Journal of the Pancreas Open Access

INTRODUCTION

The incidence of acute pancreatitis is increasing, with an overall incidence of 22.4 per 100,000 population in England, and hospital admission rate of 9.6 per year per 100,000 population [1, 2]. The majority of patients have mild acute pancreatitis which is self-limiting and respond to conservative management. Approximately 20% of patients have acute severe pancreatitis which is characterised by the presence of the persistent systemic inflammatory response syndrome and/or organ failure [3].

Vascular complications in pancreatitis range from asymptomatic venous thrombosis to catastrophic arterial bleeding. Early recognition and investigation is imperative, as prompt diagnosis and timely interventional procedures can potentially reduce mortality. Massive haemorrhage secondary to necrotizing pancreatitis is a result of ruptured pseudoaneurysms in 60% of cases [4].

Pseudoaneurysms associated with pancreatitis occur due to vessel wall erosion by enzyme-rich peripancreatic fluid released by damaged acinar cells, or contained within an adjacent pseudocyst. The incidence of pseudoaneurysm formation in chronic pancreatitis ranges between 10% and 17% [5, 6, 7, 8, 9]. In comparison, the incidence of pseudoaneurysms in acute pancreatitis is far less, and not accurately defined in the literature. Pseudoaneurysm rupture is rare, and haemorrhage may occur into the peritoneal cavity, retroperitoneum, gastrointestinal tract, into a pseudocyst, or into the pancreatic duct (haemosuccus pancreaticus) [10]. Pseudoaneurysm rupture associated with pancreatitis has a high mortality rate of up to 40% [11, 12], and is unrelated to the size of the pseudoaneurysm and the severity of pancreatitis [13].

Historically, pseudoaneurysms secondary to pancreatitis were treated surgically with an associated mortality of approximately 56% [13, 14, 15]. Due to advances in interventional radiological techniques, the paradigm has largely shifted towards endovascular treatment. The aim of this study was to report the outcomes of endovascular and percutaneous therapy in the management of pseudoaneurysms secondary to pancreatitis.

METHODS

Patients

The angiography database was used to identify all patients undergoing angiography for suspected bleeding secondary to pancreatitis between April 2005 and August 2011. Patient demographics, history, clinical presentation, underlying aetiology of pancreatitis, radiological findings, management and outcomes were retrospectively reviewed. Inclusion criteria were the presence of a pseudoaneurysm in patients with an underlying diagnosis of pancreatitis and evidence of bleeding. The median age was 57 years (range: 21-86 years), and 11 patients were male (84.6%). The most common aetiology of pancreatitis was alcohol in five patients (38.5%), followed by idiopathic (n=4, 30.8%), gallstones (n=3, 23.1%), and ethylene glycol poisoning (n=1, 7.7%). With respect to ASA status, nine patients were classed as ASA 2 (69.2%), while the remaining four patients were ASA 3 (30.8%). Nine patients had acute pancreatitis or acute on chronic pancreatitis (69.2%) as suggested by the increased amylase levels, while four patients had chronic pancreatitis (30.8%). The most common presentation was abdominal pain (n=8, 61.5%) followed by symptoms or signs of bleeding (n=5, 38.5%: gastrointestinal bleeding and anaemia). At presentation, the median haemoglobin was 8.7 g/dL (reference range: 6-11 g/dL). Five patients had evidence of pancreatic necrosis on cross-sectional imaging and ten patients spent a median of 4 days (range: 1-12 days) in the intensive care unit.

Diagnostic Modality

The diagnosis of a pseudoaneurysm was made by arterial phase computerized tomography (CT) in seven patients (53.8%), followed by portal venous phase contrast enhanced CT (PVPCT; n=4, 30.8%), duplex ultrasound (n=1, 7.7%) and catheter angiography (n=1, 7.7%; Figure 1). PVPCT failed to detect small pseudoaneurysms in a total of five out of nine patients (55.6%) which were later diagnosed on arterial phase CT. The diagnosis of a pseudoaneurysm was achieved in all patients who had an arterial phase CT. The site of the pseudoaneurysms are shown in Table 1, with the pancreaticoduodenal arteries being the most common site in this cohort (n=6, 46.1%); two patients (15.4%) had more than one pseudoaneurysm (2 and 6 pseudoaneurysms, respectively) accounting for a total of 19 pseudoaneurysms secondary to pancreatitis identified in the 13 patients.

