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1.
Acute Med ; 18(4): 260, 2019.
Artículo en Inglés | MEDLINE | ID: mdl-31912061

RESUMEN

We read with interest "Non-Cardiac Chest Pain: Management in the Ambulatory Clinic setting" (Acute Med 2019;18(3)165-70). It is useful to know about the various musculoskeletal causes of chest pain, especially where specific treatment may be available.


Asunto(s)
Dolor en el Pecho , Dolor en el Pecho/etiología , Humanos
2.
JMIR Med Educ ; 3(2): e20, 2017 Oct 31.
Artículo en Inglés | MEDLINE | ID: mdl-29089291

RESUMEN

BACKGROUND: Web-based resources are commonly used by medical students to supplement curricular material. Three commonly used resources are UpToDate (Wolters Kluwer Inc), digital textbooks, and Wikipedia; there are concerns, however, regarding Wikipedia's reliability and accuracy. OBJECTIVE: The aim of this study was to evaluate the impact of Wikipedia use on medical students' short-term knowledge acquisition compared with UpToDate and a digital textbook. METHODS: This was a prospective, nonblinded, three-arm randomized trial. The study was conducted from April 2014 to December 2016. Preclerkship medical students were recruited from four Canadian medical schools. Convenience sampling was used to recruit participants through word of mouth, social media, and email. Participants must have been enrolled in their first or second year of medical school at a Canadian medical school. After recruitment, participants were randomized to one of the three Web-based resources: Wikipedia, UpToDate, or a digital textbook. During testing, participants first completed a multiple-choice questionnaire (MCQ) of 25 questions emulating a Canadian medical licensing examination. During the MCQ, participants took notes on topics to research. Then, participants researched topics and took written notes using their assigned resource. They completed the same MCQ again while referencing their notes. Participants also rated the importance and availability of five factors pertinent to Web-based resources. The primary outcome measure was knowledge acquisition as measured by posttest scores. The secondary outcome measures were participants' perceptions of importance and availability of each resource factor. RESULTS: A total of 116 medical students were recruited. Analysis of variance of the MCQ scores demonstrated a significant interaction between time and group effects (P<.001, ηg2=0.03), with the Wikipedia group scoring higher on the MCQ posttest compared with the textbook group (P<.001, d=0.86). Access to hyperlinks, search functions, and open-source editing were rated significantly higher by the Wikipedia group compared with the textbook group (P<.001). Additionally, the Wikipedia group rated open access editing significantly higher than the UpToDate group; expert editing and references were rated significantly higher by the UpToDate group compared with the Wikipedia group (P<.001). CONCLUSIONS: Medical students who used Wikipedia had superior short-term knowledge acquisition compared with those who used a digital textbook. Additionally, the Wikipedia group trended toward better posttest performance compared with the UpToDate group, though this difference was not significant. There were no significant differences between the UpToDate group and the digital textbook group. This study challenges the view that Wikipedia should be discouraged among medical students, instead suggesting a potential role in medical education.

3.
Acute Med ; 15(4): 209-211, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-28112290

RESUMEN

A previously healthy 35-year old man presented to hospital with acute leg weakness following an alcohol binge. On assessment, tachycardia, urinary retention and bilateral upper and lower limb proximal weakness with preserved peripheral power were noted. Biochemistry revealed marked hypokalaemia, which responded to intravenous replacement, and biochemical thyrotoxicosis, leading to the diagnosis of Thyrotoxic Periodic Paralysis (TPP). Anti-thyroid therapy and beta-blockers were commenced and his neurological symptomatology resolved as he became progressively euthyroid. TPP is a rare acquired subtype of hypokalaemic periodic paralysis, typically causing proximal muscle weakness associated with thyrotoxicosis. It is most common in young Asian males. Acute treatment requires cautious oral potassium supplementation, beta-blockade, and anti-thyroid therapy. TPP is prevented by maintaining euthyroidism; otherwise recurrence is likely.


Asunto(s)
Antagonistas Adrenérgicos beta/administración & dosificación , Antitiroideos/administración & dosificación , Parálisis Periódica Hipopotasémica/tratamiento farmacológico , Potasio/administración & dosificación , Tirotoxicosis/tratamiento farmacológico , Enfermedad Aguda , Adulto , Estudios de Seguimiento , Humanos , Hipopotasemia/diagnóstico , Hipopotasemia/etiología , Parálisis Periódica Hipopotasémica/diagnóstico , Infusiones Intravenosas , Extremidad Inferior , Masculino , Monitoreo Fisiológico , Debilidad Muscular/diagnóstico , Debilidad Muscular/etiología , Medición de Riesgo , Tirotoxicosis/diagnóstico , Resultado del Tratamiento
5.
Acute Med ; 13(3): 121-5, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-25229063

