АКШ
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disease on |
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return to operating |
and 0.30±0.33 mg/L, |
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immunosuppres |
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room, prevalence |
respectively; p=0.40). |
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sion, chronic |
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of postoperative |
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moderate to |
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atrial fibrillation, |
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high-dose |
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and the duration of |
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corticosteroid |
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stay in the ICU |
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therapy, ESRD, |
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and hospital |
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patients |
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receiving IV |
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nitrates. |
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The role of |
To |
Systemat |
974 |
RCTs that compared |
The following |
ARF requiring |
Peak postsurgery |
A pooled estimate |
p=0.002 |
OR: 0.32; |
A pooled estimate showed that |
natriuretic |
systematically |
ic review |
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any form or dose of |
studies were |
dialysis, 30-d or |
serum creatinine |
showed that the use of |
for AKI |
95% CI: |
natriuretic peptide administration |
peptide |
review these |
and |
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natriuretic peptide |
excluded: (1) |
in-hospital |
levels, postsurgery |
natriuretic peptide |
requiring |
0.15 to |
was not associated with a |
administrati |
trials to |
meta- |
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with placebo in adult |
nonrandomized |
mortality |
urine output, |
was associated with a |
dialysis |
0.66 for |
statistically significant reduction |
on in CV |
ascertain the |
analysis |
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(age >18 y) patients |
trials, (2) |
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postsurgery serum |
reduction in ARF |
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AKI |
in mortality (OR: 0.59; 95% CI: |
surgery- |
role of |
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undergoing CV |
duplicate |
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aldosterone levels, |
requiring dialysis |
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requiring |
0.31 to 1.12; p=0.53). |
associated |
natriuretic |
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surgeries, and that |
publications, |
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duration of |
(OR: 0.32; 95% CI: |
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dialysis |
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renal |
peptide |
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reported at least 1 of |
(3) those |
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mechanical |
0.15 to 0.66; |
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dysfunction: |
administration |
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the following |
evaluating the |
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ventilation, and |
p=0.002). Other |
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a systematic |
in the |
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prespecified renal |
role of |
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length of ICU |
benefits were a |
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review and |
management |
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outcomes: ARF |
natriuretic |
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stay. |
reduction in |
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meta- |
of CV surgery- |
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requiring dialysis, |
peptides in a |
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postsurgery peak |
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analysis of |
associated |
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peak postsurgery |
noncardiovascu |
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serum creatinine |
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RCTs. 2009 |
renal |
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serum creatinine |
lar surgical |
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levels (WMD/OR: |
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(257) |
dysfunction. |
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levels, or |
setting (i.e., |
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−0.27; 95% CI: −0.38 |
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postsurgery urine |
major |
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to −0.16; p<0.002), an |
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output. |
abdominal |
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increase in |
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surgery and |
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postsurgery urine |
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radiocontrast |
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output (WMD/OR: |
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nephropathy |
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600; 95% CI: 330 to |
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prevention), (4) |
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870; p<0.001), a |
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experimental |
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reduction in |
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animal studies, |
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postsurgery serum |
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and (5) those |
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aldosterone levels, |
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that did not |
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and reductions in |
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report the |
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mechanical |
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prespecified |
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ventilation duration |
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renal outcomes |
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and ICU stay length. |
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(including |
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those in which |
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information on |
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renal outcomes |
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© American College of Cardiology Foundation and American Heart Association, Inc. |
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was not |
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available |
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despite |
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contacting the |
