Current status and issues of uniportal video-assisted thoracic surgery in Japan
Original Article: Lung Surgery

Current status and issues of uniportal video-assisted thoracic surgery in Japan

Kyoji Hirai1, Jitsuo Usuda2

1Department of Thoracic Surgery, Nippon Medical School Chiba Hokusoh Hospital, Inzai, Chiba, Japan; 2Division of Thoracic Surgery, Nippon Medical School, Tokyo, Japan

Contributions: (I) Conception and design: Both authors; (II) Administrative support: None; (III) Provision of study materials or patients: K Hirai; (IV) Collection and assembly of data: K Hirai; (V) Data analysis and interpretation: Both authors; (VI) Manuscript writing: Both authors; (VII) Final approval of manuscript: Both authors.

Correspondence to: Kyoji Hirai, MD. Department of Thoracic Surgery, Nippon Medical School Chiba Hokusoh Hospital, 1715 Kamakari, Inzai, Chiba 270-1674, Japan. Email: ky-hirai@nms.ac.jp.

Background: Uniportal video-assisted thoracic surgery (U-VATS) is performed routinely in some countries for respiratory diseases including lung cancer. Several studies report both advantages and disadvantages of the procedure. We review the history of U-VATS in Japan, highlight limitations of the procedure, and discuss the current status and surgical outcomes of U-VATS for anatomical lung resections performed at our institution for patients with early-stage cancer.

Methods: We performed a retrospective review of clinical factors and surgical outcomes in patients with clinical stage I non-small-cell lung cancer who underwent surgery at our institution between 2013 and 2019. We also present representative videos of the procedure performed at our institution and review limitations of the procedure as it becomes more prevalent in Japan.

Results: A total of 152 lobectomies and 33 segmentectomies were performed for clinical stage I non-small-cell lung cancer during the study period. Lobectomy and segmentectomy had a mean operative time of 145±19 and 114±17 min, intraoperative blood loss of 72±11 and 52±9 mL, drainage for 1.9±0.8 and 2.1±0.7 days, hospital length of stay of 7.8±1.4 and 6.8±1.1 days, and the number of 17±3 and 14±4 lymph nodes (LNs) were dissected, respectively. 5.9% and 3.0% of patients underwent conversion to thoracotomy in lobectomy group (LG) and segmentectomy group (SG), respectively. A total of 14 cases developed the complication (12 vs. 2 in LG and SG, respectively). There was no mortality in either group. The average of numeric rating scale (NRS) on postoperative day 30 was 2.1 and 2.4 for lobectomy and segmentectomy, respectively. The 5-year overall survival (OS) rate was 80.1% in LG and the 4-year progression-free survival (PFS) rate of segmentectomy was 94.1%.

Conclusions: We demonstrated that the outcomes of U-VATS for anatomical lung resections in patients with early-stage lung cancer was within permissible range. Our findings suggest that U-VATS anatomical lung resection may be a suitable minimally invasive option to achieve preferable treatment outcomes.

Keywords: Uniportal video-assisted thoracic surgery (U-VATS); multiport video-assisted thoracic surgery (M-VATS); minimally invasive surgery


Received: 03 January 2020; Accepted: 03 February 2020; Published: 05 July 2020.

doi: 10.21037/jovs.2020.02.07


Video 1 Surgical technique of right S3 segmentectomy (5).

Introduction

Uniportal video-assisted thoracic surgery (U-VATS) has become prevalent among thoracic surgeons in a part of countries including Japan (1-3). U-VATS and robotic-assisted thoracoscopic surgery (RATS) are two types of minimally invasive surgical techniques. Uniportal procedures are feasible although they can be technically challenging. RATS is superior to U-VATS in terms of the ability to perform procedures that require fine motor skills and to maintain wide visual fields during the procedure; however, it is not as feasible and more costly compared with U-VATS. U-VATS is also considered safer as it is easier than RATS to be converted to thoracotomy when needed. Thus, suitable procedures should be selected to meet the needs of specific cases. In the present study, we present representative videos of the procedure and review the treatment outcomes of U-VATS for anatomical lung resection that were performed at our institution for patients with early-stage lung cancer.


