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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 />

p-RIFLE at 72hrs allow to predict<br />

mortality at PICU.<br />

36. Creatinine Producti<strong>on</strong> and<br />

Creatinine Degradati<strong>on</strong> are<br />

Reduce in Patients with Acute<br />

Kidney Injury and Sepsis<br />

Rolando Claure-Del Granado, Josee<br />

Bouchard, Shar<strong>on</strong> Soroko, Glenn M<br />

Chertow, J<strong>on</strong>athan Himmelfarb, Alp T<br />

Ikizler, Emil P Paganini, Ravindra L<br />

Mehta<br />

University of California San Diego,<br />

University of M<strong>on</strong>treal, Stanford<br />

University, University of Washingt<strong>on</strong>,<br />

Vanderbilt University, Cleveland Clinic<br />

Background: Diagnosis and staging of<br />

acute kidney injury (AKI) uses serum<br />

creatinine (sCr). In a previous animal<br />

model of AKI, Doi et al have shown that<br />

sepsis dramatically decreases sCr levels<br />

and creatinine producti<strong>on</strong>. This<br />

phenomen<strong>on</strong> would limit early detecti<strong>on</strong><br />

of acute kidney injury. We evaluated the<br />

effect of sepsis <strong>on</strong> sCr levels, creatinine<br />

producti<strong>on</strong> (Pc’), and creatinine<br />

degradati<strong>on</strong> (Dc’) in patients with AKI.<br />

We hypothesized that sepsis will reduce<br />

creatinine producti<strong>on</strong> and sCr levels in<br />

AKI patients with sepsis.<br />

Methods: We analyzed data <str<strong>on</strong>g>from</str<strong>on</strong>g> 234<br />

critically ill n<strong>on</strong>-dialyzed patients with<br />

AKI <str<strong>on</strong>g>from</str<strong>on</strong>g> 5 centers included in the<br />

PICARD study. Creatinine producti<strong>on</strong><br />

was calculated using Cockcroft-Gault<br />

formula and using Moran et al formula<br />

which adjusts sCr for fluid balance.<br />

Creatinine degradati<strong>on</strong> was computed<br />

using Mitch et al equati<strong>on</strong> and adjusted<br />

for fluid balance. Results: Of the 234<br />

patients 139 were septic (59%). N<strong>on</strong>adjusted<br />

and adjusted sCr levels were<br />

lower in AKI patients with sepsis than in<br />

n<strong>on</strong>-septic patients (n<strong>on</strong>-adjusted sCr<br />

median 2. IQR [1.5 – 2.8] vs. 2.5 IQR<br />

[1.8 – 3.5] and adjusted sCr 2. IQR [1.4<br />

– 2.7] vs 2.4 IQR [1.8 – 3.6]; p < .1). Pc’<br />

was lower in septic patients than in n<strong>on</strong>septic<br />

(1,211 IQR [934 – 1,472] vs.<br />

1,278 IQR [1.17 – 1,538] mg/day; p <<br />

.1); the same was observed after<br />

adjusting Pc’ for fluid balance (1,92 IQR<br />

[828 – 1,295] vs. 1,124 IQR [892 –<br />

1,344]; p < .1). Dc’ was also<br />

significantly lower in septic than in n<strong>on</strong>septic<br />

patients [Figure 1]. C<strong>on</strong>clusi<strong>on</strong>s:<br />

Sepsis reduces creatinine producti<strong>on</strong> and<br />

reduces sCr levels in critically-ill<br />

patients with AKI. These observati<strong>on</strong>s<br />

could limit the early diagnosis of AKI.<br />

Sepsis also affects creatinine<br />

degradati<strong>on</strong>.<br />

37. AKI Superimposed On CKD After<br />

Cardiac Surgery Needs Different<br />

Cutoff Value Of Plasma NGAL<br />

Kent Doi, Masahiro Urata, Daisuke<br />

Katagiri, Seiichiro Murata, Minoru Ono,<br />

150

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