This study was conducted from May 2012 to August 2017. All the patients with cardiogenic shock who received ECMO before emergency surgery were included.
Patients would be considered for ECMO support if they have the following clinical signs: systolic blood pressure < 90 mm Hg, required two or more high-dose vasopressors, intra-aortic balloon pump counterpulsation (IABP) needed to maintain blood pressure at 90 mm Hg, peripheral vascular constriction, cold extremities, irritability, altered mental state, urine output < 30 ml/h. High-dose vasopressor included dopamine ≥ 10 µg/kg/min, adrenaline ≥ 0.05 µg/kg/min, dobutamine ≥ 1 µg/kg/min, or milrinone ≥ 0.5 µg/kg/min.
Preoperatively, all eight patients were put on ECMO using Maquet (2050 package) or Medtronic pump head, as well as the Medos membrane lung combination. The MO loop was prefilled with lactated Ringer's solution or normal saline. The pulse-arterial ECMO (VA-ECMO) mode provided circulatory assistance through the femoral arteriovenous catheters. The intubation were all made of Medtronic Carmeda coating (19 Fr or 21 Fr for vein, 15 Fr or 17 Fr for artery). Among these patients, two received percutaneous puncture catheterisation and six underwent incision catheterisation with the placement of distal irrigation. The ECMO operation was performed in the catheterisation lab for three of the patients, and in the EICU for another four patients. One patient underwent the procedure in the normal ward During ECMO, close monitoring was conducted every four hours to maintain the activated coagulation time (ACT) at 180–220 s and the activated partial thromboplastin time (APTT) at 50-60s. Appropriate sedatives such as fentanyl, propofol, and dexmedetomidine were added to the intravenous pumps. The patients’ conditions were closely monitored for any signs of recovery. All of the eight patients were supported with ECMO and mechanical ventilation. A protective lung ventilation strategy was adopted ventilator parameters were adjusted based on the blood gas results. When the patients showed good lung functions, sedation would be stopped and patients would be extubated. However, one of them awakened and had to proceed with ECMO without sedation. Bedside echocardiography was performed daily to assess the patients’ cardiac function. If patients became haemodynamically stable, we would attempt to stop the ECMO for one hour. If the patients continued to be stable with good blood circulation and cardiac function, the ECMO would be removed.
All eight patients underwent median sternotomy under general anaesthesia. Four patients underwent off-pump coronary artery bypass grafting while on ECMO with an intraoperative ACT of > 380 s. The other four patients underwent on-pump coronary artery bypass grafting and they were heparinised to achieve ACT > 480 s. Conventional ascending aorta cannulation, as well as superior and inferior vena cava cannulation, were established. The ECMO cannula was disconnected from the loop. Following that, the loop would be attached to a connector to turn it into a closed-loop self-circulation. The aortic cross-clamp was applied before starting the cardioplegia solution by cooling the heart surface with ice debris.
Surgically, three patients underwent coronary artery bypass surgery and mitral valve replacement. Another patient underwent routine mitral valve replacement with left ventricular posterior wall repair. In the operation, a sidewall clamp was first applied on the aorta while proximal stapler was used to anastomose the proximal end of the target vessel before being moved down to perform s distal anastomosis. The other four patients underwent simple coronary artery bypass grafting. All the bridging vessels used were the great saphenous veins. Of the total 15 grafts, five were for the anterior descending branch, one was for the diagonal branch, six for the circumflex branches, and three for the posterior descending branches. Mitral valve replacement was performed in four patients in which the posterior leaflet was retained and the intermittent suture was implanted. An artificial mechanical valve was used (Medtronic AP360 M24 or 26) for the patient with a ruptured posterior wall of the left ventricle as a result of visceral trauma. The valve was repaired with the intracardiac interrupted suture combined with the epicardial “sandwich” suture. All the patients were followed-up on November 30th 2017, via phone and by outpatient visits to determine their survivals and cardiac functions.