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Ann Thorac Surg 2004;78:999-1002
© 2004 The Society of Thoracic Surgeons


Original article: general thoracic

Recent results of postoperative mortality for surgical resections in lung cancer

Shun-ichi Watanabe, MDa,*, Hisao Asamura, MDa, Kenji Suzuki, MDa, Ryosuke Tsuchiya, MDa

a Division of Thoracic Surgery, National Cancer Center Hospital, Tokyo, Japan

Accepted for publication April 1, 2004.

* Address reprint requests to Dr Watanabe, Division of Thoracic Surgery, National Cancer Center Hospital, Tokyo 104-0045, Japan
syuwatan{at}ncc.go.jp


    Abstract
 Top
 Abstract
 Introduction
 Patients and methods
 Results
 Comment
 References
 
BACKGROUND: Changes in the postoperative mortality rates and causes of death for lung cancer surgery at the specialized hospital for cancer in Tokyo, Japan during the last 16 years were investigated.

METHODS: Data on 3,270 consecutive patients who underwent pulmonary resection for primary lung cancer between January 1987 and December 2002 at the National Cancer Center Hospital were retrospectively analyzed. The postoperative 30-day and in-hospital mortality rates and causes of death after pulmonary resection for lung cancer were investigated. Patients were divided into two period groups of almost equal number, the early (1,615 patients from 1987 to 1996) and the late (1,655 patients from 1997 to 2002) periods.

RESULTS: Fifty-eight operative and postoperative deaths occurred during the last 16 years. Thirty-day and in-hospital mortality were 0.6% (21/3,270) and 1.6% (58/3,270), respectively. During the last 6-year period, 30-day and in-hospital mortality were 0.5% (8/1,655) and 0.8% (21/1,655), respectively. The difference was significant between the 30-day/in-hospital mortality for pneumonectomy (3.1%/5.9%) and lobectomy (0.3%/1.3%) (p < 0.0001/p < 0.0001). The difference in mortality between lobectomy and segmentectomy or a lesser resection was not significant. The 58 deaths were caused by pneumonia/acute respiratory distress syndrome (ARDS) (36%, n = 21), bronchopleural fistula (BPF)/empyema (33%, n = 19), cerebrovascular accident (10%, n = 6), cardiac-related event (7%, n = 4), and others (14%, n = 8). The most frequent cause of death in the early period was BPF/empyema (18/45, 40%), while that in the late period was pneumonia/ARDS (6/13, 46%). Among the pneumonia/ARDS deaths in the late period (n = 6), 5 (83%) were due to acute deterioration of interstitial lung disease after lobectomy.

CONCLUSIONS: Recent postoperative mortality rates (30-day, 0.5%; in-hospital, 0.8%) in the treatment of lung cancer are quite acceptable. Special care must be taken for the patient after pneumonectomy, as reported by others. Furthermore, even after lobectomy, proper management of the patient with acute deterioration of interstitial lung disease will be required to improve the future outcome.


    Introduction
 Top
 Abstract
 Introduction
 Patients and methods
 Results
 Comment
 References
 
A limited number of reports describe postoperative mortality rates in recent decades, and most reports have defined a postoperative death as one that occurs within 30 days after the procedure. However, with the recent developments in postoperative management, many complicated patients survive more than 30 days, and their deaths can be lost in such studies. This study analyzed the change in mortality rates, including both 30-day and in-hospital mortality, after pulmonary resection for lung cancer in the specialized institution for cancer in Tokyo, Japan during the last 16 years.


    Patients and methods
 Top
 Abstract
 Introduction
 Patients and methods
 Results
 Comment
 References
 
A total of 3,270 pulmonary resections for lung cancer between January 1989 and December 2002 at the National Cancer Center Hospital, Tokyo, were studied. The postoperative mortality rates, including 30-day and in-hospital mortality, and causes of death were investigated. Thirty-day mortality was defined as a fatality that occurred within 30 days after pulmonary resection, and in-hospital mortality was defined as a fatality occurring at anytime in a postoperative hospital stay.

The 3,270 patients were divided into two period groups of almost equal number, the early (1,615 patients from 1987 to 1996) and the late (1,655 patients from 1997 to 2002) periods. A variety of analyses were performed to determine the changes in postoperative mortality in the last 16 years and to evaluate the risk factor for surgical resection for lung cancer. The result was compared with results from previous reports describing postoperative mortality in lung cancer surgery.

