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Relationship between gender and perioperative clinical features in lung cancer patients who underwent VATS lobectomy

Abstract

Objectives

Compare the differences in perioperative clinical characteristics of lung cancer patients of different genders who have undergone VATS lobectomy, and explore the impact of these differences on the short-term prognosis of patients.

Methods

A total of 338 consecutive patients with lung cancer who underwent VATS lobectomy in our hospital from August 2021 to August 2022 were retrospectively analyzed, they were divided into male group and female group. The perioperative characteristics and short-term prognosis of different groups were compared. The multivariate binary logistic regression analysis was used to analyze the risk factors.

Results

There were statistically significant differences between male and female patients in age of onset, body surface area (BSA), smoking rate, alcohol consumption rate, hypertension incidence, pulmonary function and clinical stage. There were statistically significant differences between male and female patients in operation time and lymph node dissection. The probability of postoperative complications, such as pulmonary infection, persistent air leakage and severe subcutaneous emphysema, in male patients was significantly higher than that in female patients. The average daily postoperative thoracic drainage volume in male patients was considerably higher than that in female patients, and the postoperative duration of thoracic drainage tube and hospital stay in male patients were significantly longer than those in female patients. After multiple regression analysis, low FEVI values in males was found to be an independent risk factor for postoperative complications.

Conclusions

Compared with female patients, male patients with lung cancer are more likely to have unfavorable factors such as older age, higher smoking rate, poor pulmonary function and late clinical stage of tumors when they undergoing VATS surgery treatment. The appropriate thoracic drainage time can be selected according to gender differences to shorten the length of hospital stay. The incidence of postoperative complications is higher in male patients, especially those with poor pulmonary function, and active perioperative intervention is required to reduce the incidence of postoperative complications.

Peer Review reports

Introduction

As one of the malignancies with the highest morbidity and mortality in the world, lung cancer has a 5-year survival rate of less than 20% [1].In China, lung cancer is the malignant tumor with the highest incidence and mortality rate, and the incidence and mortality rate are increasing year by year [2, 3]. Non-small cell lung cancer accounts for 85% of the pathological type in lung cancer patients [4]. For resectable lung cancer, surgical resection is the best treatment, measure, and lobectomy is the standard surgical treatment [4,5,6]. With fewer postoperative complications, shorter postoperative hospital stays, better quality of life and similar long-term survival rates than open-heart surgery, video-assisted thoracic surgery (VATS) lobectomy has been widely used in the surgical resection of patients with lung cancer [7,8,9].

There are significant gender differences in lung cancer, which are manifested in the incidence, risk factors, pathological types, clinical stages, treatment, prognosis, and pathogenesis of lung cancer [10,11,12,13,14,15], The need for gender as a stratification factor in the design of clinical trials was emphasised. Despite the large number of studies outlining gender differences in lung cancer, few reports have elaborated on the relationship between gender differences and perioperative clinical characteristics of lung cancer patients.

This study aims to provide reference for perioperative management of lung cancer patients of different genders who have undergone VATS lobectomy by studying the above issues.

Information and methodology

Clinical data and grouping

This study retrospectively analyzed the clinical data of lung cancer patients who met the study criteria and were admitted to the Department of Thoracic Surgery of West China Fourth Hospital of Sichuan University from August 2021 to August 2022.

Inclusion criteria: (1) single lesion on preoperative imaging, (2) postoperative histopathology diagnosis of primary lung cancer, (3) VATS radical resection of lung cancer (lobectomy + lymph node dissection) was performed.

Exclusion Criteria: (1) previous history of intrathoracic surgery, (2) Surgical bilobectomy or lobectomy combined with partial resection of adjacent lungs, (3) preoperative neoadjuvant therapy, (4) patients whose postoperative pathological results failed to reach R0 resection, (5) patients who converted to thoracotomy, (6) patients with incomplete clinical data.

A total of 338 patients were included in this study. Among them, 174 (51.5%) were males and 164 (48.5%) were females. The age was 26 ~ 83 years old, and they were divided into male group (n = 174) and female group (n = 164) according to gender.

Surgical and perioperative management

All patients were admitted to the hospital to improve preoperative preparation and assessment, including smoking patients need to strictly quit smoking for more than 1 week before arranging surgery, for other diseases such as hypertension, diabetes mellitus, heart disease, etc., need to ask the relevant departments to consult and guide the treatment, and only after the condition is stable can we arrange for surgical treatment. In the perioperative period, the concept of ‘Enhanced Recovery After Surgery (ERAS)’ was practiced, and all patients underwent preoperative education, preoperative nebulisation, expectorant and antispasmodic treatments, and active pulmonary exercise, and fasting on the day of surgery. VATS single-hole or three-hole lobectomy + lymph node dissection was performed, with limited fluid intake and no urinary catheter routinely placed, and a chest drain (12–22 F) was routinely placed in the 4th or 7th intercostal space after the operation, and intercostal nerve block anaesthesia was also performed. After the operation, the patients were routinely transferred to the general ward for postoperative recovery treatment, and were treated with nonsteroidal analgesics, resumed eating 6 h after the operation, and were encouraged to get out of bed at 12 h after the operation when the cardiac monitoring was withdrawn. However, for patients with preoperative pulmonary insufficiency, difficulty in tolerating single-lung ventilation during the operation and difficulty in removing the tracheal tube for a short period of time, they were transferred to the intensive care unit for ventilator-assisted respiration, and then transferred back to the general ward after the removal of the tracheal tube. After the operation, patients were strengthened with respiratory management, and were given nebulised inhalation, oxygen therapy, temporary analgesia, expectoration, prevention of infection, etc.; they were also strengthened with coughing and expectoration and respiratory exercises to promote the recovery of pulmonary function, and were actively prevented from pulmonary atelectasis, and were encouraged to get out of bed. Strengthen cough and sputum expectoration and respiratory exercise to promote lung function recovery, and actively prevent pulmonary atelectasis and lung infection; strengthen the observation and care of chest drain after operation, maintain fluid and electrolyte balance, and remove chest drain as soon as possible after complying with the guideline of removing chest drain.