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original study |
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authors). |
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Beneficial |
To determine |
Systemat |
1,290 |
The following |
Exclusion |
The number of |
The incidence of |
Fenoldopam use |
p=0.007 |
OR: 0.54; |
N/A |
impact of |
the impact of |
ic review |
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inclusion criteria |
criteria were: |
patients |
AKI and |
decreased the risk of |
(for AKI |
95% CI: |
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fenoldopam |
fenoldopam on |
and |
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were used for |
(1) studies |
progressing to |
hypotension, peak |
RRT (6.5% in the |
requiring |
0.34 to |
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in critically |
AKI, patient |
meta- |
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potentially relevant |
selecting only |
AKI that requires |
serum creatinine |
fenoldopam group vs. |
RRT); |
0.84 (for |
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ill patients |
mortality, and |
analysis |
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studies: (1) random |
patients |
at least 1 episode |
levels, long-term |
10.4% in the control |
p=0.01 (for |
AKI |
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with or at |
length of |
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allocation to |
undergoing |
of RRT, the |
survival, and the |
arm; OR: 0.54; 95% |
mortality); |
requiring |
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risk for |
hospital stay in |
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treatment, (2) |
procedures |
incidence of in- |
duration of ICU |
CI: 0.34 to 0.84; |
p<0.001(fo |
RRT); |
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ARF: a |
critically ill |
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comparison of |
with |
hospital |
and hospital stays |
p=0.007) and of all- |
r AKI). |
OR: 0.64; |
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meta- |
patients |
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fenoldopam vs. |
angiographic |
mortality |
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cause mortality |
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95% CI: |
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analysis of |
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control treatment, |
contrast media, |
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(15.1% vs. 18.9%; |
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0.45 to |
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randomized |
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and (3) performed in |
(2) nonparallel |
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OR: 0.64; 95% CI: |
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0.91 |
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clinical |
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surgical or intensive |
design (i.e., |
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0.45 to 0.91; p=0.01), |
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(mortality) |
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trials. 2007 |
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care patients (thus |
crossover) |
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as well as AKI |
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, OR: 0.43; |
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(258) |
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not including |
randomized |
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(16.0% vs. 28.3%; |
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95% CI: |
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patients administered |
trials, (3) |
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OR: 0.43; 95% CI: |
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0.32 to |
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radiocontrast dye). |
duplicate |
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0.32 to 0.59; |
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0.59 |
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publications (in |
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p<0.001). |
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(AKI). |
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this case, only |
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the article |
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reporting the |
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longest follow- |
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up was |
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abstracted), (4) |
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nonhuman |
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experimental |
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studies, and (5) |
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no outcome |
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data. |
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Fenoldopam |
To study |
RCT |
155 |
ICU patients with a |
Exclusion |
The incidence of |
N/A |
Overall in critically ill |
p=0.049 |
N/A |
There was no statistically |
mesylate in |
whether |
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serum creatinine |
criteria were a |
dialysis therapy |
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patients, 27.5% in the |
for the |
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significant difference in 21-d |
early acute |
administration |
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level increasing to |
clinical |
and/or all-cause |
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fenoldopam group |
incidence |
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mortality rates between the 2 |
tubular |
of low-dose |
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50%> a normal |
diagnosis of |
mortality at 21 d. |
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developed ATN |
of ATN in |
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groups. However, fenoldopam |
necrosis: a |
fenoldopam |
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baseline level |
ARF from |
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compared with 38.7% |
cardiac |
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reduced the incidence of ATN in |
randomized, |
during early |
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(creatinine >1.5 |
causes other |
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in the placebo group |
surgery |
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postoperative cardiothoracic |
double- |
ATN would |
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mg/dL [>133 |
than ATN, |
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(p=0.235). Similarly, |
patients |
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surgery patients with early ATN |
blind, |
decrease the |
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μmol/L]) or a 25% |
ARF after renal |
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there was no |
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(17.6% vs. 38.8%; p=0.049). |
© American College of Cardiology Foundation and American Heart Association, Inc.
