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Am. J. Respir. Crit. Care Med., Volume 162, Number 6, December 2000, 2024-2026

Talc Should Not Be Used for Pleurodesis

Richard W. Light

Saint Thomas Hospital, Vanderbilt University, Nashville, Tennessee



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At the present time, talc is one of the agents most commonly used for producing a pleurodesis in patients with either a spontaneous pneumothorax or a recurrent pleural effusion. However, questions have been raised concerning the safety of talc administered intrapleurally. In particular, there have been reports of acute respiratory distress syndrome (ARDS) occurring after talc is administered intrapleurally either as a slurry (1) or as an insufflation (5). There are at least 32 cases in the literature of ARDS occurring after administration of intrapleural talc, 17 after the use of talc slurry and the remaining 15 after talc insufflation (1). Within the first 48 h of receiving the talc, the patients developed ARDS and required mechanical ventilation. In eight instances the patient died (1, 4, 8).

The incidence of ARDS occurring after administration of intrapleural talc has varied markedly from series to series. Most of the reported cases have been from the United States. The highest incidence was that reported by Rehse and associates (6), who retrospectively reviewed 89 talc pleurodesis procedures in 78 patients. They reported that the incidence of respiratory complications or death was 33%; eight patients developed acute respiratory distress syndrome, one patient died, six patients developed dyspnea, and three patients developed re-expansion pulmonary edema (6). Although it has been suggested (10) that respiratory failure might be more common after larger doses of talc or talc slurry, Campos Milanez and coworkers reported that acute respiratory failure developed in 4 of 338 patients (1.2%) who received 2 g of insufflated talc for either recurrent pleural effusion or pneumothorax (5). It should be noted, however, that the reported incidence of respiratory complications is zero in some large series. Weissberg (10), from Israel, reported no incidences of acute respiratory distress in 360 patients who received talc pleurodesis, whereas Rodriguez-Panadero and Antony from Spain reported no cases of acute respiratory distress in 299 patients (11).

The mechanism or mechanisms by which talc produces acute lung injury is unknown. Talc is a pulverized, natural, foliated, hydrated magnesium silicate with the approximate chemical formula Mg3(Si2O5)2(OH)2. Calcium, aluminum, and iron are always present in variable amounts. Every talc deposit is unique with regard to both chemistry and morphology. When talc is processed, it is passed through mesh to eliminate the larger sized talc particles. The size of the final talc preparation depends on the size of the mesh through which it has been passed. There are more than threefold differences in the median particle size of various talc preparations used for pleurodesis, and there are also marked variations in the contaminants present in various talc preparations (12). One hypothesis is that the acute pneumonitis is related to the systemic absorption of talc, with the subsequent elaboration of inflammatory mediators, and that smaller particles are more likely to be absorbed. This hypothesis is supported by the observations in the one case reported by Rinaldo and coworkers (1) and by Campos Milanez and associates (5), who reported that there were large quantities of talc in the bronchoalveolar fluid of their patient, who presented with acute pneumonitis after talc pleurodesis. In addition, the one patient reported by Milanez Campos and colleagues, and who underwent an autopsy, had talc crystals present in almost every organ, including the ipsilateral and contralateral lung, brain, liver, kidney, heart, and skeletal muscle. Moreover, after talc is administered intrapleurally to rabbits (13) or rats (14), talc particles are found throughout the body.

From the above, it is evident that the intrapleural administration of talc, either as a slurry or as an insufflation, induces ARDS in a small percentage of patients and leads to the death of an occasional patient. Is the superiority of talc administration over other available methods of producing a pleurodesis sufficiently great to justify its continued used? Let us consider the cases separately for pleurodesis done in association with tube thoracostomy and pleurodesis done in association with thoracoscopy.

When pleurodesis is performed in conjunction with tube thoracostomy for a recurrent pleural effusion or pneumothorax, the main alternatives to talc slurry are a tetracycline derivative or bleomycin. Although it is generally accepted that talc slurry is most effective at producing a pleurodesis, there is no strong evidence that this is true. Two randomized studies (15, 16) comparing the efficacy of talc slurry and bleomycin were unable to demonstrate any significant difference in the success rates with the two agents. Heffner and associates, in reviewing the results of pleurodesis in 570 patients, were unable to demonstrate any significant difference in the success rates between talc, bleomycin, or the tetracycline derivatives (17).

