Abstract
Percutaneous pancreatic interventions performed by abdominal radiologists play important diagnostic and therapeutic roles in the management of a wide range of pancreatic pathology. While often performed with endoscopy, pancreatic mass biopsy obtained via a percutaneous approach may serve as the only feasible option for diagnosis in patients with post-surgical anatomy, severe cardiopulmonary conditions, or prior non-diagnostic endoscopic attempts. Biopsy of pancreatic transplants are commonly performed percutaneously due to inaccessible location of the allograft by endoscopy, usually in the right lower quadrant or pelvis. Percutaneous drainage of collections in acute pancreatitis is primarily indicated for infection with clinical deterioration and may be performed alone or in combination with endoscopic drainage. Post-surgical pancreatic collections related to pancreatic duct fistula or leak also often warrant therapeutic percutaneous drainage. Knowledge of appropriate indications, strategies of approach, technique, and complications associated with these procedures is critical for a successful clinical practice.
Keywords: Biopsy, Cross-section interventional radiology, Pancreas, Pancreatic cancer, Pancreatitis, Drainage
Introduction to pancreatic biopsies
Percutaneous image-guided biopsies are performed daily by most radiology practices and play a significant role in the diagnosis and management of various conditions. However, requests for image-guided biopsies of the pancreas are infrequent, as the vast majority of these are performed via an Endoscopic ultrasound (EUS) approach by gastroenterologists. Thus, radiologists may be uncertain about techniques, approaches, and potential complications for percutaneous image-guided biopsy of the pancreas. Although infrequently requested, percutaneous biopsy of the pancreas has long been reported in the literature with the first major case series published in 1982 [1]. These biopsies were not typically performed prior to the widespread availability of Computed tomography (CT) and development of rapid CT scan times and image reconstruction. However, these biopsies may be performed under either CT or Ultrasound (US) guidance, and the approach for biopsy of the native pancreas and transplant pancreas may differ. As a result, it is important for radiologists to understand the potential advantages and disadvantages of both image-guided approaches for the requested procedure.
Rationale for percutaneous vs. endoscopic biopsy approach
In the diagnostic workup of both solid and cystic pancreatic lesions, core biopsy and/or fine-needle aspiration remain essential. In most patients, the pancreas is easily accessible by endoscopy and EUS, which allows for real-time visualization of the needle. These procedures are almost always performed by gastroenterologists trained in this technique and account for the vast majority of pancreatic biopsies. As a result, gastroenterologists often have far more familiarity and experience in this procedure and routinely perform far more pancreatic biopsies than radiologists. The EUS procedure occurs via a natural orifice, which permits biopsy without a skin puncture or incision, and allows for real-time targeting of specific areas of a lesion that may improve diagnostic yield. Importantly, EUS-guided pancreatic biopsy allows for access to many portions of the pancreas without traversing multiple organs along the needle path, which may lead to less complications. These biopsies may be performed as fine-needle aspirations with a 22 gauge or 25-gauge needle, but 18-gauge core biopsies are capable of being obtained [2]. Finally, the performance of EUS is often coupled with Endoscopic retrograde cholangiopancreatography (ERCP), which allows for placement of biliary stents to relieve biliary obstruction at the same time as the diagnostic procedure.
Given that pancreatic biopsies are seldom requested to be performed by radiologists, there can be considerable hesitancy to perform the biopsy. This is primarily due to unfamiliarity of feasibility of percutaneous pancreatic biopsy, fear of potential complications, and the anatomic location of the pancreas. Percutaneous biopsies of the pancreas can be performed as either fine-needle aspirations or core biopsies, allowing for similar sample acquisition to EUS. There are several potential limitations of EUS-guided biopsy which may make a percutaneous approach the only possible or feasible option. First, not all hospitals are staffed by gastroenterologists with training in advanced endoscopy and EUS and this procedure may not be able to be offered to patients (particularly in the rural setting). However, almost all hospitals have the capability of performing CT and US-guided biopsies in radiology, which may expedite care of these patients and avoid referral to an outside hospital with EUS capabilities. In patients who are at high risk for sedation, percutaneous biopsies can often be performed with less sedation than a typical endoscopic biopsy. The percutaneous approach may be preferred if there is clinical concern for cardiopulmonary compromise during endoscopy. Also, in patients who have undergone prior gastrointestinal surgery, including Roux-en-Y gastric bypass or prior Billroth resections, retrograde access of the afferent limb may be challenging and requires the use of double-balloon enteroscopy [3]. However, the EUS is often limited by length and may not be able to successfully image portions of the pancreas depending on the patient’s gastrointestinal anatomy. In these patients, percutaneous biopsy may be the only option for a diagnosis outside of surgery. Patients who have undergone pancreas transplants also may require biopsies to evaluate for rejection, and given their typical location in the lower quadrants these pancreas biopsies necessitate a percutaneous approach. Finally, endoscopy is considered an aerosol-generating procedure, while percutaneous biopsies are generally not. This aspect became particularly important during the COVID-19 pandemic, when some institutions initially closed endoscopy suites to limit spread of the virus and conserve Personal protective equipment (PPE). Although temporary, at many institutions this led to a multidisciplinary approach to determine alternate approaches to obtain a pathological diagnosis in patients and avoid delays in diagnosis and treatment. Percutaneous biopsy under moderate sedation often utilizes less PPE than endoscopy, although there is considerable variation among institutions and may be a preferred approach in a PPE-limited setting.
