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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 />

lowest quartile, Δ< -22ng/ml), and the<br />

stable/persistent group (Δ was within<br />

IQR). In the stable/persistent group,<br />

urinary NGAL of day 1, day 2, their<br />

average, maximum and minimum values<br />

were all significantly associated with<br />

worsening kidney functi<strong>on</strong> (AUC-ROC<br />

> .9). On the other hand, <strong>on</strong>ly urinary<br />

NGAL at day 1, minimum values<br />

showed significant associati<strong>on</strong>s in the<br />

increasing group (AUC-ROC .75). In the<br />

decreasing group, urinary NGAL failed<br />

to show any significant associati<strong>on</strong> with<br />

worsening of AKI. However, relative<br />

reducti<strong>on</strong> rate was able to predict<br />

recovery <str<strong>on</strong>g>from</str<strong>on</strong>g> AKI (AUC-ROC=.72).<br />

C<strong>on</strong>clusi<strong>on</strong>: In the present study,<br />

absolute values of urinary NGAL can<br />

predict worsening AKI when increased<br />

or stable within 24 hr after ICU<br />

admissi<strong>on</strong>. Relative reducti<strong>on</strong> rate can be<br />

used to predict recovery <str<strong>on</strong>g>from</str<strong>on</strong>g> AKI when<br />

urinary NGAL decreased after ICU<br />

admissi<strong>on</strong>. These data indicate serial<br />

measurement of urinary NGAL is useful<br />

for predicting AKI worsening and<br />

recovery<br />

46. Transfusi<strong>on</strong> Related Acute Kidney<br />

Injury: Result of a Prospective<br />

Cohort Study<br />

Ladan Zand, Rodrigo Cartin-Ceba,<br />

Kianoush Kashani<br />

Mayo Clinic, Rochester, MN<br />

Background: Acute kidney injury (AKI)<br />

occurs in up to two third of intensive<br />

care unit (ICU) patients. It has been<br />

shown that blood product transfusi<strong>on</strong><br />

increases risk of acute lung injury<br />

(TRALI). C<strong>on</strong>sidering str<strong>on</strong>g associati<strong>on</strong><br />

between ALI and AKI, we evaluated the<br />

associati<strong>on</strong> between transfusi<strong>on</strong> and AKI<br />

in ICU patients. Methods: We<br />

performed a retrospective analysis of a<br />

prospectively collected cohort of<br />

c<strong>on</strong>secutive adults (>18 years of age)<br />

who were admitted to the ICU and<br />

received blood product transfusi<strong>on</strong> <str<strong>on</strong>g>from</str<strong>on</strong>g><br />

March 24 to December 25. We excluded<br />

those who developed AKI prior to<br />

receiving transfusi<strong>on</strong> or who were <strong>on</strong><br />

chr<strong>on</strong>ic hemodialysis at time of<br />

admissi<strong>on</strong>. Results: A total of 127<br />

patients met the inclusi<strong>on</strong> criteria. The<br />

median age was 64 (IQR, 53-77), 65<br />

were male (51%). A total of 49 (38%)<br />

patients developed AKI based <strong>on</strong> the<br />

AKIN criteria. In univariate analysis,<br />

there was no statistical significant<br />

difference in development of AKI based<br />

<strong>on</strong> the type of blood product that the<br />

patients received (cryoprecipitate,<br />

packed red blood cells, platelets or fresh<br />

frozen plasma). After adjustment for<br />

age, gender, baseline creatinine and<br />

presence of shock up<strong>on</strong> ICU admissi<strong>on</strong>,<br />

the transfusi<strong>on</strong> of blood products was<br />

not independently associated with<br />

development of AKI (Odds ratio 1.6,<br />

95% CI .95-1.18, p=.25). C<strong>on</strong>clusi<strong>on</strong>:<br />

In a cohort of heterogenous group of<br />

ICU patient who received blood product<br />

transfusi<strong>on</strong>, there was no increased risk<br />

of AKI.<br />

158

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