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An Intervention for Elderly in Emergency Services

3 de febrero de 2015 actualizado por: Maria del Carmen Garcia-Pena, Coordinación de Investigación en Salud, Mexico

Elderly in Emergency Services: Effectiveness of an Intervention to Improve Health Outcomes

-Can a scheme based on inter geriatricians visiting nurse consultants and reduce negative impacts on the health of elderly over 70 years ?

Descripción general del estudio

Descripción detallada

- Usual care as the comparison group

Usual care or standard refers to those processes or services that the elderly claimant receives the IMSS services network, after the acute phase of their illness has been stabilized and is defined that can be discharged from the emergency department, following clinical and therapeutic recommendations for improving their health.

  • Elders risk population for emergency

The aging population brings a major change in health conditions and social conditions around the elderly, the analysis of the elderly population is considered according to functionality and risks of old age, when it comes to care services emergency, care becomes more critical as the elderly are older, have been identified adults of 70 and over as more vulnerable to health services, especially for the emergency services as they do not exhibit classic patterns to acute events of prevalent diseases.

  • Functionality and dependence

The commitment of the functionality in adults older than 65 may be present in 5% of cases, while in over 70 years this figure rises to 50% or more. Functional impairment may be a "marker" of the effect of systemic disease on the patient and is also an indicator of severity of disease because it measures the ability of independence

The accumulation of normal aging characteristics define a threshold, which once pierced, tends to increase the propensity for loss of functional abilities due to aging. However, not everyone ages the same way, since factors such as inherited genetic capital, especially the accumulation of risks associated with lifestyle and work activities, and the opportunity to identify the disease in its period latency coupled with the accessibility and use of health services, can delay or exacerbate the loss of functionality and increase the dependency of the elderly.

  • Quality of life of older

Frailty in the elderly is a state of increased susceptibility due to less booking multiple physiological systems resulting in lower resilience, negative energy balance, sarcopenia, decreased strength and reduced exercise tolerance. Frailty is associated with adverse health outcomes such as institutionalization, falls, reduced performance status and increased mortality.

Tipo de estudio

Intervencionista

Inscripción (Actual)

1400

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

    • Distrito Federal
      • Mexico, Distrito Federal, México, 06725
        • XXI Century National Medical

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

70 años y mayores (Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • Adults 70 and over.
  • Both sexes
  • Affiliation force in the IMSS
  • Attending spontaneously or referred to the emergency department of hospitals in the study.
  • Agree to participate in the study phase in observational or intervention by signed written informed consent

Exclusion Criteria:

  1. Adults 70 and older whose income is service by:

    a. A very serious acute condition with imminent risk to life and requires immediate emergency care, cataloged by the Triage system marked by the IMSS as Red or (state the patient's functional impairment characterized by high and low, with imminent risk life or the integrity and function of some of their organs and requires immediate medical attention since his arrival to the emergency room) or require emergency care (patient condition characterized by acute and severe functional impairment, life-threatening or the integrity and function of some of their organs and requires medical attention within the next 10 minutes after arrival at the emergency department).

    • An automobile accident
    • Burn-grade II or III
    • Partial or total unconsciousness
    • Severe cognitive impairment
  2. Individuals who do not agree to participate in the study

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Investigación de servicios de salud
  • Asignación: N / A
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Único

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Sin intervención: Basal phase
Integrated measurement of all variables involved impact and frequency of prior use of health services and specifically to the emergency room, service access, patient characteristics, features for the classification of frailty, cognitive impairment and depression, why consultation, triage scale level on admission to the service and to the service variables in terms of length of stay, diagnosis and medical management, and related services with internal consultants percentage of inpatients discharged or deceased, in further analysis the researchers undertake group estimating frequency of use and the identification of factors associated with the use of emergency departments and adverse events
Participants who were assigned to the intervention will be evaluated jointly by the medical service by a medical specialist in geriatrics and a nurse trained in gerontology and geriatrics. The doctor will monitor the apparition and / or aggravation of any geriatric syndromes already established by the specialty in geriatrics, namely, polypharmacy, delirium, dementia, depression, risk of falls, etc.. The nurse will monitor and follow up in four areas I. medical issues (pressure ulcers, infusion, mobility); II. Mental and emotional state and coping strategies with hospitalization; III. functionality, and IV. Atmosphere (A. Service status, architectural difficulties for mobility, bathing etc. B. Support Network, caregiver, and C. hardship)

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in hand grip strength (HS) as a physical performance test
Periodo de tiempo: Basal and Six months
A standardized technique and digital dynamometers (Exacta TM) wil lbe used, and the best result of two tests in the dominant hand will be used for analysis. No cut-off points will be applied; instead the variable will be assessed as a continuous one with kilograms as the units of measure.
Basal and Six months

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Evaluation of individual and institutional impact
Periodo de tiempo: Six Months

Evaluate the impact of a scheme based on internal consultation geriatricians and home visiting nurses oriented elders 70 and over, in terms of individual outcomes and health services:

a. Individual Impacts:

a.1 Primary:

• Fragility

Six Months

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
Quantify hospital readmissions
Periodo de tiempo: One Year
Estimate the readmission to hospital adverse events in adults older than 70 years, underwent surgery and its comparison group from discharge from service
One Year

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Investigadores

  • Investigador principal: Carmen García-Peña, PhD, Epidemiological Research Unit and Health Services. XXI Century National Medical Center
  • Silla de estudio: Sergio Sánchez García, PhD, Epidemiological Research Unit and Health Services. XXI Century National Medical Center
  • Silla de estudio: Teresa Juarez Cedillo, PhD, Epidemiological Research Unit and Health Services. XXI Century National Medical Center
  • Silla de estudio: Rogelio Moncada Tobias, Doctor, Emergency Service. General Hospital Zone No.2
  • Silla de estudio: Nubia Franco Alvarez, Doctor, Internal Medicine. General Hospital Zone No. 2
  • Silla de estudio: José García González, Master, Department of Nephrology. Regional General Hospital No. 1
  • Silla de estudio: Ulises Pérez Zepeda, Master, Institute of Geriatrics
  • Silla de estudio: Leslie Viridiana Robles Jiménez, Doctor, National Institute of Psychiatry

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio

1 de junio de 2013

Finalización primaria (Actual)

1 de marzo de 2014

Fechas de registro del estudio

Enviado por primera vez

10 de octubre de 2012

Primero enviado que cumplió con los criterios de control de calidad

11 de octubre de 2012

Publicado por primera vez (Estimar)

15 de octubre de 2012

Actualizaciones de registros de estudio

Última actualización publicada (Estimar)

4 de febrero de 2015

Última actualización enviada que cumplió con los criterios de control de calidad

3 de febrero de 2015

Última verificación

1 de febrero de 2015

Más información

Términos relacionados con este estudio

Términos MeSH relevantes adicionales

Otros números de identificación del estudio

  • R-201 l-785-056

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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