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Aerobic capacity after lung resection in patients with COPD

Danielle C C Bedin1, Roberta P Ramos2, Elaine Brito Vieira2, Ivan Ivanaga2, Sonia M Faresin1

DOI: https://dx.doi.org/10.36416/1806-3756/e20240361

TO THE EDITOR:

Cardiopulmonary exercise testing is an important functional tool for the preoperative assessment of operability in lung resection for NSCLC.(1) Among the parameters evaluated, peak VO2 (VO2peak) has been reported to be a better predictor of postoperative complications and mortality than are resting pulmonary and cardiac function.(2) Despite advances in preoperative assessment, the magnitude of functional changes after lung resection, particularly in patients with COPD, is still matter of debate.(3,4)

We conducted a prospective study to quantify the impact of pulmonary resection on the exercise capacity of patients with COPD scheduled for lung resection surgery at our institution. All participants provided written informed consent, and the study was approved by the medical ethics committee of the institution (Reference no. 89661117.2.0000.5505).

Patients were divided into two groups: those with normal spirometry values (control group) and those with expiratory obstruction on baseline spirometry (COPD group).(5)

The preoperative assessment, which included functional analysis with spirometry, measurement of the DLCO, and cardiopulmonary exercise testing (CPET),(2) was performed before and six months after the surgical procedure. Predicted postoperative FEV1, DLCO, and VO2peak values were calculated at baseline according to segmental loss. All of the patients underwent lateral thoracotomy. For the analysis, continuous variables are presented as mean and standard deviation or as median and interquartile range, being compared by using the paired Student’s t-test, Wilcoxon test, or Mann-Whitney test, as appropriate. Two-way repeated-measures ANOVA was performed to compare functional changes between the two groups. Categorical variables are presented as absolute and relative frequencies and were compared by using Fisher’s exact test. The Kolmogorov-Smirnoff test was employed to assess the normality of the distribution of all variables. Values of p < 0.05 were considered statistically significant. All analyses were performed with the IBM SPSS Statistics software package, version 19.0 (IBM Corporation, Armonk, NY, USA).

During the study period, 18 patients underwent preoperative assessment: 10 in the COPD group and 8 in the control group. The diagnosis of COPD was defined by the presence of clinical findings consistent with the disease, a history of smoking, and an FEV1/FVC ratio below the lower limit of reference. Baseline clinical characteristics and pulmonary function test results are shown in Table 1. The complication rates in the postoperative period were similar between the two groups. In the control group, 3 patients presented with respiratory infections, whereas in the COPD group, 3 patients presented with respiratory infections and 1 presented with atrial fibrillation (p = 0.91). Similarly, there were no differences between the two groups in terms of the length of ICU stay and hospital stay (Table 1). Because there were no deaths in either group during the study period, all of the patients in our sample underwent evaluation at baseline and postoperatively. It is also noteworthy that the extent of lung resection was comparable between the two groups (Table 1).

There were no significant differences between the preoperative (baseline) and postoperative (month-six) time points, in either group, in terms of the spirometric and DLCO values (Table 1). However, the pattern of change in VO2peak (in absolute values and adjusted for body weight) was significantly different between the two groups, being significantly greater postoperatively in the control group (Table 1). These findings were reinforced by the ANOVA, which demonstrated a distinct behavior of VO2peak between the two groups and time points (p = 0.011 and p = 0.024, respectively, for the absolute and adjusted values). In addition, the decrease in VO2peak relative to the number of resected segments was greater in the control group than in the COPD group, with a median loss of 60.2 mL/min/segment in the control group and 20.3 mL/min/segment in the COPD group (p = 0.043). In the COPD group, predicted VO2peak values underestimated the actual values obtained six months after the surgery, whereas no significant difference was observed in the control group (Table 2).





In our study sample, the patients with COPD presented no significant deterioration of VO2peak after lung resection, whereas the patients with preserved lung function at baseline presented greater declines, not only in absolute values but also in VO2peak per resected segment. In addition, the predicted values of FEV1 and VO2peak overestimated the functional deterioration in the patients with COPD.

In a study of 12 patients with COPD, Bobbio et al.(6) found a 21% decrease in VO2peak at three months after lung resection. Miyoshi et al. also observed a decrease in VO2peak after lung resection, although without differentiating between patients with COPD and patients with preserved lung function at baseline. In addition, those authors revaluated exercise capacity after a shorter follow-up period. Similarly, Bolliger et al.(1) showed that the VO2peak decreased by three months after the operation but reverted to the preoperative values by six months after, without specifically addressing patients with COPD. That finding aligns with the minor changes in lung function observed in our study at six months after the surgical procedure.

In parallel with the pulmonary function tests, predicted postoperative VO2peak was similar to the actual measurements six months after surgery in the control group but was significantly lower than the actual measurements in the COPD group. These findings are consistent with those of Brunelli et al.,(8) who noted the imprecision of predicted postoperative VO2, particularly when the preoperative values are lower.