We normally perform the anatomic pulmonary resection for lung cancer through a standard posterolateral thoracotomy. In pneumonectomy cases, after closure of the main bronchial stump by suturing or stapling, we infold the stump with the membranous portion inside and oversew it with interrupted sutures, as we previously reported [1]. Then we prefer to cover the stump with a pericardial fat pad, especially for a right pneumonectomy. We have basically not used neoadjuvant preoperative therapy except for recent superior sulcus tumor cases.

Statistical analyses using the {chi}2 test was performed to evaluate the differences in mortality according to the type of resection.


    Results
 Top
 Abstract
 Introduction
 Patients and methods
 Results
 Comment
 References
 
Fifty-eight operative and postoperative deaths occurred during this period. Thirty-day and in-hospital mortality was 0.5% (21/3,270) and 1.6% (58/3,270), respectively. Among the recent 1,655 patients during the last 6-year period, 30-day and in-hospital mortality was 0.5% (n = 8) and 0.8% (n = 21), respectively (Table 1).


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Table 1. Number of Lung Resections and Mortality Rates in the Last 16 Years

 
Of the 3,270 resections, there were 355 pneumonectomies, 2594 lobectomies, and 321 segmentectomies or lesser resections. The 30-day/in-hospital mortality for pneumonectomy, lobectomy, and segmentectomy or lesser resections was 3.1%/5.9%, 0.3%/1.3%, and 0.3%/0.9%, respectively (Table 2). The difference in the 30-day/in-hospital mortality between the pneumonectomy and lobectomy group (p < 0.0001/p < 0.0001) was significant. The difference in the 30-day/in-hospital mortality between lobectomy and segmentectomy or lesser resection group (p = 0.8641/p = 0.5701) was not significant. The incidence of pneumonectomy cases decreased from 16.2% (262/1,615) in the early period to 5.6% (93/1,655) in the late period, although the in-hospital mortality of pneumonectomy has not improved between the early and late periods (6.1% vs 5.4%, p = 0.7975) (Table 3).


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Table 2. Mortality Rates According to Type of Pulmonary Resections

 

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Table 3. Changes in Number of Lung Resections and In-Hospital Mortality According to the Type of Operation

 
The 58 deaths were caused by pneumonia/acute respiratory distress syndrome (ARDS) (36%, n = 21), bronchopleural fistula (BPF)/empyema (33%, n = 19), cerebrovascular accident (10%, n = 6), cardiac-related event (7%, n = 4), and others (14%, n = 8). The most frequent cause of death in the early period was BPF/empyema (18/45, 40%), while that in the late period was pneumonia/ARDS (6/13, 46%) (Table 4). Death that was due to BPF/empyema in the late period was only 8%. Among the six deaths due to pneumonia/ARDS in the late period, five (83%) were caused by acute deterioration of interstitial lung disease (ILD).


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Table 4. Causes of Postoperative Deaths

 

    Comment
 Top
 Abstract
 Introduction
 Patients and methods
 Results
 Comment
 References
 
Lung cancer has been a major cause of death in many developed countries. Surgical resection continues to play an important roll, especially in the earlier stage lung cancer. The detection of early cancer is increasing with the development of computed tomography (CT); therefore, it is important for surgeons to collect precise data on causes of postoperative deaths and try to improve the surgical mortality.

A limited number of previous reports describe postoperative mortality rates in recent decades, and most reports have defined a postoperative death as one occurring within 30 days after the procedure, as shown in Table 5 [2–8]. However, with the development of postoperative management techniques, complicated patients tend to survive more than 30 days and their deaths can be lost in such studies. We addressed this point by collecting all postoperative in-hospital deaths beyond the 30-day limit.


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Table 5. List of Literature Describing Postoperative Mortality for Surgical Resections in Lung Cancer

 
In 1983 Ginsberg and the Lung Cancer Study Group (LCSG) [2] determined the current standards for operative mortality associated with lung cancer resection. They reported that 81 postoperative deaths occurred among 2,220 resections, and the 30-day mortality was 3.7%. In 1999 Harpole and colleagues reported a large series with a 30-day mortality of 5.2% [4]. Our overall 30-day and in-hospital mortality was 0.6% and 1.6%, respectively. During the last 6-year period, 30-day and in-hospital mortality was 0.5% and 0.8%, respectively. These results were better than those noted by others, as shown in Table 5.

We believe this may be due to following reasons:

Recent improved preoperative and postoperative care as described above could allow more patients to undergo surgery safely.

