Preoperative Carbohydrate Load and Intraoperative w3-PUFA in CAGB Surgery

Sponsor
Federal University of Mato Grosso (Other)
Overall Status
Completed
CT.gov ID
NCT03017001
Collaborator
(none)
60
4
31

Study Details

Study Description

Brief Summary

Omega-3 polyunsaturated fatty acids (w-3-PUFA) may have a potential role in enhance the postoperative balance of host immunity and reduce the incidence of postoperative atrial fibrillation (POAF). CHO drinks 2h before the induction of the anesthesia may reduce the necessity of vasoactive drugs preoperatively. the aim of this study was to investigate the effect of these two nutrients in patients undergoing CABG with cardiopulmonary bypass (CPB) on morbidity at ICU, mainly POFA. This is a double-blind controlled randomized trial.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: CHO (carbohydrate)
  • Drug: intravenous w-3 PUFA
  • Other: CHO (carbohydrate) plus intravenous w3-PUFA
Phase 2/Phase 3

Detailed Description

The authors include all patients of both sexes with medical diagnose of chronic coronary heart disease and eligible to elective CABG with age ranging from 18 to 80 years. All patients have signed the written informed consent form. We exclude those who have insulin-dependent diabetic, hepatic or renal disorders, thrombocytopenia, important dyslipidemia (triglycerides 3-fold higher than normal standard), gastro-esophageal reflux, acute coronary syndromes, allergy to fish oil, and severe malnutrition. We also exclude patients underwent off-pump CABG, combined heart procedures, reoperations, and those who received blood transfusion in the last 3 months.

Patients were randomized using a random number software available at www.graphpad.com . They were allocated for four groups: group CHO (patients received a 8h fast for solids and 2h fast with 200mL of a drink containing water plus 12.5% maltodextrin (25g) and no infusion of intraoperative w-3-PUFA); Control group (preoperative fast for solids for 8h but allowed to drink 200 mL of water until 2h before anesthesia; and no infusion of intraoperative w-3-PUFA); group CHO+w3 (patients received a 8h fast for solids and 2h fast with 200mL of a drink containing water plus 12.5% maltodextrin (25g), and an intravenous intraoperative dose of w-3-PUFA (0.2 mcg/kg) during 4h ); and group w3 (preoperative fast for solids but allowed to drink 200 mL of water until 2h before anesthesia, and an intravenous intraoperative dose of w-3-PUFA (0.2 mcg/kg) during 4h).

Only a dietitian of the hospital knew the randomization chart and informed the ward nurse to give the patient one of the two preoperative drinks before sent him to the surgical theater. . She also informed the anesthesiologist which patient would receive the intraoperative w-3-PUFA. The surgeon and his assistant team did not know which group belong each patient. A team of cardiologists and intensivists who also were blind to the study design and randomization collected all data.

Endpoints The primary endpoints were the incidence of POAF and the need of inotropic vasoactive drug (dobutamine and/or noradrenalin) for weaning from CPB (intraoperative period) and at ICU (postoperative period). As secondary endpoints the investigators looked at perioperative morbidity, hospital mortality and length of both ICU stay and total postoperative stay.

Study Design

Study Type:
Interventional
Actual Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Preoperative Carbohydrate Load and Intraoperative Omega-3 Polyunsaturated Fatty Acids Positively Impacts in Nosocomial Morbidity After CAGB Surgery. A Double-blind Randomized Trial.
Study Start Date :
Mar 1, 2014
Actual Primary Completion Date :
Jun 1, 2016
Actual Study Completion Date :
Oct 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Experimental: CHO (carbohydrate) group

Patients received a 8h preoperative fast for solids and 2h fast with 200mL of a drink containing water plus 12.5% maltodextrin (25g) and no infusion of intraoperative w-3-PUFA

Dietary Supplement: CHO (carbohydrate)
Patients in this group received a preoperative fast for solids for 6h and a drink containing water plus 12.5% maltodextrine (carbohydrate) 2h before anesthesia
Other Names:
  • maltodextrin
  • Experimental: W-3 PUFA group

    Patients received preoperative fast for solids but allowed to drink 200 mL of water until 2h before anesthesia, and an intravenous intraoperative dose of intravenous w-3-PUFA (0.2 mcg/kg)

    Drug: intravenous w-3 PUFA
    Patients in this groups received during the operation (intraoperative) a dose of intravenous w3-PUFA
    Other Names:
  • w3-fatty acids
  • Experimental: CHO plus intravenous w3-PUFA group

    Patients received a 8h fast for solids and 2h fast with 200mL of a drink containing water plus 12.5% maltodextrin (25g), and an intravenous intraoperative dose of intravenous w-3-PUFA (0.2 mcg/kg)

    Other: CHO (carbohydrate) plus intravenous w3-PUFA
    Patients in this group received a preoperative fast for solids for 6h and a drink containing water plus 12.5% maltodextrine (carbohydrate) 2h before anesthesia, plus an intravenous dose of w3-PUFA intraoperatively
    Other Names:
  • maltodextrin plus w3-fatty acids
  • No Intervention: Control

    Patients received preoperative fast for solids for 8h but allowed to drink 200 mL of water until 2h before anesthesia; and no infusion of intraoperative intravenous w-3-PUFA

    Outcome Measures

    Primary Outcome Measures

    1. The incidence of postoperative atrial fibrillation (POAF) [48 hours]

      categorical data (patients either had or not had POAF

    2. The need of inotropic vasoactive drug (dobutamine and/or noradrenalin) for weaning from cardiopulmonary bypass (intraoperative period) and at ICU (postoperative period). [48 hours]

      categorical data (patients either need or not need vasoactive drug

    Secondary Outcome Measures

    1. Postoperative morbidity [the incidence of morbidity up to 30 days after surgery]

      categorical data (patients either had or not had postoperative morbidity

    2. Length of both ICU stay [number of days up to 30 days postoperatively]

      the length in days of ICU stay

    3. Postoperative mortality [the incidence of mortality up to 30 days after surgery]

      categorical data (death or alive)

    4. Length of both hospital stay [number of days in hospital up to 30 days postoperatively]

      the length in days of hospital stay

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • The authors include all patients of both sexes with medical diagnose of chronic coronary heart disease and eligible to elective coronary artery bypass grafting (CABG)
    Exclusion Criteria:
    • The investigators exclude those who have insulin-dependent diabetic, hepatic or renal disorders, thrombocytopenia, important dyslipidemia (triglycerides 3-fold higher than normal standard), gastro-esophageal reflux, acute coronary syndromes, allergy to fish oil, and severe malnutrition. We also exclude patients underwent off-pump CABG, combined heart procedures, reoperations, and those who received blood transfusion in the last 3 months.

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Federal University of Mato Grosso

    Investigators

    • Principal Investigator: Jose Aguilar-Nascimento, MD; PhD, Federal University of Mato Grosso

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Jose Eduardo de Aguilar-Nascimento, Chair Professor, MD, PhD, Federal University of Mato Grosso
    ClinicalTrials.gov Identifier:
    NCT03017001
    Other Study ID Numbers:
    • 30493514.5.000.5165
    First Posted:
    Jan 11, 2017
    Last Update Posted:
    Jan 11, 2017
    Last Verified:
    Jan 1, 2017
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 11, 2017