Comparison of hypothermic and normothermic cardiopulmonary bypass in patients undergoing coronary artery bypass graft surgery

Year 2025, Volume: 11 Issue: 2, 289 - 295

Bişar Amaç , Mesut Engin , Ahmet Kağan As , Mustafa Abanoz , Şenol Yavuz

https://doi.org/10.18621/eurj.1582534

Abstract

Objectives: Coronary artery bypass graft (CABG) surgery operations accompanied by cardiopulmonary bypass (CPB) are the most prominent treatment options. One of the basic application principles of the CPB system is the protection of vital organs by reducing metabolic rate and oxygen consumption with hypothermia. In this study, we aimed to investigate the effects of normothermia and hypothermia applications on clinical outcomes in CABG operations performed with CPB.

Methods: This single-center study was planned retrospectively. Patients who underwent isolated CABG operation with CPB at Şanlıurfa Mehmet Akif İnan Training and Research Hospital between January 01, 2020, and January 01, 2022, were included. A total of 120 patients, 60 of whom underwent hypothermic and 60 normothermic cardiac bypass, were included in the study after applying the exclusion criteria.

Results: There was no difference between the groups in terms of age, gender, diabetes mellitus, hypertension, left ventricular ejection fraction, and body surface area characteristics (P>0.05). In the normothermia group, urea, creatinine, direct bilirubin, and lactate levels were significantly higher in the first postoperative day blood values (P=0.003, P=0.04, P=0.028, P=0.005, and P<0.001, respectively). Positive inotropic agent requirement and defibrillation requirement after cross-clamping were significantly higher in the hypothermia group (P=0.006 and P=0.045, respectively).

Conclusions: In CABB operations performed with CPB, normothermia and hypothermia applications may have beneficial effects on different clinical situations.

Keywords

Cardiopulmonary bypass, coronary artery bypass grafting, normothermia, hypothermia, postoperative term

Ethical Statement

This study was approved with the protocol dated 31/10/2022 and numbered HRÜ/22.21.05 of the Harran University Clinical Research Ethics Committee.

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