Data collection

The perioperative clinical data of patients were retrospectively collected through the electronic medical record system, including (1) Preoperative indicators: age, gender, height, weight, smoking history, chronic alcohol consumption, body mass index (BMI), body surface area (BSA), comorbidities (hypertension, diabetes, heart disease, lung disease, tumor history, etc.), tumor diameter, tumor composition, lung function (FEV1, FEV1 Pre/Ref, FEV1/FVC%); (2) Intraoperative indicators: surgical method (resection of lung lobes), intraoperative blood loss, operation time, lymph node dissection station and number, etc.; (3) Postoperative indicators: postoperative transfers to the intensive care unit, tumor stage, postoperative chest drainage tube indwelling time, mean postoperative daily chest drainage volume, postoperative cardiopulmonary complication (air leakage, pulmonary infection, chyle fistula, arrhythmia, hydrothorax, severe subcutaneous emphysema, atelectasis, respiratory failure Cardiac arrest and bronchopleural fistula were not included in this study because no cardiac arrest or bronchopleural fistula occurred) and postoperative hospital stay.

Statistical analysis

The SPSS 25.0 (IBM Corp, Armonk, NY, USA) software was used to analyze the results. The measures were expressed as x ̄ ± s, in which the independent samples t-test was used for normally distributed measures, and the Mann-Whitney U test was used for non-normally distributed measures. Count data were expressed in frequency and percentage (%), the χ2 test was used for comparison, and the Fisher exact probability method was used when the χ2 test criteria were unmet. Multivariate binary logistic regression analysis was used to analyze the risk factors for postoperative complications. P < 0.05 was statistically significant.

Ethics review

This study has been reviewed and approved by Ethical Approval of Ethics Committee of West China Fourth Hospital and West China School of Public Health, Sichuan University, approval number Gwll2024151, and the personal consent for this retrospective analysis has been waived.

Results

Baseline data comparison

A total of 338 patients were included in this study. Among them, 174 (51.5%) were males and 164 (48.5%) were females. The age was 26–83 years old. As shown in Table 1, there were 174 males and 164 females in this study. The mean age of males was 59.13 ± 9.50 years (range 28–83 years), which was significantly higher than that of females [56.19 ± 10.00 years (range 26–77 years); P = 0.006], BSA was significantly higher in males than in females [1.75 ± 0.15, (range 1.33–2.21) VS 1.57 ± 0.11, (range 1.3–1.87); P < 0.001]. There was no statistically significant difference in BMI between males and females (P = 0.477). The FEV1 in males was significantly higher than that in females [2.59 ± 0.67, (range 0.74–5.39) VS 2.02 ± 0.49, (range 0.73–3.34); P < 0.001], but the FEV1 Pre/Ref and FEV1/FVC% of males were significantly lower than those of females (P = 0.003, P < 0.001, respectively). Smoking prevalence was significantly higher in males than that in females (69% versus 6.1%; P < 0.001), and the prevalence of alcohol consumption in males was significantly higher than that in females (55.8% versus 2.4%; P < 0.001). In terms of comorbidities, the prevalence of hypertension in males was significantly higher than that in females (25.3% VS 15.9; P = 0032), and there were no significant differences in the comparison of other complications.

Table 1 Comparison of baseline data between males and females

In comparison of tumor characteristics, the mean diameter of tumors was significantly larger in males than that in females [2.78 ± 1.54 (range 0.9–7.60) VS 2.16 ± 1.10 (range 0.6–7.3); P < 0.001]. The tumor component in males was mainly solid, accounting for 65.5%, while the tumor component in females mainly was ground-glass (including pure ground-glass and mixed ground-glass), which accounted for 62.2%, the tumor component was significantly different (P < 0.001). In terms of tumor types, adenocarcinoma was the primary type in both male and female patients. Still, the proportion of adenocarcinoma in females was significantly higher than that in males (95.1% VS 75.9%, P < 0.001). There was no significant difference between males and females in the lobe location of the tumor (P > 0.05). In terms of T stage, more than half of the males had T2 or above (55.7%), while most females had T1 and below (70.1%), the difference was statistically significant (P < 0.001). There was no significant difference in the N stage between males and females (14.9% VS 8.5%, P > 0.05). In the TNM stage, the males was significantly later than that of females (P < 0.001).

