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Current morbimortality and one-year survival after pneumonectomy for infectious diseases

Abstract

Objective:

Identify the one-year survival rate and major complications in patients submitted to pneumonectomy for infectious disease.

Methods:

Retrospective data from all cases of infectious disease pneumonectomy over the past 10 years were collected from two reference centers. The authors analyzed: patient demographics, etiology, laterality, bronchial stump treatment, presence of previous pulmonary resection, postoperative complications in the first 30 days, the treatment used in pleural complications, and one-year survival rate.

Results:

56 procedures were performed. The average age was 44 years, with female predominance (55%). 29 cases were operated on the left side (51%) and the most frequent etiology was post-tuberculosis (51.8%). The overall incidence of complications was 28.6% and the most common was empyema (19.2%). Among empyema cases, 36.3% required pleurostomy, 27.3% required pleuroscopy and 36.3% underwent thoracoplasty for treatment. Bronchial stump fistula was observed in 10.7% of cases. From all cases, 16.1% were completion pneumonectomies and 62.5% of these had some complication, a significantly higher incidence than patients without previous surgery (p = 0.0187). 30-day in-hospital mortality was (7.1%) with 52 cases (92.9%) and 1-year survival. The causes of death were massive postoperative bleeding (1 case) and sepsis (3 cases).

Conclusions:

Pneumonectomy for benign disease is a high-risk procedure performed for a variety of indications. While morbidity is often significant, once the perioperative risk has passed, the one-year survival rate can be very satisfying in selected patients with benign disease.

Keywords:
Pneumonectomy; Infectious disease; Tuberculosis; survival; mortality

HIGHLIGHTS

Pneumonectomy for benign disease is a high-risk procedure performed for a variety of indications.

Patients with benign conditions would be expected to have superior long-term survival in comparison with those with malignancy.

Morbidity is often significant, with a meticulous operative technique and detailed patient management, which can be similar to a pneumonectomy performed for malignancy.

Pneumonectomy for a benign disease should continue to be considered a treatment option for carefully selected patients.

Introduction

Pneumonectomy has frequently been used for the treatment of central bronchogenic carcinoma. Under certain conditions, pneumonectomy is required to address benign lung disease, for carefully selected patients. Indications usually include complications of pulmonary Tuberculosis (TB), cystic bronchiectasis, suppurative lung disease, that immunosuppression combined with opportunistic invasive infection, and fibrosing mediastinitis.11 Owen RM, Force SD, Pickens A, Mansour KA, Miller DL, Fernandez FG. Pneumonectomy for benign disease: analysis of the early and late outcomes. Eur J Cardiothoracic Surg 2013;43(2):312–7.

Pneumonectomies for benign diseases are technically challenging procedures. Thoracic surgeons must perform in the setting of dense scar tissue and inflammatory adhesion around major vascular structures. These challenges are combined with a high rate of complications.11 Owen RM, Force SD, Pickens A, Mansour KA, Miller DL, Fernandez FG. Pneumonectomy for benign disease: analysis of the early and late outcomes. Eur J Cardiothoracic Surg 2013;43(2):312–7. The Society of Thoracic Surgeons General Thoracic Surgery Database (STS GTDB) reports that patients undergoing pneumonectomy for benign conditions are at almost three times the risk of major perioperative events when compared with lung cancer patients.22 Shapiro M, Swanson SJ, Wright CD, Chin C, Sheng S, Wisnivesky J, et al. Predictors of major morbidity and mortality after pneumonectomy utilizing the Society for Thoracic Surgeons General Thoracic Surgery Database. Ann Thorac Surg 2010;90(3):927–35. Others, however, advocate that pneumonectomy for benign disease can be performed with a favorable morbidity and mortality range from 23% to 63% and 0% to 25%, respectively.11 Owen RM, Force SD, Pickens A, Mansour KA, Miller DL, Fernandez FG. Pneumonectomy for benign disease: analysis of the early and late outcomes. Eur J Cardiothoracic Surg 2013;43(2):312–7.,33 Massard G, Dabbagh A, Wihlm JM, Kessler R, Barsotti P, Roeslin N, et al. Pneumonectomy for chronic infection is a high-risk procedure. Ann Thorac Surg 1996;62 (4):1033–8.,44 Miller DL, Deschamps C, Jenkins GD, Bernard A, Allen MS, Pairolero PC. Completion pneumonectomy: factors affecting operative mortality and cardiopulmonary morbidity. Ann Thorac Surg 2002;74(3):876–84.

