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Interact CardioVasc Thorac Surg 2008;7:398-401. doi:10.1510/icvts.2007.165696
© 2008 European Association of Cardio-Thoracic Surgery

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Institutional report - Thoracic general

Exercise capacity after lobectomy in patients with chronic obstructive pulmonary disease

Keiji Kushibe*, Takeshi Kawaguchi, Michitaka Kimura, Makoto Takahama, Takashi Tojo and Shigeki Taniguchi

Department of Thoracic and Cardiovascular Surgery, Nara Medical University School of Medicine, 840, Shijo-cho, Kashihara, Nara, 634-8522, Japan

Received 24 August 2007; received in revised form 30 October 2007; accepted 6 December 2007

*Corresponding author. Tel.: +81-744-22-3051; fax: +81-744-24-8040.

E-mail address: mdkeiji{at}m3.kcn.ne.jp (K. Kushibe).


    Abstract
 Top
 Abstract
 1. Introduction
 2. Materials and methods
 3. Results
 4. Discussion
 References
 
The aim of this study is to clarify whether patients with chronic obstructive pulmonary disease (COPD) lose less exercise capacity after lobectomy than do those without COPD, to the same extent as ventilatory capacity and lobectomy for selected patients with severe emphysema improve exercise capacity like ventilatory capacity. Seventy non-COPD patients (N group), 16 mild COPD patients (M group), and 14 moderate-to-severe COPD patients (S group) participated. Pulmonary function and exercise capacity tests were performed on the same day preoperatively and six months to one year after lobectomy. The S group lost significantly less FEV1 (forced expiratory volume in 1 s) after lobectomy than did the N or M group (P<0.0001 and P<0.005). However, their loss of exercise capacity was equivalent to that for the N and M groups. For the S group, there was a significant, negative correlation between preoperative FEV1 % of predicted and percentage change in FEV1 and maximum oxygen consumption (VO2 max) after lobectomy (r=–0.93, P<0.0001 and r=–0.64, P=0.01). In moderate-to-severe COPD patients, patients with a lower preoperative FEV1 % of predicted experienced a smaller decrease in FEV1 and VO2 max after lobectomy.

Key Words: Lung cancer; Exercise capacity; Lobectomy; Chronic obstructive pulmonary disease


    1. Introduction
 Top
 Abstract
 1. Introduction
 2. Materials and methods
 3. Results
 4. Discussion
 References
 
Despite recent advances in chemotherapy and radiotherapy, surgery remains the best treatment for patients with early-stage non-small cell lung cancer. Many patients with lung cancer are old [1] and have chronic obstructive pulmonary disease (COPD) [2]. Pulmonary resection decreases ventilatory capacity [3] and reduces exercise capacity [4–6], thereby lowering their quality of life [1].

Recent studies show that patients with COPD lose less ventilatory capacity after lobectomy than do those without COPD [7–9]. Moreover, for selected patients with severe emphysema, ventilatory capacity has even been found to improve after lobectomy for lung cancer [7, 9]. However, change in exercise capacity, an important measure of quality of life, after lobectomy in patients with COPD remains unclear. The aim of this study is to clarify whether patients with COPD lose less exercise capacity after lobectomy than do those without COPD to the same extent as ventilatory capacity and lobectomy for selected patients with severe emphysema improve exercise capacity like ventilatory capacity. In this study, we compared ventilatory capacity and exercise capacity after lobectomy for lung cancer between COPD and non-COPD (without COPD).


