跳至主要内容
临床试验/NCT00157612
NCT00157612已完成不适用

A Randomized Control Trial of a Clinical Pathway for Nursing Home Pneumonia.

McMaster University0 个研究点目标入组 680 人开始时间: 2001年1月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
680
主要终点
Hospital admission, length of stay

研究概览

简要总结

Nursing home residents are frequently transferred to hospital for management of pneumonia. This often leads to hospital related complications and is a burden on the acute care health system. The purpose of this study is to assess whether managing residents with pneumonia and lower respiratory tract infection on site in the nursing home can reduce hospital admissions and can reduce complications and improve quality of life for residents. We have randomized residents with nursing home acquired pneumonia to on-site management, using a clinical pathway, versus usual care.

详细描述

We conducted a cluster-randomized controlled trial where nursing homes were randomized to either use of a clinical pathway or usual care for management of nursing home acquired pneumonia. The clinical pathway included chest radiographs performed on-site in the nursing home by a mobile x-ray unit, use of hypodermocylysis (subcutaneous infusion) for re-hydration, administration of an oral antimicrobials, and use of pulse oximetry to assess oxygenation. The main outcomes were hospital admission rate and length of stay. Secondary outcomes included health related quality of life, rates of both infectious and non-infectious complications within four weeks of onset of symptoms; mortality rate of residents with pneumonia (death from all causes within 30 days of onset of symptoms. Time to stabilization of vital signs, as well as functional status at four weeks, were assessed.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
64 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Symptoms or signs of lower respiratory tract infection as defined by standardized criteria.

排除标准

  • Residents were excluded if they were not expected to live longer than 30 days from the date of enrollment, had a previous anaphylactic or serious allergic reaction to quinolones, had advanced directives that they are not be transferred to hospital for treatment.

研究组 & 干预措施

Intervention

Other

use of oral anti-microbials, portable chest radiographs, oxygen saturation monitoring, re-hydration and close monitoring by a research nurse

干预措施: a clinical pathway nursing home acquired pneumonia (Procedure)

Comparator

No Intervention

usual care

结局指标

主要结局

Hospital admission, length of stay

次要结局

  • complication rates,
  • mortality,
  • functional status,
  • time to stabilization of vital signs
  • Health related quality of life,

研究者

申办方类型
Other
责任方
Sponsor

相似试验