Methods

A retrospective review of a prospectively maintained database identified 212 patients with clinical stage I non-small-cell lung cancer who underwent curative thoracoscopic surgery at Nippon Medical Chiba Hokusoh Hospital between June 2012 and March 2019. One hundred and fifty-two of lobectomies and 33 of segmentectomies were performed for the patients with clinical stage I lung cancer by the same thoracic surgeon. Our indications for lung segmentectomy included peripheral clinical T1aN0M0 non-small lung cancer with a tumor less than 2 cm in diameter and a ground-glass lesion showing a solid part of less than 50% (4). In identifying the intersegmental lines, inflate-deflate method using 6- or 8-Fr pediatric-size bladder catheter via peripheral bronchus was provided. The representative procedures of uniportal segmentectomy (right anterior segmentectomy) are shown in Video 1. As for segmentectomies, simple segmentectomies were performed. In U-VATS, a 3.5–5.0 cm incision was made on the anterior to middle axillary line, followed by the attachment of a Wrap Protector (Hakko Inc., Japan). Protective procedures to the intercostal nerves were provided by the surgeon and assistants. The procedure was atraumatically performed as much as possible in order to prevent contact between the thoracoscope and forceps and intercostal nerves. The thoracoscope was mostly handled at an angle of more than 45 degrees from the chest wall. Surgery was performed using a 10- or 5-mm 30-degree oblique-viewing thoracoscope and facing/inverted dual-monitors without any specific device. The Wrap Protector mini-mini was routinely used to open incisions, and a small rib retractor was not used. The energy device, HARMONIC scalpel (Ethicon, USA) was used for mediastinal lymph node (LN) dissection. Various surgical factors (operative outcomes), the incidence of complications, postoperative complications (prolonged air leak, atelectasis, empyema, wound infection), and 60-day mortality were evaluated. Postoperative wound pain was monitored using the numeric rating scale (NRS). NRS was evaluated on postoperative day 30. Prognostic evaluation such as progression-free survival (PFS) rate and overall survival (OS) rate using Kaplan-Meier analysis in both groups was carried out.

The study was conducted in accordance with the Declaration of Helsinki (as revised in 2013). The study was approved by the institutional review board and the committee of Nippon Medical Chiba Hokusoh Hospital (No. 616). Informed consent to use the data-use agreement including surgical video was obtained from all patients before surgery.

Statistical analysis

Quantitative variables are presented as medians [± standard deviation (SD)] or ranges where appropriate. Continuous variables were compared using the Mann-Whitney U test where appropriate. The Kaplan-Meier method was used to visualize PFS and OS of segmentectomy group (SG) and lobectomy group (LG). All statistical analyses were performed with the software SPSS version 17 for Windows (IBM Corp, Armonk, NY, USA). P values of <0.05 were considered to indicate significance for all parameters.


Results

Preoperative data and resected lobe of lung

From 2013 to 2019, we performed 152 lobectomies and 33 segmentectomies by U-VATS for clinical stage I lung cancer. The preoperative patient’s characteristics are summarized in Table 1. As shown in Table 1, in LG and SG, age, sex, tumor size, forced expiratory volume 1.0 s (Fev 1.0), histology and fissure statement were indicated.

Table 1

Clinical characteristics of study population

Characteristics SG (n=33) LG (n=152) P value
Age (years) 66±4 69±8 0.74
Sex, n (%) 0.33
   Male 19 (57.6) 101 (66.4)
   Female 14 (42.4) 51 (33.6)
Tumor size (cm) 1.5±0.4 2.7±0.7 0.74
Fev1.0 (liter) 1.7±0.4 1.9±0.6 0.32
Histology, n (%) 0.38
   SC 9 (27.3) 31 (20.4)
   AD 24 (72.7) 121 (79.6)
Fissure statement, n (%) 0.29
   Developed 18 (54.5) 98 (64.5)
   Not well developed 15 (45.5) 54 (35.5)

Data are presented as mean ± SD or number (percentage). SD, standard deviation; SG, segmentectomy group; LG, lobectomy group; Fev 1.0, forced expiratory volume in 1.0 s; SC, squamous cell carcinoma; AD, adenocarcinoma.