Others have noted the high operative risk of pneumonectomy. Ginsberg and the LCSG reported a high 30-day mortality of 6.2% for pneumonectomy [2]. We observed a 30-day mortality of 3.1% and an in-hospital mortality of 5.9% for pneumonectomy, which were also significantly higher than for lobectomy. As shown in Table 3, although the mortality of pneumonectomy has not changed, the percentage of pneumonectomy in our resected cases markedly decreased from 16.2% to 5.6%, which contributed to the improvement of our mortality rates. This resulted mainly because of the increasing detection of early stage lung cancer with the development of CT scanners and the aggressive employment of bronchoplasty to avoid pneumonectomy.

As shown in Table 4, the main cause of death shifted from BPF/empyema to pneumonia/ARDS. The decreased incidence of death because of BPF/empyema, which greatly contributed to the improvement of the mortality rate, was the result of two factors. First, as described above, the incidence of pneumonectomy cases is decreasing and consequently, the number of postpneumonectomy BPF has been reduced. Second, we have improved our treatment of BPF/empyema in the late period. We make a chest wall window immediately after BPF develops, even after lobectomy, in order to completely control the infection of the intrathoracic cavity, because massive bleeding from the great vessels due to empyema easily leads to a fatal situation.

Many previous reports have described respiratory complications as a leading cause of death after pulmonary resection [2–5, 9], although none of these have described the detail of the respiratory failure. Among the deaths due to pneumonia/ARDS in our study during the late period, 83% were due to acute deterioration of ILD. All patients who developed ILD exhibited a small interstitial change on preoperative chest CT; therefore, the surgeon should check a preoperative CT to see if the patient has interstitial change and if so, should present the potential risks of acute deterioration of ILD to the patient and his or her family, and special care must be taken on postoperative management. When acute deterioration of ILD develops in the patient, the high-dose administration of steroids may be effective, as reported by Murray and colleagues [10]. Although the effect of this pharmacologic therapy is still controversial [11], an early diagnosis of interstitial pneumonia and the initiation of steroid therapy with mechanical ventilation will be mandatory to ensure survival.

In summary, recent postoperative mortality rates (30-day, 0.5%; in-hospital, 0.8%) in the treatment of lung cancer are quite acceptable. Patients after pneumonectomy showed significant high mortality as previously reported by others. Furthermore, even after lobectomy, proper management of the patient developing acute deterioration of ILD is required to improve the future outcome.


    References
 Top
 Abstract
 Introduction
 Patients and methods
 Results
 Comment
 References
 

  1. Asamura H, Naruke T, Tsuchiya R, Goya T, Kondo H, Suemasu K. Bronchopleural fistulas associated with lung cancer operations. Univariate and multivariate analysis of risk factors, management, and outcome. J Thorac Cardiovasc Surg. 1992;104:1456–1464[Abstract]
  2. Ginsberg RJ, Hill LD, Eagan RT, et al. Modern thirty-day operative mortality for surgical resections in lung cancer. J Thorac Cardiovasc Surg. 1983;86:654–658[Abstract]
  3. Deslauriers J, Ginsberg RJ, Piantadosi S, Fournier B. Prospective assessment of 30-day operative morbidity for surgical resections in lung cancer. Chest. 1994;106(6 Suppl):329S–330S[Abstract/Free Full Text]
  4. Harpole DH Jr, DeCamp MM Jr, Daley J, et al. Prognostic models of thirty-day mortality and morbidity after major pulmonary resection. J Thorac Cardiovasc Surg. 1999;117:969–979[Abstract/Free Full Text]
  5. Wada H, Nakamura T, Nakamoto K, Maeda M, Watanabe Y. Thirty-day operative mortality for thoracotomy in lung cancer. J Thorac Cardiovasc Surg. 1998;115:70–73[Abstract/Free Full Text]
  6. Fryjordet A, Klevmark B. Bronchial carcinoma. Results of treatment in 515 patients. Scand J Thor Cardiovasc Surg. 1971;5:92–96[Medline]
  7. Weiss W. Operative mortality and five-year survival rates in men with bronchogenic carcinoma. Chest. 1974;66:483–487[Abstract/Free Full Text]
  8. Romano PS, Mark DH. Patient and hospital characteristics related to in-hospital mortality after lung cancer resection. Chest. 1992;101:1332–1337[Abstract/Free Full Text]
  9. Nagasaki F, Flehinger BJ, Martini N. Complication of surgery in the treatment of carcinoma of the lung. Chest. 1982;82:25–29[Abstract/Free Full Text]
  10. Murray JF, Matthay MA, Luce JM, Flick MR. An expanded definition of the adult respiratory distress syndrome. Am Rev Respir Dis. 1988;138:720–723[Medline]
  11. Brun-Buisson C, Brochard L. Corticosteroid therapy in acute respiratory distress syndrome: better late than never? JAMA. 1998;280:182–183[Free Full Text]

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