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Esophagus. 2011 Dec; 8(4): 259–266.
Published online 2011 Sep 10. doi:  10.1007/s10388-011-0291-7
PMCID: PMC3339581

Usefulness of blood supply visualization by indocyanine green fluorescence for reconstruction during esophagectomy



Adequate blood supply for the reconstructed organ is important for safe esophagogastric anastomosis during esophagectomy. Recently, indocyanine green (ICG) has been used for visualization of the blood supply when anastomosis is performed in vascular surgery. To visualize the blood supply for reconstruction, we employed ICG fluorescence during esophagectomy.


From August 2008, 40 patients received cervical or thoracic esophagectomy. They consisted of 33 patients having esophagectomy for thoracic esophageal cancer, 3 being treated for cervical esophageal cancer, and 4 with double cancer of the thoracic and cervical regions. Before and after pulling up the reconstructed organ, 2.5 mg of ICG was injected as a bolus. Then ICG fluorescence was detected by a camera and recorded.


ICG fluorescence was easily detected in all patients at 1 min after injection. The vascular network was well visualized in the gastric wall, colonic grafts, and free jejunal grafts. In five patients, we also performed anastomosis between the short gastric vein and the external cervical vein or superficial cervical vein. The intraoperative and postoperative course of all patients was uneventful apart from three anastomotic leakages.


ICG fluorescence can be employed to evaluate the blood supply to reconstructed organs and can be useful in selecting the patients who do not need additional vessel anastomosis. However, anastomotic leakage was not reduced, so the microcirculation detected by ICG fluorescence did not necessarily provide appropriate blood supply for a viable anastomosis.

Keywords: Anastomotic leakage, Vessel anastomosis, Microcirculation
Keywords: Medicine & Public Health, Thoracic Surgery, Pathology, Surgical Oncology, Oncology, Gastroenterology


Reconstruction of the gastrointestinal tract is still a major issue in patients with gastrointestinal malignancies. In esophageal cancer surgery, anastomotic leakage is one of the important causes of death [1], and the rate of anastomotic leakage ranges from 6.2 to 27% [28]. Among several causes of anastomotic leakage, ensuring an adequate blood supply is the most important point for performing anastomosis safely after esophagectomy. In 1986, we introduced the EEA stapler for esophago-gastrostomy after resection of part of the sternum following subtotal esophagectomy [9], and the average anastomotic leakage rates from 1994 to 2008 were 4.8% (20/416).

Although all of these patients recovered, a method for effective evaluation of the blood supply to the reconstructed organs would be useful.

To assess the blood supply in reconstructed organs, laser Doppler flowmetry has been used, but sufficiently reliable measurements are not obtained [10, 11].

Indocyanine green (ICG) has long been used for the evaluation of liver function. Recently, ICG fluorescence has also been used for the detection of sentinel lymph nodes in breast cancer surgery, gastrectomy, or colorectal cancer surgery, and for visualization of the blood supply after anastomosis during vascular surgery [1217]. To visualize the blood supply of reconstructed organs during esophagectomy, we started to use ICG fluorescence in July 2008. This study was done to evaluate the efficacy of ICG fluorescence based on our experience so far.


Patient characteristics

The patients consisted of 33 having esophagectomy for thoracic esophageal cancer, 3 who were treated for cervical esophageal cancer, and 4 with double cancer of the thoracic and cervical regions. (Table 1). There were 32 men and 8 women with an average age of 66 years (range 49–81 years). Ten patients received preoperative chemotherapy, one patient received preoperative chemo-radiotherapy, and two patients had received radiotherapy several years before surgery.

Table 1
Characteristics of the patients

Operative procedures

After esophagectomy, we made a gastric tube or colonic graft and pulled it up via the retrosternal, posterior mediastinal, or subcutaneous route depending on the patient. We routinely used the retrosternal route. A gastric tube with a width of 4 cm was usually fashioned. Anastomosis was done in the cervical region by hand sewing or circular stapler (25 mm EEA) [9]. When a free jejunal graft was used, we first made a hand sewn pharyngo-jejuno anastomosis and then performed microvascular anastomosis. Finally, the jejuno-esophago anastomosis was done.

