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Идёт набор NCT07237334

A Prospective Cohort Study of Clinical and Process Outcomes of Older Adults That Transition Through the Geriatric Emergency Medicine Unit(GEM-U)

— Наблюдательное Frailty

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
Это наблюдательное исследование: исследуемое лечение участникам по протоколу не назначают.
Кому может быть актуально
Состояния в реестре: Frailty. Базовые параметры: от 75 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Ирландия
Следующий шаг
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Официальное название

A Prospective Cohort Study of the Clinical and Process Outcomes of Older Adults That Transition Through the Geriatric Emergency Medicine Unit (GEM-U)

Обзор

This study will characterise the patients using the Geriatric Emergency Medicine Unit, a unit which provides specialist care for patients aged 75 years and older attending the emergency department. It will examine how this specialist care impacts their health in terms of a number of different outcomes, such as; function, quality of life and health care usage; for example admission to the acute hospital.

Подробное описание

The emergency department is a particularly challenging and busy environment, particularly for older adults living with frailty. It is widely acknowledged throughout the literature and national healthcare strategy that these older adults require holistic, person centred care that targets the intricacies of multifaceted, complex health issues.

The geriatric emergency medicine unit (GEM-U) aims to provide such care through the framework of comprehensive geriatric assessment, with in-put from a team of healthcare disciplines. The main aim of this study is to look at how this specialist care impacts patient outcomes, such as acute admission. Clinical and process outcomes of participants will be examined using patient reported outcome measures, which will include;

1. Global measure of function (Barthel Index) 2. Delirium screen (4AT +/- Delirium Rating Scale)\* 3. Frailty status (Clinical Frailty Scale) 4. Nutritional status (Mini Nutritional Assesment) 5. Quality of life (EuroQoL-5D-5L). 6. Patient satisfaction (PSQ-18).

Participants will be followed at 30 days and 6 months post recruitment. All participants will give fully informed consent. The STrengthening the Reporting of OBservational studies in Epidemiology (STROBE) standardised reporting guidelines will be followed in the conduct and reporting of this research. Data will be statistically analysed

Первичные конечные точки

  • Our primary outcome is incidence of hospital admission at index GEM-U presentation [Срок оценки: Patients are followed at 30 days and 6 months]
Вторичные конечные точки (5)
  • Mortality [Срок оценки: Patients are followed at 30 days and 6 months]
  • Unscheduled ED revisit [Срок оценки: Patients are followed at 30 days and 6 months]
  • Unscheduled hospital visit(s) [Срок оценки: Patients are followed at 30 days and 6 months]
  • Nursing home admission [Срок оценки: Patients are followed at 30 days and 6 months]
  • Healthcare utilization (GP visit, out-patient geriatric services, PHN visit, HSCP services) [Срок оценки: Patients are followed at 30 days and 6 months]

Критерии участия

Критерии включения

  • Older adults aged ≥75 years
  • Manchester Triage System category 2-5
  • Screen positive for risk of adverse outcomes after ED visit (≥ 2 on ISAR screening tool)
  • Presenting with a medical condition
  • Reviewed by the Older Persons Integrated Care Team

Критерии исключения

  • Patients presenting with a non-medical issue including major trauma or hip fracture
  • Patients presenting with acute stroke or transient ischaemic attack
  • Patients more appropriate to another alternative pathway e.g. deep vein thrombosis pathway, low risk chest pain pathway
  • Patients with acute coronary syndrome or unstable arrthymia
  • Patients requiring care in the resuscitation room
  • Patients with head injury (unless appropriate assessment and management has been fully completed by ED team)
  • Patients with possible spinal injury (unless appropriate assessment and management has been fully completed by ED/orthopaedic team)
  • Patients with low Glasgow Coma Scale
  • Other exclusions at the discretion of the Older Persons Integrated Care team depending on team capacity and expertise
  • Exclusion criteria as set out above, are in line with those set out in the UHL Operating Policy of the Older Persons Integrated Care Team.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Модель наблюдения
Когортное

Центры проведения

Ирландия · 1 центр
  • University Hospital Limerick — Limerick

Идентификаторы

NCT: NCT07237334 · GEM-U2025

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