneity. However, a significant association was present for a number of B- and T-cell NHL subtypes. There was considerable variation in the study-specific risks which was partly explained by study design and participant characteristics. In particular, a significant positive association was present in population-based studies, which had lower response rates in cases and controls, but not in hospital-based studies. A significant positive association was present in higher-socioeconomic-status (SES) participants only. Results were very similar for the related variable of sibship size. The known correlation of high birth order with low SES suggests that selection bias related to SES may be responsible for the association between birth order and NHL.
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Orden de Nacimiento , Linfoma no Hodgkin/epidemiología , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Estudios de Casos y Controles , Femenino , Humanos , Linfoma no Hodgkin/clasificación , Masculino , Persona de Mediana Edad , Hermanos , Factores Socioeconómicos , Adulto JovenRESUMEN
BACKGROUND: Researchers in clinical trials usually pay close attention to therapist selection, training, supervision and monitoring, but the extent of this input has not been systematically documented. AIMS: To describe the extent of training and supervision activity within clinical trials, and to consider any implications for transporting therapies from research to routine clinical contexts. METHOD: Twenty-seven randomized studies examining the efficacy of CBT interventions for people with depression or anxiety disorders were selected on the basis of their quality and impact on the field. Published and unpublished sources were used to gather information about therapist selection, training and supervision within these trials. RESULTS: The review identified the extent of investment by researchers in assuring therapist expertise, adherence and competence. It also indicated inconsistencies in the clarity with which this input was reported. CONCLUSIONS: The ubiquity of intervention-specific training in research contexts risks being overlooked when commissioning evidence-based therapies in routine practice. This has clear implications for the likely effectiveness of interventions. Greater consistency in the reporting of training in clinical trials may help to draw attention to the role of training and supervision in maximizing clinical outcomes.
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Ensayos Clínicos como Asunto , Terapia Cognitivo-Conductual/educación , Educación , Pautas de la Práctica en Medicina/organización & administración , Humanos , Competencia ProfesionalRESUMEN
Adaptation paradigms highlight the dynamic nature of face coding and suggest that identity is coded relative to an average face that is tuned by experience. In low-level vision, adaptive coding can enhance sensitivity to differences around the adapted level. We investigated whether sensitivity to differences around the average face is similarly enhanced. Converging evidence from three paradigms showed no enhancement. Discrimination of small interocular spacing differences was not better for faces close to the average (Study 1). Nor was perceived similarity reduced for face pairs close to (spanning) the average (Study 2). On the contrary, these pairs were judged most similar. Maximum likelihood perceptual difference scaling (Studies 3 and 4) confirmed that sensitivity to differences was reduced, not enhanced, around the average. We conclude that adaptive face coding does not enhance discrimination around the average face.
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Discriminación en Psicología , Cara , Percepción Visual , Adaptación Psicológica , Adolescente , Adulto , Ojo/anatomía & histología , Expresión Facial , Femenino , Humanos , Masculino , Persona de Mediana Edad , Modelos Psicológicos , Reconocimiento Visual de Modelos , Estimulación Luminosa/métodos , Reconocimiento en Psicología , Umbral SensorialAsunto(s)
Carcinoma de Células Escamosas/patología , Neoplasias del Oído/patología , Oído Interno/patología , Enfermedades del Laberinto/patología , Anciano , Transformación Celular Neoplásica/patología , Enfermedades Cerebelosas/patología , Enfermedades Cerebelosas/cirugía , Ángulo Pontocerebeloso , Quiste Epidérmico/patología , Quiste Epidérmico/cirugía , Humanos , Imagen por Resonancia Magnética , MasculinoRESUMEN
The last 20 years have seen a dramatic change in the way we classify, and therefore diagnose, lymphoma. Two decades ago, the International Working Formulation enabled diagnosis and management on the basis of H&E sections alone, with no mandatory requirement for immunophenotyping, molecular studies or any other ancillary investigations. The concept of categorisation by 'clinicopathological entities' defined by clinical features, morphology, immunophenotype and more recently, genotype, began with the Kiel, and Lukes and Collins classifications in the late 1970s, becoming fully expressed in the REAL and subsequently WHO classifications. The current, multidisciplinary approach to categorisation adds significantly to the task facing the anatomical pathologist, since it requires distribution of biopsy material to all the appropriate specialised laboratories, the gathering of a range of cross-disciplinary information, the correlation of all diagnostic findings, deduction of a definitive diagnosis and, finally, integration of all the above into a single multiparameter report. In this review, we summarise the contemporary approach to the biopsy, diagnosis and reporting of lymphoproliferative disorders.