Native pancreatic biopsy
The technique percutaneous biopsy of lesions in the native pancreas was first described in a case series from 1982, which reported a diagnostic accuracy rate of 82% [1]. These biopsies may be performed as either fine-needle aspirations or core biopsies and can be performed under US or CT guidance. As with many abdominal biopsies, US may be the initial modality of choice, allowing for real-time visualization and guidance of the biopsy needle during the procedure (Fig. 1). An initial study of US-guided pancreatic mass fine-needle aspiration in 187 cases found that over 95% of samples were adequate for cytologic evaluation and a greater than 85% accuracy rate in differentiating benign and malignant processes [4]. In this study, no false-positive biopsy results were reported, but approximately 13% of cases resulted in a false-negative result [4]. The false-negative rate of US-guided percutaneous biopsy is within the range of reported false-negative results for endoscopic biopsy, with rates ranging from 5 to 19% [5–8]. In a separate retrospective review of US-guided pancreatic biopsies, a histologic diagnosis was achieved in 147/153 patients with a sensitivity of 90% and a specificity of 95% [9].
Fig. 1.
59-year-old female with suspected pancreatic mass and multiple negative prior endoscopic biopsies. Initial pre-biopsy ultrasound image A demonstrates a hypoechoic pancreatic mass located posterior to the left hepatic lobe. Ultrasound image obtained during the biopsy B demonstrates a transhepatic approach with an 18-gauge core biopsy needle successfully within the pancreatic mass
The technique for performing US-guided biopsies of the native pancreas begins with an ultrasound of the upper abdomen to determine if the lesion of interest can be visualized. Preprocedural workup for the biopsy should include a review of patient’s history and medications and assessment of the platelet count, prothrombin time, and International Normalized Ratio (INR). As per the 2019 Society of Interventional Radiology Guidelines, these biopsies are considered “high-risk” and the recommended thresholds include a platelet count of 50 × 109/L or greater and an INR value of less than 1.8 [10]. Patients are instructed to be nil per os for the exam to minimize the effect of bowel gas potentially obscuring the pancreas and to allow for safe administration of moderate sedation during the procedure. Typically, these are performed via an anterior approach with the patient in the supine position and utilize a 4 MHz curved abdominal ultrasound probe. If the lesion of interest can be localized, either a core biopsy or fine-needle aspiration procedure can be performed as per usual institutional guidelines. In some cases, a transhepatic or transgastric approach may be required and a single puncture can be utilized with a trocar technique. Typical postprocedural observation times vary among institutions without consensus, but many centers (including our own) monitor patients for 3–4-h post-biopsy.
The majority of percutaneous native pancreatic biopsies are performed under CT guidance, as the retroperitoneal location of the pancreas and patient body habitus often makes US visualization of the pancreas challenging. Unlike US, CT is not limited by these factors and allows for multiple different approaches for performing a pancreatic biopsy. For example, while CT-guided biopsies may also utilize an anterior (and potential transhepatic or transgastric) approach, they may also be performed from a lateral or posterior approach depending on the location of the pancreatic lesion (Figs. 2, 3, 4). CT-guided biopsies can be performed either utilizing CT fluoroscopy or repeating limited helical CT scans. A recent retrospective review of 82 consecutive CT-guided pancreatic biopsies reported that an anterior approach was utilized in 79.3% of cases, but only necessitated a transgastric/transhepatic approach in 14.6% [11]. In this study, almost 82% of biopsies were performed as core biopsies with a needle size ranging from 18 to 22 gauge and a mean number of three samples was obtained [11]. This resulted in a conclusive result in 82.9% of patients and demonstrated a diagnostic yield similar to EUS fine-needle/core biopsy, prompting the authors to conclude that this approach may be considered where endoscopy facilities are limited [11].
Fig. 2.
43-year-old male with suspected enhancing pancreatic head mass diagnosed on CT A during the COVID-19 pandemic with no availability of endoscopy facilities. CT-guided biopsy images B and C demonstrate a posterior pararenal approach with successful targeting and biopsy of the pancreatic head lesion
Fig. 3.
55-year-old male with history of Roux-en-Y gastric bypass suspected pancreatic head mass and superior mesenteric vein thrombosis status post failed endoscopic biopsy (A). CT-guided biopsy image B demonstrates successful pancreatic biopsy utilizing an anterolateral approach, avoiding adjacent bowel and the thrombosed superior mesenteric vein
Fig. 4.
