Methods: A total of 96 patients (58 males, 38 females; mean age 58.4±11.7 years; range, 18 to 80 years) who underwent video-assisted thoracoscopic surgery or thoracotomy in our hospital between March 2018 and March 2019 were retrospectively analyzed. Demographic and clinical characteristics and comorbidities of the patients were recorded. Quality of life of the patients was evaluated using the Short Form-36 health survey at the first postoperative month.
Results: Of the patients, 43 (44.8%) were treated by video-assisted thoracoscopic surgery and 53 (55.2%) by thoracotomy. Complications occurred in nine (20.9%) patients following video-assisted thoracoscopic surgery and in 12 (22.6%) patients following thoracotomy (p=0.840). At one month postoperatively, the patients in the video-assisted thoracoscopic surgery group had a better quality of life than those in the thoracotomy group (p<0.05).
Conclusion: Our study results suggest that both recovery and short-term quality of life seem to be better in patients undergoing video-assisted thoracoscopic surgery than in those treated by thoracotomy.
In the present study, we aimed to compare the short-term results and QoL of patients undergoing lung resection by VATS versus thoracotomy.
Surgical procedure
Thoracic computed tomography (CT) was
performed in patients with malignant tumors to determine the location of the tumor and its
relationship with the surrounding tissues. Positron
emission tomography (PET)/CT was used to evaluate
distant metastases. Fiberoptic bronchoscopy was
performed in patients with malignant tumors and in
those considered to have benign tumors requiring
endobronchial evaluation. Mediastinal evaluations
were performed via endobronchial ultrasound
and/or mediastinoscopy in patients with malignant
tumors. Pulmonary function tests, arterial blood
gas analysis, and echocardiography were routinely
performed to evaluate cardiopulmonary capacity.
Patients with cardiac comorbidities were assessed
with electrocardiography (ECG) in the cardiology
department. Patients with a forced expiratory
volume in 1 sec (FEV1) of ?40% in the preoperative
pulmonary function tests were subjected to further
pulmonary assessment (i.e., diffusing capacity of
the lung for carbon monoxide, pulmonary perfusion
scintigraphy, and the 6-min walk test).
The comorbidity score was calculated using the 19-item Charlson Comorbidity Index (CCI) which was first introduced in 1987.[12] The CCI score is an independent predictor of both the surgical mortality and long-term survival of cancer patients. A higher CCI score indicates a larger number of comorbidities. A CCI score ≥2 in lung cancer patients is considered a cut-off value for distinguishing mortality from survival.[13,14] Therefore, p atients with a CCI score of ≤2 versus >2 were evaluated separately. Complications which occurred during the first 30 days postoperatively or during hospitalization were also evaluated. The Short Form-36 (SF-36) Health Survey was used to evaluate QoL during the first month postoperatively. Comorbidities were defined as pneumonia, atelectasis, atrial fibrillation, and wound infections during hospitalization.
Statistical analysis
Statistical analysis was performed using the IBM
SPSS version 22.0 software (IBM Corp., Armonk, NY,
USA). Continuous variables were expressed in mean
± standard deviation (SD), median (min-max), while
categorical variables were expressed in number and
percentage. Parametric test assumptions (normality
and homogeneity of variance) were checked before
the groups were compared in terms of the continuous
variables. The difference between the pre- and
postoperative QoL scores was examined using a
t-test for independent groups. The difference in QoL
between the two treatment groups was examined
using the Kruskal-Wallis test. A p value of <0.05 was
considered statistically significant.
Table 1: Baseline demographic and clinical characteristics of patients
Complications occurred in nine (20.9%) patients following VATS and in 12 (22.6%) patients following thoracotomy, indicating no statistically significant difference (p=0.840). However, the QoL of patients undergoing VATS was significantly better than that of patients treated by thoracotomy. Table 2 shows the QoL of the patients undergoing the two procedures.
Table 2: Comparison of quality of life of patient groups
Subgroup analysis showed that, among patients with benign tumors, the QoL was better in the VATS group. However, in patients with malignant tumors, the VATS and thoracotomy groups did not significantly differ with respect to mental health, physical function, physical difficulty, energy vitality or the general perception of health. However, in patients with malignant tumors, the scores of emotional difficulty, social functioning, and pain were higher in the VATS group. The subgroup analysis of QoL is presented in Table 3.
