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1.
J Emerg Med ; 56(2): 191-196, 2019 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-30594351

RESUMEN

BACKGROUND: Acute appendicitis is common in the adult emergency department (ED). Computed tomography (CT) scan is frequently used to diagnose this condition, but ultrasound (US)-commonly used in pediatric diagnosis-may also have a role. OBJECTIVES: Review the clinical utility and define the frequency and diagnostic accuracy of US to diagnose appendicitis in an adult population in the ED setting. METHODS: Retrospective cohort study of patients who underwent appendiceal US in an academic, tertiary ED from July 2013-October 2015. RESULTS: There were 174 patients included, of which 39 (22%) had pathology-confirmed appendicitis. There were 25 patients who had an US scan that was positive for appendicitis, 146 (84%) were indeterminate, and 3 (1.7%) were negative. Among patients with a positive US, 25/25 (100%, 95% confidence interval [CI] 84-100%) had appendicitis, 32/146 (22%, 95% CI 16-29%) with an indeterminate US had appendicitis, and 0/3 (0%, 95% CI 0-6.2%) with a negative US had appendicitis. In the 28 definitive cases, US had a sensitivity of 64%, specificity of 2%, positive predictive value of 100%, and negative predictive value of 100%. The likelihood ratio positive and negative were 173 and 0, respectively. CONCLUSION: Our initial data suggest that an US that shows appendicitis seems to be reliable; however, a high prevalence of indeterminate studies limits the diagnostic utility as a universal approach in adult patients in the ED setting. Larger studies are needed to identify which patient populations would benefit from US as the initial imaging modality, what factors contribute to the large numbers of indeterminate results, and if any interventions may reduce the number of indeterminate results.


Asunto(s)
Apendicitis/diagnóstico , Ultrasonografía/métodos , Ultrasonografía/normas , Adolescente , Adulto , Estudios de Cohortes , Servicio de Urgencia en Hospital/organización & administración , Femenino , Humanos , Masculino , Persona de Mediana Edad , Estudios Prospectivos , Estudios Retrospectivos , Tomografía Computarizada por Rayos X/métodos , Ultrasonografía/tendencias , Estados Unidos
2.
Pathog Glob Health ; 109(6): 275-82, 2015 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-26260354

RESUMEN

We conducted a randomised single-blinded clinical trial of 100 cholera patients in Port-au-Prince, Haiti to determine if the probiotic Saccharomyces cerevisiae var. boulardii and the anti-diarrhoeal drug bismuth subsalicylate (BS) were able to reduce the duration and severity of cholera. Subjects received either: S. boulardii 250 mg, S. boulardii 250 mg capsule plus BS 524 mg tablet, BS 524 mg, or two placebo capsules every 6 hours alongside standard treatment for cholera. The length of hospitalisation plus the number and volume of emesis, stool and urine were recorded every 6 hours until the study subject was discharged (n = 83), left against medical advice (n = 11), or requested removal from the study (n = 6). There were no reported deaths or adverse study-related events. There were no statistically significant differences between the study arms and the outcomes of interest.


Asunto(s)
Antibacterianos/uso terapéutico , Bismuto/uso terapéutico , Cólera/tratamiento farmacológico , Cólera/terapia , Diarrea/prevención & control , Servicios Médicos de Urgencia/métodos , Compuestos Organometálicos/uso terapéutico , Probióticos/uso terapéutico , Saccharomyces , Salicilatos/uso terapéutico , Vibrio cholerae/efectos de los fármacos , Adulto , Antibacterianos/economía , Anticuerpos Antibacterianos , Cólera/economía , Cólera/epidemiología , Brotes de Enfermedades/economía , Servicios Médicos de Urgencia/economía , Heces/microbiología , Femenino , Fluidoterapia/economía , Haití/epidemiología , Humanos , Tiempo de Internación/economía , Tiempo de Internación/estadística & datos numéricos , Masculino , Índice de Severidad de la Enfermedad , Resultado del Tratamiento
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