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Impact of SPN on Infection Rate, Duration of Mechanical Ventilation & Rehabilitation in ICU Patients

Primary Purpose

Critically Ill

Status
Completed
Phase
Phase 3
Locations
Switzerland
Study Type
Interventional
Intervention
SPN
Sponsored by
University Hospital, Geneva
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Critically Ill focused on measuring Critically ill, nutrition, randomised controlled clinical trial, human, adult, Supplemental parenteral nutrition

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Expected ICU stay > 5 days
  • Expected survival > 7 days
  • No contraindication to EN
  • Obtained informed consent

Exclusion Criteria:

  • Refusal of consent
  • Age < 18 years
  • Short bowel syndrome
  • Significant persistent gastrointestinal dysfunction with ileus
  • High output proximal fistula (> 1.5 liter/d)
  • Patients receiving PN

Sites / Locations

  • Service of Intensive Care, Geneva University Hospital,
  • Service de Médecine Intensive Adulte et Centre des Brûlés

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

SPN group

Control gr

Arm Description

experimental arm: Supplemental Parenteral Nutrition (SPN) is added to enteral nutrition (EN) to reach 100% of their predicted energy needs from ICU day 4. In the treated group, SPN is started if at day 4 energy input by EN is < 60% of energy target in order to reach 100% of energy target by peripheral or central line. Nutritional products as currently used in our institution. SPN is composed of EN and PN, both techniques being currently used in our institution.

EN : start EN at 20-30 ml/h per day up to maximal 150 ml/h per day; or day1: 500 ml, day2: 1000 ml, day3: 1500 ml of EN dependant on gastrointestinal tolerance (gastric residue volume more than 500ml). Nutritional products as currently used in our institution.

Outcomes

Primary Outcome Measures

Documented Infection Rate
Infection, defined according to CDC criteria during the ICU and hospital stay, occurrence between day 9 and day 28

Secondary Outcome Measures

Hours on Mechanical Ventilation in All Patients
Mechanical ventilation hours during study duration (days 1-28)
Antibiotic Free Days
Number of days between day 9 to day 28 (follow-up period) free of antibiotics
Total Energy Intake During the Intervention Period , Between Day 4 and Day 8.
Percentage of energy target; in the SPN group the goal was to achieve 100% of the energy target during intervention (day 4 to day 8.The energy target was measured by indirect calorimetry in 198 patients of 305(65%),otherwise energy target was calculated by 25 kcal per kg of ideal body weight for women and 30 kcal per kg of ideal body weight for men and anamnestic body weight was used for patients with a body mass index of 20 kg/m2 or lower.
General Mortality
Days in ICU
Days in ICU
ICU Mortality
Protein Delivery During the Intervention Period From Day 4 to Day 8
Percentage of protein target between day 4 to 8. Protein target was set to 1.2 g per kg of ideal body weight a day.
Days in Hospital
hospital length of stay

Full Information

First Posted
December 3, 2008
Last Updated
April 18, 2013
Sponsor
University Hospital, Geneva
Collaborators
University of Lausanne Hospitals
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1. Study Identification

Unique Protocol Identification Number
NCT00802503
Brief Title
Impact of SPN on Infection Rate, Duration of Mechanical Ventilation & Rehabilitation in ICU Patients
Official Title
Impact of Supplemental Parenteral Nutrition (SPN) on Infection Rate, Duration of Mechanical Ventilation and Rehabilitation in Intensive Care Unit Patients: A Quality Control Program for the Implementing of New Nutrition Guidelines
Study Type
Interventional

2. Study Status

Record Verification Date
April 2013
Overall Recruitment Status
Completed
Study Start Date
May 2008 (undefined)
Primary Completion Date
July 2011 (Actual)
Study Completion Date
July 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital, Geneva
Collaborators
University of Lausanne Hospitals

