Recurrence of primary spontaneous pneumothorax following bullectomy with pleurodesis or pleurectomy: A retrospective analysis
Introduction
A pneumothorax forms when air collects in the pleural space between the lung and the chest wall. A nonspontaneous pneumothorax has an identifiable inciting event, most often being traumatic or iatrogenic. A spontaneous pneumothorax occurs despite having no readily identifiable inciting event. A primary spontaneous pneumothorax (PSP) occurs in a patient with no apparent underlying lung disease. PSPs are typically caused by rupture of subpleural blebs (<2 cm) or bullae (≥2 cm) (1).
PSP has an annual incidence of 18–28 per 100,000 in men and 1.2–6.0 per 100,000 in women (2). The goals of treating a PSP include elimination of the existing pneumothorax and minimizing recurrence (3,4). The most recent guidelines for management of PSP were published by The American College of Chest Physicians (ACCP) in 2001 and the British Thoracic Society (BTS) in 2010 (5,6). In summary, small PSPs in stable patients can be observed but a large pneumothorax (variably defined in the guidelines as >2 or >3 cm) or any pneumothorax in an unstable patient requires aspiration or a chest tube. Chest tubes can be removed once there is no air leak. In these guidelines, if the air leak persists for more than approximately 4 days, the next recommended step is surgery. Previous studies have examined trials of non-operative management ranging from 3 to 14 days (7-9). The risk of recurrence for PSPs treated with conservative treatment alone is 16–52% after the first episode and 65% after the second ipsilateral episode (10,11). Therefore, it is important to determine which surgical technique best minimizes recurrence risk.
The standard surgical approach for management of PSP is bullectomy. Classically, congenital bullae exist in the apex of the lung and wedge resection of the portion of lung containing these ruptured bullae (bullectomy) will decrease the risk of pneumothorax recurrence. In addition to bullectomy, pleurectomy or pleurodesis is performed to further decrease the risk of pneumothorax recurrence. However, there is limited data suggesting that these additional procedures offer benefit. Specifically, studies have been published showing no further decrease in pneumothorax recurrence risk following bullectomy with mechanical pleurodesis (12), chemical pleurodesis (13), or pleurectomy (14) compared to bullectomy alone. These studies are criticized for having relatively short follow-up periods (mean 18–46 months). There is currently no consensus guideline on the surgical approach which best minimizes pneumothorax recurrence risk and despite a lack of evidence, pleurodesis or pleurectomy are still commonly performed with bullectomy in patients thought to have a high recurrence risk (6). To address existing gaps in the literature, this study’s primary objective is to examine recurrence rates when pleurodesis or pleurectomy is performed with bullectomy compared to bullectomy alone in patients with PSP. We hypothesize that patients who undergo bullectomy with pleurodesis or pleurectomy will have a decreased recurrence rate compared to patients who undergo bullectomy alone. Secondary objectives include an evaluation of patient and disease factors associated with recurrence. We present the following article in accordance with the STROBE reporting checklist (15) (available at http://dx.doi.org/10.21037/jtd-20-3257).
Methods
Study design and population
This retrospective cohort study describes patient outcomes after surgical treatment for PSP at a quaternary-care hospital for the region and the only center providing thoracic surgery services. All incident cases of PSP treated with bullectomy from June 2006 to December 2018 in patients older than 17 and younger than 45 years of age were identified using the Canadian Institute for Health Information (CIHI) hospitalization records. Comparable publications limited the upper age limit for inclusion at 40 years (12,14) or 50 years (13). Chart abstraction for patient demographics and operative details was completed using electronically available medical records.
The study was conducted in accordance with the Declaration of Helsinki (as revised in 2013). The study was approved by the institutional ethics board of the Nova Scotia Health Authority (File number 1024736) and individual consent for this retrospective analysis was waived.
Measures and outcomes
The primary study outcome is pneumothorax recurrence. Recurrence was defined to occur in a participant who had already undergone bullectomy or wedge resection for PSP requiring a second surgery for ipsilateral pneumothorax either for prolonged air leak or from true recurrence. If this second surgery occurred fewer than 15 days after the initial surgery date, this was classified as a prolonged air leak. If a second surgery was performed more than 15 days following the initial surgery, it was classified a ‘true’ recurrent pneumothorax. The etiology of the clinical recurrence in each case was not captured in the original data which is why ‘true recurrence’ and ‘prolonged air leak’ are defined temporally. The cut-off of 15 days was chosen because at our centre, no patient would undergo a trial of inpatient non-operative management of an air leak exceeding 15 days, and comparable previous studies have examined trials of non-operative air leak management ranging from 3 to 14 days (7-9). There were no instances in which a patient presented following bullectomy with a clinical or radiographic ipsilateral pneumothorax recurrence and was managed non-operatively rather than undergoing a second ipsilateral surgery.