Comparison of intraoperative and postoperative data

See Table 2, the operative time was significantly longer in males than in females [124.20 ± 36.15 (range, 50–244 min) VS 114.79 ± 35.15 (range, 48–242 min); P = 0.016], but there was no significant difference between males and females in intraoperative blood loss [(101.55 ± 73.35 (range, 10-400 ml) VS 88.23 ± 83.71 (range, 20-600 ml); P = 0.12]. There was no significant difference in the station of lymph node dissection between males and females (P > 0.05), but the number of lymph nodes dissected in males was significantly higher than that in females [11.9 ± 4.55 (4–30 nodes), VS 10.74 ± 3.83 (4–23 nodes); P = 0.011]. In terms of the number of patients directly transferred to the intensive care unit after surgery, four patients in the male group and four patients in the female group were directly transferred to the intensive care unit for postoperative recovery treatment, and there was no statistically significant difference between the two groups of patients (P = 0.932).Males were significantly worse in terms of postoperative tubing time compared with females [6.02 ± 3.95 (range, 2–27 days) VS 4.47 ± 2.33 (range, 2–15 days), P < 0.001], and the length of postoperative hospital stay was significantly higher in males than in females [8.51 ± 4.38 (range, 3–33 days) VS 6.57 ± 2.51 (range, 3–17 days), P < 0.001)], the average daily chest drainage volume during the postoperative catheter period was also significantly higher in males than in females [207.79 ± 65.27 (range, 66.7-410 ml) VS 174.91 ± 58.75 (range, 50-432 ml); P < 0.001)]. Among the two groups, one male died of respiratory failure in 7 days after surgery, and there was no difference in postoperative mortality between the two groups (P = 0.332). In terms of postoperative complications, pulmonary infections, subcutaneous emphysema (6.9% VS 1.2%; P = 0.009) and persistent air leakage (12.1% VS 4.9%; P = 0.018) were more likely to occur in male (27% VS 12.2%; P = 0.001), and there was no significant difference in the comparison of other complications.

Table 2 Comparison of intraoperative and postoperative date of different groups

Univariate analysis of risk factors for postoperative complications

Pulmonary infection, subcutaneous emphysema, and persistent air leakage were included in the statistical scope of postoperative complications between the two groups (a total of 86 patients suffered from appellate complications, with an incidence rate of 25.44%). Whether the gender, BSA (≤ 1.64 and > 1.64, median 1.64), age (≤ 57 years and > 57 years, median 57 years), smoking history, chronic alcohol consumption, hypertension, FEVI (≤ 2.0 and > 2.0), FEV1 Pre/Ref (≤ 92% and > 92%, median 92%), FEV1/FVC (≤ 86.81% and > 86.81%, median 86.81%), tumor diameter (≤ 2.1 cm group and > 2.1 cm group, median 2.1 cm), tumor composition, tumor type, T stage, N stage, clinical stage of tumor, operation time (≤ 112 min group and > 112 min group, median 112 min) and number of lymph nodes dissected (≤ 10 and > 10 groups, median 10 nodes) were risk factors of postoperative complications? We performed a univariate analysis. The results showed that the gender, smoking history, chronic alcohol consumption, hypertension, FEVI, FEV1 Pre / Ref, tumor diameter, tumor composition, tumor type, T stage, N stage, clinical stage of tumor, operation time, and number of lymph nodes dissected were the risk factors for postoperative complications (P < 0.05) (Table 3).

Table 3 Univariate analysis of postoperative complications

Multivariate regression analysis of risk factors for postoperative complications

The statistically significant differences in the univariate analysis were included in the multivariate analysis for stepwise regression, and the results were showed in Table 4. The gender and FEVI were independent risk factors for postoperative complications. Males were 3.483 times more likely to develop complications after surgery than females, and the risk of complications was reduced by 65.2% for every 1 unit increase in FEV1 value.

Table 4 Multivariate analysis of postoperative complications

Discussion

The impact of gender differences on early postoperative prognosis is a complex and multifactorial issue that involves multiple physiological, psychological, and social dimensions. Firstly, there are significant anatomical and physiological differences between males and females, and these differences may affect the surgical procedure and postoperative recovery. For example, in cardiac surgery, female patients tend to have smaller coronary arteries, which may increase the difficulty of the procedure and the risk of postoperative complications [16]. 。In lung cancer surgery, women have a better prognosis for lung cancer than men due to factors such as lower smoking prevalence, lower age at disease, fewer comorbidities, and lower prevalence of squamous carcinoma compared to men [17]. Women are subject to fluctuations in oestrogen and progesterone, which may affect postoperative healing, immune function and metabolic processes [18]. Gender differences are also reflected in the immune response. Some studies have shown that women typically have a stronger immune response, which helps them to clear their bodies of pathogens and restore their health more quickly. However, in some cases, an overly strong immune response may also lead to increased autoimmune disease or inflammatory response, which can interfere with recovery after surgery [19, 20]. In terms of psychosocial factors, women are more likely than men to feel stress and anxiety in the preoperative period, and in the perioperative period, women may require more analgesic medication for pain relief and more psychological support and care [21,22,23]. A Wallis study found that gender congruence between surgeon and patient may be associated with postoperative outcomes, with female patients likely to have increased rates of postoperative mortality, complications, and readmissions when male surgeons operate on them. This may be related to gender differences in the surgeon’s assessment of the patient’s condition, surgical approach, and postoperative care regimen [24]. In summary, the impact of gender differences on early postoperative prognosis is multifaceted and complex. In order to improve patients‘ postoperative recovery outcomes and quality of life, doctors need to formulate individualised surgical and nursing care plans with full consideration of patients’ gender characteristics, physiological differences, immune responses and psychosocial factors. At the same time, there is also a need to strengthen research and exploration of gender differences in the medical field to better understand the impact of gender on postoperative recovery and to develop appropriate interventions.

