17
Hepatobiliary and pancreatic trauma
Liver trauma
Blunt and penetrating trauma are the two principal mechanisms of liver injury. Road traffic accidents account for the majority of blunt injuries, whereas knife and gunshot wounds constitute the major cause of penetrating injuries. In the UK, blunt trauma predominates by a ratio of approximately 2:1 as documented in a large Scottish epidemiological study.1 Whilst this is typical for other European centres,2 it differs from the experience in South Africa, where penetrating injuries account for 66% of liver trauma,3 and in North America, where up to 86% of liver injuries are penetrating wounds.4,5
Two types of blunt liver trauma have been described – deceleration (shearing) trauma and crush injury. Deceleration injuries occur in road traffic accidents and in falls from a height where there is movement of the liver relative to its diaphragmatic attachments.6 Crush injuries are caused by direct trauma to the liver area. The two types of injury may coexist but tend to produce somewhat different types of liver injury. Deceleration or shearing injuries create lacerations in the hepatic parenchyma, typically between the right posterior section (segments 6 and 7) and the right anterior section (segments 5 and 8), which can extend to involve major vessels. In contrast, a direct blow to the abdomen may lead to a crush injury, with damage to the central portion of the liver (segments 4, 5 and 8). Compression between the right lower ribs and the spine may also cause bleeding from the caudate lobe (segment 1). Blunt trauma can rupture Glisson’s capsule and can also lead to subcapsular or intraparenchymal haematoma formation. Penetrating injuries are usually associated with gunshot or stab wounds, with the former usually resulting in more tissue damage due to the cavitation effect as the bullet traverses the liver substance.
Classification of liver injury
The severity of liver trauma ranges from a minor capsular tear, with or without parenchymal injury, to extensive disruption involving both lobes of the liver with associated hepatic vein or vena caval injury. The American Association for the Surgery of Trauma has adopted for general use the classification of liver injury described initially in 1989 by Moore and colleagues, and revised subsequently in 19947 (Table 17.1). The hepatic injury grade is calculated from assessment of the liver injury using information derived from radiological study, operative findings or autopsy report. Where there are multiple injuries to the liver, the grade is advanced by one stage. Grade I or II injuries are considered minor; they represent 80–90% of all cases and usually require minimal or no operative treatment. Grade III–V injuries are generally considered severe and may require surgical intervention, while grade VI lesions are regarded as incompatible with survival. Schweizer et al. have described a protocol-based liver trauma management system employing this classification system that permits lesser injuries to be treated non-operatively and allows more appropriate selection of patients for operative treatment.8
Table 17.1
Hepatic injury scale used by the American Association for the Surgery of Trauma
Grade | Description | |
I | Haematoma | Subcapsular, < 10% surface area |
Laceration | Capsular tear, < 1 cm parenchymal depth | |
II | Haematoma | Subcapsular, 10–50% of surface area |
Laceration | Intraparenchymal < 10 cm in diameter, 1–3 cm parenchymal depth, < 10 cm in length | |
III | Haematoma | Subcapsular, > 50% surface area or expanding; ruptured subcapsular or parenchymal haematoma; intraparenchymal haematoma > 10 cm or expanding |
Laceration | > 3 cm parenchymal depth | |
IV | Laceration | Parenchymal disruption involving 25–75% of hepatic lobe or 1–3 Couinaud segments within a single lobe |
V | Laceration | Parenchymal disruption involving > 75% of hepatic lobe or > 3 Couinaud segments within a single lobe |
Vascular | Juxtahepatic venous injuries – retrohepatic cava, major hepatic veins | |
VI | Vascular | Hepatic avulsion |
Note: advance one grade for multiple injuries up to grade II.
The role of ‘aggressive’ high-volume fluid replacement in trauma victims has been questioned, with evidence suggesting that excessive fluid replacement is associated with adverse outcome.9 As this evidence came from an American series that included a large proportion of relatively young, previously fit adults suffering from penetrating trauma to the torso, with ready access to trauma centres, the results may not necessarily be applicable to practice in other countries.