To comprehensively select patients who would benefit from this surgical procedure, many authors have retrospectively published their experiences to identify risk factors associated with poor outcomes.11 Owen RM, Force SD, Pickens A, Mansour KA, Miller DL, Fernandez FG. Pneumonectomy for benign disease: analysis of the early and late outcomes. Eur J Cardiothoracic Surg 2013;43(2):312–7.,44 Miller DL, Deschamps C, Jenkins GD, Bernard A, Allen MS, Pairolero PC. Completion pneumonectomy: factors affecting operative mortality and cardiopulmonary morbidity. Ann Thorac Surg 2002;74(3):876–84.,55 Patel RL, Townsend ER, Fountain SW. Elective pneumonectomy: factors associated with morbidity and operative mortality. Ann Thorac Surg 1992;54(1):84–8. However, little data are reported regarding the one-year survival and the long-term outcome following pneumonectomy for benign disease.

In this retrospective analysis, 56 patients with benign lung disease who underwent pneumonectomy from two centers were included. The authors evaluate surgical outcomes of the last ten years to identify the one-year survival rate and major complications.

Materials and methods

This was a retrospective study performed at two-reference centers: Instituto do Coração (Incor), Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, and Hospital Messejana, Fortaleza. The study was approved by the Institutional Review Board (CAPPesq HCFMUSP – 33365720.2.0000.0068). The authors retrospectively reviewed the electronic medical records from two thoracic surgery databases who had undergone pneumonectomy for an infectious disease during a 10-year period. The study population consisted of all patients receiving pneumonectomy for infectious diseases. Inclusion criteria: patients undergoing pneumonectomy for infectious disease. There were no exclusion criteria in the current study. Patients who had already undergone some previous ipsilateral pulmonary resections were classified as completion pneumonectomy.

Data collection

Basic demographic information, including age, sex, comorbidities, smoking history, and etiology of infectious lung disease. Variables collected include surgical technique, bronchial stump treatment, presence of previous pulmonary resection, postoperative complications in the first 30 days, and one-year survival rate.

Surgical procedure

The procedure was performed in a standard operating room under sterile conditions. Patients underwent general anesthesia with a double-lumen endotracheal tube allowing for selective single-lung ventilation. Surgery was performed in the lateral decubitus position. The surgical procedure was performed by thoracotomy or Videothoracoscopy (VATS), decided by the surgeon. Additionally, the authors did not perform a pleuropneumonectomy, in some cases a greater pleural detachment was necessary, but this does not constitute an extrapleural pneumonectomy. One chest tube was placed after the operation and the chest tube was retained for 24 hours and kept clamped unless mediastinal adjustment of space decompression was required. The chest tube was removed gradually after the fluid collection was below 100 mL per day.

The technique of the pneumonectomy of each participating site was very similar, and in both places, this high-risk procedure was performed for an experienced thoracic surgical procedure without significant changes over the years. Moreover, both centers are reference centers for the treatment of chronic infectious diseases, one in the northeast region and another in the southeast region. However, as they are high-volume hospitals and referral centers, both have training programs for thoracic surgery. Despite having residents participating in the surgical procedure, they were always supervised and performed by the same experienced assistant team during the study period.

