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A Clinical Pathway for Nursing Home Acquired Pneumonia

This study has been completed.

Sponsors and Collaborators: Hamilton Health Sciences
Canadian Institutes of Health Research (CIHR)
Information provided by: Hamilton Health Sciences
ClinicalTrials.gov Identifier: NCT00157612
  Purpose

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.


Condition Intervention
Pneumonia
Lower Respiratory Tract Infection
Procedure: a clinical pathway for the management of nursing home acquired pneumonia

MedlinePlus related topics:   Nursing Homes    Pneumonia   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Official Title:   A Randomized Control Trial of a Clinical Pathway for Nursing Home Pneumonia.

Further study details as provided by Hamilton Health Sciences:

Primary Outcome Measures:
  • Hospital admission, length of stay

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

Estimated Enrollment:   680
Study Start Date:   January 2001
Estimated Study Completion Date:   July 2005

Detailed Description:

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.

  Eligibility
Ages Eligible for Study:   64 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

Inclusion Criteria:

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

Exclusion Criteria:

  • 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.
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00157612

Sponsors and Collaborators
Hamilton Health Sciences
Canadian Institutes of Health Research (CIHR)

Investigators
Principal Investigator:     Mark B Loeb, MD MSc FRCPC     Hamilton Health Sciences    
  More Information


Publications of Results:

Study ID Numbers:   00-1848, CRT-43826
First Received:   September 7, 2005
Last Updated:   July 19, 2006
ClinicalTrials.gov Identifier:   NCT00157612
Health Authority:   Canada: Health Canada

Keywords provided by Hamilton Health Sciences:
pneumonia  
lower respiratory tract infection  
clinical pathway  
nursing home
long-term care
randomized control trial

Study placed in the following topic categories:
Respiratory Tract Diseases
Respiratory Tract Infections
Lung Diseases
Pneumonia

Additional relevant MeSH terms:
Infection

ClinicalTrials.gov processed this record on October 10, 2008




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