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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Results
  • Discussion
  • Disclosures
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

High-grade hemostatic devices are essential for laparoscopic hepatectomy. However, these devices are not generalized in basic medical organizations. Therefore, a suite of simple and easy hemostatic devices is shown in this article, which can make the laparoscopic hepatectomy easier to perform.

Abstract

Laparoscopic hepatectomy is considered a conventional method for treating benign and malignant liver diseases because it is a minimally invasive method. Despite its non-invasive aspect, bleeding and bile leakage occur in liver parenchyma tissue resection during the operation or in the post-operation period, indicating the requirement for high-grade hemostatic devices, such as ultrasonic surgical aspiration, bipolar electrocoagulation, etc. The lack of availability of these high-grade hemostatic devices prevents laparoscopic hepatectomy from becoming a generalized procedure in basic medical organizations. In view of the situation mentioned above, a suite of simple and easy hemostatic devices is developed in this protocol, which includes a harmonic scalpel, monopole electrocoagulation, and a single lumen catheter, to innovatively perform liver parenchyma tissue resection. First of all, the porta hepatis or hepatic pedicle is occluded intermittently by a single lumen catheter, followed by clamping for 15 min and releasing for 5 min. Subsequently, using the harmonic scalpel, clamping and crushing of the liver are done to cut off the hepatic parenchyma tissue and to reveal the intrahepatic arteries, veins, and bile ducts. Lastly, the bleeding spots are coagulated by using monopole electrocoagulation at each spot. Intrahepatic pipeline structures are then visible by using these methods, which could stop bleeding easily, reduce the incidence rate of bile leakage, and improve the safety and feasibility of laparoscopic hepatectomy. Therefore, the simple and easy hemostatic devices shown here are suitable for conducting procedures in primary medical institutions.

Introduction

Hepatocellular carcinoma is one of the most common malignant tumors of the digestive system. According to the different primary sites, it can be divided into primary hepatocellular carcinoma and secondary liver cancer. Cells can metastasize from primary tumors from organs outside the liver into the liver in various ways, leading to carcinoma in the liver. It has been reported that more than 50% of metastatic cells in the liver come from colorectal cancer, while others are from breast, pancreas, lung, and stomach tumors, etc1. In recent years, many treatments for secondary liver cancer are available, including systematic chemotherapy, interventional therapy, molecular targeted therapy, surgery, etc2. However, radical resection is still the most effective treatment because it can completely remove the cancer3.

With the rapid development of laparoscopic technology, laparoscopic anatomical hepatectomy is gradually recognized by surgeons but is still not widely performed, especially in primary medical institutions. One of the reasons is the requirement for high-grade hemostatic devices. These are required to reduce the risks of bleeding and bile leakage during the operation process. Here, we present a set of simple and easy hemostatic equipment, including a single lumen catheter, harmonic scalpel, and monopole electrocoagulation, for performing laparoscopic hepatectomy. To do this, first the porta hepatis is occluded intermittently by using a single lumen catheter. Liver parenchyma tissue is then resected by using the harmonic scalpel. Bleeding spots are coagulated by monopole electrocoagulation point-to-point. This simple and easy hemostatic equipment uses a single lumen catheter to perform the pringle maneuver and utilizes the hemostasis of the harmonic scalpel and monopole electrocoagulation. The equipment can be found easily in hospitals, thereby providing added ease for performing laparoscopy or training. Thus, these simple and easy hemostatic devices are suitable for conducting procedures in primary medical institutions.

In this study, the patient was a 67-year-old male diagnosed with a moderately differentiated adenocarcinoma of the sigmoid colon metastasized in the liver. Radical resection of the sigmoid colon cancer was performed in January 2021. The pathological results were moderately differentiated adenocarcinoma with the TNM stage of pT4aN2aM1. FOLFOX chemotherapy was given four times after the operation. Following this, the patient's body condition was deemed suitable to perform laparoscopic anatomical hepatectomy to completely remove the lesion of liver metastases. The Child-Pugh grade of liver function was Grade A. For the liver reserve function test, R15 in the ICG clearance test was 1.6% (<10%). CT showed a 57 mm x 68 mm x 76 mm tumor across the dorsal part of S5 and ventral part of S6 of the liver; the three-dimensional reconstruction model is shown in Figure 1.