Management

All 13 patients underwent mesenteric angiography with an intention to treat with endovascular embolisation. Access was gained via the right common femoral artery in all patients. Two patients (15.4%) underwent a second angiographic procedure. Access was gained via the left brachial artery in one patient to allow access of a pseudoaneurysm of a small pancreatic branch of the inferior pancreaticoduodenal artery. Brachial artery access facilitates easier cannulation of branches arising from the superior mesenteric artery as this route is less tortuous. In another patient, catheterisation of both the right and left common femoral arteries was necessary because of underlying median arcuate ligament syndrome with retrograde flow through the gastro-duodenal artery into the hepatic artery via the superior mesenteric artery; simultaneous catheterisation of the superior mesenteric artery and coeliac axis was required for successful embolisation.

At angiography, transcatheter coil embolisation was attempted in 11 patients (84.6%). This was successful at the first attempt in nine patients (81.8%) and failed in two patients (18.2%). One of the patients that were successfully treated had six pseudoaneurysms, all of which were successfully embolised. One patient, who had initially been successfully embolised, had recurrence of their pseudoaneurysm four days later and was subsequently re-embolised without further complications (Figure 2). Embolisation was not performed at angiography in two patients (15.4%) because the pseudoaneurysm had thrombosed spontaneously (n=1) or was technically inaccessible (n=1). The patient with a technically inaccessible pseudoaneurysm was successfully treated with percutaneous US-guided injection of 400 IU of human thrombin (Tisseel, Baxter, Norfolk, UK).

Of the two patients that failed initial embolisation, one patient underwent angiography five days later, and the pseudoaneurysm thrombosed following repeated attempts at catheterisation. The other patient had two pseudoaneurysms and underwent percutaneous CTguided injection with 4,500 IU of bovine thrombin (Bovine Thrombin, Biomed, Lublin, Poland). Unfortunately, this patient had early recurrence and rebleed within 24 hours.

None of the patients included in this study underwent surgery.

Investigations

Patients included in this study were investigated with computerised tomography (CT). Portal venous phase contrast enhanced CT (PVPCT) was performed following a delay of 70 seconds after injection of 75 mL of intravenous iodinated contrast. Arterial phase CT was performed using 75 mL of intravenous contrast and automatic bolus tracking software (Surestart, Toshiba Medical Systems, Tokyo, Japan). The region of interest was placed over the upper abdominal aorta. Real time low dose serial monitoring scans were used to identify contrast within the aorta which then triggered the arterial phase scan and 1mm overlapping slices were obtained.

Mesenteric Angiography and Embolisation

All patients underwent angiography by a consultant interventional radiologist (P.T., P.B., J.G.P., M.D.). A variety of 4 Fr or 5 Fr mother catheters were used (Cobra or Simmons 1, Cordis, Miami Lakes, FL, USA; SOS Omni, AngioDynamics, Cambridge, UK) for initial angiography. In cases where access to smaller vessels was required, a micro-catheter (Progreat, Terumo, Tokyo, Japan) was used. Embolisation of the feeding vessel, and where necessary the draining vessel, was performed using either 0.035” or 0.018” fibered coils (Boston Scientific, Natick, MA, USA). No covered stents were used. Successful embolisation was defined as the absence of filling of the pseudoaneurysm at completion angiography, and clinical resolution of bleeding.

