Hypothermia During Cardiopulmonary Bypass Increases Need for Inotropic Support but Does Not Impact Inflammation in Children Undergoing Surgical Ventricular Septal Defect Closure.

Minimizing the systemic inflammatory response caused by cardiopulmonary bypass is a major concern. It has been suggested that the perfusion temperature affects the inflammatory response. The aim of this prospective study was to compare the effects of moderate hypothermia (32°C) and normothermia (36°C) during cardiopulmonary bypass on markers of the inflammatory response and clinical outcomes (time on ventilator) after surgical closure of ventricular septal defects. During surgical closure of ventricular septal defects under cardiopulmonary bypass, 20 children (median age 4.9 months, range 2.3-38 months; median weight 7.2 kg, range 5.2-11.7 kg) were randomized to a perfusion temperature of either 32°C (Group 1, n = 10) or 36°C (Group 2, n = 10). The clinical data and blood samples were collected before cardiopulmonary bypass, directly after aortic cross-clamp release, and 4 and 24 h after weaning from cardiopulmonary bypass. Time on ventilation as primary outcome did not differ between the two groups. Other clinical outcome parameters like fluid balance or length of stay in the intensive care were also similar in the two groups. Compared with Group 2, Group 1 needed significantly higher and longer inotropic support (P < 0.001). In Group 1, two infants had junctional ectopic tachycardia, and another had a pulmonary hypertensive crisis. Perfusion temperature did not influence cytokine release, organ injury, or coagulation. Cardiopulmonary bypass temperature does not influence time on ventilation or inflammatory marker release. However, in the present study, with a small patient cohort, patients operated under hypothermic bypass needed higher and longer inotropic support. The use of hypothermic cardiopulmonary bypass in infants and children should be approached with care.

[1]  W. Mahle,et al.  Inflammatory response after neonatal cardiac surgery and its relationship to clinical outcomes. , 2014, The Annals of thoracic surgery.

[2]  J. Kaltman,et al.  Postoperative Junctional Ectopic Tachycardia: Risk Factors for Occurrence in the Modern Surgical Era , 2013, Pacing and clinical electrophysiology : PACE.

[3]  M. Oster,et al.  Junctional Ectopic Tachycardia After Congenital Heart Surgery in the Current Surgical Era , 2013, Pediatric Cardiology.

[4]  F. Berger,et al.  Establishment of a coculture model for studying inflammation after pediatric cardiopulmonary bypass: from bench to bedside. , 2012, Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research.

[5]  A. Şaşmazel,et al.  Randomized comparison between mild and moderate hypothermic cardiopulmonary bypass for neonatal arterial switch operation. , 2012, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

[6]  C. Brizard,et al.  The influence of bypass temperature on the systemic inflammatory response and organ injury after pediatric open surgery: a randomized trial. , 2011, The Journal of thoracic and cardiovascular surgery.

[7]  A. Koster,et al.  Specific p38 inhibition in stimulated endothelial cells: a possible new anti-inflammatory strategy after hypothermia and rewarming. , 2009, Vascular pharmacology.

[8]  I. Sauer,et al.  Methylprednisolone and tacrolimus prevent hypothermia-induced endothelial dysfunction. , 2009, The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation.

[9]  K. Polderman Mechanisms of action, physiological effects, and complications of hypothermia , 2009, Critical care medicine.

[10]  Geoffrey L. Bird,et al.  Postoperative course in the cardiac intensive care unit following the first stage of Norwood reconstruction , 2007, Cardiology in the Young.

[11]  J. L. Iribarren,et al.  Tranexamic acid attenuates inflammatory response in cardiopulmonary bypass surgery through blockade of fibrinolysis: a case control study followed by a randomized double-blind controlled trial , 2007, Critical care.

[12]  G. Wernovsky Cardiology 2007 — 10th Annual Update on Pediatric Cardiovascular Disease , 2007, Cardiology in the Young.

[13]  L. Milella,et al.  Warm surgery: our experience. , 2007, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

[14]  W. Kawalec,et al.  Risk factors for cardiac arrhythmias in children with congenital heart disease after surgical intervention in the early postoperative period. , 2007, The Journal of thoracic and cardiovascular surgery.

[15]  P. Vouhé,et al.  Normothermic cardiopulmonary bypass and myocardial cardioplegic protection for neonatal arterial switch operation. , 2006, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

[16]  G. von Bernuth,et al.  Moderate hypothermia during cardiopulmonary bypass reduces myocardial cell damage and myocardial cell death related to cardiac surgery. , 2001, Journal of the American College of Cardiology.

[17]  P. Gazzaniga,et al.  Effect of normothermic versus hypothermic cardiopulmonary bypass on cytokine production and platelet function. , 2000, The Journal of cardiovascular surgery.

[18]  H. Matsuda,et al.  Role of nitric oxide in a temperature dependent regulation of systemic vascular resistance in cardiopulmonary bypass. , 2000, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

[19]  H. Hashimoto,et al.  Cardiopulmonary Bypass Produces Greater Pulmonary than Systemic Proinflammatory Cytokines , 2000, Anesthesia and analgesia.

[20]  R. Hopkins,et al.  Interleukin-6 levels in serum and lung lavage fluid of children undergoing open heart surgery correlate with postoperative morbidity , 1998, Intensive Care Medicine.

[21]  F. Deist,et al.  Hypothermia during cardiopulmonary bypass delays but does not prevent neutrophil-endothelial cell adhesion. A clinical study. , 1995, Circulation.

[22]  Y. Durandy Minimizing systemic inflammation during cardiopulmonary bypass in the pediatric population. , 2014, Artificial organs.

[23]  Thomas F. Lüscherc,et al.  Postoperative hemodynamics depend on cardiopulmonary bypass temperature: the potential role of endothelin-1. , 1997, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.