AzTrials
AzTrials

Thoracic SurgeryNCT00247793

Immunonutrition in Cardiac Surgery

A study testing Oral Impact (preoperative enteral nutritional supplement) in people with Thoracic Surgery and Cardiac Surgery, run by Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) at 1 site in Netherlands.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Effect of two preoperative oral immune-enhancing nutritional supplements in patients at high risk of infection after cardiac surgery: a randomized placebo-controlled study. Introduction: In our first study we showed that the use of a preoperative oral immune-enhancing nutritional supplement (OIENS) resulted in an… Read more about this study

Who is it for?
Ages 21 years and older
What is being tested?
Oral Impact (preoperative enteral nutritional supplement)
Type of treatment
Pill or oral medicine
How many people
Not given
Where
1 siteNetherlands
Study dates
Jul 1996to Dec 1998
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 21 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Patients undergoing cardiac surgery with the use of cardiopulmonary bypass, who met one of the following criteria
  • age >= 70 years
  • poor left ventricular function (ejection fraction < 0.4)
  • mitral valve replacement

Who cannot join

  • Age =< 21 years
  • Pregnancy
  • Insulin dependent diabetes mellitus
  • Hepatic Cirrhosis
  • Known malignancy
  • Use of chemotherapy, NSAIDs (except ASA), or corticosteroids
Show all 9Show fewer
  • Schizophrenia
  • Severe renal failure (creatinine clearance < 25 mL/h) before study entrance
  • Patients with an organ transplantation in the past

Trial locations and contacts

1 site in 1 country.

Netherlands1 site
  • Cardiopulmonary Surgery, Academic Medical Center

    Amsterdam, North Holland, 1105 AZ

Other trials in Netherlands

About this study

Official title: The Effect of Pre- and Postoperative Supplemental Enteral Nutrition in High-Risk Patients Undergoing Elective Cardiac Surgery. A Prospective Double Blind Study.

Effect of two preoperative oral immune-enhancing nutritional supplements in patients at high risk of infection after cardiac surgery: a randomized placebo-controlled study.

Introduction: In our first study we showed that the use of a preoperative oral immune-enhancing nutritional supplement (OIENS) resulted in an improved patients' host-defence with a reduction in postoperative infectious morbidity in 'high-risk' cardiac surgery patients. The use of the OIENS resulted also in less postoperative organ dysfunction. Experimental studies have shown that additional glycine results in less ischemia-reperfusion damage and that glycine has anti-inflammatory properties.

Read more

Objective: The use of an OIENS in the preoperative period in patients at high risk of infection after elective cardiac surgery with the use of cardiopulmonary bypass (CPB) results in a reduction in infections as in our first study. The addition of 9.6 gram glycine per sachet OIENS results in a further reduction in postoperative dysfunction.

Design: A prospective randomized placebo controlled study with two oral immune enhancing nutritional formula's and an isocaloric control formula. Patients: Seventy-four consecutive patients undergoing cardiac surgery with the use of an CPB who met one or more of the following inclusion criteria: Age 70 years or older, mitral valve replacement or cardiac ejection fraction less then 40%. Exclusion criteria were age < 18 years, proven malignancy, use of corticosteroids, severe renal and liver failure. Definition of a protocol violation was the intake of less then 5 L or more then 10 L of the nutritional supplement in the preoperative period.

Intervention: Patients were split up in three groups by concealed randomisation. One group received the arginine, omega3-PUFAs and nucleotides enriched formula (OIENS). Another group received the OIENS further enriched with glycine (OIENS+glyc). The control group received an isocaloric nutritional supplement without the enrichments.

Read the detailed description

Objective To study the effect of two preoperative immune enhancing nutritional supplements compared with a control nutritional supplement in 'high risk' risk cardiac surgery patients

Introduction: Elderly patients and patients with a poor ventricular function undergoing cardiac operations with hypothermic cardiopulmonary bypass (CPB), have an increased postoperative morbidity and mortality. Host defence may be diminished due to nutritional deficiencies, hypoperfusion, anaesthesia and operative trauma. Immune function is additionally depressed by the use of CPB and hypothermia. It has been suggested that L-arginine can improve postoperative outcome in cardiac surgery patients, glycine may have a role in protecting tissues against insults such as ischemia-reperfusion and hypoxia, and omega-3 polyunsaturated fatty acids (omega3-PUFA's) can limit the postoperative generalised inflammatory response.

