Utility of chronic obstructive pulmonary disease assessment test in perioperative assessment of patients with mild to moderate chronic obstructive pulmonary disease
Highlight box
Key findings
• The chronic obstructive pulmonary disease (COPD) Assessment Test (CAT) score was a significant predictor of postoperative pulmonary complications (PPCs) in patients with mild to moderate COPD.
What is known and what is new?
• The correlation between subjective symptoms and PPC incidence in COPD has not been well evaluated. We discovered that a high CAT score (≥7) was significantly associated with an increased risk of PPCs.
What is the implication, and what should change now?
• In patients with mild to moderate COPD, checking for subjective symptoms with a well-validated questionnaire and managing them appropriately could be effective in preventing PPCs, as well as existing well-established preoperative tests (e.g., pulmonary function tests, exercise testing).
Introduction
Patients with chronic obstructive pulmonary disease (COPD) have a higher incidence of lung cancer than the general population (1). COPD is a well-known risk factor for postoperative pulmonary complications (PPCs); therefore, a detailed preoperative assessment is needed to identify patients at high risk for PPCs and alternative treatment options should be considered (2-5). The risk of PPCs in COPD may vary based on the severity of symptoms, which are usually assessed using the modified Medical Research Council (mMRC) score or COPD Assessment Test (CAT) in clinical practice. Specifically, the CAT score is a widely used, simple indicator to assess patient’s quality of life and predict acute COPD exacerbations (6). However, few studies have evaluated the correlation between symptom-based scores, including the CAT score, and the incidence of PPCs.
Among several test modalities for evaluation before lung resection, spirometry, and the diffusing capacity for carbon monoxide (DLCO) are essential tests for predicting postoperative lung functions (5,7). The American College of Chest Physicians guideline recommends that patients with postoperative forced expiratory volume in one second (FEV1) or postoperative DLCO between 30% and 60% undergo a stair-climbing test or shuttle walk test (SWT), both of which are indicated for most patients with COPD (7). If the result of the SWT falls below expectation or both postoperative FEV1 and postoperative DLCO are <30%, the cardiopulmonary exercise test (CPET) should be performed (8,9). The guideline classifies patients with maximum oxygen uptake (VO2 max) <10 mL/kg/min or 35% predicted to be at high risk and recommends avoiding lung resection, while considering alternative treatment options because of the high mortality risk (7). After excluding the obviously high-risk group, patients with mild to moderate dysfunction should be evaluated using additional criteria to determine a suitable treatment option (10).
In this study, we aimed to explore the potential relationship between the CAT score and PPC in patients with mild to moderate COPD, a population commonly undergoing lung cancer surgery. Additionally, we compared the predictive values of the CAT score with those of previously well-established predictors of PPC as follows: (I) pulmonary function and exercise tests; (II) COPD composite severity index; (III) type of surgery; (IV) comorbidity index; and (V) prediction models for PPCs. We present this article in accordance with the STROBE reporting checklist (available at https://jtd.amegroups.com/article/view/10.21037/jtd-24-138/rc).
Methods
Study population
Between January 2020 and June 2022, a total of 187 patients with COPD underwent preoperative risk evaluation including CPET at the Asan Medical Center (Seoul, Korea). Exclusion criteria encompassed: (I) patients who did not undergo surgery; (II) presence of significant comorbidities (e.g., heart failure and interstitial lung disease); and (III) history of lung resection.
This retrospective study finally included 83 patients who underwent surgery for lung cancer. COPD was confirmed using spirometry with a post-bronchodilator FEV1/FVC ratio <0.7 in patients with compatible symptoms (e.g., dyspnea).
Data collection
Data including demographics, comorbidities, smoking history, symptoms, clinical tumor-node-metastasis (TNM) stage, type of lung resection surgery, and type of postoperative complications were reviewed (11). Prolonged air leak was defined as air leak for >5 days, and pneumonia was defined as clinical symptoms or signs of pneumonia and new infiltration on a chest radiograph.
