H. Hoffmann et al., PENTOXIFYLLINE DECREASES THE INCIDENCE OF MULTIPLE ORGAN FAILURE IN PATIENTS AFTER MAJOR CARDIOTHORACIC SURGERY, Shock, 9(4), 1998, pp. 235-240
Citations number
30
Categorie Soggetti
Peripheal Vascular Diseas","Emergency Medicine & Critical Care",Hematology
We assessed the safety and efficacy of intravenous pentoxifylline [3,7
-dimethyl-1-(5-oxohexyl)-xanthine] in patients at risk for developing
multiple organ failure after major cardio-thoracic surgery in a single
-center, randomized, placebo-controlled study. Of 816 consecutive pati
ents who underwent major cardio-thoracic surgery, 40 who had Acute Phy
siology and Chronic Health Evaluation II score values greater than or
equal to 19 at the first postoperative day after the surgery were incl
uded. Patients were randomized to receive either placebo (control; n =
25) or intravenous pentoxifylline treatment (pentoxifylline; n = 15)
at a dosage of 1.5 mg/kg/h as an adjunct to standard supportive therap
y. Main outcome measurements were duration of required ventilator supp
ort, intensive care unit stay, and incidence of renal failure. Thirty-
seven patients were eligible for evaluation. No significant adverse ev
ents related to pentoxifylline treatment were observed. The duration o
f mechanical ventilation was significantly greater for control patient
s (8.3 +/- 3.1 days) compared with pentoxifylline-treated patients (3.
1 +/- .9 days; p <.05). Patients treated with pentoxifylline experienc
ed fewer days on hemofiltration (1.2 +/- .8 vs. 6.8 +/- 3.3; p <.05) a
nd a shorter intensive care unit stay (5.2 +/- 1.1 vs. 11.4 +/- 3.1 da
ys). There were no intergroup differences in mortality. Mortality was
33% in the pentoxifylline group and 36% among control group patients.
In conclusion, supplemental pentoxifylline treatment may decrease the
incidence of multiple organ failure in patients at risk of systemic in
flammatory response syndrome after cardiac surgery. Additional studies
are required to determine the validity of the observed effects.