Secondary outcomes included an assessment of potential predictors of pneumothorax recurrence. These factors included age, sex, smoking status, disease severity, surgical method, contralateral pneumothorax (historical diagnosis or diagnosed during the study period), year of initial surgery, surgical approach, and performance of decortication. A priori the cases were stratified based on an assessment of disease severity. Disease severity was scored based on thoracoscopic findings at the time of surgery using Vanderschueren’s classification (14). In this validated classification scheme, stage 1 is used when no thoracoscopic abnormalities are noted, stage 2 when pleuropulmonary adhesions are seen, stage 3 when blebs are noted with a greatest dimension <2 cm, and stage 4 when bullae with a greatest dimension ≥2 cm are noted. Some operative dictations did not explicitly measure the greatest dimension of the bullae seen. In these cases, bullae described as ‘giant,’ or ‘large’ were categorized as stage 4, and blebs described as ‘small’ were categorized as stage 3. In cases for which the operative note did not adequately describe bulla size, the pathology report was used to estimate size. Those cases for which disease severity could not be determined based on the operative or pathology reports are reported as ‘Indeterminate’.
Pleurectomy was defined as the removal of the parietal pleura. The typical method of pleurectomy in this study involved using electrosurgery to circumferentially delineate a section of parietal pleural, and then peeling this pleura from the underlying structures. Mechanical pleurodesis was defined as abrasion of the parietal pleura and was typically performed by inserting a small piece of cautery scratch pad into the pleural space and using it to scratch the parietal pleura. Chemical pleurodesis is not commonly used in the operating room at this institution. Decortication was defined broadly in this study as peeling off a visceral pleural rind and/or extensive lysis of intrathoracic adhesions. The group called ‘Any Pleurectomy’ includes patients who had a partial pleurectomy in addition to some form of mechanical and/or chemical pleurodesis.
Patients in this study typically had one scheduled follow-up appointment approximately 4 to 6 weeks post-operatively. Beyond this one scheduled appointment, the patient was brought to the attention of the Thoracic Surgery group if they experienced symptoms and then underwent a chest X-ray demonstrating pneumothorax recurrence. In this catchment area, Thoracic Surgery is performed only at this quaternary centre, so pneumothorax recurrences would not be referred elsewhere.
Statistical analysis
Comparisons of proportions between study groups were made using the Chi-square tests and Fisher’s exact tests when cell sizes were less than five. T-tests were used to analyze continuous variables. Factors associated with recurrence were evaluated by logistic regression. Results were considered statistically significant at P value <0.05. All analyses were performed using SAS version 9.4 (SAS Institute, Cary, NC). To account for the time to the outcomes, we additionally re-examined our data using the Kaplan-Meier method with log-rank tests for univariable analysis and Cox regression for multivariable analysis.
Results
Two hundred and twenty-two patients were included in the study (Figure 1). Thirteen percent (28/222) were operated on for pneumothorax recurrence (Table 1). The median age was 24 years (IQR 19–32) and 73% (161/222) of patients were male. Thirty-seven percent (82/222) of patients smoked tobacco and 16% (36/222) had a history of a contralateral pneumothorax. Decortication was necessary in 16% (36/222) of initial surgeries and only three (1%) required an open thoracotomy rather than a VATS approach.
Full table
The pleurectomy and pleurodesis groups were statistically similar with four notable exceptions. For patients undergoing both mechanical pleurodesis and pleurectomy, significantly more had Vanderschueren’s stage 4 disease (44%, 8/18), and no patients had disease stage 2 (P=0.005). For the mechanical pleurodesis group, significantly more patients had a documented contralateral pneumothorax than in the other groups (30%, 18/61, P=0.010). No patients from the pleurectomy group had surgery performed from 2011–2014 and no patients in the group combining pleurectomy with some form of pleurodesis had surgery from 2015–2018 (P<0.001). Finally, decortication was performed in significantly more patients undergoing both mechanical pleurodesis and pleurectomy than for the other treatment groups (39%, 7/18, P=0.053).
