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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 />

LMWH in group B (loading dose of<br />

LMWH 4IU/kg, maintenance dose<br />

4IU/kg/hr), and regi<strong>on</strong>al citrate plus low<br />

dose of LMWH in group C(loading dose<br />

2IU/kg, maintenance dose 2IU/kg/hr).<br />

The filter survival time, the change of<br />

hemoglobin (Hb), platelet counts (PLT),<br />

and anticoagulati<strong>on</strong>-related side effects<br />

were measured. Results: Fifty-three<br />

patients completed the study and entered<br />

into data analysis, 15 in group A, 19 in<br />

group B and C. The mean APACHEII<br />

scores in each group were 16.2 ± 3.65,<br />

17.11 ± 3.5 and 17.1 ± 4.79, respectively<br />

(P>.5). There were no significant<br />

differences in age, gender, weight,<br />

baseline values of Hb, PLT, prothrombin<br />

time, activated partial thromboplastin<br />

time, blood pH, and bicarb<strong>on</strong>ate<br />

c<strong>on</strong>centrati<strong>on</strong> between 3 groups. The<br />

filter survival time were 21.22 ± 3.48h in<br />

group A, 25.1 ± 5.5 h in group B, and<br />

4.35 ± 7.8h in group C (p .5). The %age of patients with<br />

reducti<strong>on</strong> of platelet counts more than<br />

3% were 2% in group A, 31.6% in group<br />

B, and 15.7% in group C(P>.5). The<br />

mortality rate was 4% in group A, 26.3%<br />

in group B and 36.8% in group C,<br />

respectively (P>.5). There were no<br />

differences in the CVVH durati<strong>on</strong>,<br />

hospital days and ICU days between 3<br />

groups. C<strong>on</strong>clusi<strong>on</strong>: compared with<br />

anticoagulati<strong>on</strong> using <strong>on</strong>ly regi<strong>on</strong>al<br />

citrate or LMWH, regi<strong>on</strong>al citrate plus<br />

low dose of LMWH protocol is more<br />

efficacy in prol<strong>on</strong>ging filter life span,<br />

without significant increase of<br />

anticoagulati<strong>on</strong>-related complicati<strong>on</strong>s.<br />

RRT RESEARCH<br />

72. C<strong>on</strong>tinuous Venovenous<br />

Hemodialysis (CVVHD) Effluent<br />

Imipenem Levels Predict Plasma<br />

Free Imipenem Levels<br />

Seth R Bauer, Milen Amde, Michael J<br />

C<strong>on</strong>nor, Charbel A Salem, William H<br />

Fissell<br />

Cleveland Clinic, Emory University<br />

Background: Pharmacokinetic and<br />

pharmacodynamic studies typically<br />

require time-intensive sampling<br />

strategies that may exceed clinician and<br />

or Instituti<strong>on</strong>al Review Board comfort<br />

levels with blood loss due to<br />

phlebotomy. These c<strong>on</strong>cerns are<br />

heightened in the critical care<br />

envir<strong>on</strong>ment. CVVHD effluent is<br />

typically well equilibrated with plasma,<br />

and most antibiotics in comm<strong>on</strong> use in<br />

the ICU are small molecules, suggesting<br />

that effluent drug levels might predict<br />

free plasma levels. We c<strong>on</strong>ducted an<br />

IRB-approved prospective observati<strong>on</strong>al<br />

study comparing antibiotic levels in<br />

CVVHD effluent with those in plasma.<br />

Here, we present data <str<strong>on</strong>g>from</str<strong>on</strong>g> 17 patients<br />

treated with c<strong>on</strong>comitant CVVHD and<br />

imipenem. Methods: Inclusi<strong>on</strong>: Adult<br />

patients with acute or chr<strong>on</strong>ic renal<br />

failure who were receiving CVVHD in<br />

the ICU. Exclusi<strong>on</strong>: ESLD, pregnancy.<br />

Patient data: age, gender, current and<br />

admissi<strong>on</strong> weight, CVVHD doses were<br />

recorded <strong>on</strong> case report forms (CRFs).<br />

Sampling: After the fourth dose of<br />

antibiotic during uninterrupted CVVHD,<br />

trough, 3 minute post infusi<strong>on</strong> peak, and<br />

178

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