Postoperative data

The mean postoperative wound length in both groups was 4.2 cm. Distribution of lobectomies in both groups is shown in Figure 1. The most of the lobectomies in LG was right upper (RU) lobectomies and S6 segmentectomy was the most in SG. The postoperative outcomes are shown in Table 2. The data of LG are shown as follows. The median operative time was 145±19 min, and the median operative blood loss was 72±11 mL. The mean number of dissected LNs was 17±3. The mean duration of the drainage duration and postoperative hospital stay and were 1.9±0.8 and 7.8±1.4, respectively. In SG, the median operative time was 114±17 min, and the median operative blood loss was 52±9 mL. The mean number of dissected LNs was 14±4. The mean duration of the drainage duration and postoperative hospital stay and were 2.1±0.7 and 6.8±1.1, respectively. With regard to the operation time, blood loss, the number of dissected LNs, drainage duration, hospital stays, conversion rate to thoracotomy, incidence of postoperative complications including 7 prolonged air leakages lasting more than 5 days, 3 atelectasis requiring bronchoscopic suction after operation, 2 empyema requiring prolonged drainage and 2 wound infection requiring drainage. No mortality was recorded in both groups. The average of NRS on postoperative day 30 was 2.1 in LG and 2.4 in SG. According to Kaplan-Meier analysis, the 5-year OS rate and the 5-year PFS rate was 80.1% and 78.5% in LG (Figure 2 A,B) and was 100% and 94.1% (Figure 3) in SG.

Figure 1 Distribution of segmentectomy and lobectomy in U-VATS. RU, right upper; RM, right middle; RL, right lower; LU, left upper; LL, left lower; RUM, right upper and middle; RML, right middle and lower.

Table 2

Postoperative outcomes

Variables SG (n=33) LG (n=152) P value
Operation time (min) 114±17 145±19 0.32
Blood loss (mL) 52±9 72±11 0.44
The number of dissected LN 14±4 17±3 0.47
Drainage duration (days) 2.1±0.7 1.9±0.8 0.65
Hospital stay after op. (days) 6.8±1.1 7.8±1.4 0.70
Conversion to thoracotomy (%) 1 (3.0) 9 (5.9) 0.81
NRS on POD 30 2.4±0.5 2.1±0.9 0.67
Morbidity, n (%) 2 (6.1) 12 (7.9) 0.98
Mortality, n (%) 0 0

Data are presented as mean ± SD or number (percentage). Postoperative complications were including with prolonged air leak more than 5 days after surgery, atelectasis, empyema and wound infection. SD, standard deviation; SG, segmentectomy group; LG, lobectomy group; LN, lymph node; NRS, numeric rating scale.

Figure 2 Kaplan-Meier analysis of OS and PFS after U-VATS lobectomy (n=152). The 5-year OS rate (A) and the 5-year PFS rate (B) in LG was 80.1% and 78.5%. LG, lobectomy group; U-VATS, uniportal video-assisted thoracic surgery; OS, overall survival; PFS, progression-free survival.
Figure 3 Kaplan-Meier analysis of PFS after U-VATS segmentectomy (n=33). The 5-year PFS rate in SG was 94.1%. SG, segmentectomy group; U-VATS, uniportal video-assisted thoracic surgery; PFS, progression-free survival.