Modified procedure

After preparation of the gastric tube, the end of the short gastric vein was cut, and we checked the status of bleeding. If bleeding was not continuous or was very weak, there was a possible need for additional venous drainage. In order to decide whether additional drainage was likely to be effective, we performed ICG fluorescence of the gastric tube. If ICG fluorescence showed a strong microvascular network, we concluded that the gastric tube did not need additional venous drainage or arterial anastomosis. If ICG fluorescence first appeared or became stronger after cutting the short gastric vein, we concluded that additional venous drainage would be effective. If ICG fluorescence did not appear after cutting the short gastric vein, additional arterial anastomosis was added. If additional drainage or anastomosis was needed, anastomosis was performed between the short gastric vein or artery and the external cervical or superficial cervical vein.

ICG imaging

Before and after pulling up the reconstructed organ, 2.5 mg of ICG dye (Diagnogreen; Dai-Ichi Pharm, Tokyo, Japan) was injected as a bolus. Then ICG fluorescence imaging was performed with a near-infrared camera system (Photodynamic Eye; Hamamatsu Photonics K.K, Hamamatsu, Japan), and the images were recorded. In brief, images were obtained with a charge-coupled device (CCD) camera, using a light-emitting diode with a wavelength of 760 nm as the light source and a filter to eliminate light of wavelengths below 820 nm before detection [18] (Fig. 1). Images were sent to a digital video processor and then were displayed on a monitor.

Fig. 1
Near-infrared camera system


Twenty-three patients underwent thoracoscopic-assisted right thoracotomy in the left lateral position, 1 patient received left thoracotomy because of a right aortic arch, 14 patients had esophagectomy in the prone position, and 2 patients received cervical esophagectomy in the supine position. With regard to the method used for reconstruction of the esophagus, a gastric tube was employed in 36 patients, a gastric tube plus free jejunal graft in 1 patient, a free jejunal graft in 2 patients, and an ileo-colonic graft in 1 patient. In 2 patients, reconstruction was done via the posterior mediastinal route, while 5 patients were treated by the subcutaneous route, and the retrosternal route was used in 31 patients (Table 2).

Table 2
Summary of the operative procedures

Fluorescence of the reconstructed esophagus was easily detected in all patients at 1 min after ICG injection. Both arteries and veins were effectively visualized (Fig. 2a, b). Furthermore, microvessels of the gastric wall were well visualized about 2 min after ICG injection (Fig. 3a, b). The blood supply of the free jejunal grafts was also well visualized (Fig. 4a, b).

Fig. 2
ICG fluorescence image of a gastric tube before anastomosis. Blood flow in the arteries and veins is well visualized. a The gastric tube. b ICG fluorescence image. A closed arrow indicates an artery and an open arrow indicates a vein
Fig. 3
Microvessels in the gastric wall are well visualized about 2 min after ICG injection. a Image obtained under normal light. b Blood vessels and microcirculation of the gastric tube. The forceps indicates a small blood vessel in the gastric wall ...
Fig. 4
ICG fluorescence image of a free jejunal graft. a Edematous graft with repeated vascular anastomosis. b Although the graft is edematous, ICG fluorescence can visualize blood flow

In five patients, an anastomosis was added between the short gastric vein and vessels in the neck based on the ICG fluorescence findings. Subsequently, one patient required re-anastomosis because poor circulation was revealed by ICG fluorescence (Fig. 5a, b). We could also effectively visualize blood flow in the colonic graft (Fig. 6a, b).