Statistical analysis

Descriptive statistical analysis was used to summarize the characteristics of the studied patients and surgical procedures. Frequencies and percentages are presented for categorical variables, and continuous variables are summarized as the median. A comparison of risk groups was made by using χ2 analysis or a non-parametric Wilcoxon test, where appropriate. The Kaplan-Meier method was used to calculate the one-year survival rate. All statistical analyses were performed using the software SPSS (IBM Corp) version 20.0. Probability (p) values of less than 0.05 were considered statically significant.

Results

56 procedures were performed in the study, of which 32 were women 55%. The mean age was 44 years. Twenty-six patients (68%) had associated comorbidities and smoking history was the most prevalent in thirteen patients (34.2%). Patients’ baseline demographic characteristics and comorbidities are summarized in (Table 1). The most frequent etiologies were post-TB (51.8%), pulmonary aspergillosis (21.4%), bronchiectasis (19.6%), and nontuberculous mycobacteria (3.6%). 29 cases were operated on the left side (51.8%), and only one case was performed by VATS. No intraoperative complications were observed. The bronchial stump was closed by an absorbable manual suture in 44 patients (78.6%), by a stapler in 10 (17.8%), and non-absorbable suture in just two patients.

Table 1
Characteristics of study group.

The overall incidence of major complications was 28.6% and the most common were empyema 11 (19.2%) followed by postoperative bleeding 3 (5.2%) (Table 2). Among the 11 patients who developed empyema, all of them underwent a surgical procedure (pleurostomy in 4, decortication in 3, and thoracoplasty in 4). Among the 3 cases that had postoperative bleeding, 1 patient who was reoperated died due to this acute bleeding. In contrast, the other 2 patients were managed clinically with no further interventions.

Table 2
Major complications of the study group.

Bronchial Stump Fistula (BSF) was observed in 6 cases (10.7%) and 16.6% were identified in the first 14 days. In five cases, the bronchial closure technique was by absorbable manual suture and in just one case bronchus was closed by an automatic stapler. From all cases, 8 (16%) were completion pneumonectomies and 62.5% of these had empyema, which assign from this group a significantly higher incidence than patients without previous surgery (p = 0.0187). From these patients with completion pneumonectomies and empyema, the BSP was present in 5 cases (83%).

The one-year survival was 92.9% with only 04 deaths: two due to sepsis related to postoperative empyema, another due to immediate postoperative bleeding, and another due to an undetermined cause several months after hospital discharge.

Discussion

The destroyed lung is more prevalent in developing countries,66 Halezeroglu S, Keles M, Uysal A, Celik M, Senol C, Haciibrahimoglu G, et al. Factors affecting postoperative morbidity and mortality in destroyed lung. Ann Thorac Surg 1997;64(6):1635–8. and those patients are at risk of developing fatal complications like massive hemoptysis, aspergillosis, septicemia, and empyema.77 Bai L, Hong Z, Gong C, Yan D, Liang Z. Surgical treatment efficacy in 172 cases of tuberculosis-destroyed lungs. Eur J Cardiothorac Surg 2012;41(2):335–40. It was found that pneumonectomy is an effective method for preventing and treating such serious complications.88 Conlan AA, Lukanich JM, Shutz J, Hurwitz SS. Elective pneumonectomy for benign lung disease: modern-day mortality and morbidity. J Thorac Cardiovasc Surg 1995;110(4):1118–24.99 Erdogan A, Yegin A, Gürses G, Demircan A. Surgical management of tuberculosis-related hemoptysis. Ann Thorac Surg 2005;79(1):299–302. The present series of 56 patients undergoing elective pneumonectomy for a variety of chronic infectious diseases. TB was the most common etiology of infectious disease followed by pulmonary aspergillosis in the present study. Despite the high rate of major complications, the one-year survival rate was 94% and compares favorably with modern-day cancer pneumonectomy rates.55 Patel RL, Townsend ER, Fountain SW. Elective pneumonectomy: factors associated with morbidity and operative mortality. Ann Thorac Surg 1992;54(1):84–8.,1010 Ginsberg RJ, Hill LD, Eagan RT, Thomas P, Mountain CF, Deslauriers J, Fry WA, Butz RO, Goldberg M, Waters PF, Jones DP. Modern thirty-day operative mortality for surgical resections in lung cancer. J Thorac Cardiovasc Surg 1983;86(5):654–8.,1111 Harmon HA, Fergus SC, Cole FH. Pneumonectomy: review of 351 cases. Ann Surg 1976;183(6):719.