In recent years, with the widespread popularity of low-dose spiral CT of the chest, more early-stage lung cancers have been diagnosed. Surgical treatment of lung cancer has also undergone significant changes, and the long-term efficacy of thoracoscopy-assisted radical lung cancer resection is widely recognized [8]. At the same time, the combination of minimally invasive surgery and ERAS significantly reduces perioperative complications, shortens hospital stay, and improves quality of life of lung cancer patients [25, 26]. This study analysed the perioperative clinical characteristics of lung cancer patients of different genders who underwent VATS lobectomy. Compared with females, males have a higher age of disease, a higher rate of smoking and alcohol consumption, and a higher prevalence of hypertension, similar to Fibla’s study [17]. Several studies have shown that age, smoking, alcohol consumption, and hypertension were all unfavorable factors affecting the short-term prognosis of lung cancer patients [27,28,29,30]。Although the FEV1 of males was significantly higher than that of females, the FEV1 Pre/Ref and FEV1/FVC% of females were significantly higher than that of males. The proportion of females who smoke was less than 1/10 of that of males. The prevalence of lung disease in females was only 1/3 that in males, which was thought to be related to a history of smoking and underlying lung disease such as COPD. Studies have shown that relatively weak self-awareness of self-health in men, as well as signs and symptoms (e.g., cough and sputum production) that are overlooked by long-term smoking, may delay physical examination and further diagnosis, thereby delaying appropriate treatment [31, 32]. In this study, males had larger tumor diameters, more solid components, and later clinical stages than females when they underwent surgery. According to Fujikawa et al. [33], the tumor characteristics of males in this study were more aggressive, with a higher risk of recurrence and metastasis, which was not conducive to the prognosis of patients. In terms of tumour type, the prevalence of adenocarcinoma was as high as 95.1% in females, much higher than the 75.9% in males, and the type of disease in the remaining 4.9% of female patients (8 cases) was all squamous carcinoma, while the prevalence of squamous carcinoma in males was 21.8%, and the remaining 2.3% were neuroendocrine carcinoma, which is in accordance with the study of Jin [34].

In this study, males were treated with surgery for a significantly longer period than females, consistent with Gómez-Hernández’s studies [35]. In addition, males also dissected more lymph nodes during surgery than females. It is presumed to be related to a later tumor stage and a higher positive rate of lymph node metastasis in males. In terms of postoperative recovery, compared with females, males had a larger daily chest drainage volume and longer indwelling chest drains. The currently recommended daily chest drain volume varies from 200 to 500 mL [36, 37] (The drainage requirement for removal of chest drains in this study was a chest drainage volume of less than 200 ml.), however, without considering the influence of gender differences, although the daily chest drainage volume of males was significantly more than that of females, the body surface area, pleural volume and parietal pleural area of males were significantly larger than those of females, and it was currently believed that pleural effusion was mainly absorbed by the parietal pleura, and the parietal pleura had a robust compensatory ability to absorb pleural fluid [38, 39], so the ability of males to reabsorb pleural fluid was significantly greater than that of females. In this study, it was suggested that the daily chest drainage volume requirement for males could be further relaxed when evaluating the chest drain removal pointer. However, there is a lack of literature support for specific differences in chest drainage, and other controlled studies are needed. Pulmonary infection is one of the most common complications after radical lung cancer surgery. Postoperative pulmonary infection is mostly caused by the inability of patients‘ respiratory secretions to be discharged, patients’ declining resistance, poor sputum drainage, cross-infection, and anaesthesia influence. The analysis of the study showed that male, smoking history, age, longer duration of surgery, and squamous cell carcinoma are risk factors for postoperative lung infection in lung cancer patients [35, 40]. 。In this study we defined postoperative lung infection by the Melbourne Group Scale (MGS) [41], The study showed that the incidence of pulmonary infection was significantly higher in males than in females (27 versus 12.2%, P < 0.001), consistent with related studies [42]. In addition, male patients also have comorbid risk factors such as age, duration of surgery, smoking history, and squamous cell carcinoma, and it can be assumed that male patients with numerous comorbid risk factors are more susceptible to postoperative pulmonary infections. An air leak lasting 5 days or more is defined as a persistent air leak after surgery. In this study, patients had a persistent air leak of 8.6% (29/338), consistent with reports [36]. Among them, 12.1% of males and 4.9% of females had a higher probability of persistent air leakage after surgery. Risk factors for persistent postoperative air leak have been shown in several studies, including pleural adhesions, emphysema/COPD, chronic smoking history, interlobar dysplasia, upper lobectomy, older age, male sex, and low body mass index [43,44,45]。In this study, most of the males had a history of long-term smoking, a higher age and more lung disease than females, which resulted in a higher rate of persistent air leakage. Lobectomy, male sex, extensive thoracic adhesions, and advanced age are risk factors for the development of subcutaneous emphysema [46, 47], and the incidence of severe subcutaneous emphysema was 4.1% (14/338) in all patients in this study, which was significantly higher than other studies [46, 48]. At the same time, the probability of severe subcutaneous emphysema in males was about 6 times that of females. The prolonged air leakage will increase the risk of subcutaneous emphysema if the lung leaks are severe after surgery, the chest drainage is not smooth, the intrathoracic pressure increases and the intrapleural gas squeezes into the subcutaneous tissue through the pleural space, especially the loose tissue around the orifice of the closed chest drain and the incision, causing subcutaneous emphysema. The females have a lower probability of persistent air leakage after surgery, and the probability of subcutaneous emphysema is lower than that of males because there is more fatty tissue in the chest wall and a narrower intercostal space.