Thoracoscopy plus the placement of a chest tube will lead to a pleurodesis in more than 50% of patients with a malignant pleural effusion. When two studies with 61 patients were combined, thoracoscopy plus a chest tube for a few days resulted in a pleurodesis in 38 patients (62%) (18, 19). The insufflation of talc in conjunction with thoracoscopy will result in successful pleurodesis in at least 90% of patients. An alternative to talc insufflation is mechanical abrasion of the pleura. Although there are no large series evaluating thoracoscopy with pleural abrasion in the treatment of malignant pleural effusion, it has been shown in dogs that mechanical abrasion is at least as good as talc in producing a pleurodesis when the pleura is normal (20). On the basis of the above, when an attempt is made to produce pleurodesis in conjunction with a thoracoscopic procedure, pleural abrasion followed by tube thoracostomy for a couple of days is recommended.

In conclusion, the administration of talc intrapleurally, either insufflated or as a slurry, can lead to the development of the acute respiratory distress syndrome and even death. Similar problems are not seen after the intrapleural administration of the tetracycline derivatives or bleomycin or after mechanical abrasion of the pleura. Because there is no convincing evidence that talc slurry is superior to either the tetracycline derivatives or bleomycin administered via a tube thoracostomy or that talc insufflation is superior to mechanical abrasion of the pleura, talc should not be used for pleurodesis.


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REFERENCES

1. Rinaldo JE, Owens GR, Rogers RM. Adult respiratory distress syndrome following intrapleural instillation of talc. J Thorac Cardiovasc Surg 1983; 85: 523-526 [Abstract].

2. Bouchama A, Chastre JC, Gaudichet A, Soler P, Gibert C. Acute pneumonitis with bilateral pleural effusion after talc pleurodesis. Chest 1984; 86: 795 [Abstract/Free Full Text].

3. Kennedy L, Rusch VW, Strange C, Ginsberg RJ, Sahn SA. Pleurodesis using talc slurry. Chest 1994; 106: 342-346 [Abstract/Free Full Text].

4. Marel M, Skácel Z, Bednár M, Julák J, Light RW. Corynebacterium parvum, bleomycin and talc in the treatment of malignant pleural effusions. J Bon 1998; 1: 165-170 .

5. Campos Milanez JR, Werebe EC, Vargas FS, Gatineau FB, Light RW. Respiratory failure due to insufflated talc. Lancet 1987;349:251-252.

6. Rehse DH, Aye RW, Florence MG. Respiratory failure following talc pleurodesis. Am J Surg 1999; 177: 437-440 [Medline].

7. Todd TR, Delarue NC, Ilves R, Pearson FG, Cooper JD. Talc poudrage for malignant pleural effusion. Chest 1980; 78: 542-543 .

8. Nandy P. Recurrent spontaneous pneumothorax; an effective method of talc poudrage. Chest 1980; 77: 493-495 [Abstract/Free Full Text].

9. Migueres J, Jover A. Indications du talcage de plévre sous pleuroscopie au cours des pleurésies malignes récidivantes: a propos de 26 observations. Poumon-Coeur 1981; 37: 295-297 .

10. Weissberg D. Talc pleurodesis: experience with 360 patients. J Thorac Cardiovasc Surg 1993; 106: 689-695 [Abstract].

11. Rodriguez-Panadero F, Antony VB. State of the art: pleurodesis. Eur Respir J 1997; 10: 1648-1654 [Abstract].

12. Ferrer J, Villarino MA, Tura JM, Traveria J, Light RW. Comparison of size and composition of nine different talcs: its relevance for pleurodesis [abstract]. Am J Respir Crit Care Med 1998; 157: A66 .

13. Kennedy L, Harley RA, Sahn SA, Strange C. Talc slurry pleurodesis. Pleural fluid and histologic analysis. Chest 1995; 107: 1707-1712 [Abstract/Free Full Text].

14. Werebe EC, Pazetti R, De Campos JRM, Fernandez PP, Jatene FB, Vargas FS. Systemic distribution of talc after intrapleural administration in rats. Chest 1999; 115: 190-193 [Abstract/Free Full Text].

15. 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].

16. 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].

17. Heffner JE, Nietert PJ, Barbieri C. Pleural fluid pH as a predictor of pleurodesis failure: analysis of primary data. Chest 117:87-95.

18. Groth G, Gatzemeier U, Haubingen K, Heckmayr M, Magnussen H, Neuhauss R, Pavel JV. Intrapleural palliative treatment of MPEs with mitoxantrone versus placebo (pleural tube alone). Ann Oncol 1991; 2: 213-215 [Abstract/Free Full Text].

19. Sorensen PG, Svendsen TL, Enk B. Treatment of MPE with drainage, with and without instillation of talc. Eur J Respir Dis 1984; 65: 131-135 [Medline].

20. Bresticker MA, Oba J, LoCicero J III,, Greene R. Optimal pleurodesis: a comparison study. Ann Thorac Surg 1993; 55: 364-366 [Abstract].





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