Given the complexities of these operations, the most important postoperative complications reported after pneumonectomy included Bronchopleural Fistula (BPF), empyema, reoperation for bleeding, and respiratory failure.1212 Hu XF, Duan L, Jiang GN, Wang H, Liu HC, Chen C. Risk factors for early postoperativecomplications after pneumonectomy forbenign lung disease. Ann Thorac Surg 2013;95(6):1899–904. In this study, the overall incidence of major complications was 28.6% and the most common were empyema (19.2%) followed by postoperative bleeding (5.2%). The authors achieved satisfactory surgical outcomes in all patients, except one who died due to intense postoperative bleeding that in the re-operation was identified to be from a rupture of the Pulmonary Artery (PA). The final pathology of this case showed his on the PA wall. The authors don’t know if this condition could be related to the PA rupture. Published studies found that the presence of preoperative empyema, aspergillosis, massive blood loss, right pneumonectomy, reoperation for bleeding, and intraoperative dissemination were the most critical issues that lead to significant complications.1212 Hu XF, Duan L, Jiang GN, Wang H, Liu HC, Chen C. Risk factors for early postoperativecomplications after pneumonectomy forbenign lung disease. Ann Thorac Surg 2013;95(6):1899–904.,1313 Puri V, Tran A, Bell JM, Crabtree TD, Kreisel D, Krupnick AS, Patterson GA, Meyers BF. Completion pneumonectomy: outcomes for benign and malignant indications. Ann Thorac Surg 2013;95(6):1885-91.

A few authors have suggested that patients undergoing completion pneumonectomy are not at an increased risk of complications.11 Owen RM, Force SD, Pickens A, Mansour KA, Miller DL, Fernandez FG. Pneumonectomy for benign disease: analysis of the early and late outcomes. Eur J Cardiothoracic Surg 2013;43(2):312–7.,1414 Reed CE. Pneumonectomy for chronic infection: fraught with danger? Ann Thorac Surg 1995;59(2):408–11. In contrast, a more recent review of outcomes after completion of pneumonectomy noted that patients undergoing completion pneumonectomy for benign conditions were more likely to have major complications and lower median survival than those with malignancy.1313 Puri V, Tran A, Bell JM, Crabtree TD, Kreisel D, Krupnick AS, Patterson GA, Meyers BF. Completion pneumonectomy: outcomes for benign and malignant indications. Ann Thorac Surg 2013;95(6):1885-91. The present study did not find higher mortality in the completion pneumonectomy subset, however, completion pneumonectomy was more likely to have major complications such as empyema (p = 0.0187) and BPF.