ETHICS

Informed consent and Institutional Review Board approval were not required because of the retrospective nature of this study. The patients were treated according to the ethical guidelines of the “World Medical Association (WMA) Declaration of Helsinki - Ethical Principles for Medical Research Involving Human Subjects” adopted by the 18th WMA General Assembly, Helsinki, Finland, June 1964 and amended by the 59th WMA General Assembly, Seoul, South Korea, October 2008.

STATISTICS

Descriptive statistics only were evaluated: absolute and relative frequencies, median and range.

RESULTS

Outcome

All 12 patients that were successfully treated had a follow-up contrast enhanced PVPCT during hospital admission over a median of eight days (range: 1-28 days). Following discharge, further imaging was performed and radiological resolution of the pseudoaneurysm was confirmed in 11 patients (arterial phase CT: n=8; PVPCT: n=2; duplex US: n=1; loss to follow-up: n=1).

The morbidity rate following coil embolisation was 25.0% (n=3). Splenic infarction following embolisation of the splenic artery occurred in one patient. Coil migration from the splenic artery to a branch of the right hepatic artery occurred in a further patient. The coil was left in-situ as there was no evidence of thrombosis of the other hepatic artery branches. One patient developed an infected haematoma adjacent to the pseudoaneurysm which was managed by USguided percutaneous drainage.

The mortality rate in this cohort was 8.3% (n=1). Following failed transcatheter embolisation, this patient was treated with CT-guided injection of bovine thrombin, but subsequently re-bled and died of a massive pulmonary embolus 15 days after diagnosis. This patient had an underlying diagnosis of Ehlers- Danlos syndrome. Angiographic studies in patients with Ehlers-Danlos are recognised to be hazardous due to the friable nature of their arteries, and surgical intervention also carries a high risk of serious complications [16, 17].

Overall, all 12 patients demonstrated resolution of their pseudoaneurysms, either due to successful treatment or spontaneous resolution (Figure 2). The median followup after treatment was 20 months (range: 2-31 months).

DISCUSSION

Haemorrhage is a rare but potentially fatal complication in patients with pancreatitis, and often due to haemorrhage from non-pancreatic conditions such as gastritis, peptic ulcers, oesophageal varices or Mallory-Weiss tears. Bleeding pseudoaneurysms secondary to pancreatitis are an uncommon cause of haemorrhage and when it does occur it is usually into the peritoneal cavity rather than the gastrointestinal tract, making prompt and accurate diagnosis challenging [18, 19].

Duplex US and PVPCT are the most common first-line investigations in assessing acute pancreatitis. To enable detection of pseudoaneurysms, US examination must include pulsed or colour Doppler (duplex US) of all cystic masses to distinguish a pseudocyst from a pseudoaneurysm [20]. The sonographic appearance of a pseudoaneurysm changes when clot develops within its lumen rendering the diagnosis very difficult even with colour Doppler [21]. In the present series, US with colour Doppler failed to detect the presence of a pseudoaneurysm in two patients which were later diagnosed on PVPCT and arterial phase CT. Similar results have been observed in other studies, and most clinicians would conclude that the diagnostic value of Doppler US in the detection of pseudoaneurysms complicating pancreatitis is limited [22, 23]. Although PVPCT is a suitable non-invasive method for detecting pseudoaneurysms [22, 24, 25, 26], its role in the diagnosis of pseudoaneurysms is limited by its failure to identify smaller pseudoaneurysms [23, 27, 28]. In the present series, PVPCT failed to detect small pseudoaneurysms in five patients which were later diagnosed on arterial phase CT (Figure 3).

Arterial phase CT is a suitable first-line investigation for diagnosing pseudoaneurysms associated with pancreatitis with a similar sensitivity rate that of angiography [28, 29, 30]. In the present series, arterial phase CT detected all pseudoaneurysms when used as a first-line (n=2), second-line (n=4) and third-line investigation (n=1). Arterial phase CT has the additional benefit of planning further management by clearly demonstrating the arterial anatomy, providing a roadmap for further intervention. This allows for targeted visceral angiography as well as the identification of difficult cases prior to intervention. In this study, not all patients (n=3) underwent an arterial phase CT to confirm resolution of the pseudoaneurysm. One reason for this non-uniformity follow-up was due to the fact that two patients were embolised prior to 2007 when follow-up with arterial phase CT was not practiced routinely and one patient underwent a PVPCT to exclude an intra-abdominal collection where the pseudoaneurysm was shown to have resolved.

