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Ann Thorac Surg 1996;62:1655-1658
© 1996 The Society of Thoracic Surgeons


Original Articles: General Thoracic

Thoracoscopic Talc Insufflation Versus Talc Slurry for Symptomatic Malignant Pleural Effusion

Anthony P. C. Yim, MD, Anthony T. C. Chan, MB, BS, Tak Wai Lee, FRCS(E), Innes Y. P. Wan, MB, ChB, Jonathan K. S. Ho, MD

Division of Cardiothoracic Surgery, Department of Surgery, and Department of Clinical Oncology, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong

Accepted for publication July 22, 1996.


    Abstract
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 Acknowledgments
 References
 
Background. Talc has been generally accepted to be the most effective sclerosant for chemical pleurodesis, although the optimal route of administration remains unclear.

Methods. We designed a prospective, randomized study to compare video-assisted thoracoscopic talc insufflation with bedside talc slurry in the treatment of malignant pleural effusion. From September 1993 to November 1995, 57 patients were recruited and randomized to either video-assisted thoracoscopic talc insufflation under general anesthesia (n = 28) or talc slurry by the bedside (n = 29). Patients with poor general condition (Karnofsky score less than 30%), poor pulmonary function (forced expiratory volume in 1 second less than 0.5 L), or trapped lungs were excluded from this study. Five grams of purified talc was used for either video-assisted thoracoscopic talc insufflation or talc slurry.

Results. There was no statistically significant difference between the two groups of patients with respect to age, sex ratio, chest drainage duration, postprocedural hospital stay, parenteral narcotics requirement, complications, or procedure failure (ie, recurrence).

Conclusions. Video-assisted thoracoscopic talc insufflation has not been shown to be a superior approach compared with talc slurry in our study. Because the former demands more resources, we advocate that talc slurry should be considered as the procedure of choice in the treatment of symptomatic malignant pleural effusion in patients who do not have trapped lungs.


    Introduction
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 Acknowledgments
 References
 
See also page 1658.

Malignant pleural effusion is a common condition, which is often disabling and could be very difficult to treat. It represents a terminal condition with short median survival (in terms of months), and the goal of treatment is palliation [1]. Systemic chemotherapy is occasionally useful for breast and small cell lung carcinoma, but local therapy remains the mainstay of treatment. Talc has been identified as an effective sclerosant for chemical pleurodesis [2], although the optimal route of administration (dusting [3], "slurry" [4], "poudrage" [5]) remains unclear. More recently, video-assisted thoracoscopic talc insufflation (VT) has been shown to be a safe and effective approach in controlling malignant pleural effusion [6, 7]. We designed a prospective, randomized study to compare this approach with conventional bedside talc slurry (TS). Our results from a single institution form the basis of this article.


    Material and Methods
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 Acknowledgments
 References
 
From September 1993 to November 1995, 79 patients with established, symptomatic malignant pleural effusion were referred to us for treatment. Eleven patients, however, were excluded from this study because of either poor general condition (Karnofsky score less than 30%) [8] or poor pulmonary function (forced expiratory volume in 1 second less than 0.5 L). Seven patients were further excluded when trapped lung was revealed after either chest tube drainage or large-volume thoracocentesis. In addition, 4 patients who received chemotherapy or radiation therapy within 6 months before the diagnosis of malignant effusion were excluded from the study. This left 57 patients (20 men and 37 women with age ranging from 50 to 86 years) to be randomized for VT under general anesthesia (n = 28) or TS by the bedside (n = 29). We were careful in excluding patients whose dyspnea was due to tumor replacement of lung parenchyma rather than to effusion. We only selected those patients whose dyspnea improved after tube thoracostomy or large-volume thoracocentesis. Permission for the study was obtained from the Hospital Review Board, and full consent was obtained from the patients. Our techniques are briefly described below.

