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Cell saver elite

Manufactured by Haemonetics
Sourced in United States

The Cell Saver Elite is a blood cell salvage device designed to recover and reinfuse a patient's own blood during surgical procedures. It functions by collecting, washing, and concentrating the patient's blood, which can then be reinfused, reducing the need for donor blood transfusions.

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4 protocols using cell saver elite

1

Cardiopulmonary Bypass Procedure in Cardiac Surgery

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The patient was placed in the supine position with a wedge under the right chest. The femoral artery and vein were cannulated to establish CPB. After incision at the fourth intercostal space and pericardium traction, CPB commenced. The priming solution contained 1,500 mL Lactated Ringer’s injection, 500 mL Gelofusine, and 100 mL of 20% albumin. A target body temperature of 32 °C and non-pulsating perfusion utilizing a roller pump was adopted.
Furthermore, α state was used for blood gas management. After aortic clamping and antegrade perfusion of blood-containing del Nido cardioplegia (8 (link)), surgery was performed through the interatrial groove or the right atrial incision. After rewarming, norepinephrine, dobutamine, and milrinone were transfused to assist weaning from CPB if necessary. Conventional ultrafiltration was performed during CPB with a target amount of priming fluid, cardioplegia, and surgical rinsing saline. Residual blood in the surgical field and circuit were collected in an autotransfusion system (Cell Saver Elite; Haemonetics). After the hemostasis was completed, a chest tube was placed, and the incision was closed.
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2

Perioperative Cardiovascular Management

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All medications acting on the renin-angiotensin system and all diuretics were stopped on the day before surgery. General anesthesia was induced according to the protocols of the Anesthesiology Department. Anesthesia was induced and maintained in patients using target-controlled infusions of sufentanil and propofol. Atracurium was used for all anesthetics. Hemodynamic parameters were monitored with a radial artery catheter on a Philips Intellivue® MX 800. Tranexamic acid was injected before and after CPB. The CPB target flow rate was calculated using the following equation: flow (l/min) = 2.6 × body surface area. Heparin was infused before and during CPB to achieve and maintain an activated clotting time > 400 s. The protamine dose was calculated at a 1:1 rate of the heparin dose and infused at the end of CPB. Cardioplegia was applied at the surgeon's discretion. Lost blood was recovered using Cell Saver® Elite® (Haemonetics™, France) and re-transfused when possible. Vasotropic or inotropic agents, fluids and transfusion products were administered at the discretion of the anesthesiologist based on clinical, echocardiographic and biological findings. After surgery, all patients were transferred to the cardiovascular intensive care unit (ICU).
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3

Intraoperative Cell Salvage Blood Recovery

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The suction tube and blood reservoir of the IOCS machine (Cell Saver Elite, Haemonetics Corporation, MA, U.S.) was rinsed and pre-filled with 50–100 ml anticoagulant saline (heparin saline, 500 IU/ml). The negative pressure of the suction device is set at 120–150 mmHg. The anticoagulant drip rate was adjusted to about 1 drop/second, and the flow rate was adjusted according to the amount and speed of the bleeding. All intraoperative shed blood was recovered from the skin incision to tumor removal. Recovered blood was anti-coagulated and washed with sterilized saline (1500–2000 ml for 250 ml RBC). After washing, the recruited blood was filtered through PALL® leukocyte reduction filter (SB, Haemonetics Corporation, MA, U.S.). Blood products treated with IOCS–LDF are for research use only and are not returned to patients.
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4

IOCS-Based Intraoperative Blood Recovery

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The suction tube and blood reservoir of the IOCS machine (Cell Saver Elite, Haemonetics Corporation, MA, U.S. ) was rinsed and pre-lled with 50-100ml anticoagulant saline (heparin saline, 500 IU/ml ). The negative pressure of the suction device is set at 120 -150 mmHg. The anticoagulant drip rate was adjusted to about 1 drop/second, and the ow rate was adjusted according to the amount and speed of the bleeding. All intraoperative shed blood was recovered from the skin incision to tumor removal. Recovered blood was anti-coagulated and washed with sterilized saline (1500-2000 ml for 250 ml RBC).
After washing, the recruited blood was ltered through PALL ® leukocyte reduction lter (SB, Haemonetics Corporation, MA, U.S.). Blood products treated with IOCS -LDF are for research use only and are not returned to patients.
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