Measurements
The subjective symptoms of patients were assessed by using the mMRC and CAT scores. The CAT score is an 8-item, self-administered questionnaire and we used the Korean version of the CAT score (12,13). The body mass index, airflow obstruction, dyspnea, and exercise capacity (BODE) and modified BODE index (mBODE) were calculated using body mass index, FEV1, the distance of a 6-min walk test, VO2 peak (presented as a percentage of the predicted value), and mMRC grade. The VO2 peak (% of predicted value) was classified as follows: score 0 for >70% of predicted value; score 1 for 60–69% of predicted value; score 2 for 40–59% of predicted value; and score 3 for <40% of predicted value (14). Comorbidity was evaluated using the Charlson comorbidity index score. Among several prediction models for PPCs, we adopted the Assess Respiratory Risk in Surgical Patients in Catalonia (ARISCAT) score. All measurements were completed before the surgery.
Statistical analysis
Continuous variables were presented as mean ± standard deviation, and categorical variables were reported as counts and percentages. The Kolmogorov-Smirnov test was used to test data normality. For data with a normal distribution, the Student’s t-test was used. The Mann-Whitney U test was used for comparison of nonparametric data. Receiver operating characteristic (ROC) analysis and the Youden index were employed to set the optimal cut-off value. Variables with P<0.2 in univariable analysis were included for logistic regression analysis. Statistical significance was determined by the two-tailed P<0.05. We used IBM Statistical Package for the Social Sciences (version 24.0; SPSS Inc., Chicago, IL, USA) and R statistical package (version 4.3.0; R Foundation for Statistical Computing, Vienna, Austria) for data analysis.
Ethics statement
The study was conducted in accordance with the Declaration of Helsinki (as revised in 2013). The study was approved by the Institutional Review Board of the Asan Medical Center (approval No. 2021-0915), and the requirement for informed consent was waived because of the retrospective nature of the study.
Results
A total of 360 patients underwent CPET as part of their preoperative evaluation at the Asan Medical Center (Seoul, Korea). Among them, 187 patients were diagnosed with COPD. We excluded 106 patients based on the exclusion criteria, whereas the remaining 81 patients were included in the final analysis (Figure 1).
Among the 81 patients, 16 (19.8%) developed PPCs. The types of PPCs are listed in Table 1. Persistent air leakage was the most frequent complication. The baseline characteristics of patients, lung cancer stage, and type of surgery were similar between the groups with and without PPCs (Table 2).
Table 1
Complications | N [%] |
---|---|
Pneumonia | 5 [31] |
Persistent air leakage* | 8 [50] |
Bleeding | 2 [13] |
Pulmonary thromboembolism | 1 [6.3] |
*, persistent air leakage >5 days.
Table 2
Characteristics | Non-PPC group (N=65) |
PPC group (N=16) |
P value |
---|---|---|---|
Sex | 0.57 | ||
Male | 60 (92.3) | 16 (100.0) | |
Female | 5 (7.7) | 0 | |
Age, years | 67.8±7.7 | 66.9±9.1 | 0.67 |
BMI, kg/m2 | 24.8±3.6 | 23.5±3.4 | 0.21 |
Smoking history | <0.001 | ||
Never smoker | 3 (4.6) | 6 (37.5) | |
Current smoker | 18 (27.7) | 5 (31.3) | |
Ex-smoker | 44 (67.7) | 5 (31.3) | |
TNM stage | 0.40 | ||
I | 43 (66.2) | 8 (50.0) | |
II | 14 (21.5) | 6 (37.5) | |
III | 8 (12.3) | 2 (12.5) | |
Type of surgery | 0.09 | ||
Wedge resection or segmentectomy | 24 (36.9) | 2 (12.5) | |
Lobectomy | 38 (58.5) | 14 (87.5) | |
Bilobectomy | 3 (4.6) | 0 | |
Height (cm) | 166.7±6.3 | 165.7±6.0 | 0.57 |
Weight (kg) | 68.9±10.4 | 64.5±8.6 | 0.12 |
Data are presented as n (%) or mean ± SD. PPC, postoperative pulmonary complication; BMI, body mass index; TNM, tumour-node-metastasis; SD, standard deviation.
