Clinical applications of fluorescence imaging in laparoscopic surgery
Editorial

Clinical applications of fluorescence imaging in laparoscopic surgery

The laparoscopic approach has greatly improved patient care throughout various surgical subspecialties. Minimizing surgical trauma has a beneficial effect on patient recovery and decreases complications. Another advantage of laparoscopy is the improved surgical view. Not only due to improved monitors (4K), magnification and 3d view, but more recently also through image guided techniques, such as fluorescent imaging. Using specific (targeted) agents important anatomical structures can be visualized even more precisely. In this series of Laparoscopic Surgery we highlight the clinical application of fluorescence imaging throughout various laparoscopic abdominal surgical procedures. Due to the recent standard incorporation of fluorescent imaging capabilities in most mainstream laparoscopic/robotic surgery systems, the majority of laparoscopic surgeons now a days has the ability to use this technique. The principle consists of adding an exogenous fluorophore into the patient, intravenously or directly in tissue of relevance, providing highly sensitive discrimination of a relevant target within the surgical field (1). Most of the fluorescent systems use the near-infrared region (700–900 nm) as it has advantage over visible light in, for example, enhanced debt penetration (5–10 mm, depending on the tissue) and invisibility to the human eye and therefore not changing the surgical field (2). The technique had a relatively fast clinical introduction due to the availability of non-specific fluorophores methylene blue (700 nm) and indocyanine green (ICG, 800 nm) that could be used off-label (3). Although the technique is quite easy to use, in our opinion still a short learning curve must be completed of at least 20 procedures to get familiar with the technique.

A recent PubMed search (Figure 1) shows an increasing number of manuscripts that are published yearly about fluorescence and laparoscopic surgery marking its growing relevance in clinical practice. Especially non-specific ICG is frequently used due to its wide availability, good fluorescent properties, low costs and negligible adverse events. Application has been described in various fields such as biliary tract imaging (4,5), donor nephrectomies (4), colorectal surgery (6), liver surgery (7,8), lung surgery (9), gastric surgery (10,11), bowel and esophageal anastomoses (12-14), lymph node mapping (15,16), endocrine surgery (17), evaluation of perfusion of colon (18) and peritoneum (19), ureter imaging (20), tumor-specific imaging (21) and for the identification of occult pulmonary (22) or abdominal lesions (23). Specific tracers are in development that recognize vital structures or tumors and show promising results but are all still in pre-clinical phases or in clinical trials and not freely available (24).

Figure 1 Graph shows the number of published manuscripts between 1985 and April 2021 on pubmed.gov using the following search: “fluorescence AND laparoscopic AND surgery”.

The disadvantage of fluorescence imaging is the relatively low tissue penetration. Therefore, the focus of this technique is on visualizing superficial anatomical structures in addition to intraoperative ultrasound and preoperative imaging techniques rather than a stand-alone application (25). Nevertheless, applications such as lymph node detection, evaluating tissue perfusion and ureter- and biliary tract imaging can benefit from fluorescence alone. We believe that fluorescent imaging is changing intraoperative decision making and will result in more radical surgeries, better recognition of vital structures, better evaluation of tissue quality, less iatrogenic damage and therefore less morbidity and mortality and possibly even increased patient survival. Future developments must focus on enhancing the sensitivity and resolution of the cameras, and developing advanced (targeted) tracers for specific tumor detection integrating the technique with preoperative CT and PET scans and intraoperative ultrasound. Furthermore, research must focus more on the added clinical benefit of the technique, as in changing intraoperative decision making, rather than on its diagnostic performance (26).

This series include a comprehensive overview of fluorescence imaging during robotic surgery and reviews about liver surgery, colorectal liver metastases surgery, lymphadenectomy during colorectal surgery and dyes for real-time ureter imaging. We hope this series will be of interest for all readers providing useful information about the current status of fluorescence guided laparoscopic surgery. We thank Laparoscopic Surgery journal for the invitations to be guest editors and all authors for their contribution.