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Ganglios Linfáticos/patología , Trastornos Linfoproliferativos/patología , Patología Clínica/métodos , Árboles de Decisión , Femenino , Humanos , Trastornos Linfoproliferativos/clasificación , Masculino , Organización Mundial de la SaludRESUMEN
This study prospectively examines the accuracy of immunohistochemical staining in the identification of mismatch repair defective (MMRD) colorectal cancer in routine clinical practice. The potential impact of this information on decisions regarding adjuvant treatment and germline testing were quantified. A consecutive series of fresh tissue (836 cancers) was obtained from 786 individuals undergoing curative surgery for colorectal cancer at one institution. As part of normal practice, each tumour was screened for the expression of MLH1 and MSH2 by immunohistochemical staining (IHC) and relevant clinicopathological details were documented. Microsatellite instability (MSI) was assessed using standard markers. Overall, 108 (13%) tumours showed loss of staining for either MLH1 (92 tumours) or MSH2 (16 tumours). The positive predictive value of mismatch repair IHC when used alone in the detection of MSI tumours was 88%, and the negative predictive value was 97%. Specificity and positive predictive value were improved by correlation with microsatellite status. Tumour stage (HR 3.5, 95% CI 2.0-6.0), vascular space invasion (HR 1.9, 95% CI 1.2-3.0) and mismatch repair deficiency (HR 0.2, 95% CI 0.05-0.87) were independent prognostic factors in stages II and III disease. Screening by mismatch repair IHC could reasonably have been expected to prevent ineffective treatment in 3.6% of stage II and 7.6% of stage III patients. The frequency of germline mismatch repair mutations was 0.8%, representing six unsuspected hereditary non-polyposis colorectal cancer (HNPCC) cases. Routine screening of colorectal cancers by mismatch repair IHC identifies individuals at low risk of relapse, and can prevent unnecessary adjuvant treatments in a significant number of individuals. Abnormal immunohistochemistry should be confirmed by microsatellite testing to ensure that false-positive results do not adversely impact on treatment decisions.
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Disparidad de Par Base/genética , Neoplasias Colorrectales/genética , Reparación del ADN , ADN de Neoplasias/genética , Proteínas Adaptadoras Transductoras de Señales , Adulto , Distribución por Edad , Anciano , Anciano de 80 o más Años , Proteínas Portadoras/genética , Neoplasias Colorrectales/patología , Femenino , Mutación de Línea Germinal , Humanos , Técnicas para Inmunoenzimas , Masculino , Persona de Mediana Edad , Homólogo 1 de la Proteína MutL , Proteína 2 Homóloga a MutS/genética , Proteínas de Neoplasias/genética , Estadificación de Neoplasias , Proteínas Nucleares/genética , Estudios ProspectivosRESUMEN
OBJECTIVE: To describe the clinical, radiologic and histopathologic features of endolymphatic sac tumors using the St Vincent's Hospital experience with these tumors to highlight important aspects of tumor diagnosis and treatment. Possible explanations are given for the apparent increasing incidence of these tumors. STUDY DESIGN: Retrospective review of the senior author's (P.A.F.) database of skull base lesions. SETTING: Tertiary referral teaching hospital. PATIENTS: All patients with a proven diagnosis of endolymphatic sac tumor treated at St Vincent's Hospital, Sydney. OUTCOME MEASURES: Survival in months, after surgery. RESULTS: Seven cases of endolymphatic sac tumors. All were treated surgically. Mean follow-up of 70.2 months (range, 6-144 mo). CONCLUSION: Endolymphatic sac tumors are becoming increasingly recognized because of awareness of their existence as a separate entity from middle ear tumors. This has been achieved by improved imaging and histopathologic techniques. Surgery is the mainstay of treatment.
