Lee CM, Stewart L, Way LW. Postcholecystectomy Abdominal Bile Collections. Arch Surg. 2000;135(5):538-544. doi:10.1001/archsurg.135.5.538
The clinical syndromes caused by bile collections in the abdomen span a wide spectrum and their natural history and risks are not fully appreciated.
Analysis of 179 patients with bile fistulas after cholecystectomy, of which 154 patients had undrained bile collections.
To characterize the manifestations and natural history of abdominal bile collections.
A tertiary care teaching hospital.
Patients and Methods
The clinical findings in 179 patients with bile fistulas resulting from iatrogenic laparoscopic bile duct injuries and other miscellaneous operations between 1990 and 1999 were analyzed. The group of main interest consisted of 154 patients with undrained bile collections. Of these 154 patients, 21% had serious complications, including sepsis and multiorgan failure. The data were analyzed to identify the variables associated with this undesirable outcome.
Main Outcome Measures
Symptoms, physical findings, course of illness, and laboratory and imaging findings.
The clinical manifestations of intra-abdominal bile collections were initially discounted in 77% of patients, so the problem went unsuspected for a variable and often lengthy period. Abdominal pain and tenderness (bile peritonitis) gradually developed in 18% of patients with bile ascites. There were no differences in the initial clinical findings in this group compared with those who did not develop peritonitis. Nineteen percent of patients with undrained bile collections experienced serious morbidity. The initial clinical findings did not differ in these patients compared with those with a less complicated illness. Serious illness, however, was associated with the following: (1) a longer period of undrained bile (15.4 vs 9.2 days, P=.04) and (2) a higher incidence of infected bile (45% vs 7%, P=.001).
(1) Prominent abdominal pain and tenderness developed in only 21% of patients with abdominal bile collections; (2) the symptoms caused by bile collections were often subtle and their significance was overlooked, which resulted in a delay in diagnosis; (3) the early clinical findings could not distinguish patients who did become critically ill from those who did not; and (4) seriously ill patients more often had delayed drainage and infected bile. Still, failure to drain a bile collection within just 5 days resulted in serious illness in a few patients. Surgeons must watch for the clinical manifestations of bile ascites after laparoscopic cholecystectomy. This diagnosis should be suspected whenever persistent bloating and anorexia last for more than a few days; failure to recover as smoothly as expected is the most common early symptom of bile ascites. If bile collections were promptly diagnosed and drained, the rate of serious illness resulting from this complication would decline.
BILE COLLECTIONS within the peritoneal cavity have various causes, but they most often occur as a manifestation of bile duct injury or some other technical complication of laparoscopic cholecystectomy. Unless drains have been used, a bile leak leads to accumulation of bile in the abdomen. Previous reports have suggested that bile peritonitis, with guarding and rebound tenderness, is the principal manifestation of an abdominal bile collection, but this is actually an uncommon presentation early in the patient's course.1- 6 While a few patients do have such clinical findings, most have much milder symptoms, best referred to as bile ascites.7
With the advent of laparoscopic cholecystectomy, the incidence of bile duct injuries, and hence, bile collections in the abdomen, has increased.8,9 This study defines the syndromes associated with abdominal bile collections and shows how best to manage patients with this problem.
One hundred seventy-nine patients with bile fistulas were referred for evaluation to the University of California San Francisco Medical Center between 1990 and 1999. Of these 179 patients, 25 (14%) had a drain placed at the time of the first operation. The other 154 (86%) did not initially have drains placed and developed abdominal bile collections. Of this latter group, 74 had drains placed and 79 did not before a definitive operation was performed to treat the fistula. Twenty-one percent of the patients were men and 79% were women; the average age was 46 years (range, 18-86 years).
The preoperative diagnoses were chronic cholecystitis (65%), acute cholecystitis (32%), and miscellaneous (3%). The first, or index, operation was laparoscopic cholecystectomy in 94% of patients, open cholecystectomy in 3%, a nonbiliary operation in 2%, and a complex biliary operation in 1%. In 21% of patients who had a laparoscopic cholecystectomy, the procedure had been converted to an open cholecystectomy to improve exposure (4%), treat a bile duct injury (13%), or perform a common bile duct exploration (4%).
