Revised Atlanta Classifi Cation For
Revised Atlanta Classifi Cation For
org
675
G
AS
Revised Atlanta Classification T
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for OI
N
An earlier
incorrect version
of this article
appeared online.
ng of pathophysiology
necessitated substantial
revision of the classification
system (2). A draft was posted
on the Pancreas Club Web site
in 2008 (3). This draft was
referrenced in several initial
Introduct
publications in the radiology
literature (4–6). After a total of
four Web-based revisions, the
Beginning in revised Atlanta classification
2007, the system was finalized in 2012
Acute and published shortly thereafter,
Pancreatitis with updates to the earlier-cited
Classificatio draft (2).
n Working
Group
polled an
internationa
l cohort of
pancreatic
experts,
includ- ing
11
pancreatic
societies,
with the
goal of
revising the
original
1992 Atlanta
classificatio
n system for
acute
pancreatitis
(1,2).
Although the
original
Atlanta
classificatio
n system
established
common
terms for
acute
pancreatitis
and related
complicatio
ns, the
nomenclatur
e proved to
be
confusing,
leading to
incorrect
use of terms
in both
clinical
practice and
research. In
addition,
advances in
imaging and
in the
understandi
676 May-June 2016 radiographics.rsna.org
erences 2–4.
llection may become infected. ANC = acute necrotic collection, APFC = acute peripancreatic fluid collection, IEP = interstitial edematous pancreatitis, WON = walled
ay be homogeneous; follow-up computed tomography (CT) performed in 2nd week may help clarify status.
-appearing components or fat globules within fluid.
tent pancreatic leak or disconnected duct may lead to intrapancreatic pseudocyst.
criterion, but magnetic resonance (MR) imaging patients as having either severe or mild
is also appropriate. Although many patients will pancreati- tis on the basis of the presence or
meet the criteria for acute pancreatitis on the basis absence of or- gan failure, respectively (1).
of symptoms and laboratory results alone and may However, emerging evidence indicated that a
not require imaging initially, imaging may be per- large subset of patients with local complications
formed early in the disease course when the cause experienced substantial morbidity but little
of the disease is unclear, to look for causative mortality (11). Therefore, a third category was
factors such as choledocholithiasis and pancreatic added to the new classifica- tion—moderately
cancer. Imaging for the diagnosis of pancreatitis severe acute pancreatitis—to describe this
is also appropriate when abdominal pain suggests patient group (2). Organ failure and local
pancreatitis but the amylase or lipase level is not complications are not seen in patients with mild
elevated to the threshold value, which is often the pancreatitis, who are usually discharged within
case at delayed presentation (12). The onset of the 1st week, with very low mortality
pancreatitis is considered to coincide with the 1st (13). These patients rarely require CT for local
day of pain, not the day on which the patient pres- complications, and imaging may be useful only
ents for care or the day of hospital admission in assessing the cause of pancreatitis (eg, ultraso-
(2). nography [US] or MR
cholangiopancreatography for
Phases of Acute Pancreatitis choledocholithiasis) (12).
In pathophysiologic terms, acute pancreatitis is Moderately severe acute pancreatitis manifests
divided into early and late phases. The early phase in patients with transient organ failure lasting
occurs in the 1st week after onset, with the disease less than 48 hours and/or local or systemic
manifesting as a systemic inflammatory response. complica- tions. Systemic complications are
At this time, clinical severity and treatment are generally co- morbidities exacerbated by
mainly determined on the basis of type and degree pancreatitis, such as acute kidney injury in the
of organ failure. The late phase, which generally setting of chronic renal failure. Local
starts in the 2nd week and can last for weeks to complications include a variety of pancreatic and
months, occurs only in patients with moderately peripancreatic collections. Such collections
severe or severe pancreatitis, as defined by persis- generally develop in the 2nd week (the late
tent organ failure and by local complications (2). phase of pancreatitis) and are clinically
suspected in patients with unremitting or recur-
Grading of rent pain, a secondary peak in pancreatic enzyme
Severity of Acute Pancreatitis levels, worsening organ dysfunction, or sepsis
To improve the stratification of patients at the (2). These symptoms should prompt imaging
time of presentation, the pancreatitis severity studies such as (in order of preference) contrast-
scale was updated in the revised Atlanta clas- enhanced CT, contrast-enhanced MR imaging,
sification. The original classification categorized or unenhanced MR imaging (12).