Fig. 5
Before and after re-anastomosis between the short gastric vein and cervical vein. a ICG fluorescence shows no blood flow in the anastomosed vessel. b ICG fluorescence shows blood flow in the vessel after repeat anastomosis
Fig. 6
ICG fluorescence images of a colonic graft. a The ileo-colic vessels. b There is good blood flow from the middle colic vessels

During this study we evaluated ICG fluorescence using the detection of microcirculation; however, retrospective re-evaluation of the fluorescence status after the period of this study revealed that small vessels were observed in the stump of the reconstructive organ’s wall in 22 cases, (Table 3).

Table 3
The outcome of each patient

There were no severe complications in this series, but two minor and one major anastomotic leakage. In all of the leakage patients, the subcutaneous route was used for reconstruction. Retrospective analysis revealed that there was no anastomotic leakage in the cases where we could observe small vessels in the reconstructive organ’s wall. On the other hand, in 15 out of 18 cases in which we could not observe small vessels in the organ’s wall, anastomotic leakage did not occur. (Table 3).


Although surgical techniques have improved in recent decades and the incidence of anastomotic leakage has decreased to less than 10%, leakage is still one of the factors that influences the postoperative course and survival after en bloc resection of esophageal cancer [19]. Thus, in order to improve the outcome, reducing the occurrence of anastomotic leakage is a major issue in the field of esophageal surgery. The most important predictors of anastomotic leakage are ischemia of the gastric conduit and a low blood oxygen level [20]. Several reports have also suggested that tissue blood flow is worse during the intra-operative and postoperative periods among patients with leakage than those without leakage [10, 11]. Epidural anesthesia may improve blood flow to the gastric tube and reduce the occurrence of anastomotic leakage [20].

To assess the blood supply of reconstructed organs, several studies have employed laser Doppler flowmetry [10, 11, 21]. Recent progress has led to intraoperative fluorescent imaging (IFI) using the SPY system, which allows the evaluation of coronary artery bypass graft patency intraoperatively based on the detection of indocyanine green (ICG) fluorescence [15, 2224].

In the gastrointestinal field, ICG fluorescence has already been used for navigation surgery and for intraoperative detection of hepatocellular carcinoma [18, 25, 26]. In addition, Sekijima et al. [27] introduced ICG fluorescence for organ transplantation. However, detection of the microcirculation in gastrointestinal organs has not been studied much so far [28, 29].

Our results revealed that ICG fluorescence could detect organ blood flow before reconstruction and assist in evaluating the appropriate anastomotic sites. However, the incidence of anastomotic leakage was not reduced. Thus, the microvessels detected by ICG fluorescence did not always provide enough blood for a viable anastomosis. On the other hand, retrospective re-analysis revealed that there was no anastomotic leakage in cases in which we could observe small vessels in the stump of the reconstructive organ’s wall. Thus, observation of microcirculation and small vessels indicates an appropriate organ for anastomosis. However, we could observe microcirculation and small vessels in only about half of our series.

Intraoperative prostaglandin E1 treatment is also not effective for preventing anastomotic insufficiency [10]. Furthermore, gastric perfusion of less than 70% can predict the occurrence of anastomotic stricture but does not predict leakage [21]. Factors other than perfusion may also influence the process of anastomotic healing [21]. Thus, not only the blood supply, but also factors such as the route of anastomosis (retrosternal vs. posterior mediastinal or subcutaneous), the type of gastric tube (narrow or wide), the method of anastomosis (hand sewing, circular stapler, or triangulating stapling) and the tension at the anastomotic site may influence the healing of an anastomosis [10, 11, 20, 3032].

In our series, the subcutaneous route was used in five patients because of the condition of the gastric tube or various anatomical problems, and three of these five patients had leakage. Thus, the need to employ the subcutaneous route may be one of the risk factors for anastomotic leakage [7].