The biliary injuries in the patients who underwent a laparoscopic cholecystectomy were classified as follows: class 1, 8% (partial transection of the common bile duct); class 2, 21% (injury to the common hepatic duct due to clips or cautery); class 3, 54% (excision of a portion of the common duct and/or hepatic ducts); and class 4, 15% (damage to the right hepatic duct). The remaining 2% had cystic duct stump leaks (2 patients) or bile leaks from a duct in the liver bed (1 patient).
The following definitions will be adhered to in this article. Abdominal bile collection, sometimes abbreviated as "bile collection," refers to the presence of undrained bile in the abdomen and includes 2 subcategories, bile ascites and bile peritonitis. The term bile ascites is used for bile collections without prominent abdominal pain and tenderness. Bile peritonitis is the term used when a patient with an abdominal bile collection manifests prominent abdominal pain and tenderness. Bile peritonitis, as used herein, does not imply that the bile was infected.
Using the Statview 5.0 statistical program, the data were analyzed by analysis of variance, the Fisher exact test, or the χ2 test.
Of the 179 patients, 25 (14%) had a drain placed at the index operation that functioned properly, while undrained bile (ie, a bile collection) developed in 154 patients (86%). These 154 patients constitute the group of principal interest in this report, although the 25 patients with drains will also be described. Table 1 gives the symptoms in those with drained and undrained bile fistulas at initial presentation. Cholangitis was initially present in 26% of patients without drains and in 21% of patients with drains (P, not significant); 11% of patients with undrained bile had sepsis, compared with 7% of those whose fistulas were drained (P, not significant).
Bile drainage was often managed expectantly for long periods (average period, 13.9 days; range, 1-45 days) before a diagnostic workup was performed. Even when imaging studies had identified a bile fistula, these patients were followed up for an average of 30.2 days (range, 2-189 days) before a definitive repair was performed. Seventy-one percent of these patients developed symptoms during this period, most likely due to malfunction of the drains; 20% developed serious complications. One patient in this group eventually died of sepsis.
In 23 (13%) cases, the injury was recognized at the index operation. In this situation, the primary surgeon repaired the bile duct immediately (39%), placed drains and instituted nonoperative treatment (36%), or placed drains and transferred the patient to a tertiary care center for biliary reconstruction (25%).
The injury went unrecognized in 156 patients (87%) at the index operation. Of these, 139 (89%) were discharged home without a diagnosis; 25 (18%) of these patients left the hospital with bothersome malaise, anorexia, and nausea that in retrospect warranted more attention. In 35 (25%) of these patients, the diagnosis remained elusive even after the first outpatient checkup. Overall, a symptomatic bile collection was initially missed in 77% of patients; their symptoms were considered nonspecific or insignificant. The mean (± SD) time to diagnosis was 16.8 (25.0) days for all patients with intra-abdominal bile collections.
Only 5 patients (3%) had bile peritonitis as the initial presenting syndrome caused by the bile collection. The incidence of cholangitis (100% vs 25%, P=.04), sepsis (100% vs 6%, P=.004), and leukocytosis (16.2 × 109 vs 12.6 × 109, P=.03) was greater in those who initially presented with peritonitis compared with those who did not.
Patients with bile ascites who ultimately developed bile peritonitis had a higher incidence of malaise and abdominal discomfort (Table 2). Fever, abdominal tenderness, and jaundice were initially found in 45% of patients who developed bile peritonitis and in only 3% of patients who did not (P<.001). Cholangitis was initially present in 36% of patients who later developed bile peritonitis and 21% of patients who did not (P, not significant). Laboratory findings were not different and the time to diagnosis was not different between the 2 groups (Table 2).
The mean (± SD) amount of bile recovered when drains were inserted into the bile collections was 713 (901) mL. The amount was substantially larger in patients who developed bile peritonitis than in those with only bile ascites (Table 2). Bile collections greater than 500 mL were present in 79% of patients with bile peritonitis and in 13% of patients with bile ascites (P=.002). Drainage had not been instituted in 42% of patients within 7 days of the index operation and in 19% within 14 days of the index operation.
Twenty-one patients with bile collections had 1 or more of the following serious complications: sepsis (10%), abscess formation (11%), pancreatitis (3%), respiratory failure (3%), gastrointestinal bleeding (1%), transdiaphragmatic bile fistula formation (1%), necrotizing fasciitis (1%), pulmonary embolism (1%), and stroke (1%). Cholangitis developed in 25% of patients with these other serious complications. Two patients died of sepsis and multiorgan system failure.