Diagnosis of liver injury
In Feliciano et al.’s series of 1000 patients with liver trauma treated during a 5-year period, 45 patients underwent emergency room thoracotomy for control of haemorrhage related to their liver injury and all died.4 Similarly, in an 11-year review of 783 patients who sustained liver trauma in Scotland, 11 patients underwent an unsuccessful laparotomy or thoraco-laparotomy in the emergency room.1
An alternative investigation that has been advocated in initial trauma evaluation is focused assessment with sonography for trauma (FAST).10 This involves ultrasonographic assessment of the pericardium, right upper quadrant including Morrison’s pouch, left upper quadrant and pelvis. This evaluation is not designed to identify the degree of organ injury, but rather the presence of blood. A large meta-analysis of the use of emergency ultrasonography for blunt abdominal trauma reported sensitivity rates ranging from 28% to 97% and specificity rates close to 100%.11
Rozycki et al. demonstrated a significant correlation between haemoperitoneum in the right upper quadrant and injury to the liver, and suggested that adherence to a pre-agreed protocol increased the reliability of ultrasound assessment of abdominal trauma.12 Other centres have also reported that ultrasound is a reliable ‘first’ test for the assessment of a patient with suspected liver trauma.13 However, an important cautionary note comes from the study carried out by Richards et al.14 In a series of 1686 abdominal ultrasound scans for trauma, 71 patients had bowel or mesenteric injury and 30 patients had a negative ultrasound scan (43% false-negative rate). Limitations of FAST include operator dependence, poor assessment of the retroperitoneum, unreliable detection of pneumoperitoneum and difficulty in scanning obese patients or those with overlying wounds.
Computed tomography (CT) is the ‘gold standard’ investigation for the evaluation of a patient with suspected liver trauma (Fig. 17.1). The use of intravenous contrast may help in the detection of non-viable parenchyma. CT has high sensitivity and specificity for detecting liver injuries; these attributes increase as the time between injury and scanning increases, as haematomas and lacerations become better defined. Specific CT features of liver trauma have been reported by a number of authors. Fang et al. described intraparenchymal ‘pooling’ of intravenous contrast that correlated strongly to the presence of ongoing haemorrhage.15 Yokota and Sugimoto documented ‘periportal tracking’ to consist of a circumferential area of low attenuation around the portal triad.16 Periportal tracking is thought to represent blood or fluid within the condensation of the Glissonian sheath around the portal structures and indicates the presence of injury to structures in the portal triad. If the sign is present in the periphery of the liver it may alert the clinician to the presence of a peripheral bile duct injury that in turn may present as a bile leak. Addition of oral contrast does not appear to add to the diagnostic yield of CT in the assessment of liver injury.17
Figure 17.1 CT image of a 25-year-old male who sustained a blunt injury to the right chest wall but was admitted to hospital haemodynamically stable. The scan shows a substantial subcapsular haematoma associated with an intraparenchymal laceration. This patient was managed successfully without operation.
In order to maintain a balanced perspective, it is worthwhile considering some of the limitations of CT in the assessment of liver trauma. The CT-defined grade of injury may differ from the grade of liver injury found at operation, with the predominant tendency being to overdiagnose the grade of injury on CT as compared with subsequent operative findings. Croce et al. concluded that CT should not be used in isolation to estimate blood loss and that CT may not provide an accurate assessment of the extent of a liver laceration in some areas of the liver – specifically in the vicinity of the falciform ligament.18
Some authors recommend performing a whole-body CT as the standard diagnostic tool during the early phase for patients with polytrauma, advocating that this will alter treatment in up to 34% of patients with blunt trauma.19 A 30% reduction in mortality using this approach has also been reported.20 Other arguments in favour of an imaging survey are the reduction in time from admission to intervention and consistency in managing haemodynamically unstable patients.21 However, at present the logistics of such an approach are not universally applicable as it requires a CT scanner in, or very close to, the emergency department.
