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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 />

represented U-shaped curves. ED<br />

[hazard ratio (HR), 1.534] and LD (HR,<br />

1.654) as compared with ID, age (HR,<br />

1.7), diabetes (HR, 1.329), liver cirrhosis<br />

(HR, 1.596), initial central nervous<br />

system dysfuncti<strong>on</strong> (HR 1.319), sepsis<br />

(HR, 1.994), as well as pre-RRT mean<br />

arterial pressure (HR, .986), inotropic<br />

equivalent (HR, 1.8), and APACHE II<br />

scores (HR, 1.61) were identified as<br />

independent predictors for in-hospital<br />

mortality. Further, some factors were<br />

identified as predictors for entering<br />

either ED or LD groups. C<strong>on</strong>clusi<strong>on</strong>:<br />

Current study found the “U-shaped”<br />

associati<strong>on</strong> between timing of RRT<br />

initiati<strong>on</strong> and prognoses, and reminded<br />

physicians of paying more attenti<strong>on</strong> to<br />

patients with certain risk factors.<br />

78. The Affect Prescripti<strong>on</strong> and<br />

Absorpti<strong>on</strong> <strong>on</strong> Anti-epileptic<br />

C<strong>on</strong>centrati<strong>on</strong>s in Ex Vivo <strong>CRRT</strong><br />

Model<br />

Paul J McCarthy, Abiodun Orija, Keith<br />

Scott<br />

LSU Health Sciences Center -<br />

Shreveport, Shreveport, LA, USA,<br />

Banner Health, Phoenix, AZ, USA<br />

Background<br />

Neuroscience ICU’s utilize <strong>CRRT</strong> for<br />

indicati<strong>on</strong>s such as AKI, sepsis, drug<br />

intoxicati<strong>on</strong>s, volume overload,<br />

electrolyte c<strong>on</strong>trol and ICP c<strong>on</strong>trol.<br />

Many patients <strong>on</strong> <strong>CRRT</strong> require antic<strong>on</strong>vulsive<br />

medicati<strong>on</strong>s. How <strong>CRRT</strong><br />

prescripti<strong>on</strong>s affect drug c<strong>on</strong>centrati<strong>on</strong>s<br />

due to filtrati<strong>on</strong> or filter absorpti<strong>on</strong> is<br />

unknown. We tested four<br />

antic<strong>on</strong>vulsants in an ex vivo <strong>CRRT</strong><br />

model to see how mode affects clearance<br />

and filter absorpti<strong>on</strong>. The sieving<br />

coefficients and filter absorpti<strong>on</strong> of these<br />

drugs were measured in two modes.<br />

Although sieving coefficients of many<br />

drugs are reported, the filter behavior by<br />

mode of <strong>CRRT</strong> and filter interacti<strong>on</strong> is<br />

not largely Methods : Machine Setup<br />

A Prismaflex® System c<strong>on</strong>figured in<br />

CVVHDF or CVVH using a<br />

Prismaflex® M15 AN-69 filter was<br />

used. Samples were obtained <str<strong>on</strong>g>from</str<strong>on</strong>g> two<br />

runs; in the first run the blood flow rate<br />

was set at 1 ml/min with a replacement<br />

rate of 2 L/hour and no dialysate<br />

(CVVH). On the sec<strong>on</strong>d run, the blood<br />

flow rate was 1 ml/min, fluid<br />

replacement at 2 L/hour and dialysate at<br />

1L/hr, thus delivering CVVHDF. Saline<br />

was used as the replacement and<br />

dialysate. Filter absorpti<strong>on</strong> and sieving<br />

co-efficient were calculated.<br />

Medicati<strong>on</strong> Preparati<strong>on</strong><br />

A saline/Anti-epileptic mixture was<br />

c<strong>on</strong>nected to the access line of the<br />

machine. The return line was c<strong>on</strong>nected<br />

to an effluent bag.<br />

Drug Sampling & Drug C<strong>on</strong>centrati<strong>on</strong><br />

After initiating flow samples were drawn<br />

<str<strong>on</strong>g>from</str<strong>on</strong>g> three sites within the circuit; Prefilter,<br />

Post-filter and the Ultra-filtrate.<br />

Phenobarbital, phenytoin and valproate<br />

c<strong>on</strong>centrati<strong>on</strong>s were determined using a<br />

particle enhanced turbidimetric<br />

inhibiti<strong>on</strong> immunoassay technique.<br />

The sieving coefficient, filter absorpti<strong>on</strong><br />

and drug clearance were calculated for<br />

each run. Results: Phenytoin,<br />

levetiracetam and phenobarbital had<br />

high sieving coefficients with near<br />

complete drug filtrati<strong>on</strong>. Valproate had<br />

significant filter absorpti<strong>on</strong> with<br />

absorpti<strong>on</strong> of 56% and 37% respectively<br />

in CVVH and CVVHDF modes.<br />

C<strong>on</strong>clusi<strong>on</strong>s: Phenytoin, phenobarbital,<br />

and levetiracetam had low absorpti<strong>on</strong><br />

and high sieving coefficients. Valproate<br />

filter absorpti<strong>on</strong> was 56 % in CVVH and<br />

37% in CVVHDF. Anti-c<strong>on</strong>vulsive drug<br />

levels should be m<strong>on</strong>itored inn patients<br />

<strong>on</strong> <strong>CRRT</strong>. Many of these drugs are<br />

183

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