Severe disease is characterized by organ failure that
persists for more than 48 hours. Because
Table 2: Modified Marshall Scoring System
Sources.—References 2,4,14.
Note.—A score of 2 or higher indicates organ failure, with transient failure lasting less than 48 hours and persis- tent failure lasting more than 48 hours.
*Partial pressure of oxygen/fraction of inspired oxygen, or PaO2/FIO2.
IEP versus
Necrotizing Pancreatitis
In the revised classification system, new defini-
tions were created to clearly stratify acute pan-
creatitis into two subcategories based on
imaging findings: IEP and necrotizing
pancreatitis. IEP
is more common and represents nonnecrotiz-
ing inflammation of the pancreas. The entire
pancreas will enhance at contrast-enhanced
CT or MR imaging, with no unenhanced
(necrotic) areas, although enhancement of the
gland may be less avid than that of the normal
owing to interstitial edema. IEP usually manifests with
focal or diffuse pancreatic enlargement and is typically
surrounded by wispy peripancreatic inflammation or a
small amount of fluid (Fig 1). In addition, there should
be no surrounding peri- pancreatic necrotic collections
in IEP, although there may be surrounding fluid-
containing collec- tions (Fig 2).
Necrotizing pancreatitis accounts for 5%–10% of
cases of acute pancreatitis (2). It is important to
understand that necrosis may involve either the
pancreatic parenchyma or the peripancreatic tissues
and in both cases is termed necrotizing pancreatitis.
There are three subtypes of necro- tizing pancreatitis;
the subtypes are based on
the anatomic area of necrotic involvement: (a)
pancreatic only, (b) peripancreatic only, and (c)
combined pancreatic and peripancreatic. The latter
subtype is the most common, accounting for 75% of
cases. The combined subtype dem- onstrates
nonenhancing pancreatic parenchyma, as well as
nonenhancing heterogeneous peripan- creatic
collections, and typically accumulating in the lesser
sac and anterior pararenal space (Fig 3a).
Peripancreatic necrosis alone, in which the pancreas
enhances normally but the peripan- creatic tissues
show necrosis, with collections containing variable
amounts of fluid and nonliq-
Figure 2. IEP in a 43-year-old
man. Axial contrast-enhanced
CT image shows peripan-
creatic inflammation (black
arrow) and a homogeneous
fluid-attenuation collection
in the left anterior pararenal
space (white arrow), a finding
that is consistent with APFC.
lack arrow), and a large ANC in the lesser sac (white arrows). (b) Image of peripancreatic necrosis alone in an 18-year-old man shows a large, complex, heterogeneou
imaging, and nonenhanced CT may be easier weeks from onset of pain) and the presence or
in practice (12). absence of necrosis at imaging (Table 1) (2).
occur in both locations, with a coalescent collec- older than 4 weeks. Therefore, MR imaging is a
tion extending from the lesser sac into a portion valuable alternative to contrast-enhanced CT for
of parenchyma (Fig 10) (2). There is evidence planning interventions because it allows
that MR imaging outperforms CT, with higher determi- nation of the amount of necrotic debris
interreader agreement, in the assessment of the that must be removed by means of more
ratio of fluid to necrotic debris in collections aggressive inter- ventions (Fig 11) (18).