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Adenocarcinoma Papilar , Neoplasias del Oído , Saco Endolinfático , Adenocarcinoma Papilar/diagnóstico , Adenocarcinoma Papilar/patología , Adenocarcinoma Papilar/cirugía , Adulto , Anciano , Neoplasias del Oído/diagnóstico , Neoplasias del Oído/patología , Neoplasias del Oído/cirugía , Saco Endolinfático/cirugía , Femenino , Estudios de Seguimiento , Humanos , Inmunohistoquímica , Masculino , Persona de Mediana Edad , Estudios Retrospectivos , Tomografía Computarizada por Rayos X , Resultado del TratamientoRESUMEN
Lymphoma classification is based on a multiparametric approach to diagnosis, in which clinical features, morphology, immunophenotype, karyotype and molecular characteristics are important to varying degrees. While in most cases, a diagnosis can be confidently established on the basis of morphology and immunophenotype alone, a small proportion of diagnostically difficult cases will rely on molecular studies to enable a definitive diagnosis. This review discusses the various molecular techniques available including Southern blotting (SB), polymerase chain reaction (PCR), fluorescence in situ hybridisation (FISH)--including multicolour-FISH/spectral karyotyping and comparative genomic hybridisation--and also gene expression profiling using cDNA microarray technology. Emphasis is given to the analysis of antigen receptor gene rearrangements and chromosomal translocations as they relate to lymphoma diagnosis and also in the setting of minimal residual disease (MRD) detection and monitoring. Laboratories performing these tests need to have expertise in these areas of testing, and there is a need for greater standardisation of molecular tests. It is important to know the sensitivity and specificity of each test as well as its limitations and the pitfalls in the interpretation of results. Above all, results of molecular testing should never be considered in isolation, and must always be interpreted in the context of clinical and other laboratory data.
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Linfoma/clasificación , Linfoma/diagnóstico , Técnicas de Diagnóstico Molecular , Southern Blotting , Perfilación de la Expresión Génica , Humanos , Hibridación Fluorescente in Situ , Cariotipificación , Linfoma/genética , Técnicas de Diagnóstico Molecular/métodos , Hibridación de Ácido Nucleico , Análisis de Secuencia por Matrices de Oligonucleótidos , Reacción en Cadena de la Polimerasa , Sensibilidad y EspecificidadRESUMEN
We describe two young men with cystic pituitary enlargement on magnetic resonance imaging (MRI) causing hypopituitarism. The first patient presented acutely unwell with headache and vomiting associated with anterior and posterior pituitary dysfunction. The second patient presented with hypopituitarism after a long history of hypogonadism. In both cases yellow/brown fluid was found at surgery and histological examination revealed inflammatory infiltrate with foamy histiocytes, lymphocytes and multinucleated giant cells containing cholesterol clefts. Full recovery of pituitary function occurred after surgery in the first but not the second patient. The first case is the first documented case of xanthomatous hypophysitis with recovery of pituitary function following surgery. The cases differed in duration of disease, as indicated by the long history of symptoms, the histological finding of marked fibrosis and the lack of recovery of pituitary function in the second. Xanthomatous pituitary lesions categorized in the literature as xanthomatous hypophysitis, xanthogranulomatous hypophysitis and xanthogranuloma of the sellar region have overlapping histological features. Our two cases revealed histological features that do not fit completely into any of the categories but share features of all three. These findings suggest that the various xanthomatous lesions of the sellar region may be a spectrum of a common inflammatory process rather than distinct pathological entities.
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Imagen por Resonancia Magnética , Enfermedades de la Hipófisis/diagnóstico , Xantomatosis/diagnóstico , Adulto , Humanos , Inflamación/etiología , Masculino , Enfermedades de la Hipófisis/etiología , Enfermedades de la Hipófisis/patología , Enfermedades de la Hipófisis/cirugía , Xantomatosis/complicaciones , Xantomatosis/patología , Xantomatosis/cirugíaRESUMEN
Most meningiomas are slow-growing tumors that do not rapidly recur after subtotal removal. After subtotal resection of a meningioma a 47-year-old woman developed a large extracranial recurrence 1 year later. The recurrence was resected successfully. On histological examination the typical characteristics of a meningioma were absent. Based on immunohistological and ultrastructural studies, the tumor was classified as a grade III meningioma of the newly recognized rhabdoid subtype.These tumors behave aggressively and should be treated accordingly.
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The feasibility of monitoring volatile flavor compounds formed by thermal treatment of skimmed milk powder in real time by atmospheric pressure chemical ionization mass spectrometry (APCIMS) was established. Skim milk powder samples were heated isothermally (70 to 120 degrees C) at different moisture contents (2.2 and 12.7 g water/100 g dry solids). Headspace was sampled and analyzed continuously in full scan mode (30-180 amu) by APCIMS. The identity of the volatile compounds monitored by APCIMS was confirmed by coupled GC-EI-APCIMS. The concentration measured by the APCIMS was the net effect of three processes, namely formation of the compound, partition from the skim milk powder into the gas phase, and dilution due to the headspace sampling method used. Preliminary experiments established that the technique could follow the effects of heating temperature and moisture content on the formation of selected compounds from skim milk powder.