placebo- |
need for |
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increase > a baseline |
transplantation, |
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difference in the |
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controlled |
dialysis |
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level >1.5 mg/dL |
and pregnancy |
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incidence of dialysis |
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clinical trial. |
therapy and/or |
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(>133 μmol/L) |
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therapy between |
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2005 (259) |
incidence of |
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during a single 24-h |
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patients randomly |
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death at 21 d. |
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period were |
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assigned to |
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considered to have a |
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fenoldopam. |
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diagnosis of ATN. |
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Patients with ATN |
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and MAP >70 mm |
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Hg with adequate |
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central venous |
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pressure and |
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administered no |
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more than 2 |
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vasopressors were |
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eligible for study |
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enrollment. |
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Fenoldopam |
To evaluate |
RCT |
193 |
Patients were |
Exclusion |
AKI |
Need for RRT |
AKI developed in |
p=0.02 |
N/A |
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infusion for |
the |
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included if at least 1 |
criteria were |
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12.6% patients |
(ATN rate), |
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renal |
renoprotective |
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of the following risk |
defined by age |
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receiving fenoldopam |
p=0.004 |
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protection in |
effects of |
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factors was present: |
<18 y, |
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and in 27.6% patients |
(need for |
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high-risk |
fenoldopam in |
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preoperative serum |
preoperative |
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receiving placebo |
RRT) |
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cardiac |
patients at high |
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creatinine >1.5 |
use of |
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(p=0.02), whereas |
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surgery |
risk of |
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mg/dL, age >70 y, |
inotropes, |
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renal replacement |
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patients: a |
postoperative |
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diabetes mellitus on |
preoperative |
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therapy was not |
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randomized |
AKI |
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insulin treatment, or |
dialysis, and |
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required in |
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clinical |
undergoing |
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prior cardiac surgery |
known allergy |
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fenodolpam group, |
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study. 2007 |
elective |
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to fenoldopam |
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but it was started in |
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(260) |
cardiac |
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mesylate. |
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8.2% patients in |
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surgery |
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placebo group |
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requiring CPB. |
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(p=0.004). Serum |
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creatinine was similar |
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at baseline (1.8±0.4 |
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mg/dL vs. 1.9±0.3 |
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mg/dL) in the |
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fenoldopam and |
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placebo groups but |
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differed significantly |
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(p<0.001 and |
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p<0.001) 24 h |
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(1.6±0.2 mg/dL vs. |
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2.5±0.6 mg/dL) and |
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N/A |
© American College of Cardiology Foundation and American Heart Association, Inc.
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48 h (1.5±0.3 mg/dL |
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vs. 2.8±0.4 mg/dL) |
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after the operation. |
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Effects of |
To determine |
RCT |
80 |
Patients scheduled |
Exclusion |
The adequacy of |
Renal function |
There was a |
p=0.045 |
N/A |
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fenoldopam |
the effects of |
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for elective cardiac |
criteria: |
perfusion |
during and after |
significantly higher |
for the rate |
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infusion in |
fenoldopam in |
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operations on CBP, |
absence of |
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CPB (incidence of |
rate of AKI in the |
of AKI |
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complex |
a population of |
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over 18 y, and who |
written consent |
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AKI, changes in |
placebo group (10% |
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cardiac |
patients |
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had planned |
and allergy to |
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urine output, |
vs. 0%; p=0.045). |
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surgical |
undergoing |
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complex cardiac |
femoldopam. |
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changes in serum |
Urine output during |
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operations: a |
complex |
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operation (coronary |
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creatinin), in- |
and after CPB did not |
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Patients in the fenoldopam group |
prospective, |
cardiac |
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and valve operation, |
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hospital mortality, |
differ between |
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had higher oxygen delivery |
randomized, |
operations. |
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double/triple valve |
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major morbidity |
groups, nor did the |
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during CPB and a significantly |
double- |
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operation, ascending |
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renal function |
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lower perfusion pressure, |
blind, |
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aorta operation) |
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parameters. |