49-year old male with suspected pancreatic body adenocarcinoma A status post negative endoscopic biopsies. CT-guided biopsy image B demonstrates a successful lateral approach with the patient in a slightly oblique position, allowing for displacement of the colon and small bowel along the needle tract
As with any biopsy, there is always a risk of bleeding and infection. Additional unique complications related to native percutaneous pancreatic biopsy (both from an endoscopic and percutaneous approach) include post-biopsy pancreatitis and bowel perforation (Fig. 5). In the published literature, the rates of bleeding are quite low (1–2%) with only one report of a clinically significant bleeding resulting in patient death [4, 9, 11]. In most cases, bleeding was self-limited and resolved spontaneously. Additionally, no reported infectious complications were noted in the literature, although there are a limited number of manuscripts on the topic. While there is often concern for eliciting an episode of post-biopsy pancreatitis, studies suggest that this is a rare complication with an overall reported rate of post-biopsy pancreatitis ranging from 1.1 to 11% [11–14]. A study evaluating the risk of a transgastric approach to CT-guided pancreatic biopsy with a 17/18-gauge coaxial needle system found no complications aside from transient pneumoperitoneum that resolved without treatment [15]. It is important for radiologists to understand that when a core biopsy is performed via an endoscopic approach, this procedure always results in a transenteric route and violation of the bowel wall. Published data suggest that even if bowel is transgressed during a biopsy, the rate of frank peritonitis is quite low (0.3%) and the benefits of the procedure likely outweigh the risk [12, 16, 17]. Additionally, next-generation sequencing of tumors (including pancreatic tumors) is being performed with increasing frequency and allows for identification of potential targetable mutations. A study evaluating the impact of biopsy (including both percutaneous and endoscopic) on patients with inoperable pancreatic tumors found that biopsy did not adversely affect survival time and demonstrated an estimated relative risk of death in the biopsy cohort of 0.85 when compared to the non-biopsy cohort, illustrating the importance that a tissue sample can have on patient management and outcomes [18].
Fig. 5.
71-year-old male with pancreatic head mass (not shown) demonstrates an atropic but normal appearance on pre-biopsy CT image (A). Following endoscopic biopsy, CT image demonstrates new peripancreatic stranding, consistent with post-biopsy pancreatitis (B)
Transplant pancreatic biopsy
In contrast to the native pancreas, in many institutions clinicians typically rely on radiologists to perform image-guided biopsies of pancreatic allografts. A major factor in this decision is the anatomic location of the transplant pancreas, which is typically anastomosed to a loop of small bowel in the right lower quadrant or urinary bladder and often performed with a simultaneous kidney transplant. This location is challenging or impossible for endoscopists to reach and thus, a percutaneous approach is often preferred. Similar to other solid organ transplants, histopathology remains the gold standard for evaluating for and staging rejection. For pancreatic transplants, clinical criteria for rejection include monitoring of serum glucose, serum amylase, serum C-peptide level, hemoglobin A1C, and urinary amylase (if bladder drained), but these are non-specific and have a number of alternate etiologies [19]. Causes of pancreatic transplant rejection vary over time, but ultimately an allograft biopsy allows for identification of rejection and the etiology, which will guide management of the patient.
Due to the much more superficial location of the transplant pancreas when compared to the native pancreas, the vast majority of pancreas allograft biopsies are performed under ultrasound guidance. In cases where the transplant pancreas cannot be visualized under ultrasound, CT may be employed to increase confidence of visualization and targeting (Fig. 6). Ultrasound is preferred by many due to the constant peristalsis of adjacent bowel and real-time visualization of both the needle and vascular supply to the allograft (Fig. 7). Typically, once the vascular supply is identified, the needle is directed in a position away from the vasculature to minimize the risk of vascular injury, bleeding, and potential allograft compromise (Fig. 8). An initial study of 35 patients who underwent an ultrasound-guided pancreatic allograft biopsy with standardized histologic grading found a significantly increased graft and patient survival at 1 year [20]. Importantly, in this study acute rejection was only found in 11% of cases of graft loss and other important histologic findings included identification of endotheliitis, vasculitis, and confluent acinar necrosis; all of which are associated with decreased allograft survival [20]. Using the clinical criteria alone for identification of acute rejection only demonstrated a positive predictive value of 72%, highlighting the importance of biopsy [20]. The diagnostic yield of a percutaneous pancreatic allograft biopsy is high and somewhat dependent on the study and the medical provider performing the biopsy. In two larger studies where biopsies were performed by non-radiologists, the diagnostic adequacy of samples ranged from 85 to 88%, whereas a retrospective study evaluating yield of biopsies performed by radiologists found a diagnostic adequacy rate of over 96% [21–23].
Fig. 6.
Axial CT image without intravenous contrast A demonstrates a right lower quadrant pancreas transplant that was unable to be localized by ultrasound for biopsy. CT-guided biopsy image B demonstrates the patient in the oblique position with successful needle biopsy of the transplant pancreatic tail
Fig. 7.
Ultrasound images with (A) and without (B) color Doppler demonstrate a normal-appearing transplant pancreas in the right lower quadrant with successful localization of the vascular pedicle
Fig. 8.
Ultrasound with color Doppler image A demonstrates localization of a right lower quadrant pancreatic transplant for biopsy with successful identification of the vascular pedicle. Ultrasound-guided biopsy image B demonstrates successful advancement of the biopsy needle into the pancreatic transplant
As with native pancreatic biopsies, radiologists may be uncertain and concerned about the potential complications that may arise following a pancreatic transplant biopsy. Overall, the rate of post-biopsy complications ranges from 1 to 3% and the most common complication is bleeding [21–23]. Other reported complications include pancreatitis, pancreatic fistula, pancreatic leak, gross hematuria (for a transplant anastomosed to the urinary bladder), severe pain, and non-targeted biopsy. Many of these are self-limited and do not require treatment, but some cases of bleeding and pain may require overnight hospitalization and/or intervention. Following pancreatic transplant biopsies, patients are typically observed in the postprocedural recovery area for 2–3 h to monitor for signs and symptoms of bleeding and to ensure that their pain is under control.