Multivariate regression analysis showed that gender and low FEV1 were independent risk factors for postoperative complications. Therefore, in the perioperative period, we need to pay more attention to males with poor lung function, aggressive perioperative intervention in such patients. Several studies have shown that smoking increases the risk of in-hospital mortality and pulmonary complications after lung cancer resection, whereas strict preoperative smoking cessation reduces in-hospital mortality and the incidence of pulmonary complications after lung cancer resection [49,50,51]. Raupach’s studies [52] shown that a smoke-free interval of 2–6 weeks preoperatively seems to be the most favourable, however, in practice this is difficult to achieve in clinical practice as radical lung cancer surgery should not be delayed. Smoking patients in this study had a smoke-free interval of at least 1 week, and for male patients with poor lung function, a smoke-free interval of more than 2–4 weeks is recommended when their condition permits. In addition, preoperative pulmonary rehabilitation training can improve the cardiopulmonary function of lung cancer patients with poor lung function, shorten the postoperative hospital stay, and reduce the incidence of postoperative pulmonary complications and pneumonia [53,54,55]. Therefore, for male patients with poor lung function, we need to actively perform preoperative pulmonary rehabilitation training, including pharmacological rehabilitation with bronchodilators (β-2 agonists and/or anticholinergic drugs) or with β-2 agonists/inhaled corticosteroid therapy, as well as physical rehabilitation with respiratory training and endurance training. Early termination of ventilator-assisted respiratory status; continued postoperative pulmonary rehabilitation. Closer clinical monitoring is given, including pathogenetic tests, imaging tests, blood index tests, etc. Antiinfective treatment with antibiotics can be upgraded if necessary to minimise the occurrence of pulmonary complications and shorten the patient’s postoperative hospital stay.

There are some limitations to this study. First, this study was retrospective, and there was a selection bias. Data collection depended on the completeness and detail of the medical history, and some potentially important baseline patient characteristics, such as pleural adhesions, were not included in the collection database. Second, there were differences in patient selection, surgical techniques, and postoperative management between different medical groups, which might affect intraoperative and postoperative outcomes. Third, the sample size of this study was relatively small, and it was a single-center study. A multicenter study with a large sample size is needed to validate the results of this study.

Conclusion

In summary, compared with females, males with lung cancer are more likely to have unfavorable factors such as older age, higher smoking rate, poor lung function, and later clinical stage of cancer when they undergoing VATS surgery treatment. Therefore, males must enhance their self-health awareness and maintain good lifestyle habits. In perioperative surgical treatment, preoperative smoking cessation should be strict to sufficient course of treatment, preferably for more than 2 weeks without delaying the time of surgery. Pulmonary function exercises should be actively performed to improve lung function. After surgery, the appropriate time of chest drain removal can be selected according to different gender, and the length of hospital stay can be shortened. The incidence of postoperative complications is higher in men, especially those with poorer lung function, and it is important to actively perform perioperative interventions and appropriately lengthen the preparation time to reduce the incidence of postoperative complications.

Data availability

No datasets were generated or analysed during the current study.

References

  1. Bade BC, Dela Cruz CS. Lung Cancer 2020: epidemiology, etiology, and Prevention. Clin Chest Med. 2020;41(1):1–24.

    Article  PubMed  Google Scholar 

  2. Xia C, Dong X, Li H, Cao M, Sun D, He S, Yang F, Yan X, Zhang S, Li N, et al. Cancer statistics in China and United States, 2022: profiles, trends, and determinants. Chin Med J (Engl). 2022;135(5):584–90.

    Article  PubMed  Google Scholar 

  3. Wu F, Wang L, Zhou C. Lung cancer in China: current and prospect. Curr Opin Oncol. 2021;33(1):40–6.

    Article  CAS  PubMed  Google Scholar 

  4. Duma N, Santana-Davila R, Molina JR. Non-small Cell Lung Cancer: Epidemiology, Screening, diagnosis, and treatment. Mayo Clin Proc. 2019;94(8):1623–40.

    Article  CAS  PubMed  Google Scholar 

  5. Ginsberg RJ, Rubinstein LV. Randomized trial of lobectomy versus limited resection for T1 N0 non-small cell lung cancer. Lung Cancer Study Group. Ann Thorac Surg. 1995;60(3):615–22. discussion 622 – 613.

    Article  CAS  PubMed  Google Scholar 

  6. Khullar OV, Liu Y, Gillespie T, Higgins KA, Ramalingam S, Lipscomb J, Fernandez FG. Survival after Sublobar Resection versus Lobectomy for Clinical Stage IA Lung Cancer: an analysis from the National Cancer Data Base. J Thorac Oncol. 2015;10(11):1625–33.

    Article  PubMed  PubMed Central  Google Scholar 

  7. Agostini P, Lugg ST, Adams K, Vartsaba N, Kalkat MS, Rajesh PB, Steyn RS, Naidu B, Rushton A, Bishay E. Postoperative pulmonary complications and rehabilitation requirements following lobectomy: a propensity score matched study of patients undergoing video-assisted thoracoscopic surgery versus thoracotomy†. Interact Cardiovasc Thorac Surg. 2017;24(6):931–7.