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although this parameter was still |
placebo- |
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requiring a |
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within the normal range. Blood |
controlled |
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predictable CPB |
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lactate concentrations during |
study. 2010 |
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time of >90 min |
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CPB were similar in the 2 |
(261) |
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were included |
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groups. |
Fenoldopam |
To determine |
Meta- |
1,059 |
The following |
The exclusion |
The number of |
Peak serum |
Pooled estimates |
p<0.001 |
OR: 0.37; |
N/A |
reduces the |
the efficacy of |
analysis |
|
inclusion criteria |
criteria were |
patients |
creatinine levels, |
showed that |
(need for |
95% CI: |
|
need for |
fenoldopam in |
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were used for |
(1) nonparallel |
requiring at least |
and the duration of |
fenoldopam |
RRT); |
0.23 to |
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renal |
the prevention |
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potentially relevant |
design (i.e., |
1 episode of |
mechanical |
consistently and |
p<0.01 |
0.59 (need |
|
replacement |
of ARF, the |
|
|
studies: (1) clinical |
crossover) |
RRT, the |
ventilation, ICU |
significantly reduced |
(mortality) |
for RRT), |
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therapy and |
authors |
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|
trial comparing |
randomized |
incidence of in- |
and hospital stay, |
the need for renal |
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OR: 0.46: |
|
in-hospital |
performed a |
|
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fenoldopam with |
trials, (2) |
hospital |
hypotension, or |
replacement therapy |
|
95% CI: |
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death in CV |
systematic |
|
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control treatment, (2) |
duplicate |
mortality |
the use of |
(5.7% vs.13.4%; OR: |
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0.29 to |
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surgery: a |
review of |
|
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clinical trial using |
publications (in |
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vasoconstrictors. |
0.37; 95% CI: 0.23 to |
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0.75 (for |
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meta- |
RCTs and |
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random allocation or |
this case only |
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0.59; p<0.001 and in- |
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mortality) |
|
analysis. |
propensity- |
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adjustment for |
the article |
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hospital death (OR: |
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2008 (262) |
matched |
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|
covariates (for |
reporting the |
|
|
0.46; 95% CI: 0.29 to |
|
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|
|
studies in |
|
|
nonrandomized |
longest follow- |
|
|
0.75; p=0.01). These |
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|
patients |
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|
studies), and (3) |
up was |
|
|
benefits were |
|
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|
undergoing |
|
|
clinical trial in |
abstracted), (3) |
|
|
associated with |
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CV surgery. |
|
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patients undergoing |
nonhuman |
|
|
shorter ICU stay |
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CV surgery. |
experimental |
|
|
(WMD=-0.93 d [- |
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|
studies, and (4) |
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1.27; to 0.58]; |
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no outcome |
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p=0.002). |
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data as far as |
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RRT or death |
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are concerned. |
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|
Meta- |
To evaluate |
Meta- |
3,359 |
Inclusion criteria: |
N/A |
Mortality |
Need for RRT, |
There was no effect |
p=NS |
RR: 0.93; |
Improvements in serum CrCl |
analysis: |
the effects of |
analysis |
|
parallel-group RCTs |
|
|
adverse effects |
of low-dose dopamine |
|
95% CI: |
(4% relative decrease [CI: 1% to |
© American College of Cardiology Foundation and American Heart Association, Inc.
low-dose |
low-dose |
|
|
that included any pt. |
|
|
|
on mortality (RR: |
|
0.76 to |
7%]) and measured CrCl (6% |
dopamine |
dopamine (≤5 |
|
|
sample, compared |
|
|
|
0.96; 95% CI: 0.78 to |
|
1.15 (need |
relative increase [CI: 1% to |
increases |
µg/kg of body |
|
|
low-dose dopamine |
|
|
|
1.19), need for renal |
|
for RRT) |
11%]) on d 1 were clinically |
urine output |
weight per |
|
|
(≤5 µg/kg of body |
|
|
|
replacement therapy |
|
|
insignificant. |
but does not |
min) compared |
|
|
weight per min) with |
|
|
|
(RR: 0.93; 95% CI: |
|
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|
prevent |
with placebo |
|
|
placebo or no |
|
|
|
0.76 to 1.15), or |
|
|
|
renal |
or no therapy |
|
|
therapy, and |
|
|
|
adverse events (RR: |
|
|
|
dysfunction |
in patients |
|
|
recorded any of the |
|
|
|
1.13; 95% CI: 0.90 to |
|
|
|
or death. |
with or at risk |
|
|
following outcomes: |
|
|
|
1.41). Low-dose |
|
|
|
2005 (263) |
for ARF. |
|
|
all-cause mortality, |
|
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|
dopamine increased |
|
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|
requirement for renal |
|
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|
urine output by 24% |
|
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|
replacement therapy, |
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(CI: 14% to 35%) on |
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renal physiologic |
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d 1. |
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variables (urine |
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output, serum CrCl, |
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or measured CrCl on |
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d 1-, 2-, or 3- after |
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starting therapy), or |
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adverse effects. We |
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also included trials |
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in which patients |
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were allocated in |
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alternating fashion |
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or by hospital |
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registry number |
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(quasi- |
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randomization) and |
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trials with |
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pharmacologic co- |
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interventions (such |
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as mannitol, |
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diuretics, or |
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diltiazem) that were |
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equally applied to |
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both groups. |
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|
Mannitol, |
To study |
Prospecti |
100 |
Patients who |
Excluded from |
Need for RRT |
Peak serum CrCls |
Diuresis occurred in |
N/A |
N/A |
N/A |
furosemide, |
whether the |
ve |
|
manifested either |
the study were |
|
|
93.3% of mannitol- |
|
|
|
and |
need for |
|
|
acute oliguric or |
patients with |
|
|
furocemide-dopamine |
|
|
|
dopamine |
dialysis can be |
|
|
anuric renal failure |
ARF associated |
|
|
group vs. 10% in |
|
|
|
infusion in |
avoided by |
|
|
in the postoperative |
with inadequate |
|
|
diuretics group. 90% |
|
|
|
postoperativ |
infusion of the |
|
|
period, with |
cardiac output |
|
|
of diuretics group |
|
|
|
e renal |
solution of |
|
|
adequate |
and tissue |
|
|
required dialysis |
|
|
|
© American College of Cardiology Foundation and American Heart Association, Inc.