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Calor , Espectrometría de Masas/métodos , Leche/química , Gusto , Animales , Presión Atmosférica , Conservación de Alimentos , Cromatografía de Gases y Espectrometría de Masas , Polvos , VolatilizaciónRESUMEN
PURPOSE: Identification of germline mutations in mismatch repair genes is increasingly being used to guide clinical practice in hereditary non-polyposis colon cancer. The aim of this study was to retrospectively assess the clinical utility of immunostaining and microsatellite instability testing in a group of individuals in whom germline testing of hMSH2 and hMLH1 had already been performed. METHODS: Individuals were identified from the records of family cancer clinics. A total of thirty-eight tumour blocks were retrieved from 28 kindreds. DNA was extracted and PCR amplification of six microsatellite markers was performed. Immunostaining was used to examine the expression of hMSH2 and hMLH1 protein. RESULTS: Of the 32 assessable tumours, 24 (75%) showed microsatellite instability. Most of the MSI-H cancers (92%) failed to express either hMLH1 or hMSH2. Deleterious germline mutations were identified in the proband in 12 of 28 families. Missense mutations were identified in 11 cases and no mutations in six probands. CONCLUSIONS: The use of germline genetic testing is indicated for a highly selected group of individuals. MSI testing and immunostaining are extremely useful tools which significantly improve the clinical interpretation of germline results. Ambiguity regarding the significance of missense mutations in hereditary bowel cancer suggests that these findings should be interpreted with caution.
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Disparidad de Par Base , Neoplasias Colorrectales Hereditarias sin Poliposis/genética , Reparación del ADN/genética , Proteínas de Unión al ADN , Repeticiones de Microsatélite/genética , Proteínas de Neoplasias/genética , Proteínas Proto-Oncogénicas/genética , Proteínas Adaptadoras Transductoras de Señales , Adulto , Anciano , Anciano de 80 o más Años , Proteínas Portadoras , Neoplasias Colorrectales/genética , Neoplasias Colorrectales/metabolismo , Neoplasias Colorrectales/patología , Neoplasias Colorrectales Hereditarias sin Poliposis/metabolismo , Neoplasias Colorrectales Hereditarias sin Poliposis/patología , Análisis Mutacional de ADN , Femenino , Genotipo , Mutación de Línea Germinal , Humanos , Técnicas para Inmunoenzimas , Masculino , Persona de Mediana Edad , Homólogo 1 de la Proteína MutL , Proteína 2 Homóloga a MutS , Proteínas de Neoplasias/metabolismo , Proteínas Nucleares , Fenotipo , Pronóstico , Proteínas Proto-Oncogénicas/metabolismo , Estudios RetrospectivosRESUMEN
BACKGROUND: Post-transplant lymphoproliferative disease (PTLD) is a serious, often fatal complication after solid organ transplantation. Primary Epstein-Barr virus (EBV) infection is the major risk factor for PTLD after lung transplantation, with 30% to 50% of EBV-naive patients who seroconvert and are diagnosed with PTLD. METHOD: In this study, we analyzed the incidence of PTLD in lung and heart-lung transplant recipients before 1996 (historic group) and then compared the impact of long-term anti-viral prophylaxis on the development of PTLD in EBV-seronegative recipients from January 1996 to December 2000 (post-1996 group). Routine induction therapy was not given after 1995. Patients not surviving 30 days, 25 of 341 (7.3%), were excluded. RESULTS: Historic group: PTLD developed in 7 of 167 (4.2%) patients, at a mean of 394 +/- 278 (95-885) days. The mortality was 87.5% at a mean follow-up of 186 +/- 207 (17-520) days after diagnosis. Post-1996 group: Eighteen of 149 (12.3%) patients were EBV seronegative at the time of transplantation, and of these 15 (83%) began receiving continuous anti-viral prophylaxis: acyclovir or valacyclovir or ganciclovir from January 1996. None of the EBV-seronegative recipients receiving continuous anti-viral prophylaxis were diagnosed with PTLD; however, 1 of 3 (33%) of the EBV-seronegative recipients who did not receive anti-viral prophylaxis were diagnosed with PTLD. In the EBV-seronegative recipients, no deaths had been caused by PTLD at a mean follow-up of 806 +/- 534 (39-1,084) days. In the post-1996 group, PTLD developed in 1 of 131 (0.76%) EBV-seropositive recipients. CONCLUSION: Continuous, specific anti-viral prophylaxis in high-risk EBV-seronegative recipients significantly reduces the incidence of PTLD after lung transplantation in the absence of induction therapy.