Esophagus

, Volume 8, Issue 4, pp 259–266

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

  • Yutaka Shimada
  • Tomoyuki Okumura
  • Takuya Nagata
  • Shigeaki Sawada
  • Koshi Matsui
  • Ryota Hori
  • Isaku Yoshioka
  • Toru Yoshida
  • Ryusuke Osada
  • Kazuhiro Tsukada
Open AccessOriginal Article

DOI: 10.1007/s10388-011-0291-7

Cite this article as:
Shimada, Y., Okumura, T., Nagata, T. et al. Esophagus (2011) 8: 259. doi:10.1007/s10388-011-0291-7

Abstract

Background

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.

Methods

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.

Results

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.

Conclusions

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 leakageVessel anastomosisMicrocirculation

Introduction

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.

Methods

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

 

Number

Age

66 (49–81)

Sex

 Male

32

 Female

8

Tumor location

 PhMt

2

 CeMt

2

 Ce

3

 Ut

2

 Mt

19

 Lt

12

TNM stagea

 1

10

 2a

5

 2b

5

 3

18

 4

2

Preoperative treatment

 Chemotherapy

10

 Chemoradiotherapy

1

 Radiotherapy

2

 None

27

Ph pharynx, Ce cervical esophagus, Ut upper thoracic esophagus, Mt middle thoracic esophagus, Lt lower thoracic esophagus, Ae abdominal esophagus

aUICC TNM 6th edition

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

Results

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

 

Number

Reconstruction method

 Gastric tube

36

 Free jejunal graft + gastric tube

1

 Free jejunal graft

2

 Ileo-colonic graft

1

Reconstruction route

 Retrosternal

31

 Posterior mediastinal

2

 Subcutaneous

5

 Cervical

2

Additional vascular anastomosis

 Yes

5

 No

35

Surgical position

 Lateral

24

 Prone

14

 Supine

2

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 and closed arrow indicates microcirculation

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

Patient no.

Age/gender

Stage

Tumor location

Reconstruction method

Pull-up route

Method of thoracotomy

Preoperative treatment

Associated conditions

Vascular anastomosis

Anastomotic leakage

ICG (microcirculation in the stump)

ICG (small vessel in the stump)

1

59/M

T3N0M0 stage 2a

Mt

G

R

L

Observed

Observed

2

59/M

T3N1M0 stage 3

Mt

G

P

L

FP × 2

Funnel chest

Rectal cancer

Observed

Observed

3

66/M

T3N0M0 stage 2a

Lt

G

R

L

Obesity (BMI 30)

Observed

Observed

4

70/M

T1N0M0 stage 1

PhMt

G

R

L

Pharyngeal cancer, DM

Observed

Observed

5

62/M

T1N1M0 stage 2b

Lt

G

R

L

Renal failure

+

Observed

Not observed

6

70/M

T3N1M0 stage 3

Mt

G

R

L

FP × 2

Observed

Not observed

7

76/F

T3N1M0 stage 3

Mt

G

R

L

FP + 40 Gy

Observed

Not observed

8

58/M

T3N1M0 stage 3

Lt

G

R

L

Observed

Not observed

9

70/M

T3N1M0 stage 3

Lt

G

S

L

Colon cancer

+

+

Observed

Not observed

10

78/M

T3N1M0 stage 3

Mt

G

R

L

Observed

Not observed

11

56/F

T4N1M0 stage 3

Mt

G

R

L

Observed

Observed

12

76/M

T1N0M0 stage 1

Ce

J

60 Gy (9 years before)

+

Observed

Observed

13

56/F

T2N0M0 stage 2a

Ce

J

FP

+

Observed

Observed

14

68/M

T1N1M0 stage 2b

Mt

G

R

L

FP

Observed

Observed

15

62/M

T1N1M0 stage 2b

PhMt

G + J

R

L

FP

Pharyngeal cancer

+

Observed

Observed

16

71/M

T2N0M0 stage 2a

Mt

G

S

R

Right aortic arch

+

Observed

Not observed

17

81/M

T3N1M0 stage 3

Lt

G

R

L

Observed

Observed

18

67/M

T4N1M0 stage 3

CeMt

G

R

L

+

Observed

Not observed

19

54/M

T1N0M0 stage 1

Mt

G

R

L

Observed

Observed

20

67/M

T1N0M0 stage 1

Mt

C

S

L

Observed

Observed

21

76/M

T1N1M0 stage 2b

Mt

G

R

L

Observed

Observed

22

79/M

T2N0M0 stage 2a

Mt

G

R

L

Lung cancer

Observed

Not observed

23

61/F

T1N0M0 stage 1

Mt

G

R

L

Observed

Observed

24

60/M

T1N1M1 stage 4

CeMt

G

R

L

60 Gy

+

Observed

Not observed

25

67/M

T1N0M0 stage 1

Ce

G

P

L

+

Observed

Not observed

26

64/M

T2N1M0 stage 2b

AeLt

G

R

L

Observed

Not observed

27

58/M

T3N1M0 stage 3

Lt

G

R

P

Observed

Observed

28

74/M

T1N0M0 stage 1

Mt

G

R

P

Observed

Not observed

29

68/F

T1N0M0 stage 1

AeLt

G

R

P

Observed

Observed

30

65/M

T1N0M0 stage 1

UtMtLt

G

R

P

Observed

Observed

31

71/F

T3N1M0 stage 3

Mt

G

R

P

FP

Bilateral breast cancer

Observed

Not observed

32

67/M

T4N1M0 stage 3

Mt

G

S

P

DCF

+

Observed

Not observed

33

49/F

T3N1M0 stage 3

Mt

G

R

P

Observed

Observed

34

61/F

T1N1M1 stage 4

Mt

G

R

P

FP

Observed

Observed

35

70/M

T3N1M0 stage 3

Lt

G

S

P

Observed

Not observed

36

63/M

T3N1M0 stage 3

LtAe

G

R

P

Observed

Observed

37

67/M

T3N1M0 stage 3

Mt

G

R

P

FP

Observed

Not observed

38

60/M

T3N1M0 stage 3

LtAe

G

R

P

Observed

Observed

39

47/F

T3N1M0 stage 3

LtAe

G

R

P

DCF

Observed

Observed

40

68/M

T1N0M0 stage 1

Ut

G

R

P

Gastric cancer

Observed

Not observed

G gastric tube, J free jejunal graft, C colonic graft, R retrosternal, P posterior mediastinal, S subcutaneous, L left lateral position with VATS, R right lateral position with VATS, S supine position, P prone position, FP 5-FU plus cisplatin, DCF FP plus docetaxel

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).

Discussion

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

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Copyright information

© The Author(s) 2011

Authors and Affiliations

  • Yutaka Shimada
    • 1
  • Tomoyuki Okumura
    • 1
  • Takuya Nagata
    • 1
  • Shigeaki Sawada
    • 1
  • Koshi Matsui
    • 1
  • Ryota Hori
    • 1
  • Isaku Yoshioka
    • 1
  • Toru Yoshida
    • 1
  • Ryusuke Osada
    • 2
  • Kazuhiro Tsukada
    • 1
  1. 1.Department of Surgery and Science, Graduate School of Medicine and Pharmaceutical Sciences for ResearchUniversity of ToyamaToyamaJapan
  2. 2.Department of Orthopedics, Graduate School of Medicine and Pharmaceutical Sciences for ResearchUniversity of ToyamaToyamaJapan