failure |
mannitol, |
|
|
postoperative cardiac |
perfusion, |
|
|
versus only 6.7% of |
|
|
|
complicatin |
furosemide, |
|
|
output and tissue |
patients who |
|
|
mannitol-furocemide- |
|
|
|
g cardiac |
and dopamine |
|
|
perfusion were |
required |
|
|
dopamine group. |
|
|
|
surgery. |
in the early |
|
|
prospectively |
preoperative |
|
|
|
|
|
|
2000 (264) |
postoperative |
|
|
evaluated and, in |
dialysis and |
|
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|
|
period in |
|
|
100 patients, such |
patients who |
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oliguric renal |
|
|
acute renal |
depended on |
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failure. |
|
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dysfunction was |
dialysis. |
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recognized in the |
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postoperative period. |
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|
Diltiazem |
To evaluate |
RCT |
60 |
Patients undergoing |
Ex ante |
Urine output |
Excretion of |
Cumulative urine |
p<0.001 |
N/A |
Diltiazem stimulates urine |
may |
the influence |
|
|
elective cardiac |
exclusion |
|
alpha-GST, |
output in the |
(excretion |
|
output, reduces excretion of |
preserve |
of dopamine |
|
|
surgery |
criteria |
|
alpha(1)-MG, ss- |
diltiazem group |
of alpha- |
|
alpha-GST and ss-NAG and may |
renal tubular |
and diltiazem |
|
|
|
(screened the d |
|
NAG, and CrCl |
(9.0±2.8 L) increased |
GST) |
|
be useful to maintain tubular |
integrity |
on renal |
|
|
|
before surgery) |
|
|
significantly |
|
|
integrity after cardiac surgery. |
after cardiac |
function and |
|
|
|
were severe LV |
|
|
compared with |
|
|
|
surgery. |
markers for |
|
|
|
dysfunction |
|
|
placebo (7.0±1.6 L), |
|
|
|
2003 (265) |
ARF, |
|
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|
(EF <25%), |
|
|
but not compared |
|
|
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|
including |
|
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|
renal |
|
|
with dopamine |
|
|
|
|
urinary alpha- |
|
|
|
insufficiency |
|
|
(7.8±1.8 L). CrCl |
|
|
|
|
glutathion s- |
|
|
|
(creatinine |
|
|
showed no significant |
|
|
|
|
transferase |
|
|
|
>177 μmol·L– |
|
|
intergroup |
|
|
|
|
(alpha-GST), |
|
|
|
1), liver |
|
|
differences. There |
|
|
|
|
alpha-1- |
|
|
|
dysfunction |
|
|
were no significant |
|
|
|
|
microglobulin |
|
|
|
(aspartate |
|
|
intergroup differences |
|
|
|
|
(alpha (1)- |
|
|
|
aminotransferas |
|
|
in alpha (1)-MG |
|
|
|
|
MG) and N- |
|
|
|
e >40 U·L–1 or |
|
|
excretion. Alpha-GST |
|
|
|
|
acetyl-ss- |
|
|
|
alanine |
|
|
increased |
|
|
|
|
glucosaminida |
|
|
|
aminotransferas |
|
|
significantly in the |
|
|
|
|
se (ss-NAG) |
|
|
|
e >40 U·L–1), |
|
|
placebo (2.1 ± 1.8 to |
|
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|
|
after |
|
|
|
repeat cardiac |
|
|
11.4 ± 8.6 micro g x |
|
|
|
|
extracorporeal |
|
|
|
surgery, known |
|
|
L(-1)) and in the |
|
|
|
|
circulation. |
|
|
|
allergy to |
|
|
dopamine groups (2.7 |
|
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|
|
dopamine or |
|
|
± 1.8 to 13.6 ±14.9 |
|
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|
|
diltiazem, |
|
|
micro g x L(-1)), but |
|
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|
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|
|
|
|
anemia |
|
|
not in the diltiazem |
|
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|
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|
|
|
(hemoglobin |
|
|
group (1.8 ± 1.4 to |
|
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|
|
<9.0 g·dL–1), |
|
|
3.2 ± 3.2 micro g x |
|
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|
|
insulin- |
|
|
L(-1)). Forty eight h |
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|
|
dependent |
|
|
postoperatively alpha- |
|
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|
|
|
diabetes |
|
|
GST was significantly |
|
|
|
|
|
|
|
|
mellitus and |
|
|
lower in the diltiazem |
|
|
|
© American College of Cardiology Foundation and American Heart Association, Inc.