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Rationale: Enteral nutrition (EN) in the intensive care (ICU) patients is recommended as a standard of care. However, EN alone is often associated with insufficient energy intakes and increased complication rates. Recently the investigators proposed to decrease this deficit by combining EN and supplemental parenteral nutrition (SPN) whenever EN is insufficient (< 60% of their predicted energy needs) at day 3 after admission in the ICU. Objective: This study aims at: a/ investigating if the delivery of optimal nutrition support (100 % of predicted energy targets) in ICU patients by the combined administration of SPN and EN optimizes their clinical outcome; b/ implementing the new ICU nutrition guidelines. Study design: Prospective, controlled, randomized clinical study. Study site: Service of Intensive Care, Geneva University Hospital. Patient population: 220 ICU patients to be included: expected length of stay > 5 days, expected survival > 7 days, no contraindication to EN, obtained informed consent from themselves or their next of keen. Exclusion criteria: refusal of consent, age < 18 years, short bowel syndrome, significant persistent gastrointestinal dysfunction with ileus, high output proximal fistula (> 1,5 liter/d), patients receiving PN. Nutrition: At day 3 after admission, if energy input is < 60%; patients are randomized into either the "Control group" (EN alone) or the "SPN group" (EN + PN) to reach 100% of their predicted energy needs. Tight glycaemic control (target 6.0 to 8.3 mmol/l) to be achieved according to our local practice by insulin administration. Study endpoints: Primary: nosocomial infections (CDC criteria) Secondary: Mechanical ventilation duration, ICU and hospital length of stay, antibiotic free days, ICU complications (extra-renal epuration, neurological, cardiac and respiratory complications), energy and protein balance, 28 days clinical outcome.
Detailed Description
Introduction: Nutritional support of the intensive care (ICU) patients is recommended as a standard of care. It is also strongly recommended to start enteral feeding as soon as possible whenever the gastrointestinal tract is functioning (1). However, studies have repeatedly shown that with enteral support alone, insufficient energy and protein intakes often occur (2). The resulting energy and protein deficit is associated with an increased complication rate in ICU patients (3-5). Recently we proposed to decrease this deficit by promoting a combined nutrition support by enteral nutrition (EN) and supplemental parenteral nutrition (SPN) whenever EN is insufficient (6). Contrary to former beliefs, recent meta-analyses show that parenteral nutrition (PN) does not carry excess mortality (7, 8). These reports convey a concept that is a major break-through in current routine of nutritional support in ICU patients by promoting a much wider use of PN. SPN could be the optimal modality to provide the calculated energy targets if this cannot be reached by EN alone. To improve ICU patient's outcome and minimise complications, we propose to implement feeding protocols which combine both EN and PN, when EN is insufficient to cover more than 60% of caloric needs at day 4 to reach 100% of the energy targets by adding PN from day 4 (6). Hypothesis: The administration of SPN, in ICU patients receiving < 60% of targeted energy needs by EN alone, has a positive impact on their clinical outcome by optimising their nutritional support (reduced infectious complications rate, mechanical ventilation days, duration of ICU and hospital length of stay and rehabilitation). Objective: The aim of the present study is to investigate if the delivery of optimal nutrition support (100 % of predicted energy targets) in ICU patients achieved with the combined administration of SPN and EN optimizes their clinical outcome.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Critically Ill
Keywords
Critically ill, nutrition, randomised controlled clinical trial, human, adult, Supplemental parenteral nutrition

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
305 (Actual)

