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World Journal of Gastrointestinal Surgery logoLink to World Journal of Gastrointestinal Surgery
. 2023 Mar 27;15(3):338–345. doi: 10.4240/wjgs.v15.i3.338

Vascular injury during laparoscopic cholecystectomy: An often-overlooked complication

Antonio Pesce 1, Nicolò Fabbri 2, Carlo Vittorio Feo 3
PMCID: PMC10080601  PMID: 37032796

Abstract

Laparoscopic cholecystectomy is one of the most frequently performed procedures in gastrointestinal surgery worldwide. Bleeding complications due to vascular injuries represent an important cause of morbidity and mortality, especially when facing major bleeding during laparoscopy, where bleeding control can be technically challenging in inexperienced hands. Interestingly, the reported incidence rate of conversion to open surgery due to vascular lesions is approximately 0%-1.9%, with a mortality rate of approximately 0.02%. The primary aim of this article was to perform an up-to-date overview regarding the incidence and surgical management of vascular injuries during laparoscopic cholecystectomy according to the available scientific evidence.

Keywords: Laparoscopic cholecystectomy, Vascular injury, Vascular anomalies, Surgical management, Specialized hepatobiliary centers


Core Tip: The theme of biliary injuries in laparoscopic cholecystectomy and the prevention and management of bile duct lesions have been extensively exanimated. However, little attention has been given to vascular injuries. Bleeding complications due to vascular injuries represent an important cause of morbidity and mortality, as well as the negative outcomes of biliary reconstruction when associated with biliary injuries. The vascular lesions should be correctly identified, and surgeons must choose the best therapeutic option to quickly repair the vascular lesion, depending on their own surgical experience and medical center resources. Currently, the management of referrals to specialized hepatobiliary centers for multidisciplinary approaches is mandatory.

INTRODUCTION

Laparoscopic cholecystectomy (LC) is one of the most frequently performed procedures in general surgery worldwide[1]. Iatrogenic vascular and bile duct injuries still represent a major public health problem related to both medico-legal implications and health care costs[1,2]. The theme of biliary injuries in laparoscopic cholecystectomy and the prevention and management of bile duct lesions have been extensively exanimated. However, little attention has been given to vascular lesions[3]. Bleeding complications due to vascular injuries are an important cause of morbidity and mortality, especially during laparoscopy, where bleeding control can be technically challenging in inexperienced hands. Vascular injuries during laparoscopic cholecystectomy may mainly occur during trocar or Veress needle insertion or during dissection of the hepato-cystic triangle. Interestingly, the reported incidence rate of conversion to open surgery due to intra-operative vascular lesions is approximately 0%-1.9%, with a mortality rate of approximately 0.02%[3-5]. The aim of this article was to analyze and explore the incidence, diagnosis and surgical management of vascular injuries in laparoscopic cholecystectomy according to the available scientific evidence. MEDLINE and PubMed searches were performed using the MeSH terms “vascular injury”, “vascular lesion”, “vasculo-biliary injury”, and “laparoscopic cholecystectomy” to identify relevant articles (cohort studies, systematic reviews, case reports, multicenter studies) published in English, French, Spanish, and Italian over the last twenty years.