    Article  PubMed  Google Scholar 

  8. Yang HX, Woo KM, Sima CS, Bains MS, Adusumilli PS, Huang J, Finley DJ, Rizk NP, Rusch VW, Jones DR, et al. Long-term survival based on the Surgical Approach to Lobectomy for Clinical Stage I Nonsmall Cell Lung Cancer: comparison of robotic, video-assisted thoracic surgery, and Thoracotomy Lobectomy. Ann Surg. 2017;265(2):431–7.

    Article  PubMed  Google Scholar 

  9. Bendixen M, Jørgensen OD, Kronborg C, Andersen C, Licht PB. Postoperative pain and quality of life after lobectomy via video-assisted thoracoscopic surgery or anterolateral thoracotomy for early stage lung cancer: a randomised controlled trial. Lancet Oncol. 2016;17(6):836–44.

    Article  PubMed  Google Scholar 

  10. Xing X, Liao Y, Tang H, Chen G, Ju S, You L. [Gender-associated differences of lung cancer and mechanism]. Zhongguo Fei Ai Za Zhi. 2011;14(7):625–30.

    PubMed  Google Scholar 

  11. Araghi M, Fidler-Benaoudia M, Arnold M, Rutherford M, Bardot A, Ferlay J, Bucher O, De P, Engholm G, Gavin A, et al. International differences in lung cancer survival by sex, histological type and stage at diagnosis: an ICBP SURVMARK-2 study. Thorax. 2022;77(4):378–90.

    Article  PubMed  Google Scholar 

  12. Baum P, Winter H, Eichhorn ME, Roesch RM, Taber S, Christopoulos P, Wiegering A, Lenzi J. Trends in age- and sex-specific lung cancer mortality in Europe and Northern America: analysis of vital registration data from the WHO Mortality database between 2000 and 2017. Eur J Cancer. 2022;171:269–79.

    Article  CAS  PubMed  Google Scholar 

  13. Huang J, Yue N, Shi N, Wang Q, Cui T, Ying H, Wang Z, Leng J, Sui Z, Xu Y, et al. Influencing factors of lung cancer in nonsmoking women: systematic review and meta-analysis. J Public Health (Oxf). 2022;44(2):259–68.

    Article  PubMed  Google Scholar 

  14. Conforti F, Pala L, Pagan E, Corti C, Bagnardi V, Queirolo P, Catania C, De Pas T, Giaccone G. Sex-based differences in response to anti-PD-1 or PD-L1 treatment in patients with non-small-cell lung cancer expressing high PD-L1 levels. A systematic review and meta-analysis of randomized clinical trials. ESMO Open. 2021;6(5):100251.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Frega S, Dal Maso A, Ferro A, Bonanno L, Conte P, Pasello G. Heterogeneous tumor features and treatment outcome between males and females with lung cancer (LC): do gender and sex matter? Crit Rev Oncol Hematol. 2019;138:87–103.

    Article  PubMed  Google Scholar 

  16. Dumitriu LaGrange D, Tessitore E, Reymond P, Mach F, Huber C. A systematic review and meta-analysis of differences between men and women in short-term outcomes following coronary artery bypass graft surgery. Sci Rep. 2024;14(1):20682.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Fibla JJ, Molins L, Quero F, Izquierdo JM, Sánchez D, Hernández J, Bayarri C, Boada M, Guirao Á, Cueto A. Perioperative outcome of lung cancer surgery in women: results from a Spanish nationwide prospective cohort study. J Thorac Dis. 2019;11(4):1475–84.

    Article  PubMed  PubMed Central  Google Scholar 

  18. Pittet JF, Hu PJ, Honavar J, Brandon AP, Evans CA, Muthalaly R, Ding Q, Wagener BM. Estrogen alleviates sex-dependent differences in Lung Bacterial Clearance and mortality secondary to bacterial pneumonia after traumatic brain Injury. J Neurotrauma. 2021;38(8):989–99.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Zandman-Goddard G, Peeva E, Shoenfeld Y. Gender and autoimmunity. Autoimmun Rev. 2007;6(6):366–72.

    Article  CAS  PubMed  Google Scholar 

  20. Quintero OL, Amador-Patarroyo MJ, Montoya-Ortiz G, Rojas-Villarraga A, Anaya JM. Autoimmune disease and gender: plausible mechanisms for the female predominance of autoimmunity. J Autoimmun. 2012;38(2–3):J109–119.

    Article  CAS  PubMed  Google Scholar 

  21. Chang WK, Li YS, Wu HL, Tai YH, Lin SP, Chang KY. Group-based trajectory analysis of postoperative pain in epidural analgesia for video-assisted thoracoscopic surgery and risk factors of rebound pain. J Chin Med Assoc. 2022;85(2):216–21.

    Article  PubMed  Google Scholar 

  22. Chen WC, Bai YY, Zhang LH, Liu YB, Liu CY, Liang JW, He HF. Prevalence and predictors of Chronic Postsurgical Pain after Video-assisted thoracoscopic surgery: a systematic review and Meta-analysis. Pain Ther. 2023;12(1):117–39.

    Article  PubMed  Google Scholar 

  23. Eberhart L, Aust H, Schuster M, Sturm T, Gehling M, Euteneuer F, Rüsch D. Preoperative anxiety in adults - a cross-sectional study on specific fears and risk factors. BMC Psychiatry. 2020;20(1):140.

