Nutrition Therapy in Adult Patients Requiring ECMO in Australia and New Zealand
NCT ID: NCT02048046
Last Updated: 2014-01-29
Study Results
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Basic Information
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COMPLETED
109 participants
OBSERVATIONAL
2012-06-30
Brief Summary
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Another essential therapy that assists patients in their recovery from illness is the provision of artificial nutrition. This liquid formula is delivered into the stomach or as a nutritionally rich fluid provided into the vein. Until recently nutrition was under-emphasised in the critically ill, however, it has now become clear that targeted nutrition can positively affect a person's outcome and is vital during long periods of intensive care hospitalisation.
There is very limited data on how nutrition affects the outcomes of ECMO patients (positive or negative). We know from limited studies that these patients receive less nutrition than other patients, something that is particularly concerning given that less nutrition leads to a longer hospital stay and has been linked a with higher hospital mortality. We also think that adult patients on ECMO need more nutrition as they appear to lose more weight than patients with other illnesses in intensive care; however this has not been confirmed. It is thus essential that we understand the effects of this relatively simple but vital therapy on these very sick patients.
This study proposes to collect information on the current feeding practices in patients on ECMO and describe the factors that inhibit or allow provision of nutrition so that we can understand the issues that exist, develop strategies to improve delivery of nutrition and determine areas for further research.
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Detailed Description
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Our primary aims are to:
1. describe the current nutrition therapy practices and
2. profile the barriers and enablers to successful feeding in patients requiring VV (veno-venous) or VA (veno-arterial) ECMO whilst ECMO is insitu and for 7 days post ECMO removal.
Hypothesis We hypothesise that patients who receive VA or VV ECMO receive inadequate amounts of predicted nutrition requirements (including energy and protein) and are subject to frequent episodes of nutritional delivery interruption.
Study design A 12 month prospective, observational study in approximately 10 sites across Australia and New Zealand. Data will be collected from the commencement of ECMO until 7 days after its removal. All patients who are eligible for the study will have data collected by the primary dietitian or research coordinator at each site. Data collection has been confined to variables available in routine practice and easily available to the dietitian.
Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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ECMO
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Currently receiving ECMO for any reason
* Expected to remain on ECMO for ≥ 72 hours
* Expected that nutrition therapy will continue for at ≥ 72 hours
Exclusion Criteria
16 Years
ALL
No
Sponsors
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Australian and New Zealand Intensive Care Research Centre
OTHER
Responsible Party
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Locations
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The Prince Charles Hospital
Brisbane, , Australia
The Alfred Hospital
Melbourne, , Australia
Sir Charles Gardiner Hospital
Perth, , Australia
The Royal Perth Hospital
Perth, , Australia
Royal Prince Alfred
Sydney, , Australia
St Vincents, Sydney
Sydney, , Australia
Auckland City Hospital (CVICU)
Auckland, , New Zealand
Countries
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Other Identifiers
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V3 110613
Identifier Type: -
Identifier Source: org_study_id
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