Table 3: Quality of life in VATS and thoracotomy patients with benign and malignant tumors
The use of different questionnaires among studies assessing patient QoL makes it difficult to compare their results. However, randomized studies comparing VATS versus thoracotomy revealed that VATS patients had a better QoL during the first postoperative month, although the difference compared to thoracotomy patients gradually decreased after 26 weeks.[21] In the EuroQol-two dimension scale (EQ2D) study performed by Bendixen et al.,[21] the QoL of patients undergoing VATS improved during the early postoperative period and was higher than that of patients who underwent thoracotomy during the first postoperative year. Zieren et al.[22] reported that the QoL of thoracoscopy patients reached a maximum at nine months. However, whether VATS leads to a better QoL still remains controversial. Some authors have suggested that the benefits of VATS are exaggerated and that the long-term postoperative results do not significantly differ from those of open surgery.[23] Hopkins et al.[24] found that the general status, mood, and pain of patients who underwent lung resection changed from the sixth postoperative month onwards. In the long-term, there was no significant difference in the QoL between patients undergoing VATS versus thoracotomy.
In our study, the SF-36 health survey results showed that the QoL after the first postoperative month was better in the VATS than in thoracotomy patients. In the subgroup analysis, patients with benign tumors who underwent VATS had also a better QoL, while treatment with VATS resulted in significantly better scores for emotional difficulty, social functioning, and pain in patients with malignant tumors. However, this difference may be due to the heterogeneity of the study groups. In the study of Aoki et al.,[25] QoL was significantly higher in the VATS group than the thoracotomy group during the first three months postoperatively, although this difference gradually decreased from 36 months onwards. In their prospective study, Dales et al.[26] also reported a decrease in the QoL during the first three months postoperatively, while there was a subsequent improvement in the QoL as of six to nine months of surgery, similar to the preoperative period.
Nonetheless, there are some limitations to this study. First, it used a retrospective design with a relatively small sample size. Second, the preoperative QoL of the patients was unknown. Third, symptoms of depression and anxiety were unable to be evaluated, and only the short-term postoperative QoL was assessed. Finally, this study did not take into account the heterogeneity between the two groups; the thoracotomy patients in our study had a higher number of comorbidities.
In conclusion, during the first postoperative month, the quality of life of patients who underwent video-assisted thoracoscopic surgery was better than that of patients treated by thoracotomy. The difference was particularly pronounced in the subgroups of patients with benign versus malignant tumors, as patients with benign tumors who underwent video-assisted thoracoscopic surgery had improved quality of life.
Based on these findings, we can suggest that shortterm recovery is better following video-assisted thoracoscopic surgery than thoracotomy. However, further large-scale, long-term, prospective studies are warranted to confirm these findings.
Declaration of conflicting interests
The authors declared no conflicts of interest with respect to
the authorship and/or publication of this article.
Funding
The authors received no financial support for the research
and/or authorship of this article.
1) Whitson BA, Andrade RS, Boettcher A, Bardales R, Kratzke
RA, Dahlberg PS, et al. Video-assisted thoracoscopic
surgery is more favorable than thoracotomy for resection of
clinical stage I non-small cell lung cancer. Ann Thorac Surg
2007;83:1965-70.
2) Sezen CB, Kocatürk Cİ. Videothoracoscopic lobectomy
training in non-small cell lung cancer. Turk Gogus Kalp
Damar Cerrahisi Derg 2019;27:199-205.
3) Rauma V, Andersson S, Robinson EM, Räsänen JV, Sintonen H,
Salo JA, et al. Thoracotomy and VATS Surgery in Local Non-
Small-Cell Lung Cancer: Differences in Long-Term Health-
Related Quality Of Life. Clin Lung Cancer 2019;20:378-83.
4) Long H, Lin ZC, Lin YB, Situ DR, Wang YN, Rong TH.
Quality of life after lobectomy for early stage non-small cell
lung cancer--video-assisted thoracoscopic surgery versus
minimal incision thoracotomy. Ai Zheng 2007;26:624-8.
5) Rogers ML, Duffy JP. Surgical aspects of chronic postthoracotomy
pain. Eur J Cardiothorac Surg 2000;18:711-6.
