Definition:Â oxygen delivery provided by CO does not meet oxygen demand (or CI < 2.1 L/min/m2) due to inflammatory response of CPB, myocardial ischaemia from aortic crossclamp, hypo-/hyperthermia, reperfusion injury and surgical treatment (ventriculotomy).
Lowest CO usually 6-18 hrs post cross clamp removal, return to baseline after 24 hrs; approximately 25% of all children undergoing CHD have critical LCOS.
Monitoring cardiac output:
- Arterial blood pressure, but MAP ~ CO x SVR
- Cardiac filling pressures: CVP 9-12 mmHg, MPAP < 1/3 MAP, LAP 9-15 mmHg in biventricular heart without shunt
- Peripheral perfusion (capillary refill time)
- Core – peripheral temperature difference
- Urine output
- Base deficit
- Lactate trend
- Mixed venous saturation (aim SmvO2 >70% in biventricular heart without shunt)
- ECHO (EF, wall motion abnormality, valve dysfunction)
- Thermodilution (gold standard)
- Others: NIRS, oesophageal Doppler, bioimpedance measurement, arterial pulse pressure
Management strategies in LCOS:
- Exclusion of residual defects which compromise CO (ECHO)
- Pre-bypass strategies (methylprednisolone 10 mg/kg)
- Pre-surgical strategies (e.g. PFO/ASD in compromised RV function after biventricular repair, baffle fenestration in Fontan circulation)
- Post-surgical strategies: delayed sternal closure or chest reopening
- Ensure appropriate analgesia and sedation
- Consider muscle paralysis (to reduce oxygen demand)
- Preload adjustement: monitor filling pressures in regards to underlying lesion: optimise Hb (100-140 mg/dl in non-cyanotic, 140-160 mg/dl in cyanotic lesions), NaCl 0.9% bolus or albumin 4% bolus
- Pharmacological support: inodilator therapy (milrinone 0.5-1 mcg/kg/min) or phenoxybenzamine (0.5 mg/kg 8hrly) to reduce afterload; β-adrenergic drugs (dopamine 5-10 mcg/kg/min, dobutamine 5-10 mcg/kg/min, adrenaline 0.05-0.1 mcg/kg/min), but can increase diastolic dysfunction; short-term use of vasoconstrictors to maintain appropriate perfusion pressure (noradrenaline 0.05-0.1 mcg/kg/min, vasopressin 0.02-0.05 U/kg/hr) (see inotropes)
- Exclude rhythm abnormality
- Cardio-pulmonary interaction: aim for early extubation in Fontan circulation, TOF, Glenn Shunt if feasible
- Hypothermia: cooling to 34-35°C to reduce oxygen consumption
- Calcium-infusion (CaCl2 2-10 mg/kg/hr or 0.01-0.07 mmol/kg/hr), aim for Ca++Â : 1.4-1.6 mmol/l
- Triiodothyronine substitution in selected cases  in cardiac surgery
- Steroid replacement (hydrocortisone 1 mg/kg every 6 hrs)
- Consider PD
- ECLS: ECMO or VAD
References:
[1] Circulation. 1995 Oct 15;92(8):2226-35: Wernovsky et al: Postoperative course and hemodynamic profile after the arterial switch operation in neonates and infants. A comparison of low-flow cardiopulmonary bypass and circulatory arrest
[2] Eur J Cardiothorac Surg. 1999 Apr;15(4):515-8: Dalrymple-Hay et al: Induced hypothermia as salvage treatment for refractory cardiac failure following paediatric cardiac surgery
[3] Pediatr Crit Care Med. 2005 Nov;6(6):655-9: Suominen et al: Hemodynamic effects of rescue protocol hydrocortisone in neonates with low cardiac output syndrome after cardiac surgery
[4] Am Heart J. 2002 Jan;143(1):15-21: Hoffmann, Wernovsky et al: Prophylactic intravenous use of milrinone after cardiac operation in pediatrics (PRIMACORP) study. Prophylactic Intravenous Use of Milrinone After Cardiac Operation in Pediatrics
[5] J Cardiothorac Surg. 2010 Nov 17;5:112: Coskun et al: Extracorporeal life support in pediatric cardiac dysfunction
[6] Cardiology in the Young (2009), 19, 573-579: Vojitovic et al: Haemodynamic changes due to delayed sternal closure in newborns after surgery for congenital cardiac malformations
[7] Pediatr Crit Care Med. 2009 May;10(3):313-22: Bronicki et al: Cardiopulmonary interaction
[8] Curr Opin Cardiol. 2010 Mar;25(2):77-9: Absi et al: Noninvasive cardiac output monitoring in the pediatric cardiac Intensive Care Unit
[9] Crit Care Med. 2001 Oct;29(10 Suppl):S220-30: Wessel et al: Managing low cardiac output syndrome after congenital heart surgery
[10] Arch Dis Child. 2003 Jan;88(1):46-52: Tibby et al: Monitoring cardiac function in intensive care
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