The subjective symptoms of patients and results of assessment tools are presented in Table 3. Notably, the CAT scores exhibited differences between the two groups. The mean CAT score was significantly higher in the PPC group than in the non-PPC group (9.4±3.0 vs. 6.7±3.2; P=0.002). The results of pulmonary function test (FEV1, DLCO), BODE index, mBODE index, Charlson comorbidity index (CCI) score, and ARISCAT score did not differ between the two groups.
Table 3
Results | Non-PPC group (N=65) |
PPC group (N=16) |
P value |
---|---|---|---|
BODE | 0.5±0.7 | 0.5±0.7 | 0.93 |
mBODE | 1.3±1.1 | 1.2±1.1 | 0.86 |
mMRC dyspnoea scale | >0.99 | ||
Grade 0 | 47 (72.3) | 12 (75.0) | |
Grade 1 | 16 (24.6) | 4 (25.0) | |
Grade 2 | 2 (3.1) | 0 | |
CAT score | 6.7±3.2 | 9.4±3.0 | 0.002 |
CAT ≥10 | 11 (16.9) | 6 (37.5) | 0.09 |
Charlson comorbidity index | 5.5±1.2 | 5.5±1.3 | 0.91 |
ARISCAT | 48.8±8.5 | 49.5±12.6 | 0.83 |
FEV1 (GOLD group) | 0.50 | ||
GOLD 1 | 3 (4.6) | 2 (12.5) | |
GOLD 2 | 58 (89.2) | 13 (81.2) | |
GOLD 3 | 4 (6.2) | 1 (6.3) | |
FEV1 (% pred) | 68.5±9.7 | 67.6±12.4 | 0.74 |
DLCO (mL/mmHg/min) | 15.5±4.2 | 15.3±2.9 | 0.89 |
DLCO (% pred) | 74.8±15.1 | 75.7±13.8 | 0.83 |
VO2 max (mL/kg/min) | 17.9±4.5 | 18.7±4.8 | 0.53 |
VO2 max (L/min) | 1.22±0.32 | 1.21±0.35 | 0.53 |
VO2 max (% pred) (mL/kg/min) | 74.0±21.0 | 77.8±19.4 | 0.52 |
VO2 max (% pred) (L/min) | 68.0±207 | 71.6±19.0 | 0.52 |
6-min walking test (m) | 465±70 | 472±54 | >0.99 |
Missing data | 11 | 7 |
Data are presented as n (%) or mean ± standard deviation. PPC, postoperative pulmonary complication; BODE, Body Mass Index, Airflow Obstruction, Dyspnea, and Exercise capacity; mBODE, modified BODE; mMRC, modified Medical Research Council; CAT, COPD Assessment Test; ARISCAT, Assess Respiratory Risk in Surgical Patients in Catalonia; FEV1, forced expiratory volume in one second; GOLD, Global Initiative for Chronic Obstructive Lung Disease; DLCO, diffusing capacity for carbon monoxide; VO2 max, maximum oxygen uptake; COPD, chronic obstructive pulmonary disease.
