Autotransfusion system or integrated automatic suction device in minimized extracorporeal circulation: influence on coagulation and inflammatory response

Eur J Cardiothorac Surg. 2011 May;39(5):e139-43. doi: 10.1016/j.ejcts.2010.11.082. Epub 2011 Feb 21.

Abstract

Objective: To measure surrogate markers of coagulation activation as well as of the systemic inflammatory response in patients undergoing primary elective coronary artery bypass grafting (CABG) using either the so-called Smart suction device or a continuous autotransfusion system (C.A.T.S.®).

Methods: Fifty-eight patients being operated with a miniaturized circuit (minimal extracorporeal circuit, MECC) were prospectively randomized to using a so-called Smart suction device or a routine continuous autotransfusion system (C.A.T.S.®) for collection of mediastinal shed blood. The coagulation response was measured by thrombin-antithrombin complex (TAT) and D-dimer. The inflammatory response was measured by Interleukin 6 (IL-6) and complement factor 3a (C3a) at three different time points, before surgery, 2h after surgery, as well as 18 h after surgery.

Results: No serious adverse cardiovascular event was observed. Serum levels of TAT significantly differed between both groups 2h after surgery (Smart suction 16.12 ± 13.51 μg l⁻¹ vs C.A.T.S® 9.83 ± 7.81 μg l⁻¹, p = 0.040) and returned to baseline values after 18 h in both groups. Serum levels of D-dimer showed a corresponding pattern with a peak 2h after surgery (Smart suction 1115 ± 1231 ng ml⁻¹ vs C.A.T.S.® 507 ± 604 ng ml⁻¹, p = 0.025). IL-6 levels also significantly differed between both groups 2h after surgery (Smart suction 186 ± 306 pg ml⁻¹ vs C.A.T.S.® 82 ± 71 pg ml⁻¹, p = 0.072). No significant changes in serum levels of C3a over time could be observed.

Conclusions: Despite no differences in the clinical course of patients with either Smart suction or C.A.T.S.® being observed, surrogate markers of coagulation and inflammation seem to be less pronounced in patients where cardiotomy blood is not being directly reinfused. As such, C.A.T.S.® should be preferred in routine CABG, as long as no extensive volume substitution is anticipated.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Aged
  • Antithrombin III
  • Biomarkers / blood
  • Blood Coagulation / physiology*
  • Blood Transfusion, Autologous
  • Complement C3a / metabolism
  • Coronary Artery Bypass / adverse effects
  • Coronary Artery Bypass / instrumentation*
  • Coronary Artery Bypass / methods
  • Fibrin Fibrinogen Degradation Products / metabolism
  • Humans
  • Inflammation Mediators / metabolism
  • Interleukin-6 / blood
  • Middle Aged
  • Peptide Hydrolases / blood
  • Prospective Studies
  • Suction
  • Systemic Inflammatory Response Syndrome / blood
  • Systemic Inflammatory Response Syndrome / etiology*

Substances

  • Biomarkers
  • Fibrin Fibrinogen Degradation Products
  • Inflammation Mediators
  • Interleukin-6
  • antithrombin III-protease complex
  • fibrin fragment D
  • Complement C3a
  • Antithrombin III
  • Peptide Hydrolases