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* From the St. George Medical Center, Robert-Koch-Hospital, Leipzig, Germany.
Correspondence to: Steffen Kolschmann, c/o Adrian Gillissen, MD, PhD, St. George Medical Center, Robert-Koch-Hospital, Nikolai-Rumjanzew-Str 100, D-04207 Leipzig, Germany; e-mail: steffen.kolschmann{at}web.de
| Abstract |
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Methods: We report a consecutive series of 102 patients (45 women, 57 men; 20 to 83 years of age) who underwent medical thoracoscopy and TTP for recurrent MPE between 1999 and 2001. Thoracoscopy was performed utilizing local anesthesia and IV sedation (medical thoracoscopy). For pleurodesis, an average of 8 g of sterile talc powder was used. One hundred eighty-day follow-up was completed for all patients, and outcome measures included time to recurrence of the effusion and survival. Efficacy was judged by clinical examination, chest radiograph, and/or thoracic ultrasound examination. Procedure-related complications were documented.
Results: The most common primary neoplasms were lung cancer (n = 48), breast cancer (n = 16), and malignant pleural mesothelioma (n = 10). Twenty-eight patients had other types of tumors, including renal cell carcinoma, ovarian carcinoma, GI tumors, prostate, malignant lymphoma, and unknown primary cancer. At the end of the primary observation period of 180 days, 38 of 46 surviving patients (82.6%) had a successful pleurodesis. Type of primary neoplasm had no significant influence on success rate. The 30-day mortality rate was 16.7% (n = 17). Survival curves after 180 days showed significant differences, with best survival in mesothelioma and shortest life expectancy in lung cancer (p = 0.005). Adverse effects included empyema in one case and malignant invasion of the scar. No episode of talc-induced ARDS was observed.
Conclusion: Thoracoscopic talc pleurodesis is a safe and effective method to stop recurrent MPEs. Lasting pleural symphysis is obtained.
Key Words: malignant pleural effusions talc pleurodesis thoracoscopy
| Introduction |
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Pleurodesis is accepted to provide effective control of recurrent MPE. In contrast, there is no existing consensus on the best way to achieve pleurodesis. Data from an international survey among pulmonologists revealed wide variations in the use of sclerosing agents and pleurodesis practices. Talc is the most commonly used and the most effective sclerosant available for pleurodesis. However, the success rates of thoracoscopic talc poudrage (TTP) vary substantially.56789 A recent meta-analysis confirmed the superiority of talc as a sclerosing agent.10
Furthermore, reports571112 on ARDS following talc pleurodesis have raised concerns about the safety of talc in the last few years. In order to evaluate the safety and efficacy of the procedure, we reviewed the clinical outcome of 102 patients who were treated for MPE between January 1999 and 2001 in our institution.
| Materials and Methods |
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Procedure
The medical thoracoscopy was done by a pulmonary physician in an endoscopy suite assisted by two trained nurses. Patients were placed in the lateral decubitus position. The patients BP, pulse rate, and oxygen saturation were monitored continuously. Supplemental oxygen was given to the patients to maintain oxygen saturation. Lidocaine 2% was used for local anesthesia, and sedation was achieved by a combination of midazolam and fentanyl. We used a 6.5-mm thoracoscope (0° and 30°; Karl Storz; Tuttlingen, Germany) with a single 7-mm trocar. After complete aspiration of all of the remaining fluid, a thorough inspection of the pleural surface was made. The adhesions were taken down with the biopsy forceps, if possible. Biopsy specimens were made for histopathologic examination, if necessary. Under visual control, an average of 8 g of sterile asbestos-free talc (Steritalc; Novatech; France) were distributed onto the pleural surface. After removal of the thoracoscope, a thoracostomy tube (24 Charrière) was inserted. Suction (20 cm H2O) was started after 1 h, and the chest tube was left in place until < 100 mL of fluid was drained in 24 h. Chest radiography was performed the same day after the procedure and before discharge. The tumor type, initial response, and duration of suction treatment were noted. The side effects and procedure-related complications were documented.
Outcome Measures
Successful pleurodesis was described as an absence of fluid reaccumulation with long-term symptom relief. All of the cases with recurrent symptomatic effusion that needed to be drained were judged as failures, as recommended by the American Thoracic Society.1 The success rate and survival were calculated from the day of the procedure. Follow-up was obtained by periodical clinical examination combined with chest radiography and/or thoracic ultrasound in our own outpatient clinic. In addition, referring practitioners and oncologists were contacted for supplementary outcome information. Follow-up information was available for all of the patients for a period of 180 days, and follow-up continued until a maximum of 1,337 days. The primary end point was symptomatic recurrence of pleural fluid that needed to be drained.