The ROC curve for the CAT score was created to identify the optimal cut-off values for predicting PPCs in patients with COPD, and 6.5 points was the optimal cut-off value for predicting PPCs and postoperative pneumonia, respectively [PPCs; area under the ROC curve: 0.757; 95% confidence interval (CI): 0.647–0.866]. Therefore, we categorized the patients into two groups based on CAT scores (<7 and ≥7); and the group with higher CAT scores (≥7) demonstrated a significant association with the development of PPCs in the logistic regression analysis. Other variables associated with PPCs are presented in Table 4. In the multivariable logistic regression analysis, we included variables with a significance level P<0.2 identified in the univariate analysis (Table 4). Among various parameters, only higher CAT scores (≥7) emerged as an independent predictor of the development of PPCs [odds ratio (OR) =9.88; 95% CI: 1.95–50.04; P=0.005]. Additionally, we analyzed the relationship between factors and the development of only pneumonia, and likewise, higher CAT scores remained the only significant predictor of postoperative pneumonia (OR =11.74; 95% CI: 1.23–1,571.28; P=0.03) (Table S1).
Table 4
Characteristic | Univariable analysis | Multivariable analysis | |||
---|---|---|---|---|---|
OR (95% CI) | P value | OR (95% CI) | P value | ||
VO2 max (mL/kg/min) (% pred) | |||||
>15 | 1 (ref) | ||||
≤15 | 1.28 (0.39–4.23) | 0.68 | |||
6-min walking test | |||||
>400 m | 1 (ref) | ||||
≤400 m | 1.93 (0.42–8.78) | 0.40 | |||
BODE index | 1.11 (0.43–2.81) | 0.83 | |||
mBODE index | 0.94 (0.56–1.57) | 0.80 | |||
FEV1 | |||||
GOLD 1 | 1 (ref) | ||||
GOLD 2 | 0.34 (0.05–2.22) | 0.34 | |||
GOLD 3 | 0.37 (0.02–6.35) | 0.38 | |||
DLCO (% predicted) | |||||
>60% | 1 (ref) | ||||
≤60% | 1.13 (0.28–0.65) | 0.86 | |||
CAT | |||||
<7 | 1 (ref) | 1 (ref) | |||
≥7 | 8.69 (1.83–41.36) | 0.006 | 9.88 (1.95–50.04) | 0.005 | |
Weight | 0.96 (0.91–1.01) | 0.13 | 0.96 (0.90–1.03) | 0.23 | |
Type of surgery | |||||
Segmentectomy (n=17) | 1 (ref) | 1 (ref) | |||
Wedge resection (n=9) | 2.00 (0.11–36.31) | 0.64 | 1.70 (0.09–34.11) | 0.73 | |
Lobar or bilobar resection | 5.46 (0.66–45.04) | 0.12 | 5.36 (0.60–48.00) | 0.13 |
PPC, postoperative pulmonary complication; OR, odds ratio; CI, confidence interval; VO2 max, maximum oxygen uptake; BODE, Body Mass Index, Airflow Obstruction, Dyspnea, and Exercise capacity; mBODE, modified BODE; FEV1, forced expiratory volume in one second; GOLD, Global Initiative for Chronic Obstructive Lung Disease; DLCO, diffusing capacity for carbon monoxide; CAT, COPD Assessment Test; COPD, chronic obstructive pulmonary disease.
Discussion
In this study, we retrospectively analyzed patients with COPD who subsequently underwent lung resection surgery for lung cancer following preoperative evaluation. The primary objective of the study was to assess the value of the CAT score for predicting PPCs in patients with mild to moderate COPD. To our knowledge, this is the first study to comprehensively evaluate the potential of symptom-based scores, cardiopulmonary function tests, various composite severity indices, and PPC prediction models simultaneously for predicting PPCs. Our findings suggested that the CAT score holds a strong predictive value for the occurrence of PPCs in patients with mild to moderate COPD.
