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Ann Thorac Surg 2007;84:237-239
© 2007 The Society of Thoracic Surgeons
a Department of Anaesthesiology, University Hospital of Wales, Cardiff, United Kingdom
b Cardiothoracic Unit, University Hospital of Wales, Cardiff, United Kingdom
Accepted for publication March 2, 2007.
* Address correspondence to Dr Luckraz, Cardiothoracic Unit, Block C5, University Hospital of Wales, Cardiff, CF14 4XW, United Kingdom (Email: heymanluckraz{at}aol.com).
Presented at the Poster Session of the Forty-third Annual Meeting of The Society of Thoracic Surgeons, San Diego, CA, Jan 2931 2007.
| Abstract |
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Methods: A prospective randomized control trial was set up to assess the need for intercostal chest drainage after video-assisted thoracoscopic surgical lung biopsy. Patients who did not have any air leak after the procedure (lung tested while patient was still under anesthetic) was randomized to either having a chest drain or not. The study was powered at 0.9 using an alpha of 0.01.
Results: Thirty patients were recruited in each group. There were no significant differences between the two groups in terms of patients age (mean age, 59 versus 54 years), sex, history of steroid use, immediate postoperative pain scores, and wound complications. No significant pneumothoraces occurred in either group. However in the immediate postoperative phase, 28% and 15% of patients with and without chest drains, respectively, had a small (clinically not significant) pneumothorax (size <10%) on their chest radiograph. Moreover, there was significantly increased in-hospital stay in the chest drain group (median, 3 days versus 1 day; p < 0.001). At 6 weeks follow-up, all patients had fully expanded lungs bilaterally.
Conclusions: There is no need for an intercostal chest drain in patients undergoing video-assisted thoracoscopic surgical lung biopsy if no air leak is identified at the time of surgery. Patients without a drain are discharged home within 24 hours postoperatively, raising the possibility of this procedure being an outpatient procedure.
| Introduction |
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| Patients and Methods |
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Patients undergoing VATS lung biopsy were recruited preoperatively and gave written consent to be part of the study. Preoperative variables included age, sex, history of diabetes, steroid use, and side of VATS lung biopsy, whereas postoperative variables included incidence and size of pneumothorax on the postoperative chest radiograph immediately and 24 hours postoperatively, before hospital discharge, and at 6 weeks follow-up; the incidence of clinically significant pneumothorax requiring intercostal chest drain insertion; analgesic requirement; patients comfort as assessed by a visual analog pain scale; wound complication as assessed by the ASEPSIS (Additional treatment, Serous discharge, Erythema, Purulent exudates, Separation of deep tissues, Isolation of bacteria, Stay as patient prolonged over 14 days) score [2]; and in-hospital length of stay.
Video-assisted thoracoscopic surgical lung biopsy was performed using a three-port VATS incision. The biopsy was carried out using the Roticulator stapling system (Endo GIA [Autosuture, Tyco Healthcare, Norwalk, CT]).
Intraoperatively, after performing the VATS lung biopsy and before port site closure, the lung was tested for an air leak by using a size 8 mm Ryles nasogastric tube, inserted within the pleural cavity through the posterior port site with the other end positioned under water within a sterile container. The anesthetist then delivered sustained lung inflation to an airway pressure of 20 cm H2O through the double-lumen tube. All the air within the pleural space was thus evacuated. The nasogastric tube was then removed from the pleural space once the air leak stopped.
If no air leak was demonstrated, then the patient was randomized to either having an intercostal chest drain (group A) or not (group B). The randomization process was done using a sealed envelope system. If the randomization indicated the usage of a drain, then an intercostal chest drain was positioned through the anterior VATS port site. If the randomization indicated no drain usage, then no drain was inserted and the VATS port sites were closed using Steri-Strips.
If there was a persistent air leak while testing with the nasogastric tube, then the patient was not recruited in the study and an intercostal chest drain was positioned before VATS port closure, as would have been the recommended practice.
Seventy patients were approached, and 66 of them consented to be part of the study. Six of them had air leaks when the biopsied lung was tested perioperatively and were thus not randomized in the study. There was complete follow-up for all patients.
The decision for patients discharge from hospital was made by the junior staff looking after the patient and was based on the following general principles:
All patients in the drain group had their chest drain removed the day after surgery. No patients required drain insertion in the postoperative phase for pneumothorax problem. Patients stayed additional days as a result of discomfort requiring strong intravenous analgesia to achieve comfort for mobilization.
This study could not be blinded for obvious reasons. However, to minimize bias, we included a nonthoracic experienced nurse (M.P.) as an external assessor. Her contribution in the trial was to collect the visual analog pain scale score from the patients and assess the port sites using the ASEPSIS score. Our group of radiologists reported the chest radiographs as part of their daily workload, and they were unaware of whether the chest radiograph belonged to a patient in the trial or not.
| Results |
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The final histologic diagnosis was as follows: in the no-drain groupnon-specific interstitial pneumonitis (12 patients), usual interstitial pneumonia (5 patients), sarcoid (4 patients), emphysema (2 patients), extrinsic allergic alveolitis (2 patients), and bronchiolitis obliterans organizing pneumonia, collagen vascular disease, lymphoproliferative process, hamartoma, and Langerhans cell histiocytosis (1 patient each); in the drain groupusual interstitial pneumonia (7 patients), non-specific interstitial pneumonia (6 patients), emphysema (4 patients), adenocarcinoma (3 patients), extrinsic allergic alveolitis (2 patients), bronchiolitis obliterans organizing pneumonia (2 patients), respiratory bronchiolitisassociated interstitial lung disease (2 patients), and amiodarone-induced fibrosis, rheumatoid disease, sarcoidosis, and Wegeners granulomatosis (1 patient each).
| Comment |
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These findings provide the opportunity of performing this procedure as an outpatient procedure. Several authors have now investigated this policy [46]. However, although they advocated an outpatient procedure, they did not assess for air leak after lung biopsy and thus all their patients had an intercostal chest drain inserted. The drain was then removed a few hours after the procedure before the patients discharge from the hospital. This further confirms that in most patients, when there is no air leak, a chest drain is not required.
Blewett and colleagues [7] reported on their experience with an outpatient procedure. They, just as we suggested, tested the biopsied lung for air leak before deciding on the usage of an intercostal chest drain. However, they performed open lung biopsy and also inspected the cut surface for air-leak intraoperatively, a procedure that is difficult to perform under direct vision during VATS.
The economics of this practice has enormous implications. Molins and associates [6] reviewed the cost savings by their outpatient thoracic practice. This included patients undergoing VATS mediastinoscopy, lung biopsy, and bilateral thoracic sympathectomy. In their practice, patients were discharged within 6 hours of the general anesthetic, allowing a hospital total stay saving of nearly $300 per patient.
Video-assisted thoracoscopic surgical lung biopsy without the need of an intercostal chest drain is a safe procedure in well-selected patients. This reduces the discomfort experienced by patients when an intercostal chest drain is inserted and allows for the procedure to be an outpatient procedure with significant cost savings.
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