Some of the best results reported for benign pneumonectomy have come from areas where pulmonary TB is endemic, and thus experience with the operative management of these patients is vast.1515 Mohamed E, Ghaffar AA, Aboelwafa W, Mohammadien H. Indications and outcomes of pneumonectomy for benign diseases: a single-center experience. Egypt Cardiothorac Surg 2021;3(3):70–9. In this study, TB was the most common etiology of infectious disease, and the mortality rate was 7.1% for the entire cohort. In a study by Klapper and colleagues on the outcome of pneumonectomy for benign disease, they reported a 29% mortality rate for the entire cohort, and 83% of deaths were operated on an emergent or urgent bias.1616 Klapper J, Hirji S, Hartwig MG, D’Amico TA, Harpole DH, Onaitis MW, et al. Outcomes after pneumonectomy for benign disease: the impact of urgent resection. J Am Coll Surg 2014;219(3):518–24. They did not report cases of TB.1616 Klapper J, Hirji S, Hartwig MG, D’Amico TA, Harpole DH, Onaitis MW, et al. Outcomes after pneumonectomy for benign disease: the impact of urgent resection. J Am Coll Surg 2014;219(3):518–24. It has been found that mortality was reduced to less than 10% after the exclusion of the emergency cases,1717 Olcmen A, Gunluoglu MZ, Demir A, Akin H, Kara HV, Dincer SI. Role and outcome of surgery for pulmonary tuberculosis. Asian Cardiovasc Thorac Ann 2006;14(5):363–6. which is following the present results and other reports.1717 Olcmen A, Gunluoglu MZ, Demir A, Akin H, Kara HV, Dincer SI. Role and outcome of surgery for pulmonary tuberculosis. Asian Cardiovasc Thorac Ann 2006;14(5):363–6.

Although there are a few papers that have reported long-term survival rates after pneumonectomy for chronic inflammatory lung disease, the first-year survival rates in this series would seem to be satisfactory (92.9%). For high-risk patients with preoperative empyema, Shiraishi et al.1818 Shiraishi Y, Nakajima Y, Koyama A, Takasuna K, Katsuragi N, Yoshida S. Morbidity and mortality after 94 extrapleural pneumonectomies for empyema. Ann Thorac Surg 2000;70(4):1202–6. reported a 5-year survival rate of 83% and Ashour et al.1919-Ashour M. Pneumonectomy for tuberculosis. Euro J Cardiothorac Surg 1997;12 (2):209–13. reported no long-term death during 12-124 months of follow-up periods after 24 pneumonectomies for TB. In contrast, Speicher2020 Speicher PJ, Ganapathi AM, Englum BR, Onaitis MW, D’Amico TA, Berry MF. Survival in the elderly after pneumonectomy for early-stage non - small cell lung cancer: a comparison with nonoperative management. J Am Coll Surg 2014;218(3):439–49. recently reported rewarding long-term results after pneumonectomy for stage I–II NSCLC: they found that 5-year survival rates were 50%, 40%, 29%, and 19% in patients aged 50, 50–69, 70–79, and 79 years, respectively. Certainly, once the perioperative risk has passed, patients with benign conditions would be expected to have superior long-term survival in comparison with those with malignancy. Also, when the pneumonectomy is proposed for inflammatory disease in most cases the surgery is removing an already destroyed lung, in contrast for cancer, where the lung is most of the cases physiologically active, this difference can partially explain the higher incidence of complications due the accommodation in the postoperative period like the cardiac arrhythmia for lung cancer patients2121 Pricopi C, Mordant P, Rivera C, Arame A, Foucault C, Dujon A, et al. Postoperative morbidity and mortality after pneumonectomy: a 30-year experience of 2064 consecutive patients. Interact Cardiovasc Thorac Surg 2015;20(3):316–21. compared to the present data.

The adequate preoperative workup for pulmonary resections in lung infectious diseases is still in debate since the current algorithms validated for lung cancer do not correct postoperative complications.2222 Mariani AW, Vallilo CC, de Albuquerque ALP, Salge JM, Augusto MC, Suesada MM, et al. Preoperative evaluation for lung resection in patients with bronchiectasis: should we rely on standard lung function evaluation? Euro J Cardiothorac Surg 2021;59 (6):1272–8. In this population, it is important to look not only for the cardiac and pulmonary assessment risk but for other details like the nutritional status and possible airway contamination. Additionally, whenever the surgery is indicated for adjuvant treatment for TB (MDR/XDR), chronic cavitary aspergillosis, or non-tuberculosis mycobacteria a correct and rigorous medical treatment is mandatory during the perioperative period. The WHO guidelines for resistant TB, are based on a previously published meta-analysis.2323 Fox GJ, Mitnick CD, Benedetti A, Chan ED, Becerra M, Chiang CY, et al. Surgery as an adjunctive treatment for multi-drug resistant tuberculosis: an individual patient data meta-analysis. Clin Infect Dis 2016;62(7):887–95. state that the indication for adjuvant lung resection must be done if the surgery is lobectomy or less, due to the higher pneumonectomy mortality. However, recent data contrast this information, and several authors believe that for good candidates pneumonectomy can be a safe and effective adjuvant treatment for TB, leading to good results.2424 Visca D, Tiberi S, Centis R, D’Ambrosio L, Pontali E, Mariani AW, et al. Post-tuberculosis (TB) treatment: the role of surgery and rehabilitation. Appl Sci 2020;10(8):2734.