With regard to additional microvascular anastomosis, a significant increase of tissue blood flow was observed after additional venous anastomosis (mean 19%) and also after combined arterial and venous anastomosis (mean 43%) [33]. Thus, additional anastomosis between the short gastric vessels and vessels in the neck resulted in the reduction of anastomotic leakage [34]. We had a good outcome in the present series, so ICG fluorescence may provide useful information to the surgeon about whether patients require additional microvascular anastomosis or not.

Finally, imaging with the photodynamic eye has the following benefits. First, ICG is almost completely washed out within 20 min after injection, so ICG fluorescence can be assessed several times during surgery. Second, we can detect the microcirculation of a target organ as well as the adjacent organs. Third, we can select the patients who do not need additional vessel anastomosis.

In conclusion, imaging of ICG fluorescence can be used to evaluate the blood supply of reconstructed organs and can be useful in selecting the patients who do not need additional vessel anastomosis. However, the microcirculation detected by ICG fluorescence does not necessarily provide enough blood flow to maintain a viable anastomosis. In order to establish more detailed and appropriate ICG fluorescence criteria, an additional and larger study is needed.

Open Access

This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.


1. Alanezi K, Urschel JD. Mortality secondary to esophageal anastomotic leak. Ann Thorac Cardiovasc Surg. 2004;10:71–75. [PubMed]
2. Udagawa H, Akiyama H. Surgical treatment of esophageal cancer: Tokyo experience of the three-field technique. Dis Esophagus. 2001;14:110–114. doi: 10.1046/j.1442-2050.2001.00166.x. [PubMed] [Cross Ref]
3. Ando N, Ozawa S, Kitagawa Y, Shinozawa Y, Kitajima M. Improvement in the results of surgical treatment of advanced squamous esophageal carcinoma during 15 consecutive years. Ann Surg. 2000;232:225–232. doi: 10.1097/00000658-200008000-00013. [PMC free article] [PubMed] [Cross Ref]
4. Tachimori Y, Kanamori N, Uemura N, Hokamura N, Igaki H, Kato H. Salvage esophagectomy after high-dose chemoradiotherapy for esophageal squamous cell carcinoma. J Thorac Cardiovasc Surg. 2009;137:49–54. doi: 10.1016/j.jtcvs.2008.05.016. [PubMed] [Cross Ref]
5. Korst R, Port JL, Lee PC, Altorki NK. Intrathoracic manifestations of cervical anastomotic leaks after transthoracic esophagectomy for carcinoma. Ann Thorac Surg. 2005;80:1185–1190. doi: 10.1016/j.athoracsur.2005.04.020. [PubMed] [Cross Ref]
6. Atkins BZ, Shah AS, Hutcheson KA, Mangum JH, Pappas TN, Harpole DH, et al. Reducing hospital morbidity and mortality following esophagectomy. Ann Thorac Surg. 2004;78:1170–1176. doi: 10.1016/j.athoracsur.2004.02.034. [PubMed] [Cross Ref]
7. Lee Y, Fujita H, Yamana H, Kakegawa T. Factors affecting leakage following esophageal anastomosis. Surg Today. 1994;24:24–29. doi: 10.1007/BF01676880. [PubMed] [Cross Ref]
8. Sarela AI, Tolan DJ, Harris K, Dexter SP, Sue-Ling HM. Anastomotic leakage after esophagectomy for cancer: a mortality-free experience. J Am Coll Surg. 2008;206:516–523. doi: 10.1016/j.jamcollsurg.2007.09.016. [PubMed] [Cross Ref]