    Article  PubMed  PubMed Central  Google Scholar 

  24. Wallis CJD, Jerath A, Coburn N, Klaassen Z, Luckenbaugh AN, Magee DE, Hird AE, Armstrong K, Ravi B, Esnaola NF, et al. Association of Surgeon-Patient Sex Concordance with postoperative outcomes. JAMA Surg. 2022;157(2):146–56.

    Article  PubMed  Google Scholar 

  25. Khoury AL, McGinigle KL, Freeman NL, El-Zaatari H, Feltner C, Long JM. Enhanced recovery after thoracic surgery: systematic review and meta-analysis. JTCVS Open. 2021;7:370–91.

    Article  PubMed  PubMed Central  Google Scholar 

  26. Lim E, Harris RA, McKeon HE, Batchelor TJ, Dunning J, Shackcloth M, Anikin V, Naidu B, Belcher E, Loubani M, et al. Impact of video-assisted thoracoscopic lobectomy versus open lobectomy for lung cancer on recovery assessed using self-reported physical function: VIOLET RCT. Health Technol Assess. 2022;26(48):1–162.

    Article  PubMed  PubMed Central  Google Scholar 

  27. Graf SA, Zeliadt SB, Rise PJ, Backhus LM, Zhou XH, Williams EC. Unhealthy alcohol use is associated with postoperative complications in veterans undergoing lung resection. J Thorac Dis. 2018;10(3):1648–56.

    Article  PubMed  PubMed Central  Google Scholar 

  28. Shiono S, Katahira M, Abiko M, Sato T. Smoking is a perioperative risk factor and prognostic factor for lung cancer surgery. Gen Thorac Cardiovasc Surg. 2015;63(2):93–8.

    Article  PubMed  Google Scholar 

  29. Feng G, Jia Y, Zhao G, Meng F, Wang T. Risk factors for postoperative pulmonary complications in elderly patients undergoing video-assisted thoracoscopic surgery lobectomy under general anesthesia: a retrospective study. BMC Surg. 2024;24(1):153.

    Article  PubMed  PubMed Central  Google Scholar 

  30. Attaallah AF, Vallejo MC, Elzamzamy OM, Mueller MG, Eller WS. Perioperative risk factors for postoperative respiratory failure. J Perioper Pract. 2019;29(3):49–53.

    PubMed  Google Scholar 

  31. Saab MM, Noonan B, Kilty C, FitzGerald S, Collins A, Lyng Á, Kennedy U, O’Brien M, Hegarty J. Awareness and help-seeking for early signs and symptoms of lung cancer: a qualitative study with high-risk individuals. Eur J Oncol Nurs. 2021;50:101880.

    Article  PubMed  Google Scholar 

  32. Fish JA, Prichard I, Ettridge K, Grunfeld EA, Wilson C. Psychosocial factors that influence men’s help-seeking for cancer symptoms: a systematic synthesis of mixed methods research. Psychooncology. 2015;24(10):1222–32.

    Article  PubMed  Google Scholar 

  33. Fujikawa R, Muraoka Y, Kashima J, Yoshida Y, Ito K, Watanabe H, Kusumoto M, Watanabe SI, Yatabe Y. Clinicopathologic and genotypic features of Lung Adenocarcinoma characterized by the International Association for the study of Lung Cancer Grading System. J Thorac Oncol. 2022;17(5):700–7.

    Article  CAS  PubMed  Google Scholar 

  34. Jin W, Zheng L, Fan X, Wang H, Wang Q, Yang C. A comparison of three-port and four-port Da Vinci robot-assisted thoracoscopic surgery for lung cancer: a retrospective study. J Cardiothorac Surg. 2024;19(1):377.

    Article  PubMed  PubMed Central  Google Scholar 

  35. Gómez-Hernández MT, Forcada C, Varela G, Jiménez MF. Operating time: an independent and modifiable risk factor for short-term complications after video-thoracoscopic pulmonary lobectomy. Eur J Cardiothorac Surg 2022, 62(6).

  36. Novoa NM, Jiménez MF, Varela G. When to remove a chest tube. Thorac Surg Clin. 2017;27(1):41–6.

    Article  PubMed  Google Scholar 

  37. Bjerregaard LS, Jensen K, Petersen RH, Hansen HJ. Early chest tube removal after video-assisted thoracic surgery lobectomy with serous fluid production up to 500 ml/day. Eur J Cardiothorac Surg. 2014;45(2):241–6.

    Article  PubMed  Google Scholar 

  38. Miserocchi G. Physiology and pathophysiology of pleural fluid turnover. Eur Respir J. 1997;10(1):219–25.

    Article  CAS  PubMed  Google Scholar 

  39. Yalcin NG, Choong CK, Eizenberg N. Anatomy and pathophysiology of the pleura and pleural space. Thorac Surg Clin. 2013;23(1):1–10. v.

    Article  PubMed  Google Scholar 

  40. Zhang J, Zhao T, Long S, Liu X, Yu H. Risk factors for postoperative infection in Chinese lung cancer patients: a meta-analysis. J Evid Based Med. 2017;10(4):255–62.