INCIDENCE AND RISK FACTORS

Several risk factors may contribute to vascular injuries during laparoscopic cholecystectomy: Anatomical factors, including vascular anomalies, patient-related factors, the gallbladder pathology and surgeon’s experience, as summarized in Table 1. Concerning the anatomical factors, the different variants of vascular anatomy may represent a possible cause of bile duct injuries, particularly anomalies of the cystic artery and right hepatic artery (RHA). If surgeons are not aware of possible variations of the RHA, such as in the case of acute and chronic cholecystitis with unclear anatomy of Calot’s triangle, the RHA may be accidentally injured or mistaken for the cystic artery and actively cut off. In a study assessing the frequency of anatomical variations of biliary and vascular systems from Singh et al[6], the operative findings revealed 197 (26.62%) vascular anomalies, mostly related to cystic artery and RHA anatomy. Arterial anomalies are more common, occurring in at least 50% of individuals, and can be recognized only by careful dissection[7]. Based on the classification proposed by Smadja and Blumgart[8], the cystic artery is considered normally positioned when located in the center of the hepato-cystic triangle. In a recent Spanish study performed on a sample of 2000 Laparoscopic cholecystectomy procedures, Noguera et al[9] found an origin of the cystic artery from the RHA in 91.5% of cases. These data are similar to those of Bergamaschi et al[10], where, in a study of 90 consecutive human cadavers, a single artery was found in 59 of 70 specimens (84.3% of all cases).The incidence of third structures within the hepato-cystic triangle was found to be arteries in 36.2% of cases, with a reported incidence of caterpillar hump of the RHA in 12.9% of all cases and double cystic arteries in 5.7%. The most common variations of cystic artery are shown in Figure 1, according to the literature data[7-10]. Among the patient-related factors, overweight and pathological obesity, a history of biliary surgery or endoscopic procedures, and hepatic cirrhosis or chronic liver disease appear to be factors correlated with the development of perioperative complications, both for biliary and vascular structures. However, emergent cholecystectomy for acute cholecystitis increases the risk of iatrogenic lesions, as gallbladder inflammation causes a series of anatomical changes that are associated with an increased risk of iatrogenic injury. Ultimately, the surgeon’s experience plays an important role, and for this reason the importance of a correct “learning curve” for young surgeons should be stressed.

Table 1.

Summary of risk factors associated to vascular injuries

Anatomical factors
Description
Common vascular variants of cystic artery and right hepatic artery Single cystic artery[6]
Two arteries (superficial and deep)[6]
Single short cystic artery originated from caterpillar right hepatic artery[4,5,10]
Long single cystic artery not from right hepatic artery crossing anterior to the common hepatic duct[7,8]
Double cystic artery/accessory cystic artery[9]
Cystic artery seen more anteriorly than posteriorly in relation to Mascagni’s lymph node[7,9]
A constant vessel found on the postero-lateral margin of gallbladder bed[6,9]
Cystic artery coming from gastroduodenal artery, passing outside Calot’s triangle[6,9]
Patient-related factors Overweight and pathological obesity[1]
History of biliary surgery or endoscopic procedures[1]
Underlying liver disease[1]
Gallbladder pathology Acute or chronic cholecystitis[1-3]
Gallbladder anomalies (gallbladder duplication, gallbladder agenesia, left-side gallbladder)[1-3]
Surgical experience Learning curve[1,2]
Inadequate exposure[1,2,6]
Failure to recognize anatomical landmarks[2,6]

Figure 1.

Figure 1

Anatomic illustration of the most common variants of cystic artery. Common variants of cystic artery. A: Cystic artery originating from the right hepatic artery in the classical position[6-8]; B: Long cystic artery seen anteriorly to the cystic duct[6,7]; C: Cystic artery coming from the gastroduodenal artery, passing outside Calot’s triangle[6,9]; D: Long single cystic artery not from the right hepatic artery crossing anterior to the common hepatic duct[6,9]. RHA: Right hepatic artery; LHA: Left hepatic artery; PHA: Proper hepatic artery; CHA: Common hepatic artery; GDA: Gastroduodenal artery; G: Gallbladder; CHD: Common hepatic duct; CD: Cystic duct; CBD: Common bile duct; RHD: Right hepatic duct; LHD: Left hepatic duct; AA: Abdominal aorta.