9. Imamura M, Ohishi K, Mizutani N, Yanagibashi K, Naito M, Shimada Y, et al. Retrosternal esophagectomy with EEA stapler after subtotal resection of the esophagus: application and results. Dig Surg. 1987;4:101–105. doi: 10.1159/000171780. [Cross Ref]
10. Miyazaki T, Kuwano H, Kato H, Yoshikawa M, Ojima H, Tsukada K, et al. Predictive value of blood flow in the gastric tube in anastomotic insufficiency after thoracic esophagectomy. World J Surg. 2002;26:1319–1323. doi: 10.1007/s00268-002-6366-9. [PubMed] [Cross Ref]
11. Ikeda Y, Niimi M, Kan S, Shatari T, Takami H, Kodaira S. Clinical significance of tissue blood flow during esophagectomy by laser Doppler flowmetry. J Thorac Cardiovasc Surg. 2001;122:1101–1106. doi: 10.1067/mtc.2001.117835. [PubMed] [Cross Ref]
12. Kitai T, Inomoto T, Miwa M, Shikayama T. Fluorescence navigation with indocyanine green for detecting sentinel lymph nodes in breast cancer. Breast Cancer. 2005;12:211–215. doi: 10.2325/jbcs.12.211. [PubMed] [Cross Ref]
13. Tajima Y, Yamazaki K, Masuda Y, Kato M, Yasuda D, Aoki T, et al. Sentinel node mapping guided by indocyanine green fluorescence imaging in gastric cancer. Ann Surg. 2009;249:58–62. doi: 10.1097/SLA.0b013e3181927267. [PubMed] [Cross Ref]
14. Nomura S, Ohue M, Seki Y, Tanaka K, Mottori M, Kishi K, et al. Feasibility of a lateral region sentinel node biopsy of lower rectal cancer guided by indocyanine green using a near-infrared camera system. Ann Surg Oncol. 2010;17:144–151. doi: 10.1245/s10434-009-0711-2. [PubMed] [Cross Ref]
15. Taggart DP, Choudhary B, Anastasiadis K, Abu-Omar Y, Balacumaraswami L, Pigott DW. Preliminary experience with a novel intraoperative fluorescence imaging technique to evaluate the patency of bypass grafts in total arterial revascularization. Ann Thorac Surg. 2003;75:870–873. doi: 10.1016/S0003-4975(02)04669-6. [PubMed] [Cross Ref]
16. Kuroiwa T, Kajimoto Y, Ohta T. Development and clinical application of near-infrared surgical microscope: preliminary report. Minim Invasive Neurosurg. 2001;44:240–242. doi: 10.1055/s-2001-19929. [PubMed] [Cross Ref]
17. Unno N, Suzuki M, Yamamoto N, Inuzuka K, Sagara D, Nishiyama M, et al. Indocyanine green fluorescence angiography for intraoperative assessment of blood flow: a feasibility study. Eur J Vasc Endovasc Surg. 2008;35:205–207. doi: 10.1016/j.ejvs.2007.09.001. [PubMed] [Cross Ref]
18. Kusano M, Tajima Y, Yamazaki K, Kato M, Watanabe M, Miwa M. Sentinel node mapping guided by indocyanine green fluorescence imaging: a new method for sentinel node navigation surgery in gastrointestinal cancer. Dig Surg. 2008;25:103–108. doi: 10.1159/000121905. [PubMed] [Cross Ref]
19. Mariette C, Taillier G, Seuningen IV, Triboulet JP. Factors affecting postoperative course and survival after en bloc resection for esophageal carcinoma. Ann Thorac Surg. 2004;78:1177–1183. doi: 10.1016/j.athoracsur.2004.02.068. [PubMed] [Cross Ref]
20. Michelet P, Journo XBD, Roch A, Papazian L, Ragni J, Thomas P, et al. Perioperative risk factors for anastomotic leakage after esophagectomy. Chest. 2005;128:3461–3466. doi: 10.1378/chest.128.5.3461. [PubMed] [Cross Ref]
21. Pierie JP, Graaf PW, Poen H, Tweel I, Obertop H. Impaired healing of cervical oesophagogastrostomies can be predicted by estimation of gastric serosal blood perfusion by laser Doppler flowmetry. Eur J Surg. 1994;160:599–603. [PubMed]
