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The Efficacy of Early Postoperative Enteral Immunonutrition in Low-Risk Cardiac Surgery Patients

The Efficacy of Early Postoperative Enteral Immunonutrition on Immune Response and Outcomes in Low-Risk Cardiac Surgery Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04047095
Enrollment
55
Registered
2019-08-06
Start date
2015-02-01
Completion date
2021-10-01
Last updated
2022-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Surgery

Keywords

Cardiac surgery, Immunonutrition Glutamine Bioelectrical impedance, Immunological status

Brief summary

The aim of this study is to investigate the efficacy of early postoperative enteral immunonutrition on immune response and outcomes in the low operative risk cardiac surgery population with low phase angle value measured by the bioelectrical impedance analysis.

Detailed description

Study enrolls a low operative risk cardiac surgery patients who undergo elective cardiac surgery with cardiopulmonary bypass (CPB). Patient is offered to take part in a study a day prior to surgery. Information is provided regarding protocol, aim and course of study. Only signing the consent form patients could be enrolled to the study. Study consists of: Primary assessment - information about study. Consent form. Assessment of patient according to predefined criteria. Phase angle evaluation by bioelectrical impedance. (Day prior to surgery). It is a specific cohort of patients basically governed by surgery risk and the status of patients' cells. Euroscore II value was used to evaluate the risk of surgery. Bioelectrical impedance analysis derived phase angle was used to evaluate patients' cells frailty and vitality. First phase of blood sampling - blood samples were taken for evaluation immunological status (cellular and humoral) and inflammatory response (CRB, complete blood count) at the surgery day morning prior to surgery. Surgery - evaluating the course of the surgery (see exclusion criteria). Randomization - the patients will randomly selected into intervention and control groups. The patients, physicians and investigators were separate from this process. The selection sequence was computer-generated and provided to the researchers by the statistician. Intervention - patients in the intervention group received normal daily meals plus one sachet three times a day of immune nutrients (Glutamine Plus by Fresenius Kabi) for five days after the surgery. The control group was provided with normal daily meals. The patients were excluded from the study if they failed to intake all of the prescribed immunonutrients. Second phase of blood sampling - repeated taking of blood samples for evaluation immunological status (cellular and humoral) and inflammatory response (CRB, complete blood count) at the sixth day morning after the surgery. Data collection - data is recorded (demographic data of patients, co-morbidities, instrumental parameters, phase angle values, surgery course details, immunological assesment and laboratory tests, short term and long term outcomes).

Interventions

DIETARY_SUPPLEMENTImmunonutrients + normal daily meal

Glutamine Plus by Fresenius Kabi (one sachet composition: glutamine 10 g, carbohydrate 10 g, β-carotene 1.7 mg, vitamin E 83 mg, vitamin C 250 mg, zinc 3.4 mg, selenium 50 μg, and fibre 1.2 g).

DIETARY_SUPPLEMENTNormal daily meal

Normal daily meal (75-80 g protein)

Sponsors

Vilnius University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 79 Years
Healthy volunteers
No

Inclusion criteria

* Age ≥18 years; * Elective cardiac surgery with cardiopulmonary bypass: * coronary artery bypass grafting surgery (CABG); * aortic valve replacement; * mitral valve replacement; * mitral valve repair; * tricuspid valve repair; * combined operations (CABG and valve surgery); * Phase angle \<5.5⁰ (phase angle was evaluated one day prior to surgery using bioelectrical impedance analysis (InbodyS10 device).

Exclusion criteria

Preoperative: * previous cardiac surgery; * left ventricle ejection fraction \<40%; * use of preoperative intra-aortic balloon pump (IABP); * critical preoperative state; * pulmonary artery mean pressure \>55 mmHg; * diagnosis of infectious endocarditis; * pacemaker; Operative: * complicated intraoperative course (unplanned intervention or low cardiac output syndrome in the operating theatre: failure to wean from cardiopulmonary bypass (CPB) or intraoperative insertion of IABP or infusion of two or more inotropic medications with a cumulative dose of 0.2 mcg/kg/min); * surgery time \>6 h; * unplanned intervention; Postoperative: * disturbance of dietary rules.

Design outcomes

Primary

MeasureTime frameDescription
CD4+ T cellSix daysBlood samples were collected twice on the surgery and on the sixth postoperative day by sampling blood for CD4+ T cells.
CD8+ T cellSix daysBlood samples were collected twice on the surgery and on the sixth postoperative day by sampling blood for CD8+ T cells.
CD69+ T cellSix daysBlood samples were collected twice on the surgery and on the sixth postoperative day by sampling blood for CD69+ T cells.
Interleukin-1 (IL-1)Six daysBlood samples were collected twice on the surgery and on the sixth postoperative day by sampling blood for IL-1.
Interleukin-6 (IL-6)Six daysBlood samples were collected twice on the surgery and on the sixth postoperative day by sampling blood for IL-6.
Tumor necrosis factor alfa (TNFα)Six daysBlood samples were collected twice on the surgery and on the sixth postoperative day by sampling blood for TNFα.

Secondary

MeasureTime frameDescription
Duration of hospital stay28 daysShort-term postoperative outcome.
Acute kidney injury28 daysShort-term postoperative outcome.
Rate of rehospitalization2 yearsLong-term postoperative outcome.
Stroke28 daysShort-term postoperative outcome.
ICU infectious complications28 daysShort-term postoperative outcome. It was examined deep wound infections, ventilator associated and hospital acquired pneumonia, urinary tract infections, bloodstream infections, catheter-related bloodstream infections.
Duration of mechanical ventilation28 daysShort-term postoperative outcome.
Retoracotomy rate28 daysShort-term postoperative outcome.
Mortality2 yearsLong-term postoperative outcome.

Countries

Lithuania

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026