Experimental studies have shown that the use of nutritional supplements containing L-arginine, omega3-PUFA's or nucleotides, boost immune responsiveness after surgery or trauma. L-arginine is a semi-essential amino acid and precursor of nitrous oxide (NO), the most important endothelial vasodilator. In experimental studies, L-arginine improved wound healing, restored postoperative depressed macrophage function and lymphocyte responsiveness and augmented resistance to infections. Arginine protected against ischemia-reperfusion injury by increasing oxygen delivery upon reflow, thereby improving cardiac function. The intake of additional omega3-PUFA's alters cell membrane phospholipid content and prostaglandin synthesis. This might be an important factor in limiting the generalised inflammatory response and subsequent immunosuppression and capillary leakage following major surgery. Purines and pyrimidines are essential nutrients for rapidly dividing cells. The administration of nucleotides in the form of yeast-RNA has improved the host immune response to an infectious challenge. In experimental studies glycine has been proven cytoprotective in stomach, kidney, liver and cardiovascular system. The metabolic response to oral glycine is that it facilitates the uptake op glucose from the circulation.

The immunonutrients, arginine, omega3-PUFA's and yeast-RNA, have been combined into a single oral immune enhancing nutritional supplement (OIENS). In cancer surgery, trauma and critically ill patients 'post event' nutrition with this immune enhancing formula has improved immunocompetence, reduced infections and shortened length of stay in the hospital (LOSH). The onset of the effect of postoperative immune enhancing nutrition starts after 3 days and seems to be dose dependent. For this reason, it can be hypothesised that it may be beneficial to commence an oral immune enhancing nutritional supplement (OIENS) before surgery. A recent published clinical trail showed that the OIENS with these three immunonutrients in high risk cardiac surgery patients improves preoperative clinical relevant immunological parameters, reduced postoperative infectious morbidity and attenuated postoperative organ dysfunction. Recently, the three immunonutrients have been combined with glycine into a new single OIENS. Aim of the present study in 'high risk' cardiac surgery patients was to determine whether the intake of the new OIENS for minimally five days improves preoperative host defence and subsequently reduces postoperative infections and organ dysfunction.

Study design: A prospective randomized placebo-controlled three armed double blind study

Setting: Departments of cardiopulmonary surgery, anesthesiology and intensive care of the Academic Medical Center, Amsterdam, The Netherlands

Patients: Eligible patients will be included in the study after obtaining written informed consent Inclusion criteria: Patients who met one or more of the inclusion criteria: aged 70 years or more, undergoing cardiac surgery with the use of CPB, or patients with a poor left ventricular function (Ejection fraction < 0.40) or patients undergoing a mitral valve replacement.

Exclusion criteria: Age < 21 years, pregnancy, insulin dependent diabetes mellitus, hepatic cirrhosis, known malignancy, the use of chemotherapy, NSAIDs (excluding acetyl salic acid) or corticosteroids, schizophrenia, severe renal insufficiency (creatinine clearance < 25 mL/h), patients with an organ transplantation in the past

Randomization: 74 patients will be randomized by closed envelop method

Intervention: All patients will receive one of the three enteral nutritional supplements. A formula enriched with arginine, omega-3 PUFA's and nucleotides or the enriched formula further enriched with additional glycine or a control formula. Patients that needs postoperative enteral nutritional support will receive the same formula as preoperative. Patients that need no postoperative enteral nutrition nasogastric tube feeding will not receive the nutritional supplement

Endpoints: Patient compliance, infections, postperfusion phenomena, post-operative organ function (need of postoperative support e.g. inotropic, vasopressor support, fluids, myocardial infarction, ventilation parameters, renal function) time of recovery, mortality

Being tested
Oral Impact (preoperative enteral nutritional supplement)
Keywords
immunonutrition, preoperative optimization, preoperative enteral nutritional supplement, high risk, cardiac surgery, arginine, omega-3 polyunsaturated fatty acids, nucleotides, glycine, immune enhancing nutritional supplement, immune enhancing formula

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Oral Impact (preoperative enteral nutritional supplement)Drug

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Postoperative infectious morbidity

  2. Mortality

Secondary outcomes (3)
  1. Immunological measurements

  2. Postoperative organ function/support

  3. Recovery (Length of ICU stay, postoperative length of hospital stay)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Nov 2005 (estimated)
  2. Study startJul 1996
  3. Study completionDec 1998

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
IDs, dates and publications
ClinicalTrials.gov ID
NCT00247793
Sponsor's protocol ID
96.17.066
Other IDs
Mec 95/232
Status last verified
Nov 2005
First submitted
1 Nov 2005
Last updated
2 Nov 2005
Results posted
No

Publications

  • Tepaske R, Velthuis H, Oudemans-van Straaten HM, Heisterkamp SH, van Deventer SJ, Ince C, Eysman L, Kesecioglu J. Effect of preoperative oral immune-enhancing nutritional supplement on patients at high risk of infection after cardiac surgery: a randomised placebo-controlled trial. Lancet. 2001 Sep 1;358(9283):696-701. doi: 10.1016/s0140-6736(01)05836-6.