Statistical Analysis
Statistical analysis was based on data after 180 days of follow-up. The success rate and survival curves were calculated using the Kaplan-Meier method. Cases in which patients who had undergone successful pleurodesis and died before day 180 were censored, as well as those in which all patients were alive at day 180 and had undergone successful pleurodesis. The impact of different primary malignancies on the outcome was analyzed using the log-rank test. We compared the three main tumor types: lung cancer, breast cancer, and malignant pleural mesothelioma. Differences were considered significant with p values of < 0.05.
| Results |
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| Discussion |
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Unfortunately, the definition of success, as well as the length of follow-up, differs in the literature, which complicates the comparative assessment within studies. In our study, pleurodesis was successful in 82.6% of all of the cases within the follow-up period of 180 days. Three of 22 nonresponders failed to show complete reexpansion of the lung after the procedure; thus, the lungs were judged as trapped. Our findings confirmed the results by Lee et al,5 who reported in an international survey a clinical success rate of 72%. However, the success rates seen in other trials were around 90%,6789 which seems to contradict the data reported by Lee et al,5 as well as our own. This difference can be related to the inclusion criteria chosen. Because we did not exclude patients with trapped lungs, a lower success rate was observed. Also, Lee et al5 hypothesized that this apparent discrepancy might be attributable to the strict exclusion criteria in clinical studies (eg, patients with trapped lungs). Success rates seen in everyday clinical practice with more unselected patients are, therefore, likely to be lower.5 In addition, we assessed the long-term efficacy of TTP. The patients surviving the primary observation period of 180 days were additionally observed (median time, 361.5 days). In 35 of 46 patients (76%), permanent pleural symphysis was obtained. Only 24% of patients experienced a recurrence of MPE.
When referring a patient with MPE for therapy with TTP, careful selection is essential. In general, the selection criteria for pleurodesis are based on the patients performance status and the pleural fluid pH, although the latter is controversial. Sanchez-Armengol and Rodriguez-Panadero17 found a strong correlation between pleural fluid pH and survival. In contrast, Heffner et al18 stated in a meta-analysis that pleural fluid pH has insufficient predictive accuracy for selecting patients for pleurodesis. The same authors found in another study19 only a modest predictive value for pleural fluid pH as a predictor of pleurodesis failure. Because of this controversy, we decided to exclude pleural fluid pH quantification from our evaluation. The decision whether to perform TTP in our patients was based on the following criteria: (1) general medical conditions and comorbidity (eg, coagulation disorders and severity of concurrent diseases, such as cardiovascular diseases); and (2) performance status.
In our study, patients with poor performance status, which was defined as an incapability to care for themselves, were excluded, which is in accordance with Burrows et al, 3 who found the Karnofsky performance scale score to be predictive for survival. de Campos et al7 stressed the importance of excluding malnourished patients with advanced malignancy and Karnofsky performance scale scores
40 from TTP, because they have a very limited life expectancy. We observed a 30-day mortality rate of 16.7% (n = 17). Fifteen of these patients died from rapid progression of their malignant disorder and should initially have been excluded from the procedure. Additional measures to identify patients with a life expectancy of < 30 days are needed.
In our series, the response to pleurodesis did not predict the survival outcome (p = 0.44), which is in contrast to those reported in previous investigations,920 in which differences in survival between responders and nonresponders were found. As expected from the predicted median survival time (malignant pleural mesothelioma patients, 4 to 18 months; stage IIIB to IV lung cancer patients, 6 to 9 months),21 survival was strongly linked to the primary cancer diagnosis such that the 180-day survival rate was higher in patients with pleural mesothelioma than in those with lung cancer (p = 0.005).
Although TTP was reported to induce ARDS, we did not encounter such complications. The only severe adverse effect that we saw was pleural empyema in one case. This particular patient needed prolonged suction treatment and antibiotic therapy, and, subsequently, experienced a lack of response to pleurodesis. This seems comparable with the literature,7922 in which incidence rates of empyema, ranging from 0 to 4%, have been reported.
There are, however, potential limitations to our study. The retrospective study design could have introduced systemic bias, including patients who were unavailable for follow-up. This problem was eliminated by using data that were derived from a 180-day period with complete outcome information for statistical analysis. Furthermore, the quality of life was not documented in the months following the procedure. Successful pleurodesis is linked to marked improvement in dyspnea. However, the patient benefit regarding quality of life still remains to be elucidated.
In conclusion, TTP has been proven to provide safe and effective symptom control in rapidly recurrent MPEs. Lasting pleural symphysis is obtained in most cases, avoiding repetitious interventions. Therefore, TTP is a favorable method for palliation therapy in patients with advanced neoplasms due to MPE.
| Footnotes |
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Received for publication September 1, 2004. Accepted for publication February 23, 2005.
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