Protocol

The operation is routine and received ethics approval. The approvals are as follows: Approval for rapid review by the Clinical Research and Application Ethics Committee of the Second Affiliated Hospital of Guangzhou Medical University: The scientific research ethics review project "Application of simple and easy Hemostatic Devices in Laparoscopic Hepatectomy" (acceptance No.: 2022-hg-ks-02) was approved by the clinical research and application ethics committee of the Second Affiliated Hospital of Guangzhou Medical University. Its research contents and methods meet the medical ethics norms and requirements.

1. Preoperative preparation, operative position, and anesthesia

  1. Ask the patient to consume a liquid diet 1 day before the surgical operation and then abstain from eating food and drinking water at least 8 h before the surgery.
  2. Place the patient in a supine position and 30° reverse Trendelenburg position, tilted softly to the left. The principal surgeon operates from the patient's right side.
  3. Perform endotracheal intubation and give general anesthesia. Judge the anesthetic effect according to the patient's post-anesthesia and intraoperative conditions, such as complete anesthesia block, no additional drugs during operation, and stable vital signs.

2. Surgical technique

  1. Apply direct puncture to establish pneumoperitoneum in laparoscopy. Place five trocars in the following positions: observation hole in the sub-umbilical area 12 mm trocar, right anterior axillary line 5 mm trocar, right midclavicular line under the costal margin 10 mm trocar, ventral midline 10 mm and 5 mm trocar (see Figure 2).
  2. Assemble the following hemostatic devices: harmonic scalpel, monopole electrocoagulation, and single lumen catheter, to be innovatively used in liver parenchyma tissue resection (see Figure 3).
  3. Perform a Pringle maneuver. To do so, follow the steps below.
    1. Occlude the first porta hepatis intermittently by using a single lumen catheter. Clamp the lumen catheter with a hemostatic clip for 15 min, followed by releasing for 5 min.
    2. When required to release, use the harmonic scalpel to cut off the clip and take the clip out to restore blood supply to the first porta hepatis (see Figure 4).
  4. Separate the hepatic pedicles supplying the tumor. Resect and divide them one by one with a harmonic scalpel (see Figure 5).
  5. Observe the ischemia line on the liver surface, which becomes visible after the resection of the hepatic pedicles. Use the hook to mark this (see Figure 6).
  6. Resect the liver parenchyma tissue using the harmonic scalpel with clamping and crushing of the liver little by little. Observe the internal hepatic artery, vein, and bile duct now visible. Resect and divide these pipeline structures (see Figure 7).
  7. Once bleeding appears, coagulate the bleeding spots on the liver dissection surface immediately using point-to-point monopole electrocoagulation (see Figure 8).
  8. Use the right posterior hepatic pedicle as a signpost for intrahepatic parenchyma tissue resection. Reserve the main posterior hepatic pedicle (PP) and dissect the branch of pedicles (PPa) supplying the tumor (see Figure 9).
  9. To complete the operation, wash the liver surface so one can see if there are still bleeding spots. Stop the bleeding on the liver dissection surface and remove the tumor specimen from the abdominal cavity (see Figure 10).
    ​NOTE: The Paraffin pathology results of the tumor was metastatic adenocarcinoma, which is shown in Figure 11.

