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ABSTRACTS from 16th International COnference on ... - CRRT Online

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<str<strong>on</strong>g>ABSTRACTS</str<strong>on</strong>g> FROM 17 TH INTERNATIONAL CONFERENCE ON <strong>CRRT</strong>,<br />

SAN DIEGO, FEB 14-17, 2012<br />

impairment, we studied plasma and<br />

ultrafiltrate levels during c<strong>on</strong>tinuous<br />

veno-venous hemodiafiltrati<strong>on</strong><br />

(CVVHDF). Methods: A routine<br />

determinati<strong>on</strong> of citrate in plasma and<br />

dialysate using a modular analyser<br />

(Architect c8, Abbott Italia) was set up<br />

by adapting a commercial citrate lyase<br />

method. This method was modified by<br />

lowering the sample volume, with a<br />

curve linear up to 4 mmol/L. Citrate<br />

c<strong>on</strong>centrati<strong>on</strong>s were measured undiluted<br />

in systemic plasma (range .1-4 mmol/L)<br />

and with 1:2 sample diluti<strong>on</strong> in circuit<br />

plasma or ultrafiltrate (range .2-8<br />

mmol/L). In vitro we studied the<br />

distributi<strong>on</strong> of blood citrate between<br />

intra- and extracellular compartments.<br />

Ex vivo we studied citrate levels in<br />

systemic and circuit plasma and in<br />

ultrafiltrate (at , .5, 1, 3, 6, 9, 12, 24, 48<br />

and 72 hrs) of 12 septic shock patients<br />

with liver dysfuncti<strong>on</strong> <strong>on</strong> CVVHDF.<br />

Results: In order to evaluate blood<br />

distributi<strong>on</strong> of citrate between intra- and<br />

extracellular compartments, we found in<br />

vitro a significant correlati<strong>on</strong> (r .9997, y<br />

= .66 + 1.2x, n 36) between the plasma<br />

measured and the predicted citrate<br />

c<strong>on</strong>centrati<strong>on</strong>s for an exclusive<br />

extracellular distributi<strong>on</strong> (taking into<br />

account the hematocrit value).<br />

Ex vivo median systemic citrate levels<br />

were .9 (.6-.12) mmol/L (time) and .23<br />

(.18-.31) mmol/L during CVVHDF.<br />

Median sieving coefficient for citrate<br />

was .95 (.88-1.2), and did not change<br />

with different blood flow (<str<strong>on</strong>g>from</str<strong>on</strong>g> 1 to 15<br />

ml/min) and effluent volume (<str<strong>on</strong>g>from</str<strong>on</strong>g> 135<br />

to 51 ml/hour). Net citrate removal by<br />

filter significantly correlated with the<br />

effluent volume (r .85). Median citrate<br />

load entering in patient bloodstream was<br />

as low as 13.6 (9.1-19.6, n 68)<br />

mmol/hour. Citrate tests in systemic<br />

blood increased daily cost of citrate<br />

anticoagulati<strong>on</strong> <str<strong>on</strong>g>from</str<strong>on</strong>g> 2.96 to 3.51 Euro.<br />

However, due to l<strong>on</strong>ger filter survival<br />

and reduced hemorrhagic complicati<strong>on</strong>s<br />

saving costs could be potentially<br />

relevant if test availability allowed a<br />

more extended use of citrate<br />

anticoagulati<strong>on</strong>. C<strong>on</strong>clusi<strong>on</strong>: Kinetics<br />

study dem<strong>on</strong>strated that citrate did not<br />

accumulate in septic shock patients with<br />

liver dysfuncti<strong>on</strong>, where citrate losses in<br />

the ultrafiltrate can be efficiently<br />

modulated by increasing the effluent<br />

volume.<br />

13. Fulminant wils<strong>on</strong>’s crisis:<br />

plasmapharesis vs. Mars<br />

Prince Mohan, Abdallah Geara, Richard<br />

Kr<strong>on</strong>fol, Jas<strong>on</strong> L<strong>on</strong>g, Jai<br />

Radhakrishnan, Amay Parikh<br />

Columbia University<br />

Introducti<strong>on</strong>: Wils<strong>on</strong>’s disease presents<br />

with chr<strong>on</strong>ic hepatic and neurologic<br />

dysfuncti<strong>on</strong>. In rare cases, it can present<br />

with fulminant liver failure and multiple<br />

organ dysfuncti<strong>on</strong> (including renal<br />

failure, hemolytic anemia,<br />

coagulopathy). Patients have blood high<br />

levels of copper and the initial therapy of<br />

fulminant Wils<strong>on</strong>’s crisis is directed at<br />

decreasing copper levels. Since copper is<br />

albumin bound, we evaluated 2<br />

modalities of extra-corporeal copper<br />

clearance: Molecular Adsorbant<br />

Recirculating System (MARS) and<br />

plasmapheresis. This case report will<br />

explore the efficacy of copper clearance<br />

utilizing both modalities. Methods:<br />

A 25-year-old woman with known<br />

Wils<strong>on</strong>’s disease <strong>on</strong> trientine<br />

dihydrochloride presented with<br />

fulminant Wils<strong>on</strong>’s crisis due to<br />

medicati<strong>on</strong> n<strong>on</strong>compliance for the<br />

previous 1 year (acute hemolytic anemia,<br />

fulminant liver failure, acute kidney<br />

injury). Both MARS and plasmapheresis<br />

131

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