    Article  CAS  PubMed  Google Scholar 

  41. Agostini P, Naidu B, Cieslik H, Rathinam S, Bishay E, Kalkat MS, Rajesh PB, Steyn RS, Singh S. Comparison of recognition tools for postoperative pulmonary complications following thoracotomy. Physiotherapy. 2011;97(4):278–83.

    Article  CAS  PubMed  Google Scholar 

  42. Bevilacqua Filho CT, Schmidt AP, Felix EA, Bianchi F, Guerra FM, Andrade CF. Risk factors for postoperative pulmonary complications and prolonged hospital stay in pulmonary resection patients: a retrospective study. Braz J Anesthesiol. 2021;71(4):333–8.

    PubMed  PubMed Central  Google Scholar 

  43. Ponholzer F, Ng C, Maier H, Lucciarini P, Öfner D, Augustin F. Risk factors, complications and costs of prolonged air leak after video-assisted thoracoscopic surgery for primary lung cancer. J Thorac Dis. 2023;15(2):866–77.

    Article  PubMed  Google Scholar 

  44. Pompili C, Miserocchi G. Air leak after lung resection: pathophysiology and patients’ implications. J Thorac Dis. 2016;8(Suppl 1):S46–54.

    PubMed  PubMed Central  Google Scholar 

  45. Pompili C, Falcoz PE, Salati M, Szanto Z, Brunelli A. A risk score to predict the incidence of prolonged air leak after video-assisted thoracoscopic lobectomy: an analysis from the European Society of thoracic surgeons database. J Thorac Cardiovasc Surg. 2017;153(4):957–65.

    Article  PubMed  Google Scholar 

  46. Liu T, Feng J, Liu X. Risk factors for extensive subcutaneous emphysema after pulmonary resection by video-assisted thoracoscopic surgery: a case-control study. Wideochir Inne Tech Maloinwazyjne. 2023;18(3):516–23.

    PubMed  PubMed Central  Google Scholar 

  47. Wang L, Dong Y, Ji Y, Song W, Cheng C, Yang M, Che G. Clinical outcome and risk factors for subcutaneous emphysema in patients with lung cancer after video-assisted thorascopic surgery. Front Surg. 2022;9:956431.

    Article  PubMed  PubMed Central  Google Scholar 

  48. Boulemden A, Aifesehi P, Pajaniappane A, Lau K, Bajaj A, Nakas A, Waller DA, Rathinam S. Subcutaneous drain insertion in patients with post-operative extensive subcutaneous surgical emphysema: a single centre experience. Gen Thorac Cardiovasc Surg. 2013;61(12):707–10.

    Article  PubMed  Google Scholar 

  49. Mason DP, Subramanian S, Nowicki ER, Grab JD, Murthy SC, Rice TW, Blackstone EH. Impact of smoking cessation before resection of lung cancer: a society of thoracic surgeons General thoracic surgery database study. Ann Thorac Surg. 2009;88(2):362–70. discussion 370 – 361.

    Article  PubMed  Google Scholar 

  50. Thomsen T, Tønnesen H, Møller AM. Effect of preoperative smoking cessation interventions on postoperative complications and smoking cessation. Br J Surg. 2009;96(5):451–61.

    Article  CAS  PubMed  Google Scholar 

  51. Gajdos C, Hawn MT, Campagna EJ, Henderson WG, Singh JA, Houston T. Adverse effects of smoking on postoperative outcomes in cancer patients. Ann Surg Oncol. 2012;19(5):1430–8.

    Article  PubMed  Google Scholar 

  52. Raupach T, Quintel M, Hinterthaner M. [Preoperative smoking cessation in patients with lung cancer]. Pneumologie. 2010;64(11):694–700.

    Article  CAS  PubMed  Google Scholar 

  53. Lai Y, Su J, Yang M, Zhou K, Che G. [Impact and effect of Preoperative Short-Term Pulmonary Rehabilitation Training on Lung Cancer patients with mild to Moderate Chronic Obstructive Pulmonary Disease: a Randomized Trial]. Zhongguo Fei Ai Za Zhi. 2016;19(11):746–53.

    PubMed  Google Scholar 

  54. Stefanelli F, Meoli I, Cobuccio R, Curcio C, Amore D, Casazza D, Tracey M, Rocco G. High-intensity training and cardiopulmonary exercise testing in patients with chronic obstructive pulmonary disease and non-small-cell lung cancer undergoing lobectomy. Eur J Cardiothorac Surg. 2013;44(4):e260–265.

    Article  PubMed  Google Scholar 

  55. Pu CY, Batarseh H, Zafron ML, Mador MJ, Yendamuri S, Ray AD. Effects of Preoperative Breathing Exercise on postoperative outcomes for patients with Lung Cancer undergoing curative intent lung resection: a Meta-analysis. Arch Phys Med Rehabil. 2021;102(12):2416–e24272414.

    Article  PubMed  PubMed Central  Google Scholar 

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Wei Chen and Qiangqiang Zheng wrote the main manuscript text, Yi Shen, Min Liang, Yang Yuan and Yusong Lu helped perform the analysis with constructive discussions. All authors reviewed the manuscript. All authors read and approved the final manuscript.

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Correspondence to Yunfeng Zhou.

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Chen, W., Zheng, Q., Shen, Y. et al. Relationship between gender and perioperative clinical features in lung cancer patients who underwent VATS lobectomy. J Cardiothorac Surg 19, 689 (2024). https://doiorg.publicaciones.saludcastillayleon.es/10.1186/s13019-024-03211-x

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