8. Arms, Groups, and Interventions

Arm Title
SPN group
Arm Type
Experimental
Arm Description
experimental arm: Supplemental Parenteral Nutrition (SPN) is added to enteral nutrition (EN) to reach 100% of their predicted energy needs from ICU day 4. In the treated group, SPN is started if at day 4 energy input by EN is < 60% of energy target in order to reach 100% of energy target by peripheral or central line. Nutritional products as currently used in our institution. SPN is composed of EN and PN, both techniques being currently used in our institution.
Arm Title
Control gr
Arm Type
No Intervention
Arm Description
EN : start EN at 20-30 ml/h per day up to maximal 150 ml/h per day; or day1: 500 ml, day2: 1000 ml, day3: 1500 ml of EN dependant on gastrointestinal tolerance (gastric residue volume more than 500ml). Nutritional products as currently used in our institution.
Intervention Type
Dietary Supplement
Intervention Name(s)
SPN
Intervention Description
SPN : in the treated group, SPN is started if at day 4 energy input by EN is < 60% of energy target in order to reach 100% of energy target by peripheral or central line.
Primary Outcome Measure Information:
Title
Documented Infection Rate
Description
Infection, defined according to CDC criteria during the ICU and hospital stay, occurrence between day 9 and day 28
Time Frame
20 days
Secondary Outcome Measure Information:
Title
Hours on Mechanical Ventilation in All Patients
Description
Mechanical ventilation hours during study duration (days 1-28)
Time Frame
28 days
Title
Antibiotic Free Days
Description
Number of days between day 9 to day 28 (follow-up period) free of antibiotics
Time Frame
20 days
Title
Total Energy Intake During the Intervention Period , Between Day 4 and Day 8.
Description
Percentage of energy target; in the SPN group the goal was to achieve 100% of the energy target during intervention (day 4 to day 8.The energy target was measured by indirect calorimetry in 198 patients of 305(65%),otherwise energy target was calculated by 25 kcal per kg of ideal body weight for women and 30 kcal per kg of ideal body weight for men and anamnestic body weight was used for patients with a body mass index of 20 kg/m2 or lower.
Time Frame
5 days
Title
General Mortality
Time Frame
28 days
Title
Days in ICU
Description
Days in ICU
Time Frame
28 days
Title
ICU Mortality
Time Frame
28 days
Title
Protein Delivery During the Intervention Period From Day 4 to Day 8
Description
Percentage of protein target between day 4 to 8. Protein target was set to 1.2 g per kg of ideal body weight a day.
Time Frame
5 days
Title
Days in Hospital
Description
hospital length of stay
Time Frame
28 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Expected ICU stay > 5 days Expected survival > 7 days No contraindication to EN Obtained informed consent Exclusion Criteria: Refusal of consent Age < 18 years Short bowel syndrome Significant persistent gastrointestinal dysfunction with ileus High output proximal fistula (> 1.5 liter/d) Patients receiving PN
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Claudia P HEIDEGGER, MD
Organizational Affiliation
Division of Intensive Care, 1211 Geneva 14, Switzerland
Official's Role
Principal Investigator
Facility Information:
Facility Name
Service of Intensive Care, Geneva University Hospital,
City
Geneva
ZIP/Postal Code
1211
Country
Switzerland
Facility Name
Service de Médecine Intensive Adulte et Centre des Brûlés
City
Lausanne
ZIP/Postal Code
1011
Country
Switzerland

12. IPD Sharing Statement

Citations:
PubMed Identifier
17468845
Citation
Heidegger CP, Romand JA, Treggiari MM, Pichard C. Is it now time to promote mixed enteral and parenteral nutrition for the critically ill patient? Intensive Care Med. 2007 Jun;33(6):963-9. doi: 10.1007/s00134-007-0654-7. Epub 2007 Apr 28.
Results Reference
background
PubMed Identifier
23218813
Citation
Heidegger CP, Berger MM, Graf S, Zingg W, Darmon P, Costanza MC, Thibault R, Pichard C. Optimisation of energy provision with supplemental parenteral nutrition in critically ill patients: a randomised controlled clinical trial. Lancet. 2013 Feb 2;381(9864):385-93. doi: 10.1016/S0140-6736(12)61351-8. Epub 2012 Dec 3.
Results Reference
derived

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Impact of SPN on Infection Rate, Duration of Mechanical Ventilation & Rehabilitation in ICU Patients

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