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An Email Intervention to Prevent Iatrogenic Malnutrition in the ICU

Not Applicable
Completed
Conditions
Malnutrition
Interventions
Other: Feedback/Reminder email.
Registration Number
NCT02277535
Lead Sponsor
Massachusetts General Hospital
Brief Summary

This is a quality improvement research project evaluating if a targeted feedback email to clinicians impacts their nutrition delivery in the ICU.

Detailed Description

This prospective study looks to determine if a targeted email to clinicians taking care of critically ill patients will allow reduce malnutrition in the Intensive Care Units (ICU). Four ICUs will be included: medical ICU (MICU), coronary care unit (CCU) and two surgical ICUs. The investigators will rotate a 2 month period intervention amongst the aforementioned participating ICUs and follow simultaneous cohorts to evaluate the effect of our intervention (email feedback to treating clinicians) on nutrition delivery in the ICU. After the completion of the intervention, there will be a six-month follow-up of nutritional adequacy to assess the durability of changes in behavior.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
197
Inclusion Criteria
  • Clinicians taking care of patients admitted to the ICU within the past 48hrs
  • Clinicians taking care of patients in whom enteral nutrition is prescribed
Exclusion Criteria
  • Clinicians taking care of patients in whom enteral nutrition is not prescribed.

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
E-mail interventionFeedback/Reminder email.ICU clinicians caring for patients who have not yet been initiated on nutrition 48 hours after ICU admission will receive a reminder email. ICU clinicians caring for patients who accumulate a caloric deficit greater than 4000 calories or 150 g protein deficit will receive a feedback email
Primary Outcome Measures
NameTimeMethod
Patients started on nutrition within 72 h of ICU admissionAfter completing the intervention for each ICU (2 months)

The ICU admission date and EN initiation date will be collected in a data base which will later be analyzed to assess the percentange of patients initiated on EN within 72 hours of admission to the ICU. This will be reported as rates and will be compared amongst intervention and no-intervention arms using Fisher's Exact test or Chi-sq Test

Secondary Outcome Measures
NameTimeMethod
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