Acknowledgments

We greatly thank all the authors for their valuable contribution.

Funding: None.


Footnote

Provenance and Peer Review: This article was commissioned by the editorial office, Laparoscopic Surgery for the series “Clinical Applications of Fluorescence Imaging in Laparoscopic Surgery”. The article did not undergo external peer review.

Conflicts of Interest: Both authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/ls-21-11). The series “Clinical Applications of Fluorescence Imaging in Laparoscopic Surgery” was commissioned by the editorial office without any funding or sponsorship. HAM and MCB served as the unpaid Guest Editors of the series. 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.

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

  1. Vahrmeijer AL, Hutteman M, van der Vorst JR, et al. Image-guided cancer surgery using near-infrared fluorescence. Nat Rev Clin Oncol 2013;10:507-18. [Crossref] [PubMed]
  2. Hyun H, Henary M, Gao T, et al. 700-nm Zwitterionic Near-Infrared Fluorophores for Dual-Channel Image-Guided Surgery. Mol imaging Biol 2016;18:52-61. [Crossref] [PubMed]
  3. Frangioni JV. In vivo near-infrared fluorescence imaging. Curr Opin Chem Biol 2003;7:626-34. [Crossref] [PubMed]
  4. Boni L, David G, Mangano A, et al. Clinical applications of indocyanine green (ICG) enhanced fluorescence in laparoscopic surgery. Surg Endosc 2015;29:2046-55. [Crossref] [PubMed]
  5. Verbeek FPR, Schaafsma BE, Tummers QRJG, et al. Optimization of near-infrared fluorescence cholangiography for open and laparoscopic surgery. Surg Endosc 2014;28:1076-82. [Crossref] [PubMed]
  6. Son GM, Kwon MS, Kim Y, et al. Quantitative analysis of colon perfusion pattern using indocyanine green (ICG) angiography in laparoscopic colorectal surgery. Surg Endosc 2019;33:1640-9. [Crossref] [PubMed]
  7. Nakaseko Y, Ishizawa T, Saiura A. Fluorescence-guided surgery for liver tumors. J Surg Oncol 2018;118:324-31. [Crossref] [PubMed]
  8. Urade T, Sawa H, Iwatani Y, et al. Laparoscopic anatomical liver resection using indocyanine green fluorescence imaging. Asian J Surg 2020;43:362-8. [Crossref] [PubMed]
  9. Motono N, Iwai S, Funasaki A, et al. Uramoto H. Low-dose indocyanine green fluorescence-navigated segmentectomy: prospective analysis of 20 cases and review of previous reports. J Thorac Dis 2019;11:702-7. [Crossref] [PubMed]
  10. Ortega CB, Guerron AD, Yoo JS. The Use of Fluorescence Angiography During Laparoscopic Sleeve Gastrectomy. JSLS. 2018;22:e2018.00005.
  11. Ushimaru Y, Omori T, Fujiwara Y, et al. The Feasibility and Safety of Preoperative Fluorescence Marking with Indocyanine Green (ICG) in Laparoscopic Gastrectomy for Gastric Cancer. J Gastrointest Surg 2019;23:468-76. [Crossref] [PubMed]
  12. Alekseev M, Rybakov E, Shelygin Y, et al. A study investigating the perfusion of colorectal anastomoses using fluorescence angiography: results of the FLAG randomized trial. Colorectal Dis 2020;22:1147-53. [Crossref] [PubMed]
  13. Boni L, David G, Dionigi G, et al. Indocyanine green-enhanced fluorescence to assess bowel perfusion during laparoscopic colorectal resection. Surg Endosc 2016;30:2736-42. [Crossref] [PubMed]
  14. Luo RJ, Zhu ZY, He ZF, et al. Efficacy of Indocyanine Green Fluorescence Angiography in Preventing Anastomotic Leakage After McKeown Minimally Invasive Esophagectomy. Front Oncol 2021;10:619822 [Crossref] [PubMed]