    2. Materials and methods
 Top
 Abstract
 1. Introduction
 2. Materials and methods
 3. Results
 4. Discussion
 References
 
We retrospectively reviewed data for 428 patients who underwent lobectomy for non-small cell lung cancer at Nara Medical University Hospital between January 1997 and December 2005. Exclusion criteria were right middle lobectomy (n=30), failure to quit smoking postoperatively (n=10), receipt of adjuvant chemotherapy or radiotherapy (n=70), and postoperative empyema or moderate-to-severe pulmonary complications (n=21). We also excluded patients with preoperative segmental or lobar atelectasis (n=71) or a tumor more than 4 cm in diameter (n=51), because lack of function of the resected lung tissue was not necessarily due to emphysema. We also excluded five patients who had strongly impaired pulmonary function after lobectomy, with weaker function than expected, due to severe narrowing of the orifice of the right intermediate bronchus or left lower bronchus.

Of the remaining 170 patients, 30 could not perform preoperative exercise tests for the following reasons: five had severely limiting musculoskeletal disorders and 25 did not consent exercise tests. One hundred and forty patients underwent preoperative evaluation consisting of pulmonary function tests and exercise tests. Forty patients could not be re-evaluated for the following reasons: two died within 30 days after surgery, four had progressive metastatic disease, and 34 could not be contacted after surgery. Thus, 100 patients were enrolled in the study.

Pulmonary function and exercise tests were performed on the same day before surgery and again six months to one year after surgery. The mean interval between lobectomy and postoperative evaluation was 7.9±1.8 months. Exercise capacity was determined using an incremental exercise test on a cycle ergometer with breath-by-breath analysis of gas exchange (MMC 4400tc; Sensormedics Corporation; Anaheim, CA, USA). Baseline measurements were recorded after a resting period of at least 3 min on the bicycle. The exercise protocol consisted of a 10- to 15-W ramped increase in work each minute until the patient could not continue because of severe dyspnea or leg fatigue. Heart rate, electrocardiogram, and oxygen saturation were monitored during the exercise study. Continuous measurements of minute ventilation (VE), oxygen consumption (VO2), and carbon dioxide production (VCO2) were averaged every 15 s. Maximum oxygen consumption (VO2 max) and maximum minute ventilation (VEmax) were defined as the highest VO2 and VE, respectively, achieved during the exercise test. No specific postoperative rehabilitation program was provided.

Patients were divided into three groups according to the preoperative severity of COPD, which was classified using the guidelines of the Global Initiative on Obstructive Lung Disease Global Initiative for Chronic Obstructive Lung Disease (GOLD, Global initiative strategy for the diagnosis, management, and prevention of chronic obstructive pulmonary disease, available at http://www.gold.com accessed July 1, 2007). The non-COPD group (N group) comprised patients with preoperative forced expiratory volume in 1 s (FEV1)/forced vital capacity (FVC) ≥70%. The mild COPD group (M group) comprised patients with preoperative FEV1/FVC <70% and FEV1 ≥80% of predicted. The moderate-to-severe COPD group (S group) comprised patients with the preoperative FEV1/FVC <70% and FEV1 <80% of predicted.

Descriptive statistics are presented as the mean±S.D. for continuous variables. Correlations between variables were assessed using Spearman rank correlation coefficients. A P-value <0.05 was considered statistically significant. Statistical analysis was performed using the statistical software Statview 5.0 (SAS Inc., Cary, NC, USA).


    3. Results
 Top
 Abstract
 1. Introduction
 2. Materials and methods
 3. Results
 4. Discussion
 References
 
All 100 patients underwent simple lobectomy and dissection of the hilar and mediastinal lymph nodes. There were 70 patients in the N group, 16 in the M group, and 14 in the S group. There were 32 upper lobectomies (right 19, left 13), 39 lower lobectomies (right 22, left 17) in the N group and 8 upper lobectomies (right 6, left 2), 7 lower lobectomies (right 2, left 5) in the M group and 10 upper lobectomies (right 4, left 6), 4 lower lobectomies (left 4) in the S group. Patient characteristics are shown Table 1.


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Table 1 Patient characteristics

 
Table 2 shows the percentage change in pulmonary function and exercise capacity after surgery. The S group lost significantly less pulmonary function in FEV1 than did the N or M group (P<0.0001 and P<0.005, respectively). However, there were similar reductions in exercise capacity (VO2 max) and workload between groups.


