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Am. J. Respir. Crit. Care Med., Volume 162, Number 6, December 2000, 2026a-2026

REBUTTAL FROM DR. LIGHT



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I agree the ideal agent for pleurodesis should be highly effective, easy to administer, inexpensive, and not associated with serious adverse events. Dr. Sahn maintains that talc is the ideal agent. I disagree with this.

Dr. Sahn asserts that talc is clearly the most effective agent. I beg to differ. Heffner and associates reviewed the results of pleurodesis in 420 patients who received talc, tetracycline derivatives, bleomycin, or Corynebacterium parvum and, using multiple regression analysis, were unable to show that the agent selected was significantly related to pleurodesis failure (1). The failure rate with each of the agents was about 20% (1). The two studies, referenced in the original editorial, in which patients were randomized to receive talc or bleomycin, did not show a significant advantage for talc (2, 3). In general, the results with talc are slightly better than with bleomycin or a tetracycline derivative, but are they enough better to take the risk of inducing acute respiratory distress syndrome (ARDS)?

It is suggested that the ARDS picture seen after talc may not be due to talc per se. However, it is infrequent with other agents. At a symposium on pleurodesis at the 1999 American College of Chest Physicians meeting, which I cochaired with Dr. John Heffner, the audience was polled concerning their experience with talc for pleurodesis. The majority of the audience raised their hand when asked if they had seen ARDS after the administration of talc intrapleurally. When the same question was asked concerning bleomycin or the tetracycline derivatives, none raised their hands.

In conclusion, the ideal agent for pleurodesis is yet to be discovered. Talc is not the ideal agent. This inhomogeneous agent produces life-threatening respiratory failure in some individuals and therefore should not be used. The ideal agent is still to be developed. I believe that the ideal agent will not injure the pleura but will, rather, induce the mesothelial cells to produce collagen and induce a pleurodesis. Support for this contention is our observation that the intrapleural injection of transforming growth factor beta  can induce an excellent pleurodesis in rabbits without producing an inflammatory pleural effusion (4).


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1. Heffner JE, Nietert PJ, Barbieri C. Pleural fluid pH as a predictor of pleurodesis failure: analysis of primary data. Chest 2000; 117: 87-95 [Abstract/Free Full Text].

2. Noppen M, Degreve J, Mignolet M, Vincken W. A prospective, randomized study comparing the efficacy of talc slurry and bleomycin in the treatment of malignant pleural effusions. Acta Clin Belg 1997; 52: 258-262 [Medline].

3. Zimmer PW, Hill M, Casey K, Harvey E, Low DE. Prospective randomized trial of talc slurry vs bleomycin in pleurodesis for symptomatic malignant pleural effusions. Chest 1997; 112: 430-434 [Abstract/Free Full Text].

4. Light RW, Cheng D-S, Lee YC, Rogers J, Davidson J, Lane KB. A single intrapleural injection of transforming growth factor-beta 2 produces excellent pleurodesis in rabbits. Am J Respir Crit Care Med 2000; 162: 98-104 [Abstract/Free Full Text].






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Proc. Am. Thorac. Soc. Am. J. Respir. Cell Mol. Biol.
Copyright © 2000 American Thoracic Society