Percutaneous drainage in pancreatitis
Introduction
Acute pancreatitis is a common acute inflammatory process of the pancreas and has a range of severity and complications. While most episodes of acute pancreatitis are mild and will resolve within a short time period of approximately 1 week, severe pancreatitis occurs in 15–20% of patients and takes a prolonged, complex clinical course that often includes the development of pancreatic and peripancreatic collections [24–27]. The interventional approach to management of pancreatitis and local complications has evolved over the past several decades. While surgical debridement was once considered the standard therapy for symptomatic or infected collections, and minimally invasive interventions, including percutaneous drainage, have now become the preferred treatment and offer the benefits of minimizing morbidity and avoiding the poor outcomes associated with invasive surgery [25, 28].
Types of acute pancreatitis
The management of pancreatitis requires a multidisciplinary team, which includes the radiology proceduralist. Appropriate interventional management by the proceduralist requires knowledge and recognition of the classifications of pancreatitis, associated fluid collections, and the imaging features of each. The 2012 revised Atlanta classification (RAC) is an international consensus that defines the clinical and radiologic criteria for the diagnosis of acute pancreatitis and differentiates the two types of acute pancreatitis into interstitial edematous pancreatitis and necrotizing pancreatitis. The RAC also provides objective terminology to describe the morphology of pancreatic and peripancreatic collections [29].
Interstitial edematous pancreatitis (IEP) is inflammation of the pancreas without necrosis. The imaging findings of IEP are diffuse or localized pancreatic enlargement with peripancreatic edema and possibly peripancreatic fluid. The parenchyma enhances relatively homogeneously on contrast-enhanced CT and MRI. Necrotizing pancreatitis (NP) is pancreatic inflammation with necrosis of the parenchyma, peripancreatic tissues, or both. Early in the disease time course, the enhancement pattern of NP is often patchy and heterogeneous, sometimes indistinguishable from IEP. A more well-demarcated area of non-enhancing parenchyma will become evident later in the disease, indicating parenchymal necrosis. Peripancreatic necrosis is characterized by peripancreatic collections containing both fluid and heterogeneous and non-fluid components, consistent with necrotic tissue (Fig. 9) [30, 31].
Fig. 9.
Acute interstitial edematous pancreatitis and necrotizing pancreatitis in two patients. A Axial IV contrast-enhanced CT in a patient with acute IEP showing peripancreatic stranding and fluid (arrow) and mildly heterogeneous enhancement of the pancreas (arrowhead). B Axial IV contrast-enhanced CT in a patient with acute NP showing a large area of non-enhancement of the pancreas and peripancreatic stranding (arrow). A small area of enhancing pancreatic parenchyma is seen in the pancreatic head (arrowhead)
Pancreatic and peripancreatic collections
Pancreatic and peripancreatic collections are local complications identified and monitored by imaging, most commonly with Contrast-enhanced CT (CECT) or MRI [26, 27]. These collections are classified on the basis of symptom duration and designated as acute if < 4 weeks after onset and delayed if > 4 weeks after onset. Classification of the collections also depends on the type of ongoing pancreatitis—IEP or NP.
Fluid collections occurring with IEP are termed Acute peripancreatic fluid collections (APFCs) and pseudocysts. APFCs occur during the first 4 weeks in IEP. These fluid collections will appear as homogeneous fluid density and lack a defined wall. No intra-pancreatic extension is present. APFCs will usually remain sterile and resolve without drainage [29, 30, 32]. Pseudocysts occur after 4 weeks in IEP and are typically peripancreatic. Pseudocysts have a defined wall/capsule and contain no non-liquid component (Fig. 10) [29, 30].
Fig. 10.
Peripancreatic collections in interstitial edematous pancreatitis. A Axial IV contrast-enhanced CT in a patient with acute IEP and simple, homogeneous fluid density peripancreatic collections (arrow). B Axial IV contrast-enhanced CT in a patient with a history of IEP beginning 8 weeks ago showing a homogeneous fluid density peripancreatic collection (arrow) abutting the pancreatic body (arrowhead) with an enhancing capsule/rim, compatible with a pseudocyst
In NP, collections are termed Acute necrotic collections (ANC) within the first 4 weeks and walled-off necrosis (WON) after the first 4 weeks. ANCs will be heterogeneous and contain variable amounts of liquid and non-liquefied material, such as solid appearing or fatty components, consistent with necrotic debris (Fig. 11). In the early phase of pancreatitis, distinguishing between necrotic and non-necrotic collections can be difficult, but often becomes clear by the 2nd week at which time either CECT or MRI can be repeated [29]. MRI can better delineate necrotic debris within collections that is unrecognized by CT (Fig. 12) [33].
Fig. 11.
Peripancreatic and pancreatic collections in necrotizing pancreatitis. A Axial IV contrast-enhanced CT in a patient with acute NP and ANCs involving the pancreatic parenchyma (arrowhead) and the peripancreatic tissues (arrow). B Axial IV contrast-enhanced CT in a patient with NP and a large area of WON occupying the pancreatic body and tail with an enhancing capsule (arrows). Note the heterogeneous appearance of the collections in NP which contains fluid density intermixed with fat density
Fig. 12.