The initial clinical presentation was not different between those who developed serious complications and those who did not. Patients with serious complications had undrained bile present for 15.4±19.1 days, while those without serious complications had undrained bile for 9.2±10.7 days (P=.045). Serious complications developed in 45% of patients with infected bile compared with 7% of those with uninfected bile (P<.001). Severe complications were not confined to patients whose bile was allowed to go undrained for long periods: 4 patients with undrained bile developed severe complications within 5 days of the index operation.
The clinical course of patients whose bile collection was drained early (<10 days after cholecystectomy) was compared with those whose collection was drained late (≥10 days after cholecystectomy) (Table 3). Fifty-four percent of patients whose bile was drained 10 days after their cholecystectomy had fever, compared with 29% of those whose bile was drained less than 10 days after their cholecystectomy (P=.01). Infected fluid collections were more commonly found in patients whose bile was drained late (28%) than in those whose bile was drained early (7%) (P=.008).
The diagnosis of a bile fistula was made by observation of bile drainage from drains placed at the index operation (13%) or the wound (1%), or discovery of a fluid collection on ultrasound, computed tomographic (CT) scan, or HIDA scan (86%). Ultrasound scanning (69%) was the imaging test most commonly ordered, followed by CT (55%) and HIDA scans (39%). Computed tomography was the most sensitive (Table 4). The sensitivity for detecting intra-abdominal bile collections was 70% and 64%, respectively, for ultrasound and HIDA scans (Table 4). To define the biliary anatomy, a percutaneous transhepatic cholangiography was obtained in 73% of cases and endoscopic retrograde cholangiopancreatography (ERCP) in 70%. The sensitivity of percutaneous transhepatic cholangiography for detecting abnormalities was 100%, and for ERCP, 98%. While a successful ERCP was sensitive, the success rate for achieving a technically adequate study was only 87%. An exploratory laparotomy was performed (rather than percutaneous drainage) just to drain the bile collection in 14% of patients. Because these patients all had bile duct injuries, this strategy subjected these patients to 2 laparotomies instead of 1, as a second procedure was required later to repair the bile duct injury.
Most cholecystectomies are now done laparoscopically. While this is associated with less discomfort and shorter hospital stays, the incidence of bile duct injuries is more common than with open cholecystectomy.9
Bile accumulates in the abdomen in most patients with bile duct injuries because the injury most often results in a fistula that goes undetected and undrained during the original operation. Our data show that the symptoms caused by bile collections were often quite subtle. Most patients with bile collections did not present with peritonitis; instead, they had bile ascites, with mild, relatively nonspecific symptoms. Consequently, the presence of a bile collection and associated biliary injury often went unsuspected for a time until symptoms worsened and delays in diagnosis and treatment allowed bile peritonitis and serious illness to develop. Among our series, the correct diagnosis was missed initially in 77% of patients.
We could identify no criteria that allowed one to predict which patients with bile ascites would develop peritonitis. Furthermore, unlike what is widely believed, the presence of peritonitis did not predict which patients would develop serious complications. In fact, many of the patients who became seriously ill never passed through a phase that included prominent abdominal pain and tenderness. In short, it was not possible to distinguish those who would become critically ill from those who would not based on the early clinical presentation. Thus, following the abdominal findings as a strategy for determining the course of the illness was unreliable. Everyone with undrained bile was at risk.
Even when bile was issuing from a drain, the patient was sometimes managed nonoperatively for periods as long as 6 months. The presence of a drain did not guarantee that a bile collection would be avoided; drains can malfunction. Therefore, CT scans should be obtained early in the management of a patient with an unplanned external bile fistula, more or less routinely, to check on the adequacy of drainage.
Some patients in this review were known from imaging studies to have intra-abdominal bile collections, but they were followed up expectantly with the expressed hope that the bile would be reabsorbed from the abdominal space. Nevertheless, reabsorption of bile collections larger than 4 cm was rare and unpredictable. Furthermore, there is no support for such a treatment strategy in the literature.1- 8 As this and other studies show,1- 8 the morbidity and mortality rates can be high in patients with undrained bile collections. Because morbidity is greater the longer treatment is delayed, physicians caring for these patients must have a high index of suspicion for a biliary injury, learn to recognize the clinical features of bile ascites, even when mild, and investigate and treat patients who have these symptoms.