We find it interesting that, after the VO2peak decrease had been adjusted for the number of resected segments, the functional loss was three times greater in our control group than in our COPD group (60.2 mL/min/segment vs. 20.3 mL/min/segment). Previous studies of patients undergoing segmentectomy, lobectomy, or pneumonectomy have shown that greater lung tissue loss results in greater loss of pulmonary function.(1,9) However, the authors of those studies did not take the baseline ventilatory pattern or the presence of COPD into account.

Our study has limitations that should be acknowledged. It was a single-center study conducted by the same team of thoracic surgeons and pulmonologists in order to ensure uniformity in the preoperative evaluation. The postoperative tests were performed six months after surgery, a time point chosen somewhat arbitrarily on the basis of data in the literature suggesting that lung function stabilizes at three to six months after pulmonary resection.(4,10) Our results show that patients with COPD submitted to lung resection demonstrated distinct functional behavior. However, the limitations imposed by our sample size should be considered before our findings are extrapolated to other populations. In addition, our COPD group included only patients with mild or moderate COPD, which might preclude extrapolation of our results to patients with severe COPD. However, the fact that such patients were not included allowed us to speculate that the lack of room for deterioration after surgery did not explain the small size of the decrease in functional capacity in the COPD group. Furthermore, we did not correlate the functional findings with patient reported outcome measures, which could have reinforced the relevance of our findings.

In our study, the predicted postoperative VO2peak values appeared to overestimate the decrease in aerobic capacity following lung resection in patients with mild or moderate COPD. Our findings suggest that, in patients with COPD, there is a need for a more comprehensive preoperative analysis, with less emphasis on the predicted postoperative CPET values.

 
AUTHOR CONTRIBUTIONS
 
DCCB and SMF designed the study, collected the data, analyzed the data, and participated in drafting the manuscript. RPR analyzed the data and participated in drafting the manuscript. EBV and IV collected and analyzed the data.

 
CONFLICTS OF INTEREST
 
None declared.

 
REFERENCES
 
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2.           Brunelli A, Kim AW, Berger KI, Addrizzo-Haris DJ. Physiologic evaluation of the patient with lung cancer being considered for resectional surgery: Diagnosis and management of lung cancer, 3rd ed: American College of Chest Physicians evidence-based clinical practice guidelines. Chest. 2013;143(5 Suppl):166S-e190S. https://doi.org/10.1378/chest.12-2395
3.           Baldi S, Ruffini E, Harari S, Roviaro GC, Nosotti M, Bellaviti N, et al. Does lobectomy for lung cancer in patients with chronic obstructive pulmonary disease affect lung function? A multicenter national study. J Thorac Cardiovasc Surg. 2005;130(6):1616-22. https://doi.org/10.1016/j.jtcvs.2005.06.049
4.           Kushibe K, Kawaguchi T, Kimura M, Takahama M, Tojo T, Tanigucho S. Exercise capacity after lobectomy in patients with chronic obstructive pulmonary disease. Interact Cardiovasc Thorac Surg. 2008;7(3):398-401. https://doi.org/10.1510/icvts.2007.165696
5.           Global Initiative for Chronic Obstructive Lung Disease [homepage on the Internet]. Bethesda: GOLD; Global strategy for the diagnosis, management, and prevention of chronic obstructive pulmonary disease. 2015 Report. Available from: http://www.goldcopd.org
6.           Bobbio A, Chetta A, Carbognani P, Internullo E, Verduri A, Sansebastiano G, et al. Changes in pulmonary function test and cardio-pulmonary exercise capacity in COPD patients after lobar pulmonary resection. Eur J Cardiothorac Surg. 2005;28(5):754-8. https://doi.org/10.1016/j.ejcts.2005.08.001
7.           Miyoshi S, Yoshimasu T, Hirai T, Harai I, Maebeya S, Bessho T, et al. Exercise capacity of thoracotomy patients in the early postoperative period. Chest. 2000;118(2):384-90. https://doi.org/10.1378/chest.118.2.384
8.           Brunelli A, Pompili C, Refai M, Xiumè F, Salati M, Sabbatini A. Predicted versus observed peak oxygen consumption after major pulmonary resection. Ann Thorac Surg. 2012;94(1):222-5. https://doi.org/10.1016/j.athoracsur.2012.03.034
9.           Kim HK, Lee JY, Han KN, Choi YH. Pulmonary function changes over 1 year after lobectomy in lung cancer. Respir Care. 2016;61(3):376-82. https://doi.org/10.4187/respcare.04284
10.        Nagamatsu Y, Maeshiro K, Kimura NY, Nishi T, Shima I, Yamana H, et al. Long-term recovery of exercise capacity and pulmonary function after lo-bectomy. J Thorac Cardiovasc Surg. 2007;134(5):1273-8. https://doi.org/10.1016/j.jtcvs.2007.06.025

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