Video-Assisted Thoracoscopic Talc Insufflation
We modified the technique previously described using local anesthesia by Hartman and associates [6]. The procedure was performed under general anesthesia with selective one-lung ventilation and the patient in the lateral decubitus position with the table flexed at 30 degrees [9]. We routinely use a 10-mm operating telescope to minimize the number of ports made [10]. If the patient already came with a chest drain, we would use the drain site for the introduction of the telescope. Otherwise, needle aspiration was undertaken to determine the location of the fluid. We normally prefer to introduce the telescope low down in the chest (usually over the sixth or seventh intercostal space unless the diaphragm was shown or suspected to be elevated). Any residual pleural fluid was aspirated. Loculations were broken down. Fibrinous adhesions were taken down, whereas dense fibrous adhesions were selectively divided. Five grams of purified talc (Halewood Chemicals, Middlesex, UK) sterilized by dry heat was then insufflated into the chest to evenly cover the entire visceral and parietal surfaces. Initially we used a special talc atomizer (K. Storz, Culver City, CA), but we now prefer using a mucus extractor (UnoPlast, Hundested, Denmark) connected to a 50-mL syringe, which we have found to be simple, cheap, and reliable. A 28F chest drain was left in situ (placement of which was visually guided) and connected to 15 cm H2O suction. The lung was confirmed to be fully reexpanded before withdrawal of the scope. The drain was connected to 15 cm H2O suction and removed when the output was less than 50 mL in 24 hours.

Talc Slurry
Our technique was similar to that advocated by Webb and colleagues [4]. Five grams of purified talc (Halewood Chemicals) was mixed with 50 mL of normal saline solution and 10 mL of 2% lidocaine to form a suspension, which was then instilled through the chest drain. The drain was clamped for 2 hours and the patient turned in different positions. The drain was then reconnected to 15 cm H2O suction and removed when the output was less than 50 mL in 24 hours.

Follow-up
All the patients were prospectively followed up. Particular attention was paid to the postprocedural chest drainage duration, hospital stay, parenteral meperidine requirement, and periprocedural complications. After discharge, the patients were regularly seen in the clinic at 6-week intervals for the first 41/2 months and then every 3 months. Any procedural failure in terms of radiologic evidence of fluid reaccumulation was noted. Telephone interviews with the patients were made as required to record changes in symptoms. Differences between the two groups were analyzed using Mann-Whitney U tests.


    Results
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 Acknowledgments
 References
 
Our results are summarized in Table 1Go. There was no statistical difference in the demographics of the patients between the VT and TS groups in terms of age, sex ratio, and underlying pathology. There was no procedure-related mortality in either group. We found no differences between the two groups in terms of chest drainage durations, hospital stays, or parenteral meperidine requirement.


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Table 1. . Video-Assisted Thoracoscopic Talc Insufflation Versus Talc Slurry in the Treatment of Malignant Pleural Effusion
 
Three complications were encountered in the VT group: reexpansion pulmonary edema, persistent air leak, and tumor recurrence at a port site. (1) Reexpansion pulmonary edema was encountered in a 60-year-old woman with a history of ovarian carcinoma who presented with a large right pleural effusion. Large-volume thoracocentesis confirmed malignancy and conferred temporary relief. Thoracoscopically, 2 L of fluid was drained and VT was performed uneventfully. However, in the recovery room, the patient was noted to be hypoxic, and a chest roentgenogram confirmed ipsilateral pulmonary edema. She recovered after overnight ventilation and careful diuresis. (2) Persistent air leak for 8 days was encountered in a patient after extensive adhesiolysis to break down loculations. The leak stopped spontaneously without further complications. (3) Port site recurrence, which presented as a subcutaneous nodule, was noted in a patient with diffuse pleural metastasis 9 months after VT. As the nodule was asymptomatic, no further treatment was offered.

Two complications were encountered in the TS group: one acute transient respiratory failure and one wound infection. (1) Acute respiratory distress was encountered in a 73-year-old patient with chronic obstructive airway disease and stage IV lung carcinoma. It occured shortly after instillation of the talc slurry into the chest and clinically resembled exacerbation of chronic obstructive airway disease. The talc slurry was drained, and the patient improved on conservative management without needing ventilatory support. (2) The superficial wound infection resolved with local wound care.

Radiologic recurrence of effusion was noted in 1 patient 11 months after VT and in 3 patients after TS (at 6, 12, and 14 months, respectively). Nineteen patients died in the VT group, whereas 15 died in the TS group during follow-up without evidence of fluid reaccumulation. The mean follow-up is 10 months among the survivors (range, 4 to 16 months). Of the 4 patients with radiologic recurrence of effusion, only 1 patient (in the TS group) had her activity limited by dyspnea. She underwent repeat tube thoracostomy and TS treatment without further recurrence, until her death 2 months later.


