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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 />

clinically.<br />

Results- We studied 255 <strong>CRRT</strong> systems<br />

in 69 patients. There were 43 males, 26<br />

females and average age was 57 ± 12<br />

yrs. Average filter life for group 1 was<br />

18.7 ± 13.7 hrs and for group 2 it was<br />

25. ± 15.4hrs (p-value adjusted for<br />

clustering = .4). We then analyzed those<br />

with reported clotting as reas<strong>on</strong> for<br />

system disc<strong>on</strong>tinuati<strong>on</strong> (n=15) and noted<br />

a significant difference in filter patency.<br />

Average filter life for group 1 was14.3±<br />

9.5 hrs and for group 2 it was 18.7 ± 1.5<br />

hrs. (p-value adjusted for clustering =<br />

.1). C<strong>on</strong>clusi<strong>on</strong>: C<strong>on</strong>trary to<br />

c<strong>on</strong>venti<strong>on</strong>al teaching, our results show<br />

that average filter life was l<strong>on</strong>ger in<br />

those patients <strong>on</strong> CVVHD as compared<br />

to pre-diluti<strong>on</strong> CVVH. We c<strong>on</strong>clude that<br />

Pre filter CVVH may be associated with<br />

more clotting as compared to CVVHD<br />

and while choosing a system for a<br />

patient with a c<strong>on</strong>traindicati<strong>on</strong> for<br />

anticoagulati<strong>on</strong> this factor should be<br />

taken into c<strong>on</strong>siderati<strong>on</strong>.<br />

60. Saturati<strong>on</strong> Coefficient Estimate of<br />

Peramivir in a Patient Receiving<br />

C<strong>on</strong>tinuous Veno-Venous<br />

Hemodiafiltrati<strong>on</strong><br />

Michael L Bentley, Amanda C Hansen,<br />

Jean A Smith, James S Cain<br />

Department of Pharmacy, Carili<strong>on</strong><br />

Roanoke Memorial Hospital (CRMH)<br />

and Virginia Tech Carili<strong>on</strong> School of<br />

Medicine (VTCSOM), Department of<br />

Pharmacy, CRMH and VTCSOM,<br />

Department of Medicine, Secti<strong>on</strong> of<br />

Infectious Disease, CRMH and<br />

VTCSOM, Valley Nephrology Associates<br />

and VTCSOM<br />

Purpose: To estimate the saturati<strong>on</strong><br />

coefficient of peramivir in a patient<br />

receiving c<strong>on</strong>tinuous veno-venous<br />

hemodiafiltrati<strong>on</strong> (CVVHDF) during the<br />

Fall of 29. Peramivir is a potent<br />

neuraminidase inhibitor having activity<br />

against various influenza A and B<br />

subtypes. The main route of eliminati<strong>on</strong><br />

is the kidney and a dose reducti<strong>on</strong> is<br />

justified when the creatinine clearance is<br />

< 5 ml/min. Informati<strong>on</strong> <str<strong>on</strong>g>from</str<strong>on</strong>g> the<br />

manufacturer regarding dosing during<br />

c<strong>on</strong>tinuous renal replacement therapy<br />

(<strong>CRRT</strong>) did not exist at the time of this<br />

analysis. A 29-year-old female with a<br />

history of flu like symptoms presented to<br />

a local emergency department. To<br />

manage volume and provide<br />

extracorporeal renal support CVVHDF<br />

was initiated. An infectious disease<br />

c<strong>on</strong>sult was obtained to evaluate the<br />

patient for emergency use peramivir and<br />

assist in the management of<br />

Streptococcus pneum<strong>on</strong>iae pneum<strong>on</strong>ia<br />

and bacteremia. An initial peramivir<br />

dose of 6 mg followed by 48 mg every<br />

24-hours was administered<br />

intravenously. This dose was derived<br />

based <strong>on</strong> current <strong>CRRT</strong> settings and an<br />

estimated saturati<strong>on</strong> coefficient (SA) of<br />

Methods: CVVHDF was performed<br />

using a Prisma pump and an AN69 filter.<br />

During peramivir sampling, blood flow<br />

was maintained at 1 ml/minute with a<br />

dialysate flow rate of 16.7 ml/minute<br />

and a c<strong>on</strong>vective rate, using pre-filter<br />

soluti<strong>on</strong>, of 8.3 ml/minute, respectively.<br />

The mean total ultrafiltrate produced<br />

during sampling was 14.2 ml/minute. To<br />

calculate a saturati<strong>on</strong> coefficient (SA),<br />

sampling of blood and effluent were<br />

c<strong>on</strong>ducted. Pre- and post-filter as well as<br />

an effluent sample were obtained 4- and<br />

8-hours following the third dose of 48<br />

mg. Results: Using an estimated SA of<br />

1, a dose of 48 mg (following a 6 mg<br />

load) was given every 24-hours. Serum<br />

levels were obtained as described and<br />

analyzed. A linear decrease was<br />

observed over a 24-hour period (graph)<br />

169

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