|
|
|
|
|
use of diuretics |
|
|
group than in both |
|
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|
|
|
|
|
|
or calcium |
|
|
other groups. |
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|
antagonists. Ex |
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post exclusion |
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criteria were |
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perioperative |
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MI, death, and |
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low output |
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syndrome |
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requiring IABP |
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and the use of |
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aminoglycoside |
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s during the |
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study period or |
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an intolerance |
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to the study |
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drug. |
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|
Diltiazem |
To determine |
RCT |
330 |
To be included in the |
Patients were |
The incidence of |
LOS, serum |
During the first 5 d |
p=NS |
N/A |
N/A |
treatment |
whether |
|
|
study, patients’ |
excluded if |
renal failure, |
creatinine or BUN |
postoperative d, the 2 |
|
|
|
does not |
diltiazem |
|
|
hearts had to be in |
they had a |
mortality rate |
levels |
groups did not differ |
|
|
|
alter renal |
treatment |
|
|
sinus rhythm and the |
history of |
|
|
in terms of serum |
|
|
|
function |
alters renal |
|
|
patients had to be at |
chronic atrial |
|
|
creatinine or BUN |
|
|
|
after |
function in |
|
|
increased risk for |
arrhythmias or |
|
|
levels. The incidence |
|
|
|
thoracic |
patients |
|
|
developing |
second-degree |
|
|
of renal failure was |
|
|
|
surgery. |
undergoing |
|
|
postoperative |
atrioventricular |
|
|
0.6% in the diltiazem |
|
|
|
2001(266) |
major thoracic |
|
|
arrhythmias, either |
block or were |
|
|
group and 1.2% in the |
|
|
|
|
surgery. |
|
|
because they were |
taking class I or |
|
|
placebo group |
|
|
|
|
|
|
|
scheduled to |
class III |
|
|
(difference was not |
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|
|
undergo a |
antiarrhythmic |
|
|
significant). There |
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pneumonectomy or |
drugs or |
|
|
was no difference in |
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were >60 y of age |
calcium- |
|
|
the length of |
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|
and scheduled to |
channel |
|
|
hospitalization or |
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have a lobectomy. |
blockers for |
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mortality rate. |
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ischemic heart |
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disease. |
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Patients who |
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developed new |
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signs of |
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myocardial |
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ischemia or |
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infarction or |
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who required |
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|
© American College of Cardiology Foundation and American Heart Association, Inc. |
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|
inotropic support on arrival to the postanesthesia care unit were also excluded.