    Comment
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 Acknowledgments
 References
 
There is now a wealth of literature on the treatment of symptomatic malignant pleural effusion, although the optimal therapy remains unclear [1]. Options include repeated therapeutic thoracocentesis, tube thoracostomy and sclerotherapy, thoracoscopic talc insufflation, mechanical pleurodesis, pleuroperitoneal shunt, and pleurectomy. We normally reserve repeated thoracocentesis to those who are severely disabled and require continuous hospitalization (Karnofsky score less than 30%) [8] as rapid reaccumulation, protein depletion, and risk of empyema occur with this treatment. On the other hand, pleurectomy carries with it substantial morbidity and mortality [11] and is hard to justify for a palliative procedure. Pleuroperitoneal shunt has been shown to be effective [12], but it requires a very compliant patient who needs to manually pump 400 times a day. Moreover, there is a risk of shunt occlusion by blood clots or fibrin debris [13]. We therefore have reserved this approach to patients with severely (more than 25% fixed pneumothorax) trapped lung.

Of all the sclerosants available, talc is generally considered the agent of choice because of its good track record (more than 90% success rate), wide availability, and low cost [2]. The possible harmful long-term effects of talc [14] seem academic in this group of patients with limited survival. Acute respiratory failure [15] and death [16] have been anecdotally reported with TS [15] or insufflation [16]. We encountered 1 case of acute respiratory failure with TS in this series. The exact underlying mechanism remains unclear, even though it may be dose related. Kennedy and Sahn [2] recommended a 5-g dose, which is what we use. In the past we tried thoracoscopic talc insufflation under local anesthesia [6] and found it to be fairly uncomfortable for the patients. In addition, it was difficult to carry out interventions like adhesiolysis in patients who were awake with ventilating lungs.

Patients with diffuse pleural metastasis are at risk of tumor seeding at thoracoscopy port sites. Fortunately, this is relatively uncommon: 6 of 215 patients reported by Boutin and associates [17], 2 of 30 patients reported by Davidson and colleagues [18], and 2 of our patients (1 is not in this series [19]). We recommend observation if the port site recurrence is asymptomatic in view of the patient's short life expectancy; otherwise, local irradiation has been shown to provide good palliation [18].

Video-assisted thoracic surgery has provided an alternative approach in the management of a variety of thoracic conditions. Thoracoscopic talc insufflation for malignant effusions under local [6] or general anesthesia [7] has been shown to be safe and effective; here we report a randomized, prospective comparison between this approach and conventional TS.

We have not shown in our study any statistically significant difference between TS and VT in terms of hospital stay, analgesic requirement, complications, or procedure failures. It is important to note that of the 4 patients who had fluid reaccumulation, only 1 was symptomatic enough to require further treatment. We acknowledge that our sample size is small, but we emphasize that we are comparing two treatment modalities with the goal of palliation for a condition with very limited survival. A multicenter trial is underway, and it will be interesting to see if the collective experience is in agreement with our own.

There are two further points of note. First, in this study, we are focusing only on those patients with no radiologic evidence of trapped lungs. For patients with a minor degree of trapped lungs (less than 25% fixed pneumothorax), thoracoscopic decortication has been shown to be useful in achieving lung reexpansion [7]. Second, we are aware of the weakness in our study in the lack of documentation of patients' quality of life after either procedure. We have encountered problems in using standard questionnaires for our patients: they require translation into Chinese; self evaluation and the visual linear analogue scale pose difficulties to those with a low level of education or low performance status [20]; functional status is closely influenced by social and psychological factors, which are difficult to quantify; and the questionnaires have not been externally validated. We are studying some of these problems.

We have changed our practice as a result of our findings. In view of VT demanding more resources (trained thoracoscopists, general anesthesia, operating room time), we now advocate TS to be considered as the procedure of choice for patients with symptomatic malignant effusion without trapped lungs. Pleuroperitoneal shunt should be considered for those with severely trapped lung who are likely to comply with handling the device. For those patients with minor degrees of trapped lungs (less than 25% fixed pneumothorax), the thoracoscopic approach should be selectively considered [7].


    Acknowledgments
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 Acknowledgments
 References
 
We are grateful to Alex Fung, BA, for data collection and editorial assistance. This study was supported by University Funds (A/C 1635-23).