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Table 2 Percentage change in pulmonary function and exercise capacity after surgery

 
We also evaluated the correlations between the preoperative FEV1 % of predicted and the percentage change in FEV1, and between the preoperative FEV1 % of predicted and the percentage change in exercise capacity after lobectomy (Table 3). In the S group, there were significant negative correlations between preoperative FEV1 % of predicted and percentage change in FEV1 (Fig. 1, r=–0.93, P<0.0001) and between preoperative FEV1 % of predicted and percentage change in VO2 max (Fig. 2, r=–0.64, P=0.01). Among patients with COPD (M group+S group), there was a significant negative correlation between preoperative FEV1 % of predicted and percentage change in FEV1 (r=–0.60, P<0.0001).


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Table 3 Correlation between preoperative FEV1 % of predicted and percentage change in FEV1 or exercise capacity after lobectomy in COPD patients

 

Figure 1
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Fig. 1. Correlation between preoperative FEV1 % of predicted and percentage change in FEV1 in the S group. The bold line shows the best fit by linear regression. Percentage change in FEV1=78.6–12.5xpreoperative FEV1 % of predicted; R2=0.86, r=–0.93, P<0.0001.

 

Figure 2
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Fig. 2. Correlation between preoperative FEV1 % of predicted and percentage change in VO2 max in the S group. The bold line shows the best fit by linear regression. Percentage change in VO2 max=49.3–0.96xpreoperative FEV1 % of predicted; R2=0.41, r=–0.64, P=0.01.

 
We also evaluated the correlations between percentage change in FEV1 and percentage change in exercise capacity (VO2 max and workload) after lobectomy (Table 4). In both the N and M groups, there was no significant relationship between percentage change in FEV1 and percentage change in VO2 max or workload. In the S group, there was no relationship between percentage change in FEV1 and percentage change in workload, but there was a significant correlation between percentage change in FEV1 and percentage change in VO2 max (Fig. 3, r=0.61, P=0.02). This was also the case for COPD patients (M group+S group; r=0.54, P=0.002). In the all the groups, there was no significant relationship between percentage change in VO2 max and percentage change in workload (Table 4).


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Table 4 Correlation between percentage change in FEV1 and percentage change in exercise capacity after lobectomy

 

Figure 3
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Fig. 3. Correlation between percentage change in FEV1 and percentage change in VO2 max in the S group. The bold line shows the best fit by linear regression. Percentage change in VO2 max=–12.5+0.59xpercentage change in FEV1; R2=0.37, r=0.61, P=0.02.

 

    4. Discussion
 Top
 Abstract
 1. Introduction
 2. Materials and methods
 3. Results
 4. Discussion
 References
 
Staging and classification of COPD are based on FEV1. FEV1 is a simple, reliable measurement that is of unquestionable diagnostic utility and enables accurate assessment of disease progression. However, FEV1 only weakly correlates with exercise capacity and dyspnea [10, 11]. Moreover, while FEV1 is a surrogate measure for respiratory impairment, only VO2 max, or exercise capacity, is a function of blood flow and oxygen extraction and can be influenced by a number of factors involving the cardiovascular, respiratory, and/or musculoskeletal systems [12]. In patients with COPD, exercise capacity is difficult to predict based on lung function and correlates better with dyspnea and quality of life than does FEV1 [13].