Other diagnostic/therapeutic modalities for the assessment and treatment of liver injury
Angiography plays a vital role in the conservative management of liver injuries. Extravasation of contrast seen on CT requires emergency angiography and therapeutic angiographic embolisation for ongoing blood loss or haemobilia.22 Angioembolisation is also reported following damage control surgery prior to removal of packs if re-bleeding is suspected.23,24
Other diagnostic modalities may be used in specific situations. Endoscopic retrograde cholangiopancreatography (ERCP) may help in delineation of the biliary tree in patients with liver trauma, and endoscopic transpapillary stents may be used as a therapeutic modality to treat biliary leaks.25
Management of liver injury: selection of patients for non-operative management
The feasibility of non-operative management of patients with intra-abdominal solid-organ injury was first established in paediatric surgery but was subsequently extended to adult practice. Richie and Fonkalsrud described successful conservative management of four patients with liver injury in an era before the availability of CT.26 Further indirect evidence for the feasibility of a non-operative approach came from a report published by White and Cleveland27 in the same year. They reported a consecutive series of 126 patients with liver trauma, all of whom underwent laparotomy. Interestingly, 67 patients in this series (53%) had placement of a drain to the subhepatic space as their only liver-related surgical intervention at laparotomy. Subsequent studies have recognised that 50–80% of liver injuries stop bleeding spontaneously and this has led to a non-operative approach for blunt liver trauma in selected patients.
• absence of peritoneal signs;
• availability of good-quality CT;
• ability to monitor patients in an intensive care setting;
• facility for immediate surgery (and by implication, availability of an experienced liver surgeon);
• simple liver injury with < 125 mL of free intraperitoneal blood;
Farnell et al. extended the threshold of haemoperitoneum to 250 mL and described specific liver injuries suitable for non-operative management.29 Feliciano suggested subsequently that any blunt hepatic injury, regardless of its magnitude, should be managed without operation if the patient was haemodynamically stable and had a haemoperitoneum of less than 500 mL.30 The degree of liver injury amenable to successful non-operative management has gradually extended over recent years, and most authors now believe that the ultimate decisive factor in favour of non-operative management is haemodynamic stability of the patient at presentation or after initial resuscitation, irrespective of the grade of liver injury on CT or the amount of haemoperitoneum.31,32
A 22-month prospective study from Memphis of the initial non-operative treatment of haemodynamically stable blunt hepatic trauma patients compared outcome to a matched cohort of blunt hepatic trauma patients treated operatively.33 The study reported that of 136 patients with blunt trauma, 24 (18%) underwent emergency surgery. Of the remaining 112 patients, 12 (11%) failed conservative management (for causes not related to the liver injury in seven) and the remaining 100 patients were treated successfully without operation. Of these, 30% had minor injuries (grades I and II) but 70% had major injuries (grades III–V). This study concluded that non-operative management was safe for haemodynamically stable patients and that this was independent of the CT-delineated grade of the liver injury. The blood transfusion requirement and the incidence of abdominal complications were lower in the non-operatively treated group.
Reporting a single institutional experience, Boone et al. stated that 46 (36%) of 128 consecutive patients with blunt liver trauma were successfully treated non-operatively, including 23 patients with grade III and IV injuries.31 A review of 495 patients from the published literature noted a success rate for non-operative treatment of 94%.34 This was accomplished with a mean transfusion rate of 1.9 units, a complication rate of 6% and a mean hospital stay of 13 days. There were no liver-related deaths, nor were there any missed enteric injuries.
If a non-operative strategy is selected it should be borne in mind that the risk of hollow-organ injury increases in proportion to the number of solid organs injured35 and that there is a small but significant risk of delayed haemorrhage. However, it appears that the natural course of liver injuries is more analogous to that of lung or kidney injuries, rather than splenic injuries, in that any deterioration is usually gradual, with a fall in haemoglobin level or an increase in fluid requirement, rather than acute haemodynamic decompensation. Therefore, with close supervision, patients who fail with an initial non-operative approach can be detected early and treated appropriately.
Although non-operative management of haemodynamically stable patients with liver trauma has become the standard of care over the past decade, the role of in-hospital follow-up CT to monitor the injury remains controversial. Demetriades et al. reported that follow-up CT at a mean of 10 days after surgical intervention showed a 49% incidence of liver-related complications, most of which required subsequent intervention.36 However, other authors suggest there is little evidence that follow-up CT provides additional information and rarely changes management.37 In the author’s practice, in-hospital follow-up scan is not employed routinely unless the patient develops relevant symptoms or signs, but a follow-up scan 4–6 weeks later is undertaken to ensure resolution of the injury.