Various studies have established cut-off values for post-operative high mortality and morbidity based on FEV1, DLCO, SWT, and VO2 max; therefore, these tests are commonly used before pulmonary resection. However, while the usefulness of these cut-off values in discriminating patients at very high risks is well established, their relevance in predicting PPCs in mild to moderate COPD has not been sufficiently explored. In several studies, patients with VO2 max <10 mL/kg/min who underwent lung resection had an exceptionally high mortality rate of up to 100%, which is generally regarded as a criterion of inoperability (8,9,15). VO2 max between 10 and 15 mL/kg/min is associated with an increased risk of PPCs, although the incidence rate varies between studies (16,17). However, the value of VO2 max in mild to moderate COPD typically exceeds 15 mL/kg/min, which aligns with the findings of this study. No difference in VO2 max between the PPC and non-PPC groups was observed, indicating that VO2 max may not play a substantial role in predicting PPCs in mild to moderate COPD. In fact, one recent meta-analysis reported that VO2 max >15 mL/kg/min was associated with improved survival but not PPCs (18). A similar pattern was observed for DLCO. Generally, DLCO <60% of the predicted value is associated with elevated risk of mortality and PPCs (19,20). However, the result of DLCO in mild to moderate COPD is usually higher than 60% of the predicted value. In one study, DLCO in early-stage COPD was associated with higher PPC rates (OR =0.97), but the relation was not clinically meaningful (21).
In contrast, the CAT score emerged as a noteworthy predictor of PPCs, which was more reliable than spirometry. After lung surgery, limitations in respiratory muscle functions, particularly the diaphragm, and reduced ventilatory response lead to reduction in vital capacity, atelectasis, and retention of secretions (22,23). Moreover, many general anaesthetic agents interfere with mucociliary clearance and increase the production of secretions (24). In mild to moderate COPD, postoperative changes in vital capacity may be similar in almost all patients, but pre-existing differences in the functions of respiratory muscle and mucus secretions may tend to intensify these processes, leading to postoperative pneumonia. However, the most frequent complication observed in this study was persistent air leakage, which is a less explainable complication for association with CAT score than pneumonia. Previous studies have reported the association between CAT score and elevated inflammatory markers such as C-reactive protein (25-28). Even in patients with preserved respiratory function, chronic bronchitis, and a smoking history, inflammatory marker levels were correlated with CAT score and exacerbations (29). This correlation suggests that a higher CAT score may also be linked to airway inflammation, potentially contributing to delayed healing and the occurrence of air leakage. The CAT score encompasses aspects related to mucus secretion, chest tightness, breathlessness, and limitation in activities, making it an effective reflection of vulnerability of the patient to postoperative complications.
The CAT score is a very simple, easily accessible, and cost-effective tool that requires little effort in assessment compared with other tests. It is a well-validated tool for COPD and measures various factors, including respiratory symptoms and functional capacity to perform daily activities, thereby estimating the quality of life of an individual. A previous study demonstrated that a high CAT score (>10) is associated with an increased risk of respiratory failure (30). Because COPD is a category of disease with various subtypes, even patients with similar lung function have varying symptoms, functional capacity, and quality of life, which may reflect the incidence of PPCs. CAT scores may better reflect those differences than other exercise tests, composite scores, or PPC prediction models. It suggests that a well-validated, simple questionnaire may be more informative than expensive and complex tests.
Absolute contraindications of lung resection surgery are well documented in previous studies. When surgery is not contraindicated, the decision to undergo surgery is made through a comprehensive evaluation. At this point, the CAT score can play a valuable role in objectively evaluating and reflecting patient symptoms and identifying those at high risk for postoperative morbidity. Uncontrolled symptoms and subsequent reductions in functional capacity may contribute to the occurrence of PPCs; therefore, patients with more severe symptoms may require more aggressive perioperative interventions to prevent PPCs. These interventions could include customized preoperative physiotherapy, including bronchial hygiene, training of respiratory muscles and exercise, and appropriate medication (e.g., mucolytics) for patients with high CAT scores (31).
This study had several limitations. First, it was a single-center retrospective study, so inherent bias may have been present owing to the nature of the study. In addition, the study only included a small number of patients, so the predictive value of tests other than CAT scores may have been underestimated. Therefore, a prospective study including a larger population would be required to further validate our study findings.
