Inflammatory Biomarkers and Blood Physical Property Transformations Following On-Pump Coronary Artery Bypass Graft

Po-Shun Hsu1, Jia-Lin Chen2, Shih-Ying Sung1

  • 1Division of Cardiovascular Surgery, Department of Surgery, Tri-Service General Hospital, National Defense Medical Center, Taipei 114202, Taiwan.

PubMed

Insights

Coronary artery bypass graft (CABG) surgery leads to increased blood viscosity and inflammation for nearly a week post-operation. Understanding these hemorheological changes is key for improving patient recovery and outcomes.

Area of Science:

  • Cardiovascular Surgery
  • Hemodynamics
  • Inflammation Biology

Background:

  • Coronary artery bypass graft (CABG) surgery involves complex physiological changes.
  • Factors like hypothermia and hemodilution can impact blood viscosity and inflammation during CABG.
  • Postoperative hemorheological alterations require thorough investigation.

Purpose of the Study:

  • To compare hemorheological and inflammatory changes before and after CABG surgery.
  • To analyze the relationship between blood viscosity and inflammatory markers post-CABG.
  • To understand the duration of these changes in the postoperative period.

Main Methods:

  • 25 patients undergoing CABG surgery were studied.
  • Whole blood viscosity (WBV) and plasma viscosity (PV) were measured at multiple time points (pre-surgery, 2 days post, 5 days post).
  • Inflammatory markers (CRP, WBC, platelets, fibrinogen) were assessed and correlated with hemorheological data.

Main Results:

  • Significant increases in PV were observed by day 5 post-CABG.
  • WBV significantly increased on day 2 and day 5 after surgery.
  • WBV correlated significantly with fibrinogen levels on days 2 and 5, with notable inflammatory marker changes.

Conclusions:

  • Hyperviscosity, indicated by elevated PV and WBV, persists for nearly a week after on-pump CABG.
  • The interplay between inflammation and hemorheological properties is critical in the postoperative phase.
  • Further research is needed to explore mechanisms and interventions to mitigate inflammation's impact on blood viscosity post-CABG.
Abstract

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