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