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Safety and efficiency of emergency department interrogation of cardiac devices
Clinical and Experimental Emergency Medicine ; (4): 239-244, 2016.
Artículo en Inglés | WPRIM | ID: wpr-643740
ABSTRACT

OBJECTIVE:

Patients with implanted cardiac devices may wait extended periods for interrogation in emergency departments (EDs). Our purpose was to determine if device interrogation could be done safely and faster by ED staff.

METHODS:

Prospective randomized, standard therapy controlled, trial of ED staff device interrogation vs. standard process (SP), with 30-day follow-up. Eligibility criteria ED presentation with a self-report of a potential device related complaint, with signed informed consent. SP interrogation was by company representative or hospital employee.

RESULTS:

Of 60 patients, 42 (70%) were male, all were white, with a median (interquartile range) age of 71 (64 to 82) years. No patient was lost to follow up. Of all patients, 32 (53%) were enrolled during business hours. The overall median (interquartile range) ED vs. SP time to interrogation was 98.5 (40 to 260) vs. 166.5 (64 to 412) minutes (P=0.013). While ED and SP interrogation times were similar during business hours, 102 (59 to 138) vs. 105 (64 to 172) minutes (P=0.62), ED interrogation times were shorter vs. SP during non-business hours; 97 (60 to 126) vs. 225 (144 to 412) minutes, P=0.002, respectively. There was no difference in ED length of stay between the ED and SP interrogation, 249 (153 to 390) vs. 246 (143 to 333) minutes (P=0.71), regardless of time of presentation. No patient in any cohort suffered an unplanned medical contact or post-discharge adverse device related event.

CONCLUSION:

ED staff cardiac device interrogations are faster, and with similar 30-day outcomes, as compared to SP.
Asunto(s)

Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Estudios Prospectivos / Estudios de Cohortes / Estudios de Seguimiento / Desfibriladores Implantables / Comercio / Urgencias Médicas / Medicina de Emergencia / Servicio de Urgencia en Hospital / Perdida de Seguimiento / Consentimiento Informado Tipo de estudio: Ensayo Clínico Controlado / Estudio de etiología / Estudio de incidencia / Estudio observacional / Estudio pronóstico / Factores de riesgo Límite: Humanos / Masculino Idioma: Inglés Revista: Clinical and Experimental Emergency Medicine Año: 2016 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Estudios Prospectivos / Estudios de Cohortes / Estudios de Seguimiento / Desfibriladores Implantables / Comercio / Urgencias Médicas / Medicina de Emergencia / Servicio de Urgencia en Hospital / Perdida de Seguimiento / Consentimiento Informado Tipo de estudio: Ensayo Clínico Controlado / Estudio de etiología / Estudio de incidencia / Estudio observacional / Estudio pronóstico / Factores de riesgo Límite: Humanos / Masculino Idioma: Inglés Revista: Clinical and Experimental Emergency Medicine Año: 2016 Tipo del documento: Artículo