[HTML][HTML] High-dose acetylcysteine in idiopathic pulmonary fibrosis

M Demedts, J Behr, R Buhl, U Costabel… - … England Journal of …, 2005 - Mass Medical Soc
M Demedts, J Behr, R Buhl, U Costabel, R Dekhuijzen, HM Jansen, W MacNee, M Thomeer
New England Journal of Medicine, 2005Mass Medical Soc
Background Idiopathic pulmonary fibrosis is a chronic progressive disorder with a poor
prognosis. Methods We conducted a double-blind, randomized, placebo-controlled
multicenter study that assessed the effectiveness over one year of a high oral dose of
acetylcysteine (600 mg three times daily) added to standard therapy with prednisone plus
azathioprine. The primary end points were changes between baseline and month 12 in vital
capacity and in single-breath carbon monoxide diffusing capacity (DLCO). Results A total of …
Background
Idiopathic pulmonary fibrosis is a chronic progressive disorder with a poor prognosis.
Methods
We conducted a double-blind, randomized, placebo-controlled multicenter study that assessed the effectiveness over one year of a high oral dose of acetylcysteine (600 mg three times daily) added to standard therapy with prednisone plus azathioprine. The primary end points were changes between baseline and month 12 in vital capacity and in single-breath carbon monoxide diffusing capacity (DLCO).
Results
A total of 182 patients were randomly assigned to treatment (92 to acetylcysteine and 90 to placebo). Of these patients, 155 (80 assigned to acetylcysteine and 75 to placebo) had usual interstitial pneumonia, as confirmed by high-resolution computed tomography and histologic findings reviewed by expert committees, and did not withdraw consent before the start of treatment. Fifty-seven of the 80 patients taking acetylcysteine (71 percent) and 51 of the 75 patients taking placebo (68 percent) completed one year of treatment. Acetylcysteine slowed the deterioration of vital capacity and DLCO: at 12 months, the absolute differences in the change from baseline between patients taking acetylcysteine and those taking placebo were 0.18 liter (95 percent confidence interval, 0.03 to 0.32), or a relative difference of 9 percent, for vital capacity (P=0.02), and 0.75 mmol per minute per kilopascal (95 percent confidence interval, 0.27 to 1.23), or 24 percent, for DLCO (P=0.003). Mortality during the study was 9 percent among patients taking acetylcysteine and 11 percent among those taking placebo (P=0.69). There were no significant differences in the type or severity of adverse events between patients taking acetylcysteine and those taking placebo, except for a significantly lower rate of myelotoxic effects in the group taking acetylcysteine (P=0.03).
Conclusions
Therapy with acetylcysteine at a dose of 600 mg three times daily, added to prednisone and azathioprine, preserves vital capacity and DLCO in patients with idiopathic pulmonary fibrosis better than does standard therapy alone.
The New England Journal Of Medicine