AKI indicates acute kidney injury; alpha-GST, alpha-glutathion s-transferase, ARF, acute renal failure; ARI, acute renal injury; ATN, acute tubular necrosis; BUN, blood urea nitrogen;CI, confidence interval; CKD, chronic kidney disease; CK-MB, creatinine-kinase myocardial band; CPB, cardiopulmonary bypass; CrCl, Creatinine Clearance; CV, cardiovascular; d, day; EF, ejection fraction; ESRD, end-stage renal disease; IABP, intra aortic balloon pump, ICU, intensive care unit; IV, intravenous; LOS, length of stay; LV, left ventricular; MAP, mean arterial pressure; MI, myocardial infarction; N/A, not applicable; NAC, N-Acetylcysteine; NS, non significant; NYHA, New York Heart Association; OR, odds ratio; RCT, randomized controlled trial; RR, relative risk; RRT, renal replacement therapy; ss-NAG, N-acetyl-ss-glucosaminidase; U, unit; and WMD, weighted mean difference.
Data Supplement 38. Renal Dysfunction
Article Title |
Aim of |
Study |
Study |
Patient Population/Inclusion & Exclusion |
Endpoints |
Statistical Analysis |
P Values & |
OR / HR / |
Study Summary |
||
|
Study |
Type |
Size |
Criteria |
|
|
Reported |
95% CI |
RR |
|
|
|
|
|
|
Inclusion Criteria |
Exclusion Criteria |
Primary |
Secondary |
|
|
|
|
|
|
|
|
|
|
Endpoint |
Endpoint |
|
|
|
|
OPCAB and |
To |
Meta- |
27,806 |
RCTs and |
Studies involving |
Incidence of |
Peak |
The pooled effect from |
p<0.001 for |
OR: 0.61; |
In the observational |
AKI: a meta- |
critically |
analysis |
|
observational studies |
patients with ESRD |
overall AKI (as |
postoperative |
both RCT and |
both |
95% CI: 0.45 |
cohort, both overall |
analysis of |
evaluate |
|
|
comparing OPCAB |
on long term RRT |
reported by |
serum creatinine |
observational studies |
incidence of |
to 0.8 for |
AKI (OR: 0.61; 95% |
randomized |
the |
|
|
with CAB in adult |
were excluded. |
individual study |
level, nadir |
showed a significant |
overall AKI |
incidence of |
CI: 0.45 to 0.81; |
and |
outcomes |
|
|
(>18 y) patients. To |
Studies for which |
definitions), |
postoperative |
reduction in overall AKI |
and incidence |
AKI, OR: |
p<0.001) and AKI |
observational |
and |
|
|
be included, studies |
exclusion of RRT- |
incidence of |
Crcl, and change |
(OR: 0.57; 95% CI: 0.43 |
of AKI |
0.54; 95% CI: |
requiring RRT (OR: |
studies. 2009 |
conduct of |
|
|
had to report at least 1 |
dependent patients |
AKI requiring |
in postoperative |
to 0.76; p<0.001) and AKI |
requiring |
0.40 to 0.73 |
0.54; 95% CI: 0.40 to |
(267) |
clinical |
|
|
of the following renal |
with ESRD could not |
RRT. |
serum creatinine |
requiring RRT (OR: 0.55; |
RRT. |
for incidence |
0.73; p<0.001) were |
|
trials |
|
|
outcomes: AKI, AKI |
be verified were also |
|
and Crcl from |
95% CI: 0.43 to 0.71; |
|
of AKI |
significantly less in the |
|
addressing |
|
|
requiring RRT, or |
excluded. |
|
corresponding |
p<0.001) in the OPCAB |
|
requiring |
OPCAB group. |
|
the impact |
|
|
postoperative serum |
|
|
preoperative |
group compared with the |
|
RRT. |
|
|
of |
|
|
creatinine/Crcl. For |
|
|
values. |
CAB group. In RCTs, |
|
|
|
|
OPCAB |
|
|
studies that reported |
|
|
|
overall AKI was |
|
|
|
|
on AKI |
|
|
data from the same |
|
|
|
significantly reduced in |
|
|
|
|
during the |
|
|
trial in multiple |
|
|
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the OPCAB group (OR: |
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postoperat |
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publications, only the |
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0.27; 95% CI: 0.13 to |
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ive period. |
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largest study was |
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0.54; p<0.001); however, |
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included. |
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no statistically significant |
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difference was noted in |
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AKI requiring RRT (OR: |
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0.31; 95% CI: 0.06 to |
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1.59; p=0.2). |
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© American College of Cardiology Foundation and American Heart Association, Inc.
