Relationship Between Level of Hemoglobin A1c and Platelet Function in Patients Undergoing Cardiac Surgery

Sponsor
Clinical Hospital Centre Zagreb (Other)
Overall Status
Unknown status
CT.gov ID
NCT02711124
Collaborator
(none)
130
1
30
4.3

Study Details

Study Description

Brief Summary

The aim of this study is to evaluate whether increased level of hemoglobin A1c (HbA1c) correlates to higher level of platelet reactivity assessed by impedance aggregometry in patients with diabetes mellitus undergoing elective coronary artery bypass grafting (CABG).

Detailed Description

This study will be conducted at Cardiac Surgery Department, University Hospital Center Zagreb. It will be conducted in prospective observational fashion. Diabetic patients undergoing isolated, primary on-pump CABG will be consecutively recruited. Patients requiring urgent procedure will be excluded. Blood samples, both for conventional lab. findings (including HbA1c) and impedance aggregometry will be drawn prior to surgery and postoperatively on daily basis.

Cohort sample will be divided into two subgroups according to HbA1c level (Group 1 with HbA1c < 7% and Group 2 with HbA1c ≥ 7%, respectively). Respective subgroups will be compared for basic demographic data, laboratory findings including those obtained using platelet function testing, and for clinical outcomes, respectively.

Multiple-electrode aggregometry:

Whole blood aggregation will be determined using a new-generation impedance aggregometer (Multiplate analyzer; Roche Diagnostics). In brief, when platelets expose receptors on their surface they get activated and stick on the Multiplate sensor wires enhancing the electrical resistance between them. An increase in impedance is expressed in arbitrary area under the curve (AUC) units. Platelet aggregation is determined in response to stimulation with arachidonic acid (ASPI (aspirin-sensitive patients identification) test designed to evaluate the effect to acetylsalicylic acid (ASA)) and adenosine diphosphate (ADP) (ADP test designed to evaluate the effect of thienopyridines, such as clopidogrel).

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
130 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Relationship Between Level of Glycosylated Hemoglobin and Platelet Function in Patients Undergoing Coronary Artery Bypass Grafting
Study Start Date :
Feb 1, 2014
Anticipated Primary Completion Date :
Aug 1, 2016
Anticipated Study Completion Date :
Aug 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Group with hemoglobin A1c < 7

There will be no intervention administered to the group. The group will be observed for platelet function pre- and postoperatively.

Group with hemoglobin A1c ≥ 7%

There will be no intervention administered to the group. The group will be observed for platelet function pre- and postoperatively.

Outcome Measures

Primary Outcome Measures

  1. The level of preoperative HbA1c that will be a predictor of the higher prevalence of platelet resistance to the aspirin [4 days after surgery]

Secondary Outcome Measures

  1. Differences in perioperative aspirin resistance (AUC, area under the curve) between patients with insulin-dependent diabetes mellitus and patients with non-insulin-dependent diabetes mellitus [4 days after surgery]

  2. Correlation between platelet ADP receptors reactivity (AUC) and the type of diabetes [4 days after surgery]

  3. Correlation of diabetes duration and platelet reactivity (AUC) [4 days after surgery]

  4. The prevalence of major adverse cardiovascular events (MAACE) in patients with HbA1c ≥ 7% [3 months after surgery]

  5. Postoperative thoracic drainage in patients with the appropriate glucose regulation (Hba1c<7%) [within the first 5 days after surgery]

  6. Mortality [3 months after surgery]

  7. The level of HbA1c, that will represent the reliable predictor of platelet hyperreactivity and MAACE [within the 3 months after surgery]

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients undergoing isolated primary on-pump CABG

  • Elective surgery

  • Diabetic patients including insulin-dependent diabetes mellitus (IDDM) and non-insulin-dependent diabetes mellitus NIDDM

  • Patients on antiplatelet therapy (aspirin and/or clopidogrel) pre- and postoperatively

Exclusion Criteria:
  • Missing consent

  • Patients with cardiac surgical procedures other than isolated CABG

  • Patients on antiplatelet therapy other than aspirin or clopidogrel

  • Urgent surgery

  • Off-pump CABG

  • Redo CABG

Contacts and Locations

Locations

Site City State Country Postal Code
1 The University Hospital Centre Zagreb, Department of cardiac surgery Zagreb Croatia 10 000

Sponsors and Collaborators

  • Clinical Hospital Centre Zagreb

Investigators

  • Principal Investigator: Martina Zrno Mihaljević,
  • Study Chair: Bojan Biočina,
  • Study Director: Mate Petričević,

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Martina Zrno Mihaljević, MD, Principal Investigator, Surgeon at the Department of cardiac surgery, Clinical Hospital Centre Zagreb
ClinicalTrials.gov Identifier:
NCT02711124
Other Study ID Numbers:
  • KBC Zagreb
First Posted:
Mar 17, 2016
Last Update Posted:
Mar 22, 2016
Last Verified:
Mar 1, 2016
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Keywords provided by Martina Zrno Mihaljević, MD, Principal Investigator, Surgeon at the Department of cardiac surgery, Clinical Hospital Centre Zagreb
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 22, 2016