Conclusions
Our study demonstrated that the CAT score is useful in evaluating patients with COPD before lung resection surgery, as it effectively predicts the risk of developing PPCs. This suggests that patients with relatively high CAT scores may benefit from aggressive management during the perioperative period to enhance their outcomes.
Acknowledgments
Funding: None.
Footnote
Reporting Checklist: The authors have completed the STROBE reporting checklist. Available at https://jtd.amegroups.com/article/view/10.21037/jtd-24-138/rc
Data Sharing Statement: Available at https://jtd.amegroups.com/article/view/10.21037/jtd-24-138/dss
Peer Review File: Available at https://jtd.amegroups.com/article/view/10.21037/jtd-24-138/prf
Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://jtd.amegroups.com/article/view/10.21037/jtd-24-138/coif). 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 Review Board of the Asan Medical Center (approval No. 2021-0915), and the requirement for informed consent was waived because of the retrospective nature of the study.
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/.
References
- Sekine Y, Katsura H, Koh E, et al. Early detection of COPD is important for lung cancer surveillance. Eur Respir J 2012;39:1230-40. [Crossref] [PubMed]
- Gupta H, Ramanan B, Gupta PK, et al. Impact of COPD on postoperative outcomes: results from a national database. Chest 2013;143:1599-606. [Crossref] [PubMed]
- Lugg ST, Agostini PJ, Tikka T, et al. Long-term impact of developing a postoperative pulmonary complication after lung surgery. Thorax 2016;71:171-6. [Crossref] [PubMed]
- Agostini P, Cieslik H, Rathinam S, et al. Postoperative pulmonary complications following thoracic surgery: are there any modifiable risk factors? Thorax 2010;65:815-8. [Crossref] [PubMed]
- Brunelli A, Charloux A, Bolliger CT, et al. ERS/ESTS clinical guidelines on fitness for radical therapy in lung cancer patients (surgery and chemo-radiotherapy). Eur Respir J 2009;34:17-41. [Crossref] [PubMed]
- Mackay AJ, Donaldson GC, Patel AR, et al. Usefulness of the Chronic Obstructive Pulmonary Disease Assessment Test to evaluate severity of COPD exacerbations. Am J Respir Crit Care Med 2012;185:1218-24. [Crossref] [PubMed]
- Brunelli A, Kim AW, Berger KI, et al. 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:e166S-90S.
- Holden DA, Rice TW, Stelmach K, et al. Exercise testing, 6-min walk, and stair climb in the evaluation of patients at high risk for pulmonary resection. Chest 1992;102:1774-9. [Crossref] [PubMed]
- Bechard D, Wetstein L. Assessment of exercise oxygen consumption as preoperative criterion for lung resection. Ann Thorac Surg 1987;44:344-9. [Crossref] [PubMed]
- Freeman RK, Van Woerkom JM, Vyverberg A, et al. The effect of a multidisciplinary thoracic malignancy conference on the treatment of patients with lung cancer. Eur J Cardiothorac Surg 2010;38:1-5. [Crossref] [PubMed]
- Detterbeck FC, Boffa DJ, Kim AW, et al. The Eighth Edition Lung Cancer Stage Classification. Chest 2017;151:193-203.