Necrotic debris in walled-off necrosis. A Axial IV contrast-enhanced CT in a patient with WON involving the pancreatic body and tail with subtle heterogeneous density in the collection indicating necrotic debris (arrowhead). B Axial T2W sequence in the same patient obtained the next day showing comparatively more obvious necrotic debris in the same WON as indicated by heterogeneous signal intensity (arrowhead)
Infection
Infection in pancreatitis can be suspected based on clinical signs, such as fever or bacteremia, or if gas is seen within a collection on imaging (Fig. 13) [29]. Wall enhancement is not a reliable imaging finding for infection and can be seen in sterile pseudocysts and WON [30]. While any collection in pancreatitis can be sterile or infected, necrosis becomes infected more frequently and carries a mortality rate of up to 30% [25].
Fig. 13.
Gas within necrotizing pancreatitis collections due to infection. A Axial PO and IV contrast-enhanced CT showing a patient with NP with a small amount of gas in WON near the pancreatic head (arrow). No extraluminal contrast was seen to indicate bowel perforation. This patient required percutaneous drainage due to infection. B Axial non-contrast CT shows extensive gas within a large infected ANC replacing the pancreas. Percutaneous and endoscopic drainage were pursued in this patient, but ultimately surgical retroperitoneal debridement was required
Role of percutaneous intervention in pancreatitis
Historically, open surgical debridement was the mainstay therapy for infected necrosis and symptomatic sterile necrosis, but is associated with high rates of complication and mortality ranging 11–39% [34–36]. The treatment paradigm has evolved, and the traditional surgical approach has been replaced by less invasive measures, including percutaneous drainage. As minimally invasive treatment modalities for the management of pancreatitis have become more widely available, consensus practice guidelines now include recommendations regarding clinical indications for intervention, intervention strategies, and timing of intervention [25, 27, 28].
Clinical indications for drainage
Necrotizing pancreatitis
The Working Group International Association of Pancreatology/American Pancreatic Association (IAP/APA) Acute Pancreatitis Guidelines define the clinical indications for percutaneous, endoscopic, or surgical drainage of collections in necrotizing pancreatitis. Indications include (1) suspected or confirmed infected necrosis with clinical deterioration and (2) ongoing organ failure for several weeks after the onset of acute pancreatitis, in the absence of infection. Other clinical indications for drainage in necrotizing pancreatitis include (1) mechanical gastric, intestinal, or biliary obstruction, (2) persistent “unwellness,” including pain, nausea, vomiting, or nutritional failure, and (3) symptomatic disconnected duct syndrome [25–28, 37]. Disconnected duct syndrome is characterized by full transection of the pancreatic duct by necrosis resulting in symptomatic fluid collections due to leaking pancreatic fluid [37].
Sterile necrosis without clinical deterioration, organ failure, or persistent “unwellness” does not require intervention. A prospective observational cohort study of 639 patients with necrotizing pancreatitis reported that 62% of patients were successfully treated with conservative management only with a relatively low mortality rate of 7% [38].
Interstitial edematous pancreatitis
Drainage of fluid collections associated with IEP is usually not necessary, even when large APFC and pseudocysts are present, as these collections most commonly resolve without intervention [26, 32]. Rare exceptions to this principle include uncommon complications of pseudocysts, such as obstruction of the biliary or intestinal tract or prolonged symptoms, such as pain and nausea, for which drainage is indicated (Fig. 14) [27].
Fig. 14.
Pancreatic pseudocyst causing small bowel obstruction and requiring therapeutic percutaneous drainage. A Axial non-contrast CT in a patient with a large pseudocyst (arrow) in the left abdomen and multiple dilated bowel loops in the right abdomen (arrowheads). B Abdominal radiograph in standing position following placement of percutaneous drain (arrow) into the pseudocyst and persistently dilated bowel loops containing enteric contrast. C Follow-up coronal non-contrast CT 2 months later after drain removal shows a small residual pseudocyst (arrow) and resolved bowel obstruction
Intervention strategies
Multiple published series have defined the role of percutaneous catheter drainage in necrotizing pancreatitis, both as definitive monotherapy and as adjunct therapy in combination with endoscopic intervention [36, 38–41]. The recommended interventional strategy is the “step-up” approach, which begins with either percutaneous or endoscopic drainage of infected necrosis. If no clinical improvement is evident 72 h after the initial drainage and other drainable collections are present, a second drainage is performed. If additional drainage is not possible or if there is no clinical improvement after an additional 72 h, the next step is endoscopic necrosectomy or Video-assisted retroperitoneal debridement (VARD). The primary objective behind this approach is to control the infected necrosis with the least invasive measures and to postpone or avoid more invasive surgery. The step-up approach was shown to be superior to open necrosectomy for infected necrosis in the landmark Dutch PANTER trial with lower rates of new-onset organ failure, new-onset diabetes, and incisional hernia in the step-up group [36]. Trials have reported that up to 51% of patients managed with the step-up approach were adequately treated with drainage alone and did not require the next step of necrosectomy [36, 40].