The management policy for abdominal gunshot injuries in most centres continues to be a mandatory laparotomy, regardless of the clinical presentation;38 however, several studies have reported successful non-operative management of selected liver gunshot injuries.39,40 In the study by Omoshoro-Jones et al., 26.6% of patients who presented with liver gunshot injuries were managed non-operatively, with an overall success rate of 94% and a morbidity rate of 36%, of which 3% were liver related.39 This approach is associated with the risk of failure to detect concomitant intra-abdominal visceral injury and therefore should only be considered in specialist centres with experience in management of liver trauma and appropriate facilities to deal with any complications that arise.
Operative management of liver injury
Intraoperative assessment
Once the abdomen has been entered, blood and clots should be removed and packs inserted into each quadrant of the abdomen. A thorough laparotomy is performed in a systematic manner to identify all intra-abdominal injuries. Any perforations in the bowel should be sutured immediately to minimise contamination. Significant liver haemorrhage can usually be controlled initially by direct pressure using packs, although additional techniques that may be employed include: temporary digital compression of the free edge of the lesser omentum (Pringle manoeuvre; Fig. 17.2); bimanual compression of the liver; or manual compression of the aorta above the coeliac trunk. At this point, further evaluation of the extent of liver injury should be delayed until the anaesthetist has replenished adequately the intravascular volume and stabilised the blood pressure. Attempts to evaluate the liver injury before adequate resuscitation may result in further blood loss, with worsening hypotension and acidosis.
The packs can subsequently be gently removed to allow a detailed evaluation of the type and extent of the liver injury. It should be borne in mind that a subcapsular haematoma may cover an area of ischaemic tissue and that parenchymal lacerations may be associated with damage to segmental bile ducts. Many liver injuries will have stopped bleeding spontaneously by the time of surgery. However, if there is active bleeding, a Pringle manoeuvre can be used diagnostically and compression can be maintained with an atraumatic vascular clamp if haemorrhage decreases (Fig. 17.3). The clamp should be occluded only to the degree necessary to compress the blood vessels and not to injure the common bile duct. A normal liver can tolerate inflow occlusion for up to 1 hour; however, the ability of a damaged liver to tolerate ischaemia may be impaired. If haemorrhage is unaffected by portal triad occlusion, major vena cava injury or atypical vascular anatomy should be suspected. Hepatic outflow control may also be required. Access to the suprahepatic cava can be gained by an experienced liver surgeon, and slings may be placed around the hepatic veins following mobilisation of the liver from its peritoneal attachments. Total vascular occlusion of the liver requires control of the inferior vena cava below the liver in addition to the suprahepatic cava but is likely to be poorly tolerated by an injured liver.
Perihepatic packing
In situations where it is thought that definitive control of haemorrhage cannot be obtained, or patients are deemed critically unstable, coagulopathic or acidotic and therefore would not tolerate a prolonged operative procedure, perihepatic packing can be employed. This has led to the concept of damage control surgery – rapid perihepatic packing, closure of the abdominal incision with or without a Bogota bag and transferring the patient to ICU as soon as possible for continued resuscitation and rewarming. When the metabolic derangements have been corrected or improved, the patient can be taken back to theatre or transferred to a specialist centre for re-exploration and definitive treatment.41
As packing is thus a widely applicable procedure, some attention should be devoted to technical considerations. The packs should not be inserted into the liver substance itself, as this will tend to distract the edges of the parenchymal tear and encourage continued bleeding. Rather, the technique of packing involves manual closure or approximation of the parenchyma, followed by sequential placing of dry abdominal packs or a single rolled gauze around the liver and directly over the injury in an attempt to provide tamponade to a bleeding wound (Fig. 17.4). Most surgeons employ skin closure only, leaving the fascia for primary closure at the subsequent procedure for pack removal. The presence of packs, combined with massive oedema of the bowel, may lead to difficulties in wound closure. If this is encountered, a mesh can be inserted to prevent further compromise of ventilation and bowel viability, and to avoid pressure necrosis of the liver.42
Figure 17.4 (a) Placement of gauze packs around the liver to compress the fracture. (b) Closure of the incision provides additional compression. Reproduced from Berne TV, Donovan AJ. Section 10. Injury and haemorrhage. In: Blumgart LH, Fong Y (eds) Surgery of the liver and biliary tract, 3rd edn, Vol. 2. Edinburgh: Churchill Livingstone, 1994. With permission from Elsevier.