Discussion

The recent consensus report from the Uniportal VATS Interest Group (UVIG) of the European Society of Thoracic Surgeons (ESTS) describes the procedures of U-VATS for lobectomy (6). The report was generated based on questionnaires from 31 thoracic surgeons in 18 countries. According to the report, U-VATS was typically performed with <4 cm incision on the anterior axillary or middle-anterior axillary line, with a surgical assistant standing on the same side as the primary surgeon. In terms of the indications for U-VATS, 65% of the surgeons considered T1 and T2b stages to be appropriate for U-VATS and only 7% of them considered N0 to be a contraindication for U-VATS. Furthermore, only 3% of them considered that U-VATS should be contraindicated for patients at high risk of adhesion such as those with a history of pleurisy. Future studies on U-VATS should provide additional insights as to the characteristics of U-VATS. M-VATS is difficult to characterize since the specific procedures of M-VATS, such as the position and number of trocars, often vary across different institutions. On the other hand, the minimally invasive nature of U-VATS can be easily evaluated since there is only one incision made to the chest wall, thus facilitating the standardization of the procedure.

We have already performed over 200 cases of U-VATS for anatomical lung resections. Based on our experience, U-VATS is technically more suited than M-VATS for the resection of well-lobulated lungs. The technical procedures involved in U-VATS are more intuitive than M-VATS. Although there is some interreference with surgical instruments, procedural movements during U-VATS are similar to those performed during thoracotomy. In addition, some studies suggest that U-VATS may shorten the duration of RU lobectomies (7). Actually, in our study, there was no significant difference in regard with the operative outcomes of U-VATS anatomical lung resection. The conversion rates to thoracotomy were also within the permissible range. Especially as for converting U-VTAS lobectomy, we reviewed based on three reports including our data (2,8,9).

Notably, U-VATS is associated with a low risk of post-thoracotomy pain syndrome that can occur in some patients and typically lasts for over 2 months. We previously performed a retrospective study and demonstrated that the rate of post-thoracotomy pain syndrome was lower in patients who underwent U-VATS compared to those who underwent M-VATS (10). Acute pain is often caused by the presence of a drain in the surgical site, and typically resolves after the removal of the drain. Patients with narrower intercostal spaces tend to be at a higher risk of post-thoracotomy pain syndrome, and may require conversion to the dual portal procedure to avoid contact between surgical instruments and the intercostal nerves.

Currently, U-VATS is most commonly performed in China. In contrast to RATS, U-VATS can be performed within a shorter period of time, allowing to fit in 3–4 surgical cases for lung cancer in a day. Given its convenience, U-VATS is likely more optimal in terms of health care efficiency for early-stage cancer. RATS is likely more suited for cases with a narrow surgical field that require superior motor skills. In thoracic surgery, these cases may include angioplasty, bronchoplasty, and LN dissection. In fact, a study demonstrated that RATS had a superior propensity score than U-VATS in terms of the number of LNs dissected (11). We anticipate that an increasing number of workshops for U-VATS will be held in Japan, and consequently, U-VATS will become more common in institutions that do not have or have the capacity to use surgical robots.

In this report, clinical data and prognostic evaluation are originated from single center and the same surgeon operated all patients for approximately 6 years. In our experience, compared to M-VATS, U-VATS has some disadvantages in terms of surgical quality in present, however if surgeons blush up their techniques much more, this procedures will be refined and common in thoracic surgeons considering the history that spread M-VATS over the world previously.


Acknowledgments

Funding: None.


Footnote

Provenance and Peer Review: This article was commissioned by the Guest Editor (Meinoshin Okumura) for the series “Dedicated to the 36th Annual Conference of Japanese Association for Chest Surgery” published in Journal of Visualized Surgery. The article has undergone external peer review.

Conflicts of Interest: Both authors have completed the ICMJE uniform disclosure form (available at https://jovs.amegroups.com/article/view/10.21037/jovs.2020.02.07/coif). The series “Dedicated to the 36th Annual Conference of Japanese Association for Chest Surgery” was commissioned by the editorial office without any funding or sponsorship. The authors have no other 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 and the committee of Nippon Medical Chiba Hokusoh Hospital (No. 616). Informed consent to use the data-use agreement including surgical video was obtained from all patients before surgery.

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/.


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doi: 10.21037/jovs.2020.02.07
Cite this article as: Hirai K, Usuda J. Current status and issues of uniportal video-assisted thoracic surgery in Japan. J Vis Surg 2020;6:27.

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