Generally, the endoscopic transluminal/transmural approach for drainage is preferred to avoid the risk of pancreaticocutaneous fistula; however, the percutaneous approach plays an important role. Deep retroperitoneal extension of collections into the paracolic gutters and pelvis is often inadequately drained endoscopically and require percutaneous drainage (Fig. 15) [25, 27, 37, 39]. Percutaneous drainage can also provide a route for bedside irrigation and clearance of necrotic material [37]. In patients with infection who are too unstable for endoscopic management, percutaneous drainage can be critical in providing a means for source control [25].
Fig. 15.
Infected necrotizing pancreatitis requiring a combination of endoscopic and percutaneous drainage. A Coronal IV contrast-enhanced CT showing large peripancreatic and pancreatic WON containing gas (arrowheads) and an endoscopically placed cystogastrostomy (arrow). B Axial CT during CT-guided drain placement via a left retroperitoneal approach with catheter in appropriate position within the collection (arrow). This approach was chosen to provide a portal for future surgical videoscopic assisted retroperitoneal debridement; however, the patient recovered without the need for surgery
Intervention timing
If possible, delaying intervention for at least 4 weeks after the onset of acute pancreatitis is the standard recommendation by multiple published guidelines [25–28, 42]. These recommendations are primarily based on earlier literature when open necrosectomy was the treatment of choice for infected necrosis and performing surgery early (within 2–4 weeks) was associated with poor outcomes [34, 43, 44]. Delaying intervention avoids the inherent pro-inflammatory effect of surgical intervention in the early course of pancreatitis, a vulnerable clinical period when the systemic inflammatory response is driving morbidity and mortality. Delaying intervention also allows for liquefaction and encapsulation of necrosis, which can further demarcate areas of necrosis from viable pancreatic tissue. In the early stages of necrosis, when the affected pancreas is an inflammatory mass, unintentional removal of viable pancreas has been postulated as a possible etiology for increased rates of pancreatic insufficiency following necrosectomy [36, 38].
More data are needed regarding the timing of percutaneous and endoscopic intervention. While infected necrosis is considered an event occurring later in the disease course (> 4 weeks), nearly ¼ of patients will develop infected necrosis earlier [45]. Some published series using a step-up approach have also supported the benefit of delaying intervention [38], but a more recent study comparing outcomes of a step-up approach initiated that before versus after 4 weeks showed no increase in complications, similar improvement in organ failure, and a relatively low mortality in the early intervention group [46]. Early intervention with percutaneous and/or endoscopic drainage may be appropriate in select scenarios, such as clinical deterioration due to infected necrosis [37].
Image-guided aspiration
While image-guided aspiration of fluid collections in pancreatitis is feasible and safe, its utility and relevance have diminished [28, 47–49]. In the past, when necrosectomy was the treatment of choice, documented infection by aspiration was considered immediate indication for surgical management. Infected necrosis is now often managed conservatively with antibiotics, reserving intervention for clinical deterioration. Further, false-negative rates of greater than 20% have been reported with fine-needle aspiration [34, 50]. As such, published guidelines and consensus statements have recommended against routine aspiration for the diagnosis of infection [25, 27, 28]. Select clinical scenarios where aspiration might be appropriate include when fungal infection is suspected due to lack of clinical response to antibiotics [28].
Percutaneous drainage in the post-operative pancreas
Introduction
Despite modern advances in major pancreatic surgery, pancreatic fistula (e.g., leak) and abscess remain relatively common complications and are associated with increased mortality and morbidity, longer hospital stay, and increased costs [51–54]. Due to varying definitions of pancreatic fistula in the surgical literature and the overlap and grouping of terminology (e.g., fistula, leak, and abscess/infected fistula), a large range of occurrence rates have been reported, including up to 60% risk of fistula after distal pancreatectomy [55]. A now universally accepted definition and severity grading system of post-operative pancreatic fistula have been described by the International Study Group of Pancreatic Fistula. A clinically relevant fistula is defined as drain output of any measurable volume of fluid with an amylase level > 3 times the upper limit of institutional normal serum amylase, associated with a clinically relevant development/condition, such as persistent prolonged drainage > 3 weeks, infection, or related organ failure or death [51]. While the diagnosis is confirmed by drain criteria, any fluid collection or hemorrhage around the pancreatic anastomosis or resection suture line on imaging is concerning for fistula. Continuity of the collection with the pancreatic duct may also be visualized.
Pancreatic fistula pathophysiology and risk factors
Proposed mechanisms for pancreatic fistula differ based on the type of pancreatic surgery performed. Leakage of pancreatic sections from the pancreatic-intestinal anastomosis or from a traumatized surface of the gland is considered to be the sites of origin for fistula following Pancreaticoduodenectomy (PD) or Whipple procedure (Fig. 16). Several risk factors have been well established for PD fistula, including soft pancreatic texture, small ductal size, non-ductal adenocarcinoma pathology (such as duodenal or ampullary cancers), and intra-operative blood-loss greater than 1L [56]. Such risk factors have been implemented into a validated fistula risk score which influences surgical and management decisions, such as surgical drain placement and the timing of drain removal [57].
Fig. 16.