6) Taylor RS, Ullrich K, Regan S, Broussard C, Schwenkglenks
M, Taylor RJ, et al. The impact of early postoperative pain on
health-related quality of life. Pain Pract 2013;13:515-23.
7) Oh S, Miyamoto H, Yamazaki A, Fukai R, Shiomi K, Sonobe
S, et al. Prospective analysis of depression and psychological
distress before and after surgical resection of lung cancer.
Gen Thorac Cardiovasc Surg 2007;55:119-24.
8) Shigemura N, Akashi A, Funaki S, Nakagiri T, Inoue M,
Sawabata N, et al. Long-term outcomes after a variety
of video-assisted thoracoscopic lobectomy approaches for
clinical stage IA lung cancer: a multi-institutional study. J
Thorac Cardiovasc Surg 2006;132:507-12.
9) Sarna L, Evangelista L, Tashkin D, Padilla G, Holmes C,
Brecht ML, et al. Impact of respiratory symptoms and
pulmonary function on quality of life of long-term survivors
of non-small cell lung cancer. Chest 2004;125:439-45.
10) Barlési F, Doddoli C, Loundou A, Pillet E, Thomas P,
Auquier P. Preoperative psychological global well being
index (PGWBI) predicts postoperative quality of life for
patients with non-small cell lung cancer managed with
thoracic surgery. Eur J Cardiothorac Surg 2006;30:548-53.
11) Walker MS, Zona DM, Fisher EB. Depressive symptoms
after lung cancer surgery: Their relation to coping style and
social support. Psychooncology 2006;15:684-93.
12) Charlson ME, Pompei P, Ales KL, MacKenzie CR. A
new method of classifying prognostic comorbidity in
longitudinal studies: development and validation. J Chronic
Dis 1987;40:373-83.
13) Sezen AI, Sezen CB, Yildirim SS, Dizbay M, Ulutan F.
Cost analysis and evaluation of risk factors for postoperative
pneumonia after thoracic and cardiovascular surgery:
a single-center study. Curr Thorac Surg 2019;4:056-62.
14) Birim O, Kappetein AP, Bogers AJ. Charlson comorbidity
index as a predictor of long-term outcome after surgery
for nonsmall cell lung cancer. Eur J Cardiothorac Surg
2005;28:759-62.
15) Sezen CB, Bilen S, Kalafat CE, Cansever L, Sonmezoglu
Y, Kilimci U, et al. Unexpected conversion to thoracotomy
during thoracoscopic lobectomy: a single-center analysis.
Gen Thorac Cardiovasc Surg 2019;67:969-75.
16) Wildgaard K, Ravn J, Kehlet H. Chronic post-thoracotomy
pain: a critical review of pathogenic mechanisms and strategies
for prevention. Eur J Cardiothorac Surg 2009;36:170-80.
17) Mongardon N, Pinton-Gonnet C, Szekely B, Michel-Cherqui
M, Dreyfus JF, Fischler M. Assessment of chronic pain
after thoracotomy: a 1-year prevalence study. Clin J Pain
2011;27:677-81.
18) Wilson CM, Tobin S, Young RC. The exploding worldwide
cancer burden: the impact of cancer on women. Int J Gynecol
Cancer 2004;14:1-11.
19) Li WW, Lee TW, Lam SS, Ng CS, Sihoe AD, Wan IY, et al.
Quality of life following lung cancer resection: video-assisted
thoracic surgery vs thoracotomy. Chest 2002;122:584-9.
20) Gerbershagen HJ, Rothaug J, Kalkman CJ, Meissner W.
Determination of moderate-to-severe postoperative pain on
the numeric rating scale: a cut-off point analysis applying
four different methods. Br J Anaesth 2011;107:619-26.
21) 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;17:836-44.
22) Zieren HU, Zippel K, Zieren J, Müller JM. Quality of life
after surgical treatment of gastric carcinoma. Eur J Surg
1998;164:119-25.
23) Flores RM. Does video-assisted thoracoscopic surgical
(VATS) lobectomy really result in fewer complications than
thoracotomy? The biases are clear, the role of video-assisted
thoracoscopic surgery less so. J Thorac Cardiovasc Surg
2015;149:645.
24) Hopkins KG, Ferson PF, Shende MR, Christie NA, Schuchert
MJ, Pennathur A. Prospective study of quality of life after
lung cancer resection. Ann Transl Med 2017;5:204.