HEPATIC ARTERY INJURIES

Intra-operative bleeding is certainly the most common and feared complication of arterial injury during laparoscopic procedures, followed by ligation. Among hepatic artery injuries, lesions of the RHA are the most described complication that may occur during laparoscopic cholecystectomy. Hepatic artery closure is usually well tolerated without any particular consequences due to the portal flow and a dense series of collateral arterial branches coming from the hepatic hilum. However, in such cases, hepatic artery ligation can sometimes cause ischemic hepatic necrosis or liver atrophy. RHA injury is frequently encountered in association with bile duct injury, even if the true incidence of RHA injury without concomitant bile duct injury is not clear[11]. In a cadaveric study, Halasz[12] reported that the incidence of injury to the RHA or its branches was only 7%. All patients survived at least one year after cholecystectomy, and they had normal livers. For this reason, the decision to immediately repair the lesion remains controversial. RHA injuries always occur in two ways: the first is when the fundus-first approach for laparoscopic cholecystectomy is performed in the presence of severe inflammation[13]; the second is in the presence of vascular anomalies, as in the case of caterpillar hump of the RHA, where the hepatic artery may be wrongly mistaken for the cystic artery[4,5]. The most important complication of RHA injury is massive bleeding during dissection, which always leads to conversion to open surgery in inexperienced hands. In some cases, laparoscopic repair is feasible and safe[11] by suturing in cases of intra-operative bleeding or direct end-to-end anastomosis when possible in cases of ligation or clipping of the RHA.

Hepatic artery pseudoaneurysm represents another important complication after RHA injury, and it may occur in the early or late postoperative course after LC. Approximately 10% of all the reported cases of hemobilia are secondary to iatrogenic cystic artery or hepatic artery pseudoaneurysms as a consequence of an opening of cystic or RHA pseudoaneurysm within the biliary tree[14]. The exact mechanism of hepatic pseudoaneurysm formation is yet unclear: The most accredited hypotheses concern the mechanical or thermal damage during surgical dissection. Transarterial embolization represents the best therapeutic solution for hepatic artery aneurysm with a high success rate, and surgical repair should be performed in cases where the embolization attempt has failed. In many patients, an open approach in an emergency setting is performed[14], even if a laparoscopic approach is used in some cases[15].

HEPATIC VEINS, PORTAL VEIN AND MAJOR RETROPERITONEAL VESSEL INJURIES

Venous bleeding is less common than arterial bleeding. Bleeding from hepatic vein injury commonly comes from the liver bed during detachment of the gallbladder. Between 10% and 15% of patients may present a large branch of the middle hepatic vein adherent to the liver bed, leading to an increased risk of venous injury during cholecystectomy. In 1999, Misawa et al[16] first proposed an ultrasonographic assessment of the risk of injury to branches of the middle hepatic vein during laparoscopic cholecystectomy by analyzing the middle hepatic vein distance from the gallbladder bed before laparoscopy. Currently, there is controversy about the risk of injury to the branch of the middle hepatic vein during LC[17]. In a previous study, Zhang et al[18] analyzed the anatomical relationship between the gallbladder bed and the branches of the middle hepatic vein in 143 healthy volunteers by color Doppler ultrasound and found that, in most subjects, the branch of the middle hepatic vein and the gallbladder bed were well separated. Only patients with large branches of the middle hepatic vein running very close to the gallbladder bed are at risk of bleeding during laparoscopic cholecystectomy. The diameter of the distal branch of the middle hepatic vein close to the gallbladder bed is reported to vary from 0.9 mm to 3.2 mm and in some cases over 5 mm[17,19,20]. Moreover, according to Ball et al[19], the presence of chronic cholecystitis and fibrous tissue may increase the risk of significant bleeding from the liver bed. Concerning the treatment of venous injuries, bleeding from the middle hepatic vein branch during the operation can only be stopped by direct hemostatic stitches; it can be performed by laparoscopy in experienced hands or can often require conversion to open surgery[21]. In general, we strongly recommend careful dissection during the final steps of laparoscopic cholecystectomy, especially for training surgeons, when dissection becomes easier, and the surgeon may relax.

Portal vein injuries are frequently associated with biliary and RHA injuries. Compared with arterial injury after cholecystectomy, there are very few reports of isolated portal vein injury without associated biliary lesions[22]. Furthermore, as a result of its rarity, the pathogenesis of this type of injury remains unclear. The surgical repair of portal vein lesions is very difficult, often complicated by massive hemorrhage, and seldom successfully managed. When the portal vein is injured during surgery, it should be reconstructed immediately by an experienced hepato-biliary surgeon if the patient is hemodynamically stable. However, the most important complication after surgical repair of a portal vein injury is represented by acute portal thrombosis, often leading to liver infarction. For this reason, anticoagulation therapy should be started as soon as possible to avoid the progression of acute portal vein thrombosis. Liver transplantation is a salvage therapy that should only be considered in end-stage liver disease[22].