Recent experience with lung volume reduction surgery suggests that predicted postoperative FEV1 might be underestimated in patients with COPD undergoing lobectomy for lung cancer [7–9]. In addition, COPD patients with a lower FEV1 might experience a smaller loss of pulmonary function after lobectomy [7–9]. However, post-lobectomy change in exercise capacity, an important measure of quality of life, in patients with COPD remains unclear. In this study, moderate-to-severe COPD patients lost less FEV1 than did non-COPD or mild COPD patients. In addition, moderate-to-severe COPD patients with a lower preoperative FEV1 % of predicted experienced a smaller reduction in FEV1 and VO2 max after lobectomy. As COPD patients with a lower preoperative FEV1 % of predicted have more emphysematous lungs, lobectomy would produce a greater volume reduction and they would lose less FEV1 [7]. However, it is less apparent why moderate-to-severe COPD patients with a lower preoperative FEV1 % of predicted experienced a smaller reduction in VO2 max after lobectomy. VO2 max can be influenced by a number of factors involving the cardiovascular, respiratory, and/or musculoskeletal system [12]. Lobectomy loses ventilatory capacity and pulmonary blood flow. So, we suggested that change in VO2 max after lobectomy would be most affected by change in ventilatory capacity and pulmonary blood flow. As moderate-to-severe COPD patients have poor pulmonary blood flow in their emphysematous lungs, they would experience little change in pulmonary blood flow after lobectomy. Thus, for these patients, the change in VO2 max is mostly affected by change in ventilatory capacity, such that those with a lower preoperative FEV1 % of predicted would experience a smaller reduction of VO2 max after lobectomy and a smaller decrease in FEV1.

Several investigators have examined the changes in ventilatory capacity and exercise capacity at various time points between three and six months after lobectomy [4–6]. Reported reductions vary from 8% to 17% for FEV1, from 7.3% to 14% for FVC, from 0% to 13% for VO2 max, and from 0% to 12% for workload [4–6]. In the present study, in moderate-to-severe COPD patients, there was a 4.7% increase in FEV1, an 8.6% reduction in FVC, a 9.7% reduction in VO2 max, and a 6.0% reduction in workload between six months and one year after lobectomy. These patients' reduction of exercise capacity (VO2 max and workload) was equivalent to that of non-COPD and mild COPD patients. Similarly, Bobbio et al. recently showed that three months after lobectomy the FEV1 of COPD patients was not significantly altered, whereas the VO2 max was significantly reduced [14]. Larsen et al. reported that change in FEV1 is a poor predictor of change in exercise capacity [6]. In addition, Pelletier et al. reported a significant relationship between percentage change in FEV1 and percentage change in workload after major lung resections; the correlation was higher in patients with a lower preoperative FEV1 of predicted [4]. We found a significant relationship between percentage change in FEV1 and percentage change in VO2 max in moderate-to-severe COPD patients. We offer a similar explanation to that above: as in moderate-to-severe COPD patients the change in VO2 max is mostly affected by change in ventilatory capacity, change in VO2 max correlates better with change in FEV1.

Selected severe COPD patients who undergo lobectomy experience an increase in FEV1 and a decrease in FVC [7, 9]. Moreover, we and Bobbio et al. demonstrated that such patients experience a reduction in VO2 max [14]. In contrast, severe COPD patients who undergo lung volume reduction surgery achieve increased ventilatory capacity and VO2 max [15]. We suggest that the reduction of FVC and VO2 max after lobectomy in severe COPD patients is due to resection of some functioning lung tissue; if only non-functioning lung is removed, FVC and VO2 max should increase, as is the case in patients undergoing lung volume reduction surgery.

This study has certain limitations. Our study consisted of a small, retrospective analysis. Moreover, there are large discrepancies between the number of patients included in non-COPD group and that of patients included in the COPD groups. However, we believe that our findings make a contribution as a valuable addition to the field of thoracic surgery. Moreover, we also believe a large, prospective analysis could confirm these findings and clarify the more definitive conclusion about the change in exercise capacity after lobectomy in COPD patients.

In conclusion, this suggests that among moderate-to severe COPD patients, those with a lower preoperative FEV1 % of predicted experienced a smaller reduction in FEV1 and VO2 max after lobectomy, and the change in VO2 max correlated better with the change in FEV1.