3. Postoperative nursing

  1. Perform ECG monitoring after the operation. Calculate the total 24 h inflow and outflow and observe the urine volume.
    NOTE: The patient's total rehydration volume (antibiotic, amino acid, vitamin, electrolyte, etc.) was 1,750 mL 10.5 h after surgery (after surgery until 7:00 am the next day). The total liquid excretion of the patient at 10.5h after surgery was 1,900ml, including 1,700ml of urine and 200ml of drainage.
  2. On the first day after the operation, give the patient a liquid diet and instruct the patient to turn over and exercise in bed, such as turning over, patting the back, moving the legs, and other exercises, which are mainly guided by the nurses.
  3. On day 2 after the operation, assist the patient to get out of bed and carry out daily activities.
  4. On day 3 after the operation, guide the patient to walk in the corridor and increase gradually the amount of activity in combination with the recovery of the patient's condition. Implement psychological intervention according to the patient's situation to improve the patient's bad mood.
  5. Finally, according to the patient's drainage flow, remove the drainage tube. In this case, the drainage tube was removed on the 7th day after the operation when the drainage flow was 50 mL.

Results

The operation was completed within 2.5 h and the intraoperative bleeding volume was 100 mL without the blood transfusion. There were no short-term complications, and the patient was discharged from the hospital on the 8th day after the operation. The carcinoembryonic antigen (CEA) level post operation decreased to 110.64 µg/L from the pre-operation level of 1058.69 µg/L (Figure 12). Two months after the operation, the patient returned to the hospital to continue chemothe...

Discussion

Hepatectomy is one of the most important treatment methods for patients with primary liver cancer and secondary liver cancer. In 1991, Reich et al. applied laparoscopy to remove benign tumors of the liver and completed the world's first laparoscopic hepatectomy4. After years of rapid development and promotion, laparoscopic hepatectomy has become one of the mainstream methods to treat liver malignant tumors and has been widely carried out in recent years. With the advantages of less intraoperat...

Disclosures

The authors have no conflicts of interest or financial ties to disclose.

Acknowledgements

This work was supported by grants from the Science and Technology Project of Guangzhou City (202102010090).

Materials

NameCompanyCatalog NumberComments
HARMONIC ACE Ultrasonic Surgical DevicesEthicon Endo-Surgery,LLCHAR36
Hem-o-lockTeleflex Medical544233
Monopole ElectrocoagulationKANGJI MEDICAL/
single lumen ureterWELL LEAD MEDICAL CO.,LTD.12F

References

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  3. Adams, R. B., et al. Selection for hepatic resection of colorectal liver metastases: expert consensus statement[J]. HPB. 15 (2), 91-103 (2013).
  4. Reich, H., McGlynn, F., DeCaprio, J., Budin, R. Laparoscopic excision of benign liver lesions. Obstetrics and Gynecology. 78 (5), 956-958 (1991).
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  10. Cho, J. Y., Han, H. S., Yoon, Y. S., Shin, S. H. Feasibility of laparoscopic liver resection for tumors located in the posterosuperior segments of the liver, with a special reference to overcoming current limitations on tumor location. Surgery. 144 (1), 32-38 (2008).
  11. Ome, Y., Honda, G., Doi, M., Muto, J., Seyama, Y. Laparoscopic anatomic liver resection of segment 8 using intrahepatic Glissonean approach. Journal of the American College of Surgeons. 230 (3), 13-20 (2020).
  12. Ryu, T., et al. Perioperative and oncological outcomes of laparoscopic anatomical hepatectomy for hepatocellular carcinoma introduced gradually in a single center. Surgical Endoscopy. 32 (2), 790-798 (2018).
  13. Makabe, K., et al. Efficacy of occlusion of hepatic artery and risk of carbon dioxide gas embolism during laparoscopic hepatectomy in a pig model. Journal of Hepato-Biliary-Pancreatic Sciences. 21 (8), 592-598 (2014).
  14. Miyagi, S., et al. Pure laparoscopic hepatectomy combined with a pure laparoscopic pringle maneuver in patients with severe cirrhosis. Case Reports in Gastroenterology. 9 (1), 101-105 (2015).

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