The present study has several limitations, most inherent to the methodology. The main limitation of this study is its retrospective nature, which may have introduced selection biases. The small size is a similar limitation, which makes drawing definitive conclusions difficult. But to the authors’ knowledge, the size of this series compares favorably with other published series and is notable for the spectrum of disease processes that it includes.

Conclusion

Pneumonectomy for benign lung disease is a high-risk procedure that is performed for a variety of indications. While morbidity is often significant, once the perioperative risk has passed, the one-year survival rate can be very satisfying in this varied patient population. Pneumonectomy for a benign disease should continue to be considered a treatment option in selected patients.

Acknowledgment

Gonzalo Varela, M.D., Ph.D (https://orcid.org/0000-0002-4498-7842).

  • Footnote
    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.
  • Funding
    This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

References

  • 1
    Owen RM, Force SD, Pickens A, Mansour KA, Miller DL, Fernandez FG. Pneumonectomy for benign disease: analysis of the early and late outcomes. Eur J Cardiothoracic Surg 2013;43(2):312–7.
  • 2
    Shapiro M, Swanson SJ, Wright CD, Chin C, Sheng S, Wisnivesky J, et al. Predictors of major morbidity and mortality after pneumonectomy utilizing the Society for Thoracic Surgeons General Thoracic Surgery Database. Ann Thorac Surg 2010;90(3):927–35.
  • 3
    Massard G, Dabbagh A, Wihlm JM, Kessler R, Barsotti P, Roeslin N, et al. Pneumonectomy for chronic infection is a high-risk procedure. Ann Thorac Surg 1996;62 (4):1033–8.
  • 4
    Miller DL, Deschamps C, Jenkins GD, Bernard A, Allen MS, Pairolero PC. Completion pneumonectomy: factors affecting operative mortality and cardiopulmonary morbidity. Ann Thorac Surg 2002;74(3):876–84.
  • 5
    Patel RL, Townsend ER, Fountain SW. Elective pneumonectomy: factors associated with morbidity and operative mortality. Ann Thorac Surg 1992;54(1):84–8.
  • 6
    Halezeroglu S, Keles M, Uysal A, Celik M, Senol C, Haciibrahimoglu G, et al. Factors affecting postoperative morbidity and mortality in destroyed lung. Ann Thorac Surg 1997;64(6):1635–8.
  • 7
    Bai L, Hong Z, Gong C, Yan D, Liang Z. Surgical treatment efficacy in 172 cases of tuberculosis-destroyed lungs. Eur J Cardiothorac Surg 2012;41(2):335–40.
  • 8
    Conlan AA, Lukanich JM, Shutz J, Hurwitz SS. Elective pneumonectomy for benign lung disease: modern-day mortality and morbidity. J Thorac Cardiovasc Surg 1995;110(4):1118–24.
  • 9
    Erdogan A, Yegin A, Gürses G, Demircan A. Surgical management of tuberculosis-related hemoptysis. Ann Thorac Surg 2005;79(1):299–302.
  • 10
    Ginsberg RJ, Hill LD, Eagan RT, Thomas P, Mountain CF, Deslauriers J, Fry WA, Butz RO, Goldberg M, Waters PF, Jones DP. Modern thirty-day operative mortality for surgical resections in lung cancer. J Thorac Cardiovasc Surg 1983;86(5):654–8.
