Effectiveness of Sedation Management in an Australian Intensive Care Unit
NCT ID: NCT00202319
Last Updated: 2005-09-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
316 participants
INTERVENTIONAL
2001-11-30
2002-09-30
Brief Summary
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Detailed Description
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This project builds upon a significant North American study that found a substantial decrease in the duration of mechanical ventilation, length of stay and rate of tracheostomy insertion following the implementation of a structured sedation protocol by nurses. However an exact replication of the protocol is not possible due to the lack of drug availability in Australia and the preferred drug regimes of RMH intensive care consultants. In addition, there are very few studies that document patients' memories of their experience being ventilated whilst sedated, despite documented discomfort such as anxiety, panic and difficulty synchronizing with the ventilator. There is a similar lack of literature on staff perceptions during the implementation of a multidisciplinary sedation protocol.
The research questions for this study are designed to examine three areas:
1. the differences between patients receiving protocol-directed sedation management compared with non protocol-directed sedation management;
2. the differences in patient perceptions of mechanical ventilation during protocol-directed sedation management as compared to non protocol-directed sedation management following extubation, and;
3. staff perceptions of using a sedation protocol in managing critically ill mechanically ventilated patients.
The design is a prospective, randomised, controlled trial studying 316 patients. There will be 158 patients recruited to the control group and 158 patients in the experimental group. The control group will receive the current management and the experimental group will receive protocol-directed sedation management. To explore patient perceptions of their experience, the patients will be interviewed using a semi-structured questionnaire following extubation and after receiving a rating of 4 on the sedation scale for 24 or more hours. In addition, staff perceptions will be surveyed on their attitudes and perceptions of the protocol.
This study will determine the efficacy and outcomes of protocol-directed sedation management of critically ill mechanically ventilated patients in an Australian context. The study will also improve our understanding of the patients' memories and perceptions during this period, which could lead to improved clinical practices and better patient outcomes. In understanding staff perceptions of the sedation protocol and its implementation, it will assist us to identify changes to improve education for new staff and compliance issues for ongoing implementation. It may be further useful in the future development of decision-making tools and their subsequent implementation and evaluation phases.
Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Interventions
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Sedation management protocol
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* those patients readmitted to the ICU who had been on the study during a previous admission were excluded for any subsequent admissions.
17 Years
ALL
No
Sponsors
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University of Melbourne
OTHER
Australian College of Critical Care Nurses
OTHER
Abbott
INDUSTRY
Melbourne Health
OTHER
Principal Investigators
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Tracey K Bucknall, RN PhD
Role: PRINCIPAL_INVESTIGATOR
University of Melbourne
Locations
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Royal Melbourne Hospital
Melbourne, Victoria, Australia
Countries
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References
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Rose RL, Bucknall T. Staff perceptions on the use of a sedation protocol in the intensive care setting. Aust Crit Care. 2004 Nov;17(4):151-9. doi: 10.1016/s1036-7314(04)80020-1.
Bucknall TK, Manias E, Presneill JJ. A randomized trial of protocol-directed sedation management for mechanical ventilation in an Australian intensive care unit. Crit Care Med. 2008 May;36(5):1444-50. doi: 10.1097/CCM.0b013e318168f82d.
Other Identifiers
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2001.102
Identifier Type: -
Identifier Source: org_study_id