Methods: Between March 2009 and April 2012, 43 patients (34 males, 9 females; mean age 65.6±9.8 years; range 37 to 79 years) received iodopovidone pleurodesis was for the treatment of refractory pleural effusion. Pleural effusion was due to malignancy in 31 and heart failure in 12 patients. Iodopovidone (20 mL 10% plus 80 mL 0.9% NaCl) was delivered through the chest tube. The chest tube was not clamped and raised 60 cm above the chest level. The tube was removed when the amount of drainage reduced to 50 mL/day.
Results: In patients with malignant pleural effusion, iodopovidone irrigation produced significant decrease in daily pleural drainage from 574.9±169.0 mL to 71.7±25.9 mL (p=0.000), and in patients with heart failure daily drainage decreased from 588.9±138.4 mL to 63.5±12.5 mL which was also significant (p<0.001). No clinical side effect related to the procedure was observed.
Conclusion: Iodopovidone was shown to be effective in patients with refractory pleural effusions. The use of this agent without clamping the chest tube is safe, inexpensive and effective.
Iodopovidone has been used for pleurodesis to treat refractory pleural effusions and has been shown to be safe and effective in several studies, whether it was administered at the time of the thoracoscopy or applied through a chest tube.[1,6] This study was conducted to evaluate the efficacy of iodopovidone pleurodesis in 43 patients with refractory pleural effusions.
A small bore chest tube was inserted in the patients through the sixth intercostal space along the midaxillary line and was connected to an underwater sealed drainage system. The pleurodesis was performed at each patient’s bedside where they received subcutaneous 0.5-0.7 mg/kg pethidine hydrochloride (HCl) (Aldolan®, Gerot Pharmazeutika GmbH, Vienna, Austria). Previously, an intrapleural instillation of 20 mL bupivacaine (Marcain Polyamp Steripack, AstraZeneca UK Limited, London, England) had also been given. A mixture of 20 ml 10% iodopovidone and 80 ml 0.9% saline solution was then administered into the pleural cavity through the chest tube, which was not clamped, and it was kept at 60 cm above the chest wall to prevent backflow of the iodopovidone. Next, the patient was rotated in the bed to achieve a complete distribution of the iodopovidone in the cavity. After leaving the chest tube in for two hours, it was returned to its natural position and removed when the pleural drainage decreased to 50 ml/day.
Statistical analysis
Statistical analyses were performed using the Statistical
Package for Social Science (SPSS Inc., Chicago, Illinois,
USA) version 17.0 software program. Paired samples
t-tests were used to compare the mean test scores before
and after application. A value of p <0.05 was considered
to be statistically significant.
Table 1: Comparison of the amount of drainage before and after iodopovidone irrigation
Along with commonly used agents like talc, tetracycline, and doxycycline iodopovidone should be accepted as an alternative sclerosing agent[1] as it is an inexpensive and readily available agent for chemical pleurodesis.[10] Previous studies have suggested that the use of iodopovidone has a high success rate. Kelly-Garcia et al.[11] reported the use of this agent in 14 patients with a 64.2% success rate. Morales-Gómez et al.[12] performed pleurodesis with iodopovidone in 39 patients with malignant pleural effusions and achieved control of the effusions in 33 patients (91.6%). Furthermore, in the series reported by Olivares-Torres et al.,[9] complete response was observed in 50 (96.1%) out of 52 patients, with the iodopovidone pleurodesis having been performed through a tube thoracostomy or at the end of a diagnostic thoracoscopy. More recently, a study that included 43 patients with malign pleural effusions showed a success rate of 88%, and small bore catheters and large bore chest tubes were used to administer the iodopovidone into the pleural space in these cases.[13] Agarwal et a l.[10] reported comparable results in 37 patients who received iodopovidone through a chest tube. There were no reports of any recurrences of the effusions in 32 (86.5%) of their patients. In our series, iodopovidone was used for pleurodesis with a success rate of 100% in 43 patients with either benign or malignant recurrent pleural effusions.
Iodopovidone is an iodine-based topical antiseptic that may be absorbed by the thyroid gland and can appear in saliva, sweat, and milk. It undergoes minimal metabolism and is excreted practically unchanged in the urine.[9] The exact mechanism that i odopovidone uses to produce pleural symphysis is not known, but it has been suggested that this could be related to the low pH of the iodopovidone solution, which is 2.97.[14] Additionally, iodine has oxidative and cytotoxic properties that may include a potent inflammatory response to initiate the pleural symphysis.[14] The rapid reduction of the effusions in all the cases in our series supports this idea.
The main complication observed in the study of Neto et al.[14] was mild thoracic pain (16%) after iodopovidone instillation, and in the study by Olivares-Torres et al.,[9] three patients (5.8%) required opioid analgesics for pain control. Empyema is also a rarely seen complication,[14] and visual loss after iodopovidone pleurodesis was reported by Wagenfeld et al.[15] Although it has been reported that topical iodopovidone applications or the use of iodopovidone-based contrast agents may cause transient thyroid dysfunction, especially in infants, the study of Yeginsu et al.[16] determined that the intrapleural administration of iodopovidone did not affect thyroid hormone levels.[17] In our study, wed id not observe any signs or symptoms of hypothyroidism or hyperthyroidism in the patients during the follow-up period. However, four patients suffered from a minimal degree of transient chest pain.
In conclusion, we recommend the use of iodopovidone for the treatment of refractory pleural effusions since it is a cheap, effective, and safe approach.
Declaration of conflicting interests
The authors declared no conflicts of interest with
respect to the authorship and/or publication of this
article.
Funding
The authors received no financial support for the
research and/or authorship of this article.
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