The evidence suggests that if bile collections were never drained, most patients would eventually become gravely ill from superinfection. The following factors correlated with a worse outcome: length of time bile was left in the abdomen and the development of superinfection. Animal research has shown that (1) bile salts are the toxic component of bile, (2) large amounts of bile in the abdomen can be rapidly lethal, (3) mortality is greater if the bile is infected, (4) and the natural history of sterile bile in the abdomen is that it eventually becomes infected.10- 15 Our clinical data agree with these experimental observations. The longer the bile collections were left undrained, the greater the incidence of severe illness, including sepsis. Late drainage was more commonly associated with positive bile cultures.
In conclusion, we recommend adoption of a high index of suspicion for biliary tract injury in postcholecystectomy patients who have anything less than a smooth postoperative course. Vigilance should be high for the initially subtle manifestations of bile in the abdomen. Diagnostic imaging is called for even in the absence of pain, fever, leukocytosis, or abdominal tenderness. While positive findings are important, absence of expected positive findings (eg, fever or leukocytosis) is common and does not diminish the significance of the positive findings.
An abdominal CT scan should be obtained in patients who have a syndrome suggestive of bile ascites, especially after laparoscopic cholecystectomy. We are concerned about the treatment delays that followed false-negative HIDA scans, and can find no role for this test in this situtation. We favor CT over ultrasound scans as the imaging test of choice. Once the presence of intra-abdominal fluid has been confirmed by CT scan, the fluid should be percutaneously drained and cultured while the patient is still in the scanner. It is unnecessary and undesirable to perform an exploratory laparotomy solely to diagnose or drain an abdominal bile collection. Percutaneous drainage can be as thorough, and it avoids the morbidity of a laparotomy.
After a bile collection has been evacuated by drains, ERCP and percutaneous transhepatic cholangiography should be performed to define completely the cause of the bile leak and the anatomy of the biliary tree.8 Then, a specific operative treatment plan can be devised. We have previously discussed the treatment of biliary injures in detail.8 In general, cystic duct and liver bed leaks can be treated by percutaneous drainage of bile collections and endoscopic placement of a temporary biliary stent. Class 1 bile duct injuries should be treated by laparotomy and closure of the defect in the duct using fine (eg, 6-0) monofilament absorbable suture material such as Maxon (US Surgical Corp, Norwalk, Conn). There is no need for a T tube, which just adds further trauma to the duct. Class 2, 3, and 4 injuries should be treated by debridement of devitalized tissue in the hilum of the liver, mobilization of a short (ie, 5 mm) segment of the injured duct, excision of devitalized tissue at the end of the duct, followed by a Roux-en-Y hepaticojejunostomy. The anastomosis should be done in 1 layer using fine (ie, 6-0, 5-0, or 4-0), absorbable, monofilament suture. End-to-end repairs of injured bile ducts are rarely successful.
The important point of this study is that once a bile collection has been drained, the major potential for immediate serious illness has usually been eliminated. This allows the injury to be fully delineated and treatment to be planned and carried out in an unhurried manner.
Presented at the 107th Scientific Session of the Western Surgical Association, Santa Fe, NM, November 16, 1999.
Corresponding author: Lawrence W. Way, MD, 513 Parnassus Ave, Room S-550, San Francisco, CA 94143-0475 (e-mail: email@example.com).
Donald L. Kaminski, MD, St Louis, Mo: Drs Lee, Stewart, and Way have retrospectively evaluated the clinical significance of bile in the peritoneal cavity associated with biliary tract injuries. They have demonstrated that the clinical abdominal findings may be subtle and that these subtle abdominal findings frequently result in a delay in diagnosis. They indicate that suspicion should be raised when a patient is not doing well after a cholecystectomy, demonstrating anorexia, abdominal distention suggesting an ileus, and fever. These findings should raise the surgeon's suspicion and institute appropriate diagnostic studies. I have 3 theoretic disagreements with the authors' evaluation of these patients. I guess I am too old and too simple to have my misconceptions changed. The attempt to separate the presence of bile in the peritoneal cavity into patients who have ascites vs those who have peritonitis seems to me superficial and not worthwhile. Bile produces a chemical peritonitis associated with cytokine release and alterations in fluid transport across peritoneal membranes, suggesting that an inflammatory process is present. The attempt to designate bile in the peritoneal cavity as representing ascites suggests that it's innocuous, and I don't believe that bile in the peritoneal cavity is innocuous.