  • 11
    Harmon HA, Fergus SC, Cole FH. Pneumonectomy: review of 351 cases. Ann Surg 1976;183(6):719.
  • 12
    Hu XF, Duan L, Jiang GN, Wang H, Liu HC, Chen C. Risk factors for early postoperativecomplications after pneumonectomy forbenign lung disease. Ann Thorac Surg 2013;95(6):1899–904.
  • 13
    Puri V, Tran A, Bell JM, Crabtree TD, Kreisel D, Krupnick AS, Patterson GA, Meyers BF. Completion pneumonectomy: outcomes for benign and malignant indications. Ann Thorac Surg 2013;95(6):1885-91.
  • 14
    Reed CE. Pneumonectomy for chronic infection: fraught with danger? Ann Thorac Surg 1995;59(2):408–11.
  • 15
    Mohamed E, Ghaffar AA, Aboelwafa W, Mohammadien H. Indications and outcomes of pneumonectomy for benign diseases: a single-center experience. Egypt Cardiothorac Surg 2021;3(3):70–9.
  • 16
    Klapper J, Hirji S, Hartwig MG, D’Amico TA, Harpole DH, Onaitis MW, et al. Outcomes after pneumonectomy for benign disease: the impact of urgent resection. J Am Coll Surg 2014;219(3):518–24.
  • 17
    Olcmen A, Gunluoglu MZ, Demir A, Akin H, Kara HV, Dincer SI. Role and outcome of surgery for pulmonary tuberculosis. Asian Cardiovasc Thorac Ann 2006;14(5):363–6.
  • 18
    Shiraishi Y, Nakajima Y, Koyama A, Takasuna K, Katsuragi N, Yoshida S. Morbidity and mortality after 94 extrapleural pneumonectomies for empyema. Ann Thorac Surg 2000;70(4):1202–6.
  • 19
    -Ashour M. Pneumonectomy for tuberculosis. Euro J Cardiothorac Surg 1997;12 (2):209–13.
  • 20
    Speicher PJ, Ganapathi AM, Englum BR, Onaitis MW, D’Amico TA, Berry MF. Survival in the elderly after pneumonectomy for early-stage non - small cell lung cancer: a comparison with nonoperative management. J Am Coll Surg 2014;218(3):439–49.
  • 21
    Pricopi C, Mordant P, Rivera C, Arame A, Foucault C, Dujon A, et al. Postoperative morbidity and mortality after pneumonectomy: a 30-year experience of 2064 consecutive patients. Interact Cardiovasc Thorac Surg 2015;20(3):316–21.
  • 22
    Mariani AW, Vallilo CC, de Albuquerque ALP, Salge JM, Augusto MC, Suesada MM, et al. Preoperative evaluation for lung resection in patients with bronchiectasis: should we rely on standard lung function evaluation? Euro J Cardiothorac Surg 2021;59 (6):1272–8.
  • 23
    Fox GJ, Mitnick CD, Benedetti A, Chan ED, Becerra M, Chiang CY, et al. Surgery as an adjunctive treatment for multi-drug resistant tuberculosis: an individual patient data meta-analysis. Clin Infect Dis 2016;62(7):887–95.
  • 24
    Visca D, Tiberi S, Centis R, D’Ambrosio L, Pontali E, Mariani AW, et al. Post-tuberculosis (TB) treatment: the role of surgery and rehabilitation. Appl Sci 2020;10(8):2734.

Publication Dates

  • Publication in this collection
    17 Mar 2023
  • Date of issue
    2023

History

  • Received
    04 Nov 2022
  • Reviewed
    25 Dec 2022
  • Accepted
    29 Dec 2022
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