RESUMEN

Acute confusion and hyponatraemia are common presentations in acute medicine. We report two cases of anti-voltage gated potassium channel (VGKC) antibody-related limbic encephalitis highlighting the variable presentation of this condition. Both patients were thoroughly investigated with MRI scan of brain, lumbar puncture, EEG as well as infective and autoimmune screens for encephalitis. Anti-VGKC antibodies were positive for both patients and prompt treatment with immunotherapy yielded good recovery. Patients presenting with confusion and seizures who have no demonstrable infectious or metabolic cause should have investigation for an autoimmune cause expedited. In addition, psychiatric presentations with atypical features such as drowsiness should prompt similar investigations. The outcome of anti-VGKCrelated limbic encephalitis is improved with early treatment employing steroids or immunotherapy.


Asunto(s)
Encéfalo/patología , Encefalitis Límbica/diagnóstico , Imagen por Resonancia Magnética/métodos , Convulsiones/diagnóstico , Punción Espinal/métodos , Adulto , Diagnóstico Diferencial , Femenino , Humanos , Encefalitis Límbica/complicaciones , Masculino , Convulsiones/etiología
6.
Semin Dial ; 26(2): 159-63, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23432369

RESUMEN

Wikipedia, a multilingual online encyclopedia, is a common starting point for patient medical searches. As its articles can be authored and edited by anyone worldwide, the credibility of the medical content of Wikipedia has been openly questioned. Wikipedia medical articles have also been criticized as too advanced for the general public. This study assesses the comprehensiveness, reliability, and readability of nephrology articles on Wikipedia. The International Statistical Classification of Diseases and Related problems, 10th Edition (ICD-10) diagnostic codes for nephrology (N00-N29.8) were used as a topic list to investigate the English Wikipedia database. Comprehensiveness was assessed by the proportion of ICD-10 codes that had corresponding articles. Reliability was measured by both the number of references per article and proportion of references from substantiated sources. Finally, readability was assessed using three validated indices (Flesch-Kincaid grade level, Automated readability index, and Flesch reading ease). Nephrology articles on Wikipedia were relatively comprehensive, with 70.5% of ICD-10 codes being represented. The articles were fairly reliable, with 7.1 ± 9.8 (mean ± SD) references per article, of which 59.7 ± 35.0% were substantiated references. Finally, all three readability indices determined that nephrology articles are written at a college level. Wikipedia is a comprehensive and fairly reliable medical resource for nephrology patients that is written at a college reading level. Accessibility of this information for the general public may be improved by hosting it at alternative Wikipedias targeted at a lower reading level, such as the Simple English Wikipedia.


Asunto(s)
Enciclopedias como Asunto , Internet , Nefrología/educación , Educación del Paciente como Asunto , Bibliometría , Humanos
9.
Br J Hosp Med (Lond) ; 73(2): C30-2, 2012 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-22504713

RESUMEN

Rhabdomyolysis is the destruction of a significant amount of striated muscle, leading to disruptions in fluid balance, electrolytes and renal function. It may have either traumatic (such as crush injury) or non-traumatic causes. Diagnosis is typically made through the timely determination of the serum creatine kinase activity in a patient with a suggestive history or clinical features. Treatment is supportive, with generous intravenous hydration and correction of electrolyte abnormalities. Sometimes haemofiltration or dialysis is required, but the renal prognosis is generally good.


Asunto(s)
Rabdomiólisis/fisiopatología , Rabdomiólisis/terapia , Síndrome de Aplastamiento/complicaciones , Diagnóstico Diferencial , Humanos , Enfermedades Musculares/complicaciones , Rabdomiólisis/diagnóstico , Rabdomiólisis/etiología , Urinálisis
10.
J Med Internet Res ; 13(1): e14, 2011 Jan 31.
Artículo en Inglés | MEDLINE | ID: mdl-21282098

RESUMEN

The Internet has become an important health information resource for patients and the general public. Wikipedia, a collaboratively written Web-based encyclopedia, has become the dominant online reference work. It is usually among the top results of search engine queries, including when medical information is sought. Since April 2004, editors have formed a group called WikiProject Medicine to coordinate and discuss the English-language Wikipedia's medical content. This paper, written by members of the WikiProject Medicine, discusses the intricacies, strengths, and weaknesses of Wikipedia as a source of health information and compares it with other medical wikis. Medical professionals, their societies, patient groups, and institutions can help improve Wikipedia's health-related entries. Several examples of partnerships already show that there is enthusiasm to strengthen Wikipedia's biomedical content. Given its unique global reach, we believe its possibilities for use as a tool for worldwide health promotion are underestimated. We invite the medical community to join in editing Wikipedia, with the goal of providing people with free access to reliable, understandable, and up-to-date health information.