Figure 11. Necrotizing pancreatitis in a 47-year-old man in week 16 of persistent symptoms. (a)
Axial nonenhanced CT image shows pancreatic WON involving nearly the entire pancreas (arrows);
at least half of its volume appears to contain fluid. (b) Subsequent axial fat-saturated T2-weighted
MR image shows the WON (arrows) containing mostly nonliquefied debris and pancreatic necrosis,
with little fluid present. Such a collection would respond poorly to percutaneous or endoscopic
drainage and would require more aggressive therapy.
Infection
and Local Complications debated. At some institutions, fine-needle aspira-
Any collection can be sterile or infected, although tion has fallen out of favor in recent years, partly
infection occurs far more frequently in necrotic due to a shift in preference toward early conser-
collections (2). Clinically, infection is suspected vative management with percutaneous drainage,
in a previously stable patient who experiences which may delay or even obviate surgical inter-
decompensation with signs of infection (19). vention. If percutaneous drainage is performed,
The only imaging finding of an infected collec- culture of the fluid can be performed at the
tion is the presence of gas within the collection. same time (19,22). Another argument against
Wall enhancement is not a reliable indicator of fine- needle aspiration is that one must consider
infection, since it is invariably present in mature the substantial false-negative (sampling too
collections (pseudocyst and WON). An infected early) and false-positive (contamination) results
pseudocyst still lacks solid components that, if of the procedure (25% and 15%, respectively).
present, should instead lead to the diagnosis of At some institutions, fine-needle aspiration is
infected WON. The gas often appears as multiple thought to be helpful when clinical signs and
small bubbles scattered throughout the collec- imaging find- ings are confusing or complicated
tion owing to the complex nature of necrotic and the ben- efits of diagnosis of infection
collections (Figs 8, 12) (2). Infected collections outweigh the risk of iatrogenic introduction of
can also manifest with gas bubbles due to a infection (22).
pancreatic-enteric fistula, which can occasionally In addition to infection, vascular complica-
be seen when necrotic collections erode through tions are common, occurring in a quarter of
the bowel wall, most commonly in the colon and patients with acute pancreatitis, and can cause
duodenum (Fig 13) (20). In one series, an enteric substantial morbidity and mortality. Two separate
fistula occurred in 4% of patients hospitalized pathophysiologic processes lead to vascular com-
for acute pancreatitis (21). Gas within the plications. First, inflammatory reactions can lead
pancre- atic duct can also mimic gas within a to splenic vein thrombosis, the most common
pancreatic collection but generally has an vascular complication (23). Second, pancreatic
identifiable linear distribution and typically enzymes can cause vessel erosion and lead to ei-
occurs in the clinical context of recent ther spontaneous arterial hemorrhage or pseu-
endoscopic pancreatography or pancreatic duct doaneurysm of (in order of decreasing
stent placement (Fig 14). frequency) the splenic, gastroduodenal, and
The use of imaging-guided fluid collection pancreaticoduo- denal arteries (24). A detailed
aspiration or necrotic tissue fine-needle discussion of these complications is beyond the
aspira- tion to help diagnose infection prior to scope of this article, as their evaluation is not
invasive therapeutic necrosectomy has both specified under the revised Atlanta classification.
advantages and disadvantages, and the topic is We direct the reader to other excellent
still widely publications that describe these complications
(25).
Figure 12. Necrotizing pancreatitis in a 37-year-old woman. (a) Axial contrast-enhanced CT image
obtained in week 3 shows the pancreatic tail (*) and a peripancreatic ANC containing nonliquefied debris
with foci of fat attenuation (arrows). (b) Axial contrast-enhanced CT image obtained in week 6 because the
patient experi- enced decompensation and was readmitted shows organization of the collection (*) with
multiple new foci of gas, findings that are consistent with infected WON.
a high success rate (29). However, if the collec- team members recognize the expertise
tion represents WON, adequate drainage may and the standardization of terminology.
not be achieved with this approach owing to
the nonliquefied components and, therefore,
neces-
sitating more aggressive débridement through
the endoscope as a first-line therapy (Fig 11).
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Errata
May-June 2019 • Volume 39 • Number 3