    Footnotes
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 Acknowledgments
 References
 
Address reprint requests to Dr Yim, Division of Cardiothoracic Surgery, Department of Surgery, Prince of Wales Hospital, Shatin, NT Hong Kong.


    References
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 Acknowledgments
 References
 

  1. Hausheer FH, Yarbro JW. Diagnosis and treatment of malignant pleural effusions. Semin Oncol 1985;12:54–75.[Medline]
  2. Kennedy L, Sahn SA. Talc pleurodesis for the treatment of pneumothorax and pleural effusion. Chest 1994;106:1215–22.[Free Full Text]
  3. Adler RH, Sayek I. Treatment of malignant pleural effusion: a method using tube thoracostomy and talc. Ann Thorac Surg 1976;22:8–15.[Abstract]
  4. Webb WR, Ozmen V, Moulder PV, Shabahang B, Breaux J. Iodized talc pleurodesis for the treatment of pleural effusions. J Thorac Cardiovasc Surg 1992;103:881–6.[Abstract]
  5. Nandi P. Recurrent spontaneous pneumothorax: an effective method of talc poudrage. Chest 1980;77:493–5.[Abstract/Free Full Text]
  6. Hartman DL, Gaither JM, Kesler KA, Mylet DM, Brown JW, Mathur PN. Comparison of insufflated talc under thoracoscopic guidance with standard tetracycline and bleomycin pleurodesis for control of malignant pleural effusions. J Thorac Cardiovasc Surg 1993;105:743–8.[Abstract]
  7. Yim APC, Chung SS, Lee TW, Lam CK, Ho JKS. Thoracoscopic management of malignant pleural effusions. Chest 1996;109:1234–8.[Abstract/Free Full Text]
  8. Karnofsky DA, Burchenal VH. The clinical evaluation of chemotherapeutic agents in cancer. In: MacLeod CM, ed. Evaluation of chemotherapeutic agents. New York: Columbia University Press, 1949:191–205.
  9. Yim APC. Minimizing chest wall trauma in video assisted thoracic surgery. J Thorac Cardiovasc Surg 1995;109:1255–6.
  10. Yim APC, Ho JKS, Lee TW, Chung SS. Thoracoscopic management of pleural effusions revisited. Aust N Z J Surg 1995;65:308–11.[Medline]
  11. Martini N, Bains MS, Beattie EJ. Indications for pleurectomy in malignant effusion. Cancer 1975;35:734–8.[Medline]
  12. Little AG, Kadowaki MH, Ferguson MK, Staszek VM, Skinner DB. Pleuroperitoneal shunting: alternative therapy for pleural effusions. Ann Surg 1988;208:443–50.[Medline]
  13. Tsang V, Fernando AC, Goldstraw P. Pleuroperitoneal shunt for recurrent malignant pleural effusion. Thorax 1990;45:369–72.[Abstract/Free Full Text]
  14. Lange P, Mortensen J, Groth S. Lung function 22–35 years after treatment of idiopathic spontaneous pneumothorax with talc poudrage or simple drainage. Thorax 1988;43:559–61.[Abstract/Free Full Text]
  15. Bouchama A, Chastre J, Gandichet A, Soler P, Gibert C. Acute pneumonitis with bilateral pleural effusion after talc pleurodesis. Chest 1984;86:795–7.[Abstract/Free Full Text]
  16. Todd TRJ, Delarue NC, Ilves R, Pearson FG, Cooper JD. Talc poudrage for malignant pleural effusion [Abstract]. Chest 1980;78:542–3.
  17. Boutin C, Viallat JR, Cargnino P, Farisse P. Thoracoscopy in malignant pleural effusions. Ann Rev Respir Dis 1981;124:588–92.
  18. Davidson AC, George RJ, Sheldon CD, Sinha G, Corrin B, Geddes DM. Thoracoscopy: assessment of a physician service and comparison of a flexible bronchoscope used as a thoracoscope with a rigid thoracoscope. Thorax 1988;43:327–32.[Abstract/Free Full Text]
  19. Yim APC. Port site recurrence following video assisted thoracoscopic surgery. Surg Endosc 1995;9:1133–5.[Medline]
  20. Ballatori E, Roila F, Basurto C, et al. Reliability and validity of a quality of life questionnaire in cancer patients. Eur J Cancer 1993;29A(Suppl):S63–9.

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