Pancreatic fistula after Whipple for pancreatic adenocarcinoma. A Axial IV contrast-enhanced CT showing a surgical bed fluid collection (arrows) near the pancreaticojejunostomy (arrowhead). B Follow-up axial CT was obtained after percutaneous drain placement via a right retroperitoneal approach showing the catheter in appropriate position and decreased size of the collection (arrowhead)
Increased ductal pressure due to functional obstruction at the sphincter of Oddi complex has been hypothesized as the mechanism for pancreatic stump leakage following Distal pancreatectomy (DP) (Fig. 17) [58]. Lack of epidural anesthesia has been associated with an increased risk for DP fistula, which is thought to be related to reduce need for narcotic medications and resultant decreased pressure at the sphincter of Oddi. Several other risk factors for DP fistula have been reported, including age < 60, obesity, neuroendocrine or non-malignant pathology, concurrent splenectomy, and vascular resection. These risk factors, however, did not accurately predict fistula formation when implemented into a risk scoring model [59].
Fig. 17.
Pancreatic fistula after distal pancreatectomy for pancreatic neuroendocrine tumor. A Axial MRI post-contrast T1W series in a patient with a hypervascular, solid mass in the pancreatic tail (arrow). B Axial IV contrast-enhanced CT following distal pancreatectomy showing a fluid collection (arrows) in the surgical bed centered around the remnant pancreas staple line (arrowhead)
Intervention strategies
Image-guided percutaneous drainage of post-operative pancreatic collections is technically safe and effective, and the prevalence of collections requiring drainage ranges up to approximately 20% [60, 61]. The utility of routine placement of surgical drains after pancreatic resection has been questioned with conflicting reports in the surgical literature; however, the presence or absence of surgical drains does not appear to reduce the need for percutaneous drainage of fistula in interventional radiology [62–65]. High technical success rates have been reported, ranging from 97 to 100%, defined by drain placement within the collection [60, 61]. Endoscopic methods for post-operative pancreatic collection drainage have also been successful [66, 67].
Performing percutaneous drainage
Preparation and planning
Preprocedural evaluation of the patient is a critical component to any successful percutaneous drainage. The Society of Interventional Radiology Consensus Guidelines for the Periprocedural Thrombotic and Bleeding Risk can be used as a general guide for risk assessment in percutaneous pancreatic drain placement, which is classified as a deep drainage with high bleeding risk [10]. INR and platelet count, as well as anticoagulation/antiplatelet holds should be considered in conjunction with a risk/benefit profile for the procedure and the patient’s overall clinical status. Under physician supervision, moderate IV sedation can be provided by nursing staff for patient comfort and pain control during the procedure.
Imaging review is necessary to confirm the presence of a collection, to plan the approach for drainage, and for modality selection. CECT or MRI that includes an arterial phase should be obtained if there is a concern for a pseudoaneurysm masquerading as a fluid collection, which is a rare, but recognized complication in pancreatitis, often involving the splenic artery.
Access routes
Several potential access routes to peripancreatic and pancreatic collections exist, and the route should be chosen with consideration of the clinical scenario and risk of traversing other potentially avoidable structures, such as bowel and mesenteric vessels. When possible, a left retroperitoneal approach through the left anterior pararenal fascia should be chosen for percutaneous drainage in necrotizing pancreatitis. This approach minimizes the risk of peritoneal and bowel transgression and also creates a portal for future minimally invasive necrosectomy by tract endoscopy or VARD (Fig. 15) [37]. A transgastric approach may be considered if endoscopy is unavailable or if surgical anatomy, such as Roux-en-Y gastric bypass, limits endoscopic access or necessitates a percutaneous feeding tube (Fig. 18). Following PD, a collection in the deep surgical bed surrounding the pancreatic-intestinal anastomosis can be accessed through the right anterior pararenal fascia using hydrodissection for displacement of the colon [68]. Subphrenic collections are common in both the post-operative setting and pancreatitis and preferably drained via a subcostal approach to avoid pleural transgression and associated risks of fistula and empyema. If a subcostal approach is not available, selecting the most anterior and inferior intercostal access point and angling the catheter up into the collection is recommended (Fig. 19) [69].
Fig. 18.
Transgastric drainage of walled-off necrosis in a patient with Roux-en-Y gastric bypass. A Axial IV contrast-enhanced CT showing a large collection of WON (arrow) with mass effect on the gastric pouch (arrowhead) which was causing clinical symptoms of obstruction. B Axial IV contrast-enhanced CT shows that the gastric remnant (arrowheads) is anteriorly displaced by the WON. C Because the patient was nutritionally deficient and percutaneous gastrostomy tube was going to be necessary for feeding in the future, a transgastric approach for drainage was performed to both drain the WON and establish a portal for gastrostomy placement. Axial IV contrast-enhanced CT following drainage shows transgastric access by the catheter into the WON (arrows) which is now smaller. D Subsequently, the drain was removed and a gastrostomy tube was placed through the same tract (arrow)
Fig. 19.
Subcostal approach for percutaneous drainage of walled-off necrosis via ultrasound guidance. A Axial IV contrast-enhanced CT in a patient with NP and WON in the distal pancreatic body (arrow). B Ultrasound image of the left upper quadrant with the transducer angled superomedially toward the pancreas shows placement of the needle and guidewire (arrowheads) within the collection (arrow). C Oblique sagittal reformatted IV contrast-enhanced CT following percutaneous drainage shows the catheter (arrow) coursing inferior to the rib to reach the WON, minimizing the risk of pleural transgression
Image guidance
The most commonly used modalities for image-guided deep drainages are ultrasound and CT, including CT fluoroscopy. Ultrasound offers the advantages of real-time visualization of the needle and catheter reaching the collection. The multi-planar capabilities of ultrasound are particularly useful in subphrenic collections that require an oblique or angled route to avoid critical overlying structures in the axial plane. CT has higher spatial resolution and may be necessary for small and deeper collections, or when technical factors, such as body habitus, may limit the approach with US. CT gantry angulation can be a helpful tool for an angled trajectory to reach collections.
