Lipid “Rescue” Therapy

Author(s):  
Kathryn Benavides ◽  
Jonathan Babyak
Keyword(s):  
Anaesthesia ◽  
2009 ◽  
Vol 64 (2) ◽  
pp. 122-125 ◽  
Author(s):  
J. Picard ◽  
S. C. Ward ◽  
R. Zumpe ◽  
T. Meek ◽  
J. Barlow ◽  
...  

2010 ◽  
Vol 27 (8) ◽  
pp. 590-592 ◽  
Author(s):  
P. Hamann ◽  
P. I. Dargan ◽  
N. Parbat ◽  
H. Ovaska ◽  
D. M. Wood

2010 ◽  
Vol 30 (1) ◽  
pp. 25
Author(s):  
J. Picard ◽  
S.C. Ward ◽  
R. Zumpe ◽  
T. Meek ◽  
J. Barlow ◽  
...  

Author(s):  
Jun Guan Tan ◽  
Moh Sim Wong

Background Lipaemic interference on automated analysers has been widely studied using soy-based emulsion such as Intralipid. Due to the greater adoption of fish oil-based lipid emulsion for total parenteral nutrition in view of improved clinical outcomes, we seek to characterize the optical properties of SMOFLipid 20%(Fresenius Kabi, Bad Homburg, Germany), a fish-oil based emulsion, on the Roche Cobas 6000 chemistry analyser(Roche Diagnostic, Basel, Switzerland). Method Various amounts of SMOFlipid were spiked into pooled seras. We plotted Roche Cobas Serum Indices Lipaemic indices(L-index) against the amount of SMOFlipid added. We then studied the interference thresholds for AST, ALT, Albumin and renal panel analytes using SMOFlipid. We subjected five levels of spiked lipaemia to high speed centrifugation and analysed the specimens pre and post centrifugation. To postulate whether fish-oil based lipid emulsion interferes with laboratory results in the clinical setting, we calculated concentrations of SMOFlipid post lipid rescue therapy and steady state concentration of a typical TPN regime using pharmacokinetic principles. Results SMOFlipid optical behaviour is similar to Intralipid using the Serum indices L-index, with 1mg/dL of SMOFlipid representing 1 unit of L-index. Manufacturer stated interference thresholds are accurate for ALT, AST, albumin, urea and creatinine. High speed centrifugation at 60 min 21100G facilitates the removal of fish-oil based SMOFlipid. Conclusion Based on the interference thresholds we verified and pharmacokinetics parameters provided by SMOFlipid manufacturer, total parenteral nutrition may not interfere with chemistry analytes given sufficient clearance, but lipid rescue therapy will interfere. Further studies assessing lipaemic interference on immunoassays are needed


2013 ◽  
Vol 31 (10) ◽  
pp. 1536.e1-1536.e2 ◽  
Author(s):  
Mohan Punja ◽  
Stewart G. Neill ◽  
Stella Wong,

2014 ◽  
Vol 120 (3) ◽  
pp. 724-736 ◽  
Author(s):  
Michael Wagner ◽  
York A. Zausig ◽  
Stefan Ruf ◽  
Elena Rudakova ◽  
Michael Gruber ◽  
...  

Abstract Background: Cardiovascular resuscitation upon intoxication with lipophilic ion channel–blocking agents has proven most difficult. Recently, favorable results have been reported when lipid rescue therapy is performed, i.e., the infusion of a triglyceride-rich lipid emulsion during resuscitation. However, the mechanism of action is poorly understood. Methods: The authors investigate the effects of a clinically used lipid emulsion (Lipovenös® MCT 20%; Fresenius Kabi AG, Bad Homburg, Germany) on the block of the fast Na+ current (INa) induced by the lipophilic local anesthetic bupivacaine in adult rat left ventricular myocytes by using the whole cell patch clamp technique. Results: Bupivacaine at 10 µm decreased INa by 54% (−19.3 ± 1.9 pApF−1vs. −42.3 ± 4.3 pApF−1; n = 17; P < 0.001; VPip = −40 mV, 1 Hz). Addition of 10% lipid emulsion in the presence of bupivacaine produced a 37% increase in INa (−26.4 ± 2.8 pApF−1; n = 17; P < 0.001 vs. bupivacaine alone). To test whether these results could be explained by a reduction in the free bupivacaine concentration by the lipid (lipid-sink effect), the authors removed the lipid phase from the bupivacaine–lipid mixture by ultracentrifugation. Also, the resulting water phase led to an increase in INa (+19%; n = 17; P < 0.001 vs. bupivacaine), demonstrating that part of the bupivacaine had been removed during ultracentrifugation. The substantially less lipophilic mepivacaine (40 µm) reduced INa by 27% (n = 24; P < 0.001). The mepivacaine–lipid mixture caused a significant increase in INa (+17%; n = 24; P < 0.001). For mepivacaine, only a small lipid-sink effect could be demonstrated (+8%; n = 23; P < 0.01), reflecting its poor lipid solubility. Conclusion: The authors demonstrate lipid rescue on the single-cell level and provide evidence for a lipid-sink mechanism.


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