The overall population recurrence rate for PSP treated with surgery was 13% (28/222). When analyzed based on operative technique, the overall recurrence rate for bullectomy alone was 15% (19/126) and for bullectomy plus any form of pleurodesis, the recurrence rate was 9% (9/96, P=0.205). When examined by specific surgical approaches, bullectomy plus mechanical pleurodesis was 13% (8/61), bullectomy plus pleurectomy was 6% (1/17), and for bullectomy plus pleurectomy and mechanical pleurodesis the recurrence rate was 0% (0/18, P=0.302).
For the 28 patients who went on to have a second surgery for PSP, the median time from initial surgery to second surgery for recurrence was 363 days (IQR 20–1,026, Table 2). The distribution of recurrences based on number of days between the first surgery for PSP and the second surgery for recurrence is presented in Figure 2. Four (14%) patients had a second surgery within the first 15 days following the initial surgery due to prolonged air leaks. Between 16 and 30 days following the initial surgery, 6 (21%) patients had a second surgery for a recurrent PSP. Between a month and a year following the initial surgery, 4 (14%) were operated on for recurrence. Between one and two years following the initial surgery, 4 (14%) required re-operation, and between two and three years an additional four required surgery for a recurrence. Six (21%) patients required re-operation to treat a recurrence at more than three years following their initial surgery, with the longest duration between first and second surgery being 10 years (3,652 days). Nine patients had three or more surgeries. Seven out of the nine had more than two surgeries due to contralateral pneumothorax and two patients (2/9; 22%) had three surgeries due to a second ipsilateral recurrence.
Full table
Univariable and multivariable analyses (Table 3) found no associations between rate of recurrence and year of surgery, age, sex, smoking, or disease severity. On multivariable analysis using PSP treated with bullectomy alone at the time of initial surgery as a reference, patients who underwent bullectomy with mechanical pleurodesis at the time of initial surgery were found to have a lower risk of recurrence (OR 0.82, 95% CI: 0.31–2.20) and those who underwent bullectomy with any pleurectomy were found to have the lowest risk of recurrence, though these differences were not statistically significant (OR 0.15, 95% CI: 0.02–1.27, P=0.218). There were no differences in the results when re-examined using time to event analysis.
Full table
Discussion
The recurrence risk in this study for patients treated for PSP with bullectomy and pleurectomy trended lower than for patients treated with bullectomy alone, although this difference was not statistically significant. Notably, none of the 18 patients treated with bullectomy, pleurectomy, and pleurodesis experienced recurrence. Interpreting these findings is challenging because we were unable to include a zero value in our analysis. Presumably the true recurrence rate for this group is nonzero and a study containing more participants may have been able to statistically analyze this nonzero recurrence rate. Any significant difference in recurrence rates would contrast with the findings of earlier studies, which found no such effect (12-14).
The recurrence rates in this study are higher than previously reported. Recurrence was 15% for PSP treated with bullectomy alone, 13% for those treated with bullectomy and mechanical pleurodesis, and 6% for PSP treated with bullectomy and pleurectomy (with or without additional pleurodesis, Table 3). In a 2014 RCT by Min et al., recurrence following bullectomy alone was 7.5% and for bullectomy with mechanical pleurodesis was 5.9% (12). In a 2008 RCT by Rena et al., recurrence following bullectomy with apical pleurectomy was 4.6% and for bullectomy with mechanical pleurodesis was 6.2% (14). It is possible that follow-up in these earlier studies was too short to accurately capture the true recurrence rate. The mean follow-up for Min et al. was 18 months (range 6 to 24 months), and for Rena et al. was 46 months (range 24 to 66 months) (12,14). The median follow-up in the present study was 81 months (range 12 to 162 months) and 35.7% of the recurrences were recorded more than 3 years following the initial surgery (Figure 2). One recurrence was noted 10 years following the initial surgery. Follow-up periods for previous studies may be inadequately short, potentially missing a significant number of recurrences.
A recent meta-analysis found that the addition of chemical pleurodesis to VATS mechanical pleurodesis or pleurectomy with or without bullectomy was associated with a 63% lower risk of pneumothorax recurrence compared to intervention without chemical pleurodesis (16). Our institution tends not to use chemical pleurodesis as a first line agent in cases of pneumothorax recurrence and the chemical agents used in this meta-analysis were heterogeneous (variably minocycline, tetracycline, talc, and dextrose), so these results aren’t comparable to our data. However, there may additionally be a role for chemical pleurodesis to further minimize recurrence risk of PSP.