Injuries of major retroperitoneal vascular structures are uncommon but potentially life-threatening complications of laparoscopy[23-25]. Inferior vena cava and aorta injuries are frequently associated with trocar or Veress needle insertion during laparoscopic surgery. Early diagnosis and immediate conversion are mandatory for the proper management of these important injuries to minimize morbidity and mortality. Some authors have also described occasional injuries to the right renal artery with the formation of a pseudoaneurysm and consequent renal-vena cava fistula[26,27]. This often represents a late complication following laparoscopic cholecystectomy.

Another important medical complication associated with vena cava injury is venous air embolism[28]; the cardiovascular, pulmonary, and central nervous systems may all be affected, with severity ranging from no symptoms to immediate cardiovascular collapse.

CLASSIFICATION OF VASCULAR INJURIES

Several attempts have been made to uniformly classify vascular lesions, so they are always underreported, as summarized in Table 2. In early 2000, Schäfer et al[29] proposed a working classification from the Swiss Association of Laparoscopic and Thoracoscopic Surgery (SALTS) by defining vascular injuries during laparoscopy into intraoperative and postoperative bleeding complications. In 2007, Bektas et al[30] proposed the Hannover classification by underlining the importance of including additional vascular injury and the location of the biliary lesion at or above the bifurcation of the hepatic duct, as they were found to have a major impact on the extent of surgical intervention for iatrogenic bile duct injury. The Neuhaus and Strasberg-Bismuth classifications for biliary injuries do not consider vascular involvement.

Table 2.

Classifications of vascular injuries during laparoscopic cholecystectomy

Ref.
Definition of vascular injury
Schäfer et al[29], 2000 Major injury: Injury to any of the following vessels: Aorta, vena cava, portal vein, hepatic artery and splenic artery, iliac vessels, mesenteric, omental and renal vessels; the vascular injury is classified in: Intra-operative; local haemorrhage within the abdominal cavity, retroperitoneum or abdominal wall; post-operative: Bleeding occurring within 24 h after surgery
Bektas et al[30], 2007 Vascular involvement in different biliary injuries grades (types C and D): Type C tangential injury of the common bile duct: with or without vascular lesion; Type D complete transection of the common bile duct: with or without vascular lesion
Kaushik[31], 2010 Major injury: Any bleeding involving cystic artery, right hepatic artery, portal vein, superior mesenteric vein, suprahepatic veins, inferior vena cava, aorta that requires conversion to open surgery to control/repair; additional surgical procedures; need for blood transfusions
Fingerhut et al[32], 2013 Vasculo-biliary involvement by reporting the type of injured vessel
Our study Major vascular injury: Any bleeding involving right hepatic artery, portal vein, suprahepatic veins, inferior vena cava that always requires conversion to open surgery for control/repair; need for blood transfusions; associated biliary injury; need for transfer to tertiary center

In 2010, Kaushik[31] suggested a new classification system, wherein vascular injuries were divided into major and minor injuries based on the need for conversion, additional surgical procedures, or blood transfusions.

The European Association for Endoscopic Surgery (EAES) recently proposed a new classification named ATOM, including the anatomy of damage and vascular injury (A), timing of detection (To), and mechanism of damage (M)[32].