    References
 Top
 Abstract
 1. Introduction
 2. Materials and methods
 3. Results
 4. Discussion
 References
 

  1. Kurtz ME, Kurtz JC, Stommel M, Given CW, Given B. Loss of physical functioning among geriatric cancer patients: relationship to cancer site, treatment, comorbidity and age. Eur J Cancer 1997;33:2352–2358.[CrossRef][Medline]
  2. Mentzer SJ, Swanson SJ. Treatment of patients with lung cancer and severe emphysema. Chest 1999;116(Suppl_6):477S–479S.[CrossRef][Medline]
  3. Berend N, Woolcock AJ, Marlin GE. Effect of lobectomy on lung function. Thorax 1980;35:145–150.[Abstract]
  4. Pelletier C, Lapointe L, Le Blanc P. Effects of lung resection on pulmonary function and exercise capacity. Thorax 1990;45:497–502.[Abstract]
  5. Bolliger CT, Jordan P, Solèr M, Stulz P, Tamm M, Wyser Ch, Gonon M, Perruchoud AP. Pulmonary function and exercise capacity after lung resection. Eur Respir J 1996;9:415–421.[Abstract]
  6. Larsen KR, Svendsen UG, Milman N, Brenøe J, Petersen BN. Cardiopulmonary function at rest and during exercise after resection for bronchial carcinoma. Ann Thorac Surg 1997;64:960–964.[Abstract/Free Full Text]
  7. Korst RJ, Ginsberg RJ, Ailawadi M, Bains MS, Burt ME, Downey RJ, Rusch VW, Stover D. Lobectomy improves ventilatory function in selected patients with severe COPD. Ann Thorac Surg 1998;66:898–902.[Abstract/Free Full Text]
  8. Baldi S, Ruffini E, Harari S, Raviaro GC, Nosotti M, Bellaviti N, Venuta F, Diso D, Rea F, Schiraldi C, Durigato A, Pavanello M, Carretta A, Zannini P. Does lobectomy for lung cancer in patients with chronic obstructive pulmonary disease affect lung function? A multienter study. J Thorac Cardiovasc Surg 2005;130:1616–1622.[Abstract/Free Full Text]
  9. Kushibe K, Takahama M, Tojo T, Kawaguchi T, Kimura M, Taniguchi S. Assessment of pulmonary function after lobectomy for lung cancer-upper lobectomy might have the same effect as lung volume reduction surgery. Eur J Cardio-Thorac Surg 2006;29:886–890.[Abstract/Free Full Text]
  10. Bauerle O, Chrusch CA, Younes M. Mechanisms by which COPD affects exercise tolerance. Am J Respir Crit Care Med 1998;157:57–68.[Free Full Text]
  11. Carlson DJ, Ries AL, Kaplan RM. Predictors of maximum exercise tolerance in patients with COPD. Chest 1991;157:57–68.
  12. American Thoracic Society, American College of Chest Physicians. ATS/ACCP Statement on cardiopulmonary exercise testing. Am J Respir Crit Care Med 2003;167:211–277.[Free Full Text]
  13. Berry MJ, Adair NE, Rejeski WJ. Use of peak oxygen consumption in predicting physical function and quality of life in COPD patients. Chest 2006;129:1516–1522.[CrossRef][Medline]
  14. Bobbio A, Chetta A, Carbognani P, Internullo E, Verduri A, Sansebastiano G, Rusca M, Olivieri D. Changes in pulmonary function test and cardio-pulmonary exercise capacity in COPD patients after lobar pulmonary resection. Eur J Cardiothorac Surg 2005;28:754–758.[Abstract/Free Full Text]
  15. Cordova F, O'Brien G, Furukawa S, Kuzma AM, Travaline J, Criner GJ. Stability of improvements in exercise performance and quality of life following bilateral lung volume reduction surgery in severe COPD. Chest 1997;112:907–915.[CrossRef][Medline]




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