The Efficacy of Nurse-driven, Protocol Guided Ventilator Weaning in a Medical-Surgical Intensive Care Unit (ICU)

Sponsor
St. Luke's-Roosevelt Hospital Center (Other)
Overall Status
Completed
CT.gov ID
NCT00786617
Collaborator
(none)
202
6

Study Details

Study Description

Brief Summary

  1. Mechanically ventilated patients weaned by nurse-driven ventilator weaning protocol will have a mean length of stay on ventilator at least one day shorter than patients weaned by physician-initiated, non-protocol methods

  2. Mechanically ventilated patients weaned by nurse-driven ventilator weaning protocol will have al least similar Ventilator, ICU, and Hospital Length Of Stay (LOS) compared to patients weaned by physician-initiated, non-protocol method

  3. Nurse-driven ventilator weaning protocol is well accepted by other services: physicians, nurses, and respiratory therapists.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Ventilatory support is one of the most common indications for admission to ICU (1).

    The duration of mechanical ventilation is associated with several serious complications, increase mortality, prolong ICU stay, and increase hospital cost (7,8).

    Traditionally, the process of ventilator weaning is initiated and carried out my physicians.

    Recently, there have been few studies that supported the utility of protocol guided weaning algorithms. Its use have been associated with earlier initiation of weaning, leading to shorter ventilator time, and a trend for shorter ICU length-of-stay and lower hospital costs (1,2,4,9) Several studies have also shown the relative safety of utilizing nursing (3) and RT staff alone or in cooperation with medical staff in the weaning of patients from mechanical ventilation (1,2,6).

    We recently developed a nurse-driven ventilator weaning protocol for all ICUs at St. Luke's and Roosevelt hospitals. The protocol was approved by the Critical Care Committee and is implemented as of May 2007. All ICU nurses, respiratory therapists, and ICU physicians have been educated on this protocol We plan to prospectively collect data to look at length of stay on mechanical ventilation in patients weaned by nurse-driven ventilator weaning protocol. We plan to compare such data to retrospectively collected ventilator LOS data in patients weaned by physician-initiated ventilator weaning method.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    202 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    The Efficacy of Nurse-driven, Protocol Guided Ventilator Weaning in a Medical-Surgical ICU
    Study Start Date :
    Dec 1, 2007
    Actual Primary Completion Date :
    Jun 1, 2008
    Actual Study Completion Date :
    Jun 1, 2008

    Arms and Interventions

    Arm Intervention/Treatment
    Nurse-driven

    Mechanically ventilated patients weaned by nurse-driven ventilator weaning protocol

    Physician-initated

    Mechanically ventilated patients weaned by physician-initiated, non-protocol methods

    Outcome Measures

    Primary Outcome Measures

    1. Average Length of Stay on Ventilator [up to 5 months]

    Secondary Outcome Measures

    1. ICU mortality [up to 5 months]

    2. Hospital mortality [up to 5 months]

    3. Treatment intensity and resource allocation: Cost of ICU care per year [up to 5 months]

    4. Level of acceptance of nurse-driven vent weaning protocol [up to 5 months]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Receiving MV for at least 24 hours in the ICU

    • Meeting established protocol criteria for a vent wean trial

    Exclusion Criteria:
    • Patients in whom MV was actively withdrawn for terminal wean

    • Brain dead patients on MV

    • Age <18 years old

    • Transfers from other hospitals or health care facility who were ventilator dependent

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • St. Luke's-Roosevelt Hospital Center

    Investigators

    • Principal Investigator: Hassan Khouli, MD, St. Luke's-Roosevelt Hospital Center

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    St. Luke's-Roosevelt Hospital Center
    ClinicalTrials.gov Identifier:
    NCT00786617
    Other Study ID Numbers:
    • 07-122
    First Posted:
    Nov 6, 2008
    Last Update Posted:
    Mar 20, 2015
    Last Verified:
    Mar 1, 2015

    Study Results

    No Results Posted as of Mar 20, 2015