VASCULO-BILIARY INJURY

Vascular injury, in particular to the RHA, is found in approximately 12% to 61% of iatrogenic bile duct lesions, leading to high morbidity and mortality associated with altered quality of life[33-35]. It is very important to know preoperatively if a vascular lesion occurs along with a biliary lesion because the poor vascularization of the common bile duct may result in anastomotic strictures after surgical biliary tract repair, recurrent cholangitis and secondary biliary cirrhosis[33]. For these reasons, appropriate knowledge of the vascular lesion represents an important condition when the patient is referred to a specialized hepato-biliary center. In most cases, the surgical repair of biliary and vascular injuries is performed simultaneously. There are no guidelines for the timing of repair, whereas few studies have compared early vs late repair of bile duct injury[34,36,37]. In a multicenter study of the European-African Hepato Pancrea to Biliary Association (E-AHPBA), the timing of biliary reconstruction after bile duct injury with hepaticojejunostomy was not correlated with the occurrence of severe postoperative complications, re-intervention or liver-related mortality[34]. In another multicenter study, the most favorable outcomes were more frequently observed in the immediate (within the first 72 h) and (after 6 wk) reconstruction of biliary injury, and type E4 injury was found to be an independent factor of worse outcome[36]. In general, if a major bile duct transection occurs (types E1-E2 according to the Strasberg classification), the integrity of the hepatic artery, especially the RHA, should always be examined meticulously to plan early vascular reconstruction if technically possible. If revascularization is not technically feasible, biliary reconstruction close to the hilar plate is mandatory in order to minimize the possibility of anastomotic complications[38]. If the vascular lesion is discovered late, in a minority of cases, hepatectomy is needed as a salvage strategy[39,40].

DIAGNOSIS AND SURGICAL MANAGEMENT

The diagnosis of intra-operative bleeding during dissection may be obvious, but it should be correctly identified, and surgeons must choose the best therapeutic option to quickly repair the vascular lesion, depending on their own experience and medical center resources. At present, there is no clear consensus on the most suitable type or time to perform the repair, especially when vascular injury occurs in centers not specialized in complex hepato-biliary surgery; thus, the management of these complications is still a much debated topic[33]. In a recent multicenter retrospective study, the authors analyzed the management of vascular injuries during laparoscopic cholecystectomy, focusing on referral to specialized centers, time to perform the repair, and different treatment option outcomes[33]. In a cohort of 104 patients with vascular injuries, 29 patients underwent vascular repair (27.9%), 13 (12.5%) liver resection, and 1 liver transplant as a first treatment. The majority of vascular and biliary injuries occurred in non-specialized centers, and more than half were immediately transferred. The authors concluded that the management of complex vascular and biliary lesions should be mandatory in specialized centers and that late vascular repair is not necessarily associated with worse outcomes[33]. Another interesting study by Li et al[38] analyzed the effects of vascular reconstruction and hepatic re-arterialization when technically possible. In this study, successful early arterial reconstruction with or without a vascular graft (within 4 d) allowed recovery from hepatic ischemia, without any evidence of hepatic atrophy or necrosis during follow-up.

CONCLUSION

Vascular injuries represent a life-threatening complication, and they should be carefully evaluated along with biliary lesions during laparoscopic cholecystectomy. The recognition of these lesions must occur as early as possible, and the surgeon must choose the best therapeutic option for the patient according to available medical resources. Currently, the management of referrals to specialized hepato-biliary centers for multidisciplinary approaches is mandatory.

Footnotes

Conflict-of-interest statement: There are no conflicts of interest to report.

Provenance and peer review: Invited article; Externally peer reviewed.

Peer-review model: Single blind

Peer-review started: November 27, 2022

First decision: December 26, 2022

Article in press: February 22, 2023

Specialty type: Surgery

Country/Territory of origin: Italy

Peer-review report’s scientific quality classification

Grade A (Excellent): 0

Grade B (Very good): 0

Grade C (Good): C, C

Grade D (Fair): 0

Grade E (Poor): 0

P-Reviewer: Chuang SH, Taiwan; Cochior D, Romania S-Editor: Chen YL L-Editor: A P-Editor: Chen YL

Contributor Information

Antonio Pesce, Department of Surgery, University of Ferrara, Azienda USL of Ferrara, Azienda USL of Ferrara, Lagosanto 44023, Ferrara, Italy. antonio.pesce@ausl.fe.it.

Nicolò Fabbri, Department of Surgery, University of Ferrara, Azienda USL of Ferrara, Azienda USL of Ferrara, Lagosanto 44023, Ferrara, Italy.

Carlo Vittorio Feo, Department of Surgery, University of Ferrara, Azienda USL of Ferrara, Azienda USL of Ferrara, Lagosanto 44023, Ferrara, Italy.

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