Conventional angiography has long been the gold standard for the detection of pseudoaneurysms secondary to pancreatitis [28, 31] with a high sensitivity and specificity [9, 11, 27, 32, 33, 34]. Angiography also permits immediate endovascular embolisation which is considered by many authors the treatment of choice [25, 26, 31, 33, 35], with a success rate ranging from 79% to 100% [9, 32, 36]. In the present study, the embolisation success rate was 82%. Although it is less invasive and has a lower morbidity and mortality rate than surgery, there are technical limitations such as difficulty in reaching the feeding vessel. In addition, endovascular-directed therapy is associated with rare, but potentially fatal complications, such as rupture of the pseudoaneurysm during embolisation [35] or perforation of the artery with the vascular catheter [32, 37]. Previous studies have reported re-bleeding rates ranging from 6.1% to 37% [38, 39], with an associated mortality as high as 33% [22]. Other recognised complications include splenic infarction and coil migration as observed in this case series. Splenic and intestinal necrosis [39, 40], vascular dissection, and misplaced stents [29] have also been reported. The present study reported a complication rate of 25%, in-line with other published studies [22, 38, 39]. Fibered coils were used to embolise the feeding vessels and if necessary, the draining vessels. Covered stents have been advocated in the management of pseudoaneurysms arising from larger vessels with the advantage of preserving arterial flow [41, 42, 43, 44]. Covered stents however require a higher profile and stiffer delivery system than does endovascular coil embolisation, with reduced tortuosity, high calibre arteries [45]; both the size and location of the vessels supplying the pseudoaneurysms in this series were not amenable to covered stents. In addition, the preservation of arterial flow was not essential because of the rich collateral supply around the duodenum and pancreas with embolisation carrying only a small risk of infarction/ischaemia.

Another radiological alternative to embolisation is thrombin injection. Percutaneous thrombin injection was first described in the management of pseudoaneurysms of the femoral artery [46] and is now an established treatment for iatrogenic peripheral pseudoaneurysms [47]. There are numerous case reports reporting the successful management of visceral pseudoaneurysms secondary to pancreatitis delivered either by radiologically-guided percutaneous injection [48, 49, 50, 51] or endoscopic ultrasoundguided injection [52, 53, 54]. The largest series includes four patients who underwent primary percutaneous thrombin injection for low-flow pseudoaneurysms not visible on angiography but present on CT. Despite initial successful thrombosis of the aneurysms, all aneurysms recanalised within four weeks and required repeat percutaneous thrombin injections [25]. Recanalisation and late recurrences of the pseudoaneurysms after thrombin injection has also been reported in other studies [25, 48, 50] highlighting the importance of mandatory follow-up in these patients. Two patients in this case series were treated with thrombin injection, with a recurrence observed in one patient. Further studies are clearly needed to assess the efficacy and success rate of thrombin-directed therapy in pseudoaneurysms secondary to acute pancreatitis.

This study is limited by its small sample size and retrospective nature. Furthermore, only two patients were treated with thrombin injection. Therefore, firm conclusions on the outcomes of this technique cannot be made. Nevertheless, based on the results of this study and current published literature, a management algorithm has been suggested (Figure 4).

CONCLUSION

Patients with pseudoaneurysms secondary to pancreatitis are a difficult and unpredictable cohort of patients to manage, with high mortality rates associated with haemorrhage. Endovascular embolisation is a suitable first-line management strategy. The role of thrombin-directed therapy is yet to be defined. In cases where interventional radiological treatment has failed to achieve haemostasis for bleeding pseudoaneurysms, surgical management should be instituted without delay.

Sources of funding

None

Conflict of interest

None declared

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