Similarly, the attempts by the authors to distinguish bile in the peritoneal cavity as representing ascites from those patients who have peritonitis based on a retrospective analysis of clinical physical findings may not be highly reliable. Second, the terminology of bile ascites and bile peritonitis as emphasized in this article excludes the frequent presentation associated with this problem; namely, a localized collection of bile in the right upper quadrant. Many patients have a biloma, not bile ascites or bile peritonitis.
Lastly, to not correlate the type of injury and treatment from the analysis of the consequences of the presence of bile in the abdominal cavity excludes the 2 factors that in my experience are associated with determining the sequelae of the presence of bile in the peritoneal cavity; namely, is the leak controlled and is the fistula adequately drained?
I have 2 questions for the authors. Could you give us an idea how many patients required drains placed outside of the right upper quadrant? This would suggest to me that if there is seldom an indication to place a drain anywhere besides the right upper quadrant, ultrasound would allow these patients to be treated by percutaneous drainage, obviating the need for a CT scan.
Second, do you feel that serum bilirubin measurements correlate with the quantity of bile in the peritoneal cavity? Dr Lee's presentation was excellent, the article was full of wonderful information to assist surgeons in managing these patients, and I highly recommend it to you.
Mitchel P. Byrne, MD, Evanston, Ill: I have 2 questions. I wonder if this is a skewed population and if we in practice will not see this rate of bile duct injury as the cause for this problem. In normal practice, the usual cause seems to be liver bed leakage more so than bile duct injury. In those patients, repeat laparoscopy is such a simple modality that evacuates all of the bile, both in the right upper quadrant and the rest of the abdomen. It avoids the need for interventionalists, both in radiology and gastroenterology. I wonder if you have used this in selected patients. For instance, if you had operated on a patient and were confident that there was no bile duct injury, would you consider repeat laparoscopy?
William W. Turner, Jr, MD, Jackson, Mo: The authors looked at initial drainage at the index operation, but didn't present any conclusions about its efficacy or lack thereof. I would be interested to know whether they were able to draw any conclusions about the role of index procedure drainage.
Thomas A. Stellato, MD, Cleveland, Ohio: I also have a problem with the premise that suggests that a bile collection is equal to a bile duct injury. We described our own series of patients, and our paradigm is quite different from that of the authors. We feel that a CT scan should not be performed because once a collection is seen, it mandates you to percutaneous drainage. Our first image of choice is a HIDA scan. We found it be to 100% sensitive, and if a leak is identified, it doesn't necessarily mean that a bile duct injury is present. Our next step would be an ERCP to define whether an injury is present or whether is it a simple leak from a cystic duct or the gallbladder bed. In that paradigm, we have stented these patients endoscopically and do not have to resort to either reoperation or drainage at all, and all patients have recovered.
Edward H. Phillips, MD, Los Angeles, Calif: I would be interested to know how many of these patients with delayed diagnosis were treated as outpatients and/or kept overnight and discharged. The earlier a patient is discharged, obviously the more difficult it is to diagnose a bile leak. We tend to keep our patients overnight and find that the patient's heart rate is a key clinical determinant of problem. No one gets discharged with tachycardia. The tachycardia may not be due to a bile leak, a biloma, or anything serious, but we have found that a normal heart rate usually precludes a significant complication. So I was wondering whether the vital signs of these patients were looked at both prior to discharge and on follow-up at the clinic.
Ronald G. Latimer, MD, Santa Barbara, Calif: What percentage of the patients with their defined bile ascites or bile peritonitis had normal intraoperative cholangiograms?
Ernest E. Moore, MD, Denver, Colo: You provide cogent data that indicate that early recognition of the bile collection is critical to minimize the sequellae. This seems to be a compelling argument for the routine use of surveillance ultrasound by the operating general surgeon in the clinics as well as the office. You alluded to a 70% accuracy. Could you expand on the shortcomings of ultrasound, because this is certainly not consistent with surgeons' experience with ultrasound in the emergency department.
