Neurocognitive Outcome After Coronary Artery Bypass Surgery Using Minimal Versus Conventional Extracorporeal Circulation

Sponsor
AHEPA University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT01213511
Collaborator
(none)
64
1
2
41
1.6

Study Details

Study Description

Brief Summary

The aim of this study is to assess the effect of minimal (MECC) versus conventional (CECC) extracorporeal circulation on neurocognitive function after elective coronary bypass grafting (CABG) as well as whether this can be attributed to improved cerebral perfusion intraoperatively.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Coronary artery bypass grafting with the use of minimal extracorporeal circulation
  • Procedure: Coronary artery bypass grafting under conventional extracorporeal circulation
N/A

Detailed Description

Despite improvements in the biocompatibility of cardiopulmonary bypass (CPB) circuits, the activation of inflammatory systemic response can result in clinically relevant organ dysfunction. Regarding the central nervous system, prolonged hypoperfusion and microembolization during conventional CPB have been related to postoperative neurologic impairment with an incidence varying from 30% to 60%. This clinical scenario covers a spectrum from a transient subtle cognitive dysfunction to a permanent stroke. Postoperative cognitive decline (POCD) is characterized as impairment in attention, cognition, recognition, orientation, memory, and learning. It may result in prolonged hospitalization, increased morbidity and mortality, while it has an adverse impact on quality of life after surgery.

Near-infrared spectroscopy (NIRS) provides a continuous and noninvasive monitoring of regional cerebral oxygen saturation (rSO2). Recent studies have shown a significant relationship between intraoperative cerebral oxygen desaturation, indicative of cerebral ischemia, and early POCD in patients undergoing elective coronary bypass grafting (CABG) with conventional extracorporeal circulation (CECC). In an attempt to reduce CPB-inherent side effects, a minimal extracorporeal circulation (MECC) system was developed and it is evaluated in clinical practice. The aim of this pilot study was to define whether there is a difference in early postoperative neurocognitive functioning between patients being operated for CABG on MECC versus CECC systems as well as whether this can be attributed to improved cerebral perfusion intraoperatively.

Study Design

Study Type:
Interventional
Actual Enrollment :
64 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Neurocognitive Outcome After Coronary Artery Bypass Surgery Using Minimal Versus Conventional Extracorporeal Circulation
Study Start Date :
Jan 1, 2009
Actual Primary Completion Date :
Jan 1, 2011
Actual Study Completion Date :
Jun 1, 2012

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: MECC Group

Patients operated for elective coronary artery bypass grafting with the use of minimal extracorporeal circulation.

Procedure: Coronary artery bypass grafting with the use of minimal extracorporeal circulation
The MECC system (Maquet Cardiopulmonary, Hirlingen, Germany) consists of a pre-connected closed CPB circuit containing a RotaFlow centrifugal pump and a Quadrox D diffusion membrane oxygenator. A flow meter and a bubble sensor are integrated in the drive unit of the centrifugal pump. The system features a tip-to-tip heparin coating (Bioline Coating, Maquet Cardiopulmonary, Hirlingen, Germany). No arterial or venous line filters are included. Initial priming volume of the system is 500 mL, while using retrograde autologous priming (RAP) the circuit could be filled in with autologous blood, thus reducing hemodilution. Since no cardiotomy suction is used, shed blood is collected with a cell-saving device (Haemonetics Corp, Braintree, MA).

Active Comparator: CECC Group

Group of patients undergoing elective coronary bypass grafting with the use of conventional extracorporeal circulation.

Procedure: Coronary artery bypass grafting under conventional extracorporeal circulation
A standard open CPB circuit is used, consisting of uncoated PVC tubing, a hard-shell venous reservoir, a microporous membrane oxygenator (Dideco, Mirandola, Italy) and a roller pump (Stöckert S3, Munich, Germany). The circuit contains a 40 μm arterial line blood filter (Dideco, Mirandola, Italy) and it is primed with 1500 mL of a balanced crystalloid/colloid solution (1000 mL of Ringer's solution, 200 mL of mannitol 20%, and 300 mL of hydroxyethyl starch 6%). Cardiotomy as well as sump sucker are integrated to the circuit.

Outcome Measures

Primary Outcome Measures

  1. Neurocognitive outcome at 3-month follow-up [3 months]

    Neurocognitive outcome at 3-month follow-up after elective coronary artery bypass grafting with the use of minimal (MECC) versus conventional (CECC) extracorporeal circulation.

Secondary Outcome Measures

  1. Neurocognitive outcome at discharge [7-30 days]

    Neurocognitive score assessed at the time of discharge after elective coronary surgery with the use of minimal (MECC) versus conventional (CECC) extracorporeal circulation.

  2. Episodes of intraoperative cerebral desaturation [During the operation]

    Number of episodes and duration of cerebral desaturation assessed with the use of near-infrared spectroscopy after elective coronary artery bypass grafting with minimal (MECC) versus conventional (CECC) extracorporeal circulation.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • All patients scheduled for elective coronary artery bypass grafting
Exclusion Criteria:
  • history of psychiatric disorder

  • inability to undergo neuropsychological assessment

  • history of transient ischemic attack or stroke

  • carotid artery stenosis > 60% assessed by duplex ultrasonography

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of Cardiothoracic Surgery, AHEPA University Hospital Thessaloniki Greece 542 48

Sponsors and Collaborators

  • AHEPA University Hospital

Investigators

  • Principal Investigator: Kyriakos Anastasiadis, FETCS, Department of Cardiothoracic Surgery, AHEPA University Hospital, Thessaloniki, Greece
  • Study Chair: Christos Papakonstantinou, Professor, Department of Cardiothoracic Surgery, AHEPA University Hospital, Thessaloniki, Greece

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

Responsible Party:
Kyriakos Anastasiadis, Head of Cardiothoracic Department, AHEPA University Hospital
ClinicalTrials.gov Identifier:
NCT01213511
Other Study ID Numbers:
  • AHEPA_CTS-02
First Posted:
Oct 4, 2010
Last Update Posted:
Nov 28, 2013
Last Verified:
Nov 1, 2013
Keywords provided by Kyriakos Anastasiadis, Head of Cardiothoracic Department, AHEPA University Hospital

Study Results

No Results Posted as of Nov 28, 2013