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