William C. Chapman, MD, Nashville, Tenn: I would like to support the authors' comments regarding imaging and assessment of the patient who is having problems after cholecystectomy. I think there is a common tendency to attribute symptoms and fluid collections to a trivial leak from the gallbladder fossa and this approach commonly leads to late referral. So I think whether the imaging study uses CT scans, HIDA scans, or ultrasound can certainly be argued. I think the point that the authors are making is that thorough early investigation is critical to eliminate major bile leakage as a possible factor.
I have a couple of questions. First, could you tell us about the specific complications that occurred in those patients who did have infected bile, and second, what recommendations could you make for management in patients who had drains placed? Do you follow up for a prolonged interval those patients who do have bile duct injury after drain placement, or do you operate on them early after discovery of the bile duct injury?
James J. Peck, MD, Portland, Ore: My concern is the 7% of patients who were asymptomatic. What prompted you to study these patients? Were they all patients who had drains in place? What percentage had cystic duct leaks or leaks from the accessory duct in the gallbladder fossa and were really just small bilomas?
Dr Way: A main point is that surgeons expect bile in the abdomen to always produce clinical peritonitis, meaning pain and tenderness. Although bile uniformly produces histologic peritonitis, the clinical findings can range from almost no pain to severe pain. The reason for the differences from patient to patient is unknown. Thus, abdominal pain and tenderness are insensitive criteria for making the diagnosis of bile in the abdomen; for an unpredictable period, pain and tenderness are absent in most patients. In this report we have referred to abdominal bile collections without severe symptoms as bile ascites, regardless of whether the collection was localized or diffuse. Because there is risk of miscommunication unless words are used in the same way, we defined them precisely in the article.
Because the data were collected retrospectively, does this affect the validity of the conclusions? On the contrary. Retrospective data collection is a positive feature of the study. First, it would probably be impossible to conduct a study like this prospectively, but that is not the point. The advantage of the retrospective aspect is that the analysis is based on statements in the hospital records that preserve the thoughts of those caring for the patients at the moment. The character of these statements would be quite different if collected as part of a prospective study. In that case, the data would not accurately reflect existing surgical practice.
About 20% of patients had drains in places other than the right upper quadrant. The volume of bile obtained on the initial catheterization varied from about 100 mL to several liters, and the greater the volume, the more likely additional drains would be needed. The right upper quadrant drained most of the bile. If a second drain was required, it was usually in the pelvis.
The serum bilirubin level only loosely correlated with the volume of bile in the abdomen. Bilirubin levels rise because of reabsorption of bilirubin from the abdomen. They rarely exceeded 2 to 5 mg because the liver eliminates extra bilirubin according to first-order kinetics (the higher the serum bilirubin concentration, the greater the bilirubin load excreted). Because bilirubin levels remained so low, they were often dismissed as clinically insignificant.
We were dealing with a skewed population in the sense that there were few patients with leaks from the cystic duct stump or gallbladder bed. Nevertheless, the conclusions are unaffected. The principal misconceptions identified in this study are that a collection of bile (1) always produces severe pain and (2) can be left untreated as long as the patient looks and feels well. These assumptions are false regardless of the source of the leak.
In treating leaks of the cystic duct stump or the liver bed, one should not rely entirely on a bile duct stent placed at ERCP if there is also an abdominal accumulation of bile, as there usually is. Counterdrainage is indicated or serious infection may develop. Just because a bile duct stent alone has worked a few times does not mean that it will the next time. One patient who was brought to our attention, who was not part of this study, died solely because the importance of removing the abdominal bile had not been recognized. Drains placed at the index operation usually worked well.
The presence of an abdominal bile collection does not always mean a bile duct injury has occurred, but if the collection is greater than 4 cm, one should assume that there is a significant leak until an ERCP proves otherwise. From our retrospective vantage point, the surgeon remained convinced for too long that the operation was uncomplicated in many cases of leaks.
In this series, HIDA scans were misleading for the diagnosis of a bile leak and, too often, a false-negative study incorrectly suppressed tentative concerns about a possible leak. Although accurate in some cases, HIDA scans overlooked many significant leaks. Furthermore, when a HIDA scan was positive, another imaging test (ie, CT or ultrasound scan) had to be done to insert drains into the collection. Therefore, a negative HIDA scan was unreliable, and a positive scan required the alternative study anyway.