Technique
Placement of a percutaneous drainage catheter into a collection is achieved by use of the Seldinger technique or trocar technique. The Seldinger technique involves placing a hollow introducer needle percutaneously into the collection, inserting a guidewire to secure access, and then subsequent removal of the introducer needle. This is followed by sequential dilation of the tract over the guidewire, insertion of the catheter over a metal or plastic stiffener into the collection, and removal of the guidewire and stiffener. While this method requires more steps than the trocar technique, the advantage is the ability to precisely target collections with narrow windows. The trocar technique uses a catheter mounted on a sharp trocar which is directly inserted without a guidewire into the collection after superficial blunt dissection. Preceding the catheter insertion, placement of a guiding needle into the collection can provide an external reference for accurate placement of the catheter in tandem, so called the “tandem” trocar technique. The trocar technique allows the operator to quickly insert the catheter; however, this technique does not allow catheter repositioning after the first pass [70–72]. An additional modification to the trocar technique, the curved trocar technique, involves bending the metal trocar to allow intermittent visualization and redirection/adjustment of the catheter under CT fluoroscopy prior to being positioned within the collection [73].
A large range catheter size has been reported for use in pancreatic collections, and selection of the catheter size will vary depending on the contents of the collection. Generally, pancreatic collections require larger catheters for drainage due to viscous contents, possibly related to effects of amylase and lipase on fat necrosis. Small catheters (8–12 Fr) can be upsized to larger catheters (14–30 Fr) if solid necrotic components are present [61, 70]. Multiple catheters may be required for adequate drainage of complex collections. Breaking up loculations within collections can be performed by manipulation of a wire or metal stiffener during the initial drain placement [74]. Continuous or intermittent large volume irrigation with normal saline may also facilitate the drainage of complex collections when multiple drains are present. Irrigation volume may range from 0.5 to 1.5 L/drain/day depending on the collection size [71].
Drain management
Frequent and early drain monitoring on daily rounds ensures appropriate catheter function and position by assessing drain output and flushing the catheters with normal saline. If concern is raised for drain malfunction due to sudden decrease in output or failed clinical improvement, repeated cross-sectional imaging or injection under fluoroscopy can be performed. Intracavitary fibrinolytic agents, such as tissue plasminogen activator, can be instilled within the catheter to degrade fibrin bands in viscous collections and facilitate drainage [75]. When catheter output is less than 20 cc/day and the patient’s condition improves, drain removal can be considered after discussion with the multidisciplinary care team. Updated cross-sectional imaging can be obtained to ensure resolution of the collection.
Complications
Major complications in percutaneous drainage, such as uncontrolled bleeding and organ injury, are rare with reported rates of up to 4% [41, 61, 71]. Pancreaticocutaneous fistula in pancreatitis has been reported in up to 32%; however, the risk of fistula decreases when dual modality drainage is pursued with combined endoscopic and percutaneous catheters (Fig. 20) [40, 76]. An unusual complication observed in the author’s practice is breakdown/fracture of the drainage catheter by a collection associated with a pancreatic duct fistula, presumed to be related to the enzymatic contents of the collection (Fig. 21).
Fig. 20.
Pancreaticocutaneous fistula as a complication of percutaneous drainage. A Axial IV contrast-enhanced CT showing a patient with peripancreatic WON (arrow). B Axial non-contrast CT shows the percutaneous drainage catheter within the WON (arrow). C Following drain removal, the patient complained of fluid drainage at the skin through the tract of the prior drain. Axial IV contrast-enhanced CT shows persistence of the collection after drainage, now extending along the prior drain tract into the ventral abdominal wall reaching the superficial body wall (arrows)
Fig. 21.
Percutaneous drainage of a pancreatic fistula after distal pancreatectomy complicated by drainage catheter fracture. A Coronal IV contrast-enhanced CT showing a left upper quadrant fluid collection (arrow) adjacent to the pancreatic remnant staple line (arrowhead) consistent with pancreatic fistula. B–D Axial IV contrast-enhanced CT and fluoroscopic images obtained 15 days after drain placement shows fractured catheter fragments (arrow) which were subsequently retrieved in interventional radiology under fluoroscopy by loop snare
Conclusion
As illustrated above, the management of patients with abnormalities of the pancreas necessitates a multidisciplinary approach. Radiologists should not only be familiar with pancreatic imaging but also the potential advantages and disadvantages to percutaneous procedures performed on the pancreas. An interdisciplinary approach to the management of patients with pancreatitis allows for optimal patient selection and management, and radiologists should be familiar with guidelines and evidence surrounding management of percutaneous drains in peripancreatic fluid collections.
Declarations
Research involving human and animal rights
This article does not contain any studies with human or animal subjects performed by any of the authors.
Footnotes
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