- Hwang YI, Jung KS, Lim SY, et al. A Validation Study for the Korean Version of Chronic Obstructive Pulmonary Disease Assessment Test (CAT). Tuberc Respir Dis (Seoul) 2013;74:256-63. [Crossref] [PubMed]
- Hwang YI, Jung KS, Lim SY, et al. A Validation Study for the Korean Version of Chronic Obstructive Pulmonary Disease Assessment Test (CAT). Tuberc Respir Dis (Seoul) 2013;74:256-63. [Crossref] [PubMed]
- Cardoso F, Tufanin AT, Colucci M, et al. Replacement of the 6-min walk test with maximal oxygen consumption in the BODE Index applied to patients with COPD: an equivalency study. Chest 2007;132:477-82. [Crossref] [PubMed]
- Markos J, Mullan BP, Hillman DR, et al. Preoperative assessment as a predictor of mortality and morbidity after lung resection. Am Rev Respir Dis 1989;139:902-10. [Crossref] [PubMed]
- Bayram AS, Candan T, Gebitekin C. Preoperative maximal exercise oxygen consumption test predicts postoperative pulmonary morbidity following major lung resection. Respirology 2007;12:505-10. [Crossref] [PubMed]
- Smith TP, Kinasewitz GT, Tucker WY, et al. Exercise capacity as a predictor of post-thoracotomy morbidity. Am Rev Respir Dis 1984;129:730-4. [Crossref] [PubMed]
- Arbee-Kalidas N, Moutlana HJ, Moodley Y, et al. The association between cardiopulmonary exercise testing and postoperative outcomes in patients with lung cancer undergoing lung resection surgery: A systematic review and meta-analysis. PLoS One 2023;18:e0295430. [Crossref] [PubMed]
- Ferguson MK, Little L, Rizzo L, et al. Diffusing capacity predicts morbidity and mortality after pulmonary resection. J Thorac Cardiovasc Surg 1988;96:894-900. [Crossref] [PubMed]
- Ferguson MK, Dignam JJ, Siddique J, et al. Diffusing capacity predicts long-term survival after lung resection for cancer. Eur J Cardiothorac Surg 2012;41:e81-6. [Crossref] [PubMed]
- Kim ES, Kim YT, Kang CH, et al. Prevalence of and risk factors for postoperative pulmonary complications after lung cancer surgery in patients with early-stage COPD. Int J Chron Obstruct Pulmon Dis 2016;11:1317-26. [Crossref] [PubMed]
- Miskovic A, Lumb AB. Postoperative pulmonary complications. Br J Anaesth 2017;118:317-34. [Crossref] [PubMed]
- Vesovic R, Milosavljevic M, Punt M, et al. The role of the diaphragm in prediction of respiratory function in the immediate postoperative period in lung cancer patients using a machine learning model. World J Surg Oncol 2023;21:393. [Crossref] [PubMed]
- Licker M, Schweizer A, Ellenberger C, et al. Perioperative medical management of patients with COPD. Int J Chron Obstruct Pulmon Dis 2007;2:493-515. [PubMed]
- Sarioglu N, Hismiogullari AA, Bilen C, et al. Is the COPD assessment test (CAT) effective in demonstrating the systemic inflammation and other components in COPD? Rev Port Pneumol (2006) 2016;22:11-7. [PubMed]
- Kang HK, Kim K, Lee H, et al. COPD assessment test score and serum C-reactive protein levels in stable COPD patients. Int J Chron Obstruct Pulmon Dis 2016;11:3137-43. [Crossref] [PubMed]
- Yazici O, Gulen ST, Yenisey C, et al. Comparison of inflammation biomarkers among chronic obstructive pulmonary disease groups: A cross sectional study. Niger J Clin Pract 2020;23:817-24. [Crossref] [PubMed]
- Lin YH, Wang WY, Hu SX, et al. Serum C-reactive protein level in COPD patients stratified according to GOLD 2011 grading classification. Pak J Med Sci 2016;32:1453-8. [Crossref] [PubMed]
- Garudadri S, Woodruff PG, Han MK, et al. Systemic Markers of Inflammation in Smokers With Symptoms Despite Preserved Spirometry in SPIROMICS. Chest 2019;155:908-17. [Crossref] [PubMed]
- Pezzuto A, Trabalza Marinucci B, Ricci A, et al. Predictors of respiratory failure after thoracic surgery: a retrospective cohort study with comparison between lobar and sub-lobar resection. J Int Med Res 2022;50:3000605221094531. [Crossref] [PubMed]
- Kendall F, Abreu P, Pinho P, et al. The role of physiotherapy in patients undergoing pulmonary surgery for lung cancer. A literature review. Rev Port Pneumol (2006) 2017;23:343-51. [PubMed]