Coronary |
This study RCTs |
116 |
Patients with |
N/A |
Changes in renal |
Clinical |
N/A |
Serum |
N/A |
This study suggests |
artery bypass |
was |
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nondialysis-dependent |
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function |
outcomes |
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creatinine, |
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that on-pump as |
grafting with |
designed |
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renal insufficiency |
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p<0.000; |
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compared with |
or without |
to |
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with a GFR of 60 mL |
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GFR, |
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OPCAB is more |
CPB in |
compare |
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· min–1 · 1.73 m–2 or |
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p<0.000 |
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deleterious to renal |
patients with |
the effect |
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less undergoing |
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function in diabetic |
preoperative |
of off- |
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primary, elective |
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patients with |
nondialysis |
pump and |
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CABG |
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nondialysis dependent |
dependent |
on-pump |
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renal insufficiency. |
renal |
techniques |
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insufficiency: |
on renal |
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A |
function |
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randomized |
in patients |
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study. 2007 |
with |
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(268)nondialysi s- dependent renal insufficien cy with a
GFR of 60 mL · min– 1 · 1.73 m– 2 or less
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undergoin |
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g primary, |
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elective |
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CABG |
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Renal |
To |
Observa |
2,869 |
(Preoperative CrCl |
Patients on dialysis. |
Decrease in |
N/A |
Propensity match. |
p=0.2 |
N/A |
No difference in renal |
Dysfunction |
compare |
tional |
(158 |
<60 mL/min) and who |
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postop Crcl |
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outcomes between on |
in High-Risk |
the |
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OPCA |
underwent isolated |
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>25% or need |
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and off-pump. |
Patients After |
incidence |
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B) |
CABG |
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for RRT |
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On-Pump and |
of |
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postoperat |
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Coronary |
ive renal |
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Artery |
dysfunctio |
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Bypass |
n in |
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Surgery: A |
patients |
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Propensity |
with |
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Score |
preoperati |
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Analysis. |
ve renal |
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2005 (269) |
dysfunctio |
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© American College of Cardiology Foundation and American Heart Association, Inc.
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n |
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(OPACB |
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vs.on- |
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pump) |
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Coronary |
To |
Observa |
253 |
Preoperative serum |
Patients on dialysis, |
Changes in renal |
N/A |
N/A |
p<0.05 |
N/A |
Incidence of RRT |
revascularizat |
compare |
tional |
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creatinine more than |
PVD, emergency |
function |
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Greater |
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same but reduced |
ion with or |
the |
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150 µmol/L |
operation, and |
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increase in |
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increased serum |
without CPB |
incidence |
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reoperation were |
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creatinine and |
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creatinine in OPCAB |
in patients |
of |
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excluded |
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urea in the |
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vs. on-pump. |
with |
postoperat |
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on-pump |
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preoperative |
ive renal |
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group vs. |
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nondialysis- |
dysfunctio |
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OPCAB |
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dependent |
n in |
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renal |
patients |
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insufficiency. |
with |
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2001 (270) |
preoperati |
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ve |
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nondialysis |
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renal |
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insufficienc |
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y |
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(OPCAB |
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vs.onpum |
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p) |
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Does Off- |
To |
Observa |
215 |
CABG , baseline |
N/A |
Changes in renal |
N/A |
N/A |
p=0.499 |
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ARF incidence same |
Pump |
evaluate |
tional |
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creatinine>1.5 mg/dL |
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function |
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between on-pump and |
Coronary |
the impact |
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OPCAB. |
Surgery |
of CPB on |
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Reduce |
the |
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Postoperative |
incidence |
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ARF? The |
of |
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Importance of |
postoperat |
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Preoperative |
ive ARF. |
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Renal |
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Function. |
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(271) |
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AKI indicates acute kidney injury; ARF, acute renal failure; CABG, coronary artery bypass graft; CI, confidence interval; CPB, cardiopulmonary bypass; Crcl, creatinine clearance; ESRD, end-stage renal disease; GFR, glomerular filtration rate; HR, hazard ratio; ICU, intensive care unit; N/A, not applicable; OPCAB, off-pump coronary artery bypass; OR, odds ratio; PVD, peripheral vascular disease; RCT, randomized controlled trial; RR, relative risk; and RRT, renal replacement therapy.
© American College of Cardiology Foundation and American Heart Association, Inc.