TREATMENT OF SEPSIS-ASSOCIATED SEVERE ACUTE-RENAL-FAILURE WITH CONTINUOUS HEMODIAFILTRATION - CLINICAL-EXPERIENCE AND COMPARISON WITH CONVENTIONAL DIALYSIS
R. Bellomo et al., TREATMENT OF SEPSIS-ASSOCIATED SEVERE ACUTE-RENAL-FAILURE WITH CONTINUOUS HEMODIAFILTRATION - CLINICAL-EXPERIENCE AND COMPARISON WITH CONVENTIONAL DIALYSIS, Blood purification, 13(5), 1995, pp. 246-254
The syndrome of sepsis-associated severe acute renal failure is a freq
uent component of sepsis-induced multiorgan failure. Continuous hemofi
ltration techniques are often used in its dialytic manage ment but lit
tle is known about their impact. The aim of this study is to define th
e biochemical and clinical impact of continuous hemdiafiltration (CHD)
in the management of this syndrome and to retrospectively compare it
to that of conventional dialysis. A prospective, cohort study and retr
ospective comparison with historical controls was conducted at an inte
nsive care unit (ICU) of a tertiary institution. Eighty-seven consecut
ive septic patients with acute renal failure were treated by continuou
s hemodiafiltration and 40 consecutive similar patients by conventiona
l dialysis. All new cases of severe acute renal failure with sepsis we
re treated by means of continuous hemodiafiltration. Historical contro
ls were treated by means of conventional dialysis. Illness and sepsis
severity were assessed on admission and prior to initiation of teatmen
t. Biochemical variables were assessed daily. Outcome was measured as
discharge from the ICU, duration of oliguria and discharge from hospit
al. Of the 87 patients treated by hemodiafiltration, 86 had multiorgan
failure, 71 (81.6%) septic shock and 52 (59.8%) bacteremia/fungemia.
Their APACHE II score on admission was 29.9 and their mean organ failu
re score prior to treatment was 4.3. Hemodiafiltration resulted in a s
ignificant fall in mean urea and creatinine levels within 24 h and in
the correction of acidosis. The mean alveolar-arterial gradient fell f
rom 276 to 211 mm Hg (p < 0.02) within 24 h of therapy. Complications
were few and mostly related to vascular access. Hemodynamic stability
was maintained throughout all of the 18,122 h of treatment. Thirty-one
(35.6%) patients survived to hospital discharge. Comparison with conv
entionally treated historical controls showed better control of uremia
at 24 h. Among patients with an APACHE II score <30, survival was gre
ater with hemodiafiltration (51.2 vs. 26.6%; p < 0.05). This was also
true for patients with 4 or fewer failing organs (53.1 vs. 26.9%; p <
0.05). Continuous hemodiafiltration achieves rapid and reliable contro
l of uremia and acidosis in spesis-associated severe acute renal failu
re and is associated with improved gas exchange. Survival in these ext
remely ill patients approached 35%. The use of hemodiafiltration is as
sociated with better early control of uremia than with conventional he
modialysis or peritoneal dialysis. In some patient subgroups, continuo
us hemodiafiltration also appears to provide a survival advantage. The
above findings suggest that continuous hemodiafiltration may be a for
m of renal replacement therapy ideally suited to the management of sep
sis-associated severe acute renal failure.