    PubMed 11551575
  • Higgins TL, Estafanous FG, Loop FD, Beck GJ, Blum JM, Paranandi L. Stratification of morbidity and mortality outcome by preoperative risk factors in coronary artery bypass patients. A clinical severity score. JAMA. 1992 May 6;267(17):2344-8.

    PubMed 1564774
  • Kress HG, Scheidewig C, Schmidt H, Silber R. Reduced incidence of postoperative infection after intravenous administration of an immunoglobulin A- and immunoglobulin M-enriched preparation in anergic patients undergoing cardiac surgery. Crit Care Med. 1999 Jul;27(7):1281-7. doi: 10.1097/00003246-199907000-00011.

    PubMed 10446821
  • Weimann A, Bastian L, Bischoff WE, Grotz M, Hansel M, Lotz J, Trautwein C, Tusch G, Schlitt HJ, Regel G. Influence of arginine, omega-3 fatty acids and nucleotide-supplemented enteral support on systemic inflammatory response syndrome and multiple organ failure in patients after severe trauma. Nutrition. 1998 Feb;14(2):165-72. doi: 10.1016/s0899-9007(97)00429-2.

    PubMed 9530643
  • O'Leary MJ, Coakley JH. Nutrition and immunonutrition. Br J Anaesth. 1996 Jul;77(1):118-27. doi: 10.1093/bja/77.1.118. No abstract available.

    PubMed 8703621
  • Kirk SJ, Barbul A. Role of arginine in trauma, sepsis, and immunity. JPEN J Parenter Enteral Nutr. 1990 Sep-Oct;14(5 Suppl):226S-229S. doi: 10.1177/014860719001400514. No abstract available.

    PubMed 2232107
  • Engelman DT, Watanabe M, Maulik N, Cordis GA, Engelman RM, Rousou JA, Flack JE 3rd, Deaton DW, Das DK. L-arginine reduces endothelial inflammation and myocardial stunning during ischemia/reperfusion. Ann Thorac Surg. 1995 Nov;60(5):1275-81. doi: 10.1016/0003-4975(95)00614-Q.

    PubMed 8526612
  • Sato H, Zhao ZQ, McGee DS, Williams MW, Hammon JW Jr, Vinten-Johansen J. Supplemental L-arginine during cardioplegic arrest and reperfusion avoids regional postischemic injury. J Thorac Cardiovasc Surg. 1995 Aug;110(2):302-14. doi: 10.1016/S0022-5223(95)70226-1.

    PubMed 7543634
  • Jones SM, Thurman RG. L-arginine minimizes reperfusion injury in a low-flow, reflow model of liver perfusion. Hepatology. 1996 Jul;24(1):163-8. doi: 10.1002/hep.510240127.

    PubMed 8707257
  • Nonami Y. The role of nitric oxide in cardiac surgery. Surg Today. 1997;27(7):583-92. doi: 10.1007/BF02388212.

    PubMed 9306558
  • Daly JM, Weintraub FN, Shou J, Rosato EF, Lucia M. Enteral nutrition during multimodality therapy in upper gastrointestinal cancer patients. Ann Surg. 1995 Apr;221(4):327-38. doi: 10.1097/00000658-199504000-00002.

    PubMed 7726669
  • Zhong Z, Thurman RG. A fish oil diet minimizes hepatic reperfusion injury in the low-flow, reflow liver perfusion model. Hepatology. 1995 Sep;22(3):929-35.

    PubMed 7657301
  • Kulkarni AD, Rudolph FB, Van Buren CT. The role of dietary sources of nucleotides in immune function: a review. J Nutr. 1994 Aug;124(8 Suppl):1442S-1446S. doi: 10.1093/jn/124.suppl_8.1442S.

    PubMed 8064400
  • Heyland DK, Novak F, Drover JW, Jain M, Su X, Suchner U. Should immunonutrition become routine in critically ill patients? A systematic review of the evidence. JAMA. 2001 Aug 22-29;286(8):944-53. doi: 10.1001/jama.286.8.944.

    PubMed 11509059
  • Farreras N, Artigas V, Cardona D, Rius X, Trias M, Gonzalez JA. Effect of early postoperative enteral immunonutrition on wound healing in patients undergoing surgery for gastric cancer. Clin Nutr. 2005 Feb;24(1):55-65. doi: 10.1016/j.clnu.2004.07.002.

    PubMed 15681102

Questions about this trial

What is this clinical trial studying?

A study testing Oral Impact (preoperative enteral nutritional supplement) in people with Thoracic Surgery and Cardiac Surgery, run by Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) at 1 site in Netherlands.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 2 Nov 2005. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Netherlands. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Postoperative infectious morbidity. The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT00247793, which also lists 41 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Nov 2005.

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