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Compound sodium lactate

Manufactured by Baxter
Sourced in United Kingdom

Compound Sodium Lactate is a sterile, nonpyrogenic solution that contains sodium lactate and sodium chloride. It is used as a source of electrolytes and to maintain fluid and electrolyte balance.

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5 protocols using compound sodium lactate

1

Standardized Anesthesia Protocol for Canine Procedures

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For all dogs, food was removed at least eight hours prior to the procedure but access to water provided until premedication. Dog were anesthetized by a veterinary anesthesiologist (AR) using a standardized protocol. Premedication with methadone 0.3 mg/kg (Ilium Methadone 10 mg/mL, Troy Laboratories, Glendenning, NSW, Australia) IM was performed 30 min prior to induction of general anesthesia with alfaxalone (Alfaxan injection 10 mg/mL, Jurox, Glendinning, NSW, Australia) 2.2–3.2 mg/kg intramuscularly. Endotracheal intubation was used to maintain anesthesia with isoflurane (I.S.O., Veterinary Companies of Australia Pty Ltd, Kings Park, NSW, Australia) in 30% oxygen through a circle rebreathing system. End tidal isoflurane was maintained at 1.3–1.4%. Infusion of a balanced isotonic crystalloid solution (Compound Sodium Lactate, Baxter Healthcare, Toongabbie, NSW, Australia) was provided at 10 mL/kg/hour IV throughout anesthesia, along with IV fentanyl (Fentanyl injection 50 µg/mL, AstraZeneca, Macquarie Park, NSW, Australia) 2 µg/kg/hour. Arterial carbon dioxide tension was maintained between 35 and 45 mmHg by provision of mechanical ventilation by an anesthesia workstation (Datex-Ohmeda S/5 Aespire Anaesthesia Machine, GE Healthcare, Chicago, IL, USA). Active warming maintained esophageal temperature between 36.0 and 38.0 °C.
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2

Liver Flushing and Fibrin Assessment

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Before undergoing NESLiP, all livers were flushed with compound sodium lactate (Hartmann’s solution, Baxter Healthcare Ltd, United Kingdom) at room temperature to de-air the cannulas and warm and preload the liver with lactate. A small sample of vena caval effluent from this preperfusion flush from 20 consecutive livers was also collected for D-dimer analysis to assess whether fibrin was present in livers before NESLiP began.
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3

Embryo Collection and Preservation

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Embryo collection occurred on 4 commercial dairy farms situated in the central and upper provinces of the North Island, New Zealand. As part of the farms' standard breeding practice, lactating dairy cattle were artificially inseminated within 12 h of observed natural estrus. Body condition score at AI (Roche et al., 2004) , days postpartum (DPP), and change in BCS from calving to AI (BCS change) were recorded for each cow. Single embryos were subsequently recovered from the uteri 7 d after AI (Day 0) utilizing standard flushing technique. Embryos were flushed with Compound Sodium Lactate (Baxter Healthcare, Deerfield, IL) supplemented with 0.1% BSA (ICP Biotechnology, Auckland, New Zealand) and 1 mM 3-[N-morpholino] propanesulfonic acid (MOPS, Sigma Chemical Co., St. Louis, MO) . The collected flushing medium (600-800 mL) was filtered to consolidate the volume and the embryos were recovered under a Nikon SMZ1500 stereo microscope (Nikon Instruments Inc., Tokyo, Japan). Embryos were evaluated and photographed (Nikon Digital Sight DS-Fi1). All embryos that had developed to at least the morula stage by Day 7 were placed in RNAlater (Ambion Inc., Foster City, CA) and stored at -80°C until processing.
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4

Fluid Challenges for Cardiac Surgery

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This is a quasi-randomised 8, 9 , single-blinded, controlled study with an allocation ratio of 1:1. The different arms consisted of doses of 1, 2, 3 and 4 ml/kg (actual body weight) of Compound Sodium Lactate (Hartmann's Solution, Baxter, Thetford, UK) as a FC infused over 5 minutes manually using a syringe of 60 mL and a timer in the multi-parameter monitor. Patients were approached when admitted to hospital before cardiac surgery. The first 20 patients were allocated to receive 1mL/kg (total body weight), the following 20 to 2 mL/Kg and so on.
Pmsf-arm, mean arterial pressure (MAP), CO, SV, heart rate (HR) and CVP were recorded at baseline and after the FC. After the second measurement, the dose of fluids was completed according to the clinical prescription.
Clinical indication for a FC was according to the standard clinical post-operative protocol 10 (Supplemental Digital Content (SDC) Figure 1).
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5

Fluid Challenge for Hemodynamic Response

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The fluid challenge consisted of 250 ml of crystalloid (Compound sodium lactate, Baxter Healthcare Ltd, U.K) infused using a syringe of 50 ml and performing 5 boluses over 5 minutes. According to the clinical protocol, an increase in CO immediately after the fluid challenge greater than 10% was considered a positive response (R). The values recorded at baseline and immediately after the fluid challenge were used for this classification.
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