  15. Chen QY, Xie JW, Zhong Q, et al. Safety and Efficacy of Indocyanine Green Tracer-Guided Lymph Node Dissection During Laparoscopic Radical Gastrectomy in Patients With Gastric Cancer: A Randomized Clinical Trial. JAMA Surg 2020;155:300-11. [Crossref] [PubMed]
  16. Yeung TM, Wang LM, Colling R, et al. Intraoperative identification and analysis of lymph nodes at laparoscopic colorectal cancer surgery using fluorescence imaging combined with rapid OSNA pathological assessment. Surg Endosc 2018;32:1073-6. [Crossref] [PubMed]
  17. Bonnin-Pascual J, Álvarez-Segurado C, Jiménez-Segovia M, et al. Contributions of fluorescence to endocrine surgery. Cir Esp 2018;96:529-36. [Crossref] [PubMed]
  18. Wada T, Kawada K, Takahashi R, et al. ICG fluorescence imaging for quantitative evaluation of colonic perfusion in laparoscopic colorectal surgery. Surg Endosc 2017;31:4184-4193. [Crossref] [PubMed]
  19. Albers KI, Polat F, Loonen T, et al. Visualising improved peritoneal perfusion at lower intra-abdominal pressure by fluorescent imaging during laparoscopic surgery: A randomised controlled study. Int J Surg 2020;77:8-13. [Crossref] [PubMed]
  20. de Valk KS, Handgraaf HJ, Deken MM, et al. A zwitterionic near-infrared fluorophore for real-time ureter identification during laparoscopic abdominopelvic surgery. Nat Commun 2019;10:3118. [Crossref] [PubMed]
  21. Boogerd LSF, Hoogstins CES, Schaap DP, et al. Safety and effectiveness of SGM-101, a fluorescent antibody targeting carcinoembryonic antigen, for intraoperative detection of colorectal cancer: a dose-escalation pilot study. Lancet Gastroenterol Hepatol 2018;3:181-91. [Crossref] [PubMed]
  22. Newton AD, Predina JD, Nie S, et al. Intraoperative fluorescence imaging in thoracic surgery. J Surg Oncol 2018;118:344-55. [Crossref] [PubMed]
  23. Boogerd LSF, Handgraaf HJM, Lam HD, et al. Laparoscopic detection and resection of occult liver tumors of multiple cancer types using real-time near-infrared fluorescence guidance. Surg Endosc 2017;31:952-61. [Crossref] [PubMed]
  24. Hernot S, van Manen L, Debie P, et al. Latest developments in molecular tracers for fluorescence image-guided cancer surgery. Lancet Oncol 2019;20:e354-67. [Crossref] [PubMed]
  25. Keereweer S, Van Driel PBAA, Snoeks TJA, et al. Optical image-guided cancer surgery: challenges and limitations. Clin Cancer Res 2013;19:3745-54. [Crossref] [PubMed]
  26. Lauwerends LJ, van Driel PBAA, Baatenburg de Jong RJ, et al. Real-time fluorescence imaging in intraoperative decision making for cancer surgery. Lancet Oncol 2021;22:e186-95. [Crossref] [PubMed]
Hendrik A. Marsman, MD, PhD
Martin C. Boonstra, MD

Hendrik A. Marsman, MD, PhD

Department of Surgery, OLVG, Amsterdam, the Netherlands.
(Email: h.a.marsman@olvg.nl)

Martin C. Boonstra, MD, PhD

Department of Surgery, Amsterdam University Medical Center, Amsterdam, the Netherlands.
(Email: m.c.boonstra@amsterdamumc.nl)

Received: 29 April 2021; Accepted: 10 May 2021; Published: 25 July 2021.

doi: 10.21037/ls-21-11

doi: 10.21037/ls-21-11
Cite this article as: Marsman HA, Boonstra MC. Clinical applications of fluorescence imaging in laparoscopic surgery. Laparosc Surg 2021;5:27.

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