22. Balacumaraswami L, Abu-Omar Y, Choudhary B, Pigott D, Taggart DP. A comparison of transit-time flowmetry and intraoperative fluorescence imaging for assessing coronary artery bypass graft patency. J Thorac Cardiovasc Surg. 2005;130:315–320. doi: 10.1016/j.jtcvs.2004.11.033. [PubMed] [Cross Ref]
23. Rubens FD, Ruel M, Fremes SE. A new and simplified method for coronary and graft imaging during CABG. Heart Surg Forum. 2002;5:141–414. [PubMed]
24. Detter C, Russ D, Iffland A, Wipper S, Schurr MO, Reichenspurner H, et al. Near-infrared fluorescence coronary angiography: a new noninvasive technology for intraoperative graft patency control. Heart Surg Forum. 2002;5:364–369. [PubMed]
25. Ishizawa T, Bandai Y, Harada N, Muraoka A, Ijichi M, Kusaka K, et al. Indocyanine green-fluorescent imaging of hepatocellular carcinoma during laparoscopic hepatectomy: an initial experience. Asian J Endosc Surg. 2010;3:42–45. doi: 10.1111/j.1758-5910.2009.00025.x. [Cross Ref]
26. Aoki T, Tasuda D, Shimizu Y, Odaira M, Niiya T, Kusano T, et al. Image-guided liver mapping using fluorescence navigation system with indocyanine green for anatomical hepatic resection. World J Surg. 2008;32:1763–1767. doi: 10.1007/s00268-008-9620-y. [PubMed] [Cross Ref]
27. Sekijima M, Tojimbara T, Sato S, Nakamura M, Kawase T, Kai K, et al. An intraoperative fluorescent imaging system in organ transplantation. Transpl Proc. 2004;36:2188–2190. doi: 10.1016/j.transproceed.2004.09.001. [PubMed] [Cross Ref]
28. Okamoto K, Muguruma N, Kimura T, Yano H, Imoto Y, Takagawa M, et al. A novel diagnostic method for evaluation of vascular lesions in the digestive tract using infrared fluorescence endoscopy. Endoscopy. 2005;37:52–57. doi: 10.1055/s-2004-826102. [PubMed] [Cross Ref]
29. Ebihara Y, Okushiba S, Miyasaka D, Sasaki T, Kawarada Y, Kitashiro S, et al. Technical device for reconstruction after thoracic esophagectomy. Geka Chiryo. 2010;102:156–160.
30. Toh Y, Sakaguchi Y, Ikeda O, Adachi E, Ohgaki K, Yamashita Y, et al. The triangulating stapling technique for cervical esophagogastric anastomosis after esophagectomy. Surg Today. 2009;39:201–206. doi: 10.1007/s00595-008-3827-2. [PubMed] [Cross Ref]
31. Pierie JP, Graaf PW, Vroonhoven TJ, Obertop H. The vascularization of a gastric tube as a substitute for the esophagus is affected by its diameter. Dis Esophagus. 1998;11:231–235. [PubMed]
32. Lerut T, Coosemans W, Decker G, Leyn P, Nafteux P, Raemdonck D. Anastomotic complications after esophagectomy. Dig Surg. 2002;19:92–98. doi: 10.1159/000052018. [PubMed] [Cross Ref]
33. Murakami M, Sugiyama A, Ikegami T, Aruga H, Matsushita K, Ishida K, et al. Additional microvascular anastomosis in reconstruction after total esophagectomy for cervical esophageal carcinoma. Am J Surg. 1999;178:263–266. doi: 10.1016/S0002-9610(99)00161-0. [PubMed] [Cross Ref]
34. Murakami M, Sugiyama A, Ikegami T, Ishida K, Maruta F, Shimizu F, et al. Revascularization using the short gastric vessels of the gastric tube after subtotal esophagectomy for intrathoracic esophageal carcinoma. J Am Coll Surg. 2000;190:71–77. doi: 10.1016/S1072-7515(99)00234-3. [PubMed] [Cross Ref]
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