Asunto(s)
Información de Salud al Consumidor , Enciclopedias como Asunto , Salud Global , Promoción de la Salud/métodos , Internet , Salud Pública , Humanos , Difusión de la Información , Servicios de Información , Educación del Paciente como Asunto
12.
Clin Exp Med ; 9(4): 291-6, 2009 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-19543954

RESUMEN

In order to determine the glycosylation pattern for IgD, and to examine whether there are changes in the pattern of IgD and IgA1 O-glycosylation in patients with hyperimmunoglobulinaemia D and periodic fever syndrome (HIDS) during acute febrile attacks and during periods of quiescence, serum was obtained from 20 patients with HIDS and 20 control subjects. In the HIDS group, serum was obtained either during an acute febrile episode (n = 9) or during a period of quiescence (n = 11). The O-glycosylation profiles of native and desialylated IgA1 and IgD were measured in an ELISA-type system using the lectins Helix aspersa and peanut agglutinin, which bind to alternative forms of O-glycan moieties. IgD is more heavily O-galactosylated and less O-sialylated than IgA1 in healthy subjects. HIDS is associated with more extensive O-galactosylation of IgD and a reduction in O-sialylation of both IgD and IgA1. These changes are present both during acute febrile attacks and periods of quiescence. The T cell IgD receptor is a lectin with binding affinity for the O-glycans of both IgD and IgA1. The observed changes in IgD and IgA1 O-glycosylation are likely to have a significant effect on IgD/IgA1-T cell IgD receptor interactions including basal immunoglobulin synthesis, and possibly myeloid IgD receptor-mediated cytokine release.


Asunto(s)
Fiebre/inmunología , Inmunoglobulina A/sangre , Inmunoglobulina D/sangre , Deficiencia de Mevalonato Quinasa/inmunología , Adolescente , Adulto , Estudios de Casos y Controles , Ensayo de Inmunoadsorción Enzimática , Femenino , Glicosilación , Humanos , Lectinas/metabolismo , Masculino , Deficiencia de Mevalonato Quinasa/patología , Persona de Mediana Edad , Receptores Fc/metabolismo , Síndrome , Adulto Joven
14.
J Am Soc Nephrol ; 17(4): 1192-9, 2006 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-16510764

RESUMEN

In IgA nephropathy (IgAN), serum IgA1 with abnormal O-glycosylation preferentially deposits in the glomerular mesangium. The control of O-glycosylation is poorly understood. Among Ig isotypes, only IgD, produced early in B cell development, and IgA1, produced by mature B cells, are O-glycosylated. For investigation of the stage of B cell maturation at which the defect seen in IgAN arises, the O-glycosylation of serum IgA1 and IgD was studied in IgAN and controls. Serum was obtained from 20 patients with IgAN and 20 control subjects. The O-glycosylation profiles of native and desialylated IgA1 and IgD were measured in an ELISA-type system using the lectins Helix aspersa and peanut agglutinin, which bind to alternative forms of O-glycan moieties. The lectin-binding patterns of the two immunoglobulins differed in all participants, with that of IgD suggesting that it is more heavily galactosylated than IgA1. Defective O-glycosylation of IgA1, probably taking the form of reduced galactosylation, was confirmed in IgAN in this study. This undergalactosylation was not shared by IgD; in contrast, IgD carried more galactosylated O-glycans in IgAN than controls. The contrasting lectin-binding patterns of IgA1 and IgD shows that Ig O-glycosylation is differentially controlled during B cell maturation. Compared with controls, O-glycosylation in IgAN is incomplete in IgA1 but more complete in IgD. These observations show that abnormal IgA1 O-glycosylation in IgAN is not due to an inherent defect in glycosylation mechanisms but arises only at a later stage in B cell development and may be secondary to aberrant immunoregulation.


Asunto(s)
Glomerulonefritis por IGA/inmunología , Inmunoglobulina D/sangre , Adulto , Anciano , Linfocitos B/inmunología , Linfocitos B/patología , Sitios de Unión , Secuencia de Carbohidratos , Estudios de Casos y Controles , Diferenciación Celular , Ensayo de Inmunoadsorción Enzimática , Femenino , Galactosa/química , Glomerulonefritis por IGA/patología , Glicosilación , Humanos , Inmunoglobulina A/sangre , Inmunoglobulina A/química , Inmunoglobulina D/química , Lectinas , Masculino , Persona de Mediana Edad , Datos de Secuencia Molecular
15.
Lancet ; 362(9392): 1327, 2003 Oct 18.
Artículo en Inglés | MEDLINE | ID: mdl-14575983
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