No statistically significant association was found between recurrence rate and any other factors analyzed in this study. This lack of associations contrasts with previously published studies. Predictors of increased recurrence rate after surgery for PSP have previously been identified for smoking (17,18), younger age (19,20), female sex (17,18), VATS approach (21), and greater disease severity (14).
Although not statistically significant, patients found to have no thoracoscopic abnormalities (Vanderschueren’s stage 1) were more likely to recur than were patients found to have a lesion. Review of the operative reports revealed that following an initial surgery which failed to find a thoracoscopic abnormality, blebs or bullae were found in many of the second surgeries. It is possible that these lesions were missed initially. It is important to maintain a high suspicion that a targetable bulla is present even when no thoracoscopic abnormality is initially discovered. Tsou et al. found no association between performance of a pre-operative CT scan of the chest in cases of PSP and recurrence after surgery (22). Additionally, bullae detection rates are recorded to be higher during surgery (76–100%) than on pre-op CT scans (23-25). Almajid et al. reported a positive predictive value (PPV) of 86% and a negative predictive value (NPV) of 73% for detection of PSP on CT scan (26). Therefore, pre-operative CT scan does not seem to confer a superior rate of bulla detection and may not be helpful even in cases where no bullae are initially detected thoracoscopically. This recommendation against routine performance of chest CT scans is consistent with current guidelines (6,27).
This study is population-based, thus avoiding the bias associated with more restricted cohorts and suffering very little loss to follow-up. The population is young (age <45) and few health-related confounders are thought to exist in this study. In addition to the limitations inherent to a retrospective study, selection bias may exist in this analysis because the type of surgery performed for each patient was unilaterally chosen by the surgeon. The authors predicted that a surgeon’s decision about which procedure to perform may have been influenced by disease severity, which is why a priori the cases were stratified by disease severity. It is likely, however, that this stratification incompletely compensated for the selection bias. The cohort in this study was possibly too small to detect weaker associations despite the sample size being comparable to similar published studies (12-14). In comparison to the rest of Canada, the population of the Maritime provinces tends to be more rural, more Caucasian, and have a higher BMI (28-30). Despite these differences, the results of this study are generalizable to any North American population.
One limitation of this study is that we did not explicitly examine complications from the various surgical methods. Chen et al. reported on a similar population and looked at post-operative pain and chest tube drainage (13). In this study, patients reported greater pain following pleurectomy than following mechanical pleurodesis and chemical pleurodesis using minocycline on, but not following, the first post-operative day. Additionally, they report that the total chest tube drainage was significantly more following pleurectomy than following mechanical pleurodesis and chemical pleurodesis.
In summary, based on this retrospective observational analysis, no significant difference was found in the rate of recurrence of PSP treated with bullectomy and pleurectomy or bullectomy and pleurodesis. We were unable to properly assess the difference in recurrence between these rates and the rate for the bullectomy, pleurectomy, and pleurodesis group, because the recurrence rate for this group was zero. Performance of a combination of pleurectomy and mechanical pleurodesis with bullectomy may be indicated in cases of PSP suspected to be at higher risk of recurrence. A multi-centred randomized controlled trial (RCT) is necessary to further answer this question. Based on the temporal distribution of recurrences found in these data, the 2 to 3-year follow-up used in most published pneumothorax-related RCTs to date is inadequate and should be extended to 5 years of follow-up to accurately capture the recurrence rate.
Acknowledgments
An early version of this project was presented at the Dalhousie University Dept. of Surgery Research Symposium in Halifax, Nova Scotia, Canada, on June 3, 2020.
Funding: None.
Footnote
Reporting Checklist: The authors have completed the STROBE reporting checklist. Available at http://dx.doi.org/10.21037/jtd-20-3257
Data Sharing Statement: Available at http://dx.doi.org/10.21037/jtd-20-3257
Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/jtd-20-3257). The authors have no conflicts of interest to declare.
Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. The study was conducted in accordance with the Declaration of Helsinki (as revised in 2013). The study was approved by the institutional ethics board of the Nova Scotia Health Authority (File number 1024736) and individual consent for this retrospective analysis was waived.
Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
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